Doświadczenia emocjonalne rodziców w procesie diagnozy dziecka ze spektrum zaburzeń autystycznych

J. Szczepańska
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Abstract

As the population of children who are diagnosed as being on autism spectrum grows in number, so does the interest of scientists in this subject. Specialists in various fields increasingly not only focus on the children themselves but also examine their families’ situation and functioning. By doing so, they aim to understand the family as a system. Numerous empirical studies have demonstrated that when a baby with a disability is born or when it develops in an abnormal way, this becomes a source of suffering, anxiety, grief, or hostility towards the outside world. Such a situation is viewed as a crisis, a loss, and a process of mourning; working through these experiences is difficult, requires tremendous work, and requires external support in many cases. For these reasons, this paper provides a brief overview of parents’ experiences in the process of diagnosing a child; it cites the literature on the topic and shows the different paths of these experiences.
随着被诊断为自闭症谱系的儿童人数的增加,科学家对这一主题的兴趣也在增加。各个领域的专家不仅越来越关注儿童本身,而且还研究他们的家庭状况和功能。通过这样做,他们的目标是将家庭作为一个系统来理解。大量的实证研究表明,当一个残疾婴儿出生或以不正常的方式发育时,这成为痛苦、焦虑、悲伤或对外部世界怀有敌意的根源。这种情况被视为一种危机,一种损失,一种哀悼的过程;通过这些经历是困难的,需要大量的工作,并且在许多情况下需要外部支持。基于这些原因,本文简要概述了父母在诊断儿童过程中的经验;它引用了有关该主题的文献,并展示了这些经历的不同路径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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