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Who cares for the carer? The suffering, struggles and unmet needs of older women caring for husbands living with cognitive decline

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dc.contributor.author Munkejord, Mai Camilla
dc.contributor.author Stefánsdóttir, Olga Ásrún
dc.contributor.author Sveinbjarnardóttir, Eydís Kr
dc.date.accessioned 2022-06-24T01:03:48Z
dc.date.available 2022-06-24T01:03:48Z
dc.date.issued 2020-03-18
dc.identifier.citation Munkejord , M C , Stefánsdóttir , O Á & Sveinbjarnardóttir , 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 , vol. 10 . https://doi.org/10.19043/ipdj.10suppl.005
dc.identifier.issn 2046-9292
dc.identifier.other 51153481
dc.identifier.other 1f01e73b-1ea0-42f6-8e20-d981dcf0ad5d
dc.identifier.other unpaywall: 10.19043/ipdj.10suppl.005
dc.identifier.uri https://hdl.handle.net/20.500.11815/3261
dc.description.abstract Background: 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.
dc.format.extent 11
dc.format.extent 475137
dc.format.extent
dc.language.iso en
dc.relation.ispartofseries International Practice Development Journal; 10()
dc.rights info:eu-repo/semantics/openAccess
dc.subject Aldraðir
dc.subject Umönnun
dc.subject Elliglöp
dc.subject Family caregivers
dc.subject Elderly
dc.subject Dementia
dc.subject Gender
dc.title Who cares for the carer? The suffering, struggles and unmet needs of older women caring for husbands living with cognitive decline
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.19043/ipdj.10suppl.005
dc.contributor.department Faculty of Occupational Therapy


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