• 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
  •  0 items - £0.00
  • Menu
  • Skip to right header navigation
  • Skip to main content
  • Skip to secondary navigation
  • Skip to primary sidebar
  • 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
    • 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
You are here: Home / Conference / The 2020 Action Duchenne International Conference Registration is now OPEN!
The 2020 Action Duchenne International Conference Registration is now OPEN!

The 2020 Action Duchenne International Conference Registration is now OPEN!

29 July 2020 by Lynnette

We are delighted to announce that our Action Duchenne International Conference 2020 (‘the Conference’) is now open for registration.

Register

The event will inspire and educate hundreds of people from around the globe with updates on research, care and living with Duchenne muscular dystrophy.

We invite all our young people and adults living with Duchenne, members, families and friends to join and get access to amazing content, free of charge (we will welcome donations to contribute to the event costs).

#ADCONF20

For the first time ever, the Conference will be a content-packed, online event unlike anything we have produced before. It will focus on the weekend of 14/15 November, but we’ll be uploading content before the main weekend and all the plenary and breakout sessions will be easily accessible on-demand for conference attendees to view at their own convenience. 

Meeting other families, friends and our industry experts is a cornerstone of our conference, and attendees will be able to participate in interactive and engaging experiences through a new dynamic virtual conference platform. We will have interactive exhibition features and lots of opportunities to talk to researchers, pharmaceutical company staff and other attendees from the comfort and safety of your home or office.

Join our virtual conference rooms, engage with the industry experts, meet our families and friends and get access to premium content at the click of a button below.

What to expect

  • Amazing programme with updates on research, care and living with Duchenne
  • International Duchenne experts at your fingertips
  • Fully online, virtual experience to enable you to access the vital information in a safe way from anywhere in the world
  • The latest technology (it’s really whizzy!) to help you meet families, clinicians, researchers, pharmaceutical partners and exhibitors 
  • Interact ‘face-to-face’, ask your own questions and talk to everyone attending

We’ll be helping you to get the most out of the Conference, through the easy-to-use virtual platform. As always, the entire Action Duchenne team will be behind the scenes throughout the weekend to help you too!

Please register now and save the 14th and 15 November 2020 to spend with us virtually.

Register now for #ADCONF20

PS. We look forward to seeing you in person next year, at the Action Duchenne International Conference 2021.

Share this:

Category: Conference, News

Previous Post: « Practical tips to help your child or young person
Next Post: Taking Raxone? We need your input! »

Primary Sidebar

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 …

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