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首页> 外文期刊>Social Work in Mental Health >Transparency, Hope, and Empowerment: A Model for Partnering With Parents of a Child With Autism Spectrum Disorder at Diagnosis and Beyond
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Transparency, Hope, and Empowerment: A Model for Partnering With Parents of a Child With Autism Spectrum Disorder at Diagnosis and Beyond

机译:透明,希望和授权:与自闭症谱系障碍患儿的父母合作进行诊断的模型

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摘要

While models for conveying a diagnosis of Autism Spectrum Disorder (ASD) are beginning to emerge in the literature, relatively little is known about how a diagnosis is delivered and experienced by families. This study examined the experiences of parents receiving a diagnosis of ASD for their child. Based on a phenomenological approach, a purposive sample of 10 parents (8 mothers, 2 fathers) participated in in-depth, semi-structured interviews aimed at understanding their diagnostic experience. Findings revealed a lengthy, complex, and discouraging assessment and diagnostic process that resulted in parents feeling confused, disempowered, and overwhelmed. Identified themes associated with diagnosis comprised: initial recognition that a??something is differenta??; waiting, worry, and uncertainty; preference for diagnostic information in a hopeful tenor; feeling overwhelmed with information and emotion at diagnosis; processes of grief, relief, and making sense of ASD; and becoming an advocate, expert, and case manager. The importance of empowering parents by providing support, information, resources, and tools for navigating the complexity of service/treatments at the time of diagnosis was emphasized within a parent-professional partnership. A protocol for practice, focused on enhanced parental empowerment, is offered including specific clinical guidelines (what to share, how to share, and when to share) for sharing a diagnosis of ASD.View full textDownload full textKeywordsautism spectrum disorder, diagnosis, parents, empowerment, hopeRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/15332985.2012.664487
机译:虽然自闭症谱系障碍(ASD)的诊断模型已经开始出现,但是对于家庭如何进行诊断和经历诊断知之甚少。这项研究检查了父母为孩子接受ASD诊断的经历。基于现象学方法,有目的的10位父母(8位母亲,2位父亲)样本参加了旨在了解其诊断经验的深入,半结构化访谈。调查结果显示,评估和诊断过程冗长,复杂且令人沮丧,导致父母感到困惑,无能为力和不知所措。与诊断相关的已确定主题包括:最初认识到“事物有所不同”。等待,担心和不确定性;希望在希望的期限内获得诊断信息;诊断时感觉不知所措;悲伤,缓解和理解ASD的过程;并成为辩护人,专家和案件经理。在父母与专业的伙伴关系中,强调了通过提供支持,信息,资源和工具来诊断诊断时服务/治疗的复杂性来赋予父母权力的重要性。提供了一个针对实践的协议,侧重于增强父母的权能,包括用于共享ASD诊断的特定临床指南(共享内容,共享方式和共享时间)查看全文下载全文关键词自闭症谱系障碍,诊断,父母,授权,希望相关var addthis_config = {ui_cobrand:“泰勒和弗朗西斯在线”,servicescompact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,更多”,发布日期:“ ra-4dff56cd6bb1830b”} ;添加到候选列表链接永久链接http://dx.doi.org/10.1080/15332985.2012.664487

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