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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

Our impact

You are here: Home / Our impact

Thank you for attending our AGM

1 April 2024 by Lizzie Cox

Thank you for attending our AGM Action Duchenne held our AGM on 19th March 2024 and would like to thank all of our staff members, trustees and …

Thank you for attending our AGMRead More

Determination and achievement 

10 May 2022 by Lynnette

This article is written by Florence Boulton, National Director “We are all stronger, together” is a fantastic motto, but it’s even better when put …

Determination and achievement Read More

Peer to peer support – Chloe and Lyndsey

10 May 2022 by Samantha

This article is written by Duchenne parents Chloe and Lyndsey who were carefully matched by our Support team. Chloe In Jan 2021 we officially …

Peer to peer support – Chloe and LyndseyRead More

Peer-to-peer support – I don’t feel so alone anymore

9 May 2022 by Samantha

This article is written by a Duchenne Mum, Vicki, about her experience with Action Duchenne’s peer-to-peer support. Hi my name is Vicki, I have an …

Peer-to-peer support – I don’t feel so alone anymoreRead More

Peer-to-peer support – meeting a fellow mom

5 May 2022 by Lynnette

This article is written by a Duchenne Mum, Ruth, about her experience with Action Duchenne's peer-to-peer support. When my son was diagnosed with …

Peer-to-peer support – meeting a fellow momRead More

Project update: Supporting families through diagnosis and impossible decisions

1 April 2022 by Lynnette

How we’re supporting Newly Diagnosed Duchenne families through the diagnosis and the impossible decisions they are forced to make. The last year …

Project update: Supporting families through diagnosis and impossible decisionsRead More

Springing into action

8 March 2022 by Lynnette

A message from our National Director, Florence Boulton It was 2 years ago when I first joined my new team around a table in a meeting room in …

Springing into actionRead More

Join Dr. David Schonfeld Webinars

25 February 2022 by Victoria Edwards

How to talk to children about Duchenne - the early years We know how hard it is for Duchenne parents, carers and family members to find the 'right' …

Join Dr. David Schonfeld WebinarsRead More

End of project report summary – Clinical Trials Lectureship (Newcastle)

28 January 2022 by Lynnette

We are delighted to report the outcomes of our grant for a Clinical Trials Lectureship. The grant, which was supported by a consortium of seven UK …

End of project report summary – Clinical Trials Lectureship (Newcastle)Read More

Behind the scenes at Action Duchenne’s Santa’s Grotto

24 January 2022 by Lynnette

This time last year, I was proudly clicking ‘share’ on the impact report for our 2020 Christmas Campaign. We’d sprinkled a touch of magic at a time …

Behind the scenes at Action Duchenne’s Santa’s GrottoRead More

Action Duchenne brings Christmas magic to Duchenne families

21 January 2022 by Lynnette

On 17th December 2021, UK charity Action Duchenne, with support from Sporting Bears, brought light, hope and Christmas magic to 32 families living …

Action Duchenne brings Christmas magic to Duchenne familiesRead More

Happy Holidays from our National Director

16 December 2021 by Lynnette

It’s beginning to look a lot like Christmas!  This week, we’ve launched our Action Duchenne Santa’s Grotto; a little thank you to our …

Happy Holidays from our National DirectorRead More

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