RSDSA
The Reflex Sympathetic Dystrophy Syndrome Association (RSDSA) was founded in 1984 to promote public and professional awareness of Complex Regional Pain Syndrome (CRPS), also known as Reflex Sympathetic Dystrophy (RSD).Our mission is to promote public and professional awareness of CRPS 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 CRPS 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 CRPS.
Please visit our website at rsds.org for information on our other initiatives.
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Facebook Live with Todd M. Hess MD and Cammie LaValle | Minnesota Intractable Pain Bill, Advocacy
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RSDSA’s 4th Annual Virtual CRPS Awareness Walk Livestream
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Facebook Live with Cynthia Toussaint and John Garrett | CRPS, Cancer, and Caregiving
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Facebook Live with Beth Stillitano and Leanne R. Cianfrini, PhD | Managing Pain Flares
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Colleen Johnston-Devin | What do health professionals and people with CRPS need to know about CRPS?
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Can I Legally Blame Someone For My CRPS? | Bryan Pope, Esq. | RSDSA
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Healing with Bowen Therapy | Emily Deneault | RSDSA
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Facebook Live with Leanne Cianfrini, PhD | Caregiving for Individuals with a Chronic Disease
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RSDSA's 3rd Annual Virtual CRPS Awareness Walk Livestream
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Facebook Live w/ Vivianne Tawfik, MD, PhD | Updates on CRPS From Basic Science to Clinical Practice
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Facebook Live with CRPS Warriors Josh Berg, Cassie Christensen, and Kelly Considine
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Facebook Live with Steve Ariens, P.D. | Navigating the Healthcare System
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Facebook Live with Dr. Traci Patterson | CRPS in Children
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Power of Patient Advocacy | Shannon von Felden, MPP | RSDSA
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Triumph Over Tragedy | Amberly Lago | RSDSA
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