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RSDSA’s Rare Disease Week – 2020

February 24, 2020

Rare Disease Day is held annually on the last day of February to raise awareness of rare diseases. This year, Rare Disease Day is Saturday, February 29th, 2020, but RSDSA is working to spread awareness for CRPS all week long. Check out our daily virtual activities and join us if you can! Monday: Make your […]

CRPS Warriors Are Not Pretending

February 19, 2020

Written by Judi Soderberg for the RSDSA blog. How and when did you develop CRPS/RSD? For 25 years I had a shoulder issue that doctors diagnosed as Thoracic Outlet Syndrome. I tried very hard to work with that and just let it go, but the pain increased over the years. So when a vascular surgeon […]

Training for Life

February 12, 2020

This article is for those with CRPS who are searching for a different path to manage the syndrome. The path was filled with many unexpected turns, side roads, road blocks, incredible new people in my life, and constant discovery.

CRPS Guided Me to My Calling

February 12, 2020

Written by Marisol Pérez for the RSDSA blog. Hi there. This is a part of my CRPS story. I developed CRPS following a right ankle surgery in 2012. I was 25 at the time. I enjoyed the outdoors, jogging, and walking my dog (now I have three). Prior to the surgery, I was told it […]

Awareness Will One Day Bring Us a Cure

February 5, 2020

Written by Shannon Beckman for the RSDSA blog. In 2009, I was at a concert to see my favorite band. I was downstairs and I heard the music start so I ran up the stairs in my flip flops. I stumbled and ended up falling backwards, landing on the step behind me, and hyperextending my […]

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Get the latest news and
updates on CRPS
directly
from the RSDSA team

Recent Posts

Recent Posts

Get the latest news and updates on CRPS directly from the RSDSA team

Recent Posts

Recent Posts

Get the latest news and
updates on CRPS
directly
from the RSDSA team