Reflex Sympathetic Dystrophy
The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) is a non-profit organization dedicated to supporting individuals affected by Complex Regional Pain Syndrome (CRPS) through education, advocacy, and community engagement. With over 40 years of experience, RSDSA raises funds for research aimed at developing better treatments and ultimately a cure for this debilitating condition.
RSDSA fosters a strong and vibrant community for those impacted by CRPS, offering resources such as support groups, patient assistance funds, and educational presentations. Their mission is to ensure that individuals affected by CRPS receive the hope and assistance they need to manage their condition and improve their quality of life.
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