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It is only through your help that we are able to fund vital research, and offer care and support to…
News
Written by her mum Lucy, ‘Wonder Girl Carmela and Tinker the Stinker’ centres on Carmela’s exciting…
Press release
  Muscular Dystrophy UK has issued a statement following news published today that Luke Garrett,…
Press release
His Royal Highness Prince Philip, the Royal Patron of Muscular Dystrophy UK for more than 50 years…
News
On this year’s Rare Disease Day, Sunday 28 February 2021, we are showcasing the achievement of…
News
Pfizer’s ongoing clinical trial  is testing the efficacy and safety of the potential gene therapy…
Your story
He took part in #TeamOrange’s February campaign to make muscles matter by joining people all over…
Blog
My name’s Romla, I’m 21 and in my final year studying BA Politics and International Relations at…
Your story
They were shining a light on muscular dystrophy because Jack Robinson, who has Duchenne muscular…
News
Running round the street backwards for 26 minutes, picking 26 daisies, shooting 26 netballs and…