Category: Podcast

Spring has a way of looking hopeful while also trying to crawl directly into your sinuses. In this episode, I talk about what it means to live with sarcoidosis, heart issues, and the shifting realities of chronic illness through the seasons. This is about pollen, fatigue, beauty, grief, adaptation, and those quiet moments that still manage to feel like life. If you live with sarcoidosis, chronic illness, or love someone who does, this episode is a grounded look at how the body negotiates change while the world keeps blooming anyway.

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This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

After a week of rain and gray skies, I stepped outside and found myself face-to-face with a monarch butterfly—a rare, breathtaking sight that reminded me why we let dandelions grow and bees buzz in our yard. Here's why moments like these mean everything when you're living with chronic illness and still trying to find joy in the little things.

Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

A treatment built for cancer is now doing something that sounds almost unreal in autoimmune disease. In this episode, I talk through a story about CAR-T cell therapy, a woman whose body had been attacking her from multiple directions, and the uneasy hope that comes with hearing the words remission, reset, and maybe even recovery. This isn’t a miracle story, because real bodies are messier than that. But it is a story about what it means when medicine stops just managing suffering and starts asking whether the whole system can be rebooted. And for people who live inside unpredictable bodies, that question hits home.

Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

What happens when chronic illness shows up and your first instinct is to blame yourself? In this episode of Thoughts While Surviving Chronic Illness, Tate reflects on growing up with guilt, being taught to question himself, and how that old wiring followed him into life with sarcoidosis. This is a quiet, honest conversation about shame, fear, faith, and the heavy stories we attach to illness. If you have ever wondered whether you caused your condition, deserved your suffering, or somehow failed your own body, this episode is a reminder that illness is not punishment, and guilt is not something you have to carry forever.

Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research 

Chronic illness teaches you that control is often an illusion. Tests, insurance approvals, medications, and diagnoses can feel like they belong to systems far bigger than the person living inside the body.

For someone living with sarcoidosis and heart complications, routine medical tests are never really routine. They can determine whether the disease is quiet… or quietly returning.

But every once in a while something unexpected happens.

A phone call.

A decision made by someone behind the scenes.

A moment where the system that usually feels rigid suddenly bends in a human direction.

And sometimes those small moments remind you that living with chronic illness isn’t only about what the body loses… it’s also about what life quietly gives back.

Send A Text To Tate

Support the show

This podcast is narrated using an AI voice. The words, reflections, and lived experience are my own.

To respond to this episode, use the text link in the episode notes, or send longer messages through the contact form at tatebasildon.com. I’m not able to respond to solicitations, outside projects, or interview requests.

To support sarcoidosis research or learn more, please visit The Foundation For Sarcoidosis Research