Advertise on podcast: A Body Rebels: A Chronic Illness Podcast

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★★★★★

4.9

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10 reviews

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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.

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Check latest episodes from A Body Rebels: A Chronic Illness Podcast podcast

Grief and Chronic Illness: Remembering My Dad Through His Humor

2026/10/23

My dad’s birthday is coming up, and I’m remembering the humor, presence, and ordinary pleasures of the father I lost when I was thirteen. He lived with Type 1 diabetes and heart disease, and after twenty years with sarcoidosis and my own experience of heart failure, I understand parts of his life differently. From an airport breakfast to a midnight disco, these memories bring me closer to the father I miss and the grown man I wish he’d had time to know. 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

The Hidden Cost of Chronic Illness: Insurance Denials and Medical Bills

2026/10/20

Living with chronic illness brings financial costs beyond copays and prescriptions. I spend hours untangling insurance denials, prior authorizations, confusing bills, and paperwork nobody counts as work. In this episode, I talk about the energy lost to phone calls, the anxiety of not knowing what I owe, and the frustration of having complex medical care reduced to codes on a page. I also explain why I believe specialized medical decisions deserve reviewers who understand the conditions involved. 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

When My Memory Changed After a Metoprolol Dose Increase

2026/10/16

After my metoprolol dose increased to 200 mg, my wife and I began noticing troubling short-term memory problems. I was forgetting conversations and searching for things I had placed somewhere only moments earlier. In this episode, I share what those medication side effects looked like in ordinary daily life, why they frightened me, and what happened after I called my cardiologist and changed medications. 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

Chronic Illness, Brain Fog, Fatigue, and the Things I Didn’t Finish

2026/10/13

Living with chronic illness changes what an ordinary to-do list means. My iPhone reminders might show a phone call, an errand, or a message, while leaving out the fatigue, brain fog, symptoms, recovery time, and decisions surrounding each task. In this episode, I look at chronic illness and productivity through the unfinished reminders waiting on my phone, and why a list never tells the whole story of what I did with my day. 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

Will My Doctors Stop Trying If I Refuse a Lung Transplant?

2026/10/09

I canceled my lung transplant evaluation after months of research, prayer, and conversations with my wife, but I still want active medical care. Living with sarcoidosis and heart failure has made treatment decisions deeply personal, especially when recovery would ask so much of both of us. In this episode, I share why I declined the evaluation, my fear of being misunderstood by my doctors, and the care I still want as I look toward my future. 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

Chronic Illness, Depression, and Losing Friends After Diagnosis

2026/10/06

In this episode of A Body Re-bells: A Chronic Illness Podcast, I respond to a listener living with pulmonary sarcoidosis, depression, family estrangement, and the loss of friendships after diagnosis. I talk about what friendship looks like when illness stops being temporary, why suicidal thoughts deserve immediate professional support, and what happened when one of my own friendships ended after I revealed how sick I was. I also share what twenty years with sarcoidosis taught me about accepting when some people are unable to handle serious illness. 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

Still Moving: Chronic Illness, Strength, and Staying Myself

2026/10/02

On A Body Re-bells: A Chronic Illness Podcast, I tell the story of an injured mouse and Prince, my strong old cat who refused to look old. Prince was already in his late teens when our strange nighttime rescue unfolded. He later lived to twenty-one, staying strong through his final day. His goodbye changed how I remember the mouse and how I think about my own life. After twenty years with sarcoidosis, I find myself thinking less about looking brave and more about staying myself, remaining independent, and holding on to the life I value for as long as possible. 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

When Chronic Illness Makes You Forget What You Love

2026/09/29

I’ve spent much of my life becoming good at things, from school to culinary training to massage work, yet skill never answered a harder question for me: what do I love for myself? Chronic illness filled so much of my time with appointments, symptoms, tests, refills, and research, I lost touch with parts of myself unrelated to survival. In this episode, I look back at old interests, childhood dreams, and music, then explain why learning piano now feels less like another goal and more like finding something personal again. 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

I Don’t Trust Uncertainty: Chronic Illness, Control, and an ER Visit

2026/09/25

In my one hundredth episode, I end up in the emergency room after seeing blood in my urine during Labor Day weekend. I walk through the way I handled the night, from researching possible causes to arriving with twenty years of medical history ready on my phone. Somewhere between the CT scan and my medication list, I recognize a familiar pattern. Chronic illness taught me to prepare, anticipate problems, and reduce uncertainty. Those habits serve me well in medicine. I’m starting to see what happens when I carry them everywhere else. 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

Taking a Chronic Illness Break | A Body Rebels: A Chronic Illness Podcast

2026/09/05

My health has reached a point where pushing through no longer works. In this short episode, I explain why I’m ending Season Four early and taking the rest of September away from the podcast. I need my limited energy for treatment, appointments, symptoms, and the work of getting through each day. I also need space to experience this difficult period without turning every part of it into something productive. I’ll return at the end of September to begin Season Five with more stories from life inside a rebellious body. 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

Exercising With Chronic Illness: Heart Failure, Sarcoidosis, and Recovery

2026/09/01

In this episode of A Body Rebels: A Chronic Illness Podcast, I talk about exercise while living with heart failure, sarcoidosis, and severe fatigue after movement. A walk feels good while I’m outside, then the real cost shows up at home through heavy legs, harder breathing, a shower, and the need to lie down. I still want movement in my life. I also need enough energy for my private-chef work and the rest of my day. I’m learning to treat recovery as part of movement instead of proof I failed. 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

Mourning the Person I Was: Chronic Illness and Ambiguous Loss

2026/08/28

In this episode, I’m talking about ambiguous loss and the private grief of missing the person I was before chronic illness changed my body. An old pair of shoes, a photograph, or even a heavy kitchen tool can bring that earlier life rushing back. I explore how illness has changed my independence, work, relationships, and identity, and why accepting my current body doesn’t require me to erase who I used to be, deny what I’ve lost, or pretend I’m grateful for every change. 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

What a Black Bear Taught Me About Chronic Illness

2026/08/18

I’m sharing what happened when a limping black bear crossed the road in front of me on a quiet drive through rural Connecticut. Watching that injured animal continue into the woods brought my own experience with chronic illness into sharper focus. I’ve spent years measuring strength by what I could once do, how quickly I could move, and how well I could hide the struggle. That bear gave me another way to look at determination, physical limitations, acceptance, and the careful steps required to keep living in a body that has changed. 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

Prednisone Withdrawal: When My Body Finally Said Enough

2026/08/14

I missed an episode this week, and there was a very good reason. My fifth attempt to come off prednisone after twenty years hit me harder than I ever expected. With methotrexate now being used as a steroid-sparing medication, I’ve managed to reach just 2.5 milligrams of prednisone, but the pain, nausea, edema and crushing fatigue have been brutal. I’m sharing what happened when I became so exhausted at work that even standing at the stove no longer felt safe, and why I finally chose myself first. TiTIdc9RNr4bCkFaqu7v 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

The Bad Day I Fear Won’t End: Chronic Illness and an Uncertain Tomorrow

2026/08/07

When a chronic illness flare sends me back to bed with oxygen, physical exhaustion can quickly become fear about my future. I start wondering whether I’ll recover or whether my independence is slipping away permanently. I used to hide those fears from my wife because I thought I was protecting her. Now I understand that honesty means trusting her and remaining honest with myself. In this episode, I confront uncertainty, physical decline, and the frightening question of whether one terrible day could become my new reality. 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

Podcast reviews

Read A Body Rebels: A Chronic Illness Podcast podcast reviews

4.9 out of 5

10 reviews

★★★★★

Courtney @ PodLaunch 2026/08/04

Honest and thoughtful

Tate has a way of talking about hard things without making them feel heavy. As someone living with chronic migraine and as a cancer survivor on HRT, I...

★★★★★

Change happened then what? 2026/07/27

Hope despite chronic illness!

I appreciate that Tate is honest about his own experiences with chronic illness. I appreciate the honesty about the voice he uses to create his show b...

★★★★★

Living Testimonies 2026/07/25

Informative

Informative podcast about the body.

★★★★★

loving the podcast 2026/07/25

Tate makes my own journey a little easier

As someone with an auto immune disease, I really appreciate what Tate is doing with this podcast. It’s a fun, friendly voice. I can listen to on my jo...

★★★★★

Dragonsflight 2026/07/22

Interesting

Interesting storytelling

★★★★★

esandscd 2026/07/21

Enjoyable storytelling

Easy listen with good storytelling. Keep it up!

★★★★★

maj8614 2026/07/06

Putting to words what’s so hard to talk about

This is one of the most needed shows I’ve ever heard. Finally, someone is giving language to the daily highs and lows of living with chronic illness a...

★★★★☆

TexasCraig 2026/07/02

Funny about harsh subject

Interesting discussions about a harsh subject. I appreciate the host’s focus on keeping it fun.

★★★★★

Sunshine Scribe 2026/06/19

Great Podcast

A Body Rebels is honest, funny, thoughtful, and deeply validating. Tate captures what chronic illness really feels like — not as inspiration porn, but...

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