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Action Duchenne

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  • Donate
  • About Us
    • Our Purpose
    • What We Do
    • Our Impact
    • Our Team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • Get Support
    • Register for Support
      • Time Out – A Space for Mums
      • Dads Against Duchenne
      • Grandparents Together
      • Online Group Counselling Programme
    • Recently diagnosed
    • Children and Young People
    • Summer 2026 In-Person Family Days
    • 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

Join Action Duchenne for Rare Disease Day 2026

You are here: Home / Join Action Duchenne for Rare Disease Day 2026

Join Action Duchenne for Rare Disease Day 2026

Rare Disease Day Banner

Rare Disease Day is held every year on the last day in February (every 4 years it’s held on 29th February, the rarest day in the calendar). Rare Disease Day is a global movement which aims to raise awareness for the 300 million people worldwide who live with a rare disease, along with their families and carers. The long term goal is to ensure equitable access to diagnosis, treatment, healthcare, social support and opportunities for everyone affected by a rare disease. 

We want to take this opportunity to join with the international rare disease community to raise awareness, increase understanding and enhance support for the children, young people and families living with Duchenne.   

How Can You Get Involved?

There are lots of ways for you to get involved with Rare Disease Day 2026!

1. Share our posts on social media: we will be sharing lots of information leading up to 28th of February. Help us raise awareness by sharing our posts with your network. 
2. Share your colours: we are asking schools to get involved with our awareness and fundraising efforts using a Rare Disease Day slogan: “Share Your Colours”. We’ve love you to take part by holding a non-uniform day in your school or workplace during the week before Rare Disease Day, asking pupils and staff to wear their brightest colours to show their support. Get in touch with us to sign up or to find out more!
3. Share your story: stories from our community are one of the most powerful ways to raise awareness. If you’d like to tell people what it’s REALLY like to live with a rare condition, get in touch with our Communications Officer.

Become a Friend of Action Duchenne today to make sure that we can be there for EVERY family EVERY time.

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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 …

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