• 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
  • Community Summit
    • Action Duchenne Community Summit 2026 (Previously 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
  • Community Summit
    • Action Duchenne Community Summit 2026 (Previously 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
You are here: Home / Hear From Our Community / Florence's blogs / Happy Holidays from our National Director
Happy Holidays from our National Director

Happy Holidays from our National Director

16 December 2021 by Lynnette

It’s beginning to look a lot like Christmas! 

This week, we’ve launched our Action Duchenne Santa’s Grotto; a little thank you to our community and a chance for families to come together online and visit Father Christmas.  Last year, the feedback was so wonderful, we just knew we had to do it again this year! 

Impact from Christmas 2020

This year, again, places are free for all UK-based Duchenne families (made possible by our friends at Sporting Bears). I hope you will make the most of this opportunity and enjoy the magic of Christmas together as a family.

Book your place in the Grotto

Getting support over the holiday

Our offices will be closed from 12:00 GMT on Christmas Eve, re-opening on 29th December. We will then close at 12:00 GMT on New Year’s Eve, with normal hours resuming on 4th January 2022.  Over the festive period, we will be running a reduced staff, however should you need support over the next 10 days, we are here for you, as always, via info@actionduchenne.org or on 020 7250 8240. We will respond to any messages as soon as possible.

There are also other places you can seek support and advice;

  • Action Duchenne Dad’s Group
  • Action Duchenne Mum’s Group
  • Action Duchenne Grandparent’s Group
  • We have lots of great content on our website including practical tips for managing during the holidays (webinar from lockdown summer)
  • Making stretches fun (recorded with Marion Main, Lead Physiotherapist at GOSH). 
  • Watch the recordings from our recent International Conference (via the app if you have already registered, or you can register here).

Thank you

A big thank you to each and every person and organisation that have made a contribution to our charity over the last 12 months, from the volunteers, fundraisers, pharmaceutical companies and corporate partners to our social media followers, Duchenne families and of course, the children, young people and adults who live with Duchenne. 

On behalf of our trustees and team, I would like to wish you and your family a happy and healthy Christmas. 

Stay safe, 

Florence 

Making a donation this Christmas

When you make a donation to Action Duchenne at Christmas, your gift will give the children, young people, adults and their families living in the United Kingdom access to;

What your gift could provide

Thank you for your generosity, Happy Christmas!

The Action Duchenne Team

Share this:

Category: Florence's blogs, Hear From Our Community, Our impactTag: christmas

Previous Post: « Sound Force & The Velvet Tones: Concerts for Action Duchenne
Next Post: Innovative and sustainable FAIR solution for Duchenne Data Platform »

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