Robert Davidson is the first UK patient recruited to a new medical trial looking to support children with heart failure ...

Blizzard Entertainment and World of Warcraft players raised over $2 million for CureDuchenne, honoring Mats Steen, a devoted player lost to Duchenne muscular dystrophy, while promoting awareness and ...

Duchenne muscular dystrophy (DMD) treatment ifetroban led to improvements in measures of heart function in a Phase 2 clinical ...

Patient advocate Austin Leclaire, who died Feb. 1, played a pivotal role in spurring the development of the first medicines ...

Blizzard's Revenant Pack raises over $2 million for CureDuchenne! Discover how gaming communities made a real-world impact.

An Evertonian who received 1,200 cards from fellow Blues on his 12th birthday has enjoyed a VIP experience at the club’s ...

CEO Dr James Garner says at the time of the December 18 trial bombshell that knocked 85% off the value of Percheron shares, ...

Columnist Shalom Lim and his partner work to create a legacy that resonates in the world of art and disability and beyond.

A seven-year-old boy from Dublin is on his way to California to undergo testing after being diagnosed with a rare condition last year.

Despite the obstacles, Riley Herrera had a life filled with family, sports, travel, faith and hope before his death on Nov.

A Kilkenny family is urgently raising €4 million euro for life-saving treatment for their 4-year-old son. William Jonathan Moore, who was diagnosed with Duchenne Muscular Dystrophy (DMD) in 2024.

High-dose treatment with the therapy was found to cause a 3.3% overall improvement in left ventricular ejection fraction.