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  • 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
    • In-Person Support Events
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Schools
    • Siblings
    • End of Life and Bereavement
  • Annual Conference
    • Highlights from the Action Duchenne Conference 2025
    • Action Duchenne Annual International 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

Support Calendar – What’s On

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Events in May 2026

MonMonday TueTuesday WedWednesday ThuThursday FriFriday SatSaturday SunSunday
27April 27, 2026
28April 28, 2026●(1 event)

10:30 am: Parent/Carers In-Person Meet-Up: London

10:30 am – 2:00 pm
April 28, 2026

Parent/Carers In-Person Meet-Up: London
Serpentine Bar and Kitchen
Hyde Park
Serpentine Rd,
London, W2 2UH
View Location
Map Serpentine Bar and Kitchen
Register

Find out more

29April 29, 2026
30April 30, 2026
1May 1, 2026●(1 event)

10:00 am: Grandparents Together

10:00 am – 11:00 am
May 1, 2026

Grandparents Together
Register

Find out more

2May 2, 2026
3May 3, 2026
4May 4, 2026
5May 5, 2026
6May 6, 2026●(1 event)

8:00 pm: Dads Against Duchenne

8:00 pm – 9:00 pm
May 6, 2026

Dads Against Duchenne
Register

Find out more

7May 7, 2026●(1 event)

8:00 pm: Time Out - for Mums

8:00 pm – 9:00 pm
May 7, 2026

Time Out - for Mums
Register

Find out more

8May 8, 2026
9May 9, 2026
10May 10, 2026
11May 11, 2026
12May 12, 2026
13May 13, 2026●(1 event)

6:00 pm: Webinar Series 2026: Duchenne and the Brain

6:00 pm – 7:00 pm
May 13, 2026

Webinar Series 2026: Duchenne and the Brain
Register

Find out more

14May 14, 2026
15May 15, 2026●(1 event)

10:30 am: Parent/Carers In-Person Meet-Up: Leeds

10:30 am – 2:00 pm
May 15, 2026

Parent/Carers In-Person Meet-Up: Leeds
Holiday Inn Express
Kirkstall Road
Leeds, LS3 1LY
View Location
Map Holiday Inn Express
Register

Find out more

16May 16, 2026
17May 17, 2026
18May 18, 2026
19May 19, 2026
20May 20, 2026
21May 21, 2026
22May 22, 2026●(1 event)

Residential Weekend for Young People Living with Duchenne

May 22, 2026 – May 25, 2026

Register

Find out more

23May 23, 2026●(1 event)

Residential Weekend for Young People Living with Duchenne

May 22, 2026 – May 25, 2026

Register

Find out more

24May 24, 2026●(1 event)

Residential Weekend for Young People Living with Duchenne

May 22, 2026 – May 25, 2026

Register

Find out more

25May 25, 2026●(1 event)

Residential Weekend for Young People Living with Duchenne

May 22, 2026 – May 25, 2026

Register

Find out more

26May 26, 2026
27May 27, 2026
28May 28, 2026
29May 29, 2026
30May 30, 2026
31May 31, 2026

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From our community

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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 …

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 …

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