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. Our mission is to provide support, education, and hope to everyone affected by the pain and disability of CRPS/RSD while we drive research to develop better treatments and a cure. Please visit our website at rsds.org for more information on RSDSA-funded research projects and our other initiatives.