A Co Down woman is encouraging people living with a muscle wasting or weakening condition, their families and carers to join ...

“I’VE BROKEN ABOUT 34 or 35 bones. My wrist tends to hurt me very badly.” ...

The Information Day takes place on Wednesday 4 June 2025, in Lisburn, Co. Antrim, and is organised by Muscular Dystrophy UK, the leading charity for more than ...

A rare and fatal form of muscular dystrophy has long posed a devastating diagnosis for children, primarily affecting boys.

Scientists present current evidence for a new gene therapy for Duchenne muscular dystrophy called delandistrogene moxeparvovec.

The Muscular Dystrophy Association (MDA ... Circle K, Food Depot, Green Valley Grocery, Graham C-Stores, Marden's Surplus, Pete's Market, Superior Grocers, and more. This year's campaign marks a ...

We hypothesize that Duchenne muscular dystrophy and autism spectrum disorder/pervasive developmental disorder co-occur with a greater than random frequency. In this study, we set out to reject the ...

Delandistrogene moxeparvovec, a gene therapy for Duchenne muscular dystrophy (DMD), showed high dystrophin expression and a ...

NATIONAL IS TAKING PLACE TO BENEFIT THE MUSCULAR DYSTROPHY ASSOCIATION, A CAUSE THAT’S RAISED MILLIONS OF DOLLARS IN ITS 30 YEAR HISTORY. AND OUR CO ANCHOR, STEVEN GRAVES, WAS ABLE TO SIT DOWN ...

Over the last two decades, the 41-year-old Chilean has spent her days bedridden, suffering from degenerative muscular dystrophy. When she finally loses her ability to speak or her lungs fail ...

Duchenne muscular dystrophy (DMD), recognised by the World ... neurologist and epileptologist, Medical Trust Hospital, Kochi, early signs of DMD include delays in walking, toe walking, stiffness ...