The summary mentions the importance of educating clinicians and patients about bone health in Duchenne which can help to improve clinical care provided to patients.Read more
On Saturday 21 April, 180 people joined us at our information day in Cambridge. You can watch Dr Ferlini's presentation on the nanodelivery of drugs in Duchenne now
Come along to our group for families from South Asian backgrounds
Muscular Dystrophy UK wants to invite you to complete a research survey produced by Ulster University, giving your experience of caring for someone with Duchenne muscular dystrophy
An event for families from South Asian backgrounds affected by muscle-wasting conditions
Kerry from Wales, who has Facioscapulohumeral muscular dystrophy, was awarded Employment and Support Allowance (ESA) after having to attend a tribunal.
Treat-NMD Network as part of an international working group have today published updated Care Considerations for Duchenne muscular dystrophy in the Lancet.
Adam needed a specialist Strike Force Powerchair to stay on top of his game, and compete on an even playing field with other players.
ACT gets its name from one of its core messages which is to accept what is out of your own personal control, while committing to action that will improve your quality of life.
Joshua loves playing boccia and wanted to study a sports science course at University, but his care hours didn't support his education.
Muscular Dystrophy UK is holding an information and support day for families from South Asian backgrounds who are affected by muscle-wasting conditions