Evidence map›Paper›PMID 41795864›Full record

ArticleJournal of genetic counseling2026

Defining joy after a genetic diagnosis: A narrative inquiry.

Jordan Cannon Miller, Rachel Mills, Dena Phillips Swanson, Lauren E Doyle, Camerun Washington

Abstract read
In one paragraph

Article in Journal of genetic counseling, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 authors.

Jordan Cannon MillerMS Genetic Counseling Program, The University of North Carolina Greensboro, Greensboro, North Carolina, USA.ORCID 0009-0004-8810-189X
Rachel MillsMS Genetic Counseling Program, The University of North Carolina Greensboro, Greensboro, North Carolina, USA.ORCID 0000-0003-4420-9503
Dena Phillips SwansonThe University of North Carolina Greensboro, Human Development and Family Studies, Greensboro, North Carolina, USA.ORCID 0000-0001-8196-8686
Lauren E DoyleMS Genetic Counseling Program, The University of North Carolina Greensboro, Greensboro, North Carolina, USA.ORCID 0000-0001-9239-5799
Camerun WashingtonGreenwood Genetic Center, Greenville, South Carolina, USA.ORCID 0000-0001-6166-6613

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Research on patient and family experiences often focuses on the challenges associated with receiving a genetic diagnosis, including feelings of uncertainty, grief, and emotional distress. Positive or encouraging aspects of the diagnostic journey are less well described. This study aimed to identify and describe ways in which patients and their families experience joy after receiving a genetic diagnosis using a narrative methodology. Semi-structured interviews and field observations of family activities were performed with three families recruited from a pediatric genetics clinic. These methods of data collection enabled an in-depth exploration of personal stories in a natural setting as well as crystallization of the data. Interview transcripts and observation notes were inductively coded by two research team members. Through a process of re-storying, holistic codes were utilized to craft narratives of each family's journey from genetic diagnosis to joy. Overarching themes were identified that reflect the ways in which families constructed and articulated their experiences of joy. The results, presented in the form of narrative accounts and overarching themes, provide insight into how families find joy in their daily lives. Four themes were present in all family experiences: (1) focusing on the present, (2) embracing life, (3) redefining joy, and (4) normalizing their unique journey. Living in the present moment (Theme 1) allowed families to worry less about their child's future. Participating in as many activities as possible with their child enabled families to embrace life as a journey toward joy (Theme 2). Families redefined what joy meant for them (Theme 3); joy that was once found in social outings and time spent with friends evolved into simple moments of delight, like first words or their child's laugh. All three families described an amplification of joy when others outside the family normalized their experience by recognizing their child's presence and treating them with respect (Theme 4). These findings contribute to the understanding of how families adapt to and reframe their experiences after a genetic diagnosis, offering a richer and more nuanced understanding of the lived experiences of families. They also provide valuable perspectives for medical professionals seeking to provide holistic care.

Indexed as

Genetic TestingNarrationFemaleHumansfamily experiencesgenetic diagnosisjoynarrative inquiryobservational studypediatric geneticspsychosocial impacts

Identifiers

PMID41795864
PMCPMC12967724

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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.