Patients’ experiences of healthcare encounters in severe irritable bowel syndrome: an analysis based on narrative and feminist theory
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DOI: 10.1111/jocn.13400
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References listed on IDEAS
- Kay I Penny & Graeme D Smith, 2012. "The use of data‐mining to identify indicators of health‐related quality of life in patients with irritable bowel syndrome," Journal of Clinical Nursing, John Wiley & Sons, vol. 21(19pt20), pages 2761-2771, October.
- Eccleston, Chris & De C. Williams, Amanda C. & Rogers, Wendy Stainton, 1997. "Patients' and professionals' understandings of the causes of chronic pain: Blame, responsibility and identity protection," Social Science & Medicine, Elsevier, vol. 45(5), pages 699-709, September.
- Werner, Anne & Isaksen, L.W.Lise Widding & Malterud, Kirsti, 2004. "'I am not the kind of woman who complains of everything': Illness stories on self and shame in women with chronic pain," Social Science & Medicine, Elsevier, vol. 59(5), pages 1035-1045, September.
- Werner, Anne & Malterud, Kirsti, 2003. "It is hard work behaving as a credible patient: encounters between women with chronic pain and their doctors," Social Science & Medicine, Elsevier, vol. 57(8), pages 1409-1419, October.
- Kugelmann, Robert, 1999. "Complaining about chronic pain," Social Science & Medicine, Elsevier, vol. 49(12), pages 1663-1676, December.
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- Elisabet Johannesson & Eva Jakobsson Ung & Gisela Ringström & Riadh Sadik, 2019. "The experiences of physical activity in irritable bowel syndrome—A qualitative study," Journal of Clinical Nursing, John Wiley & Sons, vol. 28(17-18), pages 3189-3199, September.
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