• About Us
    • Our Purpose
    • Our Strategy
    • 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
      • Open Space
      • Group Counselling Programme
    • Recently diagnosed
    • Connect with Others
    • Support for 8-14 yrs ‘Turning Point’
    • Support for 14-25 yrs ‘Yes I Can’
    • Schools
    • Siblings
    • End of Life and Bereavement
  • AD Annual International Conference
    • Highlights from the Action Duchenne Conference 2025
    • Action Duchenne Annual International Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2025
      • Webinar Series 2025
      • 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
  • Runner Hub
  •  0 items - Free
  • 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 - Free

Action Duchenne

Header Right

  • About Us
    • Our Purpose
    • Our Strategy
    • 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
      • Open Space
      • Group Counselling Programme
    • Recently diagnosed
    • Connect with Others
    • Support for 8-14 yrs ‘Turning Point’
    • Support for 14-25 yrs ‘Yes I Can’
    • Schools
    • Siblings
    • End of Life and Bereavement
  • AD Annual International Conference
    • Highlights from the Action Duchenne Conference 2025
    • Action Duchenne Annual International Conference 2025
  • News, Webinars and Blogs
    • News
    • Webinar Series 2025
      • Webinar Series 2025
      • 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
  • Runner Hub

Welcome to our Runner Hub

You are here: Home / Welcome to our Runner Hub

Running for our small charity is incredibly rewarding. Not only can it boost your physical and mental wellbeing, but it also gives you the empowering feeling that you’re helping us support, equip, and uplift every DMD community — from diagnosis and throughout their journey.

Please note: Our injury‑prevention and nutrition guidance has been written by our Outreach Officer, Alex Berbank, a former elite athlete and trained physiotherapist. However, if you are making any sudden or significant lifestyle changes, we always recommend consulting your GP first.

We’re thrilled to have you on Team Action Duchenne. Every year, incredible people like you take on running challenges to raise vital funds for our work. We want you to enjoy every moment of this experience and to feel fully supported by us from start to finish.

Before you get going, it’s important to make sure you’ve chosen the right distance and feel genuinely excited about the challenge ahead. Asking yourself a few key questions now will be essential in helping you reach race day feeling confident and prepared.

Take a moment to check in with yourself. Consider the following:

How is your overall health right now?
How busy is your work schedule?
What other commitments or responsibilities do you have?
How will you realistically fit training into your routine?
Do you have any existing niggles or injuries that running could aggravate?
Do you have friends, colleagues or family members who can help you reach your fundraising target?
Is there anything in particular that’s worrying you?

If any of these questions raise concerns for you, please get in touch with us. We want to ensure you feel confident that you’ve chosen the right race and the right distance. And if this event isn’t quite the right fit, we’ll happily help you find an alternative challenge.

Feeling ready and excited? That’s exactly what we hope for.

If everything feels positive and you’re eager to get started — wonderful! We are here to support you with anything you need along the way.

You’re not doing this alone. You’re part of a community of Action Duchenne Champions, and we’re behind you every step of the journey.

Runs and Challenges

Read more

Training Plans and Injury Prevention

Read more

Nutrition for runners

Read more

Fundraising ideas

Read more

Share this:

Primary Sidebar

From our community

In memory of Leon Thorn

Leon’s life was full of courage, laughter, and love. Though he lived with Duchenne Muscular Dystrophy, it never defined him. Leon was brave, hilarious, kind, and endlessly determined – a gamer, a thinker, and a quiet fighter who inspired everyone around him.  In his memory, incredible friends and family came together to keep his spirit alive.  Garry, …

In Loving Memory of Christopher Whittaker 

Gemma held a fundraiser in memory of her incredible brother, Christopher Whittaker, who sadly passed away in November 2023 at the age of 28 due to Duchenne Muscular Dystrophy (DMD). Having an evening of live music, a tombola, a raffle, and bingo she raised an amazing amount of £2,230. “Everyone who knew Christopher knows how truly amazing he was—from his early years right …

Blue Monday Blog: Hear from Victoria, our Fundraising Officer and Duchenne Mum

Written by Victoria Edwards, Action Duchenne’s Fundraising Officer and mum to Dougie (who lives with Duchenne) and Allie. Feeling Blue “This Monday was Blue Monday, and wow… I really felt it. It was grey, drizzly, my son was up half the night and ended up off school from sheer tiredness. My daughter went in to …

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

Like most websites we use cookies to deliver a personalised service. To use the website as intended please accept cookies.
Privacy & Cookies Policy

Privacy Overview

This website uses cookies to improve your experience while you navigate through the website. Out of these, the cookies that are categorized as necessary are stored on your browser as they are essential for the working of basic functionalities of the website. We also use third-party cookies that help us analyze and understand how you use this website. These cookies will be stored in your browser only with your consent. You also have the option to opt-out of these cookies. But opting out of some of these cookies may affect your browsing experience.
Necessary
Always Enabled
Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.
Non-necessary
Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. It is mandatory to procure user consent prior to running these cookies on your website.
SAVE & ACCEPT