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.

Sunday, December 25, 2016

GET THE SURGERY!

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Merry Christmas everyone! I hope you are having a happy and healthy holiday season. In my last post I said I would give more information ab...

Saturday, December 17, 2016

Frequently Asked Questions About Endo

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Q: Why have I never heard about Endometriosis? A: Endometriosis is a disease that effects 10% of women, but no one seems to talk about it...

Wednesday, December 7, 2016

Ladies, Don't Let Endo Ruin Your Holiday Season

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So, the holidays are coming up as you all know, this can be some of the hardest times to have Endo. Everyone is suppose to be happy and joyo...

Sunday, November 27, 2016

Relationships With Endo

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Relationships with Endo are so hard. I have ruined several relationships because of my Endo. The worst part is, it isn't even the person...

Sunday, November 13, 2016

Girl, Take Off That Mask!

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How do you tell if someone has Endo by just looking at them? The answer to that question is you most likely can’t. Women who suffer from E...

Sunday, November 6, 2016

"Endo What?" Movie

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One day, a few weeks ago, I was in so much pain and was feeling very trapped. I could not even move and I felt like my parents did not und...

Monday, October 24, 2016

Exercise with Endo

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Exercise with Endometriosis has always been a struggle for me. This April, two months after my surgery, I started going to the gym with my...

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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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