Partners instead of patients: Women negotiating power and knowledge within medical encounters for endometriosis
This study investigated how 26 women with endometriosis navigated knowledge and power in medical encounters, finding they required doctors to acknowledge their own bodily knowledge and listen to them to facilitate effective care.
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- Information Needs of Women Affected by Endometriosis and Their Environment: Qualitative Results from Participatory Workshops 2026
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- “Oh God, I Hope She Takes Me Seriously”: How Care-Seekers With Endometriosis and Physicians Work to Perform and Undermine Epistemic Credibility and Knowledge in Endometriosis Care 2026
- Assessing healthcare needs in endometriosis: a scoping review 2025
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- 'A name to the pain': A mixed methods analysis of diagnostic delay and perceptions of diagnosis importance in Australians with endometriosis 2025
- Guideline No. 449: Diagnosis and Impact of Endometriosis - A Canadian Guideline 2024
- Directive clinique no 449 : Directive canadienne sur le diagnostic et les impacts de l’endométriose 2024
- Disregarded, devalued and lacking diversity: an exploration into women’s experiences with endometriosis. A systematic review and narrative synthesis of qualitative data 2024
- A COM-B and Theoretical Domains Framework Mapping of the Barriers and Facilitators to Effective Communication and Help-Seeking Among People With, or Seeking a Diagnosis Of, Endometriosis 2024
- "I wish I knew then what I know now" - pain science education concepts important for female persistent pelvic pain: a reflexive thematic analysis 2024
- Co-developing a digital mindfulness- and acceptance-based intervention for endometriosis management and care: A qualitative feasibility study (Preprint) 2024
- “I wish I didn’t have to defend myself for not being in pain all the time”: Healthcare Interactions between People with Endometriosis and General Practitioners about Therapeutic Cannabis Use: A Narrative Analysis 2024
- "No doctor ever asked me…so I thought it wasn't a valid concern": endometriosis patients' perspectives of barriers and facilitators to sexual health communication in general practice 2024
- Patient and Practitioner: The Impact of Social Factors on Diagnostic Delay for Endometriosis 2023
- A supportive text message intervention for individuals living with endometriosis (EndoSMS): Randomized controlled pilot and feasibility trial 2023
- Patient experiences of being advised by a healthcare professional to get pregnant to manage or treat endometriosis: a cross-sectional study 2023
- “A day-to-day struggle”: A comparative qualitative study on experiences of women with endometriosis and chronic pelvic pain 2022
- Co-design and Development of ENDOTEXT, a Supportive Text Message Intervention for Individuals Living with Endometriosis: Mixed Methods Study (Preprint) 2022
- Learning to live with endometriosis: Findings from a phenomenological study among women in Mauritius, a state in the Indian Ocean 2022
- Endometriose e psicossintomatologia: os impactos de uma doença desafiadora 2022
- Co-design and Development of EndoSMS, a Supportive Text Message Intervention for Individuals Living With Endometriosis: Mixed Methods Study 2022
- Endometriosis prevalence and incidence trends in a large population-based study in Catalonia (Spain) from 2009 to 2018 2022
- The accessibility of pelvic health physiotherapy for adolescents with persistent pelvic pain: a qualitative framework analysis 2022
- That one doctor. . . Qualitative thematic analysis of 49 women’s written accounts of their endometriosis diagnosis 2021
- ‘A day to day struggle’: A comparative qualitative study on experiences of women with endometriosis and chronic pelvic pain 2021
- “The most lonely condition I can imagine”: Psychosocial impacts of endometriosis on women’s identity 2020
- Living with Endometriosis: The Role of the Internet in Supporting the Diagnosis and Treatment Process 2020
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