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, May 21, 2021

Being In Tune with Your Body

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It's been a little over five years since I was diagnosed with endometriosis, but I started fighting for my health long before that....

Saturday, May 8, 2021

Things You Should NEVER Say to Someone with Endo

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Sometimes it's hard to know what to say to someone struggling with a chronic illness, so today I'm going to give you some insight i...

Saturday, April 24, 2021

INFERTILITY AWARENESS WEEK

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Once again, I'm doing a blog post about something I don't personally struggle with, but a lot of people with endometriosis do. This...

Saturday, April 10, 2021

WHAT IS ADENOMYOSIS?

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While I don't suffer from adenomyosis (adeno) myself, a lot of endometriosis warriors do. Adeno is actually considered the sister diseas...

Saturday, March 27, 2021

How to Advocate for Yourself!

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As many of us know all too well, being a woman seeking medical help is not easy. Years of stereotypes and sexism toward woman makes i...

Saturday, March 13, 2021

My Endo Story but Written By My Adult Self

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June 10, 2015 is a day I will never forget. I thought it was just regular period cramps, but the extreme pain never went away. T...

Wednesday, February 24, 2021

It's My Endoversary- Tips for Endo Surgery!

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Is an Endoversary a thing or did I just totally make that up? I don't know but anyway, today is my five-year anniversary of being diagno...

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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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