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Real Talk With Endo
Endometriosis affects an estimated 1 in 10 people assigned female at birth, including women, non-binary, and trans folks — and there is no cure. In honor of Endometriosis Awareness Month, Rescripted has partnered with Emma Maxwell, a tireless endo advocate, to feature personal stories from real people who have been there.
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In July 2023, I was rushed into emergency surgery for a torsed ovary with a 5cm cyst. My doctors keep saying I was okay—just a spastic pelvic floor—and wouldn’t do further testing.
I had migraines and GI issues before my first period. Heavy, painful periods followed. In 2019, an ER doctor mentioned endometriosis. My OB/GYN blamed me, suggesting therapy and antidepressants
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THE STORIES
About the Creator
Emma Maxwell
I’m Emma, a 24-year-old passionate about advocating and sharing my experiences of living with endo & adeno, among other conditions. I care so deeply about this campaign - people sharing their real and raw experiences has been so impactful throughout my journey. It’s truly why I have a diagnosis and why I do what I do.
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