My Lyme Story Part 2

from Vertigo · host Vertigo

This is the story of how I was diagnosed with Lyme disease, and what I learned along the way about the inaccuracy of ELISA and Western blot Lyme blood tests, oppression of Lyme-literate medical doctors (LLMDs), how and why the CDC and infectious disease society of America (IDSA) restrict doctors from treating Lyme, and more. This narrative is based on my experiences and only represents the situations of my life and the opinions I have formed because of those experiences. It is not intended to serve as medical advice.

Episode metadata supplied by the publisher feed · Published May 16, 2015

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My Lyme Story Part 2

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