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You, Me & Muscular Dystrophy
Leannes Wheel Life
11 episodes
6 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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All content for You, Me & Muscular Dystrophy is the property of Leannes Wheel Life and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
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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Raising Resilience: Kate & LGMD
You, Me & Muscular Dystrophy
38 minutes 10 seconds
1 month ago
Raising Resilience: Kate & LGMD

In this episode of 'You, Me and Muscular Dystrophy', host Leanne Watson speaks with Kate Johnson, a mother navigating the challenges of raising a child with Limb Girdle Muscular Dystrophy (LGMD). They discuss the journey of diagnosis, the emotional and practical challenges of parenting a child with a degenerative condition, and the importance of community support. Kate shares insights on family dynamics, sibling relationships, and the need for self-care as a caregiver. The conversation highlights the resilience of children and the hope that can be found in seeing your child happily surrounded by inclusive peers, as well as the importance of advocacy in navigating the healthcare system.

 

 

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.