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)

 
 
Thread Tools Display Modes
Prev Previous Post   Next Post Next
Old 02-09-2013, 08:29 AM #27
catra121's Avatar
catra121 catra121 is offline
Senior Member
 
Join Date: Jan 2010
Location: Illinois
Posts: 1,785
15 yr Member
catra121 catra121 is offline
Senior Member
catra121's Avatar
 
Join Date: Jan 2010
Location: Illinois
Posts: 1,785
15 yr Member
Default

Quote:
Originally Posted by *pamela* View Post
I'm also curious: can someone explain to me how tCDS has helped them? Is it mainly for helping cognitive improvement, or does it also reduce your pain level/ability to function in day-to-day life?

(sorry to be that annoying person who is overwhelmed by 48 pages and so I'm asking questions that have probably already been answered)
For me...tDCS has helped with some things and not with others. Things that have improved for me with use of tDCS:

1. Pain flares less often.
2. Pain flares last a shorter amount of time (one day vs. days or weeks).
3. Sleep went from only getting 3 hours a night with meds to now 6-8 without meds (HUGE).

I did not rely ONLY on tDCS as a treatment but since beginning it's use my balance has also improved a little (which I think is mostly due to the physical therapy and increased activity since returning to work but tDCS may have played a part as well).

Things that have not improved with use of tDCS:

1. Pain levels (flares are less often but the daily pain is the same and rises at the same triggers).
2. Hypersensitivity to touch and cold.
3. Ability to concentrate (never tried a protocol for this specifically though...may try in future).

Overall I would say that tDCS has been HUGE for me in taking back a more normal life. The increased amount of sleep and fewer flare and flares that last only a day are big deals to me for increasing my ability to function. That, however, has been my primary focus with ALL of my treatment plans for tDCS in the past 2 years...to target symptoms and the things that were preventing me from FUNCTIONING as a normal person. I still need a walker and have limitations...but I am back to work and living a "normal" life again. Prior to starting tDCS I was just beginning to get back on my feet after being in a wheelchair for almost a year.

Take care and good luck.
catra121 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Joydee (02-09-2013)
 


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
In remission right now PMCPMC Myasthenia Gravis 3 09-13-2011 05:42 PM
RA in remission. Why is SFN not better? catloucle Peripheral Neuropathy 26 03-06-2011 11:22 PM
Remission !!!! Goodn'Plenty Reflex Sympathetic Dystrophy (RSD and CRPS) 23 04-16-2010 01:51 PM
RSD in Remission Maureen Hartnett Reflex Sympathetic Dystrophy (RSD and CRPS) 7 01-07-2008 08:41 PM
ang....and remission jennyk38 Reflex Sympathetic Dystrophy (RSD and CRPS) 2 08-24-2007 07:01 PM


All times are GMT -5. The time now is 06:42 AM.


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.