A group of charities, including Muscular Dystrophy UK, is urging for the approval of a drug that can treat an underlying genetic cause of a life-limiting muscle-wasting condition.Read more
Catherine Woodhead is embarking on a huge challenge of walking the distance between Land’s End and John O’Groats (LeJog)
It is with deep sadness that Muscular Dystrophy UK has learned of the death of Valerie Patrick following a period of ill health.
CEO Catherine Woodhead has added her name to an open letter as part of the #RightNow campaign.
Breaking Covid-19 news: Extra 820,000 vulnerable people in England to be offered vaccine and advised to shield16/02/2021
A new technology called QCovid can analyse a combination of risk factors based on medical records to assess whether somebody may be more vulnerable than was previously understood.
Carmela will be presented with the Points of Light award - which recognises outstanding individual volunteers who inspire others - in a virtual ceremony next week.
PepGen’s work into molecular patches seeks to help people with Duchenne muscular dystrophy (DMD) and other muscle-wasting conditions.
A filmmaker who lives with a life-limiting muscle-wasting condition and hasn’t left the house in 10 months is taking the documentary world by storm with her film on shielding.
TalkMD is an online community where adults living with a muscle-wasting condition can share their stories, make friends and ask others for advice.
Stephanie Castelete-Tyrrell has congenital muscular dystrophy and says gaming gives her the freedom to “complete tasks that many people take for granted in the real world".
MDUK is praising a storyline of a child with mitochondrial disease in Coronation Street for sensitively and accurately capturing the reality of the muscle-wasting condition.