In their own words: The experience and needs of children in younger-onset Alzheimer's disease and other dementias families

被引:24
作者
Gelman, Caroline Rosenthal [1 ]
Rhames, Kate [2 ]
机构
[1] CUNY Hunter Coll, Silberman Sch Social Work, 2180 Third Ave, New York, NY 10035 USA
[2] Mt Sinai Hosp, PACT, New York, NY 10029 USA
来源
DEMENTIA-INTERNATIONAL JOURNAL OF SOCIAL RESEARCH AND PRACTICE | 2018年 / 17卷 / 03期
关键词
younger-onset dementia; children's experience; developmental disruption; role reversal; tailored services; CAREGIVERS; PEOPLE; PARENTS; CARERS; STRESS; IMPACT;
D O I
10.1177/1471301216647097
中图分类号
R4 [临床医学]; R592 [老年病学];
学科分类号
1002 ; 100203 ; 100602 ;
摘要
Because of the age of persons diagnosed with younger-onset Alzheimer's disease or other dementias (YOD), an important and as yet relatively little explored area of YOD, particularly in the United States, is the impact on young children of having a parent with YOD. After reviewing the small but growing research in this area, we report on findings from 12 in-depth interviews with children and well-parents in families with a parent with YOD on the experience and needs of children having a parent with this diagnosis. Children report disruption in many aspects of their lives: their developmental trajectory, emotional and psychological development, familial and broader social relationships, and financial stability. Despite these significant disruptions, and a dearth of information, resources, and services tailored to their individual and familial needs, these children demonstrate remarkable resilience and self-awareness. We discuss implications for interventions with these families.
引用
收藏
页码:337 / 358
页数:22
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