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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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Grace and Creativity: Tayla and CMS
You, Me & Muscular Dystrophy
35 minutes 54 seconds
6 days ago
Grace and Creativity: Tayla and CMS

Creative and eloquent Tayla Richardson has Congenital Myasthenic Syndrome. A rare neuro muscular disorder that presents quite similarly to many muscular dystrophies and therefore is worth sharing on You, Me & Muscular Dystrophy.

Having hundreds of periods of paralysis from her teenage years Tayla shares her unique experiences coping with a new diagnosis, working with the waves of grief, setting boundaries and exploring and honing her creativity.

Tayla has an inspirational attitude and great advice to others who may be newly diagnosed or caring for someone in that situation.


NOTES AND RESOURCES

 MDA – Muscular Dystrophy Australia - https://www.mda.org.au

 A Slight Change Of Plans podcast.    https://www.pushkin.fm/podcasts/a-slight-change-of-plans

 I Think Therefore I slam Podcast - https://podcasts.apple.com/au/podcast/i-think-therefore-i-slam/id1747139808

 The Growing Space.  https://www.thegrowingspace.com.au/

 Rare Voices Australia   https://rarevoices.org.au

 

 MORE OF TAYLA HERE

 ‘Dandelion Bouquet’ Short film: https://www.focusonability.com.au/FOA/films/3771.html 

‘Amorphous’ Short film: https://vimeo.com/1078856803

Emerging Writer’s Festival Panel: emergingwritersfestival.org.au/event/where-do-you-get-your-ideas/

Sample of spoken word Poetry: https://www.youtube.com/shorts/XmC0YtnRb7w

Russh Magazine (poetry) as finalist for Literary Showcase: https://www.russh.com/wp-content/uploads/2024/04/The_string_that_goes_unseen__excerpt_.pdf

Article in HireUP: https://hireup.com.au/news/in-the-midst-of-a-pandemic-time-is-precious-for-those/?fbclid=PAZXh0bgNhZW0CMTEAAad6iCIP3gxeHPiEzlcZ4E8ZQtuaqReuDt6fcBZQz_5o1rGFaiRvFKM-Auj3VA_aem_i-pdThP0WQ2w7N2QmEB42g

 

As a guest on podcasts ‘ListenABLE’ with Dylan Alcott and ‘I think Therefore I Slam’. 

https://www.youtube.com/watch?v=WwnICEj1ObU&feature=youtu.be

https://podcasts.apple.com/au/podcast/patreon-preview-tayla-richardson-ambiguous-loss-unequivocal/id1747139808?i=1000716533890

 

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.