Lessons From a Wonderfully Rare Community, and a Farewell

Lessons From a Wonderfully Rare Community, and a Farewell

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Lessons From a Wonderfully Rare Community, and a Farewell

Almost four years ago, my life changed. After a decade of invasive tests, hospital visits, and limited answers, I was diagnosed with endometriosis. As I navigated the medical system here in the U.K., I soon became frustrated at the multiple administrative hurdles and shockingly unsupportive doctors. After I vented my woes on my personal blog, a talented writer, also afflicted with endometriosis, contacted me. She told me she liked my writing. Her name was Serena…

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