We have one clear aim. To end Duchenne.
We are the UK's leading Duchenne muscular dystrophy (DMD) charity. We're connecting scientists, industry, the NHS and families to accelerate research and bring the best care to everyone affected by DMD.
We are the UK's leading Duchenne muscular dystrophy (DMD) charity. We're connecting scientists, industry, the NHS and families to accelerate research and bring the best care to everyone affected by DMD.
We’re going further than ever before to find effective treatments, setting our ambitions high and overcoming the barriers in our way.
We’re doing it faster, because this generation of people living with DMD can’t wait.
The only way we can achieve this is together. We collaborate with scientists and the pharmaceutical industry, bringing them together with DMD patients and families. And we work with health services to bring the best care to all.
Your donations are helping to fund life-changing research into DMD and give people living with DMD and their families the most precious gift of all, hope.
Join our mission to fund life-changing DMD treatments by fundraising, donating, or joining an event.
Get involved
We're collaborating on an initiative to improve DMD care throughout the UK.
Visit the DMD Care UK website
We fund the DMD Hub to bring more UK patients the opportunity to take part in clinical research.
Visit the DMD Hub site
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Ross took part in our annual London to Paris bike ride in 2022 following his son's DMD diagnosis
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We aim to share the most important news in drug development with the DMD community through our quarterly roundup.
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