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  • Challenge 79 for World Duchenne Awareness Day
  • About Us
    • Our vision
    • Our Strategy
    • What we do
    • Our Impact
    • Our team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Mental Health Awareness Week 2025
    • Science on Tour
    • Support Calendar – What’s On
    • Support for you and your family
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Open Space
      • Group Counselling Programme
    • Recently diagnosed
    • Connect with others
    • Support for 8-14 yrs ‘Turning Point’
    • Support for 14-25 yrs ‘Yes I Can’
    • Schools
    • Siblings
    • End of Life and Bereavement
  • AD Annual International Conference
    • SAVE THE DATE for the Action Duchenne Annual International Conference 2025
    • Highlights from the Annual Action Duchenne Annual International 2024
    • Annual International Conference 2023 Video Recordings
    • Annual International Conference 2022 Recordings
      • Adults with Duchenne
      • Growing up with Duchenne
      • The Duchenne Journey
      • What is new in Duchenne research?
  • News, Webinars and Blogs
    • News
    • Webinar Series 2025
      • Webinar Series 2025
      • Webinar recordings
    • Bite-Sized Duchenne Science Live
      • Facts about Duchenne muscular dystrophy
      • Signs and Symptoms of Duchenne Muscular Dystrophy
      • Diagnosis of Duchenne Muscular Dystrophy
      • Crucial Genetic Terminology
      • Genetics – Blueprint of Duchenne Muscular Dystrophy
      • How is Duchenne Muscular Dystrophy Inherited?
    • Blogs
  • Support Us
    • Help Make a Life Beyond Duchenne Possible – Every Month
    • Fundraising Events and Challenges
    • Take on a challenge for Duchenne
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The Wards - Family Ambassadors

The Wards – Family Ambassadors

You are here: Home / Stories / The Wards – Family Ambassadors

April 26, 2019 by Lizzie Cox

We had such an amazing time. It was incredibly difficult at times, and emotional too. But the best experience I think I’ve ever had!

Zoe Ward (Parent, Ben Nevis)

Zoe and Ben have been an amazing part of the Action Duchenne family since their gorgeous son, Dexter was diagnosed with Duchenne.

The Wards - Family Ambassadors

They have taken part in a number of fundraising events, from ascending Ben Nevis, holding a Family Fun Day, to taking part in the Modball Rally and hosting their own charity ball.

Zoe and Ben attended the 2016 Conference the year after Dexter’s diagnosis, and in 2017 bought the children along too, who were absolutely amazing and had fun with Zoe’s Mum and the other children at the family event! 

Zoe has been into the Action Duchenne offices to meet the team, get support and personalised information about potential research projects which may benefit Dexter. 

Ben’s company have also donated to Action Duchenne and we are proud to welcome them as new Action Duchenne Family Ambassadors. 

The Wards - Family Ambassadors
The Wards - Family Ambassadors

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