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Parental Life-Limiting Illness: What Do We Tell the Children?

机译:限制生育的父母疾病:我们告诉孩子们什么?

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Being diagnosed with and having a life-limiting illness is a stressful experience which is compounded when the patient has dependent children. An important aspect of the patient’s psychosocial care should include recognition that their children are also likely to experience severe stress because of the illness. However, children’s needs are often overlooked during the illness. These needs include information about the illness. Health care professionals have a significant role in supporting patients to communicate with their children. This study aims to increase our understanding of children’s experiences when a parent has a life-limiting illness by exploring bereaved children’s experiences of the support they received when their parent had a life-limiting illness, and professionals’ perspectives of the support offered to children. 7 children (aged between 9 and 24), and 16 health care professionals were interviewed about communication during parental illness. Children report needing open, clear and age appropriate conversations with parents and health care professionals to help them begin to obtain some meaning from the situation. The importance of communication is discussed, with particular reference to the role health care professionals have in supporting these conversations.
机译:被诊断患有并有生命危险的疾病是一种压力大的经历,当患者有被抚养的孩子时,这种经历会更加复杂。患者的心理社会护理的一个重要方面应该包括认识到,他们的孩子也可能因病而承受严重的压力。但是,患病期间儿童的需求经常被忽略。这些需求包括有关疾病的信息。卫生保健专业人员在支持患者与孩子沟通方面起着重要作用。这项研究的目的是通过探索失去亲人的孩子在父母患上致命性疾病时获得的抚养经验的经验,以及专业人员对子女提供的抚养费的观点,从而加深我们对父母患上生命有限的疾病的理解。采访了7名儿童(9岁至24岁)和16名医疗保健专业人员,了解父母患病期间的沟通情况。儿童报告需要与父母和医疗保健专业人员进行公开,清晰和适当的年龄对话,以帮助他们开始从这种情况中获得一些意义。讨论了交流的重要性,特别是提到了医疗保健专业人员在支持这些对话中的作用。

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