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Parents’ experiences of caring for a young person with neurofibromatosis type 1 (NF1): a qualitative study

机译:父母对1型神经纤维瘤病(NF1)年轻人的照料经验:定性研究

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摘要

Neurofibromatosis type 1 (NF1) is a variable and unpredictable genetic condition that can lead to changes to an individual’s appearance. Research has started to explore children’s and young people’s experiences of living with the condition; however, there is a lack of research with parents. This exploratory qualitative study set out to examine parents’ experiences of caring for a young person with NF1. Seven parents took part in semi structured interviews which were subjected to a thematic analysis. Three key themes were identified which related to managing the uncertainty of the condition, the impact of an altered appearance, and others’ awareness and understanding of NF1. Parents felt that understanding NF1 themselves in order to support their child was beneficial whilst a perceived lack of understanding by others was cited as a significant challenge. Parents require trustworthy information and also more widely call for greater understanding and awareness of the condition.
机译:1型神经纤维瘤病(NF1)是一种可变且不可预测的遗传病,可能导致个体外貌发生变化。研究已经开始探索儿童和年轻人在这种情况下的生活经历;但是,与父母缺乏研究。这项探索性定性研究旨在检查父母照顾NF1年轻人的经历。七个父母参加了半结构化访谈,并进行了主题分析。确定了三个关键主题,这些主题与处理条件的不确定性,外观变化的影响以及其他人对NF1的认识和理解有关。父母认为理解自己的NF1来养育自己的孩子是有益的,而认为他人缺乏理解被认为是一项重大挑战。父母需要可信赖的信息,并且更广泛地要求对这种状况有更多的了解和认识。

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