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Action Duchenne

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  • Donate
  • 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
    • Schools
    • End of Life and Bereavement
  • Annual Conference
    • Save the Date for the Action Duchenne Community Summit 2026 (Previously known as Annual International Conference)
    • 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
  • Support Us
    • Friends of Action Duchenne
    • Upcoming Events and Challenges
    • Give in memory and help us support every family, every time.
    • Organise your own event
    • Fundraising at school
    • Donate by cheque and post
    • Welcome to our Runner Hub

newly diagnosed

You are here: Home / newly diagnosed

Your invitation to the newly diagnosed Duchenne family event

10 September 2021 by Lynnette

Taking place online on Saturday 23rd October 2021 from 14:00 - 18:00 GMT, this event is a chance for families who are new to the Duchenne community to …

Your invitation to the newly diagnosed Duchenne family eventRead More

Newly diagnosed event – watch recordings

27 October 2020 by Lynnette

We were delighted to welcome so many families from across the globe to our virtual event for newly diagnosed families or those who are newcomers to …

Newly diagnosed event – watch recordingsRead More

Recognising the power of our community

12 October 2020 by Lynnette

A message from the National Director, Florence Boulton The past four weeks, since I last wrote to you all, has been a rollercoaster of extreme …

Recognising the power of our communityRead More

Newly diagnosed families special event

1 October 2020 by Lynnette

When you receive the diagnosis of Duchenne muscular dystrophy, the amount of information you receive seems overwhelming.  Here at Action …

Newly diagnosed families special eventRead More

A Life Fulfilled In Everyway (ALFIE)

12 June 2020 by Lynnette

By Duchenne Dad, Kieron Sales Hello again! First of all I’d just also like to say a big thank you to everyone that has taken time to read my …

A Life Fulfilled In Everyway (ALFIE)Read More

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