We know that the people who are most passionate about raising money to find treatments and a cure for Duchenne Muscular Dystrophy are those who live with it every day.
That's why we at Duchenne UK want to help and support you - the friends and families of those living with DMD - with raising the money to accelerate treatments and to find a cure. It's a race against time to give those with DMD a different future, but by working together we are hopeful we can do just that.
Our Family and Friends Funds provide vital support to Duchenne UK, by fundraising for us and helping us to advocate to accelerate research. They share our ambition to fund the most promising research, no matter where it is in the world, and to do so with a vision to help bring that research out of the laboratory and into the clinic where it can help patients.
Please get in touch if you are interested in joining us as a Family and Friends Fund. CLICK HERE to download our Family and Friends Funds information leaflet.
Your support means the absolute world to us.Read more
In our darkest moments we chose to not let Duchenne define either Archie or our family but instead to start fund raising and join the fight to end it.Read more
Our mission is to raise awareness and as much money as possible to fund research in order to find a cure for this cruel disease.Read more
We have set ourselves a target to raise awareness and as much money as we can to help fund research to find a cure for this cruel disease.Read more
Anna and Marc Clark are fundraising for Duchenne UK after their son Jack was diagnosed with DMD.Read more
Nick & Kirsty Ohly are determined to make a difference for their sons and all families affected by Duchenne.Read more
Our mission is to raise money for Duchenne UK and help END Duchenne IN TEN.Read more
Laura and Phil set up their family fund after their son Louis was diagnosed with Duchenne.Read more
We want to raise as much money as possible for the trials, treatments and hopefully one day a cure for all affected by this devastating disease.Read more
We are living in a time of great possibilities but time is already running out for William. Please help us save our son by donating whatever you can.Read more
We launched Muscles for Mitchell to support Duchenne charities on their mission to find potential treatmentsRead more
Dexter's parents have created Team Dex, with Duchenne UK, to raise money to go directly to the research needed to treat, cure and end DMD.Read more
The Lygo family have run, swam, climbed, cycled and walked to raise money for research into Duchenne.Read more
For Felix was set up by Alasdair Robertson and Robyn Pete after their son Felix was diagnosed with Duchenne muscular dystrophy.Read more
"Great things never happen by holding back,' says Lisa, mother of Felix. "So please don't, please donate what you can".Read more
The Crawfords are raising money for Duchenne UK to support their son Connor and many other boys like him.Read more
The Halpins are trying to give their son the best life possible and will continue to fight with Duchenne UK until we find a cure.Read more