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)

Reply
 
Thread Tools Display Modes
Old 01-10-2016, 07:14 PM #1
-Spike-'s Avatar
-Spike- -Spike- is offline
Member
 
Join Date: Sep 2015
Posts: 277
8 yr Member
-Spike- -Spike- is offline
Member
-Spike-'s Avatar
 
Join Date: Sep 2015
Posts: 277
8 yr Member
Default

Quote:
Originally Posted by RSD ME View Post
hi purple. i just wanted to let you know that my pm dr said that though the scs might be most effective the first two years of being diagnosed with rsd, that it could still help after that. i am still not ready to consider it because it is major surgery but if you feel you might want to try it, there is a trial scs that is for five days. it's still pretty invasive surgery that i am not ready to consider but maybe you should talk to you dr about it if you feel regretful for not doing it sooner. its a very difficult and personal decision to make and only you and your dr can know for sure if it's the right choice for you. i hope whatever you decide, you feel some relief from the rsd pain soon. soft hugs coming your way.
I think there is at least one person that posts here occasionally that just had her spinal cord stimulator surgery completed. Maybe that person can chime in, if they happen to read this thread.
__________________
~ No Pain is Gain ~
-Spike-
-Spike- is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
IamJenn (01-11-2016), RSD ME (01-11-2016)
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



All times are GMT -5. The time now is 01:42 PM.


Powered by vBulletin • Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise (Lite) - vBulletin Mods & Addons Copyright © 2025 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.