One Little Boy. One Big River. One Chance to Save His Life. “It’s just one little boy,” they say. But to everyone who knows 6-year-old William Jackson, he is everything. Diagnosed with Duchenne ...

DMD was first described by French neurologist Guillaume Benjamin Amand Duchenne in the 1860s. However, until the 1980s, ...

Suneel Ram is a spiritual seeker, sings in a band and was the subject of a comic novel two years ago about living with Duchenne muscular dystrophy, a rare genetic ...

When her son reached three last year, a new name loomed over their lives — Duchenne Muscular Dystrophy (DMD), a ...

With grace that extends far beyond the pageant stage, Miss Asia Pacific World 2013 Srishti Rana recently took to Instagram to champion a cause close to countless hearts—raising awareness for children ...

Suneel Ram's caregivers share some of the lessons they have learned while caring for the 28-year-old who was diagnosed with ...

Since he was a young child, Aaron Kondo has lived with muscular dystrophy. A popular history teacher at Maui High School for ...

Doing more to incorporate caregiver burden into value assessments and cost-effectiveness research of Duchene muscular dystrophy treatments was the focus of a recent International Society for ...

Trexo Robotics was honoured as Best Innovative and Tech Company of the Year, while Kiran Mann, CEO of Brar's, was nominated ...

New Delhi, Over 200 parents from 26 states across India protested at Jantar Mantar on Wednesday with their children affected ...

Children with a rare muscle wasting disease are being denied access to a groundbreaking new life-extending treatment, the Sunday Mail can reveal. Givinostat slows the progress of Duchenne muscular ...

Global Duchenne Muscular Dystrophy Drugs Market value attained USD 3.9 Billion in 2025. The market will achieve USD 6.5 ...