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.

Saturday, April 25, 2020

My Favorite Endometriosis Bloggers

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Today I wanted to share my favorite Endometriosis bloggers with you so you all can see the women I look up to in this crazy world of Endomet...

Saturday, April 11, 2020

Immunocompromised During COVID-19

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This pandemic is a scary time in the world for everyone, but please take a second to think about those who are immunocompromised, like peopl...

Saturday, March 28, 2020

Day in My Life

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Today I wanted to share a day in my life. I think a lot of people wonder what life is like living with a chronic illness. Well, my life is p...

Saturday, March 14, 2020

Easy Exercise Routine for Chronic Pain

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Exercising is always something I have struggled with. I always get in a good routine, then have a flare-up and stop going to the gym. Recent...

Saturday, March 7, 2020

Myths and Misconceptions

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Myth: Endometriosis is just a really heavy period. Women with Endo may experience a really heavy period, but that is just one of the many s...

Sunday, March 1, 2020

Endo is Not Everything

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Happy Endometriosis Awareness Month! Instead of giving you information I’ve already provided you with, I’m going to share 10 things I’ve don...

Saturday, October 5, 2019

Endometriosis in College

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As some of you know, I began college at the beginning of August and it has probably been the biggest change in my life. Although I love my c...

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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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