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dc.contributor.authorMunkejord, Mai Camilla
dc.contributor.authorStefánsdóttir, Olga Ásrun
dc.contributor.authorSveinbjarnardóttir, Eydís Kr.
dc.date.accessioned2020-04-24T07:18:39Z
dc.date.available2020-04-24T07:18:39Z
dc.date.created2020-03-19T12:22:24Z
dc.date.issued2020
dc.identifier.citationMunkejord, M. C., Stefansdottir, O. A., & Sveinbjarnardottir, E. K. (2020). Who cares for the carer? The suffering, struggles and unmet needs of older women caring for husbands living with cognitive decline. International Practice Development Journal, 10(Suppl), 1-11.en_US
dc.identifier.issn2046-9292
dc.identifier.urihttps://hdl.handle.net/11250/2652319
dc.description.abstractBackground: The Nordic welfare states have been called the ‘caring states’. However, increasingly, less money is spent on long-term care for older persons than on care for younger persons. Additionally, a strong de-institutionalisation of care coupled with an ageing at home ideology means older persons are expected to remain in their own home, even when they are frail and in need of comprehensive care. As a result, family members, particularly older women, are increasingly expected to take on caring roles, sometimes at the expense of their own health and wellbeing. Aim: The aim of this article is to examine the experiences of older women caring for a spouse living with cognitive decline in a Nordic context. Methods: A qualitative study was designed, in which 11 women in Iceland and Norway were interviewed in their own homes about their past and current experiences as care partners. Findings: Our participants reported that despite receiving home-based care services from the municipality, living with a husband with cognitive decline consisted of constantly being on the alert and assisting with various practicalities. It entailed being woken up night after night, always having to repeat the same bits of conversation, dealing with accusations of infidelity, episodes of aggression, and sometimes hallucinations, violence and fear. The women needed more information, more assistance and time away from care, and emotional and psychological support. Conclusions and implications for practice: The care partners were not treated as persons with their own care needs, and their voices were not heard. A relational person-centred approach in home-based elderly care is needed, placing the couple, not the individual, at the core of service provision. A tool for systematic collaboration between home care services and families should be developed so that both partners’ needs may be met in a more coherent and holistic way.en_US
dc.language.isoengen_US
dc.publisherFoundation of Nursing Studiesen_US
dc.relation.urihttps://www.fons.org/Resources/Documents/Journal/Vol10Suppl/IPDJ_10Suppl_005.pdf
dc.rightsNavngivelse-Ikkekommersiell 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/deed.no*
dc.subjectdamily careen_US
dc.subjectcare partneren_US
dc.subjectcouple-centred careen_US
dc.subjectdementiaen_US
dc.subjectNorwayen_US
dc.subjectIcelanden_US
dc.titleWho cares for the carer? The suffering, struggles and unmet needs of older women caring for husbands living with cognitive declineen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Authors 2020en_US
dc.source.pagenumber1-11en_US
dc.source.journalInternational Practice Development Journalen_US
dc.source.issue10en_US
dc.identifier.doihttps://doi.org/10.19043/ipdj.10Suppl.005
dc.identifier.cristin1802420
dc.relation.projectNorges forskningsråd: 287301en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse-Ikkekommersiell 4.0 Internasjonal
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