The Wilson family sat in their living room playing with their son Aadi who has SMA Type 2
 Professor Dame Kay Davies in her laboratory at the University of Oxford working with two researchers
Two delegates share laughing together in the coffee break at the Muscular Dystrophy UK 2019 conference
Volunteers taking part in a Muscular Dystrophy UK workshop
Together, fighting muscle-wasting conditions

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Access to seven new treatments

Despite the huge financial impact of the COVID-19 pandemic on our charity, we remain committed to campaigning for access to treatments. During the past year, we worked with individuals, families, clinicians and other patient groups through the assessment processes for seven new treatments, and engaged in the NICE methods review.
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Ways you can get involved


For over 50 years, we've been here for people living with muscle-wasting conditions. We couldn't do this without your help. Thank you.


Support for our work is more crucial than ever, so we've got lots of ideas about how you can help us fundraise.


Our brilliant volunteers help us deliver services, fundraise and raise awareness about muscle-wasting conditions.