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  • Challenge 79 for World Duchenne Awareness Day
  • About Us
    • Our vision
    • Our Strategy
    • What we do
    • Our Impact
    • Our team
    • Work For Us
    • Volunteer
    • The DMD Registry
    • Action Duchenne Policies
  • 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?
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  • Support Us
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You are here: Home / Uncategorized / The Abilities in Me: Duchenne muscular dystrophy by Gemma Keir
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The Abilities in Me: Duchenne muscular dystrophy by Gemma Keir
The Abilities in Me: Duchenne muscular dystrophy by Gemma Keir - Image 2
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The Abilities in Me: Duchenne muscular dystrophy by Gemma Keir

£8.99 Original price was: £8.99.FreeCurrent price is: Free.

“We are all in love with the book, I shed a tear as I read as it is so simplistic yet so cleverly and accurately written and in such a fantastic way for small children to relate to their illness, it’s beautiful.” Duchenne Mum.

This picture book is dedicated to children diagnosed with Duchenne muscular dystrophy, also known as DMD. Explore the day in the life of a young boy with Duchenne through bright, colourful illustrations and text. Perfect for teachers, parents and children alike, this book will bring awareness of the condition and teach children how to be supportive and be kind. This picture book is aimed for children aged 3 to 8 years old. This book is inspired by Ethan Sharma, age 9 with Duchenne muscular dystrophy.

We are delighted to be able to offer one book for free to families or professionals, there is a small charge for postage. If you would like to order more than one book please email dawn@actionduchenne.org 

21 in stock

SKU: 10353 Categories: Uncategorized, Education, Support
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“I thought this book was really lovely. The pictures were colourful and creative.” – Dougie Young, age 8, living with Duchenne.

“I love it, a book that helps me understand my little brother. The pictures look just like him” – Reuben, age 6.

“An amazing book that helps create awareness to DMD, and to help understand the emotional struggles our son goes through on a daily basis. Beautifully written with well designed illustrations.” – Harriet and Mark.

“This is SO COOL” – Now we have a story, about boys just like me. That’s just, amazing! I can’t wait to show all my friends at school. I LOVE it!” – Freddie, age 9, living with Duchenne.

“Being part of the rare disease community can make you feel so isolated, and with a condition such as DMD there is nothing positive out there in terms of children’s literature, until now! It has blown me away, and seeing the joy in my son’s face as he read about another boy the same as him, in an actual story, is something I will never forget. Thank you team!” – Parents of Freddie.

“What a nice book , that’s good mum!” Harrison, age 13.

“It made harrison smile to see the illustrations of others in wheelchairs. We as a family think its fabulous to have something like this for others to read.” – Mother to Harrison

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