Cover image of show Surviving Chronic Illness: Life in a Body That Rebels

Surviving Chronic Illness: Life in a Body That Rebels

Podcast by Tate Basildon

English

Health & personal development

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About Surviving Chronic Illness: Life in a Body That Rebels

Surviving Chronic Illness: Life in a Body That Rebels is a lived experience podcast about surviving sarcoidosis, heart failure, rare disease, and the strange daily reality of having a body that does not always cooperate.Hosted by Tate, a private chef, writer, husband, pet parent, and long-term sarcoidosis survivor, this podcast is not about miracle cures, medical lectures, or pretending that 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. Some episodes are reflective. Some are funny. Some are angry. Some are tender. All of them come from the lived experience of someone still figuring it out in real time.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 members, and friends who want to better understand what illness feels like 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 a podcast 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.

All episodes

73 episodes

episode Oxygen Therapy in Public and the Quiet Social Reality of Living with Sarcoidosis artwork

Oxygen Therapy in Public and the Quiet Social Reality of Living with Sarcoidosis

Wearing oxygen in public with sarcoidosis changes more than breathing. It changes the way people look at you, the way they try not to look at you, and the quiet assumptions they carry about what chronic illness is supposed to look like. In elevators, stores, and ordinary public spaces, those silent reactions tell their own story. This episode explores oxygen therapy, visible illness, social discomfort, and the strange gap between expectation and reality. It is about being seen, being misread, and learning that sometimes the hardest part of chronic illness is not the symptom itself, but what happens when the world suddenly notices it. Send A Text To Tate [https://www.buzzsprout.com/2548730/fan_mail/new] Support the show [https://www.buzzsprout.com/2548730/support] This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. If you’d like to share a quick thought about the episode, you can text the show using the link in the episode notes. I read every message, but I can’t reply by text because your number is blocked to protect your privacy. If you’d like a reply, or want to share more about your experience with sarcoidosis or chronic illness, please use the contact form at tatebasildon.com [https://tatebasildon.com/contact/]. I’m not able to respond to solicitations or outside project requests. To donate towards Sarcoidosis research or to learn more about the disease, please visit The Foundation For Sarcoidosis Research  [https://www.stopsarcoidosis.org/]

22 May 2026 - 10 min
episode The Waiting Room Anxiety Nobody Talks About: Chronic Illness Test Results and Relief artwork

The Waiting Room Anxiety Nobody Talks About: Chronic Illness Test Results and Relief

Waiting for medical test results with chronic illness can feel like sitting through an awards show you never agreed to attend. Every pause carries weight, every glance feels loaded, and your mind fills in the blanks before anyone speaks. Living with sarcoidosis and heart failure means learning how to exist in that space between testing and knowing. But sometimes, the outcome shifts. Sometimes your body gives something back. This is a story about that moment when fear loosens its grip, even briefly, and you’re reminded that relief, even temporary, still matters. Send A Text To Tate [https://www.buzzsprout.com/2548730/fan_mail/new] Support the show [https://www.buzzsprout.com/2548730/support] This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. If you’d like to share a quick thought about the episode, you can text the show using the link in the episode notes. I read every message, but I can’t reply by text because your number is blocked to protect your privacy. If you’d like a reply, or want to share more about your experience with sarcoidosis or chronic illness, please use the contact form at tatebasildon.com [https://tatebasildon.com/contact/]. I’m not able to respond to solicitations or outside project requests. To donate towards Sarcoidosis research or to learn more about the disease, please visit The Foundation For Sarcoidosis Research  [https://www.stopsarcoidosis.org/]

19 May 2026 - 8 min
episode The Guilt I Carried That Was Never Mine: Living with Chronic Illness and Letting Go artwork

The Guilt I Carried That Was Never Mine: Living with Chronic Illness and Letting Go

A moment from childhood can quietly shape how we carry guilt for decades. In this episode, I share the story of losing my stepfather at thirteen and the belief I carried for years that it was somehow my fault. Living with sarcoidosis and heart issues has taught me that emotional weight does not just live in the mind, it settles into the body. This is a reflection on how the stories we create in moments of trauma can linger, and how slowly, imperfectly, we begin to let them go. Send A Text To Tate [https://www.buzzsprout.com/2548730/fan_mail/new] Support the show [https://www.buzzsprout.com/2548730/support] This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. If you’d like to share a quick thought about the episode, you can text the show using the link in the episode notes. I read every message, but I can’t reply by text because your number is blocked to protect your privacy. If you’d like a reply, or want to share more about your experience with sarcoidosis or chronic illness, please use the contact form at tatebasildon.com [https://tatebasildon.com/contact/]. I’m not able to respond to solicitations or outside project requests. To donate towards Sarcoidosis research or to learn more about the disease, please visit The Foundation For Sarcoidosis Research  [https://www.stopsarcoidosis.org/]

15 May 2026 - 10 min
episode Why “You Don’t Look Sick” Doesn’t Offend Me: Chronic Illness, Friendship, and Looking Fine When You’re Not artwork

Why “You Don’t Look Sick” Doesn’t Offend Me: Chronic Illness, Friendship, and Looking Fine When You’re Not

Invisible illness can make ordinary social moments surprisingly complicated. A simple comment, a changed friendship, or a curious question can turn into an emotional negotiation when your body carries more than people can see. This episode explores chronic illness, invisible symptoms, privacy, boundaries, friendship, dignity, and the pressure to explain yourself. It’s about living in a body that doesn’t always advertise what it’s doing, while still wanting to be treated as a whole person, not a walking medical summary. Send A Text To Tate [https://www.buzzsprout.com/2548730/fan_mail/new] Support the show [https://www.buzzsprout.com/2548730/support] This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. If you’d like to share a quick thought about the episode, you can text the show using the link in the episode notes. I read every message, but I can’t reply by text because your number is blocked to protect your privacy. If you’d like a reply, or want to share more about your experience with sarcoidosis or chronic illness, please use the contact form at tatebasildon.com [https://tatebasildon.com/contact/]. I’m not able to respond to solicitations or outside project requests. To donate towards Sarcoidosis research or to learn more about the disease, please visit The Foundation For Sarcoidosis Research  [https://www.stopsarcoidosis.org/]

12 May 2026 - 16 min
episode The Strange Math of Chronic Illness: What Sarcoidosis Taught Me About Expectations artwork

The Strange Math of Chronic Illness: What Sarcoidosis Taught Me About Expectations

People sometimes ask how anyone living with sarcoidosis can stay positive day after day. The answer isn’t motivation, inspiration, or some magical personality trait. It’s something quieter… something most people miss entirely. Send A Text To Tate [https://www.buzzsprout.com/2548730/fan_mail/new] Support the show [https://www.buzzsprout.com/2548730/support] This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own. If you’d like to share a quick thought about the episode, you can text the show using the link in the episode notes. I read every message, but I can’t reply by text because your number is blocked to protect your privacy. If you’d like a reply, or want to share more about your experience with sarcoidosis or chronic illness, please use the contact form at tatebasildon.com [https://tatebasildon.com/contact/]. I’m not able to respond to solicitations or outside project requests. To donate towards Sarcoidosis research or to learn more about the disease, please visit The Foundation For Sarcoidosis Research  [https://www.stopsarcoidosis.org/]

8 May 2026 - 8 min
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