“If I go down, if I crumble, then everybody does” — identity crisis and emotional strain in parents of children with rare and undiagnosed conditions: a qualitative study

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Authors: Tara Maria Hoffmann, Bettina Friedrich, Celine Lewis
Cited by: 0
References: 43

Abstract

BACKGROUND: Caring for a child with a rare condition can significantly impact parents' emotional health, yet research on the emotional impact is limited. This qualitative interview study sought to investigate the lived experiences of parents who are experiencing higher psychological burden. Participants were parents of undiagnosed children undergoing whole genome sequencing (WGS) through the Genomic Medicine Service (GMS) across multiple NHS sites in England. Parents were purposively sampled to select those scoring poorly on validated measures of anxiety, family impact and/or resilience (GAD-7, PedsQL family functioning, BRS). We interviewed 24 parents after testing but prior to the return of WGS results. Questions focused on understanding their lived experience, in particular the emotional impact of their child's condition and how they coped day-to-day. RESULTS: Semi-structured interviews were transcribed and analysed using reflexive thematic analysis, leading to the generation of the central organising concept: "The construction of a caregiver identity: Torn between being a 'hero(ine)' and being a parent." Parents' experiences as caregivers often involved a significant re-evaluation of their parental role, as they sought to provide love and support while also adjusting to changes in their envisioned family life. Societal expectations, along with the complex challenges of navigating the health and social care systems, contributed to emotional strain. In particular, mothers often adapted their personal identities to embody a 'heroic' caregiving role. The anxiety caused by the uncertainty surrounding their child's condition was also found to affect parents' mental health. Areas for psychological interventions and recommendations to support parents' mental health are identified. CONCLUSIONS: Further research is needed to explore how the return of genomic sequencing results impacts parents' emotional wellbeing, and whether and which psychological counselling modalities throughout the journey might reduce emotional distress. CLINICAL TRIAL NUMBER: Not applicable.

Fields of Study & Subjects

Family and Disability Support Research Genomics and Rare Diseases BRCA gene mutations in cancer

Publication details

Journal / source
Orphanet Journal of Rare Diseases
Publisher
Springer Science and Business Media LLC
Volume
21
Issue
1
Publication date
9 June 2026
Language
EN