Get the latest news and updates on CRPS directly from the RSDSA team SearchBack to All News Recent Posts Pharmacy Benefit Managers and the DRUG Act March 2025 Legislative Update: Support the EXPERT Act A Recap of Rare Disease Week 2025 How to Complete an In Memoriam Donation to RSDSA Life Is Not a Contest. I LIVE at My Own Pace. Join Abbott On Neurostimulation for Foot Pain Webinars Through March 2024 July 11, 2023 Take note of Abbott's free national patient education event webinar series! Do You Suspect You or Your Child Has CRPS? Here is How to Self-Diagnose to Know if You Need to Seek Help July 10, 2023 The Netflix documentary Take Care of Maya has raised awareness of, and many questions about, CRPS. Sending Condolences to the Family of R. Steven Shisler, Esq. July 9, 2023 It is with deep sadness that we share the news of the passing of RSDSA board member, R. Steven Shisler, Esq. His unexpected departure has left us all in a state of profound sorrow and loss. We Will Not Stop Fighting July 3, 2023 For the record, the FDA to this date has never approved anything for the treatment of CRPS. That fact is lost on the elected and our neighbors. It’s time to change that. Don’t Allow Someone Else to Minimize Your Journey June 22, 2023 CRPS is a horrible disease. Most people, even with CRPS, don't understand CRPS fully. Don't allow someone else to minimize your journey because theirs is not as bad or the same as yours. Every warrior is a warrior. Pages: 12345678910111213141516171819202122232425262728293031323334353637383940414243444546474849505152535455565758596061626364656667686970717273747576777879808182Load More Recent Posts Pharmacy Benefit Managers and the DRUG Act March 2025 Legislative Update: Support the EXPERT Act A Recap of Rare Disease Week 2025 How to Complete an In Memoriam Donation to RSDSA Life Is Not a Contest. I LIVE at My Own Pace.
