Our Mission

Hunter’s Heart Foundation is a non-profit organization dedicated to enriching the lives of children battling Duchenne Muscular Dystrophy (DMD). We achieve this mission by providing comprehensive support and resources, championing research and treatment advancements, and raising public awareness about DMD.

What We Know

Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness due to the alterations of a protein called dystrophin that helps keep muscle cells intact. DMD is one of four conditions known as dystrophinopathies. The other three diseases that belong to this group are Becker Muscular dystrophy (BMD, a mild form of DMD); an intermediate clinical presentation between DMD and BMD; and DMD-associated dilated cardiomyopathy (heart-disease) with little or no clinical skeletal, or voluntary, muscle disease.

​DMD symptom onset is in early childhood, usually between ages 2 and 3. The disease primarily affects boys, but in rare cases it can affect girls.