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 2021. Show all posts
Showing posts with label 2021. Show all posts
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...
Saturday, June 5, 2021

How To Be a Good Advocate on Social Media (And Make Meaningful Connections to Your Audience)

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 If there is one thing the world always needs more of, it's advocates. No matter the issue, meaningful work, and change simply don't...
Saturday, January 30, 2021

How I Helped My Bladder Problems!

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 If you've been following my blog or Instagram for the last several months, then you know that I've been struggling with severe blad...
Saturday, January 2, 2021

My Health Goals for 2021

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 Happy New Year everyone!! 2020 was a hard year for everyone around the world but now is a chance to start fresh and create some goals for t...
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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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