Deb Jenssen never wanted her children to suffer from the disease that killed her brother at 28. The illness, Duchenne muscular dystrophy, initially manifests in childhood as trouble with strength and ...

The Delhi High Court has directed the central government to establish a national fund for rare diseases, ensuring effective treatment and monitoring for patients suffering from conditions like ...

The play is known as the Jackson Special. Kelly Maynard, Jackson’s mom, said he was diagnosed with Duchenne’s Muscular Dystrophy when he was five years old, which has confined him to a wheelchair. The ...

In a big homecoming night win, Hilliard Davidson's biggest play may have been a Jackson Maynard touchdown that didn't show up on the scoreboard.

I’d hoped we had time because he’s the youngest and still walking. We’d tried so hard to buy him that time, to slow down the disease progression so that he’d have skills to save, like upper body ...

Capricor Therapeutics (NASDAQ:CAPR) stock rallied 20% Friday afternoon following news the company plans to present long-term ...

Following the success of last years’ event, Corby Town Council are once again hosting a Christmas market outside the Cube.

Melanie Sanford fought to get her son Hudson a breakthrough gene therapy to stop the progression of the fatal disease ...

SAN DIEGO, Oct. 04, 2024 (GLOBE NEWSWIRE) -- (NASDAQ: CAPR), a biotechnology company developing transformative cell and ...

Precision medicine offers tailored treatments for rare diseases, addressing genetic variations and improving therapeutic ...

Piper Sandler analyst Biren Amin maintained a Buy rating on Solid Biosciences (SLDB – Research Report) today and set a price target of ...

Hereditary neuromuscular diseases encompass a diverse group of inherited disorders that affect motor neurons, peripheral ...