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Press release
Muscular Dystrophy UK has released the following statement in response to the latest NICE guidance…
Blog
This blog by Trailblazer Emma Vogelmann is the first in a series on life during the coronavirus…
Your story
Danny Parker, 17, wanted to do the 1,0000 ft jump to fundraise for Muscular Dystrophy UK because…
Blog
So just to put anyone in the picture who doesn’t know me: I was diagnosed with a rare form of…
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Working with Oliver inspired me to turn a part time, one hour a day lunch-time assistant into a…
Blog
I’d had symptoms for about 10 years – dropping things, being clumsy, gaining weight, and becoming…
Your story
Liz chairs the FSH Support Group, which we support, and helps us develop information and resources…
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Chloe Smith, whose three-year-old son, Jenson, has an undiagnosed muscle-wasting condition, knows…
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Through this agreement, people with SMA types 1, 2 and 3 can now access the treatment, although…
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As well as caring for Dregan full-time, Peter and Emma hold a number of voluntary roles for MDUK.…