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The Reflex Sympathetic Dystrophy Syndrome Association of America (RSDSA) is a national not-for-profit organization, headquartered in Milford, Connecticut, that promotes greater public and professional awareness of RSD/CRPS, a painful neurological syndrome that may affect more than 1.5 million Americans. We also fund research fellowships and evidence reports on RSD/CRPS.
Our mission is to promote public and professional awareness of Reflex Sympathetic Dystrophy Syndrome (RSD) and to educate those afflicted with the syndrome, their families, friends, insurance and healthcare providers, on the disabling pain it causes. We encourage individuals with RSD to offer each other emotional support within affiliate groups. And finally, we are committed to raising funds for research into the cause and cure of RSD.
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