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Action Duchenne

Header Right

  • About Us
    • Our Purpose
    • Our Strategy
    • 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
      • Open Space
      • Group Counselling Programme
    • Recently diagnosed
    • Connect with Others
    • Support for 8-14 yrs ‘Turning Point’
    • Support for 14-25 yrs ‘Yes I Can’
    • Schools
    • Siblings
    • End of Life and Bereavement
  • AD Annual International Conference
    • Highlights from the Action Duchenne Conference 2025
    • Action Duchenne Annual International Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2025
      • Webinar Series 2025
      • 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
  • Runner Hub

Charity of the Year

You are here: Home / Get involved / Ways you can help / Charity of the Year

Duchenne muscular dystrophy is a rare condition, not many people have heard of it before. Nominating us as your Charity of the Year is a unique opportunity for your staff to get behind our lesser known but life changing cause, showing how your company is committed to making a real difference.

Action Duchenne is at the heart of the Duchenne community. We are

  • supporting over 1,500 families a year navigate their journey from diagnosis to end of life and bereavement
  • educating and empowering parents, carers, schools and health care professionals and people living with Duchenne
  • funding innovative research projects to find better treatments and one day a cure

By partnering with us your business will also benefit from our expertise in disability rights and awareness. We can help you to create a workforce that recognises the importance of employing disabled people with rare conditions.

Why partner with us?

  • We support people nationally and locally – we work across the UK to provide virtual and face to face support, including a yearly international conference which is the largest of it’s kind in Europe
  • Our team are passionate, dedicated and experienced – many of our board and employees are Duchenne parents or live with Duchenne and are truly committed to helping your company make a difference
  • We are unique – Duchenne may be rare but it affects so many, children and adults living with the condition and also their parents or carers, siblings, friends, schools and employers.
  • We love to have fun – We know that life is here to be lived to it’s very best!

Previous Charity of the Year partnerships

Great British Beer Festival 2016 & 2022

GA Solictiors

Action Duchenne is a deserving small charity that is not only looking to improve the lives of those living with Duchenne, but also supports their families and creates a sense of community

Steve Ramsden, Managing Partner at GA Solicitors

Alderwood Recruitment

Amazing effort by Alderwood at last week’s charity bake sale for Action Duchenne, it’s great to see a charity where all their staff are so invested and attentive to those also wanting to help.

Grace Hackett, Alderwood Recruitment

Career Legal


If you would like to know more about Charity of the Year partnerships or if you are an employee who would like to nominate Action Duchenne we would love to hear from you.

Call us on 07535 498 506 and leave a message or email victoria.young@actionduchenne.org

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From our community

Blue Monday Blog: Hear from Victoria, our Fundraising Officer and Duchenne Mum

Written by Victoria Edwards, Action Duchenne’s Fundraising Officer and mum to Dougie (who lives with Duchenne) and Allie. Feeling Blue “This Monday was Blue Monday, and wow… I really felt it. It was grey, drizzly, my son was up half the night and ended up off school from sheer tiredness. My daughter went in to …

“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 …

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Action Duchenne
5th Floor, Mariner House
62 Prince Street
Bristol
BS1 4QD

07535 498 506
info@actionduchenne.org 

 

 

 

 

 

 

 

 

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