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Today I’m delighted to publish our 2022/2023 Impact Report. A year in which we rallied our…
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The use of cells in muscle research
When scientists need to study how our muscle forms and grows…
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I first became a Trustee of a charity 19 years ago for a London homeless organisation called Thames…
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Did something frustrating happen today? Or funny? Or annoying? Writing it down could help you keep…
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Carmela, who was diagnosed with LMNA congenital muscular dystrophy in 2017, is the subject of a new…
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One of the largest conferences in the field of neuromuscular research the WMS Congress brings…
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This free event, at the T3 Conference Centre, Lisburn, provided practical information and support…
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Living with CMT has limited areas of my life. Some of the everyday things that people without my…
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On Sunday 15 October Angela, with her husband Brian, will officially start Bidwells Cambridge Town…
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I decided to get involved with fundraising for Muscular Dystrophy UK (MDUK) as my dad, Edward,…