His parents Stephen and Jenny have asked Sheffield Children's NHS Foundation Trust to approve the use of drug givinostat, ...

Senior reporters Lucinda Rouse and Emily Harle discuss snippets from a recent interview Emily conducted with Andy Fletcher, chief executive of Muscular Dystrophy UK.

Charlotte and Tom Hardwick, both 33 and from Beechdale in Nottingham, have different types of muscular dystrophy and need ...

A man from Southampton who is living with a rare muscle condition has completed his first half marathon to raise vital funds ...

A man from Southampton who is living with a rare muscle condition has completed his first half marathon to raise vital funds for research.

This prevalence and incidence study is the first to be commissioned through the charity’s Neuromuscular Challenge Grants, ...

Among the notable categories is the Young Person of the Year award, sponsored by Tarana Indian Restaurant. This category ...

The young contenders for this year's award are Ioan Walters, Will Taylor, and Poppy Davies. Ioan Walters, at just 14 years old, is a young entrepreneur and photographer who uses his talents to support ...

The 41 st Microscope Ball raised over £540,000 to support people living with muscle-wasting conditions, the highest amount raised in the event’s history. ‘The Greatest Show’-themed occasion brought ...

Mother Bethany Jackson, 27, from Belfast, found out she was a carrier of Duchenne muscular dystrophy early in her pregnancy, ...

As the market ascends toward US $6.64 billion by 2033, those who align early with gene therapy platforms, scalable delivery ...

Facioscapulohumeral Muscular Dystrophy (FSHD) is a genetic disorder marked by muscle weakness, primarily in the face, shoulders, and arms. The DUX4 gene mutation leads to toxic protein production, ...