Help power our work and join us in making history

We want to help people. We want to give hope. We want a world where people's lives are no longer limited by Duchenne and Becker muscular dystrophy.

We are funding the research today which could be instrumental in finding the cure tomorrow.

When Action Duchenne was founded in 2001, the average life expectancy for a young person living in the UK with Duchenne was late teens. It is now 27. We are helping to change the future every day.

Our vision to change the face of the severe muscle-wasting condition, Duchenne can only achieved by the life-changers who support us.  We receive no government funding and everything we do is powered by you, our community. Thank you!

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