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Duchenne UK
@DuchenneUK
Duchenne UK has one clear aim – to end Duchenne, a devastating muscle-wasting disease. We are the leading Duchenne muscular dystrophy charity in the UK.
Joined October 2012
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    We're delighted to announce that our founders, Emily Reuben and Alex Johnson, have been recognised in His Majesty The King’s Birthday Honours list. They have been awarded an OBE for their services to charity and to people with Duchenne muscular dystrophy.
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    In case he is thinking of looking for a new suit, Spiderman actor Tom Holland checked out our SMART Suit when we met with @alexswish and @BrothersTrustUK to discuss its development! A huge thank you to Tom and his family for their support for the DMD community!
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    A big thank you to @eddiemarsan for recording this special message! Duchenne UK CEO Emily will be going out of her comfort zone and cycling to Paris for the first time for this year's #DuchenneDash - show her some support at bit.ly/duchennedash and help us to #EndDuchenne
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    We are delighted to announce that Her Majesty The Queen has chosen to continue her role as President of the charity following a review of Patronages by the Royal Household. 🔗duchenneuk.org/her-majesty-th… (Photo credit: Hugo Burnand)
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    Today our cofounder Emily went to speak @Saracens⁩ training ground and meet many of the amazing players and staff to explain a bit more about our work and how they can get involved in the charity partnership #togethersaracens
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    We made it! 160 cyclists 300km Over £800k raised !!! Thank you so so much to everyone involved 🚴‍♂️🚴🏻‍♀️💙💙💙💙 To donate: bit.ly/ddash18 OR text: DUCH10 £10 TO 70070 #duchennedash
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    We can't wait for tomorrows match! Thank you @Saracens for this great opportunity to raise awareness for Duchenne muscular dystrophy. @alljoinjack @DefndwilliamDMD
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    Santander support the campaign via their ambassador @J_Ennis thank you! goo.gl/80yvAw #WorldsStrongestBoys
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    Thank you @theJeremyVine @BBCRadio2 for inviting Emily on to the show and helping us to raise awareness for Duchenne muscular dystrophy
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    Thank you so much to @SkyNews for welcoming us this morning, and to the people of @PostcodeLottery for supporting the suit - helping people with Duchenne Muscular Dystrophy to restore function to their arms, helping them to chase their dreams 🙌 Now it's time to #GetEliToGlasto
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    We made it to Paris! AND WE RAISED A MILLION POUNDS! A huge HUGE well done to our incredible Dashers, and big THANKS to our amazing support team, our sponsors and all those who have donated. Please donate by following this link bit.ly/ddash19 and help us #ENDDUCHENNE
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    Breaking news! Vamorolone, the first treatment for all DMD patients regardless of ambulatory status has been approved in the UK! The drug (sold under the brand name Agamree) has been approved for the treatment of DMD in patients aged 4 yrs+ by the MHRA.
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    We are very pleased to share with you that the founders of Duchenne UK have been honoured by the Prime Minister's... fb.me/K2cXFPUE