SELLEST PODCASTIST 🔗

Saatejuhid:
Värskendamise sagedus:
weekly
Keskmine heli pikkus:
53 minutes
Külalisintervjuud
Inglise
Ameerika Ühendriigid
135 jagu
alates 2. märts 2023
episodic

VIIMANE OSA 🔗

A listener’s story becomes a conversation about autonomy, dignity, and what it means to choose your own ending. If you or someone you love is living with MS, facing relentless decline, or trying to understand Canada’s MAiD program, this episode is one you need to hear. Nix and Terry open the door…

OTSI VARASEMAID OSASID

Otsi kanali 4t Below Zero: Multiple Sclerosis Podcast viimaseid osasid.

EELMISED OSAD

MS is changing fast, and this conversation puts that progress—and the realities of living with the disease—into sharp focus. From a major campaign to accelerate MS research to the everyday challenges of stuttering, fatigue, and balance issues, this episode explores what the fight against multiple s…
Some people get one diagnosis. Amanda has survived cancer, transverse myelitis, MS, NMO, POTS, liver disease, and a life that has kept demanding more—and she’s still here, still laughing, and still building a way to help others do the same. Her story is the kind that stops a room. After a rare pan…
Ricky is a nurse, father of three, and MS advocate in southern Germany. In this conversation, he shares how a blurry eye exam led to a same-day MRI—and a life-changing diagnosis. After his 2012 diagnosis, Ricky adapted to changes in mobility while continuing to show up for his family and patients. …
Terry and Nick sit down with Thrax, also known as Tariq, for a raw conversation about living with multiple sclerosis, the frustration of being judged when you don’t “look sick,” and the mental weight of trying to keep going. Thrax shares how MS changed his work, mobility, relationships, and confide…
Black men with MS are building their own support system, and Quanta Dunn is leading the charge. His story starts with a sudden blackout in the sunlight, a life-changing diagnosis in 2014, and years of pushing through pain, fatigue, and invisible symptoms before the disease finally forced everything…
The hidden cost of emergency care is getting pushed onto residents, and it is changing how whole towns pay for ambulances. Nix and Terry break down the new local authority model, why $85 to $95 a year is only the beginning, and what happens when hospital systems disappear from the equation. They al…
The Brutal Reality of Living With MOGAD, Disability, and Hope Larry’s MOGAD story, MS overlap, and life after major medical setbacks Terry and Nix open with a candid reflection on how closely MOGAD can resemble MS, then bring on Larry to explain his diagnosis, treatment, and daily reality. This c…
Adam Powell on rebuilding life after a fast, aggressive MS diagnosis This episode features Terry, NIX, and guest Adam Powell, who shares how a devastating primary progressive MS diagnosis reshaped his life in months, not years. Adam explains how he went from a strong, independent UPS supervisor to …
Imagine living with voices in your head that everyone thinks are just signs of violence or unpredictability—yet you're an artist, advocate, and everyday person fighting to redefine what's possible. Michelle Hammer, a mental health advocate and founder of Schizophrenic NYC, shares her personal story…
Vastutamatussäte: Sellele lehele manustatud taskuhäälingusaade ja kunstiteosed pärinevad 2 Guys with MS not MS'ing around-lt, mis on selle omaniku omand ja ei ole seotud ettevõttega Listen Notes, Inc.