Hello readers! This is Verena writing again. This is something I wrote a few days ago. I like to write my thoughts on paper.

MARYLAND HEIGHTS, Mo. — Nothing lifts your spirits, quite like lifting someone else's. That's what they do every day at MDA Camp. "It's somewhere where you're not defined by your disease," said ...

Children with a rare type of muscular dystrophy received calls from doctors last week to begin treatment with a new life extending drug after a Sunday Mail campaign. Givinostat slows the progress of ...

On a Monday conference call, Sarepta CEO Doug Ingram said new long-term data should help “rebalance the discussion” ...

LOUISVILLE, Ky. (WDRB) — The Louisville Fire Department is raising money for kids living with muscular dystrophy. The annual "Fill the Boot" campaign was started more than 70 years ago through a ...

If a boy in New York has been convinced to think he’s a girl, the state Medicaid program has got you covered. But if a boy with muscular dystrophy just wants to walk again, he’s in trouble. That’s the ...

Muscular Dystrophy Association Marks Rare Disease Day by Spotlighting Community Stories Driving Progress in Research, Care, and Advocacy ...