Reflex Sympathetic Dystrophy Syndrome Association (RSDSA)
RSDSA's mission is to provide support, education, and hope to everyone affected by #CRPS / #RSD while we drive research to develop better treatment and a cure. RSDSA's mission is to provide support, education, and hope to everyone affected by CRPS/RSD. RSDSA, founded in 1984, is a national not-for-profit organization whose mission is to provide support, education, and hope to all affected by CRPS while we drive research to develop better treatment and a cure.
Founded
1984
27000
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1050649
RSDSA | 40 years of helping those affected by CRPS 40 years of helping those affected by CRPS 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. 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.
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Nerve, Muscle, and Bone Diseases Category
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