NeuroTalk Support Groups

NeuroTalk Support Groups (https://www.neurotalk.org/)
-   Reflex Sympathetic Dystrophy (RSD and CRPS) (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/)
-   -   the rash (https://www.neurotalk.org/reflex-sympathetic-dystrophy-rsd-and-crps-/16124-rash.html)

buckwheat 04-04-2007 11:06 PM

Dear Frogga,

I know my circulation is involved. Which has alot to do with the lymph system.

If are circulation is even compromised we are at risk for severe infections. Their is a Dr Andrew Wright in the UK, I have heard he is hard to get in, but you need to be a top priority. Rosie you have your whole life ahead of you, forget your Brit manners be pushy. Doc's that are hard to get in are usually good.

I beg of you not to feel bad. This horrid RSD is not a matter of shaping up or putting one foot in front of the other. I have dear friends who are healthy RN's who do not have a clue.

I know I haven't met you face to face, but you are one of the most beautiful, lovely person's I have ever known. Hugs, Roz xxx

Hippyhair 04-05-2007 06:07 AM

Rash
 
In my first and second year of RSD, I had a chest rash. It started out as a little circle on my upper rib cage and eventually spread up to my neck. Dr. said it is RSD. Then! About 6 months ago it disappeared! Maybe, because meds are working...Dr. didn't know for sure.:)

Rainbow422 04-05-2007 08:15 PM

Thanks
 
I thought it was attached to the RSD, but since none of my doctors could figure it out and did not seem to worried, I tried not to worry too. As it nagged at the back of my mind.

The only advise they had was not to itch and cause infection. Alot of help when they would start to itch. LOL

Thanks for the advice and the answers!

Gentle Hugs,

Rain :hug: :hug:


All times are GMT -5. The time now is 02:19 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.