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, February 24, 2017

One Year...

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The date February 24, 2016 is a day that I will never forget. It was the day I got my Endo surgery. It was exactly one year ago from today. ...

Thursday, February 16, 2017

Endo and Life Update

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Sorry I have been away for a while, but it has been a busy time for me so today I am going to be giving you all a little life update. Tomor...

Wednesday, January 18, 2017

Focus On Your Finals, Not Your Pain

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This week is the week that all high school students dread; finals week. The one thing that is worse than finals, is having Endo pain during...

Sunday, January 1, 2017

New Year, Less Pain...Hopefully

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Another year has come and gone and there is still no cure for Endo. This could be discouraging, but for me, I know there will be one very s...

Sunday, December 25, 2016

GET THE SURGERY!

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Merry Christmas everyone! I hope you are having a happy and healthy holiday season. In my last post I said I would give more information ab...

Saturday, December 17, 2016

Frequently Asked Questions About Endo

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Q: Why have I never heard about Endometriosis? A: Endometriosis is a disease that effects 10% of women, but no one seems to talk about it...

Wednesday, December 7, 2016

Ladies, Don't Let Endo Ruin Your Holiday Season

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So, the holidays are coming up as you all know, this can be some of the hardest times to have Endo. Everyone is suppose to be happy and joyo...

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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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