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Duchenne UK

Duchenne UK

Who we are

Duchenne UK has one clear aim, to end Duchenne.

 
As the leading Duchenne muscular dystrophy (DMD) charity in the UK, we want to find effective treatments for DMD and end its devastating impact.
 
We’re going further than anyone has before, and 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 connect the best researchers with industry, the NHS and families to advance and accelerate every stage of drug development.
Together, we will end Duchenne. 

As the leading Duchenne muscular dystrophy (DMD) charity in the UK, we want to find effective treatments for DMD and end its devastating impact. 

We’re going further than anyone has before, and 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 connect the best researchers with industry, the NHS and families to advance and accelerate every stage of drug development.


What is Duchenne muscular dystrophy? 

Duchenne muscular dystrophy (DMD) is a progressive condition diagnosed in childhood. It causes muscles in the body to gradually weaken. 

There is currently no cure for DMD, but there is hope. We are at the forefront of advancing treatments and care for everyone affected by the disease. 

For more information about our work or DMD please visit our website duchenneuk.org or watch our charity film.  


Support us

There are lots of ways you can support us. Make a donation on this page, create your own fundraising page, or visit our website to find out about the latest events and challenges you can take part in. 


Together, we will end Duchenne. 


Find out more

Charity details

Registered address
Unit G20,The Shepherds Building
Charecroft Way,London
W14 0EE

info@duchenneuk.org

http://www.duchenneuk.org

Charity number
1147094

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