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
Thanks to a grant from the Joseph Patrick Trust, Kai now has a new powerchair that caters for his complex and changing needs, and which he likens to a rather fancy sports car.
In November Muscular Dystrophy UK held an online Q&A with Demelza Stuart, Advocacy and Information Officer for Northern and a trained Occupational Therapist.