reflex sympathetic dystrophy


reflex sympathetic dystrophy Reflex Sympathetic Dystrophy


What is reflex sympathetic dystrophy?

Reflex Sympathetic Dystrophy, known as RSD, is a chronic neurological disease which affects millions of people here in this country and around the world. And the number of Reflex Sympathetic Dystrophy cases among children is alarming.


What is the International Foundation for Reflex Sympathetic Dystrophy?

This website, operated by the International Foundation for Reflex Sympathetic Dystrophy contains both educational and clinical information about Reflex Sympathetic Dystrophy (RSD) syndrome. Sections of this website include:
  • How to Help - help us fund continued research for Reflex Sympathetic Dystrophy.

  • A 40 minute video, Children with Reflex Sympathetic Dystrophy, has been recorded with recent RSD treatment innovations and has been reviewed by a panel of international experts on Reflex Sympathetic Dystrophy. This RSD video can be downloaded to your computer for viewing or you can purchase a copy of the RSD video in either VHS or DVD format. Proceeds of the video sales benefit our Reflex Sympathetic Dystrophy foundation.

  • Research Updates on Reflex Sympathetic Dystrophy - A primary mission of the Reflex Sympathetic Dystrophy Foundation is to establish an international network, with up to the minute information about ongoing RSD research, which will help educate medical professionals around the world.

  • Clinical Practice Guidelines For Reflex Sympathetic Dystrophy (third edition) - The Clinical Practice Guidelines have become a standard for managing RSD.
For a complete listing of the areas on the Reflex Sympathetic Dystrophy Foundation website, please click here. We hope this website can help educate the world and help people understand what RSD is all about.
reflex sympathetic dystrophy



HOME   |   MENU   |   DONATE   |   CONTACT US


Copyright 2003 International Research Foundation for RSD/CRPS.
All rights reserved.
For permission to reprint any information on the website, please contact the Foundation.