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Press release
Many people living with muscle-wasting conditions are “clinically extremely vulnerable” and are…
Your story
Chloe Smith, whose three-year-old son, Jenson, has an undiagnosed muscle-wasting condition, knows…
Your story
Becoming an admin member of the CMT Facebook group and connecting with MDUK has proved a life-…
Your story
My disability won’t define me
Tiffany was born with malignant hyperthermia and central core…
Blog
An interesting conversation came up in the Trailblazer’s pod of desks this week – it was about a…
Blog
Arti Dasani is 24, has Charcot-Marie-Tooth disease (CMT) and recently graduated with a degree in …
Blog
Jamie Hale is a writer and disability activist currently interning with Muscular Dystrophy UK's…