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)


advertisement
Reply
 
Thread Tools Display Modes
Old 12-16-2006, 10:13 AM #1
coachV's Avatar
coachV coachV is offline
Member
 
Join Date: Sep 2006
Location: near Allentown, PA
Posts: 209
15 yr Member
coachV coachV is offline
Member
coachV's Avatar
 
Join Date: Sep 2006
Location: near Allentown, PA
Posts: 209
15 yr Member
Default

i know of 2 people who have been involved in testing this drug.....there was someone on the old board who participated in a thalidomide study and had wonderful results from it, and i think the lenalomide is so close chemically that they're hoping for similar results....the odd thing about using it, is that thalidomide can actually CAUSE nerve damage, but still seems effective for neuropathic pain.

the lenalomide would, i think, not be part of the ongoing legal issues affecting the use of thalidomide (some of the cases involving affected children have yet to be settled) and i would guess that the company is hoping to make some money on the new version to help offset the horrendous legal costs they've been facing.

these drugs r fairly effective at slowing tumor progression....they inhibit cell splitting (which accounts for the birth defects).....the dicovery of neuropthic pain effect happened when they were treating a cancer patient who also had rsd.

i also knew of this from a person in an e-mail group that i joined years ago (the group has now disbanded)....when she used thalidomide she also had terrific results...it reduced her pain to minimal levels......her problem with it was simple.....when the study ended, she couldn't afford the pills.....her insurance company, of course, refused to pay, because of the 'experimental/investigational" loophole......the meds would have come to over $1,000 a month......that was thalidomide, and i have no idea if lenalomide would be equally prohibitive.

the people who participated in the study had to sign a long, complex agreement agreeing that they understood the risk of birth defect, agreeing to keep the medication out of the reach of children (duh!), agreeing NOT to get pregnant for, i think, at least a year, and waiving all legal action...it was far more restrictive than most drug study contracts.....so yes, i think we all have reason to be a bit spooked by the idea of using this drug.

but it's interesting, isn't it?
__________________
best to all,
liz
coachV is offline   Reply With QuoteReply With Quote
Reply


Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off


Similar Threads
Thread Thread Starter Forum Replies Last Post
Participation in Clinical Trials jeanb Parkinson's Disease 3 12-16-2006 11:03 AM
ALS current Clinical Trials list wallyw1 ALS 0 11-09-2006 08:17 AM
Worthless clinical trials BobbyB ALS 0 09-30-2006 08:24 AM


All times are GMT -5. The time now is 12:41 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.
 

NeuroTalk Forums

Helping support those with neurological and related conditions.

 

The material on this site is for informational purposes only,
and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider.


Always consult your doctor before trying anything you read here.