Endometriosis: the bloggers' tales

Other OA: bronze CC0 ⤵ 1 in-corpus citation
⚙ AI-generated summary by gemini-2.5-flash-lite, 2026-07-14 ⓘ

This paper's author discusses the difficulty of bridging the gap between healthcare professionals and patients with endometriosis due to a lack of first-hand accounts from affected women worldwide.

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Abstract

To bridge the gap – that’s what my brief for the Journal has always been. To create understanding between reproductive health professionals and health service consumers – to help the former appreciate the needs of the latter. This is why I often base my columns directly on the experiences of end-users: women patients with cervical cancer, teenage students needing sex education, purchasing customers using pharmaceutical services, being recent examples. But when the Journal Editor recently tasked me with writing about endometriosis (Box 1), I found myself unexpectedly log-jammed. Despite the fact that over 170 million women worldwide suffer, I knew no one with the condition. I didn’t even know anyone who knew anyone with the condition. And the devoted user-organisations couldn’t deliver me the numbers of globally-based, first-hand accounts that I ideally needed. Box 1 ### Facts about endometriosis

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Condition tags

endometriosis

MeSH descriptors

Blogging Blogging Endometriosis Endometriosis Abdominal Pain Abdominal Pain Abdominal Pain Endometriosis Endometriosis Endometriosis Female Female Humans Humans Social Support Social Support Women's Health Women's Health

Citation neighborhood (sparse)

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

Cites (1)

Cited by (1)

References (1)

Cited by (1)

Source provenance

europepmc
last seen: 2026-10-09T06:09:53.026058+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
pubmed
last seen: 2026-10-08T21:13:27.857801+00:00
License: CC0 · commercial use OK