Mulheres convivendo com endometriose: percepções sobre a doença
This study explored women's knowledge of endometriosis and their perceptions of quality of life post-diagnosis, finding most participants had limited understanding of the disease and viewed its impact negatively.
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This qualitative exploratory descriptive study investigated the knowledge and perceptions about quality of life after diagnosis among 13 women aged 18 to 46 years followed in a university hospital’s Pelvic Pain and Endometriosis service. Most participants reported a 1–4 year disease duration, belonged to the middle class, used contraceptive methods, had no infertility diagnosis, had irregular menstrual cycles, and had a history of prior pregnancy with many reporting abortions. The key finding was that most women did not know the disease affecting them and reported living with pain and the possibility of infertility, perceiving changes from the disease negatively. Limitations were that the study’s small, single-setting sample limits generalizability beyond these participants. This paper is centrally about endometriosis — it examines women’s perceptions and knowledge of endometriosis and how they experience quality of life after diagnosis.
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Abstract
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References (13)
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Cited by (3)
- QUALIDADE DE VIDA DAS MULHERES COM ENDOMETRIOSE: UMA REVISÃO INTEGRATIVA DE LITERATURA 2024
- ENDOMETRIOSE: DIFICULDADES NO DIAGNÓSTICO PRECOCE E SEU IMPACTO NA VIDA DAS MULHERES QUE CONVIVEM COM A DOENÇA 2023
- IMPACTOS NEGATIVOS DA ENDOMETRIOSE NA QUALIDADE DE VIDA DA MULHER ACOMETIDA: UMA REVISÃO INTEGRATIVA DE LITERATURA 2021
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- last seen: 2026-06-10T17:14:06.276822+00:00