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, October 23, 2020

BOOK REVIEW: Vagina Problems by Lara Parker

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     I just finished reading Vagina Problems: Endometriosis, Painful Sex, and Other Taboo Topics by my favorite endo blogger, Lara Parker, a...
Saturday, October 10, 2020

Going Back to College During a Pandemic

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 Before going back to college this semester, I was a little nervous, but mostly excited. In the spring, I went home for spring break and nev...
Friday, October 2, 2020

Breast Cancer Awareness Month

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 October is Breast Cancer Awareness Month and although this post isn't about endometriosis, the two are very much connected. People with...
Saturday, September 26, 2020

SHARING YOUR ENDO STORIES: Part 5 Jonnie

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“Hi, I am Jonnie (pronounced Johnny). I am 30 and divorced without a uterus. I was diagnosed with endometriosis while I was in college. At a...
Friday, September 11, 2020

BOOK REVIEW: 100 Questions and Answers About Endometriosis by Dr. David B. Redwine

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Like I said in my last book review, I have been reading a lot of books about endometriosis to better educate myself on the disease I live wi...
Saturday, August 29, 2020

SHARING YOUR ENDO STORIES: Part 4 Caroline

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“Hi, my name’s Caroline, I’m 19, and I have endometriosis. I remember my first period being very painful, but I’d been told that periods wer...
Saturday, August 15, 2020

BOOK REVIEW: Beating Endo: How to Reclaim Your Life From Endometriosis by Iris Orbuch, MD and Amy Stein, DPT

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     Beating Endo: How to Reclaim Your Life From Endometriosis by Iris Orbuch, MD and Amy Stein, DPT is different from other books on endome...
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About Me

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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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