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  • About Us
    • Our Purpose
    • Our Strategy
    • What we do
    • Our Impact
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    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
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    • Register for Support
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      • Dads Against Duchenne
      • Grandparents Together
      • Open Space
      • Group Counselling Programme
    • Recently diagnosed
    • Connect with Others
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    • Support for 14-25 yrs ‘Yes I Can’
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    • Siblings
    • End of Life and Bereavement
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    • Highlights from the Action Duchenne Conference 2025
    • Action Duchenne Annual International Conference 2025
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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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Raise Your Voice for World Duchenne Awareness Day 2024

You are here: Home / Raise Your Voice for World Duchenne Awareness Day 2024

Raise Your Voice for World Duchenne Awareness Day 2024

World Duchenne Awareness Day 2024

World Duchenne Awareness Day unites the global Duchenne community annually for advocacy, action and change. This year is a monumental milestone as it marks the first year that the United Nations have officially designated 7th September as World Duchenne Awareness Day.

Duchenne Awareness Day is held on the 7th September each year to honour the 79 exons on the dystrophin gene. An error on any one of these exons causes Duchenne. The theme this year is ‘Raise Your Voice for Duchenne’.

This year’s theme emphasises the importance of amplifying voices to advocate for the rights, inclusion and well-being of people living with Duchenne muscular dystrophy (DMD) and other dystrophinopathies. While life expectancy has increased over the last few years, there is still a long way to go in the fight for a better future for everyone living this devastating condition. 

On September 7 the World Duchenne Organisation invites everyone, irrespective of their personal connection to Duchenne, to join in creating a more inclusive world where people living with disabilities are empowered to thrive.

What can YOU do? 

Challenge 79

Enter our Challenge 79 as an individual or team – do it your way in your time

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Challenge 79 for Schools

Enter Challenge 79 as a school – we are offering all schools a visit from our Science education team plus you can also enter our design competitions

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Become an Action Duchenne Member

Become a monthly member and join us in creating our vision for lives to no longer limited by Duchenne

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Make a Donation

Make a one off donation to fund our ongoing life changing work

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Raise Your Voice

Tell us YOUR story so we can share it with the community. Email lizzie@actionduchenne.org

Share Social Media Posts

Create awareness by sharing posts on your social media

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From our community

Blue Monday Blog: Hear from Victoria, our Fundraising Officer and Duchenne Mum

Written by Victoria Edwards, Action Duchenne’s Fundraising Officer and mum to Dougie (who lives with Duchenne) and Allie. Feeling Blue “This Monday was Blue Monday, and wow… I really felt it. It was grey, drizzly, my son was up half the night and ended up off school from sheer tiredness. My daughter went in to …

“Making contact with Action Duchenne provided a lifeline”

“Making contact with Action Duchenne provided a lifeline”: Find out why Ben Dolling decided to run the London Marathon dressed as a parrot! Harry was diagnosed with Duchenne muscular dystrophy in 2019 Ben and his wife have 3 children: a daughter in year 3 and a son in his first year of university and Harry, …

The Power of Shared Experience: “Honestly, it would’ve been a much harder road without having joined this group.”   

Action Duchenne have monthly online meet-ups for Duchenne dads, mums and grandparents, facilitated by our Family Support Officers and designed to enable connection with those who truly understand. A Duchenne diagnosis can often set people apart from the support systems they usually rely on. Our support groups mean you can meet people who know exactly …

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Action Duchenne
5th Floor, Mariner House
62 Prince Street
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BS1 4QD

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