Livestream from RSDSA 2nd Annual Virtual CRPS Awareness Walk on Saturday, June 26th!

RSDSA Sponsors


The Baker Family Foundation

The Cochran Firm, National CRPS/RSD Lawyers

Michael & Lynn Coatney

Michael & Lynn Coatney


Silver Sponsors

EveryLife Foundation for Rare Diseases

Bronze Sponsors

NY Ketamine

Orange Sponsor

Maletta Pfeiffer & Associates

RSDSA's 3rd Annual Virtual CRPS Awareness Walk
 Saturday, June 11th, 2022 

We are so excited to host our 3rd annual Virtual CRPS Awareness Walk this summer!

In 2021 we had participants, donors and 57 teams, from 34 states and four countries.  Our goal was to raise $50,000, and we surpassed our goal and raised over $60,000. Thank you to all who participated, registered, & donated.

From 2020 to 2021 we increased the number of teams by 173%, and our fundraising increased by 150%! We are so grateful for the CRPS Warriors, caregivers, family, friends, and supporters who made that possible!

We hope to make this year even more successful with your help by aiming even higher and raising our goal to $75,000. We know that the CRPS community has the strength and dedication to band together and make amazing things happen!

We look forward to "seeing" you on June 11th. Although we wish we could see all CRPS Warriors in person, the benefit of our virtual walk is that you can have team members from across the country or even around the globe! This gives supporters the freedom to walk on their own schedule and still feel involved in such a wonderful experience!

  • Registration Fees: $25 for adults, $15 for children ages 5-12.
    • Register either as an individual or create a team
  • RSDSA's 3rd Annual Virtual CRPS Awareness Walk t-shirt & medal are included for all United States and Canadian registrants.
  • For questions and more information contact: Jeri Krassner, 917-597-7256 or Kelly Considine,

Did you know it is estimated that 186,000 individuals in the United States are suffering with CRPS?

These numbers are astounding and yet no cure or treatment has been found which leaves doctors "treating the symptoms" instead of looking for an underlying cause.

Living with a chronic disease, and constant pain, is daunting to say the least, but to see everyone come together to raise awareness for this rare condition is very touching. Seeing the support from so many reminds CRPS Warriors to keep fighting, and we are not alone! 

We have dealt with the burning pain; we have walked through the fire, and it is time to light it up and blaze a trail to our goal of $75,000!

We hope to see you this year!


Kelly Considine

RSDSA's 3rd Annual Virtual CRPS Awareness Walk Chair





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Learn more about RSDSA at


Facebook Lives and conferences unite CRPS Warriors and clinicians to hear about the latest treatment options. E-newsletter, In Rare Form, updates the community monthly. 


We help our community advocate for healthcare and treatments. The Advocacy Committee collaborates with other Rare Disease organizations to raise awareness.


We raise funds for research to find better treatments and a cure. Click here to read about RSDSA's current funded research grants.


We provide webinars and conferences to learn about the latest treatment options. We have two medical online courses for doctors and nurses to learn more about adult and pediatric CRPS.