Duchenne Direct

Join Today

Thank you for contacting us and supporting our work. We are in a race against time to give people with Duchenne Muscular Dystrophy a different future, but by working together we are confident we can do just that. We are passionately committed to developing and accelerating treatments for DMD, but we can only do it with your help.


Duchenne Direct is a monthly Direct Debit from you to Duchenne UK, that is spent DIRECTLY on research. 


By becoming a Duchenne Direct supporter today, you can help us End Duchenne.

Not a penny of your monthly contribution will be spent on overheads – 100% of your donations will be ring-fenced and will go directly into our exciting research projects.

By providing the charity with a regular income you allow us the flexibility to commit to the best research projects and plan for the future.


You can set up a direct debit quickly, easily and safely by clicking JOIN TODAY and following the prompts.

As a thank you for your essential support you will receive one of our World’s Strongest Boys wristbands. (Please get in touch to arrange size and delivery address). 

You will also receive quarterly updates on our research progress and discounts on our conferences and other events. 


Duchenne UK is a lean, ambitious and highly focused charity with a clear vision. 

Patients with DMD are at the heart of everything we do. Duchenne UK is run by parents, fighting every day to speed up treatments for all those living with DMD.  

Our approach is 100% focused on advancing research – and getting treatments into the clinic and to patients as quickly as possible to benefit this generation.

Our ambitious, strategic approach is backed by a robust decision-making process to ensure that every penny we spend has an impact. Our Scientific Advisory Board is comprised of some of the world's leading experts inDuchenne muscular dystrophy and our Patient Advisory Board (PAB) is made up of parents of children and young adults of different ages. 


Become a Family & Friends Fund

Join one of our fundraising events

You can contact us through our website, www.duchenneuk.org where you will also be able to find out more about how we are changing the future for those with Duchenne. Or email us, [email protected] 


Published on 2 January 2017

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