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The dement in the community: Social work practice with people with dementia revisited

机译:社区中的痴呆症:与痴呆症患者一起进行社会工作实践

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While social work practice with people with dementia and their families has a long but largely hidden history, it is an emerging area of specialism. The increased incidence, prevalence and recognition of dementia suggest that this area of practice will expand and so learning from previous practice may offer helpful insights. This paper describes and reflects upon social work practice with dements' in the 1950s in England. It draws on a reading of a small book written by a psychiatric social worker, Miss M (Muriel) H Bree, outlining her role in providing after-care to patients with neuro-syphilis who had been discharged from hospital to live with their families between 1942 and 1952 through her consideration of 275 case records and seven illustrative case studies. As a historical document, Bree's account presents a rich description of the patients and their social circumstances in post-war Britain; an account of practice from a hospital based setting that reached into the community, and of the engagement of a social worker with her clients and their family members. Threads and continuities with contemporary social work practice with people with dementia are explored; particularly work with family carers, younger people with dementia, and the value placed upon continuity of care.
机译:尽管与痴呆症患者及其家人进行社会工作实践已有很长的历史,但在很大程度上是隐藏的历史,但这是一个新兴的专业领域。痴呆症的发病率,患病率和识别率的增加表明该领域的实践将扩大,因此从以前的实践中学习可能会提供有益的见解。本文描述并反思了1950年代英格兰痴呆的社会工作实践。它借鉴了精神科社会工作者M(Muriel)H Bree小姐写的一本小书,概述了她在为出院后与家人住在一起的神经梅毒患者提供后期护理方面的作用。 1942年和1952年,她考虑了275个案例记录和七个说明性案例研究。作为历史文献,布雷的叙述对战后英国的患者及其社会状况进行了详尽的描述。来自社区的医院环境的实践经验,以及社会工作者与客户及其家人的互动的说明。探索与痴呆症患者的当代社会工作实践的脉络和连续性;特别是与家庭护理人员,患有痴呆症的年轻人一起工作,以及重视持续护理的价值。

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