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Clinical trial supported by Alex s Wish has promising results for Duchenne Muscular Dystrophy patients
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£30,000 donation from Leicestershire to help develop Covid vaccine technology to treat Duchenne Muscular Dystrophy
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Mum of boy with severe muscle-wasting disease opens up about being a carrier of his illness A lot of carriers have struggled with feeling responsible for passing it on
Updated
Emma Hallam with her son, Alex who was diagnosed with a genetic degenerative disease at the age of four. (Image: Will Johnston)
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