...
首页> 外文期刊>International psychogeriatrics >Nobody asked me how I felt: Experiences of adult children of persons with young-onset dementia
【24h】

Nobody asked me how I felt: Experiences of adult children of persons with young-onset dementia

机译:没有人问我我的感受:痴呆症患者成年子女的经历

获取原文
获取原文并翻译 | 示例
           

摘要

Background: There are few studies of young persons (< 65 years old) with dementia, and the situation of their children has been a neglected research field. The aim is explore how adult children of a parent with youngonset dementia have experienced the development of their parents' dementia and what needs they have for assistance. Method: Qualitative interviews with 14 informants (aged 20-37 years; 12 daughters, 2 sons) during 2011 were conducted and analyzed thematically. Results: The informants experienced great burdens and felt neglected during the development of their parents' dementia, both by their family and by health and social services. They emphasized a need to be seen as individuals, with their experiences, feelings, and personal needs for assistance. The stresses experienced during the development of parental dementia seemed to increase conflicts in the family. There were variations in reactions between children, depending on age, gender, family structure and relationships, responsibilities, personal relations with both parents, and whether there was an adult primary caregiver. The length of time living together with the parent with dementia seemed to increase the stress and burden to the children. They expressed a great need for information and support. Conclusion: The findings strengthen the notion of the need for family-oriented support, combined with personcentered care for the children according to their needs. In addition, group meetings and contact with other young people in the same stage of life could be of interest for some.
机译:背景:对患有痴呆症的年轻人(<65岁)的研究很少,其孩子的状况一直是被忽视的研究领域。目的是探讨患有年轻性痴呆症的父母的成年子女如何经历其父母痴呆症的发展以及他们需要什么帮助。方法:2011年对14名线人(年龄在20-37岁; 12名女儿,2个儿子)进行了定性访谈,并进行了主题分析。结果:在父母痴呆症的发展过程中,举报人承受了沉重的负担,并被家人,健康和社会服务所忽视。他们强调需要被视为具有个人经验,感情和个人援助需求的个人。父母痴呆症发展过程中所承受的压力似乎加剧了家庭中的矛盾。儿童之间的反应会有所不同,具体取决于年龄,性别,家庭结构和关系,责任,与父母双方的个人关系以及是否有成人的主要照顾者。与患有痴呆症的父母一起生活的时间似乎增加了孩子的压力和负担。他们表示非常需要信息和支持。结论:这些发现强化了需要以家庭为导向的支持的观念,并结合以人为本的对儿童的照料。此外,一些人可能会参加小组会议并与生活在同一阶段的其他年轻人接触。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号