ABOUT THIS 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.
Update frequency:
weekly
Average audio length:
53 minutes
Guest interviews
English
United States
132 episodes
since March 2, 2023
episodic
LATEST EPISODE 🔗
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. …
SEARCH PAST EPISODES
Search past episodes of 4t Below Zero: Multiple Sclerosis Podcast.
PREVIOUS EPISODES 🔗
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…
How a Small Community and Podcast Became My Healing Sanctuary
Join us as we dive into Jenny's inspiring journey living with multiple sclerosis, from her initial diagnosis after electrocution to her current advocacy and podcasting efforts. We explore the importance of acceptance, supportive healthc…
Most parents hope their kid’s biggest worry is missing dessert or losing at hide and seek. But for Erica, the fears started way earlier—like when her nine-year-old was diagnosed with pediatric MS before she even knew what it was. This isn’t your typical story; it’s a rollercoaster through shocking …
Disclaimer: The podcast and artwork embedded on this page are from 2 Guys with MS not MS'ing around, which is the property of its owner and not affiliated with or endorsed by Listen Notes, Inc.
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