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The experience of caring for a partner with young onset dementia: How younger carers cope

机译:照顾年轻痴呆症患者的伴侣的经验:年轻的照顾者如何应对

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摘要

A growing body of literature suggests that the social context of experiencing dementia at a younger age may influence carers' and particularly partners' subjective experience and coping strategies. The current paper aims to explore the coping strategies adopted by six carers in order to adapt to changes in their relationship with their partner with young onset dementia. All were recruited from the north west of England and interpretative phenomenological analysis was used to analyse the data. Four major themes were evident: (I) 'this is not happening': the use of denial as a coping strategy; (2) 'let's not have anymore of this demeaning [treatment]': stigma in young onset dementia; (3) 'I've had to fight every inch': struggling to maintain control of events and emotions; (4) 'what will become of me?': carers' adaptation to loss. Comparisons with existing literature are made and implications for clinical practice are considered.
机译:越来越多的文献表明,在年轻时经历痴呆症的社会环境可能会影响护理者,尤其是伴侣的主观经验和应对策略。本论文旨在探讨六个照护者所采取的应对策略,以适应与他们与年轻发作性痴呆的伴侣之间关系的变化。所有这些都是从英格兰西北部招募来的,并且使用解释性现象学分析来分析数据。四个主要主题显而易见:(I)“这没有发生”:使用拒绝作为应对策略; (2)“让我们不再有这种贬低[治疗]”:年轻发作性痴呆的耻辱; (3)“我必须竭尽全力”:努力保持对事件和情感的控制; (4)“我会变成什么样?”:照顾者对损失的适应。与现有文献进行比较,并考虑对临床实践的影响。

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