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, January 29, 2022

I'M IMMUNOCOMPROMISED AND GOT COVID

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After only one week back at college for the spring semester, I tested positive for covid after dodging it for almost two years. This tim...

Saturday, December 18, 2021

End of Semester Update!

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I'm back everyone and I apologize for my absence this past semester! I think it has been a crazy time for most people, especially those...

Sunday, October 24, 2021

ORGANIZATIONAL TIPS!

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This doesn't have much to do with chronic illness, but I want to share my organizational tips with you today. However, these methods he...

Sunday, September 26, 2021

Back to School with a Chronic Illness- Tips

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It's that time of year again when all of us students are getting in the swing of school. I know I certainly am. I know better than most...

Saturday, September 11, 2021

Back to School!

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Some of you may have noticed that I took a month off from posting and that’s because the beginning of school has been crazy. The day I moved...

Friday, July 30, 2021

Chatty Catch Up (COVID, School, Keeping Busy, and Health Update)!

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I've been really busy with work this week and getting ready to go on vacation next week, so we're doing a quick, chatty blog post t...

Saturday, July 17, 2021

WHAT IS CUPPING THERAPY?

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Many of you have heard me talk about cupping therapy (or cupping) here and on my Instagram, but I've learned that most people don'...

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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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