• 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

#WDAD2020: The brain and Duchenne

You are here: Home / #WDAD2020: The brain and Duchenne
Gary Fegan Duchenne Parent and Chair of the Board of Trustees for Action Duchenne

Those living with Duchenne muscular dystrophy are more likely to experience learning difficulties and behavioural issues but nobody is exactly sure why. Scientists have shown that some forms of dystropin (the protein missing in Duchenne) are produced in the brain, but what it does and whether it’s important isn’t really understood.

To mark World Duchenne Awareness Day 2020 we’re highlighting some of the issues in Duchenne and how they can be managed.

Behaviour & attention – many families we speak to have difficulty managing their child or young person’s attention, learning and behaviour. Watch this fascinating recording to find out more.

Memory – from Kim’s game to pairs, Lego to shopping lists, find out simple but practical ways to help your young person develop their memory here.

Emotion – the frontal lobes have important functions in guiding our actions, reactions and responses. We hope this session recording helps you deal with the psychological effects of life with Duchenne.

Posture – wheelchairs, seating, orthotics and other equipment can be confusing and daunting for families. Take a look at this session recording which we hope you find helpful.

The initial focus following a diagnosis with Duchenne is understandably on the devastating physical prognosis.  In time, the learning and behaviour side of the condition can become more apparent presenting a series of other challenges for child and parent alike.  

A diagnosis of Autism or ADHD can unlock additional and targeted support at school and if you suspect your child may have particular behaviours or problems, for example in social interactions and obsessive or repetitive actions, you should push hard for an assessment.  Our upcoming conference on 14 and 15 November is also a great opportunity to hear from professionals in this field and I would really encourage parents and carers, as well as teaching and learning support staff, to sign up for this year’s groundbreaking online event.

Mark Silverman, Duchenne Parent and Action Duchenne trustee   

Find out more from the comfort of your own home

The brain and Duchenne is a key topic you can learn about at the virtual Action Duchenne International Conference 2020. Over the weekend of 14 and 15 November 2020, we’ll start with the science – finding out why dystrophin is in the brain and what it’s doing. We’ll talk about learning difficulties and behavioural issues faced by those living with Duchenne and their families, and how these can be managed and individuals supported.

You can register for the event below, tickets are free and all are welcome.

Share this:

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