The Megan Palmer Foundation
Advancing Care for the Muscular Dystrophy Community
Building Hope, Empowering lives
The Megan Palmer Foundation is dedicated to supporting individuals living with muscular dystrophy through community, advocacy, awareness, and meaningful support that helps no one face the disease alone.
30+
Distinct genetic subtypes identified
1 in 14,500
People affected worldwide (est.)
8 years
Average wait for a confirmed diagnosis
Limb-Girdle Muscular Dystrophy
Limb-Girdle Muscular Dystrophy — known as LGMD — is not a single disease. It’s a family of more than 30 rare genetic conditions, each caused by a mutation in a different gene, all sharing the same devastating effect: the progressive weakening and wasting of the muscles around the hips and shoulders.
Upcoming Events
Join us in making a difference by participating in our upcoming events in support of those living with muscular dystrophy. Together, we can build a stronger future for individuals and families affected by muscular dystrophy — we hope to see you there!