A single-dose gene replacement therapy is found to improve movement ability in children over 2 years of age and teenagers with spinal muscular atrophy, according to research published in Nature ...

Indore: The district administration will soon extend facilities like physiotherapy and medication to children suffering from muscular dystrophy, said collector Shivam Verma at a workshop on ...

The funds will go to the government's Invest America plan. In a major philanthropic move, billionaires Michael and Susan Dell are donating $6.25 billion to deposit $250 into savings accounts for up to ...

Kate Gosselin is breaking down how she budgets for Christmas as a single mom to eight kids, a system she developed after what she described as a "sickening" financial collapse. The former "Jon & Kate ...

Jason Mast is a general assignment reporter at STAT focused on the science behind new medicines and the systems and people that decide whether that science ever reaches patients. You can reach Jason ...

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 ...

Jason Mast is a general assignment reporter at STAT focused on the science behind new medicines and the systems and people that decide whether that science ever reaches patients. You can reach Jason ...

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 ...

"I don't like the attention at all," said Shep, as his family and friends call him, who gets a lot of it at school. "It just annoys me, that every day I'm asked, 'Hey, why do you need a wheelchair?' ...

• The "Fill the Boot" fundraiser ran from 3-6 p.m. and supports research, cures and local families affected by muscular dystrophy • Donations can still be made online through a QR code and dedicated ...

WOODBRIDGE, Conn.--(BUSINESS WIRE)--Cure Rare Disease (CRD), a 501(c)(3) nonprofit biotechnology company developing genetic therapies for ultra-rare neuromuscular diseases, today announced that the ...