• 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

#ADCONF20 announcement

3 June 2020 by Lynnette

We want to announce that the Action Duchenne International Conference will take place online this year. Following the Government's latest update, …

#ADCONF20 announcementRead More

National charity launches campaign for COVID-19 answers

28 May 2020 by Samantha

PRESS RELEASE Action Duchenne, the first national charity established to support those living with Duchenne muscular dystrophy (DMD), has launched …

National charity launches campaign for COVID-19 answersRead More

Open letter from the First Minister of Scotland

28 May 2020 by Samantha

Advice for those Shielding Thank you for your email and attached letter of 18th of May to the First Minister regarding shielding advice for …

Open letter from the First Minister of ScotlandRead More

Take part in important survey

27 May 2020 by Samantha

Impact of COVID-19 on transition planning for young people with additional support needs ARC Scotland, Lead …

Take part in important surveyRead More

Survey for individuals living with swallowing difficulties and neuromuscular disease

21 May 2020 by Samantha

Do you live with a neuromuscular condition? Do you experience swallowing difficulties as part of your neuromuscular condition? If you answer …

Survey for individuals living with swallowing difficulties and neuromuscular diseaseRead More

The Vampires Diaries’ Kat Graham supports charity single

19 May 2020 by Lynnette

Musician, actress and producer, Kat Graham has congratulated Jonathon Inkin on the launch of his charity single 'Horizons'. In the beautiful …

The Vampires Diaries’ Kat Graham supports charity singleRead More

Support our campaign for COVID-19 answers

14 May 2020 by Lynnette

COVID-19 has deeply affected the families we support. Most people living with Duchenne muscular dystrophy have been classified as clinically …

Support our campaign for COVID-19 answersRead More

North Eastern lad releases debut single

13 May 2020 by Lynnette

We are excited to share with you the debut single from the super talented, Newcastle lad Alex James. Being in a wheelchair performing is pretty …

North Eastern lad releases debut singleRead More

IMPaCCt Study – Investigating the impact of COVID-19 on Caregivers and patients.

13 May 2020 by Samantha

Researchers at Queen’s University Belfast and University of Aberdeen are conducting an online international survey to gain an understanding of the …

IMPaCCt Study – Investigating the impact of COVID-19 on Caregivers and patients.Read More

Looking forward to meeting again

11 May 2020 by Lynnette

A message from the National Director, Florence Boulton It was a relief this weekend to hear the Prime Minister announce the start of a process for …

Looking forward to meeting againRead More

Translarna MAA COVID-19 update

5 May 2020 by Neil

Translarna can treat Duchenne caused by a nonsense mutation (about 10-13% of cases). The drug is available in England and Wales via a Managed Access …

Translarna MAA COVID-19 updateRead More

Patron Martin Bashir backs fundraising single

24 April 2020 by Lynnette

We are incredibly excited to announce details of ‘Horizons’, an inspirational new song, recorded by Jonathon Inkin, a 21 year old living with Duchenne …

Patron Martin Bashir backs fundraising singleRead More

  • « Go to Previous Page
  • Page 1
  • Interim pages omitted …
  • Page 26
  • Page 27
  • Page 28
  • Page 29
  • Page 30
  • 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