Help Keep Dylan Moving: Support His Fight Against Duchenne Muscular Dystrophy

Our 15-year-old son, Dylan is living with a rare, devastating and life limiting disease called Duchenne Muscular Dystrophy (DMD). This progressive muscle-wasting disease has already taken a significant toll on his body, limiting his mobility and impacting his quality of life.

Despite the challenges, Dylan remains brave, resilient, and full of hope. Recently, we discovered a promising treatment available in the United States that may help preserve his mobility and slow the progression of this cruel disease. It offers a lifeline—not just for his body, but for his future.

However, this treatment comes at a very high cost. As parents, we are doing everything in our power to fund Dylan’s treatment but we simply cannot cover the full expense alone.

We are reaching out to our community, friends, and kind-hearted supporters to ask for your help. Any contribution—no matter how small—will go directly toward Dylan’s treatment and care.

Please help us give Dylan the best chance to keep moving, to keep dreaming, and to keep living a full life.

Thank you from the bottom of our hearts for your support.

Greg, Terri and Dylan.