To find effective treatments for Duchenne muscular dystrophy we need to go further than anyone ever has. We’re going to do it faster too, because this generation of boys can’t wait. We need your help, because the only way we can do this is together!
Join us, and be part of the end of Duchenne.
London - Paris, 24hrs, 300kms.
Take part in a challenge, do something fun or attend one of our events.
Challenges, activities and events
If you have a loved one with DMD, you can set up your own dedicated fund or make a donation.
Family & Friends Funds
Find out how your company can get involved and help us to accelerate vital research.
Corporate support
Your regular donations will help us to change the lives of those affected by DMD.
Set up a monthly donation
Take part in our annual bike ride from London to Paris in May 2024.
Take part
Get in touch with our friendly team for fundraising information and support.
Contact us
could provide a newly diagnosed family with a vital DMD Family Information Pack.
could pay for a family to attend a Duchenne UK Parent Information Day.
could pay for one hour of life-changing DMD research by a senior researcher.
could pay for a week of support from a clinical research nurse
"In 2013 we found out by a routine visit to hospital that Felix, one of our four children, had an incurable terminal disease, DMD.
After hiding and crying and keeping our pain locked away we now see a future not to be feared: it's to do something, it's to raise money, to make people aware, to fight for Felix and enjoy the future with him."
Lisa, Felix's mum
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