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 02-06-2007, 07:27 PM #11
GalenaFaolan's Avatar
GalenaFaolan GalenaFaolan is offline
Member
 
Join Date: Dec 2006
Location: Florida
Posts: 445
15 yr Member
GalenaFaolan GalenaFaolan is offline
Member
GalenaFaolan's Avatar
 
Join Date: Dec 2006
Location: Florida
Posts: 445
15 yr Member
Default

Awesome! They have clothes, like comfy sweatpants, wrist bands, pens, bags, etc. It's awesome. As soon as I get some money free I'm going to get another sticker (the one I have has been there so long it's beginning to fall off!) and maybe a few other things.

Hugs,
Karen
__________________
Laugh until you cry, don't cry until you laugh.

Living, loving and laughing with RSD for 14 years and counting.
GalenaFaolan is offline   Reply With QuoteReply With Quote

advertisement
Old 02-08-2007, 08:03 PM #12
InHisHands InHisHands is offline
Member
 
Join Date: Dec 2006
Posts: 808
15 yr Member
InHisHands InHisHands is offline
Member
 
Join Date: Dec 2006
Posts: 808
15 yr Member
Exclamation Hello, INSIGHT!

Quote:
Originally Posted by Insight View Post
Dear Hands,

I just sent a long message about our daughter's experiences with RSD, but I'm not sure it got sent. I'll briefly re-state the message just in case. Our daughter was tremendously helped by Dr. David Sherry of the Children's Hospital of Philadelphia. His waiting list was too long, so we bought his DVD and gave it to a local physical therapist in our (large) city. Dr. Sherry graciously offered to have his staff and him consult with our PT. Our PT put our daughter thru 3.5 gruelling weeks of full-time (9AM - 4PM) physical therapy. Some improvements started after a few days. Dr. Sherry recommended that she not have any pain meds or anesthesia, so our daughter toughed it out on her own. Full function returned by the end of treatment. Her pain decreased during treatment, but didn't fully dissapate until several months later (after her treatment had already ended). About one year has passed and our daughter is symptom-free. Hope this is helpful.
Hi there. I would love to talk some more with you regarding this. I tried to reply to your message, but I got a message saying that you cannot receive PM's.

I'd love to ask you some questions. Are you willing to talk some? Maybe we could start a thread to discuss it, or email.

Hope to hear from you. I am a teen, and so I'd love to discuss your daughter's treatment/ results.

Thanks.
InHisHands 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



All times are GMT -5. The time now is 09:05 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.