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

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

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

Alena Jones shares how living with FSHD taught her that a diagnosis does not define her future or erase her dreams.

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

Columnist Patrick Moeschen says it took LGMD and several weeks in the hospital to remind him that being alive is a wonderful ...

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.

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

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 ...

Scientists can now explain why treatment with one steroid slows growth in young boys with Duchenne MD, while use of a newer one doesn't.