Together, we will fight for

Every Child with Duchenne Muscular Dystrophy

Building awareness, supporting families, and funding life‑changing research — so no family faces Duchenne alone.

Our Why

Connor’s Fight

Connor’s Fight was created after our son, Connor, was diagnosed with Duchenne Muscular Dystrophy at age two. We exist to unite communities, support families, and accelerate research that brings us closer to a world where Duchenne no longer takes our children too soon.

What We Do

Turning Connor’s Story into Action

We combine awareness, support, advocacy, and research funding to create real, tangible change for children and families living with Duchenne Muscular Dystrophy.

Awareness & Education

We share Connor’s story and the stories of others to shine a light on Duchenne Muscular Dystrophy — a condition many have never heard of, despite its severity. Through events, speaking engagements, and community initiatives, we help others understand the realities families face.

Funding Life‑Changing Research

Research is the only path toward better treatments and, someday, a cure. We raise funds to support innovative scientific efforts that aim to slow disease progression and extend both quality of life and longevity.

Advocacy

We work with local and national leaders to push for better funding, improved access to care, and policies that support families affected by DMD. No one’s voice should go unheard.

Family Support

Families navigating Duchenne deserve guidance and connection. We provide information, resources, and support to help families access care, understand treatment options, and feel less alone.