Thanks to you, children are winning their fight against juvenile myositis.

"I see first-hand every day that Cure JM is an organization like no other. Cure JM is laser-focused on its mission, and every gift is stewarded to improve the lives of children living with Juvenile Myositis." – Nikki H., Addie’s Mom

"Cure JM is not only a wonderful organization for parents and support, but through fundraising, they are able to find more research grants and get us closer to a CURE! Cure JM gives all of us with kids JM HOPE!" – Sue C., Kristen’s Mom

"I was able to meet other teens living with JM at Walk Strong to Cure JM and other events. This means a lot when you have a rare disease. What a great group of people working together for a cure!" – Marco D., Teen Patient

"As a mom of a newly diagnosed child, I felt scared and lost, and I needed information and support. That’s when I found Cure JM, and they were able to supply all of that for me. Cure JM is more than an organization; it’s a family!" – Angie D., Adrie’s Mom

"Cure JM has done an incredible job supporting us and others in the JM community. They thoughtfully connect families, effectively raise funds, drive important research, and so much more." – Todd M., Natalie's Dad

"Cure JM has been integral to my daughter's support network. In fact, they are the only advocacy group for this rare disease. Cure JM's strong leadership chain is nothing less than stellar…I am confident in the foundation's ability to fight for a cure. – Jason P., Maggie's Dad

"With such a rare disease, it comforts me that there is an organization out there fighting for a cure, doing the research, raising awareness, and connecting all of us so that we do not feel alone. I've worked with hundreds of non-profits throughout my career, and Cure JM is one of the most dedicated, passionate, and organized." – Deema L. Zeina's Mom