Celebrating 25 Years of Action Duchenne

Celebrating 25 Years of Action Duchenne

“As we celebrate 25 years of supporting families affected by Duchenne Muscular Dystrophy, we want to take this opportunity to reflect on the impact we have achieved together, share the progress we are making today and look to the future with ambition, collaboration and hope to ensure every family receives the support they need and that progress continues for generations to come.”
Katie Endacott, CEO

We are excited to announce that it’s our 25th birthday and you’re invited to our celebrations! There are lots of ways you get involved throughout the year. We’ve got our ‘Evening with Action Duchenne’ coming up on 20th October, our birthday party on Friday 13th November at the Community Summit, and much more to come!