A lift door failing to open ahead of a concert illustrates the issues with accessibility that columnist Betty Vertin's sons face regularly.

DMD patients who switched to the experimental therapy deramiocel in a trial showed slower declines in upper limb function ...

The FDA has given the go-ahead for a trial testing an oral therapy that aims to aid muscle regeneration in adults with FSHD, ...

Share this page with email Share this page on Facebook Share this page on X Share this page on Reddit Print Preferred Source on Google Last week, I lost my dear friend Aloysius Teo, who passed away at ...

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

The realization that they were not alone set the tone for MDA Engage: Chicago, a free symposium held Sept. 26 in suburban ...

New treatments for muscular dystrophy are moving forward, but some promising therapies have fallen short in trials, two ...

In the past six months, FSHD has destroyed the muscles in columnist Robin Stemple's arms and hands, and now he fears he can't play piano.

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

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 ...

Share this page with email Share this page on Facebook Share this page on X Share this page on Reddit My name is Jake Levin. I am 23 years old, and I live with Duchenne muscular dystrophy. I graduated ...