• 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
  •  0 items - £0.00
  • Menu
  • Skip to right header navigation
  • Skip to main content
  • Skip to secondary navigation
  • Skip to footer

Before Header

  • My account
  •  0 items - £0.00

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
    • 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

Conference

You are here: Home / Conference

Overview of dystrophin restoring approaches

2 February 2024 by Lizzie Cox

Overview of the role of dystrophin in Duchenne and Beckers MD, the therapeutic options and challenges in treating neuromuscular diseases. …

Overview of dystrophin restoring approachesRead More

Overview of inflammation and fibrosis reducing strategies

2 February 2024 by Lizzie Cox

The role of inflammation and fibrosis in DMD myopathy and the latest therapeutic strategies for reducing muscle degeneration. …

Overview of inflammation and fibrosis reducing strategiesRead More

Dystrophinopathy: Female Carriers

2 February 2024 by Lizzie Cox

The importance of understanding the genetics of female carriers, the prevalence of clinical symptoms and how they're caused, and the services …

Dystrophinopathy: Female CarriersRead More

Genetics of Duchenne muscular dystrophy: Why, hows and mutations

2 February 2024 by Lizzie Cox

An introduction to the genome and genetics of Duchenne muscular dystrophy: why it occurs, the types of mutations, and how it is tested for. …

Genetics of Duchenne muscular dystrophy: Why, hows and mutationsRead More

Thank you for attending the Action Duchenne Annual International Conference 2023!

14 November 2023 by Lizzie Cox

…

Thank you for attending the Action Duchenne Annual International Conference 2023!Read More

Welcome to the Annual Action Duchenne International Conference 2023

10 November 2023 by Florence Boulton

Welcome to the Annual Action Duchenne International Conference 2023 On behalf of the whole team at Action Duchenne, I would like to give you the …

Welcome to the Annual Action Duchenne International Conference 2023Read More

Registration is OPEN for the Action Duchenne Annual International Conference 2023

30 June 2023 by Lizzie Cox

Registration is OPEN for the Action Duchenne Annual International Conference 2023 FREE tickets for Duchenne families as well as every young …

<strong>Registration is OPEN for the Action Duchenne Annual International Conference 2023</strong>Read More

Ask the pharmaceutical companies your questions ahead of Action Duchenne’s 2023 Annual International Conference

25 May 2023 by Lizzie Cox

Ask the pharmaceutical companies your questions ahead of Action Duchenne's 2023 Annual International Conference To make sure you get your voice …

Ask the pharmaceutical companies your questions ahead of Action Duchenne’s 2023 Annual International ConferenceRead More

More than Hanging Out

9 December 2022 by Lizzie Cox

More than Hanging Out Blog by Jess Breeze, Programme Assistant When I spent an amazing day with the Sporting Bears on 19th March, (see blog here …

More than Hanging OutRead More

The Action Duchenne International Conference 2022; Opening Remarks

11 November 2022 by Robbie Handley

Our international conference has now officially started! After months of hard work and dedication from our amazing team to get the event on, we are so …

The Action Duchenne International Conference 2022; Opening RemarksRead More

Questions at the Conference

23 September 2022 by Lynnette

Action Duchenne is providing a platform for you, the Duchenne community, to ask questions from the leading Pharmaceutical companies driving …

Questions at the ConferenceRead More

Conference agenda

20 September 2022 by Lynnette

Join us for two days in November as we explore the latest research, treatments and updates. Watch presentations, Q&A sessions and join discussions …

Conference agendaRead More

  • « Go to Previous Page
  • Page 1
  • Page 2
  • Page 3
  • Page 4
  • Page 5
  • Go to Next Page »

Footer

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

07535 498 506
info@actionduchenne.org 

 

 

 

 

 

 

 

 

Subscribe to our mailing list

Do you consent to receiving regular email updates? *
Email Format
  • Accessibility
  • Privacy Policy
  • Terms & Conditions

© Action Duchenne - Registered Charity No 1101971 - Scottish Charity No SC043852