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.

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More info about Sarcoidosis and to donate toward research: The Foundation For Sarcoidosis Research 

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