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 * Home
 * About
   * History
   * Board of Directors
   * Scientific Advisory Committee
   * Annual Report
 * Living With CRPS
   * Definition of CRPS
   * How CRPS is Diagnosed
   * Signs & Symptoms
   * Resources
   * Post-Diagnosis Steps
   * Coping Strategies
   * Resources for Caregivers
   * For Youth
 * Research
   * Clinical Treatment Guidelines
   * Treatments
   * Educational Presentations
   * Research Grants
 * Community
   * Support Groups
   * Jenkins Patient Assistance Fund
   * Carolyn’s Cards
   * Send a Child to Camp
   * CRPS Warriors Memorial
 * Media
   * Newsletters
   * Community Updates
   * Information Packages
   * Brochures & Cards
   * Therapy Resources
 * Advocacy




40 YEARS OF HELPING THOSE
AFFECTED BY CRPS

Donate Now


LIVING WITH CRPS

RSDSA gives those affected by CRPS education, advocacy and hope! From signs &
symptoms, to diagnosis, to living with CRPS long term, this section has health
and lifestyle information for adults and youth living with this painful and
debilitating condition – as well as for their families and caregivers.

Learn More


RESEARCH

RSDSA raises funds for research to find better treatments – and a cure – for
CRPS. We also work with research groups and healthcare professionals worldwide
to foster collaboration, communication and awareness. Here you’ll find the
latest studies and articles about progress and breakthroughs

View Research


COMMUNITY

CRPS can be isolating. RSDSA ensures that those affected by CRPS are not alone.
We’ve built a strong, vibrant community that participates in conferences,
fundraising events, mentoring, support groups and other activities that help
them take control of life with CRPS. Join us.

Learn More


OUR MISSION

Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) mission is to provide
support, education, and hope to all affected by the pain and disability of CRPS,
while we drive research to develop better treatments and a cure.




UPCOMING EVENTS

Walk Strong 2024
April 27, 2024

Join Burning Hope and RSDSA in walking a 3k in support of the CRPS Community.
All proceeds will aid in research and treatment options for those suffering from
CRPS.

View Details
Young Adult Retreat: Denver
May 31, 2024

RSDSA's 2024 Young Adult Retreat will take place in Denver, Colorado from
Friday, May 31st to Monday, June 3rd!

View Details
The Coalition Against Pediatric Pain’s (TCAPP) Pediatric Pain Week
July 16, 2024

The 2024 camp will be from July 16-20 at The Center for Courageous Kids in
Scottsville, Kentucky!

View Details
View All Events


CORPORATE PARTNERS

Diana and Peter Smith, In Memory of Stephanie Theresa Smith
Dr. & Mrs. Lawrence and Judy Zager, In Loving Memory of Hunter Lia Zager
Lynn & Michael Coatney


RECENT VIDEOS

5TH ANNUAL RSDSA LONG ISLAND CRPS AWARENESS WALK & EXPO RADIO INTERVIEW

THE EXPERIENCE AND IMPACT OF HAVING CRPS AND THE NEED FOR EARLY DIAGNOSIS &
TREATMENT

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RSDSA is a registered 501(c)3 non-profit organization. For donation purposes,
our EIN is 22-2559139.

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