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.

Monday, October 24, 2016

Exercise with Endo

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Exercise with Endometriosis has always been a struggle for me. This April, two months after my surgery, I started going to the gym with my...

Friday, October 14, 2016

My Endometriosis Story: End?

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My surgery was scheduled for February 24, 2016. I will never forget that date. It was a very easy surgery but I do not remember a lot of ...

Tuesday, October 11, 2016

My Endometriosis Story: Middle

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In my previous posts, I talked about how my gynecologist did not really do anything to help my situation. Finally, the gynecologist though...

Monday, October 10, 2016

My Endometriosis Story: Hospital Visits

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Over the summer, I go to a two week overnight theatre camp. This was in August and I started getting the pain in June. This camp is my fa...

Sunday, October 9, 2016

My Endometriosis Story: Beginning

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For those who do not know, the dictionary definition of Endometriosis is a condition resulting from the appearance of endometrial issue out...

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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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