BENEFITING: Cure JM Foundation
In August, our son Nate was diagnosed with Juvenile Dermatomyositis a form of Juvenile Myositis (JM), a rare and painful autoimmune disease affecting approximately 17,000 children in the United States. Although there are treatments for the symptoms of JM, there is currently no cure.
Last weekend we held a fundraiser to raise money for Cure JM Foundation, a 501(c)(3) non‑profit organization specifically created to support families affected by this disease and fund research toward a cure. Please consider making an on-line donation to help find a cure. One day we hope no child will have to suffer from the pain of JM.