Members of the RSDSA community tend to be doers as individuals and groups are organizing events across the U.S. The events create greater awareness of this little-known syndrome – and raise the funds necessary to help RSDSA support research and provide patient assistance.
Those who participate in our events find that it feels great to get involved and join with others who are passionate about finding better treatments and a cure for CRPS/RSD. Doing something is empowering. You can make a difference. And by helping others, you help yourself!
Take a moment to view our upcoming events and return here often to see what’s going on in your area. Feel free to contact us if you would like to host an event in your town.
9Facebook Live with Brad Yates Wednesday, December 9th at 7pm (EST) at 7:00 pm