Evidence map›Paper›PMID 42265703›Full record

ArticleOrphanet journal of rare diseases2026

"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.

Tara Maria Hoffmann, Bettina Friedrich, Celine Lewis

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Tara Maria HoffmannPopulation, Policy and Practice Department, UCL Great Ormond Street Institute of Child Health, London, UK.
Bettina FriedrichPopulation, Policy and Practice Department, UCL Great Ormond Street Institute of Child Health, London, UK.
Celine LewisPopulation, Policy and Practice Department, UCL Great Ormond Street Institute of Child Health, London, UK. celine.lewis@ucl.ac.uk.ORCID http://orcid.org/0000-0001-7169-1521

Funding

National Institute for Health and Care Research NIHR300099
6 · The paper itself

Abstract

backgroundCaring 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.

resultsSemi-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.

conclusionsFurther 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.

Indexed as

ParentsRare DiseasesAdultAnxietyCaregiversChildEmotionsFemaleHumansMaleQualitative ResearchStress, PsychologicalWhole Genome SequencingEmotional wellbeingFamily dynamicsGenomic sequencingMental healthParent caregiversPsychological counsellingPsychosocial insightsRare conditionUncertaintyUndiagnosed condition

Identifiers

PMID42265703
PMCPMC13602518

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.