Our mission at Jett Foundation is to extend and enrich the lives of individuals affected by Duchenne muscular dystrophy and other neuromuscular disorders.

We fulfill this mission by partnering with individuals and families through empowering educational programming, transformational direct service experiences, and by accelerating development of life-changing treatments.


Family Workshops

Bringing together families, clinicians, and industry partners for a day of Duchenne information and resources.

jett giving fund

Assisting families affected by Duchenne muscular dystrophy in purchasing vital medical and accessibility equipment.

camp promise

A free, week-long camp for kids, teens, and adults with neuromuscular disorders.


JeTT foundation updates: