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
Why I Walked Away From Support Groups (And Found My Voice Instead)
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Welcome to A Body Rebels, formerly Surviving Chronic Illness.
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.
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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