This November, the Muscular Dystrophy Association (MDA) is honoring family caregivers who provide essential support for people living with muscular dystrophy, ALS, and more than 300 related ...

Columnist Shalom Lim is grateful for the opportunity to use his lived experience to do good work on behalf of people with DMD ...

Brett and Erin Bullers were literally speechless after their son, Nicholas, was diagnosed with Duchenne muscular dystrophy in 2007. “Someone tells you that your 3-year-old will be in a wheelchair by 8 ...

See more of our trusted coverage when you search. Prefer Newsweek on Google to see more of our trusted coverage when you search. Max, Rowan and Charlie Vertin's muscles have been slowly collecting ...

“He couldn't run well or jump,” Kris said. “The pediatrician chalked it up to slow development.” It wasn't until Jared had blood work done later that year when doctors discovered the full story: Jared ...

Chase Andrews, 10, was diagnosed with a common but severe form of muscular dystrophy in April 2018. A tornado inspired them to seek help to pay the $15K-per-session stem cell therapy. A GoFundMe page ...

Bone Health Specialist “Bone health is very important, because many people with muscular dystrophies are at risk of falling,” says Lauren Elman, MD, director of the Muscular Dystrophy Association ...