95 Episodo

  1. Episode 95: A Job, Physical Challenge and Where I'm at

    Publicado: 27/11/2022
  2. Episode 94: Taking Back My Mental Power

    Publicado: 27/10/2022
  3. Episode 93: Insight into Vulnerability and Avoidance

    Publicado: 13/9/2022
  4. Episode 92: Health Challenges, Confidence and What's Important

    Publicado: 11/8/2022
  5. Episode 91: Confidence after a fall and Volunteering

    Publicado: 28/4/2022
  6. Episode 90: Happy Birthday & Toilet Fall

    Publicado: 14/4/2022
  7. Episode 89: Another Fall and Keep Going

    Publicado: 7/4/2022
  8. Episode 88: What a Day looks like with Limb Girdle Muscular Dystrophy

    Publicado: 31/3/2022
  9. Episode 87: Body Changes, Chloe Skiing and Being Alone

    Publicado: 23/3/2022
  10. Episode 86: Fatigue and My Mind

    Publicado: 17/3/2022
  11. Episode 85: Living Life or Living from Stories

    Publicado: 11/3/2022
  12. Episode 84: Tripped by My Cat

    Publicado: 2/3/2022
  13. Episode 83: Fatigue, Pushed by a 5 year old, and Chloe sees the future

    Publicado: 24/2/2022
  14. Episode 82: Button Pusher

    Publicado: 16/2/2022
  15. Episode 81: Meditation, Judgmental Johnny and Time Does Not Heal All Wounds

    Publicado: 10/2/2022
  16. Episode 80: Happiness is Healing, Chloe's 6th Birthday and Sleepy Mind with Muscular Dystrophy

    Publicado: 27/1/2022
  17. Episode 79: Changing the mentality of "How do I get rid of muscular dystrophy" to "How do I live with it"

    Publicado: 21/1/2022
  18. Episode 78: Getting Covid and having Limb Girdle Muscular Dystrophy

    Publicado: 13/1/2022
  19. Episode 77: What have I learned from myself in 2021 with Limb Girdle Muscular Dystrophy

    Publicado: 22/12/2021
  20. Episode 76: Having a Mobility Scooter Means What and A Cinderella Play

    Publicado: 15/12/2021

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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.

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