Hosted by Leannes Wheel Life · 🇺🇸 US · EN-AU · 17 episodes
Established thought leaders with verified media credentials.
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.
Leannes Wheel Life hosts You, Me & Muscular Dystrophy, a society show with 17 episodes published.
You, Me & Rare Disease ep. 2 of 2 acknowledging International Rare Disease Day 28th February On You, Me & Rare Disease episode 2 of 2 we feature insights from Carly Findlay, OAM, Clare Reilly and Leanne Watson. Their per
Welcome to You, Me & Rare Disease episode 1 of 2 – as a special breakout theme to You Me & Muscular Dystrophy to acknowledge rare diseases day 28th of February. We begin this fabulous series with with a discussion with f
Avery Roberts and Kelly Berger discuss with passion, humour and thoughtful insight about how they drive, dance and thrive through life with Congenital Muscular Dystrophy.We talk about adaptive driving, making dance histo
In this thoughtful and insightful podcast episode, we dive into the world of resilience and personal growth with the talented Chris Anselmo. Known for his articulate and vulnerable writing and public speaking on overcomi
Tugba is warm and bright person who shares how she broke out of her self-imposed bubble to live life fully and autonomously while living with congenital muscular dystrophy from birth. She is now setting and achieving man
In this conversation, Leanne Watson speaks with Joshua Ruff, a young man in charge of his life, creatively designing and showcasing his beautiful Henle Gardens while living with Duchenne muscular dystrophy . Joshua gener
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 Dy
Diagnosed at age 35 vibrant Paul Bugeja shares his personal journey with Facioscapulohumeral Muscular Dystrophy (FSHD). In this conversation with humour and enthusiasm Paul reflects on the signs of FSHD that were present
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
In this conversation, Leanne and her husband Gary Watson discuss the profound impact of Leanne's neurological muscle wasting disease (LGMD) on their marriage and lives. They explore themes of resilience, adaptation, and
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
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,
I very much enjoy Kalvin Hopper ‘s articulate and unassuming discussion of life for a sporty man in his mid 20s with facioscapulohumeral dystrophy (FSHD). He speaks candidly about acceptance, community support, and findi
In this conversation, Leanne Watson speaks with Linda Williams, a mother and primary caregiver to her son Harrison, who has Duchenne muscular dystrophy. They discuss the challenges and realities of living with DMD, inclu
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 mus
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 conn
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 dystro
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You, Me & Muscular Dystrophy is hosted by Leannes Wheel Life. The show is categorised under society (culture) and has published 17 episodes.
You, Me & Muscular Dystrophy has published 17 episodes.
You, Me & Muscular Dystrophy regularly covers society, culture, personal. It sits in the society category, with a culture focus.
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Episodes of You, Me & Muscular Dystrophy average 32 minutes. a focused format where a clear narrative arc and tight preparation matter most.
Our data rates You, Me & Muscular Dystrophy's guest bar at 80/100 (Premium tier). Established thought leaders with verified media credentials. Sign in to PitchCentric to see how your own Pod Score compares against this show.
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