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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.
Little Hercules Foundation – FacebookLittle Hercules Foundation is a register...
North Sydney students collect aluminum can tabs for teenager with muscular dystrophyJean and Alfred Landry are shown with Fe...
Stand for Duchenne CanadaStand for Duchenne Canada is a not-for-p...
CureDuchenne – FacebookCureDuchenne is a nonprofit organization...
Kristin Engelstad, MS, CGCKristin Engelstad is a clinical study co...
CureDuchenne E-storeYou can now buy T- shirts and other av...