父母共同患有多发性先天性关节挛缩症的女童的社会应对经验

M. Abed
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引用次数: 0

摘要

多发性先天性关节挛缩症,通常被称为AMC,是一种由关节多次挛缩所识别的疾病。与这种障碍相关的症状跨越了不同程度的严重程度。然而,撇开身体上的问题不谈,智力是不受干扰的。本文的目的是集中在调查与这种情况下生活的孩子的社会应对经验,采用定性的方法来研究。本研究采用个案研究设计,运用现象学的理论框架。一个样本用于数据收集,特别是一个被诊断患有关节挛缩症的儿童,她的应对经历与她的父母分享。在审查数据时,采用了专题分析。这项研究具有重要意义,因为它试图了解患有这种疾病的儿童以及整个残疾儿童群体。从这项研究中出现的关键问题包括社会关系的作用,父母在社会化中的作用,以及他人对AMC的看法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Social Coping Experiences of a Female Child with Arthrogryposis Multitplex Congenita Shared by her Parents
Arthrogryposis Multiplex Congenita, commonly referred to as AMC, is a disorder recognised by multiple contractures of the joints. The symptoms associated with the disorder span across various levels of severity. Regardless of the physical problems, however, intelligence remains undisturbed. The aim of this paper is centred on investigating the social coping experiences of a child living with this condition, adopting a qualitative approach to the research. A case study design was adopted for the research, with the theoretical framework applied known as Phenomenology. One sample was used for the data collection, notably a child diagnosed with Arthrogryposis, with her coping experiences shared by her parents. When examining the data, thematic analysis was applied.  This study has significance in the fact it seeks to develop an understanding of children living with this condition, as well as for the disabled child population as a whole. The key issues seen to arise from this study include the role of social relationships, the role of the parent in socialisation, and the perceptions of others concerning AMC.
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