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 05-14-2009, 12:21 AM #1
loretta loretta is offline
Senior Member
 
Join Date: Feb 2007
Posts: 1,090
15 yr Member
loretta loretta is offline
Senior Member
 
Join Date: Feb 2007
Posts: 1,090
15 yr Member
Default

Hi Kate,
I'm sorry you have had spread in your hand and arm. Are you in physical therapy?
It's really important to get treatment early, it's the best and usually the only time for possible remission. Does your Dr. have a plan for you? Our limbs can permanently lock up without treatment. So important to keep moving, massage therapy is also very good along with p.t. I've also used swimming as a way to keep from freezing up. I've had RSD 13 years now and full body. Only have left hand partially froze up like a claw. Am grateful I stayed with pt along with desensitizing my limbs. It took time to find a good RSD Dr, but so important.
I miss wearing my wedding rings too and other special rings.
If you live close to a large city, a RSD support group really can be a wealth of encouragement and information. We have guest speakers that are Drs. Pharmacists, etc and I've found a lot of coping skills here on the NT and local group. You can find location and phone number on the internet thru RSDSA by giving you zip code. Take care, loretta
loretta is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
Dew58 (05-14-2009)
Old 06-02-2009, 05:00 AM #2
baseballfan baseballfan is offline
Junior Member
 
Join Date: Mar 2009
Location: California
Posts: 94
15 yr Member
baseballfan baseballfan is offline
Junior Member
 
Join Date: Mar 2009
Location: California
Posts: 94
15 yr Member
Default

Quote:
Originally Posted by loretta View Post
Hi Kate,
I'm sorry you have had spread in your hand and arm. Are you in physical therapy?
It's really important to get treatment early, it's the best and usually the only time for possible remission. Does your Dr. have a plan for you? Our limbs can permanently lock up without treatment. So important to keep moving, massage therapy is also very good along with p.t. I've also used swimming as a way to keep from freezing up. I've had RSD 13 years now and full body. Only have left hand partially froze up like a claw. Am grateful I stayed with pt along with desensitizing my limbs. It took time to find a good RSD Dr, but so important.
I miss wearing my wedding rings too and other special rings.
If you live close to a large city, a RSD support group really can be a wealth of encouragement and information. We have guest speakers that are Drs. Pharmacists, etc and I've found a lot of coping skills here on the NT and local group. You can find location and phone number on the internet thru RSDSA by giving you zip code. Take care, loretta
Hi Lorerta,

No I am not in any pt. I am waiting for the insurance company to approve a sympathetic nerve block. Yes I live by a large city and my psych doc gave me a list of RSD groups that meet in my area. thanks

Kate
baseballfan 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
Spread from an LP? dshue Reflex Sympathetic Dystrophy (RSD and CRPS) 3 01-19-2009 04:21 PM
RSD spread MominPainRSD Reflex Sympathetic Dystrophy (RSD and CRPS) 7 01-10-2009 03:09 PM
Spread allentgamer Reflex Sympathetic Dystrophy (RSD and CRPS) 23 07-23-2007 02:54 AM
For those of you who had spread LisaM Reflex Sympathetic Dystrophy (RSD and CRPS) 16 11-01-2006 09:25 PM
Spread allentgamer Reflex Sympathetic Dystrophy (RSD and CRPS) 8 09-29-2006 10:36 AM


All times are GMT -5. The time now is 11:09 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.