I’m participating in Reflex Sympathetic Dystrophy Syndrome Association (RSDSA)'s 7th Annual Walk for CRPS. When I first received my diagnosis for this rare, neuorpathic disability, RSDSA was a great resource of information for me.They provide community, advocacy, and education. They also give money to research to find better treatments.

If you can think of others who might be interested in making a donation, please share this with friends or on social media!  RSDSA is a great organization and you’d be helping them (and me!) by spreading the word. 

Thank you so much for helping me reach my goal, and for supporting RSDSA. We couldn’t do it without you!