Category: Podcast

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.

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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 

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

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 

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

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 

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

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 doctor’s waiting room is usually boring. Mine briefly turned into a low-budget suspense film because my portable oxygen backpack looked like it was smoking. Living with sarcoidosis and chronic illness means getting used to equipment, routines, and symptoms that feel normal to you but deeply suspicious to everyone else. What started as an ordinary appointment became one of those strange public moments where illness stops being private and starts becoming a spectacle. It was awkward, absurd, and, honestly, a little funny. Because sometimes the only way to survive the weirdness of living inside a body that makes its own rules is to laugh before somebody calls security.

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