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, December 18, 2020

My Pelvic Floor Physical Therapy Experience...

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Many of you who follow me on Instagram have asked recently if I could share my pelvic floor physical therapy experience and what I do at my ...

Saturday, December 5, 2020

Endometriosis Gift Guide

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With the holiday season upon us, I decided to do something I've never done before and made an endometriosis gift guide! This will consi...

Friday, November 20, 2020

Update On My Bladder Problems

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If you follow my Instagram, you may know that I have been struggling with bladder pain and frequency for the last couple of months. It is n...

Saturday, November 7, 2020

Food Guilt

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Something that I have been struggling with a lot lately is food guilt. I mean this in the terms of eating things that I know will caus...

Friday, October 23, 2020

BOOK REVIEW: Vagina Problems by Lara Parker

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I just finished reading Vagina Problems: Endometriosis, Painful Sex, and Other Taboo Topics by my favorite endo blogger, Lara Parker, a...

Saturday, October 10, 2020

Going Back to College During a Pandemic

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Before going back to college this semester, I was a little nervous, but mostly excited. In the spring, I went home for spring break and nev...

Friday, October 2, 2020

Breast Cancer Awareness Month

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October is Breast Cancer Awareness Month and although this post isn't about endometriosis, the two are very much connected. People with...

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About Me

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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