PROTECT Rare Act – Providing Realistic Opportunity To Equal and Comparable Treatment for Rare Act Over 7,000 rare diseases affect more than 30 million people in the United States. CRPS…
Written by Lisa Van Allen, Chair of the RSDSA Advocacy Committee, for the RSDSA blog. Building relationships with your Members of Congress is important to ensuring that CRPS patients are…
Join Burning Hope in walking a 3k in support of the Complex Regional Pain Syndrome (CRPS) Community. All proceeds will benefit RSDSA & Burning Hope, helping to advance care and…
by Pradeep Chopra, MD for the RSDSA blog. Edited for clarity. There is a lot of discussion about the newest medicine on the market. Suzetrigine, marketed under the brand name…
RSDSA is hosting a livestream with Philip Getson, D.O. on Wednesday, March 5th at 7p Eastern. He will join us to speak about the latest developments with CRPS and answer…
