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The England Rare Diseases Action Plan is the first of four action plans, which will cover each of…
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Tens of thousands more people in the UK than previously thought are living with rare, muscle-…
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A drug that helps treat Spinal Muscular Atrophy (SMA) will be funded for use on the NHS in Scotland…
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MDUK is delighted to announce the winners of its President’s Awards 2021, in recognition of those…
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The fashion fitness brand Tikiboo has launched two bright and bold muscle-themed activewear…
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This semester (September-December 2021), I have been studying here in London at the Foundation for…
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It was a chance to bring together care advisors from across the UK to discuss the impact of the …
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Muscular Dystrophy UK has today shared a set of climate change principles that we will use to …
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The questionnaire sets out 23 actions that have been developed for the implementation of the UK…
Your story
Lucy Anderson’s father, Philip Anderson, has a progressively disabling muscle wasting condition,…