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 12-27-2015, 07:41 PM #4
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

When my RSD spread and got much worse a few years ago I went to group E...got almost no sleep...never more than 15-30 minutes at a stretch and basically fell asleep due to pure exhaustion after several days of no sleep. Then the dr put me on amitriptyline and I went to group D...getting a solid stretch of 3 hours each night which isn't much but compared to the hellish several months prior I felt a lot better. Then I did tDCS treatments and I was able to get off the amitriptyline and was getting 6 hours a night consistently...occasionally more with just occasional bad nights during flare ups.

In October I fell off the top of a 10ft ladder at work and tore my rotator cuff...Right before thanksgiving I started physical therapy which made the shoulder much worse. Now...for the past month...I've been back to group E and it SUCKS. Can't sleep at all with this new pain even with the pain meds. They gave me flexoril for a couple weeks in the beginning to help me sleep but once I ran out of that I've been in hell with my sleep patterns. Insomnia is now my constant companion again and it's taking a hell of a toll on me where my pain levels are concerned. My RSD has been flaring more often and I've been house bound for a month now. Using the Quell device helps a little but I can't do many of my other pain management things at home due to those same things hurting the shoulder. We all deal with so much pain and I am used to that...but this shoulder pain on TOP of everything else has thrown me into a tail spin. Hoping it gets better soon because I will tell you that sleep makes a HUGE difference in my ability to cope with the RSD day in and day out...it's essential and not getting it right now is a killer...
catra121 is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
-Spike- (12-27-2015), BioBased (12-27-2015), PurpleFoot721 (12-27-2015)
 


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
Sleep Patterns? Breaker814 Reflex Sympathetic Dystrophy (RSD and CRPS) 11 03-24-2012 06:10 AM


All times are GMT -5. The time now is 12:50 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.