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.
Duchenne UK was founded by parents and we are fighting every day to find treatments for our children and everyone living with DMD. We do this with the relentless determination of a mother and the rigorous focus of a scientist.
We are funding research, accelerating treatments, and supporting families along the way. At the heart of it all are our boys, men and rare girls living with DMD.
Donate now and bring forward the day when we will end Duchenne.
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 2022.
Take part
Get in touch with our friendly team for fundraising information and support.
Contact us
This festive season, give a gift with a difference and bring hope to families affected by Duchenne muscular dystrophy.
Duchenneber is a whole month dedicated to raising awareness and funds to fight DMD.
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
Sign up for the latest news on DMD research, upcoming events and ways to get involved.
