Guest writer Steve Way wants to share the things he wishes people had said to him following his diagnosis of muscular ...

Increasing pain and weakness are making it more and more challenging for columnist Robin Stemple to move his body, especially ...

Columnist Shalom Lim discusses a new independent film in which all of the disabled characters were played by actors with ...

Rayna Haque reflects on her brother Anjar's life with LGMD, including his passion for wrestling, and his legacy of love and ...

For DJ Kevin Kaelin, who lives with Duchenne muscular dystrophy, the power of music lets the crowd see beyond his physical ...

As columnist Betty Vertin prepares to move into a new house, she finds the most relaxing to do is go to DMD clinic visits with her sons.

Speech therapy for muscular dystrophy can serve as part of multidisciplinary care when the condition affects speech, communication, or swallowing. In some types of muscular dystrophy, weakness of the ...

Scientists now have evidence to explain why treatment with the corticosteroid prednisone — but not the newer steroid Agamree (vamorolone) — drives bone loss in young boys with Duchenne muscular ...

Tell us a little about yourself and your experience with muscular dystrophy. Your answers help us share information, resources, and community content that are more relevant to you. It only takes about ...

I have lived with limb-girdle muscular dystrophy (LGMD) type 2E/R4 for more than 40 years. Initially, apart from stretching and visiting a neuromuscular clinic twice a year, I didn’t think much about ...

With seven children — Lexi, 25; Max, 20; Chance, 19; Rowen, 17; Charlie, 15; Mary, 11; and Callie, 4; three of whom have Duchenne muscular dystrophy (DMD) — I have entered the zone of a veteran parent ...