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 11-10-2014, 11:33 AM #1
zookester's Avatar
zookester zookester is offline
Member
 
Join Date: Jun 2013
Posts: 583
10 yr Member
zookester zookester is offline
Member
zookester's Avatar
 
Join Date: Jun 2013
Posts: 583
10 yr Member
Default

Quote:
Originally Posted by ShaggyChic_1201 View Post
Thanks Zooster. Can you say more please. Does the uv protection clothing stop the pain, (a laser defense system, so to speak ) or prevent further harm?
Hey ShaggyChic,

lol.. I feel so connected to you because you are the first person to ever describe that sun through the window thing that I so dread in the summer time. haha.. we are soul mates Anyways yes, the UV clothing has seemed to reduce the laser feeling and more importantly it has kept the rash at bay that usually forms with any sun exposure. My doctors refer to it as livedo reticularis a lace like rash under the skin or a vascular rash. I don't have it on my upper body just my legs and because of tactile stimulation causing great pain, I only wear leggins or yoga type pants because the even pressure is much less painful than the tapping of loose fitting clothing. I have found Athleta, REI and Patagonia (and I'm sure others) have a good assortment of the type of UV protected clothing that has textures I can tolerate. I have since started wearing the shirts with UV protection just as a precaution/prevention. It's weird because most people I have spoken to either have sensitivity to cold or heat but few both.. so this has been an added challenge trying to find middle ground.

Regarding ice therapy - for me it seems quite logical that ice would cause problems since our blood flow is compromised by CRPS and using ice would only make this worse. I was also formerly a mountain climber and have seem many people lose fingers and have subsequent neuropathy due to frost bite so it makes sense to me. Personally I have found that the use of moist heat works best even though my legs burn constantly the moist heat is still more soothing than anything else I have found. Warm epsom salt baths also really help when pain is severe and the magnesium in it is very beneficial to the body for a number of reasons.

I hope this helps,
Tessa
zookester is offline   Reply With QuoteReply With Quote
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


Similar Threads
Thread Thread Starter Forum Replies Last Post
The Cold, Hard Facts of PD - Is It Partly Caused by the Cold? reverett123 Parkinson's Disease 9 07-07-2011 03:31 PM
Ice Cold Leg Lisa in Ohio Reflex Sympathetic Dystrophy (RSD and CRPS) 8 09-03-2010 09:56 PM
@#$% Cold! cyclelops Peripheral Neuropathy 138 01-20-2010 12:32 PM
Does this dog know it is cold outside? Vowel Lady Pets & Wildlife 1 01-11-2008 02:14 AM


All times are GMT -5. The time now is 10:17 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.