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This December, we're asking you to give the gift of hope instead of buying cards, gifts, or hosting a party, by helping to fund life-changing research for Duchenne muscular dystrophy (DMD).

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Owen aged 7 with his Duchenneber drawing Owen aged 7 with his Duchenneber drawing
Charlie aged 4 with his festive drawing for Duchenneber

Why get involved?

DMD is a severe muscle-wasting disease. It is the most common and severe form of muscular dystrophy, usually diagnosed in early childhood.

There is currently no effective treatments or cure, but there is hope.

Duchenne UK is going further to find effective treatments for DMD and end its devastating impact. We’re doing it faster, too, by accelerating access to these treatments and therapies for this generation of patients. 

Give the gift of hope to families affected by DMD this festive season and together, we will end Duchenne.

How you can help

By getting involved in Duchenneber, you’ll be funding vital research to give our boys, rare girls and young men living with DMD hope for the future.

There are lots of ways to support Duchenne UK and Duchenneber this year:

Follow and share!

Follow Duchenne UK on our Instagram and Facebook pages where we will be posting some festive artwork made by children in the DMD community and sharing what they’re most looking forward to this December. 

If your child would like to feature, or if you are planning a festive fundraiser for Duchenneber, we would love to know more. Send your pictures to [email protected] or tag us in your social posts using @DuchenneUK and #Duchenneber. 

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Duchenneber gallery

Published on 16 November 2021

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