Children diagnosed with Juvenile Myositis bravely face a body fighting itself. Right now, there is no cure and no FDA-approved treatments. This is where you can change lives.
JM is a rare, life-threatening auto-immune disease that attacks children’s muscles and skin. It can cause pain, weakness, the inability to walk, disfigurement, organ failure, and can even lead to death.
Cure JM, the ONLY organization solely dedicated to supporting the most promising JM research and improving the lives of every family fighting JM. Because JM is rare, research is almost entirely funded through private donations from people like you.
Right now, we’re funding research at more than 29 prestigious research institutions, pushing research forward at an unprecedented pace. We’re living in times of great scientific progress and we need to push forward now, so children will have better treatments and we can all get closer to a cure. Our research goals are within our grasp…but we need your help. Please consider making a gift today. One reason that Cure JM is a top-rated charity is because since inception over 90% of our revenues go directly to programs, including research.
We say, "A Cure Can't Wait," well, neither can our kids.