SOBRE ESTE PODCAST 🔗
An international podcast about living with Multiple Sclerosis.
2 Guys with MS not MS'ing around. Hosted by Nick and Terry, discussing and attempting to normalize the conversation around life with a chronic and invisible illness.
2 Guys with MS not MS'ing around. Hosted by Nick and Terry, discussing and attempting to normalize the conversation around life with a chronic and invisible illness.
Frequência de atualização:
weekly
Duração média do áudio:
53 minutes
Entrevistas com convidados
Inglês
Estados Unidos da América
134 episódios
desde 2 de Março de 2023
episodic
ÚLTIMO EPISÓDIO 🔗
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…
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EPISÓDIOS ANTERIORES 🔗
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…
Finding Strength and Hope with Montel Williams: A Conversation on MS, Mental Health, and Resilience
In this episode, we have an inspiring conversation with Montel Williams, a daytime Emmy-winning television host, decorated military veteran, and groundbreaking advocate for MS awareness and mental he…
Aviso: O podcast e a arte incorporada nesta página são de 2 Guys with MS not MS'ing around, que é propriedade de seu proprietário e não é afiliado ou endossado por Listen Notes, Inc.
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