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It’s Interpersonal: Family Relationships Genetic Risk and Caregiving

机译:人际交往:家庭关系遗传风险和护理

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摘要

My research program considers family relationships across the life course: in early life, with a focus on disease prevention—leveraging genetic risk information and relationships to motivate health-promoting behaviors—and in later life, with a focus on informal caregiving—identifying characteristics of those most vulnerable to, or resilient from, caregiver stress. It is fortuitous, if not tragic, then, that my research and personal worlds collided during my mother’s final 8 months of life. Here, I discuss how this experience has shifted my thinking within both arms of my research program. First, I consider the state of the science in family health history, arguing that the current approach which focuses on an individual’s first- and second-degree relatives does not take us far enough into the relational landscape to activate communal coping with disease risk. Second, I discuss caregiving from a family systems perspective. My family’s experience confirmed the importance of using a systems approach and highlighted a need to identify underlying variability in members’ expectations of caregiving roles. In so doing, I capture the significance of understanding the multiple perspectives that frame a context in which families adapt and cope with risk and disease diagnoses.
机译:我的研究计划考虑了整个生命过程中的家庭关系:在生命的早期阶段,侧重于疾病预防-利用遗传风险信息和亲缘关系来促进健康行为;在晚年的生活中,侧重于非正式护理-识别家庭的特征。最容易受到照顾者压力或能从照顾者压力中恢复过来的人。不幸的是,即使不幸,我的研究和个人世界在母亲生命的最后8个月中发生了冲突。在这里,我将讨论这种经历如何在我的研究计划的两个方面改变了我的思想。首先,我考虑了家庭健康史上的科学状况,认为当前针对个人一等和二等亲属的方法不足以使我们深入关系领域,以激发社区应对疾病风险的能力。第二,我从家庭系统的角度讨论照料。我家人的经验证实了使用系统方法的重要性,并强调需要确定成员对照护角色的期望的根本差异。通过这样做,我抓住了理解构成家庭适应和应对风险和疾病诊断的环境的多种观点的重要性。

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