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Action Duchenne

Header Right

  • 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
    • In-Person Support Events
    • 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
campaign for action duchenne

Campaign for Action Duchenne

You are here: Home / Get involved / Campaign for change / Campaign for Action Duchenne

Campaigning definition ‘An organised course of action to achieve a goal‘

Action Duchenne lead our families, friends and supporters to work together to make change happen.

We know that through working together we can get our voices heard. We campaign in parliament to improve access to treatments and medicines. We work tirelessly to improve standards of care for people living with Duchenne, which directly improves their quality and length of life.

Action Duchenne’s Access to Medicines and Campaigns Strategy is targeted at the UK Government, NHS and treatment access policy makers.

Action Duchenne played a key role in the Managed Access Agreement for translarna; the first treatment licensed for those living with Duchenne and eligible with nonsense mutations. This was a long-fought campaign with ourselves and the community at the forefront.  We are considered a true stakeholder by the key decision makers. We have lead the way and have a proven track record in making change happen.

We build strong partnerships with the community to maximise our shared knowledge with our membership organisations Genetic and Neurological Alliance. We seek to influence policy by identifying factors that must be changed and bring about change by influencing policymakers, key decision makers in the access of potential treatments and also the NHS environment. We influence policy across the health service, public health and ensure it supports the quality of life for all young people living with Duchenne Muscular Dystrophy.

Take action

  • Call us 020 7250 8240
  • Contact your MP 
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From our community

Turning Challenges into Change – Our Story with Action Duchenne

I was introduced to Action Duchenne by the Muscle Team in Newcastle shortly after Oliver’s diagnosis in 2017. In those early, overwhelming days, their support meant everything. Members of the Support Team would call just to let me talk, vent, cry — whatever I needed. They were simply there, and that’s why I choose to support them every …

Louise’s London Marathon Story

Louise’s London Marathon Story Written by Louise Ruddick “My relationship with Action Duchenne came about very spontaneously at the beginning of January this year. My brother, George, was diagnosed with Duchenne back in 1992, just before his third birthday. He was obviously too young to be aware however the impact that it had on our …

Parent Story: Scott and Vicki share their story of their son’s diagnosis of Duchenne and their family’s journey.

Parent Story: Scott and Vicki share their story of their son’s diagnosis of Duchenne and their family’s journey. “I was just sitting in the room and the doctor’s mouth was moving but I couldn’t hear anything that was coming out of it”  Parents Scott and Vicki have two children, Josh and Layla. When Josh was just …

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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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