Episodes
7
Jan. 13, 2026
Why I Stopped Watching The Last of Us on Max
This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body Rebels More info about Sarcoidosis and to donate toward research: The Foundation For Sarcoidosis Research
6
Jan. 9, 2026
When Life Cancels Your Walk and Sends a Rainbow Instead.
A chef living with chronic illness discovers that sometimes life’s soggy disappointments lead to unexpected beauty—like when a canceled dog walk turns into a rainbow moment that slaps you with perspective. A story about resilience, humor, and finding color in the drizzle. This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body Rebels More info about Sarcoidosis and to donate toward research: The Foundation For Sarcoidosis Research
5
Jan. 6, 2026
Swimming with Jellyfish: A Childhood Memory of Risk, Wonder, and the Sea
As a child, I dove into a jellyfish-filled cove off the Atlantic coast, defying fear and instinct. In this personal mini memoir, I explore the unforgettable day the ocean chose not to sting me—blending themes of childhood courage, memory, and our mystical bond with nature. To Comment, please visit https://tatebasildon.com/2025/05/21/swimming-with-danger/ This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body Rebels More info about S...
4
Jan. 1, 2026
Stop Saying These “Compliments” — They’re Not Kind, They’re Just Loud
Some of the most painful moments don’t come from cruelty, but from “kindness” said out loud without a second thought. Living with sarcoidosis has taught me that certain compliments land more like paper cuts than comfort—and once you hear them, you can’t un-hear them. This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body Rebels More info about Sarcoidosis and to donate toward research: The Foundation For Sarcoidosis Research
3
Dec. 30, 2025
Learning to Sit With the Quiet: How Silence Became My Survival Skill While Living With Sarcoidosis
Living with sarcoidosis has a way of changing how you hear the world. When your body is already loud with symptoms, appointments, and internal negotiations, silence stops feeling empty and starts feeling necessary. This reflection explores how quiet moments—unexpected, unplanned, and deeply human—became one of my most reliable survival tools. This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body Rebels More info about Sarcoidosis an...
2
Dec. 26, 2025
When TikTok “Doctors” Go Rogue: Real Healing Isn’t a Trend
Herbal and homeopathic medicine can absolutely help chronic illness like sarcoidosis and heart failure—but TikTok wellness hacks and unverified “miracle cures” are another story. In a world where influencers push detoxes, conspiracies, and half-baked science, it’s time to talk about what real healing looks like—and why you should trust research, not ring lights. This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body Rebels More info ...
1
Dec. 23, 2025
Dear Prudence, Who Hurt You? When Online Advice Goes Off the Rails and Lands in a Pot of Mush
Some days, while easing into the morning and pretending the world makes sense, I stumble across online advice so astonishing it makes sarcoidosis feel like the most logical part of my life. And recently, “Dear Prudence” delivered guidance so unhinged—I had to sit there blinking like a confused owl, wondering who exactly we’ve trusted with our emotional emergencies. This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body Rebels More in...
21
Dec. 19, 2025
The “What If” Game and the Man Who Didn’t Know He Was Sick Yet
There was a version of me in 2002—forty years old, a working chef, exhausted in ways that made no logical sense, and listening to doctors insist that every alarming symptom was “stress.” Now that sarcoidosis is a familiar part of my vocabulary, looking back on that time feels like watching a movie where you want to yell at the character to turn around. Revisiting that moment made me rethink the “what if” game entirely and wonder how differently life looks when you finally know what your body was...
20
Dec. 16, 2025
The Vacation That Tried to Break Me (But I’m Still Here, Sarcoidosis and All)
Living with sarcoidosis can feel like starring in a long-running medical sitcom where the plot twists pop up at the most inconvenient times, including when you’re on vacation trying to rest. Without giving too much away, let’s just say my quiet beach getaway took an unexpected turn—and you’ll have to read the full post to see how a simple trip turned into something far stranger. This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. Contact A Body ...
19
Dec. 12, 2025
What You Don’t See: A Chef’s Reflection on Living With Sarcoidosis
Living with sarcoidosis is like starring in a medical drama no one else can see—one where you look perfectly fine on the outside while your organs do the cha-cha backstage. Back in 2011, when all of this felt new and terrifying, I kept most of it to myself. Now, looking back from 2025, I can’t help but revisit how invisible everything looked… especially to everyone who insisted I “didn’t look sick.” There’s a lot more to the story, but you’ll have to come inside for the rest. This podcast is na...