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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

机译:谁关心照顾者?老年女性的痛苦,斗争和未满足的需求,以认知下降

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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.
机译:背景:北欧福利国家被称为“关怀国家”。然而,越来越多的金钱对于老年人来说,在长期护理而不是对年轻人的照顾。此外,在归属意识形态上与老龄化相结合的强烈解除制度化意味着老年人,也有望在自己的家中留在自己的家中,即使它们是虚弱,需要全面的护理。因此,家庭成员,特别是年长的女性,越来越希望承担关怀的角色,有时以自己的健康和健康为代价。目的:本文的目的是审查在北欧背景下的认知下降的配偶的老妇人的经验。方法:设计了一个定性学研究,其中11名冰岛和挪威的妇女在自己的家庭中接受了关于他们过去和当前经历作为护理合作伙伴的看法。调查结果:我们的与会者报告说,尽管在从市政家庭接受家庭护理服务,但与认知下降的丈夫生活在警惕和协助各种实用性上居住。它必须在夜晚醒来,总是不得不重复相同的谈话,处理不忠,侵略事件的指责,有时是幻觉,暴力和恐惧。妇女需要更多信息,远离护理的更多信息,以及情感和心理支持。结论和对实践的影响:护理合作伙伴未被视为自身护理需求的人,他们没有听到他们的声音。需要一种以家庭为基础的老人护理的居中性的方法,将这对夫妇放置在服务条款的核心处。应开发家庭护理服务和家庭之间系统合作的工具,以便以更加连贯和整体的方式满足合作伙伴的需求。

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