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Action Duchenne

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  • 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
    • In-Person Support Events
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Open Space
      • Group Counselling Programme
    • Recently diagnosed
    • 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 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

Leave a legacy donation

You are here: Home / Leave a legacy donation

Action Duchenne was established in 2001 to support children, young people, adults, and their families living with Duchenne muscular dystrophy. It is a community-led charity, proud to work with partner organisations to address the unmet needs of the community through designing programmes and services that maximise resources.

THE FUTURE: OUR 10 YEAR AMBITION

It’s important for all children born in the years to come to be free from a life limited by Duchenne muscular dystrophy. We will work towards;
● The availability of better treatments
● Improved care and life expectancy
● Families having the knowledge they need
● People gaining acceptance more quickly than they do today
● A significantly increased science education and research programme
● Appropriate support pathways for families starting at diagnosis and continuing throughout their lives
● Opportunities for people living with Duchenne don’t have to be sought, they just exist – university, jobs etc.
● A much wider reach for all our projects – nationally and internationally
● Respite centre(s) available for families

Leave a gift in your Will

Leaving a gift in your Will helps to create this future, and keep the important work we have started going. The donation can be as small or large as you like, every gift makes a difference to our cause. Should you wish to, you can choose to leave a legacy for a specific project or activity close to your heart.

How to leave a gift in your Will to us

  1. Decide what type of gift you want to to leave us – Pecuniary gifts – a set amount of money, Residuary gifts – a percentage, or the whole, of your estate (what’s left after other specified gifts, costs, and tax) or Specific gifts – a specific object, asset or property
  2. Get advice and read guides on making a Will from a source that you trust
  3. Contact your solicitor or Will writer and provide them with details of our charity and the gift you would like to leave us.

It was a hugely helpful day for us in clarifying a lot about our son’s potential future and reassuring us that there is more hope than we imagined.

Science Education Workshop Participant

If you would like to discuss leaving a gift in your will please contact fundraising@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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