Community Support
Duchenne Communities
Connect with organizations created to help families living with DMD
My advice to new parents that found out that their son has [Duchenne] muscular dystrophy is that they’re not alone.
– Gil, Landon’s dad
CureDuchenne
A nonprofit organization offering education and support programs for parents, caregivers, clinicians, and physical therapists
Jett Foundation
A nonprofit organization that empowers people and families impacted by DMD through the development of transformative programming, educational opportunities, and ongoing support
My advice to new parents that found out that their son has [Duchenne] muscular dystrophy is that they’re not alone.
– Gil, Landon’s dad
Muscular Dystrophy Association
A voluntary health organization that provides access to support and programs that empower the lives of people living with neuromuscular diseases
Parent Project Muscular Dystrophy
A nonprofit organization connecting the Duchenne community to news, resources, advancements in research, and each other
The Akari Foundation
A nonprofit organization specializing in DMD that educates and empowers the Hispanic community by providing resources, awareness, advocacy, and education entirely in Spanish