Living with dementia in Aotearoa New Zealand: Samoan families’ perspectives

Fuafiva Fa’alau, Andrew Peteru, Jacinta Fa’alili-Fidow, Mary Roberts, Sharyn Wilson
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Abstract

There is very little research about dementia in Aotearoa (New Zealand) New Zealand (NZ) Pacific communities, but information available suggests that Pacific people are presenting with dementia at a younger age and with more severe cognitive symptoms than do non-Pacific. The Samoan ethnic group is NZ’s largest Pacific population. This study explores experiences and understanding of dementia from family sessions with 25 people from 10 Samoan families living with dementia. Thematic analysis of the interviews showed there was no Samoan concept for dementia as a disease of the brain that required special medical attention; instead, Samoan elders spoke of memory loss as part of ageing, signifying the end to one’s purpose in life. A formal medical diagnosis saw family members honouring their obligations to care for their loved one at home, often at great cost. Culturally appropriate services, incorporating Samoan concepts of care and ageing, were rarely available.
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在新西兰奥特亚罗瓦与痴呆症患者共同生活:萨摩亚家庭的观点
有关奥特亚罗瓦(新西兰)-新西兰(新西兰)太平洋社区痴呆症的研究很少,但现有资料表明,与非太平洋裔人相比,太平洋裔人患痴呆症的年龄更小,认知症状更严重。萨摩亚人是新西兰最大的太平洋裔群体。本研究通过与来自 10 个萨摩亚痴呆症患者家庭的 25 名患者进行家庭访谈,探讨他们的经历和对痴呆症的理解。对访谈进行的主题分析表明,在萨摩亚人的概念中,痴呆症并不是一种需要特别医疗照顾的脑部疾病;相反,萨摩亚长者认为记忆丧失是衰老的一部分,意味着人生目标的终结。正式的医学诊断表明,家庭成员有义务在家照顾他们的亲人,这往往需要付出巨大的代价。结合萨摩亚人的护理和老龄化概念的文化上适当的服务很少提供。
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CiteScore
2.40
自引率
10.50%
发文量
72
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