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, 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...
Sunday, July 19, 2020

BOOK REVIEW: Living with Endometriosis by Samantha Bowick

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Recently I've been reading a lot of books about endometriosis (more book reviews coming soon) to better inform and educate myself about ...
Sunday, July 5, 2020

SHARING YOUR ENDO STORIES: Part 2 Ellie

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“Hi I'm Ellie, I'm 24. I was 12 years old when I started my period and 13 years old when I started on the pill. For me starting the ...
Sunday, June 28, 2020

SHARING YOUR ENDO STORIES: Part 3 Hannah

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“Hi, I’m Hannah and I’m 20 years old! When I was 11 years old I got my first period. I was so excited to tell my mom that I was “finally was...
Saturday, June 20, 2020

SHARING YOUR ENDO STORIES: Part 1 Amrita

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“From the time I got my period at the age of 12, everything was normal. I’d have regular periods with hardly any pain or discomfort but life...
Friday, June 5, 2020

HOW TO HELP: Full List of BLM Resources (SHARE!)

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This week I decided to take a break from the endo content because there are more important things going on. I have seen a lot of different l...
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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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