MDA 2026 keynote speaker John Crowley discussed with MD News Today the progress made in neuromuscular disease and the future challenges.

A little boy was diagnosed with a life-limiting, muscular condition after his parents realised he was unable to jump.

If you’ve landed on this page, your child or grandchild probably said a weird word you've never heard before in your life, ...

Atamyo Therapeutics, a biotechnology company specializing in the development of next-generation gene therapies for limb-girdle muscular dystrophy (LGMD), announced at the MDA (Muscular Dystrophy ...

A little boy from Sheffield was diagnosed with a life-limiting, muscular condition after his parents realised he struggled to jump. Kairo Barranco, seven, was diagnosed with Duchenne muscular ...

The Kia Sorento is a muscular SUV with room for the whole family and a hybrid powertrain to save the family money.What's ...

A RECOMMENDATION for the HSE not to cover the cost of a drug to help children with a rare muscular disease has been blasted by families. Last year, The Irish Sun highlighted the plight of ...

Dr. Phil’s “Liar, Liar” episodes spotlight Sarah Delashmit, the Illinois woman who faked cancer and other illnesses for years ...

The president and CEO of the Muscular Dystrophy Association talks about what she's most excited about in neuromuscular disease research.

UCL’s Professor Francesco Muntoni has received the 2026 Novo Nordisk Prize for his pioneering research offering hope to children with Duchenne muscular dystrophy.

It was tragedy and heartache that led this WA truckie to sell his butcher shop and take to the road to follow his dream.

The first and only approved achondroplasia therapy to provide continuous systemic exposure to CNP over the weekly dosing intervalCommercial availability expected during early part of Q2 2026Rare Pedia ...