'No one agrees except for those of us who have it': endometriosis patients as an epistemological community

other OA: bronze public-domain-us ⤵ 1 in-corpus citation
AI-generated summary by gemini-2.5-flash-lite, 2026-07-18

This paper analyzes the epistemological strategies, particularly the centrality of experience, employed by women within an endometriosis patient community to develop and evaluate knowledge about their disease.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

Abstract

This paper contributes to the literature on patients' claims-making work by analysing the epistemological strategies and standards used by members of an endometriosis patient community. It draws upon focus group research with members of a support group for endometriosis sufferers, and an open-ended survey of an e-mail list for women with the disease. Lynn Hankinson Nelson's (1993) concept of epistemological community is used to examine standards and practices for developing and evaluating knowledge used by women with endometriosis. Particular attention is paid to the use and centrality of the notion of experience within this community.

My notes (saved in your browser only)

Condition tags

endometriosis

MeSH descriptors

Consumer Health Information Endometriosis Knowledge Patient Participation Self-Help Groups Body Image Consumer Health Information Endometriosis Female Health Knowledge, Attitudes, Practice Humans Patient Participation Physician-Patient Relations Sociology, Medical

Citation neighborhood (sparse)

Too few in-corpus citations on either side for a chart; here are the lists.

Cited by (1)

Cited by (1)

Source provenance

europepmc
last seen: 2026-08-30T06:09:04.529024+00:00
pubmed
last seen: 2026-05-13T22:14:42.556217+00:00
unpaywall
last seen: 2026-05-14T19:30:52.867331+00:00
License: public-domain-us · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine