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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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Embracing life: Shae Mankey and FSHD
You, Me & Muscular Dystrophy
25 minutes 55 seconds
2 weeks ago
Embracing life: Shae Mankey and FSHD

In this conversation, Leanne speaks with the delightful Shae Mankey about her experiences living with Facioscapulohumeral Muscular Dystrophy (FSHD). They discuss Shae’s career transition to Accessible Accommodation, the impact of childhood disability on her dreams and future aspirations. Shae speaks about the decision not to have children and her love for her husband, family and dog, ending with great advice for those newly diagnosed with muscular dystrophy.

 

SHOW NOTES

Accessible Accommodation

https://www.accessibleaccommodation.com/

 

The Accessible Group – Facebook 

https://www.facebook.com/groups/accessiblegroup

 

 

 

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.