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World Duchenne Awareness Day 2025

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World Duchenne Awareness Day 2025

World Duchenne Awareness Day Logo

September 7th is World Duchenne Awareness Day or WDAD. Each year, an annual campaign aims to increase awareness of Duchenne and Becker muscular dystrophy. World Duchenne Awareness Day raises awareness and inspires action to improve the lives of people living with Duchenne and Becker muscular dystrophy.

There is still relatively little awareness of the impact of Duchenne on the lives of those living with it. World Duchenne Awarness Day aims to change this. In 2024, The United Nations has marked a momentous milestone for the global rare disease community by officially designating September 7th as World Duchenne Awareness Day. The adoption of the resolution “World Duchenne Awareness Day” is the UN’s first formal acknowledgment of a day dedicated to a rare disease.

We would love you to join us for WDAD 2025, and here are a few ways you can get involved.

Family: the heart of care

This year the theme for World Duchenne Awareness Day is “Family: The Heart Of Care”. This theme recognises that a Duchenne journey is shaped by the amazing people who travel the journey alongside someone living with Duchenne.

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Challenge 79

We invite you and your family to take part in Challenge 79—a simple, creative way to raise awareness and feel connected with the global Duchenne community.

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Bad Shirt Friday

A fun, simple way to support the Duchenne community and raise vital funds—by wearing your worst (or most brilliantly bold) shirt. Whether it’s bright, loud, clashing or downright questionable, we want to see it on Friday 5th September.

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From our community

“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 …

Guest Blog: Birthday Boy

By Jack Waddington We are pleased to feature a very special guest blog for World Duchenne Awareness Day 2025. This blog has been written by Jack Waddington. Jack’s younger brother Sam lived with Duchenne after he passed away, Jack has written a memoir about growing up with him. In his own words, “it’s about the …

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