WALK WITH JOHN'S TEAM TO CURE JDM
John began his journey with fighting Juvenile Dermatomyositis (JDM) 4 years ago, at just 18 months old. Since his diagnosis, John has been nothing but brave and inspiring as he's endured numerous doctor's visits, blood draws, and medications to keep his symptoms at bay and stop it from spreading. While there is currently no cure for JDM, we continue to support research for better treatments and hopefully one day a cure!
We are participating in the 3rd annual Walk Strong Across America and invite you to show your support by making a gift and walking with us on or before July 4th - from the comfort of your home, in your yard, or around your neighborhood.
Cure JM families, friends and supporters are coming together to raise $750,000 for Juvenile Myositis research. Reaching this important milestone will help ensure no promising research is left on the table in 2022.
Right now, there are no FDA-approved treatments and no cure for Juvenile Myositis, but together we can change that.
Like many rare diseases, research is only made possible by friends and family like you. With your support we can:
-Pursue promising new treatments
-Fund clinical trials
-Expand our Centers of Excellence
-Launch our NEW Clinical Care Network, which will expand excellent JM care to children around the country
Gifts will be matched by the Leetz Family Match. Every dollar makes a difference and gifts will be put straight to work to advance research for better treatments, better care, and, ultimately, a cure.
All proceeds benefit Cure JM Foundation, a non-profit dedicated to finding a cure for JDM.
Support the fight against JDM today!
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