Kelsey Saxon shares how she went from surviving to healing after her son received gene therapy for Duchenne muscular ...

Neuromuscular disease patients and families should help shape drug development from the start, per a panel discussion at MDA Engage.

Elliott Johnson, a podcaster living with Duchenne, along with his able-bodied cohost, advocates across a wider community.

Share this page with email Share this page on Facebook Share this page on X Share this page on Reddit My name is Cody Chalfan. I’m 26, from Columbus, Ohio, and I live with Duchenne muscular dystrophy ...

Rather than giving up something he enjoys, columnist Shalom Lim has learned how to adapt to change in the way he accesses ...

Columnist Betty Vertin pays tribute to her 11-year-old daughter, Mary, who is wise beyond her years and always steps in to help.

In recognition of Muscular Dystrophy Awareness Month in September, the Muscular Dystrophy Awareness Month campaign features a ...

Today, we’re diving into living well with muscular dystrophy: real-world hacks and daily realities. We’re skipping the clinical lecture format and focusing instead on peer-driven, practical strategies ...