Our mission is deeply personal—to help find a cure for Duchenne Muscular Dystrophy and bring hope to families facing this devastating disease. After losing our son, Ryan, last year, we have committed ourselves to turning grief into purpose. Duchenne takes strength, mobility, and ultimately lives far too soon, and no family should have to endure that loss. Everything we do is in Ryan’s honor—raising awareness, funding research, and pushing forward with urgency so that one day, a cure is not just possible, but real. This mission is for him, and for every child and family still fighting.