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
 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 10-19-2011, 01:51 AM #1
kimberlyluv kimberlyluv is offline
Junior Member
 
Join Date: Oct 2011
Location: utah
Posts: 11
10 yr Member
kimberlyluv kimberlyluv is offline
Junior Member
 
Join Date: Oct 2011
Location: utah
Posts: 11
10 yr Member
Smirk rsd and cprs 2

i am new to this site! i have had rsd and cprs 2 for 7 years now i am on crutches have benn for 7 years also it has ruined my life i went into a clinic to get a pain shot in my hip and the nurse missed and went into my sciatic nerve and also the medication she used was so strong as like acid ruined my sciatic nerve i felt stabbing shocking pain from my buttocks to my foot and here i am 7 years later and it has spread! i have tried therapy that makes it worse!! tens unit wont use eve again that is to painful i have not sat down for 7 years or laid in a bed i lean over my bed or table so nothing touching my right leg and buttocks and now its in the left leg moving in arms hands! i get about hour of sleep every 2 weeks if i am lucky! i ahte it the pain is unbarable it has hurt my kids i cant do much with them no more my ten year old cant remem me sitting on a couch hugging her playing with her on the floor she was 3 when i happened!no insurance dont get u no where!! i have had my downs with it very depress run down no enery so tired!! and hate watching everyone do things i use to do i cant no more!! i am trying the new treatment called calmare today i am nervous but the doc that is doing it is also doing it for free he wanted to do the stimulator for free but could not get one donaited! but i herd the longer u have had it and the more it has spread have a hard chance of it working! i no its not a guarantee worth a try anything is! my pain mana and specailist that was treating just retired so have no doct right now! very upset about that because i got no warning! so dont no where to go where i can afford but no it dont get easier and the pain gets worse and worse!! this life i have lived for over 7 years is killing me and not fair to my kids or husband but glad my husband has stuck by my side!! anyone who knows of any new treatments medications anything let me know!! i am legally disabled now but of course did not have enough work credits to get on medicare was short 4 hate how that works so trying to get baack on medicaid and also need a doc asap!!
kimberlyluv is offline   Reply With QuoteReply With Quote
 


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
specialist of CPRS in San Francisco/Bay Area? rsinha Reflex Sympathetic Dystrophy (RSD and CRPS) 3 10-18-2011 09:10 PM
CPRS Conference FYI HopeLivesHere Reflex Sympathetic Dystrophy (RSD and CRPS) 2 06-17-2007 07:20 PM


All times are GMT -5. The time now is 06:31 PM.

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.