A Body Rebels: A Chronic Illness Podcast
A Body Rebels is a lived-experience podcast about sarcoidosis, heart failure, rare disease, chronic illness, and the strange daily reality of living in a body that does not always cooperate.
I’m Tate — a private chef, writer, husband, pet parent, and long-term sarcoidosis survivor. This podcast is not about miracle cures, medical lectures, or pretending a positive attitude fixes everything. It is about the honest middle of chronic illness: the fatigue, fear, grief, humor, stubbornness, absurdity, and small victories that come with surviving day after day.
These are first-person stories about illness, identity, marriage, work, memory, resilience, and learning how to live inside a life that changed without asking permission.
This podcast is for people living with chronic illness, sarcoidosis, rare disease, heart failure, autoimmune conditions, invisible illness, or any body that feels like it has gone off-script. It is also for caregivers, spouses, family, and friends who want to understand illness from the inside.
If you are tired of toxic positivity, pity, miracle-cure noise, and being told to “just stay strong,” you are in the right place.
This is for the sick, the tired, the stubborn, the scared, the sarcastic, the hopeful, and everyone trying to build a life in a body that rebels.
A Body Rebels: A Chronic Illness Podcast
The High Price of Staying Alive: Sarcoidosis, Chronic Illness, Insurance, and America’s Health Care Circus.
Use Left/Right to seek, Home/End to jump to start or end. Hold shift to jump forward or backward.
Ever notice how sarcoidosis doesn’t just come for your lungs (or your heart, if it’s feeling ambitious)—it comes for your calendar, your energy, and your bank account too? This is the story of what “good insurance” looks like when the bills have six digits, the premiums creep up like a horror-movie soundtrack, and you realize staying alive in America is a subscription plan you never asked for… but can’t cancel.
This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.
More info about Sarcoidosis and to donate toward research: The Foundation For Sarcoidosis Research
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