Interview with Jon Powton

April 10, 2018 by abzali123

Hear from the fantastic Jon Powton when he spoke with Peter Duffy at the #ADConf17 about his life, fostering and living with Becker muscular dystrophy.

YouTube Video https://www.youtube.com/watch?v=8qvq-UsVMRo

Reflections and Hope

As we approach the festive season and the end of 2024, I have been reflecting on a year filled with triumphs and challenges. It has been a time of uncertainty, but also one of progress, resilience, and hope for the Duchenne community. In this blog, I would like to share some key highlights from the …

Action Duchenne Selected for ‘Season of Soul’ Initiative by Jaguar Land Rover Solihull

Action Duchenne is deeply honoured to be chosen as one of the charities for JLR Solihull’s ‘Season of Soul’ initiative. Ian Taylor, a Duchenne dad and JLR employee, nominated Action Duchenne and shared with the JLR team the challenges that families living with Duchenne muscular dystrophy face, as well as the impactful work of Action …

Winter Wishes

Winter Wishes at Hyde Park On the 27th November, we were thrilled to offer complimentary tickets to 8 of our families to the Winter Wishes event at the Hyde Park Winter Wonderland. This is an accessible event, where groups that may otherwise have a difficult time attending the event can have a magical day out, …

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