- Title
- "You don't know until you get there": The positive and negative "lived" experience of parenting an adult child with 22q11.2 deletion syndrome
- Creator
- Goodwin, Jane; McCormack, Lynne; Campbell, Linda E.
- Relation
- Health Psychology Vol. 36, Issue 1, p. 45-54
- Publisher Link
- http://dx.doi.org/10.1037/hea0000415
- Publisher
- American Psychological Association
- Resource Type
- journal article
- Date
- 2017
- Description
- 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.
- Subject
- velo-cardio-facial syndrome; 22q11.2 Deletion Syndrome; IPA; traumatic distress; psychological growth
- Identifier
- http://hdl.handle.net/1959.13/1330073
- Identifier
- uon:26300
- Identifier
- ISSN:0278-6133
- Rights
- This article may not exactly replicate the final version published in the APA journal. It is not the copy of record.
- Language
- eng
- Full Text
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