Endo Is Not The End

Taylor is a 24-year-old young professional living with endometriosis, heart arrhythmias, pelvic floor dysfunction, sleep apnea, and severe allergies. Working in politics and government, she uses her lived experience to connect with others and advocate for healthcare policy and women’s rights.

Friday, January 23, 2026

Grad School & Chronic Illness/Pain

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As I enter the final days before starting my last semester of graduate school, I can’t help but reflect on all the obstacles I’ve faced over...
Tuesday, January 20, 2026

Fear & The Psychological Symptoms Surrounding Chronic Illness

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Have you ever gone to bed not knowing if you’d wake up in the morning? I have. Many times. That’s the reality of living with heart problems....
Friday, January 16, 2026

Feeling Invisible

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Having an invisible illness, or multiple in my case, is a uniquely lonely experience. No matter how hard others try to understand, no matter...
Friday, January 9, 2026

I’m Excited for Heart Surgery (Here’s Why)

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My biggest goal going into 2026 is to have my third heart surgery for my arrhythmias, this time for atrial fibrillation, and finally say goo...
Friday, January 2, 2026

Journaling & 2026 Health Goals

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Journaling used to scare me. I never wanted to be left alone with my thoughts, because that’s when the pain would creep in and take over. I ...
Tuesday, December 23, 2025

How to Support a Loved One with Chronic Illness

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The holidays are supposed to be a joyful time of coming together and spending time with loved ones. But for people with chronic illness, the...
Friday, March 25, 2022

It's Been a Hard Month...

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Well, Endometriosis Awareness Month hasn't been treating me very kindly. I feel like whenever I start to get better, something else happ...
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About Me

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Taylor Sprague
Taylor is a 24-year-old young professional navigating life with multiple chronic health conditions, including endometriosis, heart arrhythmias, pelvic floor dysfunction, sleep apnea, and severe allergies. Through her lived experience, she uses this space to connect with others facing similar challenges and to educate readers about chronic illness, self-advocacy, and the realities of living in a body that doesn’t always cooperate. Professionally, Taylor works in politics and government, where she is a strong advocate for accessible, equitable healthcare policy and women’s rights. This blog sits at the intersection of personal storytelling and public policy, blending vulnerability with advocacy in the hope that no one feels alone in their diagnosis, and that lived experiences help drive meaningful change.
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