You, Me & Muscular Dystrophy
Exploring muscular dystrophy one story at a time. Sharing the lives of the wonderful people that make up the muscular dystrophy community in my unique podcast series talking to people, their families and caregivers that live with the many forms of muscular dystrophy. If you or anyone you know would like to be involved in this podcast, I'd love to hear from you. My contact details will be in the notes below and I'm also on Instagram and Facebook under Leanne's Wheel Life.
Episodes
How does a music loving, car enthusiast become a published author and an active disability advocate ?
Brad Miller shares his aspirations, inspirations and wonderful advocacy work and what it means to live with Becker muscular dystrophy from a young age.
We covered many topics such as the importance of creative outlets and community, bullying, anxiety, car racing, music and much more in this 10 question chat.
I really enjoyed my tim...
In You, Me and Muscular Dystrophy I will ask the same 10 questions to various people that have some form of muscular dystrophy or are caregivers of someone with muscular dystrophy or otherwise move in the muscular dystrophy world.
Together we can provide a sense of community and support for people in all the stages of the dystrophy journey and for others to understand how they can support us. Also providing an understanding to thos...
Welcome to You, Me and Muscular Dystrophy—a series where we ask 10 questions to people impacted by the many forms of muscular dystrophy, uncovering how our diagnoses and journeys can be both different and yet deeply connected.
In this very first episode, I hand the mic to my daughter Amy, who turns the tables and interviews me. She kicks things off by asking: “Who are you, and what’s your connection to muscular dystrophy?”
I share my...
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