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.

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...
Thursday, February 24, 2022

MY SIX YEAR ENDOVERSARY

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 I say this every year, but I can't believe today marks six years since I was diagnosed with endometriosis! It feels like yesterday, but...
Saturday, February 12, 2022

Prioritizing Friends in College (while having a chronic illness)

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 I'm happy to report to you that since the last time we spoke, I am doing much better! I have been back on the daily grind of doing my i...
Saturday, January 29, 2022

I'M IMMUNOCOMPROMISED AND GOT COVID

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    After only one week back at college for the spring semester, I tested positive for covid after dodging it for almost two years. This tim...
Saturday, December 18, 2021

End of Semester Update!

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 I'm back everyone and I apologize for my absence this past semester! I think it has been a crazy time for most people, especially those...
Sunday, October 24, 2021

ORGANIZATIONAL TIPS!

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 This doesn't have much to do with chronic illness, but I want to share my organizational tips with you today. However, these methods he...
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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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