Senior reporters Lucinda Rouse and Emily Harle discuss snippets from a recent interview Emily conducted with Andy Fletcher, chief executive of Muscular Dystrophy UK.
Mother Bethany Jackson, 27, from Belfast, found out she was a carrier of Duchenne muscular dystrophy early in her pregnancy, ...
His parents Stephen and Jenny have asked Sheffield Children's NHS Foundation Trust to approve the use of drug givinostat, ...
This prevalence and incidence study is the first to be commissioned through the charity’s Neuromuscular Challenge Grants, ...
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 ...
Charlotte and Tom Hardwick, both 33 and from Beechdale in Nottingham, have different types of muscular dystrophy and need ...
Membership recognizes individuals who have demonstrated outstanding professional achievements and commitment to service ...
A man from Southampton who is living with a rare muscle condition has completed his first half marathon to raise vital funds for research.
A man from Southampton who is living with a rare muscle condition has completed his first half marathon to raise vital funds ...
Families affected by a rare muscle-wasting condition may soon benefit from a new treatment with fewer side effects than ...
The Medicines and Healthcare products Regulatory Agency (MHRA) National Institute for Health and Care Excellence (NICE) Scottish Medicines Consortium (SMC) (on behalf of NHS boards in Scotland) ...
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