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.

Showing posts with label relationships. Show all posts

Friday, January 16, 2026

Feeling Invisible

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Having an invisible illness, or multiple in my case, is a uniquely lonely experience. No matter how hard others try to understand, no matter...

Friday, January 2, 2026

Journaling & 2026 Health Goals

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Journaling used to scare me. I never wanted to be left alone with my thoughts, because that’s when the pain would creep in and take over. I ...

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...

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 ...

Monday, March 11, 2019

Happy Endometriosis Awareness Month!

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Hey everyone! Wow, it's been a while. I've been super busy with school and figuring all the college stuff out. Well, it's that...

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...

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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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