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Articles

The third shift: Health, work and expertise among women with endometriosis

Pages 194-206 | Received 20 Aug 2008, Accepted 14 Apr 2009, Published online: 17 Dec 2014

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Meredith Nash. (2023) Breaking the silence around blood: managing menstruation during remote Antarctic fieldwork. Gender, Place & Culture 30:8, pages 1083-1103.
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Sarah Grogan, Emma Turley & Jennifer Cole. (2018) ‘So many women suffer in silence’: a thematic analysis of women’s written accounts of coping with endometriosis. Psychology & Health 33:11, pages 1364-1378.
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Emilie Zaslow. (2012) REVALORIZING FEMININE WAYS OF KNOWING. Information, Communication & Society 15:9, pages 1352-1372.
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Sally Lindsay & Hubertus J.M. Vrijhoef. (2009) A sociological focus on ‘expert patients’. Health Sociology Review 18:2, pages 139-144.
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Sarah Delaney, Sylvia Huntley-Moore & Patricia Cronin. (2024) Exercising power in the self-management of COPD: A narrative inquiry. Patient and user perspectives. Patient Education and Counseling 118, pages 107990.
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Fred Brouns, Annelotte Van Haaps, Daniel Keszthelyi, Koen Venema, Marlies Bongers, Jacques Maas & Velja Mijatovic. (2023) Diet associations in endometriosis: a critical narrative assessment with special reference to gluten. Frontiers in Nutrition 10.
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Simon Lindgren & Lorna Richardson. (2023) Endometriosis pain and epistemic community: Mapping discourses in online discussions among sufferers. Social Science & Medicine 326, pages 115889.
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Payal Kanwar Chandel, Pawan Kumar Maurya, Sajad Hussain, Divya Vashistha & Shreya Sharma. (2023) Endometriosis and Depression: A Double Agony for Women. Annals of Neurosciences, pages 097275312311520.
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Katherine Ellis, Deborah Munro & Rachael Wood. (2022) The experiences of endometriosis patients with diagnosis and treatment in New Zealand. Frontiers in Global Women's Health 3.
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Lara Owen. (2022) Stigma, sustainability, and capitals: A case study on the menstrual cup. Gender, Work & Organization 29:4, pages 1095-1112.
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Eliza Brown. (2022) Less Like Magic, More Like a Chore: How Sex for the Purpose of Pregnancy Becomes a Third Shift for Women in Heterosexual Couples* 1 . Sociological Forum 37:2, pages 465-485.
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Youngsub Yoon, Min‐Ae Park & Sihyun Park. (2021) Seeking adaptation from uncertainty: Coping strategies of South Korean women with endometriosis. Research in Nursing & Health 44:6, pages 970-978.
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Adrienne Pichon, Kayla Schiffer, Emma Horan, Bria Massey, Suzanne Bakken, Lena Mamykina & Noemie Elhadad. (2021) Divided We Stand. Proceedings of the ACM on Human-Computer Interaction 4:CSCW3, pages 1-24.
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Nicky Hudson, Caroline Law, Lorraine Culley, Helene Mitchell, Elaine Denny, Wendy Norton & Nick Raine‐Fenning. (2020) Men, chronic illness and healthwork: accounts from male partners of women with endometriosis. Sociology of Health & Illness 42:7, pages 1532-1547.
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K.M. Saulnier. (2020) Telling, Hearing, and Believing: A Critical Analysis of Narrative Bioethics. Journal of Bioethical Inquiry 17:2, pages 297-308.
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Jenny Vennberg Karlsson, Harshida Patel & Asa Premberg. (2020) Experiences of health after dietary changes in endometriosis: a qualitative interview study. BMJ Open 10:2, pages e032321.
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Rebecca O’Hara, Heather Rowe & Jane Fisher. (2019) Self-management in condition-specific health: a systematic review of the evidence among women diagnosed with endometriosis. BMC Women's Health 19:1.
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Elaine Denny, Annalise Weckesser, Georgina Jones, Stavroula Bibila, Jane Daniels & Siladitya Bhattacharya. (2018) Women’s experiences of medical treatment for endometriosis and its impact on PRE-EMPT trial participation: a qualitative study. Pilot and Feasibility Studies 4:1.
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Rizwana Roomaney & Ashraf Kagee. (2016) Salient aspects of quality of life among women diagnosed with endometriosis: A qualitative study. Journal of Health Psychology 23:7, pages 905-916.
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Bianca Brijnath & Josefine Antoniades. (2016) “I'm running my depression:” Self-management of depression in neoliberal Australia. Social Science & Medicine 152, pages 1-8.
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Kate Young, Jane Fisher & Maggie Kirkman. (2015) Women's experiences of endometriosis: a systematic review and synthesis of qualitative research. Journal of Family Planning and Reproductive Health Care 41:3, pages 225-234.
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Hedyeh Riazi, Najmeh Tehranian, Saeideh Ziaei, Easa Mohammadi, Ebrahim Hajizadeh & Ali Montazeri. (2014) Patients’ and physicians’ descriptions of occurrence and diagnosis of endometriosis: a qualitative study from Iran. BMC Women's Health 14:1.
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Francine Toye, Kate Seers & Karen Barker. (2014) A meta-ethnography of patients' experiences of chronic pelvic pain: struggling to construct chronic pelvic pain as ‘real’. Journal of Advanced Nursing 70:12, pages 2713-2727.
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Lorraine Culley, Caroline Law, Nicky Hudson, Elaine Denny, Helene Mitchell, Miriam Baumgarten & Nick Raine-Fenning. (2013) The social and psychological impact of endometriosis on women's lives: a critical narrative review. Human Reproduction Update 19:6, pages 625-639.
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E. A. F. Dancet, L. Ameye, W. Sermeus, M. Welkenhuysen, W. L. D. M. Nelen, L. Tully, B. De Bie, J. Veit, H. Vedsted-Hansen, K. T. Zondervan, C. De Cicco, J. A. M. Kremer, D. Timmerman & T. M. D'Hooghe. (2011) The ENDOCARE questionnaire (ECQ): a valid and reliable instrument to measure the patient-centeredness of endometriosis care in Europe. Human Reproduction 26:11, pages 2988-2999.
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