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 02-10-2010, 07:59 PM #6
keep smilin keep smilin is offline
Member
 
Join Date: Aug 2009
Posts: 851
15 yr Member
keep smilin keep smilin is offline
Member
 
Join Date: Aug 2009
Posts: 851
15 yr Member
Heart I feel silly!!!!!

Quote:
Originally Posted by loretta View Post
Hi Cindi, Wow you have been snowed on and snowed on again. It only looks beautiful if you don't have to go to work in it, if you still have electricity, have food stocked, lots of games for the kids, don't have RSD,
rent some funny movies for the kids. turn the fireplace on and have a little Dom, we don't have RSD so we can have it. I would like some of our vacations that I don't have in an album yet, and finish that project-it would be so much fun. Have Michael bluble on and other favorite CD's.
Now reality,could you call in for refill and it would be ready when someone is able to get out? Does the Pharmacy have a delivery service to patients.
Are you presently taking an anti-anxiety med? They work well on the sympathetic nervous system thus lowering pain level. The anti-depressant med like cymbalta does the same-lower anxiety thus lowers pain meds. Some towns have Pick Up and Delivery Service. That would be in the yellow pages.
Take care, I'm staying in, I'm in a flare too Cindi. I have a lesion on the back of my leg, last year I had two and they got infected, bad news. I'm also have hot spots.
I am totally mobile, except left hand got delayed in treatment so have 50% range of motion. But I can type, cut my own food. I'm grateful. I have terrible headaches. My plan is to have HBOT this summer. My Dr. just opened two clinics that each have a HBOT. So saving up for it now.
Hope you get thru this mixed up weather with as little pain as possible.Take care, loretta with soft hugs
I sure feel really silly asking this..but can someone explain to me exactly what a flare feels like????????????? I am trying to pin point what it may be but my RSD pain is constant and continual..same heightened mean pain with the hot/cold temperatures never ending..Ole' KS need some straightening out.....I am RSD totaled!!

luv, Kathy
keep smilin is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
cindi1965 (02-11-2010), Kakimbo (02-11-2010), loretta (02-11-2010), SandyS (02-11-2010)
 


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
How far does a flare go? 4cordelia Multiple Sclerosis 4 09-10-2010 05:48 PM
pseudo flare while still in a flare? legzzalot Multiple Sclerosis 9 09-29-2009 05:58 AM
First Flare Catch Multiple Sclerosis 5 02-06-2008 02:22 PM
My first flare or? Catch Multiple Sclerosis 6 02-05-2008 01:55 PM
Flare! coyote Fibromyalgia and Chronic Fatigue 5 09-18-2006 08:40 PM


All times are GMT -5. The time now is 02:50 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.