In 2016, our family received life changing news when four of our boys - two sets of brothers - were diagnosed with Becker Muscular Dystrophy, a rare form of muscular dystrophy. Like many families facing a neuromuscular disease diagnosis, we were overwhelmed with questions and uncertainty about what the future would hold.

As we learned more about the disease, we realized awareness is one of the most powerful tools we have. We made it our mission to educate our community, inspire hope, and turn that awareness into action.

Today, our nonprofit brings people together through fundraising events, community partnerships, and educational outreach to support those affected by neuromuscular diseases. The funds we raise help advance research and are donated to organizations such as the Muscular Dystrophy Association (MDA) and other organizations working toward better treatment- and ultimately a cure.

Every event, every donation, and every conversation bring us one step closer to a future where no family has to face this alone.