• Donate
  • About Us
    • Our Purpose
    • What We Do
    • Our Impact
    • Our Team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • Summer 2026 In-Person Family Days
    • Schools
    • End of Life and Bereavement
  • Community Summit
    • Action Duchenne Community Summit 2026 (Previously 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
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • Summer 2026 In-Person Family Days
    • Schools
    • End of Life and Bereavement
  • Community Summit
    • Action Duchenne Community Summit 2026 (Previously 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

Annual International Conference 2019

Slides and Presentations

The Action Duchenne International Conference 2019 had 43 separate sessions (plus loads of activities for children and teenagers), meaning even those in attendance didn’t get to see everything!

Here we have compiled as many of those presentations as we can, so that the whole international Duchenne community can benefit from them. Please note some of these have been edited (and some we can’t publish at all) as they often contain information and results that have not yet been made available to the wider public.

Developing Effective Treatments for All

Looking at the real world – developing new outcome measures. (Victoria Selby and Laurent Servais)

The age of genomic medicine (Patrick Short)

Gene therapy – the latest updates and a look to the future (Neil Bennett, Jean-Francois Briand and Francesco Muntoni)

Exon skipping technology in Duchenne (Annemieke Aartsma-Rus, Graham McClorey, Aurelie Goyenvalle and Ian Woodcock)

Company updates (Capricor, Catabasis, Italfarmaco, Pfizer, PTC, ReveraGen, Roche, Santhera, Sarepta, Wave)

Action Duchenne update (Neil Bennett)

An update on basic research and why it’s still important (Neil Bennett, Keith Foster and Linda Popplewell)

Company and Researcher Q+A (Capricor, Catabasis, PTC, ReveraGen, Roche, Santhera, Sarepta, Wave)

Developing Effective Treatments for All (continued…)

Stem cell therapies in Duchenne (Neil Bennett, Yung-Yao Lin and Saverio Tedesco)

Clinical trial experiences, considerations and ethics (Bobbie Farsides, Stefan Spinty and Families)

Using existing drugs to treat Duchenne (Steve Winder and Jarod Wong)

Building a Community

Newly diagnosed: Duchenne 101 (Annemieke Aartsma-Rus)

Carriers: genetics and implications (Neil Bennett and Angela Stringer)

Physiotherapy (Marion Main and Jose Longatto)

Talking to your children about Duchenne: diagnosis, treatment, hopes and dreams (David Schonfeld)

Carriers: reproduction (Michela Guglieri)

Learning and behaviour in Duchenne (James Poysky)

Psychology (Gabriella Rands)

A More Inclusive Society

Accessible gaming for Duchenne (Vivek Gohil)

Manual handling (Julie Hewitt and Disability Living Foundation)

Practical inclusion tips for school (Clair Warner)

IEPS and EHCPs (Clair Warner)

Sibling stories (Clare Kassa and siblings)

What to do in an emergency (Jarod Wong and Stefan Spinty)

Air travel with a disability (Chris Wood)

Duchenne education programme (Alban Squires)

Wishes of teens and adults with Duchenne (David Abbott, 2018 presentation)

Back to #ADCONF19
Share this:

Primary Sidebar

From our community

Honouring George and Finding Community

Honouring George and Finding Community Remembering George one year on. “If I’d never experienced George having Duchenne, I wouldn’t be half the person I am now. He taught me so much about life. I truly believe that boys with Duchenne are just the most awesome people in the world.”  On Sunday 26th April 2026, Louise Ruddick ran the …

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 …

Footer

Action Duchenne
2nd Floor
South
One Castle Park
Tower Hill
Bristol
BS2 OJA

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