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Send Kids to Camp!

Help overcome the shortfall to keep vital programs strong​

“In the back of my head, I worried Stella would be disappointed to see others doing things she couldn’t do due to her extra equipment. … That was NOT the case as she was involved in every aspect of camp. I believe she is truly a changed person because of this one week of camp and she can’t wait to go back!” 

Like you, the Muscular Dystrophy Association (MDA) believes everyone deserves the chance to live life more independently. MDA Summer Camps give kids and young adults living with neuromuscular diseases a whole week to enjoy some of the best things about being kids — at no cost to their families. 

Right now, a shortfall is putting pressure on MDA programs. As we get ready for summer camp, we need to raise significant funds for special expenses like accessible camp facilities and qualified medical professionals. Your gift today gives more kids like Stella a life-changing week and keeps research, advocacy, and care programs going strong. Thank you!