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PO Box 502
Milford, CT 6460
The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) is a non-profit organization founded to promote greater public and professional awareness of complex regional pain syndrome (CRPS), formerly known as reflex sympathetic dystrophy syndrome (RSD) and support research into the causes and cure of complex regional pain symdrome/reflex sympathetic dystrophy (CRPS/RSD). The association's mission also includes the establishment and organization of support groups for affected individuals and their families; and promotion of awareness of reflex sympathetic dystrophy syndrome among healthcare professionals and the general public. Founded in 1984, the association provides a referral service to physicians, offers a pen pal service, and promotes patient advocacy. RSDA offers a variety of educational materials and services including an information packet, a quarterly newsletter, a statistical report on reflex sympathetic dystrophy syndrome derived from member questionnaires, reference articles, brochures, booklets, and videos. The association also provides educational in-service conferences for healthcare professionals and patients and has published clinical practice guidelines for the diagnosis, treatment, and management of RSD/CRPS.
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