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Raising Awareness of Complex Regional Pain Syndrome since 1984.
     

Team RSDSA at the 2009 Achilles Walk for Hope & Possibility
June 28, 2009 | Central Park, New York City

Click here for 2009 Forms, Online Registration, and to view Team RSDSA's Firstgiving Pages!
 


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The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) was founded in 1984 to promote public and professional awareness of Complex Regional Pain Syndrome (CRPS), also known as Reflex Sympathetic Dystrophy (RSD).

Our website is designed to give patients, family members, and healthcare professionals the most up-to-date information on treatment, legislation, support groups, research, fundraising, and patient stories. RSDSA does not accept advertising for this website. Our website is funded by RSDSA membership revenue.

The website is not intended to provide advice on personal medical matters or to substitute for consultation with a physician.

Recent News

Registering Online and Fundraising for the 2009 Achilles Walk for Hope & Possibility in NYC

FDA: Botox and Botox Cosmetic (Botulinum toxin Type A) and Myobloc (Botulinum toxin Type B): Boxed Warning Required

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Achievements

We are producing a DVD that will instruct physical and occupational therapists how to restore function in people with CRPS.

We participated in the Achilles Walks for Hope & Possibility in Cincinnati and New York City, as well as numerous walks and fundraising events across the country.

For more Achievements, click here.

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© 2009 RSDSA | Please contact the webmaster with questions or comments about this site.
Updated May 7, 2009
 

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