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  • About Us
    • Our Purpose
    • What We Do
    • Our Impact
    • Our Team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Support Calendar – What’s On
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • In-Person Support Events
    • Schools
    • End of Life and Bereavement
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    • Highlights from the Action Duchenne Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2026
    • 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?
    • Hear From Our Community
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    • Upcoming Events and Challenges
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News

You are here: Home / News

Join National Director Florence Boulton as part of our Vitality London 10,000 Team!

20 June 2023 by Lizzie Cox

Join National Director Florence Boulton as part of our Vitality London 10,000 Team! On September 24th 2023, the hugely popular Vitality London …

Join National Director Florence Boulton as part of our Vitality London 10,000 Team!Read More

D.AD’s Night – Dads Against Duchenne

18 June 2023 by Alex

D.AD's Night - Dads Against Duchenne It is a difficult place being a Dad in Duchenne and there isn’t much opportunity to speak with others face to …

D.AD’s Night – Dads Against DuchenneRead More

Join our At Home Superheroes!

15 June 2023 by Lizzie Cox

Join our At Home Superheroes! Ivelina, mum of Presian ( 5 year old DMD hero ), tells us what motivated her family to sign up for the Superheroes …

Join our At Home Superheroes!Read More

My viewpoint as a bereaved parent by Angela Stringer

8 June 2023 by Angela Stringer

Is it wrong to feel relieved now that I am bereaved?  I wish my son was still here and to be able to enjoy his company.  Sadly not.  …

My viewpoint as a bereaved parent by Angela StringerRead More

Thank you to our volunteers

1 June 2023 by Lizzie Cox

Thank you to our volunteers 1st - 7th of June is National Volunteers Week and we want to say thank you! In 2022/23 the team here at Action …

Thank you to our volunteersRead More

Fighting for the future

31 May 2023 by Lizzie Cox

Fighting for the future While we continue our much needed day to day work supporting our families, I want to share with you the recent developments …

<strong>Fighting for the future</strong>Read More

Join us for the second half of Yes I Can Online

29 May 2023 by Lizzie Cox

Join us for the second half of Yes I Can Online We are now half way through our 12 online sessions. So far we've heard from Alex James and …

Join us for the second half of Yes I Can OnlineRead More

Isaac White tells us all about his first fundraising event for Action Duchenne

26 May 2023 by Lizzie Cox

Isaac White tells us all about his first fundraising event for Action Duchenne "Party Planning is what I was born to do! Enjoy!" On Friday …

Isaac White tells us all about his first fundraising event for Action DuchenneRead More

Ask the pharmaceutical companies your questions ahead of Action Duchenne’s 2023 Annual International Conference

25 May 2023 by Lizzie Cox

Ask the pharmaceutical companies your questions ahead of Action Duchenne's 2023 Annual International Conference To make sure you get your voice …

Ask the pharmaceutical companies your questions ahead of Action Duchenne’s 2023 Annual International ConferenceRead More

Roche UK issues statement to the Duchenne Community following Sarepta’s Update on Regulatory Review of SRP-9001 gene therapy.

25 May 2023 by Mehreen Arif

Roche UK issues statement to the Duchenne Community following Sarepta's Update on Regulatory Review of SRP-9001 gene therapy. Following the update …

Roche UK issues statement to the Duchenne Community following Sarepta’s Update on Regulatory Review of SRP-9001 gene therapy.Read More

Sarepta Therapeutics Announces Update on Regulatory Review of SRP-9001

24 May 2023 by Mehreen Arif

Sarepta Therapeutics Announces Update on Regulatory Review of SRP-9001 Sarepta Therapeutics, today provided the following update on the Biologics …

Sarepta Therapeutics Announces Update on Regulatory Review of SRP-9001Read More

PepGen Announces Clearance by Health Canada of CTA for PGN-EDO51 to Begin the Phase 2 Clinical Trial, CONNECT1-EDO51, for the Treatment of Duchenne Muscular Dystrophy

19 May 2023 by Mehreen Arif

PepGen Announces Clearance by Health Canada of CTA for PGN-EDO51 to Begin the Phase 2 Clinical Trial, CONNECT1-EDO51, for the Treatment of Duchenne …

PepGen Announces Clearance by Health Canada of CTA for PGN-EDO51 to Begin the Phase 2 Clinical Trial, CONNECT1-EDO51, for the Treatment of Duchenne Muscular DystrophyRead More

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