Beyond Labels and Limitations
Ein Podcast von John Graybill
Kategorien:
95 Folgen
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Episode 55: What I have learned from having Limb Girdle Muscular Dystrophy
Vom: 21.7.2021 -
Episode 54: Finding beauty in Limb Girdle Muscular Dystrophy is a choice
Vom: 14.7.2021 -
Episode 53: Digestive Issues and Limb Girdle Muscular Dystrophy
Vom: 7.7.2021 -
Episode 52: Keeping the mindset of "I'm going to beat Limb Girdle Muscular Dystrophy" alive
Vom: 30.6.2021 -
Episode 51: What do you do for a living when you have Limb Girdle Muscular Dystrophy
Vom: 23.6.2021 -
Episode 50: How Can I be Grateful when I have Limb Girdle Muscular Dystrophy
Vom: 16.6.2021 -
Episode 49: Donavon Decker, LGMD2D, and his participation in Gene Therapies
Vom: 9.6.2021 -
Episode 48: What I Learned from My Cat
Vom: 2.6.2021 -
Episode 47: Meet Brad Williams, Ph.D, who also has Limb Girdle Muscular Dystrophy 2B/R2
Vom: 26.5.2021 -
Episode 46: Healing in Brazil at the Casa De Dom Inacio
Vom: 19.5.2021 -
Episode 45: Robert Schwartz, "Your Souls Plan", Discovering the Real Meaning of the Life You Planned Before You Were Born
Vom: 12.5.2021 -
Episode 44: Using Limb Girdle Muscular Dystrophy to find Me
Vom: 5.5.2021 -
Episode 43: Meet Amanda, who was misdiagnosed with Limb Girdle Muscular Dystrophy
Vom: 28.4.2021 -
Episode 42: How suffering shows up in parenting for me
Vom: 21.4.2021 -
Episode 41: Meet Dr. Vovanti Jones, who has Limb Girdle Muscular Dystrophy
Vom: 14.4.2021 -
Episode 40: Rollin with Henry Eichner
Vom: 7.4.2021 -
Episode 39: When is it time to stop working when you have limb girdle muscular dystrophy
Vom: 31.3.2021 -
Episode 38: Tips & Tricks with Limb Girdle Muscular Dystrophy
Vom: 24.3.2021 -
Episode 37: One year follow up and what's troubling now
Vom: 17.3.2021 -
Episode 36: Shopping for Clothes and Shoes
Vom: 10.3.2021
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.