Duchenne Muscular Dystrophy is a genetic terminal muscle wasting disease. It has no cure but a few treatments to slow down the progression of the disease. It typically is fatal in the late teens to 20s. Spreading awareness, fundraising, and supporting boys impacted by this disease helps bring hope!

This campaign directly supports a family with a little boy impacted by this disease. Owen is a sweet 4 year old boy who was diagnosed with DMD nearly 3 years ago. He is also impacted by autism which is a common condition seen with DMD.

He is more than his diagnosis! He loves tractors, Chevy's, and all things with wheels. He adores spending time outside, cooking in his pretend kitchen, drawing, and playing with his little brother.

He receives weekly infusion therapy, weekly physical, speech, and occupational therapy, and almost monthly appointments for his care. Though we are blessed with amazing insurance, travel and copays can still quickly pile up.

Any funds from this campaign are saved for his medical and travel expenses! Thank you for your support.

We pray that a cure is found in Owen's lifetime. Duchenne's shouldn't be a hopeless end...