Supporting the CRPS Community
The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) is a 501(c)3 not-for-profit organization based in Milford, CT, founded in 1984. Our mission is to provide support, education, and hope to all affected by the pain and disability of CRPS/RSD, while driving research to develop better treatments and a cure.
RSDSA is governed by a national Board of Directors and guided by a Scientific Advisory Committee, and we mail out hundreds of introductory packets via physical mail and email on an annual basis.
Board of Directors
Scientific Advisory Committee
RSDSA is a 501(c)(3) not-for-profit organization. Founded in 1984, we are the oldest organization dedicated to supporting the CRPS/RSD community, funding research to find better treatments and ultimately a cure for this rare disease that afflicts people with chronic, potentially debilitating pain.
In addition to viewing our audit and annual accomplishments, you may find additional information about our activities and success stories throughout our website. We are also available to speak with you one-to-one about support opportunities. Thank you for your interest in RSDSA.
Here is our 2021 and 2020 audit for your review, as well as our 2022 initiatives and accomplishments.