Goodwin Jane, McCormack Lynne, Campbell Linda E
School of Psychology, University of Newcastle.
Health Psychol. 2017 Jan;36(1):45-54. doi: 10.1037/hea0000415. Epub 2016 Sep 22.
22q11.2 deletion syndrome (22q11DS), a complex genetic syndrome associated with more than 180 features, presents complex challenges for parents including gaining a diagnosis. This phenomenological study sought the "lived" interpretations of parents supporting an adult child with 22q11DS, a poorly researched area.
Interpretative phenomenological analysis informed a detailed and open exploration of parenting a child through to adult life with 22q11DS. Using in-depth semistructured interviews, 8 parents (2 male, 6 female) of adult children with 22q11DS were individually interviewed; providing the data set for transcription and thematic analysis.
Losing "I" Finding "self," overarched 6 subordinate themes that emerged from participants' articulated descriptions of psychological distress and psychological growth. Distress in parenting a child with 22q11DS was experienced through stigma, loss, grief, and guilt. Progressively, stigma undermined independence, friendships, and instinctual judgement. Ill-informed hierarchical structures experienced as layers of obstruction and lack of awareness of the syndrome triggered angry advocacy for their child. Diagnosis brought opposing relief and grief. In time, they came to value their unique "accomplishments," collected on their journey with 22q11DS, and in turn, consciously valued authentic "self" expressed through empathy, humility, gratitude, and pride.
Parental distress through societal, educational, and health care invalidation persisted for decades for all participants. Conversely, distress facilitated psychological growth for redefining "self" and role as parents over time. Building on this phenomenological cameo, future research can educate against the plight of 22q11DS families. It can enlighten health care professionals in buffering against associated stigma, blame, and self-doubt, and in fostering psychological well-being. (PsycINFO Database Record
22q11.2缺失综合征(22q11DS)是一种与180多种特征相关的复杂遗传综合征,给包括确诊在内的家长们带来了复杂的挑战。这项现象学研究探寻了抚养患有22q11DS成年子女的家长们的“亲身”解读,这是一个研究较少的领域。
解释现象学分析为深入且开放地探索抚养患有22q11DS的子女直至成年的养育过程提供了指导。通过深入的半结构化访谈,对8位患有22q11DS成年子女的家长(2名男性,6名女性)进行了单独访谈;提供了用于转录和主题分析的数据集。
失去“我”,找到“自我”,这一主题涵盖了从参与者对心理困扰和心理成长的清晰描述中浮现出的6个从属主题。抚养患有22q11DS的子女所经历的困扰表现为污名化、失落、悲伤和内疚。逐渐地,污名化损害了独立性、友谊和本能判断。被误解为层层阻碍的信息层级结构以及对该综合征的缺乏认识引发了为子女愤怒维权的行为。确诊带来了矛盾的解脱和悲伤。随着时间的推移,他们开始重视在与22q11DS相伴的旅程中所取得的独特“成就”,进而有意识地重视通过同理心、谦逊、感恩和自豪所表达的真实“自我”。
对于所有参与者而言,社会、教育和医疗保健方面的忽视所导致的家长困扰持续了数十年。相反,这种困扰促进了心理成长,使得家长们能够随着时间的推移重新定义“自我”和父母角色。基于这一现象学简述,未来的研究可以让人们了解22q11DS家庭的困境。它可以启发医疗保健专业人员减轻相关的污名化、指责和自我怀疑,并促进心理健康。(PsycINFO数据库记录