Beyond Labels and Limitations
En podcast af John Graybill
![](https://is1-ssl.mzstatic.com/image/thumb/Podcasts115/v4/4c/b1/76/4cb17636-16e5-26c7-699f-5e1fccf1d4ac/mza_8718642472020513424.png/300x300bb-75.jpg)
Kategorier:
95 Episoder
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Episode 95: A Job, Physical Challenge and Where I'm at
Udgivet: 27.11.2022 -
Episode 94: Taking Back My Mental Power
Udgivet: 27.10.2022 -
Episode 93: Insight into Vulnerability and Avoidance
Udgivet: 13.9.2022 -
Episode 92: Health Challenges, Confidence and What's Important
Udgivet: 11.8.2022 -
Episode 91: Confidence after a fall and Volunteering
Udgivet: 28.4.2022 -
Episode 90: Happy Birthday & Toilet Fall
Udgivet: 14.4.2022 -
Episode 89: Another Fall and Keep Going
Udgivet: 7.4.2022 -
Episode 88: What a Day looks like with Limb Girdle Muscular Dystrophy
Udgivet: 31.3.2022 -
Episode 87: Body Changes, Chloe Skiing and Being Alone
Udgivet: 23.3.2022 -
Episode 86: Fatigue and My Mind
Udgivet: 17.3.2022 -
Episode 85: Living Life or Living from Stories
Udgivet: 11.3.2022 -
Episode 84: Tripped by My Cat
Udgivet: 2.3.2022 -
Episode 83: Fatigue, Pushed by a 5 year old, and Chloe sees the future
Udgivet: 24.2.2022 -
Episode 82: Button Pusher
Udgivet: 16.2.2022 -
Episode 81: Meditation, Judgmental Johnny and Time Does Not Heal All Wounds
Udgivet: 10.2.2022 -
Episode 80: Happiness is Healing, Chloe's 6th Birthday and Sleepy Mind with Muscular Dystrophy
Udgivet: 27.1.2022 -
Episode 79: Changing the mentality of "How do I get rid of muscular dystrophy" to "How do I live with it"
Udgivet: 21.1.2022 -
Episode 78: Getting Covid and having Limb Girdle Muscular Dystrophy
Udgivet: 13.1.2022 -
Episode 77: What have I learned from myself in 2021 with Limb Girdle Muscular Dystrophy
Udgivet: 22.12.2021 -
Episode 76: Having a Mobility Scooter Means What and A Cinderella Play
Udgivet: 15.12.2021
Welcome to the podcast for Beyond Labels & Limitations. John talks about living a life with Muscular Dystrophy BL&L, started as an organization to raise money dedicated exclusively to Limb-Girdle Muscular Dystrophy 2A (LGMD2A) and to educate on the disease course and associated struggles of LGMD2A, as recounted through my personal experiences.