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首页> 外文期刊>Child: care, health and development >Parents' voices: 'why and how we advocate'. A meta-synthesis of parents' experiences of advocating for their child with autism spectrum disorder
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Parents' voices: 'why and how we advocate'. A meta-synthesis of parents' experiences of advocating for their child with autism spectrum disorder

机译:父母的声音:“我们为什么以及如何倡导”。父母代言自闭症谱系障碍儿童经验的综合研究

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Parenting a child with autism spectrum disorder (ASD) can be stressful, and accessing services can add to this stress. Self-efficacy, agency and advocacy are important for parents when accessing and using services. To develop insight into parental advocacy, a meta-synthesis was undertaken to consolidate the literature focussing on parents' experiences of advocating for their child with ASD. A qualitative meta-synthesis was conducted. Fifteen databases were systematically searched by using key terms related to ASD, children, parents/carers, advocacy and qualitative studies. Twenty-four studies were identified and appraised using an adapted version of the Critical Appraisal Skills Programme tool. Data were synthesized into themes through the steps of review, meta-aggregation, integration and interpretation. Two overarching concepts emerged, illustrating both the challenging nature of advocacy and the associated personal and societal benefits. These two concepts are supported by eight themes: a life-long, all-encompassing challenge; advocacy as a parental coping strategy; advocacy involving working to create a future; balancing roles and needs; isolation versus support; personal impacts of advocacy; benefits of advocacy; and the barriers to advocacy. The experience of advocacy for parents with a child with ASD is complex and intensive, presenting both personal and societal benefits, as well as challenges for parents. In supporting individuals with ASD and family well-being, service providers need to have an understanding of the advocating role of parents and ensure that opportunities exist for their voices to be heard during service delivery.
机译:为患有自闭症谱系障碍(ASD)的孩子做父母可能会感到压力,使用服务可能会增加这种压力。自我效能,代理和倡导对于父母在访问和使用服务时很重要。为了深入了解父母的主张,进行了元综合研究,以巩固文献,重点关注父母为ASD提倡子女的经验。进行了定性的元合成。通过使用与ASD,儿童,父母/照顾者,倡导和定性研究有关的关键术语,系统搜索了15个数据库。使用关键评估技能计划工具的改编版对24项研究进行了识别和评估。通过审查,元汇总,整合和解释的步骤将数据合成为主题。出现了两个总体概念,说明了倡导的挑战性以及相关的个人和社会利益。这两个概念得到八个主题的支持:一个终生,无所不包的挑战;倡导作为父母的应对策略;倡导创造未来的工作;平衡角色和需求;孤立与支持;宣传的个人影响;宣传的好处;以及宣传的障碍。对患有自闭症儿童的父母进行倡导的经历是复杂而深入的,既给个人和社会带来好处,也给父母带来了挑战。在为个人提供自闭症和家庭幸福的支持时,服务提供商需要了解父母的倡导角色,并确保在提供服务期间存在机会让他们的声音被听到。

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