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Action Duchenne’s main aim has always been to find a cure for Duchenne and Becker, to raise awareness through fundraising and campaigning, and to develop the necessary protocols. Action Duchenne continues to fundraise, campaign and provide support and educational expertise to young people and families affected by Duchenne.
Action Duchenne has a team of 10 permanent staff dedicated to meeting the main challenge set by the founders – Dr Janet Hoskin and Nic Catlin : To be a leader in supporting innovative research to cure and treat Duchenne.
Action Duchenne works across the UK, the EU, the US and the southern hemisphere seeking answers and support from all parts of the duchenne community: researchers, clinicians, physicians, pharmacological companies and other duchenne charities.
Evox Therapeutics wins funding from Duchenne UK to explore exosome-mediated delivery of dystrophinEvox Therapeutics Ltd, a leading exosome...
The Muscular Dystrophy AssociationThe Muscular Dystrophy Association is co...
Hope for Gus FoundationHope For Gus Foundation was founded by p...
Muscular Dystrophy Family FoundationSince 1958, Muscular Dystrophy Family Fo...
Brothers with rare condition painting postcards to fund custom vehicleTwo brothers in Cambridge with a rare ge...
RARE on the Road – Interactive WebinarParticipants will engage in interactive ...