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Hanging on to Some Autonomy in Decisionmaking: How do Spouse Carers Support this?

机译:悬挂在决策中的一些自主权:配偶照顾者如何支持这一点?

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In Australia, the majority of people with dementia live in the community with informal care provided by family, commonly a spouse. A diagnosis of dementia is a threat to one’s personhood and is often accompanied by perceptions of future dependency, which will involve the inability to carry out conventional roles and complete everyday tasks including making decisions. Being able to make decisions, however, is part of being a ‘person’ and it is through relationships that personhood is defined and constructed. In face-to-face interviews with seven couples (a carer and person with dementia dyad) and two spouse carers, this study explored why, and how, spouse carers support continued involvement in decision-making for people with dementia. The findings highlight the importance of loving and respectful relationships in the development of strategies to support continued decision-making for people with dementia.
机译:在澳大利亚,大多数人患有痴呆症的人生活在社区,由家庭提供的非正式护理,通常是配偶。 痴呆症的诊断是对一个人的态度的威胁,并且往往伴随着对未来依赖的看法,这将涉及无法开展传统角色并完成日常任务,包括做出决定。 然而,能够做出决定是成为“人”的一部分,并且通过人际关系的关系是一个人的关系。 本研究探讨了与七对夫妻(护理人员和痴呆症Dyad的人)和两个配偶照顾者进行面对面访谈,以及如何,配偶照顾者支持继续参与痴呆症的人民的决策。 调查结果突出了爱情和尊重关系在制定战略方面的重要性,以支持痴呆症的持续决策。

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