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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
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    • Webinar Series 2025
      • Webinar Series 2025
      • Webinar recordings
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      • 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?
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Family Science Education Day

You are here: Home / News / Family Science Education Day
Family Science Education Day

April 3, 2025 by Lizzie Cox

Family Science Education Day

On Saturday 22nd March, we welcomed some of our amazing families to our Family Science Education Day at the Think Tank Science Museum in Birmingham. After enjoying a light lunch together, the children and young people took part in a brilliant science workshop with Sublime Science. Parents and carers had a chance to meet, chat and support each other alongside AD staff Sadia, Kelly and Ravi. Everyone had the opportunity to check out the exhibits at the museum before heading to their hotels to get ready for the Charity Dinner Dance in the evening. 


It was wonderful to be able to bring families together to share experiences, develop friendships and have some fun! Thank you so much to everyone who was able to join us and made it such a memorable day. 

Charity Dinner Dance

Ruth Talyor and her dedicated committee organised their second charity dinner dance in aid of Action Duchenne. This wonderful event was held in Aston Villa Football Ground on Saturday 22nd March and included a 3 course meal, band, auction, raffle and disco. Action Duchenne staff Sadia, Kelly and Victoria were delighted to be among the guests, along with the families from our Science Education Day.  We will share more photos and experiences from the evening over the coming weeks, but for now we want to thank Ruth and Ian Taylor and the Dinner Dance Committee for everything they put in to organising such an amazing event, and to everyone who came along to share in the experience. 

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You can find links to our online support groups , support for schools and to register for our newly launched webinar series.

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We need YOUR support so that we can continue to support those living with Duchenne muscular dystrophy. Find out how YOU could support us by becoming a valued member, making a donation or fundraising for us here.

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