Raising money for Duchenne Muscular Dystrophy

Do you want to join me in making a difference? I'm raising money in aid of Duchenne UK and every donation will help. Thank you in advance for your contribution to this cause that means so much to me.

More information about Duchenne UK: Duchenne UK has one clear aim, to end I am a family member of a club, that I dont want to be in!! In 2023 I became a confirmed family member of the DMD club, but really I had been in it since 2019. I didn"t even know what Duchenne Muscular Dystrophy (DMD)was, until my grandson was diagnosed with it. He was falling alot, unable to jump & hop, waddling when he walked up an incline & he had times of extreme fatigue. The horror of reading what DMD has in store for my beautiful, innocent little boy breaks my heart. How can I make a difference to this incurable neuromuscular condition? How can I support my grandson & immediate family? How do I share this information with my friends? We have to live with HOPE. We have to advocate for further research for a cure & better treatments & best care. Please can you, my community, join with me in the DMD club & help me make that difference.Duchenne.

Duchenne muscular dystrophy (DMD) is a progressive muscle-wasting disease.

As the leading DMD charity in the UK, Duchenne UK is at the forefront of advancing treatments and care for everyone affected by the disease to end its devastating impact.

Duchenne UK is going further than anyone has before, and doing it faster because this generation of people living with DMD can't wait.

Together, we will end Duchenne.