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That’s why we’re joining a global alliance on 15 September, International Myotonic Dystrophy…
Your story
Joseph Moan has been blind from birth. When their eldest son Jack was diagnosed with Duchenne…
Your story
Sam Tisbury, from Brentwood, has a strong connection with MDUK through supporting his Uncle Bryon,…
Blog
David Howard, who has facioscapulohumeral muscular dystrophy (FSHD), is excited to be taking on the…
News
To mark World Duchenne Awareness Day 2021 on Tuesday 7 September, we were joined in our Muscles…
News
In the week of World Duchenne Awareness Day 2021 we are delighted to be able to announce that the…
Publication
It is only through your help that we are able to fund vital research, and offer care and support to…
Blog
I am pleased to announce that the Journal for Neuromuscular Disorders has accepted for publication…
Your story
Phil Carroll was diagnosed with Duchenne muscular dystrophy in 2003, when he was nine years old.…
Your story
It was not just the pandemic which changed everything last year for Jack Partridge, who was…