4.5 Article

You Don't Know Until You Get There: The Positive and Negative Lived Experience of Parenting an Adult Child With 22q11.2 Deletion Syndrome

Journal

HEALTH PSYCHOLOGY
Volume 36, Issue 1, Pages 45-54

Publisher

AMER PSYCHOLOGICAL ASSOC
DOI: 10.1037/hea0000415

Keywords

velo-cardio-facial syndrome; 22q11.2 Deletion Syndrome; IPA; traumatic distress; psychological growth

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Objectives: 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. Method: 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. Results: 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. Conclusion: 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.

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