• Challenge 79 for World Duchenne Awareness Day
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    • SAVE THE DATE for the Action Duchenne Annual International Conference 2025
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      • Facts about Duchenne muscular dystrophy
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Action Duchenne

Header Right

  • Challenge 79 for World Duchenne Awareness Day
  • About Us
    • Our vision
    • Our Strategy
    • What we do
    • Our Impact
    • Our team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Mental Health Awareness Week 2025
    • Science on Tour
    • Support Calendar – What’s On
    • Support for you and your family
      • 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
    • SAVE THE DATE for the Action Duchenne Annual International Conference 2025
    • Highlights from the Annual Action Duchenne Annual International 2024
    • Annual International Conference 2023 Video Recordings
    • Annual International Conference 2022 Recordings
      • Adults with Duchenne
      • Growing up with Duchenne
      • The Duchenne Journey
      • What is new in Duchenne research?
  • 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?
    • Blogs
  • Support Us
    • Help Make a Life Beyond Duchenne Possible – Every Month
    • Fundraising Events and Challenges
    • Take on a challenge for Duchenne
    • Shop
You are here: Home / Work for Good

Work for Good

Action Duchenne has joined Work for Good, an online platform that makes it easy for small businesses to support our life-changing work.

How to get involved

The team at Work for Good are on hand to support you every step of the way.

  • Your business has the power to make a positive impact, whatever you do and whatever your size.
  • Whether you’re a sole-trader or small business. Work for Good have made it easy for you to support Action Duchenne.
  • They take care of the legal requirement that is needed for sales fundraising, known as a Commercial Participation Agreement, leaving you to get on with what you do best.
  • By raising funds through your sales, you can sustainably support Action Duchenne and make a real difference.
  • Work with purpose. Work for good.
Find out more and start fundraising now

From the first phone call, I felt completely understood and supported. Speaking to other DMD parents who work for Action Duchenne has truly been a lifeline for me, and they have never wavered in their support and patience

Lizzie | Duchenne Mum | Member

Our impact

We are proud to bring you an update of the work we are doing here at Action Duchenne, and to explain the tangible progress we are making.

These past few months we have started delivering key parts of the ‘All-through Support’ project, including; 

  • support webinar double-bill on trauma and bereavement
  • over 600 1-2-1 support calls and meetings with Duchenne families in the past 6 months
  • carefully ‘match-making’ Duchenne families with others in a similar position
  • hosting The Friday Hive, an open, drop-in peer-to-peer support group on Fridays 10-12 during term time
  • planning the transition to adulthood project
  • new team-mates have joined our ranks; Alex (Outreach Officer) and Dr Mehreen (Chief Scientific Officer) 
  • collaborating with partner organisations, both from within the Duchenne community and from other specialised areas. 

Earlier this month, we were proud to solidify our status as an agile charity, by announcing an increase in our expenditure on charitable activities to 88.7p in every £1 we raise!

This is a great achievement for us, and one that sets us apart from other charities which may be struggling following the pandemic’s devastation to the third sector. 

Donations we receive are vital to help Action Duchenne bring our life-changing work to more and more people across the UK.

Your support will enable Duchenne families to attend important support and education events like the Conference and Science Education Programme, take part in our transition to adulthood residential and access our world-class support services as soon as they are diagnosed. And help us to achieve our vision ‘a world where lives are no longer limited by Duchenne muscular dystrophy’
 

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Action Duchenne
Wellesley House
Duke of Wellington Avenue Royal Arsenal
London
SE18 6SS

07535 498 506
info@actionduchenne.org 

 

 

 

 

 

 

 

 

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