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dc.contributor.authorBakken, Anne Karen
dc.contributor.authorMengshoel, Anne Marit
dc.contributor.authorSynnes, Oddgeir
dc.contributor.authorStrand, Elin Bolle
dc.date.accessioned2023-06-16T07:34:28Z
dc.date.available2023-06-16T07:34:28Z
dc.date.created2023-06-15T11:17:16Z
dc.date.issued2023
dc.identifier.citationInternational Journal of Qualitative Studies on Health and Well-being. 2023, 18 (1), 2223420-?.en_US
dc.identifier.issn1748-2623
dc.identifier.urihttps://hdl.handle.net/11250/3071718
dc.descriptionThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.en_US
dc.description.abstractBackground: The condition known as chronic fatigue syndrome or myalgic encephalomyelitis (CFS/ME) is poorly understood. Simplified medical models tend to neglect the complexity of illness, contributing to a terrain of uncertainty, dilemmas and predicaments. However, despite pessimistic pictures of no cure and poor prognosis, some patients recover. Purpose: This study’s purpose is to provide insight into people’s experiences of suffering and recovery from very severe CFS/ME and illuminate understanding of how and why changes became possible. Methods: Fourteen former patients were interviewed about their experiences of returning to health. A narrative analysis was undertaken to explore participants’ experiences and understandings. We present the result through one participant’s story. Results: The analysis yielded a common plotline with a distinct turning point. Participants went through a profound narrative shift, change in mindset and subsequent long-time work to actively pursue their own healing. Their narrative understandings of being helpless victims of disease were replaced by a more complex view of causality and illness and a new sense of self-agency developed. Discussion: We discuss the illness narratives in relation to the disease model and its shortcomings, the different voices dominating the stories at different times in a clinically, conceptually, and emotionally challenging area.en_US
dc.language.isoengen_US
dc.publisherTaylor & Francisen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectpersistent physical symptomsen_US
dc.subjectpersonal experiencesen_US
dc.subjectcontested diagnoseen_US
dc.subjectqualitative interviewsen_US
dc.subjectvery severe CFS/MEen_US
dc.subjectnarrative analysisen_US
dc.subjectillness narrativesen_US
dc.subjectrecovery processen_US
dc.titleAcquiring a new understanding of illness and agency: a narrative study of recovering from chronic fatigue syndromeen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Groupen_US
dc.source.pagenumber1-18en_US
dc.source.volume18en_US
dc.source.journalInternational Journal of Qualitative Studies on Health and Well-beingen_US
dc.source.issue1en_US
dc.identifier.doidoi.org/10.1080/17482631.2023.2223420
dc.identifier.cristin2154802
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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