Center for Medical Ethics and Health Policy Staff Publications

Language

English

Publication Date

1-1-2026

Journal

Sociology of Health and Illness

DOI

10.1111/1467-9566.70142

PMID

41549371

PMCID

PMC12813254

PubMedCentral® Posted Date

1-18-2026

PubMedCentral® Full Text Version

Post-print

Abstract

People living with endometriosis, a disease in which tissue similar to the lining of the uterus grows elsewhere in the body, often experience prolonged diagnostic journeys because of symptom variability, normalisation of period pain and other symptoms, and lack of awareness of the condition. In this article, we analyse the endometriosis diagnostic journey through the lens of epistemic injustice. Drawing on in-depth interviews with 52 people living with endometriosis in the United States, we introduce the concept of diagnostic buck-passing to characterise the phenomenon wherein individuals who seek treatment for their symptoms end up stuck in a cycle of seeing different providers across ranging specialities, which ultimately delays their diagnosis. We describe diagnostic buck-passing and the conditions that give rise to its emergence, grounding our conceptualisation in endometriosis diagnosis. Utilising concepts of undone science and wilful ignorance, we demonstrate how endometriosis diagnosis becomes a site of hermeneutical injustice due to a long history of underinvestment in women's health research and resultant knowledge gaps in clinical care.

Keywords

Humans, Endometriosis, Female, Adult, Interviews as Topic, Qualitative Research, United States, Middle Aged, Delayed Diagnosis

Published Open-Access

yes

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