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You, Me & Muscular Dystrophy
Leannes Wheel Life
10 episodes
5 days ago
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.
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Personal Journals
Society & Culture
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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.
Show more...
Personal Journals
Society & Culture
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The Power of Community: Cerys Davage & LGMD
You, Me & Muscular Dystrophy
27 minutes 44 seconds
1 month ago
The Power of Community: Cerys Davage & LGMD

In this conversation, Cerys Davage ( YouTube@unbalanced with Cerys Davage) shares her personal journey with Limb Girdle Muscular Dystrophy (LGMD), and what LGMD means to her beyond the physical. How her love of teaching, music and performance has shaped and enhanced the community and supports she has around her. Cerys exudes warmth, humility and wisdom in this enlightening chat with Leanne.Show Notes & LinksUnbalanced Podcast Instagram. https://www.instagram.com/unbalancedpodcast/Daniel Ferguson LGMD foundation. https://dffoundation.com.au/LGMD awareness foundation. https://www.lgmd-info.orgCure lgmd2I Foundation. https://curelgmd2i.com

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.