Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) is a 501(c)(3) not-for-profit organization, based in Milford, Connecticut, founded 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.
- Conducts conferences throughout the United States to provide the latest knowledge on research and treatments
- Connects individuals with CRPS/RSD with one another, 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 USPS and email annually.
RSDSA is governed by a national Board of Directors and guided by a Scientific Advisory Committee.
RSDSA is led by one full-time professional and four part-time staff. Contact Jim Broatch, MSW, Executive Vice President, Director with any questions.
Read the latest RSDSA annual report.