Question:

Is there a best way to do this? I read some builders twist the component lead with other leads or wires going into that eyelet  before soldering.If so, use needle nose pliers? Any danger of weakening the component lead by doing this.Any  advice will be appreciated.The eyelet board is G10 fiberglass and laid out for a Pro 5E5.How about soldering with the component side down? thanks,

Response:

>Is there a best way to do this? I read some builders twist the >component lead with other leads or wires going into that eyelet  before >soldering.If so, use needle nose pliers? Any danger of weakening the >component lead by doing this.Any  advice will be appreciated.The eyelet >board is G10 fiberglass and laid out for a Pro 5E5.How about soldering >with the component side down? thanks,

There is no reason to twist parts together – in fact it’s bad idea. You won’t get the part out after you do that, and you stress the lead for nothing. You can put parts on either or even both sides if you want. The only thing to watch out for is what’s called a "flux joint".  Sometimes flux from the solder will occupy the space inside the eyelet and prevent a part from being soldered. It will look ok but one lead will be loose, held only by flux. Be careful to solder EACH lead in the eyelet when there are a bunch together, and use a pick to remove all of the flux later. (Always a good idea.) Bob Graduate of 3 week Pace advanced soldering course.

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thanks Bob for that information.I did not know to watch for rosen joints or to solder each lead separately.I’ll do some practice beforehand.No twisting of leads for me.

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To avoid a "flux joint" you do what? Will keeping the heat on it a few extra seconds burn it off? PL

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> To avoid a "flux joint" you do what? Will keeping the heat on it a few > extra seconds burn it off? PL

Phil : What Bob said, just make sure each lead gets individual attention.  No "group" soldering.  I’ve got an old Gibson with one eyelet that has about 7 components going into it and it was a real mess to deal with when I had a problem in that location.  I was a real novice at the time, and I ended up with what I now understand to be a bad solution.  Even though it worked, I’m not sure I’ll ever get it apart again without using cutters and a very hot iron.  Just take your time and pay attention.  You’ll do just fine. Phil S.

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>To avoid a "flux joint" you do what? Will keeping the heat on it a few >extra seconds burn it off? PL

No, you can’t ‘burn off’ flux, you will just over heat your parts and board. If you burn a fiberglass board it will turn to carbon ( a very good conductor ) and self destruct when you power up! I guess you haven’t had a soldering course…   this is what you do… 1   Clean the leads and eyelet, insert all the leads required. 2  use a tip large enough to cover the eyelet and leads, some small PCB tips designed for computer boards are too small.  I use a 1/4" tip at 800F but that’s me… and use the bigger .068 ( I think it is ) solder. 3  Clean the tip on a wet sponge before EVERY joint. 4  Wet the tip with solder and then apply it to the eyelet and one lead, count to 2 or 3 5  Apply solder to the junction of the tip and lead and eyelet and wait for it to melt – should be counting to 4 or 5 by now. 6  Push 1/4 to 1/2 inch of solder into the eyelet, move the tip around a bit… REMEMBER how much solder you used on the best looking joint and use that as your guide. 7  If there are more leads, move the tip onto them and apply the solder to them until it melts. You won’t have to apply too much more solder, just get them wet as well. 8  inspect the joint with a x10 loupe, solder should connect all leads to the eyelet. 9  Scrape off all of the flux with a dentist pick. NOTE:  You DON’T want a hill of solder on top of the joint, you want a VALLEY where you can see all the leads and the eyelet, and a good solder connection to all parts. There should not be a hole thru the joint either, but actually that is NOT important, as the leads solder on the sides of the eyelet. Also, inspect the other side of the board to see if the solder flowed through. That’s where you’ll find a flux joint – no flow through… Bob Amp builder

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thanks for all the help.I learned a lot.My iron has interchangable heating elements of 45Watts at 900F,33W 800F and 23W at 700F.I have a 1/4inch tip.Any advice on making the solder joints to the brass grounding plate?I know to keep the brass plate away from the chassis. When making the joints to the brass plate how do you keep the wire from moving, any good methods?I really appreciate all you taking time to answer this, I have a lot invested in this Pro 5E5 and want a professional type job when I am finished.Ted Weber said to run a large wire soldered to the brass plate going to the transformer  mounting bolt ground (where your heavy current grounds are connected) Phil L.. .

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> thanks for all the help.I learned a lot.My iron has interchangable > heating elements of 45Watts at 900F,33W 800F and 23W at 700F.I have a > 1/4inch tip.Any advice on making the solder joints to the brass > grounding plate?I know to keep the brass plate away from the chassis. > When making the joints to the brass plate how do you keep the wire from > moving, any good methods?I really appreciate all you taking time to > answer this, I have a lot invested in this Pro 5E5 and want a > professional type job when I am finished.Ted Weber said to run a large > wire soldered to the brass plate going to the transformer  mounting > bolt ground (where your heavy current grounds are connected) Phil L.. > .

Phil: For most work, the 30-35W option is the most appropriate. For the brass plate, you will need as much heat as you can muster for a good connection.  One strategy is to install the bolt and a decent loop of braided copper as your very first step, before any other parts are in the way.  Use a propane torch to heat it up if the 45W iron proves to be too cold.  Careful not to discolor the chassis (it’s ugly, that’s all).  Then, you will be able to attach your ground leads to the braided copper with an ordinary iron.  To connect to the tranny bolt, terminate the wire with a ring terminal, insuring that it won’t slip off. Regards, Phil S.

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> thanks for all the help.I learned a lot.My iron has interchangable > heating elements of 45Watts at 900F,33W 800F and 23W at 700F.I have a > 1/4inch tip.Any advice on making the solder joints to the brass > grounding plate?I know to keep the brass plate away from the chassis. > When making the joints to the brass plate how do you keep the wire from > moving, any good methods?I really appreciate all you taking time to > answer this, I have a lot invested in this Pro 5E5 and want a > professional type job when I am finished.Ted Weber said to run a large > wire soldered to the brass plate going to the transformer  mounting > bolt ground (where your heavy current grounds are connected) Phil L.. > .

Phil: you might want to download the PDF manual on this page and check page 14.  It is Heathkit’s standard instructions on how and how not to make a proper solder.  Very similar to Bob’s excellent advice, but a bit more descriptive. http://www.heathkit-museum.com/ListArchive/msg02419.html Regards, Phil S.

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> thanks for all the help.I learned a lot.My iron has interchangable > heating elements of 45Watts at 900F,33W 800F and 23W at 700F.I have a > 1/4inch tip.Any advice on making the solder joints to the brass > grounding plate?I know to keep the brass plate away from the chassis. > When making the joints to the brass plate how do you keep the wire from > moving, any good methods?I really appreciate all you taking time to > answer this, I have a lot invested in this Pro 5E5 and want a > professional type job when I am finished.Ted Weber said to run a large > wire soldered to the brass plate going to the transformer  mounting > bolt ground (where your heavy current grounds are connected) Phil L.. > .

Tin the connection with the iron holding down the wire, then drop the solder and grab a spudger to hold the wire down as you withdraw the iron. Or you can drill holes in the brass plate in order to facilitate soldering wires to it. For an eyelet build, the way Fender did it was to solder from the back, upside down.  This results in very easily inspectable joints.  Your 1/4" tip is too big, you need a size or two smaller tip for general eyelet work… I use a 1/8" chisel on an Ungar 35w element and handle.  Your connections should look like a smooth shiny bubble from the component side.  This is called a ‘wet’ connection, and is the main goal of soldering. I use a q-tip to apply a very light surface coat of (electronics!) paste flux to the completed eyelet connection before soldering. Hit it hard and fast with a hot iron and solder and get off it quick… the quicker you make the connection, the cooler the surrounding components remain.  Ironically, (!) this means having a hotter iron.  Rich uses a 200w gun for this reason, among others (raised by wolves). I’ll bet the irons used by the little old ladies on Fender’s production line were not wimpy! __ Steve .

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>thanks for all the help.I learned a lot.My iron has interchangable >heating elements of 45Watts at 900F,33W 800F and 23W at 700F.I have a >1/4inch tip.Any advice on making the solder joints to the brass >grounding plate?I know to keep the brass plate away from the chassis. >When making the joints to the brass plate how do you keep the wire from >moving, any good methods?I really appreciate all you taking time to >answer this, I have a lot invested in this Pro 5E5 and want a >professional type job when I am finished.Ted Weber said to run a large >wire soldered to the brass plate going to the transformer  mounting >bolt ground (where your heavy current grounds are connected) Phil L.. >.

Generally, I use an alligator clip or two to hold parts to solder. You can usually rig up something if you have a small vacuum base bench vise and other vice grips and things… or you can practice soldering on the fly, using a few fingers to hold each object. Sometimes I arrange the solder so I can push it down with my nose onto the joint… keep the solder on the big reel… To solder on a metal plate (I used to solder RF cavities, with 1/8" wire on a thick aluminum and brass plate, I used about 3 ’stove’ irons at once) you need to first tin the wire with fresh solder and flux, and then heat the plate up till you can make a puddle of solder on it, and quickly set the wire into the puddle using the iron tip to hold it and then a screwdriver blade or something, as you remove the iron… hold your breath and don’t let anything move till it sets!   It’s best to practice this quite a bit… Try soldering resistors to your stove… so at least you’ll have an ohm on the range… Bob enjoying a beer on Labor Day

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>Generally, I use an alligator clip or two to hold parts to solder.

AT LAST..some one mentioned roach..em, ‘alligator’ clips. I do alot of high $ part work, and when ya play that stupid game, you HAVE to produced the ‘gold plated tin wired, silver’ mOjO the customer is paying for.  * U * wanna burn out that $$ of level part.  Not me.  Clip everything..everywhere.. One must work tension so they don’t damage, and ONLY use non-plated copper.  Radididideio-ish-shucker has them. But I have to say, anyone not saving all this soldering data on file is an idiot.  In the OFD, this didn’t happen. PRATICE..PRATICE..PRATICE..  less IS more.. Thanks to all who help everyone.  Learn or be sold to.. JJTj

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- Hide quoted text — Show quoted text ->Generally, I use an alligator clip or two to hold parts to solder. > AT LAST..some one mentioned roach..em, ‘alligator’ clips. > I do alot of high $ part work, and when ya play that stupid > game, you HAVE to produced the ‘gold plated tin wired, silver’ > mOjO the customer is paying for.  * U * wanna burn out that > $$ of level part.  Not me.  Clip everything..everywhere.. > One must work tension so they don’t damage, and ONLY use > non-plated copper.  Radididideio-ish-shucker has them. > But I have to say, anyone not saving all this soldering > data on file is an idiot.  In the OFD, this didn’t happen. > PRATICE..PRATICE..PRATICE..  less IS more.. > Thanks to all who help everyone.  Learn or be sold to.. > JJTj

Hi, When delicate things needs soldering, heat sinking is needed like alligator clip but it’s heat conducing could prevent good soldering depending on situation. Some times I hold things together with laundry hanging clip which is made of wood(non-heat conducting). I used to solder per mil-spec. Tony

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> Is there a best way to do this? I read some builders twist the > component lead with other leads or wires going into that eyelet  before > soldering.If so, use needle nose pliers? Any danger of weakening the > component lead by doing this.Any  advice will be appreciated.The eyelet > board is G10 fiberglass and laid out for a Pro 5E5.How about soldering > with the component side down? thanks,

I have had a young fellow helping out here for the last two months.  I loose my intern to a music college is a week or two. When I take in an intern or apprentice, the first two weeks is nothing but soldering. I have a whole demo routine I go through that is not covered in the books. So, let me give you all a fast short form version of this, because I type like a snail, and I don’t have time to write a complete book here on the subject.  But, this will get you started. First, use Google to find the PDF file of the Weller Soldering Manual. Next, the selection of the right iron for the job, is most important. ALWAYS have more heat than you need. I’m not very big on soldering irons.  When you see me at work, I pack a pair of Weller 8200-N shootin irons in dual cross draw holsters style.  Yes, some days I have the cowboy hat on too. With a new tinned tip on one of my shootin irons, it will reach 1000 degrees F.  Yet, I use it on PC boards all the time.  But, NOT at 1000 degrees F. I like shooting irons for the temp control, and the fact they are only in use when the trigger is pulled.  For you energy conservation minded, it’s the only way to cut down on phantom load from the work bench. Now, let’s smoke up the room with a little soldering. You are going to need the following: 1. A high intensity light, to light up your work close up. 2. A spool of Radio Shack 60/40 solder .062 dia   3. A 100 watt iron or Weller 8200-N 4. A piece of *CLEAN* & *SMOOTH* pine board at least 8 inches square 5. A LEVEL work area 6. Basic hand tools to handle working with wire 7. 6 feet of standard stranded lamp cord Now, that you have collected these items, we have to round up some stuff for an EXPERIMENT. This is actually more important than anything you can find printed on the subject of soldering. You are going to need the following: A small corn flakes bowl filled half way with water. One loaded pepper shaker One bar of soap from the bathroom soap dish Now, put that bowl of water on the work surface with the high intensity light over it. Shake pepper from the pepper shaker and cover the surface of the water well.  Notice it floats. Why.  Because there is a SKIN on the surface of the water.  Which, is caused surface tension. Look very closely at the surface of the water around the pepper with the high intensity light. You may see that the surface between the pepper grains is not quite flat. You can also float a sewing needle on that skin, if in placing the needle on it, you don’t break the skin. But, pepper good enough for what we have to do. NOW, while looking very closely at the surface again, touch only the corner of that bar of soap to the surface of the water in the CENTER of the bowl. Watch what happens very closely. Yes, the soap broke the surface tension.   If that pepper had not been there, you would not have known, that happened. OK, now you can throw that experiment into the kitchen sink, we’re done with that now. The reason for the experiment is to show you what surface tension is, and tell you that solder when liquid, has the same surface tension. Now, I’m going to show you that too. Make sure that piece of pine board is CLEAN and SMOOTH on BOTH sides.  To make sure it’s smooth, you could hit it with some 320 fine sand paper, to insure proper results.  Which, may vary from the ideal. <lesson one> 1. Place that pine board under the high intensity lamp. 2. Peel off the spool of solder a straight length of solder approximately 12" long. 3. In the center of the pin e board, 1/3 from the LEFT SIDE, place the tip of the iron. 4. Now fast as it will melt, feed the solder to the tip, and make a BLOB about 3/8" in size. 5. Pull the iron from the solder, and very quickly, look at the surface very closely!!!!!! Can you SEE the surface.   Can you SEE is swirling and moving. As the solder cools, did you notice the motion slows and stops. Did you notice, if the air is very still, how bright the surface is when it reaches room temperature. Most important, notice the final SHAPE of the BLOB.   That SHAPE is caused by the surface tension.   A drop of water on glass has a very similar shape, for the sam reason. Notice the amount of rosin on the wood around the solder blob. <lesson two> Remove the blob, and place it off to the side for now. Again, to the letter, do the following: 1. Peel off the spool of solder a straight length of solder approximately 12" long. 3. In the center of the pin e board, 1/3 from the RIGHT SIDE, place the tip of the iron. 4. Now fast as it will melt, feed the solder to the tip, and make a BLOB about 3/8" in size. 5. Pull the iron from the solder, and very quickly, look at the surface very closely!!!!!! So, we have just performed a repeat of what we did before.  Only, this time, on a new surface to the right side of the board. Now, here is what we are going to do. 6. Place the tip back into that BLOB, and keep it there. 7. Move the BLOB around with the tip of the iron. As you keep on doing this, NOTICE the SHAPE of the BLOB. NOTICE, the change in the SURFACE, the longer you keep doing this. It’s OK if you BURN the board and make a little smoke. KEEP GOING. When it really starts getting UGLY, see if you can use the tip of the iron and divide it into two EQUAL ugly parts. Then, let them BOTH cool to room temperature. Now, what happened here is you lost the surface tension the rosin makes possible.  You just boiled it off. How many times have you seen that before.   OK, what do you do if you boil off the rosin and are left with this mess doing a soldering task. Well, there are two things you can do.  That’s why you have those two ugly solder BLOBS still sitting there. <lesson three> 1. Pop one of the solder BLOBS off the board. 2. Place that solder BLOB to the left where the rosin sits from lesson one. 3. Place the tip of the iron into the ugly blob, and roll it around in the rosin. 4. When it rolls around as a ball again, pull the tip and let it cool undisturbed. So, we still have that other UGLY blob sitting over there on the right side of the board yet. What do we do with that one. 5. Peel off some solder from the spool, and place the tip of the iron into the last ugly blob of solder. 6. Add a little bit of solder to the blob as you roll it around. 7. When it has that ball shape again, pull the iron, and let it cool to room temperature undisturbed. Notice how little solder was needed to get that ball shape back again. Notice how both those solder blobs almost look the same. Now place the blob we placed off to the side before, in the middle of these two for comparison. <lesson four> 1. Knock the blobs of the board, and turn it over. 2. Cut lengths of solder to 1/4, 3/8, 1/2, 5/8, 3/4, 1", 1 1/4. 3. Place them on the board in order of size. 4. Grab that HOT iron, and coat the tip with solder. 5. knock of the excess and touch it to the end of the shortest length of solder. Watch closely. What happened. 6. knock of the excess and touch it to the end of the Next shortest length of solder. Watch closely. What happened. 7. Repeat till the last piece of solder is touched. Well, I guess we learned here, that solder it attracted to the heat. The more the heat, the more the attraction. <summary> Without rosin, there is no soldering. You boil off the rosin, you are taking too long.   I solder in a micro second, what take others 5-10 seconds to do. Lowering the heat is not the answer. It takes longer for the solder to reach FLOW temperature, and the parts being soldered will now reach higher temperatures. This should get you started with the right approach. Regards, Rich Koerner, Time Electronics. http://www.timeelect.com Specialists in Live Sound FOH Engineering,        Music & Studio Production, Vintage Instruments, and Tube Amplifiers

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> >Generally, I use an alligator clip or two to hold parts to solder.

just how high dollar? maybe you should use this instead of alligator clips http://video.google.com/videoplay?docid=3831751197741115059&q=solder&… > AT LAST..some one mentioned roach..em, ‘alligator’ clips.

http://workmanship.nasa.gov/lib/insp/2%20books/links/sections/601%20G…

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>just how high dollar? maybe you should use this instead of alligator >clips >http://video.google.com/videoplay?docid=3831751197741115059&q=solder&…

Well, not THAT hi $.  Great vid.. > AT LAST..some one mentioned roach..em, ‘alligator’ clips. >http://workmanship.nasa.gov/lib/insp/2%20books/links/sections/601%20G…

Well, I ment here.  I like the idea of wood’n ones, never thought of it B4.  Another great link, btw.. SO much to learn from online.  I learned 80% the OTHER way, you kids 2day better grab all the knowledge ya can.. JJTj …It is history in the making… ……and it’s in the Key of ‘ A ‘.. …what more can any civilized man want…

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-snip interesting demo- >I solder in a micro second, what take others 5-10 seconds to do.

That reminds me of when I took my course in the 80s, when it came time to practice on 16 pin DIPs, I still had my 1/4" chisel tip in the iron. The instructor told me to change it, it was too big for IC work. Already having 20 years experience, I told him "No problem, I can do this easy!" He said "Oh yeah?"  and I promptly soldered in the chip in about 30 seconds, about 2 seconds per pin. "I love the high thermal mass I get from this tip" I said.  He turned to the rest of the class and said "You people use the small tip until you have the experience!" One demo I use to show people how to solder is to get them to solder a wire to a dirty penny – one time as is (almost impossible), the next time with liquid RA flux. One guy wanted to take the soldered wire and penny with him, he was so proud of it!

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>One demo I use to show people how to solder is to get them to solder a wire to a >dirty penny – one time as is (almost impossible), the next time with liquid RA >flux. One guy wanted to take the soldered wire and penny with him, he was so >proud of it!

ONCE you learn how to do that with the right tools, you learn the right tools for the job(s).. JJTj

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> http://workmanship.nasa.gov/lib/insp/2%20books/links/sections/601%20G…

Would everyone PLEASE send this link to Fender, Marshall, Vox, Mesa Boogie, Ampeg, etc….  to improve the quality of their products. Regards, Rich Koerner, Time Electronics. http://www.timeelect.com Specialists in Live Sound FOH Engineering,        Music & Studio Production, Vintage Instruments, and Tube Amplifiers

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My way, after 30 years of soldering, to keep parts in the eyelet from moving is to use aluminum tape (strips off the roll)to hold all in place, and remove when done. Works like a dream. Give it a try. Chris Calvin Associates

– Hide quoted text — Show quoted text -> thanks for all the help.I learned a lot.My iron has interchangable > heating elements of 45Watts at 900F,33W 800F and 23W at 700F.I have > a > 1/4inch tip.Any advice on making the solder joints to the brass > grounding plate?I know to keep the brass plate away from the > chassis. > When making the joints to the brass plate how do you keep the wire > from > moving, any good methods?I really appreciate all you taking time to > answer this, I have a lot invested in this Pro 5E5 and want a > professional type job when I am finished.Ted Weber said to run a > large > wire soldered to the brass plate going to the transformer  mounting > bolt ground (where your heavy current grounds are connected) Phil > L.. > .

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Question:

>Your system in NYC seems to me to be better than most cities.  I had not heard >of it before.  I have long been an advocate of requiring behavior changes for >those to who we give money.  Certainly taking meds for the mentally ill should >be a requirement and supervised.  The addicted need to be proved to be drug >free. >Nonetheless, I thought this one man’s idea is worth exploring.  For those who >went to the web site, there was a picture of the 100 sq ft room with a bunk >bed, an easy chair, a chest of drawers with a TV on it looked quite >comfortable.  I assume there would have to be a shared bathroom nearby. >-Connie

Grouping all the homeless in some kind of colony will only replicate the problems the shelters experience.  The strong will prey on the weak, the disturbed on the sane, drugs will continue to flow.  Far better to have an incentive program and disperse the housing in small units through the community.  With adequate monitoring and support for a long period of time.

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>>Unitarians don’t have a creed, >You said it.  Not a religion.  A cult.

Unitarianism is as far from a cult as you can get.   Cult: Adherents of an exclusive system of religious beliefs and practices An interest followed with exaggerated zeal Unitarians do not share an exclusive system of religious beliefs and practices, nor are they zealous in promoting their religion. Unitarianism is the direct opposite of a cult — there is nothing to hold its members to the church except the fellowship they may find there with others, each of whom forms his or her personal spiritual path. What’s more, each Unitarian congregation is unique.  Ministers are elected by the congregation and serve at its pleasure.  Unlike in a cult, the minister has no authority whatsoever over individual members and their beliefs. A cult attempts to attract members to an exclusive, closed belief system and to maintain total control over members’ lives.  Something like Jim Jones or the Moonies.   You are just blowing hot air on this one, Jim.

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>Like I said, Rita. The mouse behind the refrigerator. Would you >consider Scientology a religion? The Scientologists do. Whatever >floats your boat is fine with me, but what was it Sordo said, "Secular >Humanism"? Maybe Philosophy is a better term for what you believe, >than "Religion" — sort of a convergence of liberal politics and quasi >religion.

Scientology charges people to go up in its ranks.  So, no, I don’t consider it a religion but rather a cult.  However, this may be an arbitrary distinction.  Religion has a spiritual dimension and if you can experience that only in a religion with an arbitrary authority and creed, then more power to you.  But you can hardly deny others to form beliefs as in "the spirit of the universe" or "the oneness of mankind" or feelings of being one with nature and all humans who have come before and will come after.  Why should these beliefs not be called religion?  Why must religion be defined as bowing to some belief system imposed from without oneself?  Why are those who formulated the major or minor religions better suited to deal with spiritual matters than each individual?  Unitarians do have ministers but they serve as guides, not authority figures. Our services are eclectic and there are study groups on Buddhism, Christianity, etc., and people listen, learn, participate and decide for themselves on the spiritual path they wish to take. But if you want to discuss spirituality in concrete terms, it really can’t be done very well at all. I’m sorry you don’t understand, but then people are in general taught to think of religion as being synonymous with a fixed belief system imposed from without.  Seems you are one of those people.  Seen that way, it is a very limiting concept, giving power over one’s beliefs to others. Obviously, Unitarians find their religion helpful to them in living their lives and in joining with others on a spriritual quest. It is not a religion that appeals to those who want absolute certainty of belief and some authority to tell them what is right or wrong.  We don’t prosylyte — people come to the UU churches from many other religious backgrounds. I asked our minister, "Is there any point of belief on which all UUs agree?" and his answer was very UU, "Probably not."

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- Hide quoted text — Show quoted text – >We haven’t a perfect solution, but gradually the city began a >sort of incentive system — homeless signed up in day drop in >shelters or regular homeless shelters for drug and alcohol treatment >programs and for medical care and counseling if mentally ill.  Most >seem to be one or the other, at least to some degree, or both. >Then after "proving themselves" by working on these problems, they >were helped to sign up for SSI if eligible by virtue of disability, >or public assistance and/or to get some kind of employment. >Finally those who stuck with the program were offered some kind of >subsidized housing — usually a room or very small apartment, >and sometimes in buildings with social workers, mental health people >looking in, sometimes not. >My daughter tells me a study has been done that shows that just giving >the homeless a decent place to live seems to be as successful as having >them go through the various treatment options.  But it is only one study. >And even if it works in that those given housing with no strings attached >become stabilized, this certainly would function as a honey pot to attract >more homeless to any area offering this.  Resources for housing and funds >are limited in cities and given the fact that the climate in SF is more >agreeable than in many parts of the country, I agree you would have an >influx.  A more nuanced and step by step approach with the individual having >to meet certain behavioral goals would seem to me to be far better.

Your system in NYC seems to me to be better than most cities.  I had not heard of it before.  I have long been an advocate of requiring behavior changes for those to who we give money.  Certainly taking meds for the mentally ill should be a requirement and supervised.  The addicted need to be proved to be drug free. Nonetheless, I thought this one man’s idea is worth exploring.  For those who went to the web site, there was a picture of the 100 sq ft room with a bunk bed, an easy chair, a chest of drawers with a TV on it looked quite comfortable.  I assume there would have to be a shared bathroom nearby. -Connie

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> Tiny houses seen as answer for homeless > Advocate says the units would work if government would just bend rules a bit. > By Herbert A. Sample — Bee San Francisco Bureau > Published 2:15 am PDT Saturday, July 3, 2004

The U.S. had those 150 years ago. They were called slave quarters. The current idea is simply a cop out.  Reagan cut Federal money for mental institutions, driving most of these people onto the streets.  So a majority of homeless people need mental help. The idea of building shacks for homeless people can do nothing but incease crime, violate zoning laws,  reduce property values, and piss people off.

Response:

– Hide quoted text — Show quoted text -> Tiny houses seen as answer for homeless > Advocate says the units would work if government would just bend rules a bit. > By Herbert A. Sample — Bee San Francisco Bureau > Published 2:15 am PDT Saturday, July 3, 2004 >The U.S. had those 150 years ago. They were called slave quarters. >The current idea is simply a cop out.  Reagan cut Federal money for mental >institutions, driving most of these people onto the streets.  So a majority >of homeless people need mental help. >The idea of building shacks for homeless people can do nothing but incease >crime, violate zoning laws,  reduce property values, and piss people off.

It is a very bad idea.  Better idea is to provide housing, with services such as mental health care and so forth in small residences around the city.  We have some of these in New York City, and they work out well. But we don’t have enough of them.  We also have a system where people have to prove themselves to be taking medication and be stable before being assigned permanent housing.  There are only so many resources to go around, and the homeless themselves need to cooperate in the process.  So people have to live in shelters and work up to permanent housing, with mental health treatment and/or drug treatment programs, and developing some source of income, be it some kind of employment or SSI.

Response:

Is this one of those ideas that is based on the idea if you build it they will come?  What happens if you buid it and they do not come?  Iseem to recall that is basic idea has been tried before in Los Angeles.  How successful was that effort.

– Hide quoted text — Show quoted text -> Tiny houses seen as answer for homeless > Advocate says the units would work if government would just bend rules a bit. > By Herbert A. Sample — Bee San Francisco Bureau > Published 2:15 am PDT Saturday, July 3, 2004 > SAN FRANCISCO – It’s not much bigger than a large garden shed, but Jim Reid – > building contractor, perennial candidate and thinker of unorthodox ideas – > believes it can be one solution to this city’s vexing homeless problem. > The not-so-simple trick is convincing everyone else. > Reid’s brainchild is to build hundreds of 100-square-foot homes he calls > Shelter Ones in neighborhoods around San Francisco as residences for homeless > persons willing to perform some manual labor in return. >  As a concept, there are some here who think Reid may be onto something. The > Board of Supervisors in April asked city agencies to analyze the notion, and > what they found were minor qualms and one big hurdle: State-mandated minimum > floor space requirements for dwellings. > But Reid labors on, in any forum he can, confident that he has discovered an > answer to a complicated problem if only government would bend a bit. > "Government has no common sense," he said in an interview. "I mean, they look > at this house and they say, ‘It’s illegal.’ But it’s really needed." And though > no one is quite ready to give the go-ahead for Reid’s concept yet, it has its > supporters. > "Yeah, he’s endured a lot of ridicule, but they’re cute little houses," said > Barbara Meskunas, president of the Coalition for San Francisco Neighborhoods, > an influential group whose imprimatur Reid would need if his idea were to get > off the ground. > "I’m sure his little house is a whole lot better than some of the in-law units > that are in most of our neighborhoods," she added. "They’re certainly better > than many of the single-room-occupancy hotels that we put homeless people in." > Reid, 54, has been pushing his Shelter One concept for years now through his > nonprofit firm, Habitat for the Homeless, and during two quixotic campaigns for > mayor, last year and in 1999. To prove his point to the skeptics, he built and > lived for a time in a prototype. > The wood-frame cottage sports a kitchenette and an enclosed bathroom – though > the tub appears a bit smaller than normal and the sink sits above the toilet. > Across from the kitchenette is a "loft bed" above a seating area with a small > window. Nearby is a tiny closet with a combination washer-dryer. > Reid insists Shelter Ones could be built for as little as $6,000 if the > materials and construction labor are donated, or $30,000 if not, excluding land > costs. Larger versions would be two and three times larger. > The Taj Mahal they aren’t. But Reid explains that for some homeless people, a > tiny house would be better than the street or shelters. And for low-income > couples, the larger varieties could help them get started as homeowners. > "People don’t have a choice," Red said. "You could buy a 2,000-square-foot > house that costs a half a million dollars or rent a place. That’s all. And I > would like to give people a choice of renting 600 square feet or buying 300 > square feet." > Reid may be convinced of his idea’s worth as an answer to homelessness, but > others aren’t so sure. > "I’ve got a problem with it as housing," said Paul Boden, executive director of > the Coalition on Homelessness, citing Reid’s proposal that Shelter One > residents perform neighborhood cleanup duties in lieu of rent. "I don’t have a > problem with it as (temporary) shelter." > Sam Davis, an architecture professor at the University of California, Berkeley, > said he doubts the city and neighborhood groups would allow enough Shelter Ones > to be built to put a sizable dent in homelessness. > Further, he said the homes lack the on-site social services included with the > "supportive housing," the city now focuses on. Yet, Davis included Reid’s idea > in an upcoming book on designing living spaces for the homeless. > "I think what’s interesting about him and people like him is they are using the > knowledge that they have, they’re using their skills and expertise, to try and > attack the problem," he said. > When city building inspectors took a look at the prototype, they found glitches > that seemed correctable, such as missing plumbing fixtures and the lack of a > heating system. > The big hurdle, they noted, was a state law that requires a minimum of 220 > square feet of usable floor space for an "efficiency" unit. Shelter One has > only 50 square feet, but Reid says there is an exemption for homeless housing. > Then, of course, there are city zoning ordinances to deal with. > "The obvious issue here is, do you want to create a double standard for people > who live in complying houses and for people … who don’t?" said Laurence > Kornfield, chief building inspector for the city. "That would be for the state > Legislature to consider." > Reid says he’ll prod local legislators to look into the issue. In the meantime, > he’s a fervent as ever about Shelter One. That focus has led some observers to > consider him and his idea a bit eccentric, though Reid characterizes it > somewhat differently. > "No one’s thinking outside the box on this, and they have to," he said. > "Smaller is the answer." > http://www.sacbee.com/content/news/story/9871234p-10793495c.html (includes > picture)

Response:

, >"Respect the best in all religions", eh ?    Who is it that decides >just what is best and worst ?      I’ve always heard that the world is >made up of two kinds of people.  Good and Bad.   The Good (Religious) >decide who is who.    So, according to you,  I see the Unitarians are >more religious than I thought :-)

Individual decide what they want to "take" from this religion or that. What’s wrong with that?  After all, religions were formed by specific individuals and some parts of them are worth considering, while others are not — in each person’s judgement. Unitarians simply do not expect members to agree on everything. There is no overriding "creed". >A wise man once said something  to the effect:    "To respect >everything is to respect nothing".

And that is certainly true.  We all make value judgments on what is worth respecting.  If you want perfect unanimity, then join a religion that demands that and adhere to its teachings 100%. We all have choices.  There is a choice to accept some one authority on religion and the choice to decide what one believes on one’s own. – Hide quoted text — Show quoted text –

Response:

>Unitarians don’t have a creed,

You said it.  Not a religion.  A cult. but they do have general principles. – Hide quoted text — Show quoted text ->Some are deists, some agnostics, some atheists.  Unitarians respect >the best in all religions, although mouse religions have escaped my >notice to date.  Perhaps tomorrow? >Officially: >With its historical roots in the Jewish and Christian traditions, Unitarian >Universalism is a liberal religion — that is, a religion that keeps an open >mind to the religious questions people have struggled with in all times and >places. We believe that personal experience, conscience and reason should be the >final authorities in religion, and that in the end religious authority lies not >in a book or person or institution, but in ourselves. We are a "non-creedal" >religion: we do not ask anyone to subscribe to a creed. >So, Jeff, you may think Unitarians have no right to call themselves >a religion, but it seems for you a religious person must accept some >religious "authority"?  Or that a person can’t be a "spiritual" person >without accepting some religious authoirty?  Or that a person can’t find >his or her own way on questions of God and the meaning of existence? >With that view, Unitarians would differ. >The principles most Unitarians share are: >We, the member congregations of the Unitarian Universalist Association, covenant >to affirm and promote >    * The inherent worth and dignity of every person; >    * Justice, equity and compassion in human relations; >    * Acceptance of one another and encouragement to spiritual growth in our >congregations; >    * A free and responsible search for truth and meaning; >    * The right of conscience and the use of the democratic process within our >congregations and in society at large; >    * The goal of world community with peace, liberty, and justice for all; >    * Respect for the interdependent web of all existence of which we are a >part. >The living tradition which we share draws from many sources: >    * Direct experience of that transcending mystery and wonder, affirmed in all >cultures, which moves us to a renewal of the spirit and an openness to the >forces which create and uphold life; >    * Words and deeds of prophetic women and men which challenge us to confront >powers and structures of evil with justice, compassion, and the transforming >power of love; >    * Wisdom from the world’s religions which inspires us in our ethical and >spiritual life; >    * Jewish and Christian teachings which call us to respond to God’s love by >loving our neighbors as ourselves; >    * Humanist teachings which counsel us to heed the guidance of reason and the >results of science, and warn us against idolatries of the mind and spirit. >    * Spiritual teachings of earth-centered traditions which celebrate the >sacred circle of life and instruct us to live in harmony with the rhythms of >nature. >Grateful for the religious pluralism which enriches and ennobles our faith, we >are inspired to deepen our understanding and expand our vision. As free >congregations we enter into this covenant, promising to one another our mutual >trust and support.

Response:

>Rita, >    In a wager you can’t have three winning scenarios.  You either win or >you lose.  Pascal is taking the position that he prefers not to plead >ignorance since that would not have a winning scenario, it would be the >same as a loss.  Therefore, Pascal is embracing known probabilities >rather than hoping the quarter lands on its edge. >Bob >Ol’Original

We know the odds for the toss of a coin.  That is knowable.  The existence of God is quite a different matter — a concept that can be disputed on many grounds.  One God, whose God, many Gods?  Which God must one believe in?  The Roman Catholic God, the Southern Baptist God, the Jehovah Witness God, the Mormon God, Allah, Jesus?  It assumes we know the mind of that God in relation to human beings, if indeed there is one.  Almost all religions have at one time or another condemned unbelievers to hellfire for refusing not just to believe in their God, but for failing to follow this or that rule of their belief system. Pascal’s premise is that there is one true religion and that one who does not espouse it will suffer in the afterlife. It presumes a God who will punish those who don’t blindly assent to his existence. That, to me, is irrational, since if there is a God he or she would not be the kind of being who would punish humans for not knowing the unknowable.  It is based on fear of hell.  And it is not rational to me that a God who created us all would be that kind of petty tyrant, if indeed a God exists.  That would mean God plays very nasty games. Refusing to give us firm evidence of his or her existence, yet making us assent on the basis of no real knowledge. I prefer a religion that centers on the search for how to lead a good life on this earth.  Nothing I have read about the major religions of the world gives me a reason to live by faith and faith alone in any of them. It seems cowardly to me to make a wager that is against reason — and Pascal says that God’s existence can’t be known by reason — in order to avoid possible punishment in the afterlife.  It is an argument based on fear. Voltaire protested that there is something unseemly about the whole Wager. He suggests that Pascal’s calculations, and his appeal to self-interest, are unworthy of the gravity of the subject of theistic belief.

Response:

– Hide quoted text — Show quoted text ->Rita, >        You might want to consider this: >God either exists or He doesn’t. Either I believe in God or I don’t. Of >the four possibilities, only one is to my disadvantage. To avoid that >possibility, I believe in God.  Blaise Pascal >   Would that god be Allah?  or Zeus?  or Ctulhu?  Careful now, >you mustn’t take any chances.   Better believe in all of them. >Ctulhu is even worse than Jehovah when he gets annoyed >with people: you’d better not tick him off.

Sorry I’m late but the subject, "houses for the homeless" threw me off.  Although most predominant in Japan, many in the far east prefer exactly this, believe in them all, it’s good for business. Rochester Minnesota USA

Response:

Rita,         In a wager you can’t have three winning scenarios.  You either win or you lose.  Pascal is taking the position that he prefers not to plead ignorance since that would not have a winning scenario, it would be the same as a loss.  Therefore, Pascal is embracing known probabilities rather than hoping the quarter lands on its edge. Bob Ol’Original – Hide quoted text — Show quoted text ->Rita, >       You might want to consider this: >God either exists or He doesn’t. Either I believe in God or I don’t. Of >the four possibilities, only one is to my disadvantage. To avoid that >possibility, I believe in God.  Blaise Pascal >Bob >Ol’Original > There is a 3rd choice — one simply does not know. > And feels no need to take on Pascal’s wager.

– In times of change, there is no incentive so great, and no medicine so powerful as hope for a better tomorrow.

Response:

– Hide quoted text — Show quoted text ->Tiny houses seen as answer for homeless >Advocate says the units would work if government would just bend rules a bit. >By Herbert A. Sample — Bee San Francisco Bureau >Published 2:15 am PDT Saturday, July 3, 2004 >SAN FRANCISCO – It’s not much bigger than a large garden shed, but Jim Reid – >building contractor, perennial candidate and thinker of unorthodox ideas – >believes it can be one solution to this city’s vexing homeless problem. >The not-so-simple trick is convincing everyone else. >Reid’s brainchild is to build hundreds of 100-square-foot homes he calls >Shelter Ones in neighborhoods around San Francisco as residences for homeless >persons willing to perform some manual labor in return. > I wish someone would spend as much time and money in sending them back > to Mexico as they do dreaming up all of these Socialist programs. > You house all of these, next year there wil be just as many new ones > looking for a handout.

I don’t suppose you have some statistics to back up what you just said, that the vast majority of the homeless are illegal aliens.

Response:

Rita,         You might want to consider this: God either exists or He doesn’t. Either I believe in God or I don’t. Of the four possibilities, only one is to my disadvantage. To avoid that possibility, I believe in God.  Blaise Pascal Bob Ol’Original – Hide quoted text — Show quoted text ->>>Since I volunteered for some time at my church’s >>For someone who has daily preached secular fundamentalism >>against every religion known to man in this news group, don’t >>you think it’s a little disingenuous to claim membership in any >>church ? >>Inquiring minds want to know. >Ah, but Rita’s church doesn’t believe in anything :-) >Obviously a liberal establishment. > You expected maybe I’d be a Southern Baptist?  I have the > same religion as: >         Abigail Adams* >         John Adams* >         John Quincy Adams >         Ethan Allen >         John C. Calhoun >         William S. Cohen >         Paul H. Douglas >         Millard Fillmore* >         Benjamin Franklin* >         Horace Greeley* >         Thomas Jefferson* >         Thomas Paine >         William J. Perry >         Paul Revere* >         Josiah Quincy (1722-1864) >         Elliot L. Richardson >         Leverett Saltonstall >         Adlai Stevenson (1900-1965)* >         William Howard Taft* >         Daniel Webster* >         Henry David Thoreau >         Henry Wadsworth Longfellow >         Nathaniel Hawthorne >         Ralph Waldo Emerson >         Charles Darwin >         Alexander Graham Bell >         John Dewey > And many others who believed in "nothing at all":) > * People marked with an asterisk have appeared on postage stamps (in most cases, > US stamps).

– In times of change, there is no incentive so great, and no medicine so powerful as hope for a better tomorrow.

Response:

>Rita, >    You might want to consider this: >God either exists or He doesn’t. Either I believe in God or I don’t. Of >the four possibilities, only one is to my disadvantage. To avoid that >possibility, I believe in God.  Blaise Pascal

   Would that god be Allah?  or Zeus?  or Ctulhu?  Careful now, you mustn’t take any chances.   Better believe in all of them. Ctulhu is even worse than Jehovah when he gets annoyed with people: you’d better not tick him off.

Response:

- Hide quoted text — Show quoted text ->>>>>Since I volunteered for some time at my church’s >>>>For someone who has daily preached secular fundamentalism >>>>against every religion known to man in this news group, don’t >>>>you think it’s a little disingenuous to claim membership in any >>>>church ? >>>>Inquiring minds want to know. >>>Ah, but Rita’s church doesn’t believe in anything :-)     >>>Obviously a liberal establishment.   >>You expected maybe I’d be a Southern Baptist?  I have the >>same religion as: >>    Abigail Adams* >>    John Adams* >>    John Quincy Adams >>    Ethan Allen >>    John C. Calhoun >>    William S. Cohen >>    Paul H. Douglas >>    Millard Fillmore* >>    Benjamin Franklin* >>    Horace Greeley* >>    Thomas Jefferson* >>    Thomas Paine >>    William J. Perry >>    Paul Revere* >>    Josiah Quincy (1722-1864) >>    Elliot L. Richardson >>    Leverett Saltonstall >>    Adlai Stevenson (1900-1965)* >>    William Howard Taft* >>    Daniel Webster* >>        Henry David Thoreau >>        Henry Wadsworth Longfellow >>        Nathaniel Hawthorne >>        Ralph Waldo Emerson >>        Charles Darwin >>    Alexander Graham Bell >>    John Dewey >>And many others who believed in "nothing at all":) >>* People marked with an asterisk have appeared on postage stamps (in most cases, >>US stamps). > *P*H*O*N*E*Y* >Rita is a Unitarian — which means she is pretty much free to believe >in God, or Buddha, or the mouse behind her refrigerator. Personally, I >think referring to Unitarianism as a "religion" is a stretch, but to >each his own. >Correct me if I’m wrong, Rita.

Unitarians don’t have a creed, but they do have general principles. Some are deists, some agnostics, some atheists.  Unitarians respect the best in all religions, although mouse religions have escaped my notice to date.  Perhaps tomorrow? Officially: With its historical roots in the Jewish and Christian traditions, Unitarian Universalism is a liberal religion — that is, a religion that keeps an open mind to the religious questions people have struggled with in all times and places. We believe that personal experience, conscience and reason should be the final authorities in religion, and that in the end religious authority lies not in a book or person or institution, but in ourselves. We are a "non-creedal" religion: we do not ask anyone to subscribe to a creed. So, Jeff, you may think Unitarians have no right to call themselves a religion, but it seems for you a religious person must accept some religious "authority"?  Or that a person can’t be a "spiritual" person without accepting some religious authoirty?  Or that a person can’t find his or her own way on questions of God and the meaning of existence? With that view, Unitarians would differ. The principles most Unitarians share are: We, the member congregations of the Unitarian Universalist Association, covenant to affirm and promote     * The inherent worth and dignity of every person;     * Justice, equity and compassion in human relations;     * Acceptance of one another and encouragement to spiritual growth in our congregations;     * A free and responsible search for truth and meaning;     * The right of conscience and the use of the democratic process within our congregations and in society at large;     * The goal of world community with peace, liberty, and justice for all;     * Respect for the interdependent web of all existence of which we are a part. The living tradition which we share draws from many sources:     * Direct experience of that transcending mystery and wonder, affirmed in all cultures, which moves us to a renewal of the spirit and an openness to the forces which create and uphold life;     * Words and deeds of prophetic women and men which challenge us to confront powers and structures of evil with justice, compassion, and the transforming power of love;     * Wisdom from the world’s religions which inspires us in our ethical and spiritual life;     * Jewish and Christian teachings which call us to respond to God’s love by loving our neighbors as ourselves;     * Humanist teachings which counsel us to heed the guidance of reason and the results of science, and warn us against idolatries of the mind and spirit.     * Spiritual teachings of earth-centered traditions which celebrate the sacred circle of life and instruct us to live in harmony with the rhythms of nature. Grateful for the religious pluralism which enriches and ennobles our faith, we are inspired to deepen our understanding and expand our vision. As free congregations we enter into this covenant, promising to one another our mutual trust and support.

Response:

>Rita, >    You might want to consider this: >God either exists or He doesn’t. Either I believe in God or I don’t. Of >the four possibilities, only one is to my disadvantage. To avoid that >possibility, I believe in God.  Blaise Pascal >Bob >Ol’Original

There is a 3rd choice — one simply does not know. And feels no need to take on Pascal’s wager.

Response:

– Hide quoted text — Show quoted text -> >> Tiny houses seen as answer for homeless > >> Advocate says the units would work if government would just bend rules >a bit. > >> By Herbert A. Sample — Bee San Francisco Bureau > >> Published 2:15 am PDT Saturday, July 3, 2004 > >The U.S. had those 150 years ago. They were called slave quarters. > >The current idea is simply a cop out.  Reagan cut Federal money for >mental > >institutions, driving most of these people onto the streets.  So a >majority > >of homeless people need mental help. > >The idea of building shacks for homeless people can do nothing but >incease > >crime, violate zoning laws,  reduce property values, and piss people off. > It is a very bad idea.  Better idea is to provide housing, with services > such as mental health care and so forth in small residences around the > city.  We have some of these in New York City, and they work out well. > But we don’t have enough of them.  We also have a system where people have > to prove themselves to be taking medication and be stable before being > assigned permanent housing.  There are only so many resources to go >around, > and the homeless themselves need to cooperate in the process.  So people > have to live in shelters and work up to permanent housing, with mental > health treatment and/or drug treatment programs, and developing some >source > of income, be it some kind of employment or SSI. >And what about those people who are homeless who do not have a mental health >problem.  Do all of the homeless have mental health problems, or have drug >problems?

No, but most are "damaged" in some profound way.  Many have physical health problems that are quite severe.  Those that have none of these problems usually are homeless only for short periods.  Obviously those who have no health or drug problems, and are relatively young, don’t need the same kind of services. They may be homeless for short periods, but will find their way back on their own.  They are a small percentage of the problem. I once did not believe this but visiting homeless shelters and working in one showed me otherwise.  I am talking about the single longterm homeless population.  There are many homeless families with children who simply can’t pay the rent.  But they are not the homeless on the streets.

Response:

– Hide quoted text — Show quoted text ->Is this one of those ideas that is based on the idea if you build it they >will come?  What happens if you buid it and they do not come?  Iseem to >recall that is basic idea has been tried before in Los Angeles.  How >successful was that effort. >> Tiny houses seen as answer for homeless >> Advocate says the units would work if government would just bend rules a >bit. >> By Herbert A. Sample — Bee San Francisco Bureau >> Published 2:15 am PDT Saturday, July 3, 2004 >> SAN FRANCISCO – It’s not much bigger than a large garden shed, but Jim >Reid – >> building contractor, perennial candidate and thinker of unorthodox ideas – >> believes it can be one solution to this city’s vexing homeless problem. >> The not-so-simple trick is convincing everyone else. >> Reid’s brainchild is to build hundreds of 100-square-foot homes he calls >> Shelter Ones in neighborhoods around San Francisco as residences for >homeless >> persons willing to perform some manual labor in return. >>  As a concept, there are some here who think Reid may be onto something. >The >> Board of Supervisors in April asked city agencies to analyze the notion, >and >> what they found were minor qualms and one big hurdle: State-mandated >minimum >> floor space requirements for dwellings. >> But Reid labors on, in any forum he can, confident that he has discovered >an >> answer to a complicated problem if only government would bend a bit. >> "Government has no common sense," he said in an interview. "I mean, they >look >> at this house and they say, ‘It’s illegal.’ But it’s really needed." And >though >> no one is quite ready to give the go-ahead for Reid’s concept yet, it has >its >> supporters. >> "Yeah, he’s endured a lot of ridicule, but they’re cute little houses," >said >> Barbara Meskunas, president of the Coalition for San Francisco >Neighborhoods, >> an influential group whose imprimatur Reid would need if his idea were to >get >> off the ground. >> "I’m sure his little house is a whole lot better than some of the in-law >units >> that are in most of our neighborhoods," she added. "They’re certainly >better >> than many of the single-room-occupancy hotels that we put homeless people >in." >> Reid, 54, has been pushing his Shelter One concept for years now through >his >> nonprofit firm, Habitat for the Homeless, and during two quixotic >campaigns for >> mayor, last year and in 1999. To prove his point to the skeptics, he built >and >> lived for a time in a prototype. >> The wood-frame cottage sports a kitchenette and an enclosed bathroom – >though >> the tub appears a bit smaller than normal and the sink sits above the >toilet. >> Across from the kitchenette is a "loft bed" above a seating area with a >small >> window. Nearby is a tiny closet with a combination washer-dryer. >> Reid insists Shelter Ones could be built for as little as $6,000 if the >> materials and construction labor are donated, or $30,000 if not, excluding >land >> costs. Larger versions would be two and three times larger. >> The Taj Mahal they aren’t. But Reid explains that for some homeless >people, a >> tiny house would be better than the street or shelters. And for low-income >> couples, the larger varieties could help them get started as homeowners. >> "People don’t have a choice," Red said. "You could buy a 2,000-square-foot >> house that costs a half a million dollars or rent a place. That’s all. And >I >> would like to give people a choice of renting 600 square feet or buying >300 >> square feet." >> Reid may be convinced of his idea’s worth as an answer to homelessness, >but >> others aren’t so sure. >> "I’ve got a problem with it as housing," said Paul Boden, executive >director of >> the Coalition on Homelessness, citing Reid’s proposal that Shelter One >> residents perform neighborhood cleanup duties in lieu of rent. "I don’t >have a >> problem with it as (temporary) shelter." >> Sam Davis, an architecture professor at the University of California, >Berkeley, >> said he doubts the city and neighborhood groups would allow enough Shelter >Ones >> to be built to put a sizable dent in homelessness. >> Further, he said the homes lack the on-site social services included with >the >> "supportive housing," the city now focuses on. Yet, Davis included Reid’s >idea >> in an upcoming book on designing living spaces for the homeless. >> "I think what’s interesting about him and people like him is they are >using the >> knowledge that they have, they’re using their skills and expertise, to try >and >> attack the problem," he said. >> When city building inspectors took a look at the prototype, they found >glitches >> that seemed correctable, such as missing plumbing fixtures and the lack of >a >> heating system. >> The big hurdle, they noted, was a state law that requires a minimum of 220 >> square feet of usable floor space for an "efficiency" unit. Shelter One >has >> only 50 square feet, but Reid says there is an exemption for homeless >housing. >> Then, of course, there are city zoning ordinances to deal with. >> "The obvious issue here is, do you want to create a double standard for >people >> who live in complying houses and for people … who don’t?" said Laurence >> Kornfield, chief building inspector for the city. "That would be for the >state >> Legislature to consider." >> Reid says he’ll prod local legislators to look into the issue. In the >meantime, >> he’s a fervent as ever about Shelter One. That focus has led some >observers to >> consider him and his idea a bit eccentric, though Reid characterizes it >> somewhat differently. >> "No one’s thinking outside the box on this, and they have to," he said. >> "Smaller is the answer." >> http://www.sacbee.com/content/news/story/9871234p-10793495c.html (includes >> picture) > Jerry, my guess is that if they build it — they will come. San > Francisco already has ten times as many homeless per capita as New > York. The Board of Supes seems to be shooting for twenty.

Well, I am not so sure about that, but I guess that depends on how many are homeless and where they live.  Easier to remain homeless when you live in a place like Hawaii, then it is in New York City I would imagine.  And I guess the same thing can be said about those living in Los Angeles vs. those living in San Francisco.  So, maybe there will make good use of thee dwellings…only time will tell of course.

Response:

> Jerry, my guess is that if they build it — they will come. San > Francisco already has ten times as many homeless per capita as New > York. The Board of Supes seems to be shooting for twenty.

That’s primarily because of the Winter temperature, nothing else. That’s why homelessness is a national problem, not a local or State prolem.

Response:

- Hide quoted text — Show quoted text ->>Since I volunteered for some time at my church’s >For someone who has daily preached secular fundamentalism >against every religion known to man in this news group, don’t >you think it’s a little disingenuous to claim membership in any >church ? >Inquiring minds want to know. >Ah, but Rita’s church doesn’t believe in anything :-)     >Obviously a liberal establishment.  

You expected maybe I’d be a Southern Baptist?  I have the same religion as:         Abigail Adams*         John Adams*         John Quincy Adams         Ethan Allen         John C. Calhoun         William S. Cohen         Paul H. Douglas         Millard Fillmore*         Benjamin Franklin*         Horace Greeley*         Thomas Jefferson*         Thomas Paine         William J. Perry         Paul Revere*         Josiah Quincy (1722-1864)         Elliot L. Richardson         Leverett Saltonstall         Adlai Stevenson (1900-1965)*         William Howard Taft*         Daniel Webster*         Henry David Thoreau         Henry Wadsworth Longfellow         Nathaniel Hawthorne         Ralph Waldo Emerson         Charles Darwin         Alexander Graham Bell         John Dewey And many others who believed in "nothing at all":) * People marked with an asterisk have appeared on postage stamps (in most cases, US stamps).

Response:

– Hide quoted text — Show quoted text ->>>Since I volunteered for some time at my church’s >>For someone who has daily preached secular fundamentalism >>against every religion known to man in this news group, don’t >>you think it’s a little disingenuous to claim membership in any >>church ? >>Inquiring minds want to know. >Ah, but Rita’s church doesn’t believe in anything :-)     >Obviously a liberal establishment.   >You expected maybe I’d be a Southern Baptist?  I have the >same religion as: >    Abigail Adams* >    John Adams* >    John Quincy Adams >    Ethan Allen >    John C. Calhoun >    William S. Cohen >    Paul H. Douglas >    Millard Fillmore* >    Benjamin Franklin* >    Horace Greeley* >    Thomas Jefferson* >    Thomas Paine >    William J. Perry >    Paul Revere* >    Josiah Quincy (1722-1864) >    Elliot L. Richardson >    Leverett Saltonstall >    Adlai Stevenson (1900-1965)* >    William Howard Taft* >    Daniel Webster* >        Henry David Thoreau >        Henry Wadsworth Longfellow >        Nathaniel Hawthorne >        Ralph Waldo Emerson >        Charles Darwin >    Alexander Graham Bell >    John Dewey >And many others who believed in "nothing at all":) >* People marked with an asterisk have appeared on postage stamps (in most cases, >US stamps).

   There should be an asterisk after J.Q. Adams.  I have a couple of sets of 22-cent stamps showing all the American presidents through Lyndon Johnson.    Thomas Paine should definitely appear on a postage stamp – he’s long overdue.  Maybe anticipated objections from conservative religious groups have forestalled that. He’s certainly overwhelmingly more important to American history than Paul Revere.    Darwin is on some British paper currency, some of the five- or ten-pound notes, I think.

Response:

– Hide quoted text — Show quoted text ->> Tiny houses seen as answer for homeless >> Advocate says the units would work if government would just bend rules a bit. >> By Herbert A. Sample — Bee San Francisco Bureau >> Published 2:15 am PDT Saturday, July 3, 2004 >The U.S. had those 150 years ago. They were called slave quarters. >The current idea is simply a cop out.  Reagan cut Federal money for mental >institutions, driving most of these people onto the streets.  So a majority >of homeless people need mental help. >The idea of building shacks for homeless people can do nothing but incease >crime, violate zoning laws,  reduce property values, and piss people off. > It is a very bad idea.  Better idea is to provide housing, with services > such as mental health care and so forth in small residences around the > city.  We have some of these in New York City, and they work out well. > But we don’t have enough of them.  We also have a system where people have > to prove themselves to be taking medication and be stable before being > assigned permanent housing.  There are only so many resources to go around, > and the homeless themselves need to cooperate in the process.  So people > have to live in shelters and work up to permanent housing, with mental > health treatment and/or drug treatment programs, and developing some source > of income, be it some kind of employment or SSI.

And what about those people who are homeless who do not have a mental health problem.  Do all of the homeless have mental health problems, or have drug problems?

Response:

>Jerry, my guess is that if they build it — they will come. San >Francisco already has ten times as many homeless per capita as New >York. The Board of Supes seems to be shooting for twenty.

I have followed the homeless problem in NYC for more than 20 years.  We used to have a problem like SF of countless homeless living on the streets, panhandling and frightening and annoying the public.  Our subways stations had homeless sleeping there and on every train one seemed to encounter several begging in the cars.  We still have a few non-conformists who prefer to live on the street.  I was panhandled the other day by a Muslim woman of all things, but that was the first time in months and months I’ve been approached for money.  I very much doubt she was living on the streets, however.  In my neighborhood I occasionally see a homeless man sacked out in front of the OTB (off track betting run by the state), but this is rare. We haven’t a perfect solution, but gradually the city began a sort of incentive system — homeless signed up in day drop in shelters or regular homeless shelters for drug and alcohol treatment programs and for medical care and counseling if mentally ill.  Most seem to be one or the other, at least to some degree, or both. Then after "proving themselves" by working on these problems, they were helped to sign up for SSI if eligible by virtue of disability, or public assistance and/or to get some kind of employment. Finally those who stuck with the program were offered some kind of subsidized housing — usually a room or very small apartment, and sometimes in buildings with social workers, mental health people looking in, sometimes not. My daughter tells me a study has been done that shows that just giving the homeless a decent place to live seems to be as successful as having them go through the various treatment options.  But it is only one study. And even if it works in that those given housing with no strings attached become stabilized, this certainly would function as a honey pot to attract more homeless to any area offering this.  Resources for housing and funds are limited in cities and given the fact that the climate in SF is more agreeable than in many parts of the country, I agree you would have an influx.  A more nuanced and step by step approach with the individual having to meet certain behavioral goals would seem to me to be far better. Since I volunteered for some time at my church’s shelter for homeless men I did get to know the population (and also many years ago actually inspected city shelters for the Coalition for the Homeless.)  So I not a "do gooder" with no appreciation of the problems.  But a structured approach over time does work with most and that is the best any city can hope for so long as there are shortages of affordable housing overall. Compared to problems many cities face today, the old cheap hotels that sold a bed for a night on skid rows for a dollar or two, begin to look not so bad:)  Gentrification took care of those and now the Bowery in Manhattan is upscale.  

Response:

Tiny houses seen as answer for homeless Advocate says the units would work if government would just bend rules a bit. By Herbert A. Sample — Bee San Francisco Bureau Published 2:15 am PDT Saturday, July 3, 2004 SAN FRANCISCO – It’s not much bigger than a large garden shed, but Jim Reid – building contractor, perennial candidate and thinker of unorthodox ideas – believes it can be one solution to this city’s vexing homeless problem. The not-so-simple trick is convincing everyone else. Reid’s brainchild is to build hundreds of 100-square-foot homes he calls Shelter Ones in neighborhoods around San Francisco as residences for homeless persons willing to perform some manual labor in return.  As a concept, there are some here who think Reid may be onto something. The Board of Supervisors in April asked city agencies to analyze the notion, and what they found were minor qualms and one big hurdle: State-mandated minimum floor space requirements for dwellings. But Reid labors on, in any forum he can, confident that he has discovered an answer to a complicated problem if only government would bend a bit. "Government has no common sense," he said in an interview. "I mean, they look at this house and they say, ‘It’s illegal.’ But it’s really needed." And though no one is quite ready to give the go-ahead for Reid’s concept yet, it has its supporters. "Yeah, he’s endured a lot of ridicule, but they’re cute little houses," said Barbara Meskunas, president of the Coalition for San Francisco Neighborhoods, an influential group whose imprimatur Reid would need if his idea were to get off the ground. "I’m sure his little house is a whole lot better than some of the in-law units that are in most of our neighborhoods," she added. "They’re certainly better than many of the single-room-occupancy hotels that we put homeless people in." Reid, 54, has been pushing his Shelter One concept for years now through his nonprofit firm, Habitat for the Homeless, and during two quixotic campaigns for mayor, last year and in 1999. To prove his point to the skeptics, he built and lived for a time in a prototype. The wood-frame cottage sports a kitchenette and an enclosed bathroom – though the tub appears a bit smaller than normal and the sink sits above the toilet. Across from the kitchenette is a "loft bed" above a seating area with a small window. Nearby is a tiny closet with a combination washer-dryer. Reid insists Shelter Ones could be built for as little as $6,000 if the materials and construction labor are donated, or $30,000 if not, excluding land costs. Larger versions would be two and three times larger. The Taj Mahal they aren’t. But Reid explains that for some homeless people, a tiny house would be better than the street or shelters. And for low-income couples, the larger varieties could help them get started as homeowners. "People don’t have a choice," Red said. "You could buy a 2,000-square-foot house that costs a half a million dollars or rent a place. That’s all. And I would like to give people a choice of renting 600 square feet or buying 300 square feet." Reid may be convinced of his idea’s worth as an answer to homelessness, but others aren’t so sure. "I’ve got a problem with it as housing," said Paul Boden, executive director of the Coalition on Homelessness, citing Reid’s proposal that Shelter One residents perform neighborhood cleanup duties in lieu of rent. "I don’t have a problem with it as (temporary) shelter." Sam Davis, an architecture professor at the University of California, Berkeley, said he doubts the city and neighborhood groups would allow enough Shelter Ones to be built to put a sizable dent in homelessness. Further, he said the homes lack the on-site social services included with the "supportive housing," the city now focuses on. Yet, Davis included Reid’s idea in an upcoming book on designing living spaces for the homeless. "I think what’s interesting about him and people like him is they are using the knowledge that they have, they’re using their skills and expertise, to try and attack the problem," he said. When city building inspectors took a look at the prototype, they found glitches that seemed correctable, such as missing plumbing fixtures and the lack of a heating system. The big hurdle, they noted, was a state law that requires a minimum of 220 square feet of usable floor space for an "efficiency" unit. Shelter One has only 50 square feet, but Reid says there is an exemption for homeless housing. Then, of course, there are city zoning ordinances to deal with. "The obvious issue here is, do you want to create a double standard for people who live in complying houses and for people … who don’t?" said Laurence Kornfield, chief building inspector for the city. "That would be for the state Legislature to consider." Reid says he’ll prod local legislators to look into the issue. In the meantime, he’s a fervent as ever about Shelter One. That focus has led some observers to consider him and his idea a bit eccentric, though Reid characterizes it somewhat differently. "No one’s thinking outside the box on this, and they have to," he said. "Smaller is the answer." http://www.sacbee.com/content/news/story/9871234p-10793495c.html (includes picture)

Response:

Question:

- Hide quoted text — Show quoted text – > 737 gets new toilets designed to please > It’s potty time: more sink space and no seats slamming shut > The Jetsons might have had it better, but but Boeing’s new 737 toilets are a > huge leap from that grubby early-80s look. The waste bin won’t snap back on your > hand anymore, so make sure you tidy up. > By Jon Bonn

Question:

I believe that 6-mp is cheaper than Asacol.  my copay for Imuran is 15 dollars, but 35 for  the Asacol.  (also, 2 pills per day vs 9)

Response:

> I believe that 6-mp is cheaper than Asacol.  my copay for Imuran is 15 dollars, > but 35 for  the Asacol.  (also, 2 pills per day vs 9)

AFAIK there is no generic manufacturer of Asacol which is likely a big reason why it is so much more expensive than 6-MP or azathioprine.

Response:

Good luck with your increased meds.  I take 9 asacol plus I take imuran too.   6-MP and imuran are sister drugs, so the affects are the same.   When on the immunosuppressants, try to stay away from  people who are sick (hard in a large company, I know…)  One question, why would your gastro advise against telling your  boss?   I work at a large company and am very open about my condition and my medical appointments.   I have never had any problems with any managers bein upfront about my crohn’s.   Good luck.  I hope all goes well.

Response:

That’s very expensive. I picked up 125 pills last week and it was marked $220.00 Canadian. That’s $1.76 each or about $1.30 US each. Actually I paid nothing. My insurance company was billed directly. I only pay the first $10.00 Canadian per family member per year. This is one of the best drug plans I have heard of. — Paul Visit our photo albums at http://www.laflammefamily.ca To reply, replace "deadspam.com" with "laflammefamily.ca" — – Hide quoted text — Show quoted text – > Without the insurance, it’s about $3.50/pill. My portion of the bill (30%) > is roughly $80/month. You doctor may start you at a lower dosage, plus your > insurance is probably more generous than mine, so your bill may be lower. > Good luck. > Obviously, nothing is more important than a person’s health. How much > does 6-MP cost? I’m just trying to budget for the additional cost. > > I’m now on 100mg of 6MP (originally at 50mg) and most have few in any > side > > effects if they can tolerate the drug in the first place (your blood > tests > > will demonstrate this within the first week). > > And…as a fellow Type A personality, I can tell you that you *can* > manage > > your mind much more than you think when it comes to UC (I assume that’s > your > > condition). You gotta psych yourself up before work every day along with > all > > the other things you do. But once in a while when things go awry it’s > nice > > knowing that I have a change of clothes with me at all times (at the > > desk–not the car). > > To hell with the additional cost of the 6MP–this is your health, what’s > > more important than that? > > > My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > > > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > > > stressful job, and work for a large corporation and my condition seems > > > to be getting worse (still mild compared to most of you), spending > > > more time in the bathroom (making me consistently later for work and > > > people notice), harder to control bowels, and fatigue/nausea/weakness > > > are worse (in part to IBD and medicine). It’s the first time I’m > > > really experiencing the quality of my life deteriorating like I read > > > about on here all the time. > > > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > > > after next colonscopy to see if my colon inflammation has been > > > reduced. I will do what it takes to avoid steroids and surgery and > > > have started sleeping more, eating better, and exercising as much as > > > possible (really hard when all you want to do is lay down and relax). > > > My Gastro. thinks my type A personality and anxiety are making my > > > condition worse and it may contribute, but I think you can only manage > > > your mind so much. > > > Please share your experiences of going from Asacol to 6-MP or about > > > 6-MP in general. I am especially about the side-effects, cost (10 > > > co-pay for Asocal now), and whether or not monthly blood tests will > > > give me know choice but to tell my boss (gastro. advised me not too, > > > but the numerous medical appt’s are getting suspicious, don’t want it > > > to affect my compensation and reputation).

Response:

this may not work for you, but it has worked for me.  The Gym.  I’ve been finding the more I work out(especially in the mornign, but thats hard for me, working on it), my UC has relaxed, my body is less stressed, less fatigue, less weakness.  I know you said you are exercise more..but maybe it’s not enough? I’ve found that if I go 2-3 time a week(min.) my body feels so much better. Yes it’s a time sink, but by going I maximize my time outside of the gym.  I also like this I recently read: Today’s Fitness Tip of the Day. Brought to you by Bally Total Fitness. If you find yourself dreading your usual workout, procrastinating like mad and searching frantically for an excuse to cancel, make yourself a deal. Commit to working out for only 15 minutes – and if you still don’t feel like exercising at that point, you can stop without feeling guilty. Chances are, however, that once you’ve put in your 15 minutes, you’ll feel reinvigorated and want to continue for another 15 or 30 minutes or longer. best wishes -joel

– Hide quoted text — Show quoted text -> Vanny- Most of what you said makes sense, but your following > paragpragh needs clarification: > "If you choose to go down this route they must be made aware that it > might mean that you will be off work for a few if not several months > and that if you are working you might need to lie down regularly, need > to be in close proximity of the toilet and will be on chemotherapy." > Why would I need to take months off of work? Need to lie down oftem? > And why the hell would I need chemotherapy? Last time I checked chemo. > was only for cancer patients. Are you talking about side-effects of > 6-MP or just telling me how shitty (no pun intended) my work life > could be in the future? Are you speaking from personal experience? > – sinikal

– Hide quoted text — Show quoted text -> Hi Sinikal, > I would forget the Type A personality thing and just accept that you have > IBD and it is progressing. This means that you need to increase the > medication and for long-term safety reasons go on to a steroid sparing > regime. If you do not do this, from the description you have given, you will > just get worse and worse. You are probably going to have to accept that you > will have to take time off work because the 6-MP and similar take 1-4 months > to kick in so you are likely to get worse before you get better. > With respect to telling your work. I would be careful here because a lot of > people including employees, friends and relatives are unaware of IBD and > what it means. An IBDer looks physically OK – I mean no broken bones, no > litres of blood gushing out of visible wounds and thus because we are > ‘tired’ all the time we are quickley categorised as being psychologically > ill – a neat escape route even for the so-called specialists. > If you know that you can talk to somebody at work in confidence then do it. > A large corporation must have a doctor or welfare officer and I would start > there – take some literature with you just in case they need educating. If > you then want to tell your boss you might be best advised to do it in the > presence of the work’s doctor or welfare officer. If you choose to go down > this route they must be made aware that it might mean that you will be off > work for a few if not several months and that if you are working you might > need to lie down regularly, need to be in close proximity of the toilet and > will be on chemotherapy. Discuss this with your partner, relatives and with > your doctor again. He must have had a reason for advising you against it. > My personal experience regarding telling employers has been more negative > than positive. For me there was little understanding and I was expected to > work the same 12 hour days that everyone else is expected to work and to > still be smiling/standing at the end of the day. Of course, others here have > had all the support in the world from their employers throughout the course > of their illness. On the otherhand, others have been nudged out of their > jobs – like me at one company. > All the best, > Vanny > My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

Response:

You may or may not need time off from work depending on how sick you are and how far you will push yourself when you are that sick.  6MP is a chemotherapy drug.  In low doses, it is used as an immunosuppressant, in higher doses it is used for chemotherapy most commonly for leukemia.  Because you will take it in much lower doses than are used in chemotherapy, you may not experience all of the negative side effects.   As Vanny said, it is best to start on this regiment and avoid steroids if at all possible; the long term side effects are devastating.  6MP takes between 3-6 months to begin working, so the sooner you start, the better it will be for you. Good luck! :)  mgbio – Hide quoted text — Show quoted text – > Vanny- Most of what you said makes sense, but your following > paragpragh needs clarification: > "If you choose to go down this route they must be made aware that it > might mean that you will be off work for a few if not several months > and that if you are working you might need to lie down regularly, need > to be in close proximity of the toilet and will be on chemotherapy." > Why would I need to take months off of work? Need to lie down oftem? > And why the hell would I need chemotherapy? Last time I checked chemo. > was only for cancer patients. Are you talking about side-effects of > 6-MP or just telling me how shitty (no pun intended) my work life > could be in the future? Are you speaking from personal experience? > – sinikal >Hi Sinikal, >I would forget the Type A personality thing and just accept that you have >IBD and it is progressing. This means that you need to increase the >medication and for long-term safety reasons go on to a steroid sparing >regime. If you do not do this, from the description you have given, you will >just get worse and worse. You are probably going to have to accept that you >will have to take time off work because the 6-MP and similar take 1-4 months >to kick in so you are likely to get worse before you get better. >With respect to telling your work. I would be careful here because a lot of >people including employees, friends and relatives are unaware of IBD and >what it means. An IBDer looks physically OK – I mean no broken bones, no >litres of blood gushing out of visible wounds and thus because we are >’tired’ all the time we are quickley categorised as being psychologically >ill – a neat escape route even for the so-called specialists. >If you know that you can talk to somebody at work in confidence then do it. >A large corporation must have a doctor or welfare officer and I would start >there – take some literature with you just in case they need educating. If >you then want to tell your boss you might be best advised to do it in the >presence of the work’s doctor or welfare officer. If you choose to go down >this route they must be made aware that it might mean that you will be off >work for a few if not several months and that if you are working you might >need to lie down regularly, need to be in close proximity of the toilet and >will be on chemotherapy. Discuss this with your partner, relatives and with >your doctor again. He must have had a reason for advising you against it. >My personal experience regarding telling employers has been more negative >than positive. For me there was little understanding and I was expected to >work the same 12 hour days that everyone else is expected to work and to >still be smiling/standing at the end of the day. Of course, others here have >had all the support in the world from their employers throughout the course >of their illness. On the otherhand, others have been nudged out of their >jobs – like me at one company. >All the best, >Vanny >My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 >months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, >stressful job, and work for a large corporation and my condition seems >to be getting worse (still mild compared to most of you), spending >more time in the bathroom (making me consistently later for work and >people notice), harder to control bowels, and fatigue/nausea/weakness >are worse (in part to IBD and medicine). It’s the first time I’m >really experiencing the quality of my life deteriorating like I read >about on here all the time. >I’m nervous about stepping up to a stronger drug (he recommended 6-MP) >after next colonscopy to see if my colon inflammation has been >reduced. I will do what it takes to avoid steroids and surgery and >have started sleeping more, eating better, and exercising as much as >possible (really hard when all you want to do is lay down and relax). >My Gastro. thinks my type A personality and anxiety are making my >condition worse and it may contribute, but I think you can only manage >your mind so much. >Please share your experiences of going from Asacol to 6-MP or about >6-MP in general. I am especially about the side-effects, cost (10 >co-pay for Asocal now), and whether or not monthly blood tests will >give me know choice but to tell my boss (gastro. advised me not too, >but the numerous medical appt’s are getting suspicious, don’t want it >to affect my compensation and reputation).

Response:

Vanny- Most of what you said makes sense, but your following paragpragh needs clarification: "If you choose to go down this route they must be made aware that it might mean that you will be off work for a few if not several months and that if you are working you might need to lie down regularly, need to be in close proximity of the toilet and will be on chemotherapy." Why would I need to take months off of work? Need to lie down oftem? And why the hell would I need chemotherapy? Last time I checked chemo. was only for cancer patients. Are you talking about side-effects of 6-MP or just telling me how shitty (no pun intended) my work life could be in the future? Are you speaking from personal experience? – sinikal – Hide quoted text — Show quoted text – > Hi Sinikal, > I would forget the Type A personality thing and just accept that you have > IBD and it is progressing. This means that you need to increase the > medication and for long-term safety reasons go on to a steroid sparing > regime. If you do not do this, from the description you have given, you will > just get worse and worse. You are probably going to have to accept that you > will have to take time off work because the 6-MP and similar take 1-4 months > to kick in so you are likely to get worse before you get better. > With respect to telling your work. I would be careful here because a lot of > people including employees, friends and relatives are unaware of IBD and > what it means. An IBDer looks physically OK – I mean no broken bones, no > litres of blood gushing out of visible wounds and thus because we are > ‘tired’ all the time we are quickley categorised as being psychologically > ill – a neat escape route even for the so-called specialists. > If you know that you can talk to somebody at work in confidence then do it. > A large corporation must have a doctor or welfare officer and I would start > there – take some literature with you just in case they need educating. If > you then want to tell your boss you might be best advised to do it in the > presence of the work’s doctor or welfare officer. If you choose to go down > this route they must be made aware that it might mean that you will be off > work for a few if not several months and that if you are working you might > need to lie down regularly, need to be in close proximity of the toilet and > will be on chemotherapy. Discuss this with your partner, relatives and with > your doctor again. He must have had a reason for advising you against it. > My personal experience regarding telling employers has been more negative > than positive. For me there was little understanding and I was expected to > work the same 12 hour days that everyone else is expected to work and to > still be smiling/standing at the end of the day. Of course, others here have > had all the support in the world from their employers throughout the course > of their illness. On the otherhand, others have been nudged out of their > jobs – like me at one company. > All the best, > Vanny > My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

Response:

Without the insurance, it’s about $3.50/pill. My portion of the bill (30%) is roughly $80/month. You doctor may start you at a lower dosage, plus your insurance is probably more generous than mine, so your bill may be lower. Good luck.

> Obviously, nothing is more important than a person’s health. How much > does 6-MP cost? I’m just trying to budget for the additional cost.

– Hide quoted text — Show quoted text -> I’m now on 100mg of 6MP (originally at 50mg) and most have few in any side > effects if they can tolerate the drug in the first place (your blood tests > will demonstrate this within the first week). > And…as a fellow Type A personality, I can tell you that you *can* manage > your mind much more than you think when it comes to UC (I assume that’s your > condition). You gotta psych yourself up before work every day along with all > the other things you do. But once in a while when things go awry it’s nice > knowing that I have a change of clothes with me at all times (at the > desk–not the car). > To hell with the additional cost of the 6MP–this is your health, what’s > more important than that? > > My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > > stressful job, and work for a large corporation and my condition seems > > to be getting worse (still mild compared to most of you), spending > > more time in the bathroom (making me consistently later for work and > > people notice), harder to control bowels, and fatigue/nausea/weakness > > are worse (in part to IBD and medicine). It’s the first time I’m > > really experiencing the quality of my life deteriorating like I read > > about on here all the time. > > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > > after next colonscopy to see if my colon inflammation has been > > reduced. I will do what it takes to avoid steroids and surgery and > > have started sleeping more, eating better, and exercising as much as > > possible (really hard when all you want to do is lay down and relax). > > My Gastro. thinks my type A personality and anxiety are making my > > condition worse and it may contribute, but I think you can only manage > > your mind so much. > > Please share your experiences of going from Asacol to 6-MP or about > > 6-MP in general. I am especially about the side-effects, cost (10 > > co-pay for Asocal now), and whether or not monthly blood tests will > > give me know choice but to tell my boss (gastro. advised me not too, > > but the numerous medical appt’s are getting suspicious, don’t want it > > to affect my compensation and reputation).

Response:

Obviously, nothing is more important than a person’s health. How much does 6-MP cost? I’m just trying to budget for the additional cost. – Hide quoted text — Show quoted text – > I’m now on 100mg of 6MP (originally at 50mg) and most have few in any side > effects if they can tolerate the drug in the first place (your blood tests > will demonstrate this within the first week). > And…as a fellow Type A personality, I can tell you that you *can* manage > your mind much more than you think when it comes to UC (I assume that’s your > condition). You gotta psych yourself up before work every day along with all > the other things you do. But once in a while when things go awry it’s nice > knowing that I have a change of clothes with me at all times (at the > desk–not the car). > To hell with the additional cost of the 6MP–this is your health, what’s > more important than that? > My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

Response:

Hi Sinikal, I would forget the Type A personality thing and just accept that you have IBD and it is progressing. This means that you need to increase the medication and for long-term safety reasons go on to a steroid sparing regime. If you do not do this, from the description you have given, you will just get worse and worse. You are probably going to have to accept that you will have to take time off work because the 6-MP and similar take 1-4 months to kick in so you are likely to get worse before you get better. With respect to telling your work. I would be careful here because a lot of people including employees, friends and relatives are unaware of IBD and what it means. An IBDer looks physically OK – I mean no broken bones, no litres of blood gushing out of visible wounds and thus because we are ‘tired’ all the time we are quickley categorised as being psychologically ill – a neat escape route even for the so-called specialists. If you know that you can talk to somebody at work in confidence then do it. A large corporation must have a doctor or welfare officer and I would start there – take some literature with you just in case they need educating. If you then want to tell your boss you might be best advised to do it in the presence of the work’s doctor or welfare officer. If you choose to go down this route they must be made aware that it might mean that you will be off work for a few if not several months and that if you are working you might need to lie down regularly, need to be in close proximity of the toilet and will be on chemotherapy. Discuss this with your partner, relatives and with your doctor again. He must have had a reason for advising you against it. My personal experience regarding telling employers has been more negative than positive. For me there was little understanding and I was expected to work the same 12 hour days that everyone else is expected to work and to still be smiling/standing at the end of the day. Of course, others here have had all the support in the world from their employers throughout the course of their illness. On the otherhand, others have been nudged out of their jobs – like me at one company. All the best, Vanny My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, stressful job, and work for a large corporation and my condition seems to be getting worse (still mild compared to most of you), spending more time in the bathroom (making me consistently later for work and people notice), harder to control bowels, and fatigue/nausea/weakness are worse (in part to IBD and medicine). It’s the first time I’m really experiencing the quality of my life deteriorating like I read about on here all the time. I’m nervous about stepping up to a stronger drug (he recommended 6-MP) after next colonscopy to see if my colon inflammation has been reduced. I will do what it takes to avoid steroids and surgery and have started sleeping more, eating better, and exercising as much as possible (really hard when all you want to do is lay down and relax). My Gastro. thinks my type A personality and anxiety are making my condition worse and it may contribute, but I think you can only manage your mind so much. Please share your experiences of going from Asacol to 6-MP or about 6-MP in general. I am especially about the side-effects, cost (10 co-pay for Asocal now), and whether or not monthly blood tests will give me know choice but to tell my boss (gastro. advised me not too, but the numerous medical appt’s are getting suspicious, don’t want it to affect my compensation and reputation).

Response:

My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, stressful job, and work for a large corporation and my condition seems to be getting worse (still mild compared to most of you), spending more time in the bathroom (making me consistently later for work and people notice), harder to control bowels, and fatigue/nausea/weakness are worse (in part to IBD and medicine). It’s the first time I’m really experiencing the quality of my life deteriorating like I read about on here all the time. I’m nervous about stepping up to a stronger drug (he recommended 6-MP) after next colonscopy to see if my colon inflammation has been reduced. I will do what it takes to avoid steroids and surgery and have started sleeping more, eating better, and exercising as much as possible (really hard when all you want to do is lay down and relax). My Gastro. thinks my type A personality and anxiety are making my condition worse and it may contribute, but I think you can only manage your mind so much. Please share your experiences of going from Asacol to 6-MP or about 6-MP in general. I am especially about the side-effects, cost (10 co-pay for Asocal now), and whether or not monthly blood tests will give me know choice but to tell my boss (gastro. advised me not too, but the numerous medical appt’s are getting suspicious, don’t want it to affect my compensation and reputation).

Response:

- Hide quoted text — Show quoted text – > My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

hi i am on 9 tabs of asacol…and now on 6mp..i was on 100mg of 6mp but liver function tests werent good so i am on 50mg..i did have a bad bout in may and had to be on pred as well for a while…i am also going to be starting cipro tomorrow.. 1) i dont think your personality and stress have much to do with the ibd..i HATE it when people start down that road…my bouts can come about in the most relaxing times..and i have been really healthy in some terrible times..ibd comes and goes…so i wouldnt pay much mind to that …and you are right..u can only manage your mind so much 2) side effects from 6mp..the worst is the nausea..it was like being pregnant for me..the same kind of feelings…he prescribed compazine for me and i still have to take it almost every day..but not 3 a day now..usually just one also..u can take 6mp all at once if u are on more than one..and you can take it at night..i checked first with the pharmacist when i didnt reach my md..then my md said that also..if u take it at night u are less likely to feel sick get some crackers or something..and coke, gingerale..peppermint iced tea helps me a lot..so does coke..cheezits help the nausea for me..if u keep something in your tummy u wont feel so bad 3) u willhave to have frequent blood tests…usually every 2 weeks to start..then moving on to every 6 weeks..depending on if there are changes..i was on it several months before there were some problems showing on the tests..he lowered the dosage…and the problems seemed to go… 4)it has helped me a lot..tho i was even better on 100mg..on that amount..i didnt bleed much or often, the diarrhea stopped, the pain mostly stopped; the joint and muscle problems got a lot better..i wasnt even taking the relafen for joints when i was on more 6mp..on less..i am back to it.. 5) it works by knocking out your immune system..GET A FLU SHOT..and i am also given an pneumonia shot…every couple of years…and try to avoid crowds..and being around sick people…wash your hands a lot..especially after work, travel etc….rest a lot..well i know u are trying to ..and just put up with the side effects..i think its well worth it..i just wish i could take 100mg as i was so much bettr on it.. good luck…oh..it doesnt do anything mixing with the asacol to my knowledge..i dont have a lot of side effects from 9 tabs of asacol..12 bothered me..tummy pain etc..but 9 seems ok..i lose some hair now and then..thats all.. take care and good luck.. annie

Response:

well, i will tell you honestly. my experience was with azathioprime, very similar to 6-mp.  my experience was a bad one. i had major muscle group soreness that left be bed-ridden until the drug wore off.  when we tried it again, i got what felt like chest pains, i thought i was having a heart attack.  my g.i. warned me of these side effects but felt they are rare.  they are, until they hit you.  these can occure with no warning, and they did with me.  so i guess they are rare, but they certainly hit me. i used pentasa, which just releases a little earlier in the g.i. track.  i don’t know how much good it was doing. i am on methotrexate and remicade now.  i am in remission and i am able to tolerate the mtx pretty well. i had been getting bloods every 2 weeks on the aza.  i get bloods every month on mtx. jeff

– Hide quoted text — Show quoted text -> My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

Response:

I have left sided UC.  I was diagnosed in June ‘03.   I have been on a prednisone yo-yo since being diagnosed.  I have been on 6MP for 6 weeks now and I am doing fine.  I have not noticed any side effects.  My blood tests have shown that everything is doing good.  I am still at 35mg of prednisone and tapering down.  I also take 12 asacols a day and a Librax before each meal (I also have IBS).  My bleeding seems to have stopped and number of BM’s is down.  I am hoping that the 6MP will be able to keep me in remission and that I can get off the prednisone.  Every time I get to a low dose of prednisone I flare up again. I believe the side effects of the 6MP will be less than the side effects of long term high dose prednisone! Rod

– Hide quoted text — Show quoted text -> My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

Response:

I’m now on 100mg of 6MP (originally at 50mg) and most have few in any side effects if they can tolerate the drug in the first place (your blood tests will demonstrate this within the first week). And…as a fellow Type A personality, I can tell you that you *can* manage your mind much more than you think when it comes to UC (I assume that’s your condition). You gotta psych yourself up before work every day along with all the other things you do. But once in a while when things go awry it’s nice knowing that I have a change of clothes with me at all times (at the desk–not the car). To hell with the additional cost of the 6MP–this is your health, what’s more important than that?

– Hide quoted text — Show quoted text -> My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

Response:

Hi, I am on Pentasa (similar to Asacol) and 6MP.  I have had some minor problems with the 6MP, especially if the dosage is too high.  The monthly blood work is crucial for me for this reason.  Many others can graduate to less strict monitoring once they are stable on a dosage.  My nutritionist has been instrumental in recommending supplements to take to help my liver cope with metabolizing the 6MP.  For me it is all worthwhile because it has brought my fistulizing CD into remission.  Good luck! :)  mgbio – Hide quoted text — Show quoted text – > My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 > months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, > stressful job, and work for a large corporation and my condition seems > to be getting worse (still mild compared to most of you), spending > more time in the bathroom (making me consistently later for work and > people notice), harder to control bowels, and fatigue/nausea/weakness > are worse (in part to IBD and medicine). It’s the first time I’m > really experiencing the quality of my life deteriorating like I read > about on here all the time. > I’m nervous about stepping up to a stronger drug (he recommended 6-MP) > after next colonscopy to see if my colon inflammation has been > reduced. I will do what it takes to avoid steroids and surgery and > have started sleeping more, eating better, and exercising as much as > possible (really hard when all you want to do is lay down and relax). > My Gastro. thinks my type A personality and anxiety are making my > condition worse and it may contribute, but I think you can only manage > your mind so much. > Please share your experiences of going from Asacol to 6-MP or about > 6-MP in general. I am especially about the side-effects, cost (10 > co-pay for Asocal now), and whether or not monthly blood tests will > give me know choice but to tell my boss (gastro. advised me not too, > but the numerous medical appt’s are getting suspicious, don’t want it > to affect my compensation and reputation).

Response:

My Gastro. upped my Asacol intake to 9 pills daily from 6 (400mg) 3 months ago. I was diagnosed in March ‘03. I’m 28, have a high-profile, stressful job, and work for a large corporation and my condition seems to be getting worse (still mild compared to most of you), spending more time in the bathroom (making me consistently later for work and people notice), harder to control bowels, and fatigue/nausea/weakness are worse (in part to IBD and medicine). It’s the first time I’m really experiencing the quality of my life deteriorating like I read about on here all the time. I’m nervous about stepping up to a stronger drug (he recommended 6-MP) after next colonscopy to see if my colon inflammation has been reduced. I will do what it takes to avoid steroids and surgery and have started sleeping more, eating better, and exercising as much as possible (really hard when all you want to do is lay down and relax). My Gastro. thinks my type A personality and anxiety are making my condition worse and it may contribute, but I think you can only manage your mind so much. Please share your experiences of going from Asacol to 6-MP or about 6-MP in general. I am especially about the side-effects, cost (10 co-pay for Asocal now), and whether or not monthly blood tests will give me know choice but to tell my boss (gastro. advised me not too, but the numerous medical appt’s are getting suspicious, don’t want it to affect my compensation and reputation).

Response:

Question:

- Hide quoted text — Show quoted text – > I don’t think it’s barbaric. It’s not too painfull a procedure, at least in > my case it isn’t. > I asked the doctor about the sedation. He said it’s not a problem to get one > (although it’s not a total sedation), but he preferes not to give it. > Reason: although not likely, it is possible that something goes wrong during > the colonoscopy. It’s possible to damage or even puncture the colon. When > the patient is awake he can constantly give feedback: "this is starting to > hurt a bit, this doesn’t feel good, back up a little". Things like that. > And during the scope it’s possible to talk to your doctor. The professor of > the department was called in to look along and I was able to tell him about > my meds and the current complaints I have. > My scope didn’t go that well by the way. Turns out there is a lot of scar > tissue / narrowings in the last part of the colon. Still have to get the > result from my doc. But I think my bad health of the last months were caused > by the narrowings, not by active disease (so the high dose of prednisone was > probably not right either). > — > Martin > The Netherlands > http://home.wanadoo.nl/m.dahlhaus/ > hi martin

i am sorry your scope didnt go that well..but if its not active disease at leat that is something.. i am not put totally under either cos i have epilepsy..for one thing..but i am given enough versed and demerol that i really dont care what happens..i can also talk to the doctor while undergoing it..a couple of times i have worn my glasses and watched the monitor as well…i am having one in january when we visit boston..not looking forward to it..but now its at the point where the prep is the worst of the whole thing..that and waiting in that cold waiting room in that skimpy jonny and having to pee…which i always do…on and off the stretcher clutching my jonny ..i call them ‘jillies’ cos its for me a female..anyway..its not fun…but not barbaric either.. take care martin..we are still hoping to get to see u ..when alan has his sabbatical.. hugs..annie

Response:

Well, I’m not going anywhere ;-) — Martin The Netherlands http://home.wanadoo.nl/m.dahlhaus/ – Hide quoted text — Show quoted text -> take care martin..we are still hoping to get to see u ..when alan has > his sabbatical.. > hugs..annie

Response:

more power to you, martin. just wanted to say that there’s nothing wrong with sedation.  (im purposely not talking about my scope saga now…long story) but i HAVE had a sigmoidoscopy, and it was EXCRUTIATING.  But that was just me. I screamed at the top of my lungs.  There’s no way my doctor will touch me without me being sedated ever again. we all have our own thresholds. :) peace

Response:

Of course, when you’re in a lot of pain during a scope there’s nothing wrong with being sedated. But when it’s just a bit uncomfortable then the docs in the Netherlands advice not to be sedated. The doctor did say I must have a high pain threshold… cause it didn’t look too good in there ;-) — Martin The Netherlands – Hide quoted text — Show quoted text -> more power to you, martin. > just wanted to say that there’s nothing wrong with sedation.  (im > purposely not talking about my scope saga now…long story) but i HAVE > had a sigmoidoscopy, and it was EXCRUTIATING.  But that was just me. I > screamed at the top of my lungs.  There’s no way my doctor will touch > me without me being sedated ever again. we all have our own > thresholds. > :) peace

Response:

I don’t think it’s barbaric. It’s not too painfull a procedure, at least in my case it isn’t. I asked the doctor about the sedation. He said it’s not a problem to get one (although it’s not a total sedation), but he preferes not to give it. Reason: although not likely, it is possible that something goes wrong during the colonoscopy. It’s possible to damage or even puncture the colon. When the patient is awake he can constantly give feedback: "this is starting to hurt a bit, this doesn’t feel good, back up a little". Things like that. And during the scope it’s possible to talk to your doctor. The professor of the department was called in to look along and I was able to tell him about my meds and the current complaints I have. My scope didn’t go that well by the way. Turns out there is a lot of scar tissue / narrowings in the last part of the colon. Still have to get the result from my doc. But I think my bad health of the last months were caused by the narrowings, not by active disease (so the high dose of prednisone was probably not right either). — Martin The Netherlands http://home.wanadoo.nl/m.dahlhaus/ – Hide quoted text — Show quoted text ->>What’s all this about IV’s in the other posts? >>I’ve had several colonoscopies over the years >but was never sedated >>they asked me if I wanted to be sedated, but as I was alone in the hospital >>and came there by car I declined. >>It’s not comfortable, but I’ve survived it so far ;-) >>And when not sedated you can watch the whole thing on a monitor, including >>tissue samples <G> >>Not trying to scare you by the way, you’ll be fine. The prep is the worse >>part, and maybe the bloated feeling afterwards… >>I’m going to faint now… I’m a little bit hungry… ;-) >>– >>Martin > Dear Martin: >   I’m sorry, but that does sound a bit barbarric to me.  Thank God that in this > country sedation is the standard.  In fact you usually  have to ask to NOT be > sedated!  I won’t have one without it!  Be well and good luck tomorrow! God > bless. > Love. >   Margie > CD Class of 67 > UC Class of 96

Response:

actually don, you never mentioned the prep, but in all honesty, that is the worst of it. did you ever have an iv?  it is that simple, you get a "cocktail"in your arm and you might even get to watch the montor if you ask the doc nice.  you won’t feel a thing. probably 2 worst things, yet they are mearly minor inconveniences.  i had a sore b hole the next day.  felt like i had gotten "reamed".  it was uncomfortable, took nothing and it was gone in a day.  the air the blow in to you, you end up "farting" out afterwards, again, minor inconvenience. believe me, you will likely want to eat after, go for it. i have been thru many tests and exams, this one is by far NOT the worst, not even a close second! good luck to you, sit back, relax, don’t worry.  you get thru the prep, the rest is a piece of pie…err, i mean cake. jeff

– Hide quoted text — Show quoted text -> I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

Response:

> I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

Hi Don. Had it done twice. This was my experience: *** Step 1. Insert IV. It usually doesn’t hurt until you’ve had about 100 a year and your veins are trashed. Once it’s in, it’s over. No pain. Don’t worry. You’ll only feel a quick pain, and it doesn’t even last a second. After years and years of IVs your veins will become deteriorated and it will hurt, the veins will bust and clot, like mine do. It’s not fun. The best thing to do to insure that you have no problems is to keep water constantly going thru the IV. It keeps the channel opened clearly and avoids clotting. Pumping drugs thru a clotted veins HURTS. Don’t listen to that garbage about "fluid lock;" it doesn’t usually work for longer than 10-30 minutes. *** Step 2. Waiting. You’ll probably be wheeled into a tiny cubicle where everyone is waiting to have their colonoscopies. I hate waiting. *** Step 3. Getting prepped. They’ll take you to the operating room. You’ll get some gas and they’ll hook you up to some GOOD drugs. *** Step 4. They’ll do the colonoscopy, but you’ll be on planet mars having dinner with Frank Zappa and Luke Skywalker. Trust me. *** It’s over. You’re recoving. All is good. -Best of wishes to ya

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> I use to Visicol tablets to clean me out….much more tolerable than > the salt water!  Good Luck!

I prefer the salt water stuff. I think it was called sodium sulfate or something. It was a lot better than drinking like 4 gallons of golytely! ;)

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Thanks for your advice. I have never had an IV in the hand and only had one once in my arm for a CT scan. It hurt. I am just very scared which is embarassing since I am 31 and male. Someone my age had a colonoscopy at the same hospital I will be having mine and died a year ago. I did not know them. They had a different doctor though. I found out they will gove me demerol and versed. What is it like when you get these? I heard the demerol burns when you get it. I have the procedure done the day before Thanksgiving at 8:00 a.m. WIll I be in pain afterwards? Will I go home and sleep all day?

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it is a piece of cake any pain you have (you may have zero) you will not remember the demerol doesnt hurt or burn going in it is given via IV typically

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Demeral can burn sometimes but when they put the demerol and versed in you won’t care.  I love this cocktail.  You shouldn’t feel any pain other than to put the iv in and then they will give you the other meds so you won’t care.  I do recommend having someone take you.  I am not allowed to drive myself after this test.  The reaction afterwards like sleeping and anything else is different with everyone.  I don’t anymore.  UM MOM Susan

– Hide quoted text — Show quoted text -> Thanks for your advice. I have never had an IV in the hand and only > had one once in my arm for a CT scan. It hurt. > I am just very scared which is embarassing since I am 31 and male. > Someone my age had a colonoscopy at the same hospital I will be having > mine and died a year ago. I did not know them. They had a different > doctor though. > I found out they will gove me demerol and versed. What is it like when > you get these? I heard the demerol burns when you get it. > I have the procedure done the day before Thanksgiving at 8:00 a.m. > WIll I be in pain afterwards? Will I go home and sleep all day?

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I had my 2nd colonscopy last week and did fine once again. Its no big deal because you’re asleep for the entire thing. I’m 27 years old and hate IVs as well but trust me, that’s the worst part of it. Just don’t look at it while they insert it or you might get sick. I’d like to point out that colonscopies are much better than a sigmoidoscopy simply because you’re asleep and don’t remember anything. There is no pain during or after the surgery. Best of luck – Hide quoted text — Show quoted text – > Thanks for your advice. I have never had an IV in the hand and only > had one once in my arm for a CT scan. It hurt. > I am just very scared which is embarassing since I am 31 and male. > Someone my age had a colonoscopy at the same hospital I will be having > mine and died a year ago. I did not know them. They had a different > doctor though. > I found out they will gove me demerol and versed. What is it like when > you get these? I heard the demerol burns when you get it. > I have the procedure done the day before Thanksgiving at 8:00 a.m. > WIll I be in pain afterwards? Will I go home and sleep all day?

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What’s all this about IV’s in the other posts? I’ve had several colonoscopies over the years (and will have one tomorrow, just finished the last glass of prep) but was never sedated. The last time they asked me if I wanted to be sedated, but as I was alone in the hospital and came there by car I declined. It’s not comfortable, but I’ve survived it so far ;-) And when not sedated you can watch the whole thing on a monitor, including tissue samples <G> Not trying to scare you by the way, you’ll be fine. The prep is the worse part, and maybe the bloated feeling afterwards… I’m going to faint now… I’m a little bit hungry… ;-) — Martin The Netherlands http://home.wanadoo.nl/m.dahlhaus/ – Hide quoted text — Show quoted text -> I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

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> I had my 2nd colonscopy last week and did fine once again. Its no big > deal because you’re asleep for the entire thing. I’m 27 years old and > hate IVs as well but trust me, that’s the worst part of it. Just don’t > look at it while they insert it or you might get sick. I’d like to > point out that colonscopies are much better than a sigmoidoscopy > simply because you’re asleep and don’t remember anything. There is no

you are right about that! > pain during or after the surgery. Best of luck

– Hide quoted text — Show quoted text -> Thanks for your advice. I have never had an IV in the hand and only > had one once in my arm for a CT scan. It hurt. > I am just very scared which is embarassing since I am 31 and male. > Someone my age had a colonoscopy at the same hospital I will be having > mine and died a year ago. I did not know them. They had a different > doctor though. > I found out they will gove me demerol and versed. What is it like when > you get these? I heard the demerol burns when you get it. > I have the procedure done the day before Thanksgiving at 8:00 a.m. > WIll I be in pain afterwards? Will I go home and sleep all day?

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it is possible (i just heard of this the other day) that you can be allergic to the plastic used for the iv.  there are more than one type, ask for a different one.  can’t say i know my plastics in iv’s.  if there is a "standard", have them try an alternate.  i hear there are alternates. jeff

– Hide quoted text — Show quoted text -> Thanks for your advice. I have never had an IV in the hand and only > had one once in my arm for a CT scan. It hurt. > I am just very scared which is embarassing since I am 31 and male. > Someone my age had a colonoscopy at the same hospital I will be having > mine and died a year ago. I did not know them. They had a different > doctor though. > I found out they will gove me demerol and versed. What is it like when > you get these? I heard the demerol burns when you get it. > I have the procedure done the day before Thanksgiving at 8:00 a.m. > WIll I be in pain afterwards? Will I go home and sleep all day?

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>terrified and have never had it done before. I am terrifed of needles >and never been put to sleep >When they give me the Demerol and Vesed will I pass out? Will it be >painful afterwards? Will I be able to walk to the car? Will I be able >to eat the next day? >What is it like when they gove you the drugs?

Dear Don;    Please don’t tear yourself up worrying.  First of all, if you are not accustomed to IV needles, so much the better.  This means that your veins are probably in terrific shape and the nurse will have no problem getting the IV in.  So you will feel little to no pain. (By  the way, you are talking to a big baby here who has had CD for over 30 years and STILL can’t get used to the tests)  Anyway….after the IV is in, as soon as the doctor is ready, he will or rather the anesthesiologist will ask you a few questions, and then, ever so gently they inject the Demerol and Versed so you neveer even feel it go in. No, you don’t just "pass out’  however, as the doctor askes you to count or something, you will fall almost immediately asleep.  Not abruptly, not frighteningly, just very gently.  Then before you know it, they will be waking you up in the Recovery Room.  They keep you there usually until you are pretty well over the anesthetic and you can tolerate a little apple juice and jello. You will feel bloated and you will need to just fart away!  That is the only way you will be able to release the pressure.  You might be a little groggy the rest of that day, but by the next day you will be more than able to eat your weight worth in turkey and stuffing etc.  So, be well, try not to worry and God bless.  Have a wonderful Thanksgiving.  OH!!!!  One more thing….if you don’t bring someone with you to drive you home they won’t do it for you that day. You have to have someone with you to drive you home.  Byeeeee!   Margie CD Class of 67 UC Class of 96

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>>What’s all this about IV’s in the other posts? >I’ve had several colonoscopies over the years >but was never sedated >they asked me if I wanted to be sedated, but as I was alone in the hospital >and came there by car I declined. >It’s not comfortable, but I’ve survived it so far ;-) >And when not sedated you can watch the whole thing on a monitor, including >tissue samples <G> >Not trying to scare you by the way, you’ll be fine. The prep is the worse >part, and maybe the bloated feeling afterwards… >I’m going to faint now… I’m a little bit hungry… ;-) >– >Martin

Dear Martin:   I’m sorry, but that does sound a bit barbarric to me.  Thank God that in this country sedation is the standard.  In fact you usually  have to ask to NOT be sedated!  I won’t have one without it!  Be well and good luck tomorrow!  God bless. Love.   Margie CD Class of 67 UC Class of 96

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Don’t worry about it. When I had my barium enema, it was "supposed" to be a terribly uncomfortable procedure. I fell asleep. Ditto the colonoscopy – they sedated me so that I wasn’t aware of a thing.  I was well enough to go home a couple of hours afterwards, and ate a large meal. Honestly, it shouldn’t be a problem at all.  If anything, those couple of seconds before you fall asleed from the anaesthetic feel amazing! Duncan – Hide quoted text — Show quoted text – > I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

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Don’t be scared–it’s a safe, routine procedure. You’ll be able to walk to the car–you probably won’t even be that drowsy after a few minutes of sleeping it off before leaving the hospital. One temporary problem is that they shoot gas up your gut so you’ll be feeling very bloated for several hours–maybe even having cramps from bloating before you can expel all the gas; the whole expulsion process may take up to several hours, but after that you’ll be fine.

– Hide quoted text — Show quoted text -> I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

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Don…I think the worst part of it all is drinking the stuff the day before to flush you out. It is very salty/nasty tasting.. I learned to chill it as much as possible and stand over the kitchen sink and slam it. You will have to drink about 3/4 of a gallon of the stuff. It gives you the chills and makes you need to go right then so make sure the bathroom is always free for the first few hours.  My colonosocopy was in 1998 so I don’t know if the routine has changed at all.  I think the stuff was orange or cherry flavored but that doesn’t help the taste much.  The IV in your hand doesn’t hurt at all (just don’t watch ‘em put it in). The procedure meds just make you very sleepy. Good Luck to ya and have a good turkey day!!!  You will feel fine then..don’t forget to cheer on the Green Bay Packers too!!! Doobie

– Hide quoted text — Show quoted text -> I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

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I use to Visicol tablets to clean me out….much more tolerable than the salt water!  Good Luck!

– Hide quoted text — Show quoted text -> Don…I think the worst part of it all is drinking the stuff the day before > to flush you out. It is very salty/nasty tasting.. I learned to chill it as > much as possible and stand over the kitchen sink and slam it. You will have > to drink about 3/4 of a gallon of the stuff. It gives you the chills and > makes you need to go right then so make sure the bathroom is always free for > the first few hours.  My colonosocopy was in 1998 so I don’t know if the > routine has changed at all.  I think the stuff was orange or cherry flavored > but that doesn’t help the taste much.  The IV in your hand doesn’t hurt at > all (just don’t watch ‘em put it in). The procedure meds just make you very > sleepy. > Good Luck to ya and have a good turkey day!!!  You will feel fine > then..don’t forget to cheer on the Green Bay Packers too!!! > Doobie > I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

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Yes there are lots of other stuff to take then what you had.  I prefer the pills Visacol.  They are big and there’s a lot of them but no taste at all. UM MOM Susan

– Hide quoted text — Show quoted text -> Don…I think the worst part of it all is drinking the stuff the day before > to flush you out. It is very salty/nasty tasting.. I learned to chill it as > much as possible and stand over the kitchen sink and slam it. You will have > to drink about 3/4 of a gallon of the stuff. It gives you the chills and > makes you need to go right then so make sure the bathroom is always free for > the first few hours.  My colonosocopy was in 1998 so I don’t know if the > routine has changed at all.  I think the stuff was orange or cherry flavored > but that doesn’t help the taste much.  The IV in your hand doesn’t hurt at > all (just don’t watch ‘em put it in). The procedure meds just make you very > sleepy. > Good Luck to ya and have a good turkey day!!!  You will feel fine > then..don’t forget to cheer on the Green Bay Packers too!!! > Doobie > I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

Response:

I am having one the day before Thanksgiving at 8:00 a.m. I am terrified and have never had it done before. I am terrifed of needles and never been put to sleep. I am having it for constipation and bloating that has lasted over a year. When they give me the Demerol and Vesed will I pass out? Will it be painful afterwards? Will I be able to walk to the car? Will I be able to eat the next day? What is it like when they gove you the drugs? This is embarassing. I am a male and 31 years old but I am scared.

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Hi Don.  I think we were all scared the first time but don’t worry it’s not bad.  You will get a iv put in so just don’t look when it’s done.  When they put you to sleep you won’t feel a thing.  After you wake up they take you by wheel chair outside for your driver to take you home.  You can not drive yourself as you will still be sleepy probably.  When you get home if your tired sleep but you are probably going to want to eat first.  You should be fine afer the test other than maybe a little tired until all the med is out. Try to drink so you can flush it out of you.  As for eating the next day too you shouldn’t have any problems enjoying yourself.  The only needle will be the iv anything else should be put through it.  Just try to relax about it and you will be ok.  My son, who was 23 and feared needles was given gas to chill him out for the iv and then he didn’t have any problems except hunger and being tired.  He was in the army at the time.  Good luck with the test and have a Happy Thanksgiving.  UM MOM Susan

– Hide quoted text — Show quoted text -> I am having one the day before Thanksgiving at 8:00 a.m. I am > terrified and have never had it done before. I am terrifed of needles > and never been put to sleep. I am having it for constipation and > bloating that has lasted over a year. > When they give me the Demerol and Vesed will I pass out? Will it be > painful afterwards? Will I be able to walk to the car? Will I be able > to eat the next day? > What is it like when they gove you the drugs? > This is embarassing. I am a male and 31 years old but I am scared.

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Question:

: The baggage reclaim wasn’t too far, so everything seemed to go quickly. : Had to wait for the luggage for a moment though, but the good thing with : small flights like these are that there is really _no way_ they can : screw it up. You might think so, but just a few weeks back a friend of mine flew Tampere-Copenhagen on an Air Botnia Saab 2000 identical to yours. He was told he couldn’t take his (IATA-sized) carry-on bag containing his laptop on board, so he put it in the hold… and he never saw it again.  Total damages awarded: 400 euros.  Whee. I’m flying HEL-CPH-SIN on SAS tonight, and will be holding on to my gear with both hands… Cheers, — Jani Patokallio  >O._,  A jug of wine, a loaf of bread, and Thou!

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<SNIP> > Did the check-in. Person at the counter advised that she can’t > check me or my bag through to Newark, and that I had to pick my > luggage up at Stockholm, and re-check in with it.

I am surprised by this – might have something to do with the additional security requirements for USA flights. <SNIP> > Great view at the archipelago from the plane; the sea was still covered > with ice and ice roads were visible.

I have to agree. The Finland-Stockholm route is beautiful in Winter and Summer. In summer I always try to find the Silja/Viking line ferries. <SNIP> – Hide quoted text — Show quoted text -> Back to check-in, and in to the airside. > I missed the corridor leading to the right gate at first, > and went the wrong way. Arlanda seems to be bit confusing, > especially if you’re in a hurry. > But I quickly noticed that when the gate numbers didn’t seem > right at all, and turned back. > The gate for the Newark flight was pretty far away, so it > was a long walk. And that part of the airport was deserted; > there were empty halls and empty corridors, and not a single > person in sight. That makes you feel a bit unsure, if you’re > going to the right direction, especially if you don’t know > the airport, like me.

Since I use Arlanda all the time I never think of this. However it is laid out in a Strange way. Another example is that the terminals are numbers 2 to 5, with no number 1 terminal (and Number three is really only a pier). It will get better though, as they are currently re-building, and Arlanda will be split into Arlanda North and Arlanda South, with the piers labelled with a Character. You went out via the F pier – which is used for Non-schengen flight just now. The long walk you had to the plane will shortly be replaced by an equally long walk, but with shops and open spaces, etc. > The flight was about half full. There were a lot of empty > seats everywhere, which is a big difference compared to > British Airways, which I’ve usually flown before to the US.

In the last 3 months, almost every flight I’ve been on has been half empty. Before that almost all was full. I think SAS are hurting bad. > The plane looked a bit crummy, and dirty. Maybe it was one > of the older ones. It was a 767.

Been there, done that. Their 767’s are really past their sell by date. They have not invested in the inside or the outside, as they are to be replaced soon (in fact one of the USA routes, not sure if its ORD or EWR from Stockholm,has already been replaced with a brand spanking new A330). > And I do like the BA’s entertainment system better, where > each seat has a screen. I guess the other one’s OK, if you > happen to sit in the right seat, but many times you don’t.

The A330 will be a big difference – seat back screens, with lots of movies, features, games, moving maps and real life camera’s (forward and down). Flew on a SAS A340 to Japan, and it was a BIG difference. > Why is it that no matter where I sit, I’m usually one of the last > people on my flight to get through immigration? It’s not that > I take long there, but I always get the line that’s the slowest.

I know the feeling – but then again it’s not limited to immigration with me – supermarkets, banks, McDonalds, etc, etc, etc > Here is a big difference with the customs between the US > and the European countries I’ve been in. In the US, they > seem to pick people for inspection continuously, whereas this > is not the case in Europe, especially in Finland. Here they > pick people pretty much only if they suspect something.

Haven’t been stopped in the USA or Europe for over 9 years, so can’t comment > Good view though; I could see Manhattan from the terminal. Nice > rocking chairs too. Great idea, they should do that at other > airports too.

Last time I was in EWR, I went to the SAS lounge, had the SAS 767 directly outside the lounge window, leaving just enough space to see the IKEA store. Hardly felt like flying after that as I was already in Sweden.. > Didn’t sleep a bit in the plane. I can never sleep in the plane, > I don’t know why. It’s not that I’m nervous. Maybe I should try > those noise-cancelling headphones, if it’s the noise that > bothers me.

Try eye shades and ear plugs. You still don’t sleep much, but its a lot better than without (and cheaper than the headphones). > So, in order to keep me occupied, when everyone was asleep, I > went to the bathroom and looked through everyhing that was there. > Has anyone ever noticed, how much stuff there actually is there? > I mean, there’s paper, then there’s another kind of paper, > trash bags, sanitary napkins (not that I need those). Then there > was air refreshener (had to try that too), different kinds of > soap. Toilet bowl liners… They thought of everything. Too > bad there wasn’t a window, or I would’ve just stayed there. > Nice and quiet, privacy, and sometimes more room than in your > own seat. A new class is born; toilet class.

You should try and visit the front toilets on SAS’s renovated MD80/90’s, their 737’s and A321’s. You would even have a window view to keep you happy in toilet class. Joking aside, their toilets are far and away the best I’ve ever seen (wood panelling, space, windows, etc). > All in all; SAS was slightly worse in my book than British > Airways. But only because of food and entertainment system.

Years since I’ve flown long distance on BA, but I’m sure you’re right. The A330 will make a big difference, and I must say, a A330/767 size (width) of plane beats a 777/747/MD-11 for me. > Previously I’ve flown British Airways HEL-LHR-JFK, but this > seemed to be a much better route. I saved money and a lot > of time with this routing. Sometimes it does pay to go > for the smaller airports, instead of the big ones.

You sound like a perfect target for Ryanair !!!! Good report GinGan – Hide quoted text — Show quoted text -> — > Mikko Peltoniemi; Film & Video Editor, Avid Technician > Looking to edit in the US or Finland. > http://editor.is.dreaming.org

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> I am surprised by this – might have something to do with the additional > security requirements for USA flights.

I don’t understand it, though. I think you don’t have to do it flying through Copenhagen.  > I have to agree. The Finland-Stockholm route is beautiful in Winter  > and Summer. In summer I always try to find the Silja/Viking line  > ferries. Saw a couple, just outside of Stockholm… Plus saw the iceroads too: http://mikkopel.dyndns.org:1000/maailmalta/maailmalta.html#b22-vayla > flight just now. The long walk you had to the plane will shortly be replaced > by an equally long walk, but with shops and open spaces, etc.

Ok, so that’s why it was all deserted? I guess, in the future, when they finish the terminal and the shops open, there will be more people. But now it was just weird, when no-one was around… > Been there, done that. Their 767’s are really past their sell by date. They > have not invested in the inside or the outside, as they are to be replaced > soon (in fact one of the USA routes, not sure if its ORD or EWR from > Stockholm,has already been replaced with a brand spanking new A330).

You mean they are already replacing them? Well, I guess if you want to keep up in times, it’s about time to start offering the new entertainment systems already. Especially since it will take a while (and money) to replace all of the planes. Good thing anyway, so I don’t have to buy a laptop just for entertaining myself on a plane! > Haven’t been stopped in the USA or Europe for over 9 years, so can’t comment

I’ve been only stopped once, but still every time I go I see the customs people pulling passengers off the line, and I’ve never seen that in Europe. > You should try and visit the front toilets on SAS’s renovated MD80/90’s, > their 737’s and A321’s. You would even have a window view to keep you happy > in toilet class. Joking aside, their toilets are far and away the best I’ve > ever seen (wood panelling, space, windows, etc).

Why is that anyway that usually there aren’t windows there? Maybe people don’t like it, and feel like they’re being watched. :) > You sound like a perfect target for Ryanair !!!! Good report

Oh no way! :) — Mikko Peltoniemi; Film & Video Editor, Avid Technician Looking to edit in the US or Finland. http://editor.is.dreaming.org

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I’ll put some pictures from this trip on my home page next week, when I get them developed. That is, if they’re any good… The address is at the bottom. I arrived at the airport on March 28th for a morning flight to Stockholm with Air Botnia less than an hour early. Turku airport is small, pretty much all the flights that leave are Air Botnia’s flights to Stockholm and Copenhagen and Finnair’s flights to Helsinki. Only a handful of people were at the caf

Question:

 I guess my Higher Power lets me pout for awhile, then shows me the gifts…. ((((((Donnah))))))  The pouting is called a "pity party" and we all need them from time to time.  I think we need pity parties because they drain out enough of our unessential junk that just brings us down.  When the junk is drained out, we are ready to see things as they really are.  There are good reasons for our down times. You have a wonderful way of expressing your feelings, Donnah and because of that you will get through all of your turmoils in  good shape!  You go girl!! I’m so glad Nick saw the light and is now able to see how much he truly values you. Have fun picking out that wonderful new crutch!  I love my forearm crutches!  They were so much easier than a walker or the regular crutches when I was not able to put weight on my leg. Take care Donnah!! Carol

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Carol, thank you, thank you!!  I also chose the forearm crutches, but will be using just one for my left side. I was so thrilled at the difference in my posture and less pain in the back and hip …and I am finding out there is a greater side to Nick then I knew existed…it probably got lost in the turmoil of all the surgeries, infections, etc…..so instead of leaving him ’cause his attitude stunk, I am staying in this comfortable old home….we are taking it very slowly and that makes me very content….. donnah

– Hide quoted text — Show quoted text – >  I guess my Higher Power lets me pout for awhile, then shows me the > gifts…. > ((((((Donnah))))))  The pouting is called a "pity party" and we all > need them from time to time.  I think we need pity parties because > they drain out enough of our unessential junk that just brings us > down.  When the junk is drained out, we are ready to see things as > they really are.  There are good reasons for our down times. > You have a wonderful way of expressing your feelings, Donnah and > because of that you will get through all of your turmoils in  good > shape!  You go girl!! > I’m so glad Nick saw the light and is now able to see how much he > truly values you. > Have fun picking out that wonderful new crutch!  I love my forearm > crutches!  They were so much easier than a walker or the regular > crutches when I was not able to put weight on my leg. > Take care Donnah!! > Carol

Response:

Donnah, you always amaze me at the way you manage to bring humor into even your whines and the way you have of so beautifully saying what you are going through.  Even more so, I am inspired by the way you manage to so quickly turn to the positive.  And it is wonderful that this has at least brought some healing for you and Nick.  Something good coming out of such difficulties is a real gift. (((((Donnah))))) — Nann remove the Gator cheer to email me I like nonsense; it wakes up the brain cells. – Dr Suess

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Yahoooooooo!!! Really good to read this Donnah!  May Nick continue to be gentle and may you both find new love and respect for each other!!! Hugs! Donna G

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…..so instead of leaving him ’cause his attitude stunk, I am staying in this comfortable old home….we are taking it very slowly and that makes me very content….. donnah Donnah, that is the very BEST news! Best wishes to you both. Gwen

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thanks…at this point I ‘m just glad I have some one to do windows LOL…sorry, warped aren’t I.. it’s actually been all right…he still has his head and I have some of mine ..and he has started a new job…going back to wok with behaviorally disturbed kids….and I HELPED!!…if he could handle me the past month, he can handle anything.. seriously, he was offered top salary to go to work there..2nd shift which is what I will be working when I return although our days off are not the same….won’t  have time to do anything but be friendly :)

– Hide quoted text — Show quoted text -> Yahoooooooo!!! > Really good to read this Donnah!  May Nick continue to be gentle and may > you both find new love and respect for each other!!! > Hugs! > Donna G

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Gwen, thank you! donnah

– Hide quoted text — Show quoted text -> …..so instead of leaving him ’cause his attitude stunk, I > am staying in this comfortable old home….we are taking it very slowly and > that makes me very content….. > donnah > Donnah, that is the very BEST news! Best wishes to you both. > Gwen

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Thank you, Nann. I have much to be grateful for…so very much. donnah

– Hide quoted text — Show quoted text -> Donnah, you always amaze me at the way you manage to bring humor into even > your whines and the way you have of so beautifully saying what you are going > through.  Even more so, I am inspired by the way you manage to so quickly > turn to the positive.  And it is wonderful that this has at least brought > some healing for you and Nick.  Something good coming out of such > difficulties is a real gift. > (((((Donnah))))) > — > Nann > remove the Gator cheer to email me > I like nonsense; it wakes up the brain cells. – Dr Suess

Response:

Happened to run into my old neurologist today [that is one sweet man]. His specialty is MS and I was surprised to see him as he has retired. He told me he only comes in one day a week for research now — all of his patients have been sorted to others. So I asked him. He said maybe I meant Zocor [it is a drug for high cholesterol]. He says they have found cholesterol drugs seem to help with MS energy. Although drugs for depression are given too for depression. Still haven’t looked for that article which was posted here but at least we will be looking for the right drug. :) Duckie

… Zoloft helping MS patients

Response:

I take Zocor for Cholesterol, and you must have your liver checked the same as with some of the arthritis medications. Gwen

Response:

Tell Nick prayers are ongoing for success on his new job. You two having the same work hours will be good. Gwen

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Duckie, thanks! I’ll google asap…donnah

– Hide quoted text — Show quoted text -> Happened to run into my old neurologist today [that is one sweet man]. > His specialty is MS and I was surprised to see him as he has retired. He > told me he only comes in one day a week for research now — all of his > patients have been sorted to others. So I asked him. > He said maybe I meant Zocor [it is a drug for high cholesterol]. He says > they have found cholesterol drugs seem to help with MS energy. Although > drugs for depression are given too for depression. > Still haven’t looked for that article which was posted here but at least > we will be looking for the right drug. :) > Duckie > … Zoloft helping MS patients

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>.2nd shift which is >what I will be working when I return although our days off are not the >same..

Sugar-With this new diagnosis, do you think it might be time to apply for SS Disability.  I know you dont want to give in to what is happening to your body, but maybe conserving your resourse, should be moved up your list of priorities?  Just a thought. Char "Remember, I’m pulling for ya’.  We’re all in this together."  Red Green

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I’m thinking too, Char….really want to wait until my follow up with the neuro so I can make an "informed decision". ….or at least something close to it donnah

– Hide quoted text — Show quoted text ->.2nd shift which is >what I will be working when I return although our days off are not the >same.. > Sugar-With this new diagnosis, do you think it might be time to apply for SS > Disability.  I know you dont want to give in to what is happening to your body, > but maybe conserving your resourse, should be moved up your list of priorities? >  Just a thought. > Char > "Remember, I’m pulling for ya’. >  We’re all in this together."  Red Green

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> I’m thinking too, Char….really want to wait until my follow up with the > neuro so I can make an "informed decision". > ….or at least something close to it > donnah

I’m glad to hear you’re thinking about it.  Whichever way it goes for now, it can help to come to terms with the possibility. — Nann remove the Gator cheer to email me I like nonsense; it wakes up the brain cells. – Dr Suess

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Nann, it hurts my hair to think so hard…but, I have to be realistic…falling because of my knee giving out is not a good thing…and I drove yesterday and it dislocated..mucho pain putting it back…now have an elephant leg..can’t stand ice so I did the heat thing today and the pee pill and the swelling is some what better.. ..and found out that once I start meds for the MS it can make the surgery more dangerous…but they can watch for the fever from the happy gas ((Nann)) I bragged too much about the weather…I have my heat on now!…well, that will teach me to crow within earshot of Mother Nature… praying you and Mike are feeling safe and good and hopeful and patient donnah

– Hide quoted text — Show quoted text -> I’m thinking too, Char….really want to wait until my follow up with the > neuro so I can make an "informed decision". > ….or at least something close to it > donnah > I’m glad to hear you’re thinking about it.  Whichever way it goes for now, it > can help to come to terms with the possibility. > — > Nann > remove the Gator cheer to email me > I like nonsense; it wakes up the brain cells. – Dr Suess

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>..falling because of my knee giving out is not a good thing…and >I drove yesterday and it dislocated..

Your knee dislocated and you put it back in place yourself?  Oh, damn, damn, DAMN that must have hurt. You are way tougher than I am girl. Char "Remember, I’m pulling for ya’.  We’re all in this together."  Red Green

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LOL..not tougher..just wanted to get home asap…and I wasn’t doing the firemen bit again no matter how good looking they are…hmmm, was in more pain then I thought if I didn’t want them around <G> it’s better today although it could pass as a ham hock… donnah

– Hide quoted text — Show quoted text ->..falling because of my knee giving out is not a good thing…and >I drove yesterday and it dislocated.. > Your knee dislocated and you put it back in place yourself?  Oh, damn, damn, > DAMN that must have hurt. > You are way tougher than I am girl. > Char > "Remember, I’m pulling for ya’. >  We’re all in this together."  Red Green

Response:

My grandson’s shoulder dislocated twice in a basketball game, and he got it back both times, but the muscles in his arm and back were very sore for a couple of weeks.  Imagine you are going to be sore for some time too, Donnah. Sure sorry that happened. Gwen

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thanks, Gwen..I’m going to charm school for old gimps soon…donnah

– Hide quoted text — Show quoted text -> My grandson’s shoulder dislocated twice in a basketball game, and he got it > back both times, but the muscles in his arm and back were very sore for a > couple of weeks.  Imagine you are going to be sore for some time too, Donnah. > Sure sorry that happened. > Gwen

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Donnah-That is just wonderful news about you and Nick.  That has got to have removed a huge stone from you heart and mind. You are an amazing lady, and you are going to come through this with flying colors.  You have been thru worse and survived.  You will come thru this too. Prayers continuing for you Sweetie. God Bless- Char "Remember, I’m pulling for ya’.  We’re all in this together."  Red Green

Response:

My heart is lifted at the news about Nick. Looks like he grew tall during that ER visit. And even better — it showed you both how much he loves you. Better days are coming. While I can still remember it — days ago, I heard a tidbit on the news about Zoloft helping MS patients with their symptoms. Can someone route out that bit of medical info for Donnah. To tired to at the moment — physical therapy was this afternoon and since 8:30am there has been banging going on in the downstairs bathroom. Looks like the medicine cabinet, counter top and sink cabinet, lots of wall and the tiles that covered them are all in the dumpster. Tub is still there — guess that is tomorrow’s work. Hugs to you Donnah. Sorry my mind trailed off like that. Duckie – Hide quoted text — Show quoted text – > Thanks to all of you for the hugs and cards and emails and love and > support….I am swimming out of this ocean of depression toward the > shoreline….am so grateful for all of you.. > each of you has a unique gift in the way you give support and advice…and > that is so good…as I need it, it is provided at just the right time… > what a talented and giving family we are… > …you dried my tears and gave me hope > …you helped me believe in my ability to handle it > …you were unconditional in your love > …you were tolerant of my tantrums–aka CoJo > …you surrounded me with the protection of a family that has been there, > done that and that’s more precious than gold or chocolate > all of you stay in my prayers, my sunset songs, my mediations….for > foot-stomping joy…for trust in yourself and your Higher Power…for > gratitude that life is still to be enjoyed…that you know that you are > loved by a group of people who choose to love, forgive, accept… > I am rich > …I did not win the lottery yet > …seeing double gives me many more wildflowers to see > …"          "          "        ” more cardinals and chickadees > … ditto for stud muffins, lobster boys, and the cabannas > It also makes me read my beloved books slowly enough to truly grasp the > meanings and/or develop my own > The fuzzy thinking has cleared many of my intolerances and prejudices…ones > that I didn’t know I had ! > Hopefully I will get my new crutch soon and will have the security of more > than the toothpick I am using…and my RD encouraged me to go to my DME > place and get what I felt comfortable with…not telling me what to get > And this is a BIGGIE…Nick went through a shock when they were working on > me at the ER and the days following…when he realized that he may lose me > in a different way than just moving out…he asked me to forgive him for his > past actions and volunteered to take care of me no matter what….this after > the neuro told him I would need extra help until they finalized the dx and > started treatment…he never left my side except to eat and go home to > sleep.. > he has treated me with respect..has made no complaints..we have learned to > laugh together again.. > …we have a budding FRIENDSHIP….I do not think of what may or may not > develop… > …we are sharing our joy at the first grandchild being born > …baseball has started—did you see me throw out the >    first ball? LOL…girl throw! > I guess my Higher Power lets me pout for awhile, then shows me the gifts…. > as Fra Giovanni said in the 1500 hundreds…." everything we call a trial, a > sorrow or a duty, believe me..the gift is there and so is the wonder of an > overshadowing presence." > donnah > — > If You Are Going Through Hell… > Keep Going!

–   _(‘>  (_<_)           _   _(‘< -quack  (_<_)     _    __(‘< *QUACK!* <_{__)   _(‘< "|,,|_"  (_<_)   _(‘< "AFLAC!"  (_<_)

Response:

{{{{{Donnah}}}}} So glad to hear the good news.  Sometimes it takes a "wake-up call", doesn’t it? Cindy R.

– Hide quoted text — Show quoted text -> Thanks to all of you for the hugs and cards and emails and love and > support….I am swimming out of this ocean of depression toward the > shoreline….am so grateful for all of you.. > each of you has a unique gift in the way you give support and advice…and > that is so good…as I need it, it is provided at just the right time… > what a talented and giving family we are… > …you dried my tears and gave me hope > …you helped me believe in my ability to handle it > …you were unconditional in your love > …you were tolerant of my tantrums–aka CoJo > …you surrounded me with the protection of a family that has been there, > done that and that’s more precious than gold or chocolate > all of you stay in my prayers, my sunset songs, my mediations….for > foot-stomping joy…for trust in yourself and your Higher Power…for > gratitude that life is still to be enjoyed…that you know that you are > loved by a group of people who choose to love, forgive, accept… > I am rich > …I did not win the lottery yet > …seeing double gives me many more wildflowers to see > …"          "          "        ” more cardinals and chickadees > … ditto for stud muffins, lobster boys, and the cabannas > It also makes me read my beloved books slowly enough to truly grasp the > meanings and/or develop my own > The fuzzy thinking has cleared many of my intolerances and prejudices…ones > that I didn’t know I had ! > Hopefully I will get my new crutch soon and will have the security of more > than the toothpick I am using…and my RD encouraged me to go to my DME > place and get what I felt comfortable with…not telling me what to get > And this is a BIGGIE…Nick went through a shock when they were working on > me at the ER and the days following…when he realized that he may lose me > in a different way than just moving out…he asked me to forgive him for his > past actions and volunteered to take care of me no matter what….this after > the neuro told him I would need extra help until they finalized the dx and > started treatment…he never left my side except to eat and go home to > sleep.. > he has treated me with respect..has made no complaints..we have learned to > laugh together again.. > …we have a budding FRIENDSHIP….I do not think of what may or may not > develop… > …we are sharing our joy at the first grandchild being born > …baseball has started—did you see me throw out the >    first ball? LOL…girl throw! > I guess my Higher Power lets me pout for awhile, then shows me the gifts…. > as Fra Giovanni said in the 1500 hundreds…." everything we call a trial, a > sorrow or a duty, believe me..the gift is there and so is the wonder of an > overshadowing presence." > donnah > — > If You Are Going Through Hell… > Keep Going!

Response:

yeah, it does, Cindy R….that it does! donnah

– Hide quoted text — Show quoted text -> {{{{{Donnah}}}}} > So glad to hear the good news.  Sometimes it takes a "wake-up call", doesn’t > it? > Cindy R. > Thanks to all of you for the hugs and cards and emails and love and > support….I am swimming out of this ocean of depression toward the > shoreline….am so grateful for all of you.. > each of you has a unique gift in the way you give support and advice…and > that is so good…as I need it, it is provided at just the right time… > what a talented and giving family we are… > …you dried my tears and gave me hope > …you helped me believe in my ability to handle it > …you were unconditional in your love > …you were tolerant of my tantrums–aka CoJo > …you surrounded me with the protection of a family that has been there, > done that and that’s more precious than gold or chocolate > all of you stay in my prayers, my sunset songs, my mediations….for > foot-stomping joy…for trust in yourself and your Higher Power…for > gratitude that life is still to be enjoyed…that you know that you are > loved by a group of people who choose to love, forgive, accept… > I am rich > …I did not win the lottery yet > …seeing double gives me many more wildflowers to see > …"          "          "        ” more cardinals and chickadees > … ditto for stud muffins, lobster boys, and the cabannas > It also makes me read my beloved books slowly enough to truly grasp the > meanings and/or develop my own > The fuzzy thinking has cleared many of my intolerances and > prejudices…ones > that I didn’t know I had ! > Hopefully I will get my new crutch soon and will have the security of more > than the toothpick I am using…and my RD encouraged me to go to my DME > place and get what I felt comfortable with…not telling me what to get > And this is a BIGGIE…Nick went through a shock when they were working on > me at the ER and the days following…when he realized that he may lose me > in a different way than just moving out…he asked me to forgive him for > his > past actions and volunteered to take care of me no matter what….this > after > the neuro told him I would need extra help until they finalized the dx and > started treatment…he never left my side except to eat and go home to > sleep.. > he has treated me with respect..has made no complaints..we have learned to > laugh together again.. > …we have a budding FRIENDSHIP….I do not think of what may or may not > develop… > …we are sharing our joy at the first grandchild being born > …baseball has started—did you see me throw out the >    first ball? LOL…girl throw! > I guess my Higher Power lets me pout for awhile, then shows me the > gifts…. > as Fra Giovanni said in the 1500 hundreds…." everything we call a trial, > a > sorrow or a duty, believe me..the gift is there and so is the wonder of an > overshadowing presence." > donnah > — > If You Are Going Through Hell… > Keep Going!

Response:

Thanks to all of you for the hugs and cards and emails and love and support….I am swimming out of this ocean of depression toward the shoreline….am so grateful for all of you.. each of you has a unique gift in the way you give support and advice…and that is so good…as I need it, it is provided at just the right time… what a talented and giving family we are… …you dried my tears and gave me hope …you helped me believe in my ability to handle it …you were unconditional in your love …you were tolerant of my tantrums–aka CoJo …you surrounded me with the protection of a family that has been there, done that and that’s more precious than gold or chocolate all of you stay in my prayers, my sunset songs, my mediations….for foot-stomping joy…for trust in yourself and your Higher Power…for gratitude that life is still to be enjoyed…that you know that you are loved by a group of people who choose to love, forgive, accept… I am rich …I did not win the lottery yet …seeing double gives me many more wildflowers to see …"          "          "        ” more cardinals and chickadees … ditto for stud muffins, lobster boys, and the cabannas It also makes me read my beloved books slowly enough to truly grasp the meanings and/or develop my own The fuzzy thinking has cleared many of my intolerances and prejudices…ones that I didn’t know I had ! Hopefully I will get my new crutch soon and will have the security of more than the toothpick I am using…and my RD encouraged me to go to my DME place and get what I felt comfortable with…not telling me what to get And this is a BIGGIE…Nick went through a shock when they were working on me at the ER and the days following…when he realized that he may lose me in a different way than just moving out…he asked me to forgive him for his past actions and volunteered to take care of me no matter what….this after the neuro told him I would need extra help until they finalized the dx and started treatment…he never left my side except to eat and go home to sleep.. he has treated me with respect..has made no complaints..we have learned to laugh together again.. …we have a budding FRIENDSHIP….I do not think of what may or may not develop… …we are sharing our joy at the first grandchild being born …baseball has started—did you see me throw out the    first ball? LOL…girl throw! I guess my Higher Power lets me pout for awhile, then shows me the gifts…. as Fra Giovanni said in the 1500 hundreds…." everything we call a trial, a sorrow or a duty, believe me..the gift is there and so is the wonder of an overshadowing presence." donnah — If You Are Going Through Hell… Keep Going!

Response:

Question:

>Re Woolite and travelling: interesting to read everyone’s comments. A >small warning — Woolite, while great for hand-washing and more kind >to the skin than detergents, is still known in the industry as being a >threat to the dye in cotton knits and woven fabrics (fading).

Good heavens, I had no idea!  Could you direct me to a site where this can be checked out?  Appreciate your help.  (I don’t do a lot of bathroom sink washing with Woollove, but just in case…!) >The family of the cranky banker have been known to use bars of hotel >hand soap to wash small stuff. It seems to work well.

Yes, but more rinsing required.  I often do the same, actually, when traveling.  (Note: take a stopper with you; ISTR there are countries where no stopper is provided for the basin; never could figure that one out!) — Polar

Response:

>>Re Woolite and travelling: interesting to read everyone’s comments. A >small warning — Woolite, while great for hand-washing and more kind >to the skin than detergents, is still known in the industry as being a >threat to the dye in cotton knits and woven fabrics (fading).

snip Since Woolite markets a product for dark clothes I expect some damage could occur from repeated washings. Frank Matthews

Response:

Re Woolite and travelling: interesting to read everyone’s comments. A small warning — Woolite, while great for hand-washing and more kind to the skin than detergents, is still known in the industry as being a threat to the dye in cotton knits and woven fabrics (fading). The family of the cranky banker have been known to use bars of hotel hand soap to wash small stuff. It seems to work well. Cranky

Response:

– Hide quoted text — Show quoted text -> > > Have you tried one of those shop-vac barber thingies?  It seems > > > you’d do perfectly with such a bowl cut.  Me?  I tell them what I > > > want four or six times a year.  Sometimes I get it. I usually > > > like it a little bit closer than 4" under my nose though.  ;-) > > That’s not a bowl cut, it’s just a symmetrical shag.  My son has a > > flowbee, but there’s something wrong with the blade(s). > That’s what I wuz thinking about.  Symetrical shag… We had > carpets like that years ago.  ;-) > > > > I’ve had a quart of Pert Plus forever, but it makes my hair feel icky so I > > > > use Tresseme from Costco instead. > > > I’ve been using Clarol Herbal Essence since I was a kid, millions > > > of moons ago.  It doesn’t even taste all that bad (ok, I don’t > > > eat it).  My wife uses all the expen$ive junk.  I have more hair. > More hair than your wife?  Lordy.

Yeah, it’s sometimes a problem.  I don’t have long hair either. :-( – Hide quoted text — Show quoted text -> > That smells good too.  My mom hs a tiny bottle, and it’s too precious to > > waste just on hair-washing.  So they still make it? > You may be thinking about different stuff.  This is the stuff I > used 35+ years ago.  There were other versions inbetween that > *stunk* like a skunk.  Yes the original is now available.  The > wife has no problems finding it in the supermarket.  She was > buying it a half dozen at a time when she found it, but it’s now > readily available again. > Good, I’ll get some when my gallon of Tresseme is gone. > It’s not eye friendly like baby shampoo, but it’s not so bad near > the mouth.  I have a full beard so gacky tasting things aren’t in > the plan.  My wife doesn’t so she uses gacky tasting things. ;-) > If grownups can’t wash their hair without getting soap in their eyes, they > deserve a little pain.  

Well, sometimes before the morning coffee a little pain is motivating. ;-) —   Keith

Response:

– Hide quoted text — Show quoted text -> "Sanjay Punjab" asked: > In regards to international travel, why do so many people recommend > woolite for washing clothes in a hotel sink? > Because your hands are going to be in that water.  Woolite is made for > that. > Isn’t a small bottle of liquid tide more effective in cleaning >  clothes > in a sink? > For the clothes, yes.  For your hands, no way.  Liquid Tide is NOT made > for hand washing (in either sense of the word).  Your dermatologist > will verify this, and may get to after you are done if you insist on > using it to hand wash. > Is it practical to use a small amount of liquid fabric softener when > washing clothes in the sink? > Again, same story. > Thanks > john cline ii, who hopes that helps (and who once washed dishes with > Wisk back when he was in college and ended up almost having to visit > the dermatologist…strong burning and redness, extreme drying)

But then, Wisk may be helpful for removing those annoying ink stains when Bics leak in shirt pockets on long airline flights. <r&d>

Response:

>Hmm…ISTR that shampoo is formulated differently than liquid soap for >clothes.  Anybody have the skinny on this?

You’d definitely want to use a shampoo that doesn’t leave any form of conditioner etc on the hair.  Almost all do; when you wash your hair with something that removes grease and dirt as effectively as clothes detergent, it feels like straw.  It doesn’t with shampoo, and hence…shampoo leaves stuff on there that you don’t necessarily want on your clothes.   On the other hand, clothes detergents also add stuff to the clothes that you don’t want on your hair.  Clean white clothes are not "whiter than white", they’re just white.  Those that are,  are coated with fluorescent molecules.  (That’s why so many clothes "glow" under black light in a nightclub). A bar of good old sunlight might be just as good? — Ken Tough

Response:

> But then, Wisk may be helpful for removing those annoying ink stains > when Bics leak in shirt pockets on long airline flights.

Busted. Not that a BIC would ever leak. john cline ii who notes that only about four people will understand all that, but that’s okay, and hopefully none of them use orange ink

Response:

>WTH is "Rogy?" Oh wait, I know, you got your > fingers tangled up in the wonderful wizardry > of that wireless keyboard from your WebTV > tee hee hee unit….

It’s a *tidbit* and sometimes it gets confused and thinks it’s an adult and can post on rta.  One can tell a *tidbit* by it’s *tee hee hees*.<g BTW, it have no problem with my typing skills, *ROGY*.  If it’s not your name…..why do you always respond when I use it????? Mary

Response:

> In regards to international travel, why do so many people recommend > woolite for washing clothes in a hotel sink?

My guess would be that it rinses out easily.  If you’ve ever tried to wash fabric with liquid dishwashing detergent, you know that it takes LOTS more time and water (perhaps 10x) to rinse the stuff out than it did to wash it in the first place. > Isn’t a small bottle of liquid tide more effective in cleaning clothes > in a sink? > Is it practical to use a small amount of liquid fabric softener when > washing clothes in the sink?

Why wouldn’t it be?  Other than the nuisance of carrying a bottle of it around, of course. — Cheers, Bev     He’s your god.  They’re your rules.  *You* burn in hell!

Response:

> >Hmm…ISTR that shampoo is formulated differently than liquid soap for >clothes.  Anybody have the skinny on this? > You’d definitely want to use a shampoo that doesn’t leave any > form of conditioner etc on the hair.  Almost all do; when you > wash your hair with something that removes grease and dirt as > effectively as clothes detergent, it feels like straw.  

Not necessarily.  I washed my hair with Dawn for years and then decided that I could splurge on cheap shampoo that smells good.  No difference that I can see, but my idea of hair styling is telling the cutter "make it all four inches long" and then trying to explain that three different ways because she can’t understand something that simple. I’ve had a quart of Pert Plus forever, but it makes my hair feel icky so I use Tresseme from Costco instead. — Cheers, Bev     He’s your god.  They’re your rules.  *You* burn in hell!

Response:

You are so tired. I bet you look just like the character Alice on "The Brady Bunch."

Response:

>You are so tired. I bet you look just like the > character Alice on "The Brady Bunch."

Rogy…..you really must let us know which one of us you are insulting. No fair hurting some innocent poster’s feelings if you mean me.   Dear one are you sure you are not looking into your own mirror.  I’m not tired and I sure don’t look like "Alice"! Do you? <g Mary

Response:

– Hide quoted text — Show quoted text -> >Hmm…ISTR that shampoo is formulated differently than liquid soap for > >clothes.  Anybody have the skinny on this? > You’d definitely want to use a shampoo that doesn’t leave any > form of conditioner etc on the hair.  Almost all do; when you > wash your hair with something that removes grease and dirt as > effectively as clothes detergent, it feels like straw.   > Not necessarily.  I washed my hair with Dawn for years and then decided > that I could splurge on cheap shampoo that smells good.  No difference > that I can see, but my idea of hair styling is telling the cutter "make it > all four inches long" and then trying to explain that three different ways > because she can’t understand something that simple.

Have you tried one of those shop-vac barber thingies?  It seems you’d do perfectly with such a bowl cut.  Me?  I tell them what I want four or six times a year.  Sometimes I get it. I usually like it a little bit closer than 4" under my nose though.  ;-) > I’ve had a quart of Pert Plus forever, but it makes my hair feel icky so I > use Tresseme from Costco instead.

I’ve been using Clarol Herbal Essence since I was a kid, millions of moons ago.  It doesn’t even taste all that bad (ok, I don’t eat it).  My wife uses all the expen$ive junk.  I have more hair. —   Keith

Response:

- Hide quoted text — Show quoted text -> > >Hmm…ISTR that shampoo is formulated differently than liquid soap for > > >clothes.  Anybody have the skinny on this? > > You’d definitely want to use a shampoo that doesn’t leave any > > form of conditioner etc on the hair.  Almost all do; when you > > wash your hair with something that removes grease and dirt as > > effectively as clothes detergent, it feels like straw. > Not necessarily.  I washed my hair with Dawn for years and then decided > that I could splurge on cheap shampoo that smells good.  No difference > that I can see, but my idea of hair styling is telling the cutter "make it > all four inches long" and then trying to explain that three different ways > because she can’t understand something that simple. > Have you tried one of those shop-vac barber thingies?  It seems > you’d do perfectly with such a bowl cut.  Me?  I tell them what I > want four or six times a year.  Sometimes I get it. I usually > like it a little bit closer than 4" under my nose though.  ;-)

That’s not a bowl cut, it’s just a symmetrical shag.  My son has a flowbee, but there’s something wrong with the blade(s).   > I’ve had a quart of Pert Plus forever, but it makes my hair feel icky so I > use Tresseme from Costco instead. > I’ve been using Clarol Herbal Essence since I was a kid, millions > of moons ago.  It doesn’t even taste all that bad (ok, I don’t > eat it).  My wife uses all the expen$ive junk.  I have more hair.

That smells good too.  My mom hs a tiny bottle, and it’s too precious to waste just on hair-washing.  So they still make it? — Cheers, Bev "Anonymity is a shield from the tyranny of the majority."    – U.S. Supreme Court, McIntyre v Ohio Elections,1995

Response:

> In regards to international travel, why do so many people recommend > woolite for washing clothes in a hotel sink?

pretty sure it’s just because woolite markets itself as a "hand wash" detergent, but I don’t think it really matters, just whatever detergent or soap you like, it’s all marketting. — edt

Response:

– Hide quoted text — Show quoted text -> > > >Hmm…ISTR that shampoo is formulated differently than liquid soap for > > > >clothes.  Anybody have the skinny on this? > > > You’d definitely want to use a shampoo that doesn’t leave any > > > form of conditioner etc on the hair.  Almost all do; when you > > > wash your hair with something that removes grease and dirt as > > > effectively as clothes detergent, it feels like straw. > > Not necessarily.  I washed my hair with Dawn for years and then decided > > that I could splurge on cheap shampoo that smells good.  No difference > > that I can see, but my idea of hair styling is telling the cutter "make it > > all four inches long" and then trying to explain that three different ways > > because she can’t understand something that simple. > Have you tried one of those shop-vac barber thingies?  It seems > you’d do perfectly with such a bowl cut.  Me?  I tell them what I > want four or six times a year.  Sometimes I get it. I usually > like it a little bit closer than 4" under my nose though.  ;-) > That’s not a bowl cut, it’s just a symmetrical shag.  My son has a > flowbee, but there’s something wrong with the blade(s).  

That’s what I wuz thinking about.  Symetrical shag… We had carpets like that years ago.  ;-) > > I’ve had a quart of Pert Plus forever, but it makes my hair feel icky so I > > use Tresseme from Costco instead. > I’ve been using Clarol Herbal Essence since I was a kid, millions > of moons ago.  It doesn’t even taste all that bad (ok, I don’t > eat it).  My wife uses all the expen$ive junk.  I have more hair. > That smells good too.  My mom hs a tiny bottle, and it’s too precious to > waste just on hair-washing.  So they still make it?

You may be thinking about different stuff.  This is the stuff I used 35+ years ago.  There were other versions inbetween that *stunk* like a skunk.  Yes the original is now available.  The wife has no problems finding it in the supermarket.  She was buying it a half dozen at a time when she found it, but it’s now readily available again. It’s not eye friendly like baby shampoo, but it’s not so bad near the mouth.  I have a full beard so gacky tasting things aren’t in the plan.  My wife doesn’t so she uses gacky tasting things. ;-) —   Keith

Response:

- Hide quoted text — Show quoted text -> > Have you tried one of those shop-vac barber thingies?  It seems > > you’d do perfectly with such a bowl cut.  Me?  I tell them what I > > want four or six times a year.  Sometimes I get it. I usually > > like it a little bit closer than 4" under my nose though.  ;-) > That’s not a bowl cut, it’s just a symmetrical shag.  My son has a > flowbee, but there’s something wrong with the blade(s). > That’s what I wuz thinking about.  Symetrical shag… We had > carpets like that years ago.  ;-) > > > I’ve had a quart of Pert Plus forever, but it makes my hair feel icky so I > > > use Tresseme from Costco instead. > > I’ve been using Clarol Herbal Essence since I was a kid, millions > > of moons ago.  It doesn’t even taste all that bad (ok, I don’t > > eat it).  My wife uses all the expen$ive junk.  I have more hair.

More hair than your wife?  Lordy. > That smells good too.  My mom hs a tiny bottle, and it’s too precious to > waste just on hair-washing.  So they still make it? > You may be thinking about different stuff.  This is the stuff I > used 35+ years ago.  There were other versions inbetween that > *stunk* like a skunk.  Yes the original is now available.  The > wife has no problems finding it in the supermarket.  She was > buying it a half dozen at a time when she found it, but it’s now > readily available again.

Good, I’ll get some when my gallon of Tresseme is gone. > It’s not eye friendly like baby shampoo, but it’s not so bad near > the mouth.  I have a full beard so gacky tasting things aren’t in > the plan.  My wife doesn’t so she uses gacky tasting things. ;-)

If grownups can’t wash their hair without getting soap in their eyes, they deserve a little pain.   — Cheers, Bev If he had any brains, he’d take them out and play with them.

Response:

In regards to international travel, why do so many people recommend woolite for washing clothes in a hotel sink? Isn’t a small bottle of liquid tide more effective in cleaning clothes in a sink? Is it practical to use a small amount of liquid fabric softener when washing clothes in the sink? Thanks

Response:

"Sanjay Punjab" asked: > In regards to international travel, why do so many people recommend > woolite for washing clothes in a hotel sink?

Because your hands are going to be in that water.  Woolite is made for that. > Isn’t a small bottle of liquid tide more effective in cleaning clothes > in a sink?

For the clothes, yes.  For your hands, no way.  Liquid Tide is NOT made for hand washing (in either sense of the word).  Your dermatologist will verify this, and may get to after you are done if you insist on using it to hand wash. > Is it practical to use a small amount of liquid fabric softener when > washing clothes in the sink?

Again, same story. > Thanks

john cline ii, who hopes that helps (and who once washed dishes with Wisk back when he was in college and ended up almost having to visit the dermatologist…strong burning and redness, extreme drying)

Response:

This is about as relevant to RTA as that sushi argument (six vs. eight pieces.)

Response:

> In regards to international travel, why do so many people recommend > woolite for washing clothes in a hotel sink? > Isn’t a small bottle of liquid tide more effective in cleaning clothes > in a sink?

I generally just use a basic shampoo – it works well, and saves me having to carry extra stuff.

Response:

>I generally just use a basic shampoo – it works > well, and saves me having to carry extra stuff.

I prefer to just pack a small bottle of the same detergent I use at home.  The poster was right about Tide.  We can’t use it because it is very harsh not only to hands but other parts of the body.  Many travelers have told me they prefer just using shampoo as the above poster writes. It is not harmful to the hands and will do just as good a job.  I have also used this on trips. As to Rogy……would you prefer we discuss your sushi??<g  This is relevent to rta, IMO, because I carry my detergent on the "plane" and I would guess the other posters are flyers too. Mary

Response:

WTF is "Rogy?" Oh wait, I know, you got your fingers tangled up in the wonderful wizardry of that wireless keyboard from your WebTV tee hee hee unit….

Response:

>> In regards to international travel, why do so many people recommend > woolite for washing clothes in a hotel sink? > Isn’t a small bottle of liquid tide more effective in cleaning clothes > in a sink? >I generally just use a basic shampoo – it works well, and saves me having >to carry extra stuff.

Hmm…ISTR that shampoo is formulated differently than liquid soap for clothes.  Anybody have the skinny on this? To Sanjay:  There’s a product called "Woolove" that is just the same as Woolite, but much less expensive.  All stores used to carry it right next to the Woolite, but this time I had to check a few stores before I found it.  Green bottle. As to Tide vs. Woolite, it depends partly on how dirty the clothes are.  If you’re just swishing them through to remove the daily dust and sweat, I’d go for Woolite/love; milder on the clothes. — Polar

Response:

Question:

– Cyberhugs, DianeW

– Hide quoted text — Show quoted text -> I was on the plaquenil/MTX/azulfidine combo for a couple months, and it > really finally did seem to be working and allowing me to reduce my prednisone > dosage.  Then the infections started.  When I had a resistant sinus infection, > a UTI, _and_ a skin abcess all at once, I finally had enough.  The rheumie > agreed, and we reduced the MTX to 10mg.  No infections, but it didn’t _do_ > anything other than make me want to yarf.  So we’ve dropped the MTX and the > Plaquenil because I’ve been on the highest dosage for 7 years now and need > to take a vacation from it.  Started Arava at 10mg (half dose) with no loading > dose.  I’ve had too many GI tract problems to do the normal dosing.  I’ve > registered with Amgen to get in line for Enbrel.  Hopefully, it won’t be > months (I plan to get the rheumie to sign me off for a priority spot).  If > the wait is too long, we may have to try Remicade, but it’s not a great > prospect given my problems with MTX.  After looking at the study results for > Humira, neither of us wants me to be the lab rat.  I already have lupus-like > symptoms, so Humira seems like a really bad idea in my case.  And he’s yet to > have _anyone_ want to try Kineret. > We’re ordering me a second walker to use inside the house (there’s steps > up to the porch, then a step up to the doorjamb–this is a rental house, we’re > not paying to put a ramp in here).  George is upset that I’ve fallen one too > many times in the house, so now I’ll be using a walker indoors too.  At least > the cats don’t think the walker is a toy.  A couple of my falls were from the > cats trying to play with my cane. ;} > On the other hand, we’ve had our 11th wedding anniversary, and he’s still a handicapped > now!"  Once he understood why I was getting hysterical over little nothing > things, he’s been entirely supportive ever since.  He’s currently twisting his > boss’s arm over getting me an attendant for a couple hours each day when he’s > gone on business trips.  Which means that when he gets back, the sink won’t > be full of dirty dishes and the bedroom won’t be taken over by a pile of > unwashed laundry.  Less stress for me, less stress and worry for him.  He > even threatened to not go if they didn’t pay for an attendant.  His boss, > and the boss’s boss agree, it’s corporate management that were dragging their > feet.  He doesn’t leave until February, so we have enough time to finish > re-arranging the house so I can get around unassisted. > After the two monster projects are done, the next thing on the agenda is > to start looking for a new house.  If we _owned_ our house, we wouldn’t > feel like we were wasting money to build ramps, put in a dishwasher, and > buy a front-loading washing machine.  At least this place is all on one > level, though there’s no way the walker will ever fit into the bathroom. > I haven’t been posting or even reading much lately because simply getting > through each day has taken too much out of me.  Hopefully that’ll get better. > During my adjustment phase, I’ve been using gallows humor to keep from going > totally over the edge.  George is now urging me to offer some of the artwork > I’ve done lately as tshirts (probably through CafePress).  I’ll post those > seperately. > Damn, this winter has just sucked for too many of us.  Hope we _all_ see > better days soon. > — > Head Muso, White Rats Morris, Faultline Morris > Member, Knights of Xenu (1995).  Chaos Monger and Jill of All Trades. > "A head-on collision between Morticia Adams and Martha Stewart"

Response:

{{{{{LEE}}}}}  Gosh I’m sorry to hear that things are so tough for you right now.  When I don’t see much from someone I like to think they are doing well.  I’ve been thru the walker thing in the house and it’s really helpful once you get the hang of it and some accoutrements to help you carry things. That and remembering where you left it when you get up and walk away cause you aren’t used to using it.  I actually use my manual wheelchair more in the house than I do the walker, but that’s due to the broken foot and fatigue.  I use my feet to move the wheelchair around.  I use the walker when I’m out when I can walk ok but need more help than a cane.  What kind of walker did you get?  Does it have a seat on it or a basket or such?  I really like to use the walker when I have to go someplace like the post office and I’m likely to have to stand in line.  I have a seat to sit on while I wait and a small basket to hold what I’m trying to carry.  I’ve found a clear tray also that will hold a drink!  Have you decorated it yet? The Christmas I was using mine, I had it all decorated!  Bells and all. Think of all the holidays to come to give yourself a little cheer! I hope Enbrel works for you.  It was a great thing for me.  Got me out of bed and moving again.  I had to add Arava with it this year and that’s been a good thing also.  The number of swollen joints is down to two from almost all.  I started it without the loading dose also.  Due to a bout of bronchitis I’ve had to stop both of them (last Monday) and so far nothing except fatigue has returned.  Hopefully, this will end soon. Hang in there and know we are thinking about you! — Cyberhugs, DianeW

– Hide quoted text — Show quoted text -> I was on the plaquenil/MTX/azulfidine combo for a couple months, and it > really finally did seem to be working and allowing me to reduce my prednisone > dosage.  Then the infections started.  When I had a resistant sinus infection, > a UTI, _and_ a skin abcess all at once, I finally had enough.  The rheumie > agreed, and we reduced the MTX to 10mg.  No infections, but it didn’t _do_ > anything other than make me want to yarf.  So we’ve dropped the MTX and the > Plaquenil because I’ve been on the highest dosage for 7 years now and need > to take a vacation from it.  Started Arava at 10mg (half dose) with no loading > dose.  I’ve had too many GI tract problems to do the normal dosing.  I’ve > registered with Amgen to get in line for Enbrel.  Hopefully, it won’t be > months (I plan to get the rheumie to sign me off for a priority spot).  If > the wait is too long, we may have to try Remicade, but it’s not a great > prospect given my problems with MTX.  After looking at the study results for > Humira, neither of us wants me to be the lab rat.  I already have lupus-like > symptoms, so Humira seems like a really bad idea in my case.  And he’s yet to > have _anyone_ want to try Kineret. > We’re ordering me a second walker to use inside the house (there’s steps > up to the porch, then a step up to the doorjamb–this is a rental house, we’re > not paying to put a ramp in here).  George is upset that I’ve fallen one too > many times in the house, so now I’ll be using a walker indoors too.  At least > the cats don’t think the walker is a toy.  A couple of my falls were from the > cats trying to play with my cane. ;} > On the other hand, we’ve had our 11th wedding anniversary, and he’s still a handicapped > now!"  Once he understood why I was getting hysterical over little nothing > things, he’s been entirely supportive ever since.  He’s currently twisting his > boss’s arm over getting me an attendant for a couple hours each day when he’s > gone on business trips.  Which means that when he gets back, the sink won’t > be full of dirty dishes and the bedroom won’t be taken over by a pile of > unwashed laundry.  Less stress for me, less stress and worry for him.  He > even threatened to not go if they didn’t pay for an attendant.  His boss, > and the boss’s boss agree, it’s corporate management that were dragging their > feet.  He doesn’t leave until February, so we have enough time to finish > re-arranging the house so I can get around unassisted. > After the two monster projects are done, the next thing on the agenda is > to start looking for a new house.  If we _owned_ our house, we wouldn’t > feel like we were wasting money to build ramps, put in a dishwasher, and > buy a front-loading washing machine.  At least this place is all on one > level, though there’s no way the walker will ever fit into the bathroom. > I haven’t been posting or even reading much lately because simply getting > through each day has taken too much out of me.  Hopefully that’ll get better. > During my adjustment phase, I’ve been using gallows humor to keep from going > totally over the edge.  George is now urging me to offer some of the artwork > I’ve done lately as tshirts (probably through CafePress).  I’ll post those > seperately. > Damn, this winter has just sucked for too many of us.  Hope we _all_ see > better days soon. > — > Head Muso, White Rats Morris, Faultline Morris > Member, Knights of Xenu (1995).  Chaos Monger and Jill of All Trades. > "A head-on collision between Morticia Adams and Martha Stewart"

Response:

>The jury is still out for >me on this injectible MTX.  Last weekend was a horrible blur of dizziness

Diana-Sure hope things settle down for you soon.  Maybe it is going to be time soon, to try something else?  How about Arava?  Remember Ken Mc has had a near miracle from it.  And it really helped me for a while.  Maybe you will get lucky!! Char "Remember, I’m pulling for ya’.  We’re all in this together."  Red Green

Response:

>Have you decorated it yet? >The Christmas I was using mine, I had it all decorated!  Bells and all. >Think of all the holidays to come to give yourself a little cheer!

I already have headlights on it (they’re krypton bicycle lights).  Added them after I almost got run over crossing the street one night.  Right now, I have the Gimp Jolly Roger banner hung across the backrest bar.  This one has a basket, but I found small things tended to fall through the bars, so I added a zip-up duffel bag inside the basket.  It’s black with cherries embroidered all over it. [smirk]  The guys tell me I need to add a hood ornament to the front of the basket now.  I’ve got a set of miniature cadillac fins that I’m painting to match the candy apple red finish.  I’ll probably also add big red LEDs to the tail lights.  When that’s finished, all the decorations will transfer over to the new walker (when it arrives, should be in a week or so). k/1 – a woman after my own heart!  cool!  i’d love to see a photo of that walker of yours!!! kate

Response:

((DeeTee)) – Hide quoted text — Show quoted text – > me on this injectible MTX.  Last weekend was a horrible blur of dizziness > (went to ER on Tuesday with stroke symptoms – nothing found.  Now have > appointment with GP for blood pressure stuff (I’m only on THREE meds for it > now. Clearly they’ve stopped working.) I stayed home from church today > ’cause I keep trying to lose breakfast.  So I am hoping it’s just an > adjustment phase. > Keep us informed, > DeeTee > DeeTee and Bob Taggart > http://home.earthlink.net/~bdtaggart/ > I was on the plaquenil/MTX/azulfidine combo for a couple months, and it > really finally did seem to be working and allowing me to reduce my > prednisone > dosage.  Then the infections started.  When I had a resistant sinus > infection, > a UTI, _and_ a skin abcess all at once, I finally had enough.  The rheumie > agreed, and we reduced the MTX to 10mg.  No infections, but it didn’t _do_ > anything other than make me want to yarf.  So we’ve dropped the MTX and > the > Plaquenil because I’ve been on the highest dosage for 7 years now and need > to take a vacation from it.  Started Arava at 10mg (half dose) with no > loading > dose.  I’ve had too many GI tract problems to do the normal dosing.  I’ve > registered with Amgen to get in line for Enbrel.  Hopefully, it won’t be > months (I plan to get the rheumie to sign me off for a priority spot).  If > the wait is too long, we may have to try Remicade, but it’s not a great > prospect given my problems with MTX.  After looking at the study results > for > Humira, neither of us wants me to be the lab rat.  I already have > lupus-like > symptoms, so Humira seems like a really bad idea in my case.  And he’s yet > to > have _anyone_ want to try Kineret. > We’re ordering me a second walker to use inside the house (there’s steps > up to the porch, then a step up to the doorjamb–this is a rental house, > we’re > not paying to put a ramp in here).  George is upset that I’ve fallen one > too > many times in the house, so now I’ll be using a walker indoors too.  At > least > the cats don’t think the walker is a toy.  A couple of my falls were from > the > cats trying to play with my cane. ;} > On the other hand, we’ve had our 11th wedding anniversary, and he’s still > a > handicapped > now!"  Once he understood why I was getting hysterical over little nothing > things, he’s been entirely supportive ever since.  He’s currently twisting > his > boss’s arm over getting me an attendant for a couple hours each day when > he’s > gone on business trips.  Which means that when he gets back, the sink > won’t > be full of dirty dishes and the bedroom won’t be taken over by a pile of > unwashed laundry.  Less stress for me, less stress and worry for him.  He > even threatened to not go if they didn’t pay for an attendant.  His boss, > and the boss’s boss agree, it’s corporate management that were dragging > their > feet.  He doesn’t leave until February, so we have enough time to finish > re-arranging the house so I can get around unassisted. > After the two monster projects are done, the next thing on the agenda is > to start looking for a new house.  If we _owned_ our house, we wouldn’t > feel like we were wasting money to build ramps, put in a dishwasher, and > buy a front-loading washing machine.  At least this place is all on one > level, though there’s no way the walker will ever fit into the bathroom. > I haven’t been posting or even reading much lately because simply getting > through each day has taken too much out of me.  Hopefully that’ll get > better. > During my adjustment phase, I’ve been using gallows humor to keep from > going > totally over the edge.  George is now urging me to offer some of the > artwork > I’ve done lately as tshirts (probably through CafePress).  I’ll post those > seperately. > Damn, this winter has just sucked for too many of us.  Hope we _all_ see > better days soon. > — > Head Muso, White Rats Morris, Faultline Morris > Member, Knights of Xenu (1995).  Chaos Monger and Jill of All Trades. > "A head-on collision between Morticia Adams and Martha Stewart"

Response:

(((((((((((((((((((((Lee)))))))))))))))))))  praying for enbrel for you! and you’re right, it has been a sucky-poo winter for a bunch on the ng. time for change! kate

I was on the plaquenil/MTX/azulfidine combo for a couple months, and it really finally did seem to be working and allowing me to reduce my prednisone dosage.  Then the infections started.  When I had a resistant sinus infection, a UTI, _and_ a skin abcess all at once, I finally had enough.  The rheumie agreed, and we reduced the MTX to 10mg.  No infections, but it didn’t _do_ anything other than make me want to yarf.  So we’ve dropped the MTX and the Plaquenil because I’ve been on the highest dosage for 7 years now and need to take a vacation from it.  Started Arava at 10mg (half dose) with no loading dose.  I’ve had too many GI tract problems to do the normal dosing.  I’ve registered with Amgen to get in line for Enbrel.  Hopefully, it won’t be months (I plan to get the rheumie to sign me off for a priority spot).  If the wait is too long, we may have to try Remicade, but it’s not a great prospect given my problems with MTX.  After looking at the study results for Humira, neither of us wants me to be the lab rat.  I already have lupus-like symptoms, so Humira seems like a really bad idea in my case.  And he’s yet to have _anyone_ want to try Kineret. We’re ordering me a second walker to use inside the house (there’s steps up to the porch, then a step up to the doorjamb–this is a rental house, we’re not paying to put a ramp in here).  George is upset that I’ve fallen one too many times in the house, so now I’ll be using a walker indoors too.  At least the cats don’t think the walker is a toy.  A couple of my falls were from the cats trying to play with my cane. ;} On the other hand, we’ve had our 11th wedding anniversary, and he’s still a handicapped now!"  Once he understood why I was getting hysterical over little nothing things, he’s been entirely supportive ever since.  He’s currently twisting his boss’s arm over getting me an attendant for a couple hours each day when he’s gone on business trips.  Which means that when he gets back, the sink won’t be full of dirty dishes and the bedroom won’t be taken over by a pile of unwashed laundry.  Less stress for me, less stress and worry for him.  He even threatened to not go if they didn’t pay for an attendant.  His boss, and the boss’s boss agree, it’s corporate management that were dragging their feet.  He doesn’t leave until February, so we have enough time to finish re-arranging the house so I can get around unassisted. After the two monster projects are done, the next thing on the agenda is to start looking for a new house.  If we _owned_ our house, we wouldn’t feel like we were wasting money to build ramps, put in a dishwasher, and buy a front-loading washing machine.  At least this place is all on one level, though there’s no way the walker will ever fit into the bathroom. I haven’t been posting or even reading much lately because simply getting through each day has taken too much out of me.  Hopefully that’ll get better. During my adjustment phase, I’ve been using gallows humor to keep from going totally over the edge.  George is now urging me to offer some of the artwork I’ve done lately as tshirts (probably through CafePress).  I’ll post those seperately. Damn, this winter has just sucked for too many of us.  Hope we _all_ see better days soon. — Head Muso, White Rats Morris, Faultline Morris Member, Knights of Xenu (1995).  Chaos Monger and Jill of All Trades. "A head-on collision between Morticia Adams and Martha Stewart"

Response:

>I use my feet to move the wheelchair around.  

Hah.  When I’m in very long lines, I do this with the walker.  Gets some odd looks since of course, you have to scoot along backwards. >I use the walker >when I’m out when I can walk ok but need more help than a cane.  What kind >of walker did you get?  Does it have a seat on it or a basket or such?  

I got a four-wheeled model made by Otho-Nova.  This one’s the Cruiser Deluxe. The second one we’re ordering will be the Junior model, which is about 3 inches shorter.  The handles are at the right height for me, but my feet don’t quite rest on the floor if I sit down on the seat.  This one will be fine for in the house.  In fact, the new one is this model: http://www.walgreens.com/store/product.jhtml?PRODID=376665&CATID=100283 The current one is also red. I’ll stow the shorter one in the car and use it when I’m out and about. Having a chair that doesn’t have a seat that’s too soft or saggy and has a back support in the right place has already saved me a couple times.  The chairs at our local clinic are all slouch chairs and I can’t get up if I sit in them for more than a few minutes. >I really like to use the walker when I have to go someplace like the post >office and I’m likely to have to stand in line.  I have a seat to sit on >while I wait and a small basket to hold what I’m trying to carry.  I’ve >found a clear tray also that will hold a drink!  

Heh.  Jody keeps telling me that I need to get a cup holder for mine.  I’m gonna dig around at the local non-slimey wheelchair repair place and see if they can come up with a quick-release cane holder and a cup holder for me. >Have you decorated it yet? >The Christmas I was using mine, I had it all decorated!  Bells and all. >Think of all the holidays to come to give yourself a little cheer!

I already have headlights on it (they’re krypton bicycle lights).  Added them after I almost got run over crossing the street one night.  Right now, I have the Gimp Jolly Roger banner hung across the backrest bar.  This one has a basket, but I found small things tended to fall through the bars, so I added a zip-up duffel bag inside the basket.  It’s black with cherries embroidered all over it. [smirk]  The guys tell me I need to add a hood ornament to the front of the basket now.  I’ve got a set of miniature cadillac fins that I’m painting to match the candy apple red finish.  I’ll probably also add big red LEDs to the tail lights.  When that’s finished, all the decorations will transfer over to the new walker (when it arrives, should be in a week or so). >I hope Enbrel works for you.  It was a great thing for me.  Got me out of >bed and moving again.  I had to add Arava with it this year and that’s been >a good thing also.  The number of swollen joints is down to two from almost >all.  I started it without the loading dose also.  Due to a bout of >bronchitis I’ve had to stop both of them (last Monday) and so far nothing >except fatigue has returned.  Hopefully, this will end soon.

Hope so.  Hope that I _get_ the Enbrel in a reasonable time.  No one at our clinic has managed to receive it yet, but that may be because the pharmacy is clueless about the patients needing to register.  I called Amgen’s 888 number and registered myself.  The packet should get here sometime this week, then I get it signed and mail it back. >Hang in there and know we are thinking about you!

Thank you. — Head Muso, White Rats Morris, Faultline Morris Member, Knights of Xenu (1995).  Chaos Monger and Jill of All Trades. "A head-on collision between Morticia Adams and Martha Stewart"

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me on this injectible MTX.  Last weekend was a horrible blur of dizziness (went to ER on Tuesday with stroke symptoms – nothing found.  Now have appointment with GP for blood pressure stuff (I’m only on THREE meds for it now. Clearly they’ve stopped working.) I stayed home from church today ’cause I keep trying to lose breakfast.  So I am hoping it’s just an adjustment phase. Keep us informed, DeeTee DeeTee and Bob Taggart http://home.earthlink.net/~bdtaggart/

– Hide quoted text — Show quoted text -> I was on the plaquenil/MTX/azulfidine combo for a couple months, and it > really finally did seem to be working and allowing me to reduce my prednisone > dosage.  Then the infections started.  When I had a resistant sinus infection, > a UTI, _and_ a skin abcess all at once, I finally had enough.  The rheumie > agreed, and we reduced the MTX to 10mg.  No infections, but it didn’t _do_ > anything other than make me want to yarf.  So we’ve dropped the MTX and the > Plaquenil because I’ve been on the highest dosage for 7 years now and need > to take a vacation from it.  Started Arava at 10mg (half dose) with no loading > dose.  I’ve had too many GI tract problems to do the normal dosing.  I’ve > registered with Amgen to get in line for Enbrel.  Hopefully, it won’t be > months (I plan to get the rheumie to sign me off for a priority spot).  If > the wait is too long, we may have to try Remicade, but it’s not a great > prospect given my problems with MTX.  After looking at the study results for > Humira, neither of us wants me to be the lab rat.  I already have lupus-like > symptoms, so Humira seems like a really bad idea in my case.  And he’s yet to > have _anyone_ want to try Kineret. > We’re ordering me a second walker to use inside the house (there’s steps > up to the porch, then a step up to the doorjamb–this is a rental house, we’re > not paying to put a ramp in here).  George is upset that I’ve fallen one too > many times in the house, so now I’ll be using a walker indoors too.  At least > the cats don’t think the walker is a toy.  A couple of my falls were from the > cats trying to play with my cane. ;} > On the other hand, we’ve had our 11th wedding anniversary, and he’s still a handicapped > now!"  Once he understood why I was getting hysterical over little nothing > things, he’s been entirely supportive ever since.  He’s currently twisting his > boss’s arm over getting me an attendant for a couple hours each day when he’s > gone on business trips.  Which means that when he gets back, the sink won’t > be full of dirty dishes and the bedroom won’t be taken over by a pile of > unwashed laundry.  Less stress for me, less stress and worry for him.  He > even threatened to not go if they didn’t pay for an attendant.  His boss, > and the boss’s boss agree, it’s corporate management that were dragging their > feet.  He doesn’t leave until February, so we have enough time to finish > re-arranging the house so I can get around unassisted. > After the two monster projects are done, the next thing on the agenda is > to start looking for a new house.  If we _owned_ our house, we wouldn’t > feel like we were wasting money to build ramps, put in a dishwasher, and > buy a front-loading washing machine.  At least this place is all on one > level, though there’s no way the walker will ever fit into the bathroom. > I haven’t been posting or even reading much lately because simply getting > through each day has taken too much out of me.  Hopefully that’ll get better. > During my adjustment phase, I’ve been using gallows humor to keep from going > totally over the edge.  George is now urging me to offer some of the artwork > I’ve done lately as tshirts (probably through CafePress).  I’ll post those > seperately. > Damn, this winter has just sucked for too many of us.  Hope we _all_ see > better days soon. > — > Head Muso, White Rats Morris, Faultline Morris > Member, Knights of Xenu (1995).  Chaos Monger and Jill of All Trades. > "A head-on collision between Morticia Adams and Martha Stewart"

Response:

I was on the plaquenil/MTX/azulfidine combo for a couple months, and it really finally did seem to be working and allowing me to reduce my prednisone dosage.  Then the infections started.  When I had a resistant sinus infection, a UTI, _and_ a skin abcess all at once, I finally had enough.  The rheumie agreed, and we reduced the MTX to 10mg.  No infections, but it didn’t _do_ anything other than make me want to yarf.  So we’ve dropped the MTX and the Plaquenil because I’ve been on the highest dosage for 7 years now and need to take a vacation from it.  Started Arava at 10mg (half dose) with no loading dose.  I’ve had too many GI tract problems to do the normal dosing.  I’ve registered with Amgen to get in line for Enbrel.  Hopefully, it won’t be months (I plan to get the rheumie to sign me off for a priority spot).  If the wait is too long, we may have to try Remicade, but it’s not a great prospect given my problems with MTX.  After looking at the study results for Humira, neither of us wants me to be the lab rat.  I already have lupus-like symptoms, so Humira seems like a really bad idea in my case.  And he’s yet to have _anyone_ want to try Kineret.   We’re ordering me a second walker to use inside the house (there’s steps up to the porch, then a step up to the doorjamb–this is a rental house, we’re not paying to put a ramp in here).  George is upset that I’ve fallen one too many times in the house, so now I’ll be using a walker indoors too.  At least the cats don’t think the walker is a toy.  A couple of my falls were from the cats trying to play with my cane. ;} On the other hand, we’ve had our 11th wedding anniversary, and he’s still a now!"  Once he understood why I was getting hysterical over little nothing things, he’s been entirely supportive ever since.  He’s currently twisting his boss’s arm over getting me an attendant for a couple hours each day when he’s gone on business trips.  Which means that when he gets back, the sink won’t be full of dirty dishes and the bedroom won’t be taken over by a pile of unwashed laundry.  Less stress for me, less stress and worry for him.  He even threatened to not go if they didn’t pay for an attendant.  His boss, and the boss’s boss agree, it’s corporate management that were dragging their feet.  He doesn’t leave until February, so we have enough time to finish re-arranging the house so I can get around unassisted.   After the two monster projects are done, the next thing on the agenda is to start looking for a new house.  If we _owned_ our house, we wouldn’t feel like we were wasting money to build ramps, put in a dishwasher, and buy a front-loading washing machine.  At least this place is all on one level, though there’s no way the walker will ever fit into the bathroom. I haven’t been posting or even reading much lately because simply getting through each day has taken too much out of me.  Hopefully that’ll get better. During my adjustment phase, I’ve been using gallows humor to keep from going totally over the edge.  George is now urging me to offer some of the artwork I’ve done lately as tshirts (probably through CafePress).  I’ll post those seperately. Damn, this winter has just sucked for too many of us.  Hope we _all_ see better days soon. — Head Muso, White Rats Morris, Faultline Morris Member, Knights of Xenu (1995).  Chaos Monger and Jill of All Trades. "A head-on collision between Morticia Adams and Martha Stewart"

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Question:

Solor powered laptop chargers have been available for quite sometime. Try a Google search for a few retailers. -david – Hide quoted text — Show quoted text – > My question > How good is a solar cell? > Would it be viable to have a desk with a solar panel attached so it > could charge/run a laptop and/or mobile phone? > I suppose it could use ambiant lighting but of needed an intense beam > of light could be projected from a wall. > What do you all think?

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Thank you Anthony , This about answers all the questions. I suppose it is also the same reason the chocolate teapot was never a big hit . Many thanks Bill – Hide quoted text — Show quoted text – > … > How good is a solar cell? > Pretty good. Most commercially sold solar PV panels run about 12 to 15% > efficiency and are guaranteed to last 20 to 25 years. > Would it be viable to have a desk with a solar panel attached so it > could charge/run a laptop and/or mobile phone? > Yes, as long as you operate it outside in the sunlight. A typical > laptop may require from 20 to 40 watts and cell phones are usually > less than a watt or two. There are many common PV panels that are > rated at 40+ watts and which measure about 1 foot by 4 feet in size. > Depending on your equipment you may only need one or two of these > panels to power your equipment. This is pretty common for RV’s. > I suppose it could use ambiant lighting but of needed an intense beam > of light could be projected from a wall. > Indoor lighting is often less than 1/100th the intensity of sunlight. > You get as much power from a solar cell as you provide light so you > will get 1/100th (or less) of the power from your panel with typical > indoor light. You would need either a much larger panel or much more > intense light. > If you use light from an electric lamp then it’s likely you will lose > 95% of the energy inside the lamp and the panel will only be able to > convert 15% of the remaining 5% (except for special situations). It’s > likely you’ll wind up with less than 1% of the electricity you started > with. You would do better to run an extension cord. > What do you all think? > I’m not at all certain what you are asking but there is a reason why > solar powered watches never caught on for coal miners. > Anthony

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My question How good is a solar cell? Would it be viable to have a desk with a solar panel attached so it could charge/run a laptop and/or mobile phone? I suppose it could use ambiant lighting but of needed an intense beam of light could be projected from a wall. What do you all think?

Response:

… > How good is a solar cell?

Pretty good. Most commercially sold solar PV panels run about 12 to 15% efficiency and are guaranteed to last 20 to 25 years. > Would it be viable to have a desk with a solar panel attached so it > could charge/run a laptop and/or mobile phone?

Yes, as long as you operate it outside in the sunlight. A typical laptop may require from 20 to 40 watts and cell phones are usually less than a watt or two. There are many common PV panels that are rated at 40+ watts and which measure about 1 foot by 4 feet in size. Depending on your equipment you may only need one or two of these panels to power your equipment. This is pretty common for RV’s. > I suppose it could use ambiant lighting but of needed an intense beam > of light could be projected from a wall.

Indoor lighting is often less than 1/100th the intensity of sunlight. You get as much power from a solar cell as you provide light so you will get 1/100th (or less) of the power from your panel with typical indoor light. You would need either a much larger panel or much more intense light. If you use light from an electric lamp then it’s likely you will lose 95% of the energy inside the lamp and the panel will only be able to convert 15% of the remaining 5% (except for special situations). It’s likely you’ll wind up with less than 1% of the electricity you started with. You would do better to run an extension cord. > What do you all think?

I’m not at all certain what you are asking but there is a reason why solar powered watches never caught on for coal miners. Anthony

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> > Does anybody know of a web site that gives the basics of Solar energy, like how > it works in basic form it is a subject I know nothing about and I mean NOTHING > and would like to cheers G > I went to Alta Vista at http://altavista.digital.com/ and searched for the phrase "solar energy basics" > 2,746,270 matches were found. > John Hughes

Yeah.  That’s why you don’t go to Alta Vista.  The boolean search does an "or", apparently, between solar and energy and basics. Instead, you go to Infoseek and search on "solar".  You get a load of pages.  Then you click on the button to search only those pages and enter "energy".  You get less pages.  You click the button to search only those pages again.  You search on "basics".  I think I ended up with about 17 pages. Good luck. DPH

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>Instead, you go to Infoseek and search on "solar".  You get a load of pages.  Then you click on the button >to search only those pages and enter "energy".  You get less pages.  You click the button to search only >those pages again.  You search on "basics".  I think I ended up with about 17 pages.

Or make it quicker with "+solar +energy +basics"

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Does anybody know of a web site that gives the basics of Solar energy, like how it works in basic form it is a subject I know nothing about and I mean NOTHING and would like to cheers G

Response:

> Does anybody know of a web site that gives the basics of Solar energy, like how > it works in basic form it is a subject I know nothing about and I mean NOTHING > and would like to cheers G

I went to Alta Vista at http://altavista.digital.com/ and searched for the phrase "solar energy basics" 2,746,270 matches were found. John Hughes

Response:

: >Hi, my name is Masasumi Oga. I’m new to this newsgroup. : >I’m interested in solar power. I want to know how can we get electric : >energy from solar heat. However, I don’t have any knowledge about it. : >Is there anyone who has any information on solar power? : > : >Thank you. : You get a barf load of heliostatic mirrors to reflect the sunlight onto a : target mass which has a working fluid running through it. The 5 megawatt : Luz plant used a flamable oil called therminol. You use the hot oil to : boil water to run a steam turbine. Worked great, well other than that it : took an inordinate amount of land per usable watt generated. Oh yeah & the : therminal blew up once injuring 7 people & costing millions of dollars. : Opps, also It may have required more energy to construct & maintain than : it ever produced. This is NOT the technology of today! The biggest solar termal plats are build in California cald SEGS each 80MW, all together  app. 350 MW. The mirrors are build by Flachglas Solar Germany from Pilkington Group. This plants don’t use heliostatic mirrors but line focusing parabolic troughs. More info in: The Yearbook of Renewable Energies 1994 London Best Regards mt. — —–WWW http://www.heim2.tu-clausthal.de/USERS/Martin.Tschierschke/  –

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> Hi, my name is Masasumi Oga. I’m new to this newsgroup. > I’m interested in solar power. I want to know how can we get electric > energy from solar heat. However, I don’t have any knowledge about it. > Is there anyone who has any information on solar power? > Thank you.

There are also photovoltaic cells to get energy from the sun. Do you know what it is ? Pedro :-)

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>Hi, my name is Masasumi Oga. I’m new to this newsgroup. >I’m interested in solar power. I want to know how can we get electric >energy from solar heat. However, I don’t have any knowledge about it. >Is there anyone who has any information on solar power? >Thank you.

You get a barf load of heliostatic mirrors to reflect the sunlight onto a target mass which has a working fluid running through it. The 5 megawatt Luz plant used a flamable oil called therminol. You use the hot oil to boil water to run a steam turbine. Worked great, well other than that it took an inordinate amount of land per usable watt generated. Oh yeah & the therminal blew up once injuring 7 people & costing millions of dollars. Opps, also It may have required more energy to construct & maintain than it ever produced. —       Karl Johanson,  Victoria B.C. Canada -It’s okay to disagree with me. However, once I explain where you’re wrong you’re supposed to become enlightened & change your mind. Congratulating me on how smart I am is optional.

Response:

Hi, my name is Masasumi Oga. I’m new to this newsgroup. I’m interested in solar power. I want to know how can we get electric energy from solar heat. However, I don’t have any knowledge about it. Is there anyone who has any information on solar power? Thank you.

Response:

>Hi, my name is Masasumi Oga. I’m new to this newsgroup. >I’m interested in solar power. I want to know how can we get electric >energy from solar heat. However, I don’t have any knowledge about it. >Is there anyone who has any information on solar power? >Thank you.

You get a barf load of heliostatic mirrors to reflect the sunlight onto a target mass which has a working fluid running through it. The 5 megawatt Luz plant used a flamable oil called therminol. You use the hot oil to boil water to run a steam turbine. Worked great, well other than that it to an inordinate amount of land per usable watt generated. Oh yeah & the treminal blew up once injuring 7 people & costing millions of dollars. Opps, also It may have required more energy to construct & maintain than it ever produced. —       Karl Johanson,  Victoria B.C. Canada -It’s okay to disagree with me. However, once I explain where you’re wrong you’re supposed to become enlightened & change your mind. Congratulating me on how smart I am is optional.

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   : It covers the thin-film amorphous silicon cells currently produced by    : United Solar Systems of Troy, Michigan, which achieve now a remarkable    : 10.2 percent efficiency.    I thought thin-film amorphous, while cheaper to produce, had a shorter    lifespan and lost efficiency over time.  Am I mistaken? No, you’re not.  Example:  I own one of Real Goods’ amorphous panels — when I bought it last year they were calling it a "10W" panel.  The rating sticker on it said "max pwr 1400mA at 10V" or something — anyway, it initially did put out 14W, as per the manufacturer’s rating.  However, over the first month the output decayed to approximately [the RG rating of] 10W.  Over the past year, the output has gradually decreased until now, almost exactly a year after I installed it, peak output is about 4.5W. You pay more for polycrystalline or crystalline cells — but it’s more than worth it for the more durable technology. — –Craig DeForest

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: It covers the thin-film amorphous silicon cells currently produced by : United Solar Systems of Troy, Michigan, which achieve now a remarkable : 10.2 percent efficiency. I thought thin-film amorphous, while cheaper to produce, had a shorter lifespan and lost efficiency over time.  Am I mistaken? : The DOE, which is partially funding  USS research, predicts that the cost : of photovoltaic power besed on these panels could be brought down to : 12 to 16 cents per kilowatt/-hour. But when will it happen? Five years? Ten?  I’m hoping for five years at the outside since that is when I’m planning on building a home which will be off grid.

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: There was a short article in Business Week, Nov 8th comparing solar power : to other alternative energy sources.  There are also various associations : in the US and Canada which can give you more info. And there is also an interesting short article titled "Solar cells make a leap in cost-effectiveness" in Scientific American, April 94, p90. It covers the thin-film amorphous silicon cells currently produced by United Solar Systems of Troy, Michigan, which achieve now a remarkable 10.2 percent efficiency. The DOE, which is partially funding  USS research, predicts that the cost of photovoltaic power besed on these panels could be brought down to 12 to 16 cents per kilowatt/-hour. A fascinating technology, at long last coming of age. __ philippe

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I m working on a solar energy paper and was wondering where I could find the following: (1) GIFS of solar panels, etc. (2) good articles on the viability of solar power commercially as well as technically Azam Ali

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There was a short article in Business Week, Nov 8th comparing solar power to other alternative energy sources.  There are also various associations in the US and Canada which can give you more info.

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– Hide quoted text — Show quoted text -> Most of the studies for large scale solar power plants concluded that > it would be possible to be competative when the capital cost of the > system dropped below $1700 / kw capacity for components with a 50 year > life. > Most solar cells are rated at 5 year life — breakage being the prime > limit. > Even in the sunniest part of the US (ElPaso tx) you would only get 8 > KW hrs per day from each sq yd of collector(times 5% effiecient). Peak > power of 20 kw (100 amp – 240 volt system) would be expensive. > Imagine : 20 kw requires — 20 sq yd / .05 * cosine of latitude => 800 > sq yd  per household or 4 times the area of the average house. >A more practical near term approach is to put enough cells to cover >average loads on the roof angled at about the latitude off of >horizontal. That eliminates the need for most of your multiply by >cosine of latitude fudge factor.

No as easy as you suggest. The collector area could be adjusted by angular adjustment  – but the roof could not be covered because of shadowing effects. Solar Thermal Tower systems ended up with solar collectors only covering about 1/4 of the ground of the installation — the rest was space to prevent blocking sunlight to other mirrors. And as those who installed solar water heaters know — it is expensive to get a plumber to work on your roof. And it hurt to cut down the tall oak tree for more heat for the shower. >It also makes sense to size the system for average loads instead of >peak loads. That reduces it to about a 2 kw system or 80 sq yd.  solid >state invertors that made 60hz power from the DC could easily sync >with the power lines so you could sell any excess pwoer to the power >company, and you would be connected to the grid when you needed more >than 2 kw power.

Except that no electric company wants to have the village idiot feeding 5000 watts into the grid with the wrong phase or power factor — there is a tendency to blow whole substations if you are not constantly monitoring what you feed into the lines. >I have a 2.2kW programable PID controller in my shop that converts >220V 60Hz 1 phase power to DC then to 220V 3 phase power at any >frequency I want from 0.5Hz to 360Hz.  It cost $410.  An invertor that >only had to generate 220V synced powerline frequency could easily by >1/2 the price if produced in quatity. >I don’t personally think the price of a solar cell installation makes >economic sense for somone who is on the power grid, but we are getting >closer.  For the average homeowner, adding spiffy things like fuel >cells or large battery banks to the system drives the price and >maintenance up to the point where they are a long ways from making >economic sense.

Agreed that the aux equipment to balance out the few hours of peak solar production creates horrible costs — but they would have to be paid either by user with a private system — or by the utility to have standby peak power equal to total peak power produced by all networked solar systems. To pick up the load on the cold windy nights when the sun does not shine. There is no free lunch; someday the idiots in California will wake up and realize the truth, in the meantime there will be more of the same crazy ideas infecting the Ivory Towers and latte shops in the rest of the country.

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– Hide quoted text — Show quoted text ->>     "We can produce this for less than $200 for 200 watts, making it the >>first approach that we believe can truly compete with fossil fuels," Swanson >>says of the cubes. In the future, far fewer cubes could be used for personal >>power plants. >A dollar a watt. I dont know where you live  but here in Florida >I am paying $0 .10 a kw  thats 10 cents for a thousand watts. In >North Carolina it was 3 or 4 cents a kw plus a demand charge during >peak nours >Ed Christie > I’m afraid Jerry is up to his tricks again.  We don’t buy > electricity by the watt or kilowatt, we buy it by the > kilowatt-hour (did Jerry claim to be an engineer?).  With Jerry’s > data no comparison is possible because we don’t know the life of > the fuel cell/solar panel (how many hours will it put out the > rated wattage before it fails).  For now, the best we have is a > reference in the original post to three times the cost of oil and > gas. > Rochester Minnesota USA

I think you folks are misreading why I posted this article from ABC News.  I posted the article because it was the first time I had heard of using solar power in combination with a fuel cell.  The cost issue was irrelevant to me because this technology will only be successful if it can compete with other sources of energy.  Glenn, your point is a good one, i.e. reliability.  But again, let me suggest it is just another obstacle for this technology to overcome.  In the end, price and performance will determine if there is widespread use of this idea. But for the sake of discussion, let us assume they can come reduce cost significantly.  By the way, I think the criticism of the cost quoted in the article is accurate (could it be that once again the ABC reporter who is probably a technological dummy, is using the acquisition cost, not the recurring cost).  Think of the application of this technology in the underdeveloped world.  If they succeed in reducing the acquisition cost significantly (I am assuming of course the recurring cost is very small), that would mean in even the most remote regions of a country, they could have electricity.  Think about how that can transform these countries if their people could have electricity.  But there is another major problem for that to work and that is, the device would have require very little maintenance.

Response:

>     "We can produce this for less than $200 for 200 watts, making it the >first approach that we believe can truly compete with fossil fuels," Swanson >says of the cubes. In the future, far fewer cubes could be used for personal >power plants.

A dollar a watt. I dont know where you live  but here in Florida I am paying $0 .10 a kw  thats 10 cents for a thousand watts. In North Carolina it was 3 or 4 cents a kw plus a demand charge during peak nours Ed Christie —–= Posted via Newsfeeds.Com, Uncensored Usenet News =—– http://www.newsfeeds.com – The #1 Newsgroup Service in the World! —–==  Over 80,000 Newsgroups – 16 Different Servers! =—–

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[snip] > I don’t personally think the price of a solar cell installation makes > economic sense for somone who is on the power grid, but we are getting > closer.  For the average homeowner, adding spiffy things like fuel > cells or large battery banks to the system drives the price and > maintenance up to the point where they are a long ways from making > economic sense.

Agree, but the equation differs for industrial users. F’rinstance, hereabouts several plants are getting heavily into co-generation, reducing both their dependence on the grid and their costs. The industrials have an advantage over the homeowner in that they have a heat source which they are now recognizing should be used rather than allowed to float wastefully up the smokestack. Same thing applies to solar arrays. Given the ‘average’ lot size of a suburban home, there just isn’t enough room for an economically viable array. The industrials and government, however, typically have much more real estate available. Prediction: As electricity costs escalate, more and more co-generation will become the norm, and the monopoly of the electric companies will be broken. It’s interesting to speculate on the affect this development will have on prices.

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– Hide quoted text — Show quoted text ->>     "We can produce this for less than $200 for 200 watts, making it the >>first approach that we believe can truly compete with fossil fuels," Swanson >>says of the cubes. In the future, far fewer cubes could be used for personal >>power plants. >A dollar a watt. I dont know where you live  but here in Florida >I am paying $0 .10 a kw  thats 10 cents for a thousand watts. In >North Carolina it was 3 or 4 cents a kw plus a demand charge during >peak nours >Ed Christie >I’m afraid Jerry is up to his tricks again.  We don’t buy >electricity by the watt or kilowatt, we buy it by the >kilowatt-hour (did Jerry claim to be an engineer?).  With Jerry’s >data no comparison is possible because we don’t know the life of >the fuel cell/solar panel (how many hours will it put out the >rated wattage before it fails).  For now, the best we have is a >reference in the original post to three times the cost of oil and >gas.   >Rochester Minnesota USA

Most of the studies for large scale solar power plants concluded that it would be possible to be competative when the capital cost of the system dropped below $1700 / kw capacity for components with a 50 year life. Most solar cells are rated at 5 year life — breakage being the prime limit. Even in the sunniest part of the US (ElPaso tx) you would only get 8 KW hrs per day from each sq yd of collector(times 5% effiecient). Peak power of 20 kw (100 amp – 240 volt system) would be expensive. Imagine : 20 kw requires — 20 sq yd / .05 * cosine of latitude => 800 sq yd  per household or 4 times the area of the average house.

Response:

– Hide quoted text — Show quoted text ->     "We can produce this for less than $200 for 200 watts, making it the >first approach that we believe can truly compete with fossil fuels," Swanson >says of the cubes. In the future, far fewer cubes could be used for personal >power plants. >A dollar a watt. I dont know where you live  but here in Florida >I am paying $0 .10 a kw  thats 10 cents for a thousand watts. In >North Carolina it was 3 or 4 cents a kw plus a demand charge during >peak nours >Ed Christie

I’m afraid Jerry is up to his tricks again.  We don’t buy electricity by the watt or kilowatt, we buy it by the kilowatt-hour (did Jerry claim to be an engineer?).  With Jerry’s data no comparison is possible because we don’t know the life of the fuel cell/solar panel (how many hours will it put out the rated wattage before it fails).  For now, the best we have is a reference in the original post to three times the cost of oil and gas.   Rochester Minnesota USA

Response:

Harnessing the Sun’s Power New Technology May Run Fossil Fuels Into the Ground By Jim Goldman ABC News S U N N Y  V E I L, Cal., Jan. 6 – There’s an excitement going on in the environmental movement over the development in solar energy- a development that some hope will eventually run rings around fossil fuels. STORY HIGHLIGHTS Simple and Effective- So Far Technicians have developed a solar powered flying wing that will be able to stay aloft for six months at a time.      The airplane generates all of its own energy, and stores its own energy, which has been the problem for solar up until now, and can exist completely independently of outside energy sources.      Engineers say the technology that powers the aircraft could solve some of the energy industry’s biggest challenges-generating and then storing solar energy and making it cost-effective.      A working prototype of a fuel cell coupled with this new, high-tech solar panels made from silicon or refined sand. The flat silicon solar panels are arranged in a cube- and that with the fuel cell ends up being about the size of a Rubik’s cube. Just 10 of those cubes would be enough to generate enough electrical power for an entire house.      According to Dick Swanson, CEO of Sun Power, they’re talking about the future of power being sunlight, which is free, and sand, which is probably the most prevalent material on the planet.      This is how it works: The sun’s energy splits water into hydrogen and oxygen during the day. Then, a fuel cell then brings the two gases back together to make electricity at night.      "This energy storage system is actually a fairly elegant, simple system, we think," says John Delfrate of NASA. Simple and Effective- So Far The flying wing is one example which some day could be used to monitor the environment and relay telecommunications data.      Power plants will be next, using thousands of solar cell cubes.      "We can produce this for less than $200 for 200 watts, making it the first approach that we believe can truly compete with fossil fuels," Swanson says of the cubes. In the future, far fewer cubes could be used for personal power plants.      "It takes about ten of these to power one house," Swanson says.      For now, solar power still costs as three times as much as oil and gas. Analysts say that is the final challenge the industry needs to overcome before it comes a realistic energy alternative.

Response:

Does anyone out there have any good information about Solar Power for the home?  I have been considering installing a Photovoltaic Solar Panel or two on the roof of the house which my wife and I are building.  I am interested in just how much power these panels will produce.   I have found a panel on the advertised on the Internet which claims to have a power rating on 260 watts.  This is for a panel about 6 x 4 feet.  I am pretty stupid when it comes to electrical consumption.  Is this a significant amount of juice?  Will it make a noticable impact on our electric bill?  Just how much juice is 260 watts? If anyone has experience with solar power, please let me know.

Response:

> Just how much juice is 260 watts?

Well, consider a 250 watt light bulb.  Just about THAT much. —                                                 Brett Carver                                                 (707) 577-4344

Response:

Cost effectiveness depends a lot on where you’re located (e.g. weather conditions, cost of power) and how you can orient the collector system. Most places where solar power is feasible have local organizations that you can contact for info and references (e.g. for contractors that have experience building solar-friendly houses).  If you live in the Northern California area the Northern California Solar Energy Association (NCSEA) can http://www.ihpva.org/ncsea.     Sam – Hide quoted text — Show quoted text – >Does anyone out there have any good information about Solar Power >for the home?  I have been considering installing a Photovoltaic >Solar Panel or two on the roof of the house which my wife and I are >building.  I am interested in just how much power these panels will >produce. >I have found a panel on the advertised on the Internet which >claims to have a power rating on 260 watts.  This is for a panel about >6 x 4 feet.  I am pretty stupid when it comes to electrical >consumption.  Is this a significant amount of juice?  Will it make a >noticable impact on our electric bill?  Just how much juice is 260 >watts? >If anyone has experience with solar power, please let me know.

Response:

Get the Real Goods catalog — the firm is located in Ukiah, CA…website info about solar power plus tech support.  

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Humm, I’m not so sure where Kirk is getting his stats. My wife is in the energy consulting field (a mechanical engineer), and I’ve accompanied her to a couple of the Solar ‘9x conventions, so I’ll throw in my $0.02. I’m not sure where you live, but Solar ‘98 is being held in Alberquerque, NM in June, I think. Check out http://www.sni.net/solar/ > . >Does anyone out there have any good information about Solar Power > . >for the home? > Yes. Except for certain very special circumstances, (IE, when other power > sources are unavailable or hideously expensive) it’s a rip-off. I refer > here specifically to solar panels for electricity, not reasonably > plausible schemes like using solar energy to directly warm a building or > to heat (or pre-heat) water. Those can work, sometimes brilliantly. Solar > panels, on the other hand, are a hopeless disaster if conventional "juice" > is available.

The question that will help decide how much $$$ this saves is does your state allow net metering. i.e. if you generate excess power during the day, can you run you meter backwards (there are a few different schemes for this) and supply power to the power company). The advantage here is that you are giving back during the periods of peak demand/cost, and only using power from the grid during times of lowest demand/cost (night). I have heard of situations where at the end of the year the home owner comes out being owed money by the power company. If you need to buy batteries to store the power, costs go up rapidly. > . I have been considering installing a Photovoltaic > . >Solar Panel or two on the roof of the house which my wife and I are > . >building.  I am interested in just how much power these panels will > . >produce. > The key question is: how long does it take for you to recoup your > investment? The nasty answer is: about 20 years if you already have > electrical power available at ten cents a kWh or less. > Note that 20 years is approximately twice the design lifetime of most > solar panels… so you will be just about half way through the payback > period when you have to go out and buy the most expensive parts all over > again.

Many of the solar panels comming out now have rated lifetimes of 30 years. > If your power costs more than .10/kWh, the payback declines > proportionately. If it costs less, the payback stretches out. Regardless, > because solar panels do deteriorate over time, the payout period is > essentially infinite: you NEVER save any money. (unless you are paying > maybe .50/kWh) > . >I have found a panel on the advertised on the Internet which > . >claims to have a power rating on 260 watts.  This is for a panel about > . >6 x 4 feet.  I am pretty stupid when it comes to electrical > . >consumption.  Is this a significant amount of juice? > No.

I decent figure would be about 2 KW for your average home. your peak will be about this. Again the real issue is, "do you have net metering?" – Hide quoted text — Show quoted text -> . > Will it make a > . >noticable impact on our electric bill? > No. > . Just how much juice is 260 > . >watts? > It is approximate 1/4 kilowatt. When the panel is running and producing > full power it will be "saving" you about 2.5 _cents_/hour. Assuming that > it can deliver full power for 8 hours a day (a hopelessly optimistic > assumption), it will thus save you a walloping 20 CENTS a day, or $73/ > year. You can never get this kind of performance in the real world — in > most cases you would not break even, ever. This is not a good investment. > And don’t forget — the panel will need an inverter to convert the low > voltage DC from the panel into higher voltage AC that your appliances > want. This wastes energy, making the payback numbers even worse. > Generally, you can take the cost of the panel and invest it in a mediocre > investment (a randomly selected stock or mutual fund) and make more than > that. > . >If anyone has experience with solar power, please let me know. > Fortunately, I can run a calculator, so I haven’t even been suckered by > the mythical savings of solar panels.

There are ways to waste money with solar, and ways to save money. Many people have a mental block against it, and you will never convince them otherwise. If you believe in the idea of solar power, go head, it will make you feel good. And when all states allow net metering, you will be ready to hook up on day one.         Cheers,                 Sid > — > | The picture atop of this message, if present, was > | made by "Saving Face" for the Macintosh, available at: > | http://www.santafe.edu/~smfr/utils.html

– Sid Hellman  - Systems Analyst/Programmer –  at the Passcal Instrument Center          Lamont-Doherty Earth Observatory of Columbia University

Response:

>I have never >heard of an actual documented instance when photovoltaic power "paid" >anybody except solar panel sellers.

Most of the PV installations I’ve heard of are in remote areas where it would cost a small fortune to bring in a power line, which changes the payback equation considerably. The exceptions to this get a lot of publicity, but they seem to be rare. Also, every PV installation I’ve ever heard of is combined with an aggressive load-reduction program, including things like special super-insulated refrigerators, all-flourescent lighting, heating systems that don’t require pumps or blowers, and sometimes even appliances (eg washing machines) that have been retro-fitted with high-efficiency motors in place of the usual induction motors. These things aren’t cheap, but watt-for-watt they’re cheaper than PV panels. If you’re on the grid, try some of this stuff first, and then see if you still want the PV panels. Also, they often include generators for backup and occasional high-energy uses (like power tools). If you’re on the grid, buy the generator first– it will come in handy during power failures.

Response:

> . Humm, I’m not so sure where Kirk is getting his stats. > From looking at the prices in vendor catalogs, and doing elementary > arithmetic. Try it sometime.

As I mentioned, the math changes dependent upon your local. > (snip) > . > . The question that will help decide how much $$$ this saves is does > . your state allow net metering. i.e. if you generate excess power > . during the day, can you run you meter backwards (there are a few > . different schemes for this) and supply power to the power > . company). The advantage here is that you are giving back during the > . periods of peak demand/cost, and only using power from the grid during > . times of lowest demand/cost (night). > The numbers do not work out on this — because your electricity costs more > to produce than the power company’s does — and they generally _buy_ your > power at a lower rate than they sell power to you at.

That is dependant on the state. Some states mandate that they buy back at wholesale, some at retail.  If you are lucky enough to be one of the retail states, it makes great economic sence. And even if you have to sell at wholesale, there is always the warm fuzzy feeling you will get knowing that you are helping the environment. (said with a little bit of PC sarcasm, but I do also buy into this.) > .  I have heard of situations where > . at the end of the year the home owner comes out being owed money by > . the power company. If you need to buy batteries to store the power, > . costs go up rapidly. > "I have heard of" sounds a lot like "a friend of a friend". I have never > heard of an actual documented instance when photovoltaic power "paid" > anybody except solar panel sellers.

I’ve seen talks on this subject at meetings, where the talks are based upon scientific research. Do I have it in front of me? no. So accept it if you want. – Hide quoted text — Show quoted text -> . > > . > . I have been considering installing a Photovoltaic > . > . >Solar Panel or two on the roof of the house which my wife and I are > . > . >building.  I am interested in just how much power these panels will > . > . >produce. > . > > . > The key question is: how long does it take for you to recoup your > . > investment? The nasty answer is: about 20 years if you already have > . > electrical power available at ten cents a kWh or less. > . > > . > Note that 20 years is approximately twice the design lifetime of most > . > solar panels… so you will be just about half way through the payback > . > period when you have to go out and buy the most expensive parts all over > . > again. > . > . Many of the solar panels comming out now have rated lifetimes of 30 years. > Then how come they only have 10-year warranties?

Good question, but from what I’ve seen, most failures are due to misuse. i.e. walking on them, shotgun blast, etc, All it takes if one section of one panel to be damaged, and since most panels are wired in series, the entire panel is dead. (I work in environmental monitoring, where we set up sites in remote locations, run by solar panels. I’ve yet to see a panel die of natural causes. YMMV) – Hide quoted text — Show quoted text -> . > . > > . > If your power costs more than .10/kWh, the payback declines > . > proportionately. If it costs less, the payback stretches out. Regardless, > . > because solar panels do deteriorate over time, the payout period is > . > essentially infinite: you NEVER save any money. (unless you are paying > . > maybe .50/kWh) > . > > . > . >I have found a panel on the advertised on the Internet which > . > . >claims to have a power rating on 260 watts.  This is for a panel about > . > . >6 x 4 feet.  I am pretty stupid when it comes to electrical > . > . >consumption.  Is this a significant amount of juice? > . > > . > No. > . > . I decent figure would be about 2 KW for your average home. your peak > . will be about this. Again the real issue is, "do you have net > . metering?" > The average home only uses 2kW peak? You have a peculiar notion of the > "average home". Perhaps the "average home" with no electric kitchen > appliances, no electric heating (including bathroom heat), and 100% > fluorescent lighting. 2kW is less than 9 amps — the average home is wired > for 200A service.

I’m sorry, I meant to type "above this" not "about this". The net metering issue is meant to imply if you have the grid as a backup source, you don’t need to account for peak in your solar panel purchase, only average. I just talked to my wife (the mechanical/energy engineer for those of you joining us now) She stated that with 3 kw, and good conservation habits/appliances you can handle most of your load requirements except for peak. – Hide quoted text — Show quoted text -> . > > . > . > Will it make a > . > . >noticable impact on our electric bill? > . > > . > No. > . > > . > . Just how much juice is 260 > . > . >watts? > . > > . > It is approximate 1/4 kilowatt. When the panel is running and producing > . > full power it will be "saving" you about 2.5 _cents_/hour. Assuming that > . > it can deliver full power for 8 hours a day (a hopelessly optimistic > . > assumption), it will thus save you a walloping 20 CENTS a day, or $73/ > . > year. You can never get this kind of performance in the real world — in > . > most cases you would not break even, ever. This is not a good investment. > . > > . > And don’t forget — the panel will need an inverter to convert the low > . > voltage DC from the panel into higher voltage AC that your appliances > . > want. This wastes energy, making the payback numbers even worse. > . > > . > Generally, you can take the cost of the panel and invest it in a mediocre > . > investment (a randomly selected stock or mutual fund) and make more than > . > that. > . > > . > . >If anyone has experience with solar power, please let me know. > . > > . > Fortunately, I can run a calculator, so I haven’t even been suckered by > . > the mythical savings of solar panels. > . > > . > . There are ways to waste money with solar, and ways to save money. > True. The best way to save money is to avoid photovoltaics at all cost. > . Many > . people have a mental block against it, and you will never convince > . them otherwise. > As opposed to "True Believers" who can’t stand cost-benefit analysis"

trust me, I’m not a True Believer. The problem I have with the solar engery field is that it has many "granola types" in it. They will espouse the value if making collectors out of dung and chewing gum and how it will also channel the sun god’s love through your home…. But, the field also has researchers from many companies and universities. I think you would all be surprised how many oil companies are in the business, mostly on the wings, but they are interested. When you go to one of these solar energy meetings you will see technical talks on the Stirling Engine Efficiencies right next door to talks on Straw Bale Construction (warning new flame war…) However it was these "pioneers" who kept the field alive for all those long years, so that the engineers and scientists still have something to sink their teeth into. > . If you believe in the idea of solar power, go head, it will make you > . feel good. > Good and broke. > . And when all states allow net metering, you will be ready > . to hook up on day one. > Sure — if you want to sell .50/kWh electricity for .06/kWh.

Please see my comment about wholesale vs retail on a state by state basis.                 Cheers,                         Sid – Hide quoted text — Show quoted text -> — > | The picture atop of this message, if present, was > | made by "Saving Face" for the Macintosh, available at: > | http://www.santafe.edu/~smfr/utils.html

Response:

> And even if you have to sell at wholesale, there is always the warm > fuzzy feeling you will get knowing that you are helping the > environment. (said with a little bit of PC sarcasm, but I do also buy > into this.)

You’re only doing something for the environment if the net gain once you consider the environmental impact of the manufacture, installation, and operation of the PV’s amortized over the electricity generated during their life is better than that of the commercially produced electricity. This is one of the big fallacies of to a lesser extent electric vehicles and to a huge extent the abuse of Ethanol as a so-called renewable resource via the corn farming lobby. > I just talked to my wife (the mechanical/energy engineer for those of > you joining us now) She stated that with 3 kw, and good conservation > habits/appliances you can handle most of your load requirements except > for peak.

Three 3KW average is still a far cry from 260W peak.   As pointed out, that depending what you are using for heat/hot-water, you may make a bigger personal cost-impact and environmental gain using your solar collecting area to generate hot water rather than electricity.

Response:

> > And even if you have to sell at wholesale, there is always the warm > fuzzy feeling you will get knowing that you are helping the > environment. (said with a little bit of PC sarcasm, but I do also buy > into this.) > You’re only doing something for the environment if the net gain > once you consider the environmental impact of the manufacture, > installation, and operation of the PV’s amortized over the > electricity generated during their life is better than that > of the commercially produced electricity.

The picture is usually gets more complicated as you look more closely. The idea of electric cars being better than fossil fuels is that you may be able to make large power plants cleaner/mile than your car. But this depends on lot of stuff including the type of power plant. When I was in grad school, we read a paper (from the 70’s I believe) that tried to rank various types of power generation according to health risk. They actually cacluated "deaths/KWH" for most major power sources. The highest? Hydro. The deaths there had to do with the worker’s deaths and the dangers in working at the dams. (this may have changed in 2 decades). – Hide quoted text — Show quoted text -> This is one of the big fallacies of to a lesser extent electric > vehicles and to a huge extent the abuse of Ethanol as a so-called > renewable resource via the corn farming lobby. > I just talked to my wife (the mechanical/energy engineer for those of > you joining us now) She stated that with 3 kw, and good conservation > habits/appliances you can handle most of your load requirements except > for peak. > Three 3KW average is still a far cry from 260W peak. >   As pointed out, that > depending what you are using for heat/hot-water, you may make > a bigger personal cost-impact and environmental gain using > your solar collecting area to generate hot water rather > than electricity.

My only point was that solar can be cost effective. We are only going to do it if NY State enact net metering at retail pricing. As for solar hot water, these systems generally need more maintainance than most home owners are willing to do.                 Cheers,                         Sid

Response:

Does anyone out there have any good information about Solar Power for the home?  I have been considering installing a Photovoltaic Solar Panel or two on the roof of the house which my wife and I are building.  I am interested in just how much power these panels will produce.   I have found a panel on the advertised on the Internet which claims to have a power rating on 260 watts.  This is for a panel about 6 x 4 feet.  I am pretty stupid when it comes to electrical consumption.  Is this a significant amount of juice?  Will it make a noticable impact on our electric bill?  Just how much juice is 260 watts? If anyone has experience with solar power, please let me know.

Response:

> Just how much juice is 260 watts?

Well, consider a 250 watt light bulb.  Just about THAT much. —                                                 Brett Carver                                                 (707) 577-4344

Response:

Cost effectiveness depends a lot on where you’re located (e.g. weather conditions, cost of power) and how you can orient the collector system. Most places where solar power is feasible have local organizations that you can contact for info and references (e.g. for contractors that have experience building solar-friendly houses).  If you live in the Northern California area the Northern California Solar Energy Association (NCSEA) can http://www.ihpva.org/ncsea.     Sam – Hide quoted text — Show quoted text – >Does anyone out there have any good information about Solar Power >for the home?  I have been considering installing a Photovoltaic >Solar Panel or two on the roof of the house which my wife and I are >building.  I am interested in just how much power these panels will >produce. >I have found a panel on the advertised on the Internet which >claims to have a power rating on 260 watts.  This is for a panel about >6 x 4 feet.  I am pretty stupid when it comes to electrical >consumption.  Is this a significant amount of juice?  Will it make a >noticable impact on our electric bill?  Just how much juice is 260 >watts? >If anyone has experience with solar power, please let me know.

Response:

Get the Real Goods catalog — the firm is located in Ukiah, CA…website info about solar power plus tech support.  

Response:

Humm, I’m not so sure where Kirk is getting his stats. My wife is in the energy consulting field (a mechanical engineer), and I’ve accompanied her to a couple of the Solar ‘9x conventions, so I’ll throw in my $0.02. I’m not sure where you live, but Solar ‘98 is being held in Alberquerque, NM in June, I think. Check out http://www.sni.net/solar/ > . >Does anyone out there have any good information about Solar Power > . >for the home? > Yes. Except for certain very special circumstances, (IE, when other power > sources are unavailable or hideously expensive) it’s a rip-off. I refer > here specifically to solar panels for electricity, not reasonably > plausible schemes like using solar energy to directly warm a building or > to heat (or pre-heat) water. Those can work, sometimes brilliantly. Solar > panels, on the other hand, are a hopeless disaster if conventional "juice" > is available.

The question that will help decide how much $$$ this saves is does your state allow net metering. i.e. if you generate excess power during the day, can you run you meter backwards (there are a few different schemes for this) and supply power to the power company). The advantage here is that you are giving back during the periods of peak demand/cost, and only using power from the grid during times of lowest demand/cost (night). I have heard of situations where at the end of the year the home owner comes out being owed money by the power company. If you need to buy batteries to store the power, costs go up rapidly. > . I have been considering installing a Photovoltaic > . >Solar Panel or two on the roof of the house which my wife and I are > . >building.  I am interested in just how much power these panels will > . >produce. > The key question is: how long does it take for you to recoup your > investment? The nasty answer is: about 20 years if you already have > electrical power available at ten cents a kWh or less. > Note that 20 years is approximately twice the design lifetime of most > solar panels… so you will be just about half way through the payback > period when you have to go out and buy the most expensive parts all over > again.

Many of the solar panels comming out now have rated lifetimes of 30 years. > If your power costs more than .10/kWh, the payback declines > proportionately. If it costs less, the payback stretches out. Regardless, > because solar panels do deteriorate over time, the payout period is > essentially infinite: you NEVER save any money. (unless you are paying > maybe .50/kWh) > . >I have found a panel on the advertised on the Internet which > . >claims to have a power rating on 260 watts.  This is for a panel about > . >6 x 4 feet.  I am pretty stupid when it comes to electrical > . >consumption.  Is this a significant amount of juice? > No.

I decent figure would be about 2 KW for your average home. your peak will be about this. Again the real issue is, "do you have net metering?" – Hide quoted text — Show quoted text -> . > Will it make a > . >noticable impact on our electric bill? > No. > . Just how much juice is 260 > . >watts? > It is approximate 1/4 kilowatt. When the panel is running and producing > full power it will be "saving" you about 2.5 _cents_/hour. Assuming that > it can deliver full power for 8 hours a day (a hopelessly optimistic > assumption), it will thus save you a walloping 20 CENTS a day, or $73/ > year. You can never get this kind of performance in the real world — in > most cases you would not break even, ever. This is not a good investment. > And don’t forget — the panel will need an inverter to convert the low > voltage DC from the panel into higher voltage AC that your appliances > want. This wastes energy, making the payback numbers even worse. > Generally, you can take the cost of the panel and invest it in a mediocre > investment (a randomly selected stock or mutual fund) and make more than > that. > . >If anyone has experience with solar power, please let me know. > Fortunately, I can run a calculator, so I haven’t even been suckered by > the mythical savings of solar panels.

There are ways to waste money with solar, and ways to save money. Many people have a mental block against it, and you will never convince them otherwise. If you believe in the idea of solar power, go head, it will make you feel good. And when all states allow net metering, you will be ready to hook up on day one.         Cheers,                 Sid > — > | The picture atop of this message, if present, was > | made by "Saving Face" for the Macintosh, available at: > | http://www.santafe.edu/~smfr/utils.html

– Sid Hellman  - Systems Analyst/Programmer –  at the Passcal Instrument Center          Lamont-Doherty Earth Observatory of Columbia University

Response:

>I have never >heard of an actual documented instance when photovoltaic power "paid" >anybody except solar panel sellers.

Most of the PV installations I’ve heard of are in remote areas where it would cost a small fortune to bring in a power line, which changes the payback equation considerably. The exceptions to this get a lot of publicity, but they seem to be rare. Also, every PV installation I’ve ever heard of is combined with an aggressive load-reduction program, including things like special super-insulated refrigerators, all-flourescent lighting, heating systems that don’t require pumps or blowers, and sometimes even appliances (eg washing machines) that have been retro-fitted with high-efficiency motors in place of the usual induction motors. These things aren’t cheap, but watt-for-watt they’re cheaper than PV panels. If you’re on the grid, try some of this stuff first, and then see if you still want the PV panels. Also, they often include generators for backup and occasional high-energy uses (like power tools). If you’re on the grid, buy the generator first– it will come in handy during power failures.

Response:

> . Humm, I’m not so sure where Kirk is getting his stats. > From looking at the prices in vendor catalogs, and doing elementary > arithmetic. Try it sometime.

As I mentioned, the math changes dependent upon your local. > (snip) > . > . The question that will help decide how much $$$ this saves is does > . your state allow net metering. i.e. if you generate excess power > . during the day, can you run you meter backwards (there are a few > . different schemes for this) and supply power to the power > . company). The advantage here is that you are giving back during the > . periods of peak demand/cost, and only using power from the grid during > . times of lowest demand/cost (night). > The numbers do not work out on this — because your electricity costs more > to produce than the power company’s does — and they generally _buy_ your > power at a lower rate than they sell power to you at.

That is dependant on the state. Some states mandate that they buy back at wholesale, some at retail.  If you are lucky enough to be one of the retail states, it makes great economic sence. And even if you have to sell at wholesale, there is always the warm fuzzy feeling you will get knowing that you are helping the environment. (said with a little bit of PC sarcasm, but I do also buy into this.) > .  I have heard of situations where > . at the end of the year the home owner comes out being owed money by > . the power company. If you need to buy batteries to store the power, > . costs go up rapidly. > "I have heard of" sounds a lot like "a friend of a friend". I have never > heard of an actual documented instance when photovoltaic power "paid" > anybody except solar panel sellers.

I’ve seen talks on this subject at meetings, where the talks are based upon scientific research. Do I have it in front of me? no. So accept it if you want. – Hide quoted text — Show quoted text -> . > > . > . I have been considering installing a Photovoltaic > . > . >Solar Panel or two on the roof of the house which my wife and I are > . > . >building.  I am interested in just how much power these panels will > . > . >produce. > . > > . > The key question is: how long does it take for you to recoup your > . > investment? The nasty answer is: about 20 years if you already have > . > electrical power available at ten cents a kWh or less. > . > > . > Note that 20 years is approximately twice the design lifetime of most > . > solar panels… so you will be just about half way through the payback > . > period when you have to go out and buy the most expensive parts all over > . > again. > . > . Many of the solar panels comming out now have rated lifetimes of 30 years. > Then how come they only have 10-year warranties?

Good question, but from what I’ve seen, most failures are due to misuse. i.e. walking on them, shotgun blast, etc, All it takes if one section of one panel to be damaged, and since most panels are wired in series, the entire panel is dead. (I work in environmental monitoring, where we set up sites in remote locations, run by solar panels. I’ve yet to see a panel die of natural causes. YMMV) – Hide quoted text — Show quoted text -> . > . > > . > If your power costs more than .10/kWh, the payback declines > . > proportionately. If it costs less, the payback stretches out. Regardless, > . > because solar panels do deteriorate over time, the payout period is > . > essentially infinite: you NEVER save any money. (unless you are paying > . > maybe .50/kWh) > . > > . > . >I have found a panel on the advertised on the Internet which > . > . >claims to have a power rating on 260 watts.  This is for a panel about > . > . >6 x 4 feet.  I am pretty stupid when it comes to electrical > . > . >consumption.  Is this a significant amount of juice? > . > > . > No. > . > . I decent figure would be about 2 KW for your average home. your peak > . will be about this. Again the real issue is, "do you have net > . metering?" > The average home only uses 2kW peak? You have a peculiar notion of the > "average home". Perhaps the "average home" with no electric kitchen > appliances, no electric heating (including bathroom heat), and 100% > fluorescent lighting. 2kW is less than 9 amps — the average home is wired > for 200A service.

I’m sorry, I meant to type "above this" not "about this". The net metering issue is meant to imply if you have the grid as a backup source, you don’t need to account for peak in your solar panel purchase, only average. I just talked to my wife (the mechanical/energy engineer for those of you joining us now) She stated that with 3 kw, and good conservation habits/appliances you can handle most of your load requirements except for peak. – Hide quoted text — Show quoted text -> . > > . > . > Will it make a > . > . >noticable impact on our electric bill? > . > > . > No. > . > > . > . Just how much juice is 260 > . > . >watts? > . > > . > It is approximate 1/4 kilowatt. When the panel is running and producing > . > full power it will be "saving" you about 2.5 _cents_/hour. Assuming that > . > it can deliver full power for 8 hours a day (a hopelessly optimistic > . > assumption), it will thus save you a walloping 20 CENTS a day, or $73/ > . > year. You can never get this kind of performance in the real world — in > . > most cases you would not break even, ever. This is not a good investment. > . > > . > And don’t forget — the panel will need an inverter to convert the low > . > voltage DC from the panel into higher voltage AC that your appliances > . > want. This wastes energy, making the payback numbers even worse. > . > > . > Generally, you can take the cost of the panel and invest it in a mediocre > . > investment (a randomly selected stock or mutual fund) and make more than > . > that. > . > > . > . >If anyone has experience with solar power, please let me know. > . > > . > Fortunately, I can run a calculator, so I haven’t even been suckered by > . > the mythical savings of solar panels. > . > > . > . There are ways to waste money with solar, and ways to save money. > True. The best way to save money is to avoid photovoltaics at all cost. > . Many > . people have a mental block against it, and you will never convince > . them otherwise. > As opposed to "True Believers" who can’t stand cost-benefit analysis"

trust me, I’m not a True Believer. The problem I have with the solar engery field is that it has many "granola types" in it. They will espouse the value if making collectors out of dung and chewing gum and how it will also channel the sun god’s love through your home…. But, the field also has researchers from many companies and universities. I think you would all be surprised how many oil companies are in the business, mostly on the wings, but they are interested. When you go to one of these solar energy meetings you will see technical talks on the Stirling Engine Efficiencies right next door to talks on Straw Bale Construction (warning new flame war…) However it was these "pioneers" who kept the field alive for all those long years, so that the engineers and scientists still have something to sink their teeth into. > . If you believe in the idea of solar power, go head, it will make you > . feel good. > Good and broke. > . And when all states allow net metering, you will be ready > . to hook up on day one. > Sure — if you want to sell .50/kWh electricity for .06/kWh.

Please see my comment about wholesale vs retail on a state by state basis.                 Cheers,                         Sid – Hide quoted text — Show quoted text -> — > | The picture atop of this message, if present, was > | made by "Saving Face" for the Macintosh, available at: > | http://www.santafe.edu/~smfr/utils.html

Response:

> And even if you have to sell at wholesale, there is always the warm > fuzzy feeling you will get knowing that you are helping the > environment. (said with a little bit of PC sarcasm, but I do also buy > into this.)

You’re only doing something for the environment if the net gain once you consider the environmental impact of the manufacture, installation, and operation of the PV’s amortized over the electricity generated during their life is better than that of the commercially produced electricity. This is one of the big fallacies of to a lesser extent electric vehicles and to a huge extent the abuse of Ethanol as a so-called renewable resource via the corn farming lobby. > I just talked to my wife (the mechanical/energy engineer for those of > you joining us now) She stated that with 3 kw, and good conservation > habits/appliances you can handle most of your load requirements except > for peak.

Three 3KW average is still a far cry from 260W peak.   As pointed out, that depending what you are using for heat/hot-water, you may make a bigger personal cost-impact and environmental gain using your solar collecting area to generate hot water rather than electricity.

Response:

> > And even if you have to sell at wholesale, there is always the warm > fuzzy feeling you will get knowing that you are helping the > environment. (said with a little bit of PC sarcasm, but I do also buy > into this.) > You’re only doing something for the environment if the net gain > once you consider the environmental impact of the manufacture, > installation, and operation of the PV’s amortized over the > electricity generated during their life is better than that > of the commercially produced electricity.

The picture is usually gets more complicated as you look more closely. The idea of electric cars being better than fossil fuels is that you may be able to make large power plants cleaner/mile than your car. But this depends on lot of stuff including the type of power plant. When I was in grad school, we read a paper (from the 70’s I believe) that tried to rank various types of power generation according to health risk. They actually cacluated "deaths/KWH" for most major power sources. The highest? Hydro. The deaths there had to do with the worker’s deaths and the dangers in working at the dams. (this may have changed in 2 decades). – Hide quoted text — Show quoted text -> This is one of the big fallacies of to a lesser extent electric > vehicles and to a huge extent the abuse of Ethanol as a so-called > renewable resource via the corn farming lobby. > I just talked to my wife (the mechanical/energy engineer for those of > you joining us now) She stated that with 3 kw, and good conservation > habits/appliances you can handle most of your load requirements except > for peak. > Three 3KW average is still a far cry from 260W peak. >   As pointed out, that > depending what you are using for heat/hot-water, you may make > a bigger personal cost-impact and environmental gain using > your solar collecting area to generate hot water rather > than electricity.

My only point was that solar can be cost effective. We are only going to do it if NY State enact net metering at retail pricing. As for solar hot water, these systems generally need more maintainance than most home owners are willing to do.                 Cheers,                         Sid

Response:

Does anyone out there have any good information about Solar Power for the home?  I have been considering installing a Photovoltaic Solar Panel or two on the roof of the house which my wife and I are building.  I am interested in just how much power these panels will produce.   I have found a panel on the advertised on the Internet which claims to have a power rating on 260 watts.  This is for a panel about 6 x 4 feet.  I am pretty stupid when it comes to electrical consumption.  Is this a significant amount of juice?  Will it make a noticable impact on our electric bill?  Just how much juice is 260 watts? If anyone has experience with solar power, please let me know.

Response:

> Just how much juice is 260 watts?

Well, consider a 250 watt light bulb.  Just about THAT much. —                                                 Brett Carver                                                 (707) 577-4344

Response:

Cost effectiveness depends a lot on where you’re located (e.g. weather conditions, cost of power) and how you can orient the collector system. Most places where solar power is feasible have local organizations that you can contact for info and references (e.g. for contractors that have experience building solar-friendly houses).  If you live in the Northern California area the Northern California Solar Energy Association (NCSEA) can http://www.ihpva.org/ncsea.     Sam – Hide quoted text — Show quoted text – >Does anyone out there have any good information about Solar Power >for the home?  I have been considering installing a Photovoltaic >Solar Panel or two on the roof of the house which my wife and I are >building.  I am interested in just how much power these panels will >produce. >I have found a panel on the advertised on the Internet which >claims to have a power rating on 260 watts.  This is for a panel about >6 x 4 feet.  I am pretty stupid when it comes to electrical >consumption.  Is this a significant amount of juice?  Will it make a >noticable impact on our electric bill?  Just how much juice is 260 >watts? >If anyone has experience with solar power, please let me know.

Response:

Get the Real Goods catalog — the firm is located in Ukiah, CA…website info about solar power plus tech support.  

Response:

Humm, I’m not so sure where Kirk is getting his stats. My wife is in the energy consulting field (a mechanical engineer), and I’ve accompanied her to a couple of the Solar ‘9x conventions, so I’ll throw in my $0.02. I’m not sure where you live, but Solar ‘98 is being held in Alberquerque, NM in June, I think. Check out http://www.sni.net/solar/ > . >Does anyone out there have any good information about Solar Power > . >for the home? > Yes. Except for certain very special circumstances, (IE, when other power > sources are unavailable or hideously expensive) it’s a rip-off. I refer > here specifically to solar panels for electricity, not reasonably > plausible schemes like using solar energy to directly warm a building or > to heat (or pre-heat) water. Those can work, sometimes brilliantly. Solar > panels, on the other hand, are a hopeless disaster if conventional "juice" > is available.

The question that will help decide how much $$$ this saves is does your state allow net metering. i.e. if you generate excess power during the day, can you run you meter backwards (there are a few different schemes for this) and supply power to the power company). The advantage here is that you are giving back during the periods of peak demand/cost, and only using power from the grid during times of lowest demand/cost (night). I have heard of situations where at the end of the year the home owner comes out being owed money by the power company. If you need to buy batteries to store the power, costs go up rapidly. > . I have been considering installing a Photovoltaic > . >Solar Panel or two on the roof of the house which my wife and I are > . >building.  I am interested in just how much power these panels will > . >produce. > The key question is: how long does it take for you to recoup your > investment? The nasty answer is: about 20 years if you already have > electrical power available at ten cents a kWh or less. > Note that 20 years is approximately twice the design lifetime of most > solar panels… so you will be just about half way through the payback > period when you have to go out and buy the most expensive parts all over > again.

Many of the solar panels comming out now have rated lifetimes of 30 years. > If your power costs more than .10/kWh, the payback declines > proportionately. If it costs less, the payback stretches out. Regardless, > because solar panels do deteriorate over time, the payout period is > essentially infinite: you NEVER save any money. (unless you are paying > maybe .50/kWh) > . >I have found a panel on the advertised on the Internet which > . >claims to have a power rating on 260 watts.  This is for a panel about > . >6 x 4 feet.  I am pretty stupid when it comes to electrical > . >consumption.  Is this a significant amount of juice? > No.

I decent figure would be about 2 KW for your average home. your peak will be about this. Again the real issue is, "do you have net metering?" – Hide quoted text — Show quoted text -> . > Will it make a > . >noticable impact on our electric bill? > No. > . Just how much juice is 260 > . >watts? > It is approximate 1/4 kilowatt. When the panel is running and producing > full power it will be "saving" you about 2.5 _cents_/hour. Assuming that > it can deliver full power for 8 hours a day (a hopelessly optimistic > assumption), it will thus save you a walloping 20 CENTS a day, or $73/ > year. You can never get this kind of performance in the real world — in > most cases you would not break even, ever. This is not a good investment. > And don’t forget — the panel will need an inverter to convert the low > voltage DC from the panel into higher voltage AC that your appliances > want. This wastes energy, making the payback numbers even worse. > Generally, you can take the cost of the panel and invest it in a mediocre > investment (a randomly selected stock or mutual fund) and make more than > that. > . >If anyone has experience with solar power, please let me know. > Fortunately, I can run a calculator, so I haven’t even been suckered by > the mythical savings of solar panels.

There are ways to waste money with solar, and ways to save money. Many people have a mental block against it, and you will never convince them otherwise. If you believe in the idea of solar power, go head, it will make you feel good. And when all states allow net metering, you will be ready to hook up on day one.         Cheers,                 Sid > — > | The picture atop of this message, if present, was > | made by "Saving Face" for the Macintosh, available at: > | http://www.santafe.edu/~smfr/utils.html

– Sid Hellman  - Systems Analyst/Programmer –  at the Passcal Instrument Center          Lamont-Doherty Earth Observatory of Columbia University

Response:

>I have never >heard of an actual documented instance when photovoltaic power "paid" >anybody except solar panel sellers.

Most of the PV installations I’ve heard of are in remote areas where it would cost a small fortune to bring in a power line, which changes the payback equation considerably. The exceptions to this get a lot of publicity, but they seem to be rare. Also, every PV installation I’ve ever heard of is combined with an aggressive load-reduction program, including things like special super-insulated refrigerators, all-flourescent lighting, heating systems that don’t require pumps or blowers, and sometimes even appliances (eg washing machines) that have been retro-fitted with high-efficiency motors in place of the usual induction motors. These things aren’t cheap, but watt-for-watt they’re cheaper than PV panels. If you’re on the grid, try some of this stuff first, and then see if you still want the PV panels. Also, they often include generators for backup and occasional high-energy uses (like power tools). If you’re on the grid, buy the generator first– it will come in handy during power failures.

Response:

> . Humm, I’m not so sure where Kirk is getting his stats. > From looking at the prices in vendor catalogs, and doing elementary > arithmetic. Try it sometime.

As I mentioned, the math changes dependent upon your local. > (snip) > . > . The question that will help decide how much $$$ this saves is does > . your state allow net metering. i.e. if you generate excess power > . during the day, can you run you meter backwards (there are a few > . different schemes for this) and supply power to the power > . company). The advantage here is that you are giving back during the > . periods of peak demand/cost, and only using power from the grid during > . times of lowest demand/cost (night). > The numbers do not work out on this — because your electricity costs more > to produce than the power company’s does — and they generally _buy_ your > power at a lower rate than they sell power to you at.

That is dependant on the state. Some states mandate that they buy back at wholesale, some at retail.  If you are lucky enough to be one of the retail states, it makes great economic sence. And even if you have to sell at wholesale, there is always the warm fuzzy feeling you will get knowing that you are helping the environment. (said with a little bit of PC sarcasm, but I do also buy into this.) > .  I have heard of situations where > . at the end of the year the home owner comes out being owed money by > . the power company. If you need to buy batteries to store the power, > . costs go up rapidly. > "I have heard of" sounds a lot like "a friend of a friend". I have never > heard of an actual documented instance when photovoltaic power "paid" > anybody except solar panel sellers.

I’ve seen talks on this subject at meetings, where the talks are based upon scientific research. Do I have it in front of me? no. So accept it if you want. – Hide quoted text — Show quoted text -> . > > . > . I have been considering installing a Photovoltaic > . > . >Solar Panel or two on the roof of the house which my wife and I are > . > . >building.  I am interested in just how much power these panels will > . > . >produce. > . > > . > The key question is: how long does it take for you to recoup your > . > investment? The nasty answer is: about 20 years if you already have > . > electrical power available at ten cents a kWh or less. > . > > . > Note that 20 years is approximately twice the design lifetime of most > . > solar panels… so you will be just about half way through the payback > . > period when you have to go out and buy the most expensive parts all over > . > again. > . > . Many of the solar panels comming out now have rated lifetimes of 30 years. > Then how come they only have 10-year warranties?

Good question, but from what I’ve seen, most failures are due to misuse. i.e. walking on them, shotgun blast, etc, All it takes if one section of one panel to be damaged, and since most panels are wired in series, the entire panel is dead. (I work in environmental monitoring, where we set up sites in remote locations, run by solar panels. I’ve yet to see a panel die of natural causes. YMMV) – Hide quoted text — Show quoted text -> . > . > > . > If your power costs more than .10/kWh, the payback declines > . > proportionately. If it costs less, the payback stretches out. Regardless, > . > because solar panels do deteriorate over time, the payout period is > . > essentially infinite: you NEVER save any money. (unless you are paying > . > maybe .50/kWh) > . > > . > . >I have found a panel on the advertised on the Internet which > . > . >claims to have a power rating on 260 watts.  This is for a panel about > . > . >6 x 4 feet.  I am pretty stupid when it comes to electrical > . > . >consumption.  Is this a significant amount of juice? > . > > . > No. > . > . I decent figure would be about 2 KW for your average home. your peak > . will be about this. Again the real issue is, "do you have net > . metering?" > The average home only uses 2kW peak? You have a peculiar notion of the > "average home". Perhaps the "average home" with no electric kitchen > appliances, no electric heating (including bathroom heat), and 100% > fluorescent lighting. 2kW is less than 9 amps — the average home is wired > for 200A service.

I’m sorry, I meant to type "above this" not "about this". The net metering issue is meant to imply if you have the grid as a backup source, you don’t need to account for peak in your solar panel purchase, only average. I just talked to my wife (the mechanical/energy engineer for those of you joining us now) She stated that with 3 kw, and good conservation habits/appliances you can handle most of your load requirements except for peak. – Hide quoted text — Show quoted text -> . > > . > . > Will it make a > . > . >noticable impact on our electric bill? > . > > . > No. > . > > . > . Just how much juice is 260 > . > . >watts? > . > > . > It is approximate 1/4 kilowatt. When the panel is running and producing > . > full power it will be "saving" you about 2.5 _cents_/hour. Assuming that > . > it can deliver full power for 8 hours a day (a hopelessly optimistic > . > assumption), it will thus save you a walloping 20 CENTS a day, or $73/ > . > year. You can never get this kind of performance in the real world — in > . > most cases you would not break even, ever. This is not a good investment. > . > > . > And don’t forget — the panel will need an inverter to convert the low > . > voltage DC from the panel into higher voltage AC that your appliances > . > want. This wastes energy, making the payback numbers even worse. > . > > . > Generally, you can take the cost of the panel and invest it in a mediocre > . > investment (a randomly selected stock or mutual fund) and make more than > . > that. > . > > . > . >If anyone has experience with solar power, please let me know. > . > > . > Fortunately, I can run a calculator, so I haven’t even been suckered by > . > the mythical savings of solar panels. > . > > . > . There are ways to waste money with solar, and ways to save money. > True. The best way to save money is to avoid photovoltaics at all cost. > . Many > . people have a mental block against it, and you will never convince > . them otherwise. > As opposed to "True Believers" who can’t stand cost-benefit analysis"

trust me, I’m not a True Believer. The problem I have with the solar engery field is that it has many "granola types" in it. They will espouse the value if making collectors out of dung and chewing gum and how it will also channel the sun god’s love through your home…. But, the field also has researchers from many companies and universities. I think you would all be surprised how many oil companies are in the business, mostly on the wings, but they are interested. When you go to one of these solar energy meetings you will see technical talks on the Stirling Engine Efficiencies right next door to talks on Straw Bale Construction (warning new flame war…) However it was these "pioneers" who kept the field alive for all those long years, so that the engineers and scientists still have something to sink their teeth into. > . If you believe in the idea of solar power, go head, it will make you > . feel good. > Good and broke. > . And when all states allow net metering, you will be ready > . to hook up on day one. > Sure — if you want to sell .50/kWh electricity for .06/kWh.

Please see my comment about wholesale vs retail on a state by state basis.                 Cheers,                         Sid – Hide quoted text — Show quoted text -> — > | The picture atop of this message, if present, was > | made by "Saving Face" for the Macintosh, available at: > | http://www.santafe.edu/~smfr/utils.html

Response:

> And even if you have to sell at wholesale, there is always the warm > fuzzy feeling you will get knowing that you are helping the > environment. (said with a little bit of PC sarcasm, but I do also buy > into this.)

You’re only doing something for the environment if the net gain once you consider the environmental impact of the manufacture, installation, and operation of the PV’s amortized over the electricity generated during their life is better than that of the commercially produced electricity. This is one of the big fallacies of to a lesser extent electric vehicles and to a huge extent the abuse of Ethanol as a so-called renewable resource via the corn farming lobby. > I just talked to my wife (the mechanical/energy engineer for those of > you joining us now) She stated that with 3 kw, and good conservation > habits/appliances you can handle most of your load requirements except > for peak.

Three 3KW average is still a far cry from 260W peak.   As pointed out, that depending what you are using for heat/hot-water, you may make a bigger personal cost-impact and environmental gain using your solar collecting area to generate hot water rather than electricity.

Response:

> > And even if you have to sell at wholesale, there is always the warm > fuzzy feeling you will get knowing that you are helping the > environment. (said with a little bit of PC sarcasm, but I do also buy > into this.) > You’re only doing something for the environment if the net gain > once you consider the environmental impact of the manufacture, > installation, and operation of the PV’s amortized over the > electricity generated during their life is better than that > of the commercially produced electricity.

The picture is usually gets more complicated as you look more closely. The idea of electric cars being better than fossil fuels is that you may be able to make large power plants cleaner/mile than your car. But this depends on lot of stuff including the type of power plant. When I was in grad school, we read a paper (from the 70’s I believe) that tried to rank various types of power generation according to health risk. They actually cacluated "deaths/KWH" for most major power sources. The highest? Hydro. The deaths there had to do with the worker’s deaths and the dangers in working at the dams. (this may have changed in 2 decades). – Hide quoted text — Show quoted text -> This is one of the big fallacies of to a lesser extent electric > vehicles and to a huge extent the abuse of Ethanol as a so-called > renewable resource via the corn farming lobby. > I just talked to my wife (the mechanical/energy engineer for those of > you joining us now) She stated that with 3 kw, and good conservation > habits/appliances you can handle most of your load requirements except > for peak. > Three 3KW average is still a far cry from 260W peak. >   As pointed out, that > depending what you are using for heat/hot-water, you may make > a bigger personal cost-impact and environmental gain using > your solar collecting area to generate hot water rather > than electricity.

My only point was that solar can be cost effective. We are only going to do it if NY State enact net metering at retail pricing. As for solar hot water, these systems generally need more maintainance than most home owners are willing to do.                 Cheers,                         Sid

Response: