• 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 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

News

You are here: Home / News

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. The event …

The 2020 Action Duchenne International Conference Registration is now OPEN!Read More

Summer ‘holiday’ after lock-down

28 July 2020 by Lynnette

A message from the National Director, Florence Boulton At the start of what would normally be the season for summer ‘holidays’, my thoughts go to …

Summer ‘holiday’ after lock-downRead More

Impact of Aviva fundraising campaign

17 July 2020 by Lynnette

Thank you to everyone who supported our recent fundraising campaign through the Aviva Community Fund UK. We are delighted to let you know we …

Impact of Aviva fundraising campaignRead More

Dr Shuko Joseph awarded the Lorber Prize

15 July 2020 by Samantha

We are delighted to share the news that; Dr Shuko Joseph has won the Lorber Prize for best paediatric research paper for her work on growth and …

Dr Shuko Joseph awarded the Lorber PrizeRead More

Patron backs Duchenne science project

15 July 2020 by Lynnette

Our Patron and hugely talented actress, Helena Bonham Carter is supporting our Aviva Community Fund project. I’m absolutely delighted to back this …

Patron backs Duchenne science projectRead More

Open letter from Minister for Health, Northern Ireland

8 July 2020 by Lynnette

In May, we sent out letters directly to Prime Minister Boris Johnson, Secretaries of State for Health, Education and Work and Pensions, as …

Open letter from Minister for Health, Northern IrelandRead More

Thank you to the staff and pupils at Immanuel College

8 July 2020 by Samantha

A very special thank you to Eddie Curtis, 14, who bravely gave a presentation to 700 pupils at his school about Duchenne muscular dystrophy, and the …

Thank you to the staff and pupils at Immanuel CollegeRead More

Remembering BJ Doherty

7 July 2020 by Samantha

We were so very shocked and saddened to hear the news of BJ Doherty's passing in January 2019. BJ was an incredible friend, father and husband, …

Remembering BJ DohertyRead More

Scottish Powerchair Football Association cheque presentation

28 June 2020 by Samantha

Massive thanks to Action Duchenne for coming up to give us a donation, much appreciated and we hope you enjoy watching some Powerchair Football It …

Scottish Powerchair Football Association cheque presentationRead More

Cross Party Group meeting on Palliative Care

28 June 2020 by Samantha

On 5 June 2019, Our Scottish Advocacy Officer John Miller attended the Cross Party Group meeting on Palliative Care. This meeting explored the …

Cross Party Group meeting on Palliative CareRead More

Send us your questions

25 June 2020 by Lynnette

In May, we launched our COVID-19 campaign #weneedanswers where we asked the Prime Minister, Secretaries of State for Health, Education and Work and …

Send us your questionsRead More

Open letter from Deputy First Minister and Cabinet Secretary for Education and Skills

25 June 2020 by Lynnette

In May, we sent out letters directly to Prime Minister Boris Johnson, Secretaries of State for Health, Education and Work and Pensions, as …

Open letter from Deputy First Minister and Cabinet Secretary for Education and SkillsRead More

  • « Go to Previous Page
  • Page 1
  • Interim pages omitted …
  • Page 25
  • Page 26
  • Page 27
  • Page 28
  • Page 29
  • Interim pages omitted …
  • Page 49
  • 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