CureDuchenne, led by CEO Debra Miller, is at the forefront of research for Duchenne muscular dystrophy, which is a rare and fatal neuromuscular disease.

The Jeffrey Foundation was started in 1972 by Alyce Morris Winston. At the time, Winston was a young mother who could not ...

SAGINAW TWP., Mich. (WJRT) - A Saginaw Township woman with muscular dystrophy is working hard to make her dreams come true, ...

It does not necessarily reflect the view of The Herald. A woman whose grandad lives with muscular dystrophy will join thousands of others for a charity 10k in Oxford this May to support people ...

New research led by the University of Portsmouth has revealed how Duchenne muscular dystrophy (DMD), best known for causing ...

Suneel Ram's caregivers share some of the lessons they have learned while caring for the 28-year-old who was diagnosed with ...