Why I Walked Away From Support Groups (And Found My Voice Instead)

Living with sarcoidosis is already its own exhausting full-time job, so the idea of a support group sounded…promising. Or at least not disastrous. But back in the early 2010s, when my lungs and heart were misbehaving like rebellious teenagers, the search for “people like me” turned into something far stranger than comforting. I won’t spoil the whole story here, but let’s just say it involved Christmas ornaments, long train rides, and me realizing the person I actually needed to find was somewhere else entirely. Maybe someone like you.

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This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

When Hospital Check-In Feels Like an Interrogation: A Chef, an MRI, and Too Many Personal Questions

Before my MRI next week, a simple online check-in turned into a bizarre quiz about my private life, sprinkled with the usual sarcoidosis-related precautions—but what came next left me blinking at the screen and wondering who exactly was getting scanned here. Let’s just say the questions took a turn I did not see coming.


Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

Losing My Voice but Not My Humor: Living With Sarcoidosis, Symbicort, and a Stubborn Set of Lungs

Sarcoidosis may steal your breath, your energy, and—if you’re lucky—your voice, but it can’t take your sense of humor. As a chef living with chronic illness and heart failure, I’ve learned to navigate breathing tests, inhalers, and vocal cord drama with sarcasm, garlic, and a pinch of grit. Here’s what happens when Symbicort and I go another round in the fight for air—and why I still keep cooking, writing, and laughing through it all.

Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

Losing My Voice but Not My Humor: Living With Sarcoidosis, Symbicort, and a Stubborn Set of Lungs

Sarcoidosis may steal your breath, your energy, and—if you’re lucky—your voice, but it can’t take your sense of humor. As a chef living with chronic illness and heart failure, I’ve learned to navigate breathing tests, inhalers, and vocal cord drama with sarcasm, garlic, and a pinch of grit. Here’s what happens when Symbicort and I go another round in the fight for air—and why I still keep cooking, writing, and laughing through it all.

Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

The New Trend in Unhygienic: 72-Hour Deodorant and the Death of Daily Showers

Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research