School of Healthcare, University of Leeds, UK.
Department of Nursing and Midwifery, Sheffield Hallam University, UK.
Br J Health Psychol. 2020 May;25(2):324-338. doi: 10.1111/bjhp.12409. Epub 2020 Mar 9.
Objective Despite increased research into how caring for a child diagnosed with juvenile idiopathic arthritis (JIA) affects mothers, more needs to be known about ways in which such experiences transform their lives. Insight into the experiences of such mothers was sought through analysis of interviews with eight mothers and one father caring for a child with JIA. Design The study is situated within a larger project involving families with a child with JIA. A social constructionist approach was adopted and grounded theory including a 'negative case,' guided gathering and analysing data. Individual, semi-structured interviews were conducted based on the research question: 'What is it like to be the mother of a child with juvenile idiopathic arthritis?' Results Findings suggest that mothers find difficulty living up to the 'ideal mother' expected within Western society when forced to provide competing demands of age-related, yet illness-relevant care. The unpredictable nature of JIA means mothers face a lack of understanding from professionals so become hyper-vigilant, 'battling' on behalf of their ill child. A self-perpetuating loop develops if this is misperceived as being overprotective, leaving mothers vulnerable to being judged 'neurotic'. However, with experience, often at an emotional cost, such mothers' confidence in managing the competing demands of caring for their ill child increases such they can navigate a positive journey from 'neurotic' to 'managing' mother. Conclusions Understanding this process could help health care professionals reduce stressful experiences faced by mothers when caring for a chronically ill child. Statement of contribution What is already known on this subject? Mothers of chronically ill children are often diagnosed with anxiety and depression. Such mothers will have taken over managing their child's condition, and this can include negative experiences within the health care system. Qualitative methods enable deeper understanding of the experiences of mothers of chronically ill children. What does the study add? Potentially gendered position of mothers of children with chronic conditions. Taken for granted assumptions implicitly underpin interactions between mothers and some professionals. Greater partnership between mothers and professionals ultimately improves the care of the ill child.
目的 尽管越来越多的研究关注照顾被诊断为幼年特发性关节炎(JIA)的儿童如何影响母亲,但仍需要更多地了解这些经历如何改变她们的生活。通过分析 8 位母亲和 1 位父亲照顾患有 JIA 的孩子的访谈,了解这些母亲的经历。
设计 本研究位于一个涉及 JIA 患儿家庭的更大项目中。采用社会建构主义方法,并采用扎根理论,包括“负面案例”,指导数据收集和分析。根据研究问题进行了个人半结构化访谈:“作为一个患有幼年特发性关节炎的孩子的母亲是什么感觉?”
结果 研究结果表明,当被迫提供与年龄相关但与疾病相关的护理时,母亲发现自己难以满足西方社会中“理想母亲”的期望。JIA 的不可预测性意味着母亲面临专业人员缺乏理解,因此变得高度警惕,代表生病的孩子“战斗”。如果这被误解为过度保护,就会形成一个自我延续的循环,使母亲容易受到评判“神经质”。然而,随着经验的积累,通常是在情感上付出代价,母亲对管理照顾生病孩子的竞争需求的信心增加,使她们能够从“神经质”的母亲转变为“管理”母亲。
结论 了解这一过程可以帮助医疗保健专业人员减轻母亲在照顾慢性病儿童时面临的紧张经历。
声明 关于这个主题已经知道了什么? 慢性疾病儿童的母亲通常被诊断出患有焦虑症和抑郁症。这些母亲将已经接管了管理孩子病情的工作,这可能包括在医疗保健系统中经历的负面情况。定性方法可以更深入地了解慢性病儿童母亲的经历。 这项研究增加了什么? 患有慢性疾病儿童的母亲潜在的性别化地位。一些专业人员与母亲之间的互动隐含着不言而喻的假设。母亲和专业人员之间更大的合作关系最终会改善患病儿童的护理。