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RSDSA: More than 30 Years of Helping Those Affected by CRPS/RSD

Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) is an international 501 (c) 3 not-for-profit organization, based in Milford, Connecticut, formed in 1984. Our mission is to provide support, education, and hope to all affected by the pain and disability of CRPS/RSD, while we drive research to develop better treatments and a cure.

RSDSA:

  • Conducts conferences throughout the United States to provide the latest knowledge on treatment and research
  • Connects individuals with CRPS/RSD with each other, as too often individuals with CRPS/RSD have never met someone else with the same disorder
  • Provides hope and tools for now and the future.

RSDSA has a toll-free number, 877-662-7737 and we mail out hundreds of informative introductory packets via postal mail or email annually.

RSDSA is governed by a national Board of Directors and guided by a Scientific Advisory Committee.

RSDSA is led by two full-time professionals and three part-time staff. Contact Jim Broatch, MSW, our Vice President, Director or Samantha Barrett, Special Events Coordinator.

Read the latest RSDSA annual report.