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 10-01-2013, 12:11 AM #11
Sylmeister Sylmeister is offline
Junior Member
 
Join Date: Aug 2013
Location: Albuquerque
Posts: 60
10 yr Member
Sylmeister Sylmeister is offline
Junior Member
 
Join Date: Aug 2013
Location: Albuquerque
Posts: 60
10 yr Member
Default

Hi William, I have only had RSD for a little over 10 years. How awful for you, so much time. I've had a lot of the last week with sort of mind blowing pain. I think because, as you mentioned, winter is coming. Fall used to be my favorite time of year, but we have had about 3 days in the last week, that were considerably cooler and I have been a wreck. It's not even cold, it's startlingly beautiful, but my pain has been awful and it's got me thinking of all of the things I can't do. Not something I usually dwell on. Hang on and get some fleece socks. That is my cold weather friend. I can't stand socks with even a tiny bit of elastic. I could scream with things that touch with any firmness. Fleece socks are soft and warm and they don't really touch my feet or ankles, they just snuggle me softly. I think I have about 10 pair now. They last years and since I moved to a higher elevation last year, I love them even more. If I had a sewing machine or knew how to sew, I'd seriously make them and mail you all a pair. They are that awesome.

Welcome ad hope to hear from you here. Pulling off 18 years tells me you are a pro at managing this curse.
Warm wishes, Sylvia
Sylmeister is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Brambledog (10-01-2013)

advertisement
Old 10-01-2013, 01:46 AM #12
AZ-Di's Avatar
AZ-Di AZ-Di is offline
Member
 
Join Date: Mar 2013
Location: Arizona
Posts: 453
10 yr Member
AZ-Di AZ-Di is offline
Member
AZ-Di's Avatar
 
Join Date: Mar 2013
Location: Arizona
Posts: 453
10 yr Member
Default

Hi William,
Like all the others here I'm sorry for the circumstances that brought you here but welcome. Everyone here is so supportive and helpful!
I don't know what I'd do without this group!

I feel even worse for the spread to your kidney. What I've been told about preventing spread is take Vitamin C 500 -1000 mg. daily. I've had several nerve blocks & I don't know if that prevents it or not. I've only been diagnosed for 9 months and so far very little spread.

The people really do understand what you're going through even if they can't fix it. We can be ourselves here and don't have have to put on the brave face all of the time.
AZ-Di is offline   Reply With QuoteReply With Quote
Reply

Tags
chronic, crps, pain, rsd


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
New Member Yorkieville New Member Introductions 7 07-07-2011 02:55 PM
New Member with PCS AllInMyHead New Member Introductions 3 07-06-2011 05:50 AM
New member vigwig New Member Introductions 11 05-10-2008 02:40 PM
new member sunniecher New Member Introductions 7 05-09-2008 09:44 AM
new member Traceeg New Member Introductions 5 03-23-2008 12:30 PM


All times are GMT -5. The time now is 12:39 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.