Last month, my primary care physician (PCP) referred me to a cardiologist for suspected postural orthostatic tachycardia syndrome (POTS)…
Claire Richmond
Claire Richmond was diagnosed with acute intermittent porphyria in 2017 after living with unexplained pain for 19 years. She was 32 years old and quickly learned there’s no guidebook for incorporating a strange rare disease into her life. When she could no longer work full time, she struggled to find her purpose. That’s when she began to write. Claire hopes speaking her truth will build connections and generate hope. She lives in Des Moines, Iowa, with her family and rescue poodle.
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Articles by Claire Richmond
It’s that time of year again, when many of my friends and those on social media are making vision boards…
Like others, I’m guilty of hating on 2020. In relation to in-person gatherings, I’ll be the first to admit I’ve…
Last week, we decorated for the holidays. Mugs of cocoa steamed on the dining room table, and jolly holiday tunes…
As a person with an invisible illness living in an ableist society, my chronic pain and its effects on…
My upcoming holidays are going virtual. Right now, families like mine across the world are making hard calls about how…
The COVID-19 pandemic canceled a wedding we had scheduled for last June. When my fiancé, Michael, and I told friends…
It was love at first sight when I met my standard poodle, Lenny Bruce, but what I never imagined is…
My fiancé, Michael, is my caregiver. He tends to my needs during acute hepatic porphyria attacks, provides emotional support,…
I recently found myself (masked up) at Walmart in a tiny Iowa town. These days, I don’t frequent big-box stores,…