We wouldn’t be able to fight muscle-wasting conditions without your support, and without gifts in wills, around 25 percent fewer families would be helped by Muscular Dystrophy UK.

Meet Ethan

Ethan has congenital fibre type disproportion with the faulty gene being ACTA1. While he is a typical little brother, he is also a unique little boy. Doctors call him ‘child 3’, as at the time of diagnosis he was only the third child in Europe that they knew of with this specific diagnosis. Read more…

 

Meet Abbi

She can walk but she cannot jump and she battles to get up after sitting. Sometimes even a strong gust of wind could knock Abbi’s frail little body over. Her muscles will weaken and waste over time and she will most likely use a wheelchair full-time through her teen years. And she’ll struggle to breathe unaided. Read more…

 

When the time is right for you to make your will, please remember Muscular Dystrophy UK.

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