• Donate now
  • Support Calendar – What’s On
  • Contact us
  • About us
    • Our vision
    • What we do
    • Our Impact
    • Our team
    • Work for us
    • Volunteer
    • The DMD Registry
  • Celebrating our Action Duchenne Champions
  • Get Support
    • Recently diagnosed
    • Group Counselling Programme
    • Connect with others
      • Online support sessions
      • Support for 14-25 yrs ‘Yes I Can’
      • Support for 8-14 yrs ‘Turning Point’
    • Science on Tour 2023
    • Schools
    • Siblings
    • End of Life & Bereavement
  • International Conference
    • 2022 Recordings
  • News, Blogs & Webinars
    • News
    • Blogs
    • Webinar recordings
  • Challenge 79
  • Support Us
    • Make a Pledge
  • Shop
  •  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

  • BECOME A MEMBER
  • SHOP
  • My account
  •  0 items - Free

Action Duchenne

Header Right

  • About Us
    • Our vision
    • Our Strategy
    • What we do
    • Our Impact
    • Our team
    • Work for us
      • Volunteer for us
    • Volunteer
    • The DMD Registry
    • Celebrating our Action Duchenne Champions
  • Get Support
    • Mental Health Awareness Week 2025
    • Science on Tour
    • Support Calendar – What’s On
    • Support for you and your family
      • 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
    • SAVE THE DATE for the Action Duchenne Annual International Conference 2025
    • Highlights from the Annual Action Duchenne Annual International 2024
    • Annual International Conference 2023 Video Recordings
    • Annual International Conference 2022 Recordings
      • Adults with Duchenne
      • Growing up with Duchenne
      • The Duchenne Journey
      • What is new in Duchenne research?
  • 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?
    • Blogs
  • Support Us
    • Rare Disease Day 2025 – More than you can imagine
    • Make a Pledge
    • Become an Action Duchenne member
    • Take on a challenge for Duchenne
    • Fundraising Events and Challenges
  • Shop

Dads Against Duchenne

You are here: Home / Events / Dads Against Duchenne

February 21, 2024 by Lizzie Deeble

Dads Against Duchenne

8:00 pm – 9:00 pm
July 1, 2024

It is a difficult place being a Dad in Duchenne and there isn’t much opportunity to speak with others face to face. 

We're going to be launching a virtual Dad’s night hosted by myself to give Duchenne dads some time and space to just talk to other guys in the same position. 

 

I hear that finding time to unwind after a stressful week is gold dust and seems to be shrinking. We need to change that. Making time to relax and unwind is just as important as anything else when we’re in a stressful situation. It’s why sleep is always recommended and any olympic athlete will have rest days built into their schedule. We need to do the same. The virtual dads night is about just relaxing with other men who are in the same situation. It doesn't always have to be about duchenne either. I know myself sometimes when I've been in a tough place the last thing i feel like doing is unloading everything and talking through it bit by bit. In these cases it’s just nice to have a laugh with a few mates who get it, and would be ok with me talking about it if I wanted to but will also understand if i didn't. After speaking to a lot of dads I feel like we have that community together we just need a place to hang out. 

 

I’m hoping that the Dads night is a place to get to know other people who get that, I genuinely have different conversations with dads. You have different priorities and often different ambitions that you’ve been forced to change and adapt. But you’re not alone in that. Personally I challenge any dad to get in contact with me if they feel like they are the only one facing a problem with duchenne and ill find you 15 other Dads thinking the exact same thing. With this dads night I’m confident i can show you that in person, even if it is just virtual. 

 

There's no set agenda each week, it’s as open ended as going to the pub or for a meal with mates. We can talk about the big stuff one week and maybe even the football , or the music we grew up on the next. The content isn't what matters, what matters is that we are surrounded by a great team on these nights, and together there’s not a problem Duchenne throws at us or our families that we can’t deal with. Together, united, Dads Against Duchenne.

 

More information

Register

iCal

Google Calendar

View full calendar

Event Categories: DAD's

Primary Sidebar

From our community

Mental Health and Community – Duchenne Dads and Male Mental Health

Written by Partnerships and Outreach Manager Alex Berbank You can listen to the audio recording of this blog here: It’s somewhat of a buzz term currently. We know it’s an area that has been neglected in the past but has anything changed and currently as a bloke today, how do you realise when you need …

An Action Duchenne Spring Update

An Action Duchenne Spring Update As we head into May, welcoming warmer days and lighter evenings, it’s a time to reflect back over the first few months of 2025 as well as look ahead to the many exciting events still to come. Webinar Series 2025 A highlight of the year so far, The Action Duchenne …

Coping with Diagnosis with David Schonfeld

March marked a special milestone at Action Duchenne as we kicked off our brand-new webinar series! Each month, we are diving deeper into the important themes related to Duchenne muscular dystrophy (DMD) care, and we could not have asked for a better start. We were incredibly fortunate to have the brilliant Professor. David Schonfeld joined …

Footer

Action Duchenne
Wellesley House
Duke of Wellington Avenue Royal Arsenal
London
SE18 6SS

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