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Social Action Partners: Peer support for children and young people with intellectual disability and their families in Victoria

机译:社会行动伙伴:为维多利亚州的智障儿童和青少年及其家庭提供同伴支持

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摘要

This project used a social action research approach with two groups of Victorian children and young people with intellectual disability aged 9-22 and their parents. The groups conducted research and provided peer support about their experiences with self-directed disability support. The intentions were to build capacity among children, young people and families for the transition to a policy context of self-directed support under the National Disability Insurance Scheme (NDIS) and to build capacity within the disability community for self-direction, strengthen peer support and develop research competence. Three facilitator organisations ran two workshops with each group. Data was generated and collected through discussion, artefacts from the workshops, feedback forms, demographic surveys, notes written by the facilitators and teleconferences with the facilitators. The findings cover the extent to which children, young people and parents had used self-directed disability support and their thoughts about its future possibilities for them, as well as children and young people’s reflections on their participation in school, work, volunteering, relationships and their aspirations for the future – for children and young people, funding and support were a means to achieving their goals in these life areas. The findings also cover the experience and outcomes of information sharing, mentoring, role modelling and the opportunity for dedicated dialogue and discussion time available in the groups formed for the project.The project’s findings have policy implications for children, young people and parents’ access to self-directed support options in the future; their control over managing their support; how to better cater to information needs; the importance of peer support, information sharing and opportunities for discussion in developing capacity for self-directed support; and the need to focus decisions about support arrangements on the aspirations of children and young people.
机译:该项目采用社会行动研究方法,对两组维多利亚州的9-22岁智障儿童和青少年及其父母进行了研究。这些小组进行了研究,并就他们在自我指导的残疾支持方面的经验提供了同行支持。目的是在儿童,年轻人和家庭中建立能力,以过渡到根据国家残疾保险计划(NDIS)提供自我支持政策的背景,并在残疾社区内部建设自我指导的能力,加强同伴支持并发展研究能力。三个主持人组织与每个小组一起举办了两个研讨会。通过讨论,研讨会的人工制品,反馈表,人口调查,主持人撰写的笔记以及与主持人的电话会议来生成和收集数据。研究结果涵盖了儿童,年轻人和父母使用自残式残疾支持的程度以及他们对他们未来的可能性的想法,以及儿童和年轻人对他们参与学校,工作,志愿服务,关系和生活的思考。他们对未来的期望–对于儿童和年轻人,资金和支持是实现他们在这些生活领域中目标的一种手段。研究结果还涵盖了信息共享,指导,角色榜样的经验和成果以及项目组中有机会进行专门对话和讨论的时间。该项目的研究结果对儿童,年轻人和父母获取信息的政策产生了影响未来的自我指导支持方案;他们控制自己的支持;如何更好地满足信息需求;同伴支持,信息共享和讨论机会在发展自我支持能力方面的重要性;以及需要将有关支助安排的决定重点放在儿童和年轻人的愿望上。

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