Search the RSDSA Website Search Blog We’re Hiring A Social Media Intern for Spring 2025! December 4, 2024 Reflex Sympathetic Dystrophy Syndrome Association’s (RSDSA) mission is to provide support, education, and hope to all affected by the pain and disability of CRPS, while we drive research to develop… Event Facebook and YouTube Live with Dr. Lisa Van Allen Join RSDSA for our first Facebook and YouTube Live of the year as we speak with Dr. Lisa Van Allen on Thursday, January 16th at 4:00p Eastern / 3:00p Central… Event Young Adult Weekend Retreat: Nashville RSDSA’s 2025 Young Adult Weekend Retreat will take place June 27 – June 30th, in Nashville! Young adults with CRPS between the ages of 18 to 32 will spend the… Blog You Are Your Expert January 21, 2025 Written by Laura Swan, LMFT for the RSDSA blog. How and when did you develop CRPS/RSD? In 2003, a physician did a shockwave procedure on my elbow. I was on… Blog Advocacy Update | House Bill 6094 Protect Rare January 23, 2025 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… Pages: 12345678910111213141516171819202122232425262728293031323334353637383940414243444546474849505152535455565758596061626364656667686970717273747576777879808182838485868788899091929394959697
