Run for Action Duchenne!

You can be part of our vision, a world where lives are no longer limited by Duchenne muscular dystrophy.

In 2023, run for Action Duchenne and you will be warmly welcomed into our community of amazing supporters and Duchenne families. Every penny you raise will help children, young people and adults living with Duchenne muscular dystrophy, a rare muscle wasting condition.

With the money you raise

*£20 Could pay for a newly diagnosed family to receive an initial support telephone call and vital information pack.

*£50 Could fund one full hour of research.

*£100 Could contribute to bringing a Duchenne science education event to our families across the UK

*£500 Could help us develop and deliver a support and education webinar

Registration is now free with code ADFREE entered at the checkout. We suggest that our runners set minimum of £100 to support our vital work.

*Deadline to register is 12 noon on 18th September*

Want to enter as a team? A Team Leader needs to register first. We will then contact the team leader with their unique link to send others inviting them to join their team! As a team you can pick your own fundraising target, we recommend teams aim for a minimum of £400.

Supporting you to smash your target

As a much treasured supporter we provide you with

  • The start of what we hope will be an amazing journey with our charity!
  • Support from you from the moment you sign up and throughout your whole journey. We will make sure you know the impact your hard work and commitment is having on our vision.
  • Peer support and training tips from other Action Duchenne runners.
  • Fundraising support, ideas and materials to help you generate and smash your target. You can download our fundraising pack to help you get started.
  • An Action Duchenne running vest or t-shirt for you to wear with pride during training and on the day!
 

registrations are not available

There are currently no entry options available for this event.

 

Your support is life changing for people living with Duchenne and their families, and we also hope to bring you one of the most rewarding experiences of your life.

If you have any questions at all, or need some support to sign up, please contact [email protected].

We look forward to getting to know you!