Reflex Sympathetic Dystrophy Syndrome Association

The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) is a national 501(c)(3) non-profit organization dedicated to providing support, education, and hope to those affected by Complex Regional Pain Syndrome (CRPS), formerly known as Reflex Sympathetic Dystrophy (RSD). Founded in 1984, the association focuses on promoting public and professional awareness of the condition to facilitate early diagnosis and treatment. RSDSA actively funds and supports research aimed at discovering better treatments and a potential cure for CRPS. They provide a variety of resources, including support groups, educational conferences, and advocacy initiatives to improve the quality of life for patients and their families. The organization serves as a critical link between the patient community, medical professionals, and researchers.