CRPS is one of the most painful and least understood conditions known to medicine – and because of that, many individuals face their diagnosis feeling isolated, afraid, and unsure where to turn. For thousands of people across the country, RSDSA becomes the first steady source of clarity, community, and hope. It is only through your support we can continue this great work.
This year, supporters like you helped RSDSA:
- Create resources and education for individuals and families living with this rare condition
- Provide guidance and community connections for people navigating their CRPS journey
- Deliver expert-led livestreams, online support, and educational materials to improve understanding and outcomes
- Increase awareness among healthcare providers and advocates
- Strengthen national networks so no one must walk this path alone
- Grow our patient assistance programs
But there is still so much more work to be done.
Because CRPS is rare, individuals often struggle for years searching for clear information, appropriate care, and a supportive community. For more than 40 years, RSDSA has funded research, centralized credible resources, and laid a foundation that many organizations rely on today.
As we look toward 2026, we are committed to doing even more – expanding education, strengthening advocacy, and growing our patient assistance programs, to name just a few. None of this is possible without your dedicated support.
Your year-end gift has a direct and meaningful impact.
Please visit rsds.org/donate to make your year-end contribution today.