Resources- Specific Diagnosis Card Catalog- Reflex Sympathetic Dystrophy Syndrome
Who to Contact
RSDSA - Reflex Sympathetic Dystrophy Syndrome Association of America
P.O. Box 502
Milford, CT 06460
(203) 877-3790
E-mail: patient.representative@rsds.org
Web: www.rsds.org
The Reflex Sympathetic Dystrophy Syndrome Association of America (RSDSA) is a national not-for-profit organization, headquartered in Milford, Connecticut, that promotes greater public and professional awareness of RSD/CRPS, a painful neurological syndrome that may affect more than 1.5 million Americans. We also fund research fellowships and evidence reports on RSD/CRPS.
Our mission is to promote public and professional awareness of Reflex Sympathetic Dystrophy Syndrome (RSD) and to educate those afflicted with the syndrome, their families, friends, insurance and healthcare providers, on the disabling pain it causes. We encourage individuals with RSD to offer each other emotional support within affiliate groups. And finally, we are committed to raising funds for research into the cause and cure of RSD.
Where to go to Chat with Others?
RSD
This is a list for people that have Reflex Sympathetic Dystrophy (RSD). This is a list to share information, and gain support for those that suffer with RSD.
RSD-CRPS of America
Founded to provide a place to discuss treatments, medications and vent with others who suffer from this painful disease.
RSD Hope - Teens
A support group for kids and teenagers suffering from reflex sympathetic dystrophy (RSD)
RSD Support
A safe place to discuss RSD and life with RSD.
Learn More About It
Reflex Sympathetic Dystrophy Syndrome Fact Sheet from NIH
An Introduction to Reflex Sympathetic Dystrophy Syndrome (RSDS)
Links
RSDSA-Reflex Sympathetic Dystrophy Syndrome Association of America
Reflex Sympathetic Dystrophy Syndrome Association of California
RSD UK
Awareness, Education and Support for those involved with RSD/CRPS issues
The International Reflex Sympathetic Dystrophy Foundation
Living with RSD and Fibromyalgia
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