Bleed: Destroying Myths and Misogyny in Endometriosis Care by Tracey Lindeman
This paper examines the historical and ongoing myths and misogyny that have historically hindered endometriosis care and proposes a path toward improved treatment and patient support.
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This article is a personal narrative and commentary by Tracey Lindeman that critiques the systemic dismissal of pain experienced by patients with endometriosis. Lindeman argues that medical misogyny and entrenched myths contribute to significant delays in diagnosis and inadequate care for those affected by the condition. The text highlights the emotional and physical toll of being unheard by healthcare providers, framing the struggle as part of a broader pattern of gender bias in medicine. This paper is centrally about endometriosis — specifically addressing the social and cultural barriers to proper care and validation for patients.
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References (4)
- “Do mad people get endo or does endo make you mad?”: Clinicians’ discursive constructions of Medicine and women with endometriosis via openalex
- Endometriosis in Canada: It Is Time for Collaboration to Advance Patient-Oriented, Evidence-Based Policy, Care, and Research via openalex
- W1546365706 via openalex
- W4230683478 via openalex
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- openalex
- last seen: 2026-06-10T17:14:06.276822+00:00
- unpaywall
- last seen: 2026-08-23T06:29:45.520198+00:00