Over 40 years of helping
those affected by CRPS
Living With CRPS
RSDSA gives those affected by CRPS education, advocacy and hope! From signs & symptoms, to diagnosis, to living with CRPS long term, this section has health and lifestyle information for adults and youth living with this painful and debilitating condition – as well as for their families and caregivers.
Research
RSDSA raises funds for research to find better treatments – and a cure – for CRPS. We also work with research groups and healthcare professionals worldwide to foster collaboration, communication and awareness. Here you’ll find the latest studies and articles about progress and breakthroughs
RSDSA Message Board Community
The RSDSA Message Board intends to provide a supportive environment for individuals affected by CRPS, including patients, caregivers, friends, family members, and advocates. Join to meet others and ask questions related to your journey.
Our Mission
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 better treatments and a cure.
Upcoming Events
We’re excited to bring our national walk and day of awareness to a town near you! Learn more about registering and donating.
RSDSA's 2026 Young Adult Weekend Retreat will take place June 26 – June 29 in Scottsdale!
Our inaugural "The CRPS Connection – Strategies and Skills for Living with CRPS" event will take place October 2-5 in Philadelphia!
Corporate Partners
Recent Videos
CRPS + Mental Health with Gabi Baylor, APCC, CRC
