Join Us in the Fight Against Duchenne Muscular Dystrophy

March 18 & 19, 2027

Join us as we come together for a cause that truly changes lives. Duchenne Muscular Dystrophy (DMD) is a 100% fatal disease with currently no cure. This progressive muscle-wasting disorder affects thousands of boys, robbing them of their strength, mobility, and, eventually, their lives.

In 2020, Dan and Paula Florczykowski founded Finn’s Friends in response to their son Finn’s devastating diagnosis. As they traveled the country seeking the best care, attending events, and connecting with other families, they quickly realized the overwhelming financial and emotional burden placed on families affected by this debilitating disease.

Finn’s Friends has worked tirelessly to raise awareness and funds through multiple fundraising initiatives. Our vision is to provide direct family assistance while supporting multi-disciplinary Duchenne specialty clinics that offer comprehensive care to those affected.

The Impact We’ve Made: Our collective efforts have resulted in life-changing assistance for families, including Accessible vans, Wheelchairs, Home modifications, Service dogs, and Travel & transportation assistance.

Be Part of the Fight: We invite you to join us on this journey. Your support helps us continue funding critical resources and providing hope to families battling Duchenne. Together, we can make a difference.

Donate. Advocate. Support. 💚 Visit Finnsfriends.net to learn more and get involved!

DSO Network Event/Concert 2027