Writing Through the Fire: Endometriosis, Indie Authorship, and Becoming the Dragon
Author Mackenzie writes about creativity, chronic pain and finding a voice while living with stage 4 endometriosis.
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Ngā kōrero | Lived experience · reflection · community
Stories worth hearing.
Honest writing from those affected by endometriosis, shared to reduce isolation, build understanding and help others feel less alone.
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The Prison You Can't See
Nicole’s poem gives language to the pain, isolation and determination that can accompany endometriosis.
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Cass shares the frustration of being dismissed, the importance of self-advocacy and the relief of finally receiving answers.
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Will it ever stop?
Madison reflects on years of symptoms, dismissal and persistence before receiving an endometriosis diagnosis.
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Cat People (Putting out Fire)
Helena writes about the emotional, physical and financial impact of living with endometriosis and trying to access care.
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Michelle shares more than two decades of pain, dismissal and the toll that navigating care has taken.
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Learning to Listen to My Body
Ruby writes about six years of dismissal, learning to trust her body and finding comfort in community after diagnosis.
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You Are Not Alone- Baby Loss Awareness Day
Founder Yessenia Sandoval shares her experience of endometriosis, PCOS and pregnancy loss for Baby Loss Awareness Day.
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7 Years of let down
Nikki describes seven years of dismissal, pain and persistence—and the importance of continuing to ask for help.
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Real experiences, shared with care
These articles reflect each writer’s personal experience and language at the time of writing. They are not medical advice and may describe treatments, outcomes or views that differ from current general information.
EWA adds clear content notes and support information where a story includes potentially distressing material, while keeping the writer’s voice intact.
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