One in 5000 newborn boys in the world is affected by a rare and fatal disease: Duchenne Muscular Dystrophy (DMD). Seems like a small group, but the 250.000 patients around the globe think big and have big dreams. Duchenne Parents have set up organizations in their countries, and all of them work day by day to guarantee access to care, to improve research, to educate patients and families.

September 7 is World Duchenne Awareness Day. On this day we raise awareness for Duchenne and Becker muscular dystrophy around the globe.  As every year, we have a special theme that deserves more attention.

The WDAD 2024 theme is ‘Raise your voice for Duchenne’. With this year’s theme, WDAD supports creating a society that provides equal opportunities for all. This year we organize the 11th edition.

 

 

Past activities on World Duchenne Awareness Day

2025: Family, the heart of care

Documentary highlighting how love, community, and determination shape life with Duchenne

2024: Raise your voice for Duchenne

Documentary sharing the stories of three individuals from different corners of the world

2023: Breaking Barriers

Documentary sharing how people living with DMD/BMD are each breaking barriers in their lives

2022: Women & Duchenne

Educational conference where we highlight all the aspects connected with Duchenne and the female world.

2021: Adult Life & Duchenne

World Duchenne Awareness Day 2021 theme: Duchenne adults living their lives to the fullest.

2020: Duchenne and the Brain

Livestream where experts share their knowledge on DMD/BMD and learning and behavioral issues.

2020: Together we are stronger

Promo video for WDAD 2020 to raise global awareness for Duchenne and Becker Muscular Dystrophy.

2019: Nutrition in DMD

Information to increase understanding of nutrition and supplement use in Duchenne Muscular Dystrophy.

2019: Bring Your Light

A global collaboration of Duchenne families to raise awareness on DMD and BMD in the general public.

2018: Standards of Care

Making Duchenne Care information accessible for as many people as possible and more specific for children as well.

2017: Duchenne Dreams

By telling the dreams of the DMD boys worldwide it was possible to inform and involve the civil society to be part of this commitment for a better future.

2016: Early Diagnosis

The third edition of WDAD was focused on early diagnosis: identifying and communicating early signs of Duchenne in order to guarantee a good quality of life to the children.

2015: Duchenne Stories

By telling the dreams of the DMD boys worldwide it was possible to inform and involve the civil society to be part of this commitment for a better future.

2014: Faces of Duchenne

For the first edition of the World Duchenne Awareness Day in 2014, it was essential to explain to the civil society what is Duchenne muscular dystrophy, what does it mean to live with this disease day by day.