Families affected by the condition and a dedicated support crew walked 92km across Perth over four days to raise funds and ...

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 ...

It's known as the 'Super Bowl of Bodybuilding' - a weekend where weightlifters all gather in Columbus, Ohio to flex and put on display their hard work in achieving the 'perfect physique.' ...

Team IMPACT partnerships often last long beyond the 2-year contract between children and the teams that sign them.

Nine inspiring Toowoomba women have opened up about the lessons that have shaped them and their advice for the next generation to celebrate International Women’s Day on March 8.

Phil Farley has survived 25 years with an untreatable disease that typically kills it victims within three years of diagnosis.

If you asked a hundred random Hoosiers where to find one of America’s best automotive museums, probably ninety-nine of them ...

Luke Criado, a 12-year-old from San Antonio, is battling Duchenne Muscular Dystrophy while staying active in power soccer.

In early March 2026, Tenaya Therapeutics reported a reduced full-year net loss of US$90.6 million and highlighted encouraging preclinical and Phase 1 data for its HDAC6 inhibitor TN-301 in Duchenne ...

Precision BioSciences, Inc. (Nasdaq: DTIL), a clinical stage gene editing company utilizing its novel proprietary ARCUS® platform to develop in vivo gene editing therapies for high unmet need diseases ...

Sheffield boy Kairo Barranco, seven, was diagnosed with Duchenne muscular dystrophy in September 2024.