In this powerful follow-up to last week’s conversation on advocacy, Mikey takes a deeper dive into one of the hardest — and most important — parts of navigating chronic illness and rare disease: learning how to advocate for yourself. Whether you’ve been dismissed by a doctor, questioned by strangers online, or left second-guessing your own symptoms, this episode is for you. Mikey shares raw, personal experiences of being gaslit by medical professionals, invalidated online, and underestimated ...
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In this powerful follow-up to last week’s conversation on advocacy, Mikey takes a deeper dive into one of the hardest — and most important — parts of navigating chronic illness and rare disease: learning how to advocate for yourself. Whether you’ve been dismissed by a doctor, questioned by strangers online, or left second-guessing your own symptoms, this episode is for you. Mikey shares raw, personal experiences of being gaslit by medical professionals, invalidated online, and underestimated ...
Hey besties! This is the very first episode of Mikey’s House, and I’m so glad you’re here. In today’s episode, we’re starting things off strong with an honest, cozy introduction. I’ll be sharing who I am, why I started this podcast, and what you can expect from this space moving forward. After documenting my life with a neurodegenerative disease online for the past few years, I wanted to create a safe, unfiltered, and welcoming place where we can talk about everything. No censors. No pressure...
Mikey's House
In this powerful follow-up to last week’s conversation on advocacy, Mikey takes a deeper dive into one of the hardest — and most important — parts of navigating chronic illness and rare disease: learning how to advocate for yourself. Whether you’ve been dismissed by a doctor, questioned by strangers online, or left second-guessing your own symptoms, this episode is for you. Mikey shares raw, personal experiences of being gaslit by medical professionals, invalidated online, and underestimated ...
