Striving to Limit the Impact: Parenting an Adult Child Who Has Multiple Sclerosis-A Grounded Theory Study.

Q1 Nursing International journal of MS care Pub Date : 2023-11-01 Epub Date: 2023-11-08 DOI:10.7224/1537-2073.2021-053
Camilla Holden, Peter Hewitt, Rachel Tams
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Abstract

Background: Multiple sclerosis (MS) is a chronic, progressive autoimmune inflammatory disorder. Its impact is felt not only by individuals but also by their families; however, little is known about the effect on their parents. This study of a cohort from the United Kingdom aimed to develop a conceptual understanding of the parental role and how it changes over time when an adult son or daughter has MS via firsthand accounts.

Methods: Twelve parents of adults with MS were recruited from a UK hospital providing outpatient services to people with MS and a branch of a national MS charity. A social constructivist grounded theory approach informed audio-recorded semistructured interviews and subsequent data analysis.

Results: In this sample, parents of adults with MS strove to limit the impact of MS on their son or daughter by undertaking practical caring activities and providing emotional support. The developed theoretical model illustrates how, in their efforts to meet this aim, parents experienced competing demands between prioritizing their child's needs and managing the effects on their life, between managing the emotional experience and protecting their child from the burden of their experience, and between an intensified instinct/desire to help while maintaining their child's independence.

Conclusions: Findings indicate that parents may be uniquely affected by their adult son or daughter having MS, advocating for their inclusion in research and clinical interventions addressing family adjustment to MS. Further research is needed to ascertain the generalizability of these findings in comparable samples and to determine the impact of sociodemographic and cultural variables on the observed phenomena.

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努力限制影响:养育患有多发性硬化症的成年子女-一项有根据的理论研究
多发性硬化症是一种慢性进行性自身免疫性炎症性疾病。它的影响不仅体现在个人身上,也体现在他们的家庭身上;然而,人们对其对父母的影响知之甚少。这项针对英国队列的研究旨在通过第一手资料了解父母的角色,以及当成年儿子或女儿患有多发性硬化症时,父母的角色如何随着时间的推移而变化。从英国一家为多发性硬化症患者提供门诊服务的医院和一家国家多发性痴呆症慈善机构的分支机构招募了12名多发性麻痹症成年人的父母。以社会建构主义为基础的理论方法为录音的半结构访谈和随后的数据分析提供了信息。在这个样本中,患有多发性硬化症的成年人的父母努力通过开展实际的关爱活动和提供情感支持来限制多发性痴呆症对他们的儿子或女儿的影响。所开发的理论模型说明,在努力实现这一目标的过程中,父母如何在优先考虑孩子的需求和管理对他们生活的影响之间,在管理情感体验和保护孩子免受经验负担之间,经历竞争性的需求,以及在保持孩子独立的同时增强帮助的本能/愿望之间。研究结果表明,父母可能会受到其成年儿子或女儿患有多发性硬化症的独特影响,主张将其纳入研究和临床干预措施,以应对多发性痴呆症的家庭适应。需要进一步的研究来确定这些发现在可比样本中的可推广性,并确定社会人口和文化变量对观察到的现象的影响。
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来源期刊
International journal of MS care
International journal of MS care Nursing-Advanced and Specialized Nursing
CiteScore
3.00
自引率
0.00%
发文量
40
期刊最新文献
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