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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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#1 | ||
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Senior Member
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Simply hard to believe....
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#2 | ||
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In Remembrance
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Mike,
As always, Thanks for the 'Heads Up'! What can we do, to whom can we write? We don't want to see this go down in WA, nor trickle to other states! Again, My Thanks! Pete asb |
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"Thanks for this!" says: | fmichael (12-06-2010) |
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Senior Member
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Quote:
Pete - What to do? First things first, I invite anyone to go the Dr. Okie's "perspective article" with a fine tooth comb and send some scathing letters to the editor of the NEJM, not that they will be published. Better yet, encourage your doctors to do so. Off hand, I think the best attack is a numbers game: I suspect there are far many more people in intractable pain in this country than who perish through recreational abuse if these drugs: by several orders of magnitude. Whether our population is equaled by a group of abusers in Appalachia is another matter, but then the argument becomes the immorality of condemning some to pain just so other can't have what passes for fun. (Somewhere, the cold hand of Calvin has to be involved in this one.) For specific information, the best source right now appears to be the American Pain Foundation. Here's their page on the subject: http://www.painfoundation.org/take-a...fforts/wa.html Purdue Pharmaceuticals (maker of OxyContin) probably has a good hand on the numbers as well. It's a corporate sponsor of the RSDSA, so Jim Broatch might be a good point of contact. Just a few thoughts . . . Mike |
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"Thanks for this!" says: | AintSoBad (12-07-2010) |
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#4 | ||
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Elder
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I cannot believe in this country, that this type of thing could happen. Evidently none of the people sponcering this bill have never had pain of any kind much less NP, or the hurtfull conditions people have all over this country. The ignorance of those folks is frightening. Most people who use opiods for true pain are not doing it because they want to, they do it because they have to, to be able to have some kind of quality to their lives. We should write to our state senators and maybe become more active in protesting such bills. This would place unfair restrictions on pain specialists, and take time away from the patients.
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