Abstract
In this article, I examine the uterus as an object in relation to endometriosis
and the epistemological struggle of sufferers to have their pain taken seriously.
Defined by endometrial-like tissue outside the uterus, endometriosis
affects multiple organs, causes severe pain, and is often undiagnosed for
years. While outsiders frequently describe the condition, patient voices
remain marginal. Using illness autoethnography and my experience in
Germany, I show how delegitimized embodied knowledge shapes the identify
work of coping with endometriosis. Medical gaslighting, stigma, limited
literacy, and shame increase dismissal of symptoms and vulnerability.
Recognizing the gendered framings of endometriosis can reshape how
people cope with it.
and the epistemological struggle of sufferers to have their pain taken seriously.
Defined by endometrial-like tissue outside the uterus, endometriosis
affects multiple organs, causes severe pain, and is often undiagnosed for
years. While outsiders frequently describe the condition, patient voices
remain marginal. Using illness autoethnography and my experience in
Germany, I show how delegitimized embodied knowledge shapes the identify
work of coping with endometriosis. Medical gaslighting, stigma, limited
literacy, and shame increase dismissal of symptoms and vulnerability.
Recognizing the gendered framings of endometriosis can reshape how
people cope with it.
| Original language | English |
|---|---|
| Pages (from-to) | 1-18 |
| Number of pages | 18 |
| Journal | Medical Anthropology |
| Early online date | 22 Jan 2026 |
| DOIs | |
| Publication status | E-pub ahead of print - 22 Jan 2026 |
Keywords
- Autoethnography, chronic living, endometriosis, gender bias, Germany, uterine vulnerability
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