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'We didn't know it would get that bad': South Asian experiences of dementia and the service response.

机译:“我们不知道情况会变得如此糟糕”:南亚痴呆症的经历和服务反应。

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The aim of the present paper was to examine some views and experiences of dementia among older South Asian people, as well as their families and carers, and to explore central issues of service support. Data were collected in Scotland through interviews with 11 professionals working with South Asian people with dementia, and four case studies of South Asian people with a diagnosis of dementia, as well as their families and carers. The case studies demonstrated overwhelmingly negative experiences of dementia, with poor quality of life, desperate needs for support, lack of access to appropriate services, little knowledge of dementia, and isolation from community and family life. The interviews with professionals described a strong demand for services, a need to develop awareness and knowledge about dementia in South Asian communities, and a need to promote more culturally sensitive, individually responsive services. Similarities between South Asian people and the non-South Asian population include stresson carers, increasing isolation, problematic diagnostic practices, lack of knowledge and demand for service support. Differences include limited use of non-National Health Service (NHS) support, dealing with later stages of dementia at home, particularly negative views about residential care, culturally based attitudinal differences and use of the term 'dementia' in English as neutral rather than stigmatising. The present authors suggest that there is little knowledge and experience of dementia in South Asian communities, as well as restricted access to appropriate services, despite the efforts of voluntary sector and NHS special projects. There is demand for services, especially at home. Services need to develop individual responsiveness for effective working in a diverse society.
机译:本文的目的是研究南亚老年人以及他们的家人和护理人员中痴呆症的一些观点和经验,并探讨服务支持的核心问题。在苏格兰,通过采访11位与南亚痴呆症患者一起工作的专业人员,以及对南亚患有痴呆症诊断者及其家庭和护理人员的四个案例研究,收集了苏格兰的数据。案例研究表明,痴呆症绝大多数是负面的,生活质量差,急需支持,缺乏适当的服务,对痴呆症的了解很少以及与社区和家庭生活隔离。对专业人士的采访描述了对服务的强烈需求,在南亚社区中对痴呆症的认识和知识发展的需求,以及促进对文化更加敏感的,对个人敏感的服务的需求。南亚人与非南亚人之间的相似之处包括压力人照顾者,日益孤立的情况,有问题的诊断做法,缺乏知识和对服务支持的需求。差异包括:有限使用非国家卫生服务(NHS)支持,在家中处理痴呆症的后期阶段,尤其是对寄宿医疗的负面看法,基于文化的态度差异以及英语中的“痴呆症”一词为中性而非污名化。本作者建议,尽管志愿部门和NHS特殊项目做出了努力,南亚社区对痴呆症的知识和经验很少,而且获得适当服务的机会有限。对服务的需求特别是在家庭中。服务需要发展个人的响应能力,以便在多元化的社会中有效工作。

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