Evidence map›Paper›PMID 41387006›Full record

ArticleBMJ open2025

Sources and consequences of self-doubt in patients with Ehlers-Danlos syndrome: a qualitative study in Europe and North America.

Colin M E Halverson, Samantha L Vershaw, Clair A Francomano, Tom Doyle

Abstract read
In one paragraph

Article in BMJ open, 2025. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Colin M E HalversonIndiana University School of Medicine, Indianapolis, Indiana, USA.
Samantha L VershawCenter for Bioethics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Clair A FrancomanoMedical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Tom DoyleIndiana University School of Medicine, Indianapolis, Indiana, USA doylet@iu.edu.ORCID http://orcid.org/0000-0002-8565-0648

Funding

Improving Care for Rare Genetic Diseases: Patient-Provider Communication and Patient Validation in the Ehlers-Danlos SyndromesK01HG012408 · NHGRI · INDIANA UNIVERSITY INDIANAPOLIS · PI Colin Michael Egenberger Halverson · 2022 to 2026
$836k
NHGRI NIH HHS K01 HG012408
6 · The paper itself

Abstract

objectivesTo examine how clinicians' scepticism regarding patients' self-reports of subjective symptoms can be internalised, leading to psychosocial and medical harms.

designIn-depth, semi-structured qualitative interviews with the resulting data analysed using reflexive thematic analysis.

participants43 individuals with Ehlers-Danlos syndrome (EDS) from Europe and North America completed a pre-survey, and 39 of those participants completed interviews for this study. Purposive sampling was used to obtain approximately equal numbers of participants with hypermobile EDS and the molecularly defined types of EDS.

resultsPatients with both hypermobile and molecularly defined types of EDS reported high levels of self-doubt, with 73% of survey respondents questioning the extent-and even reality-of their private experiences of pain. Participants attributed much of their self-doubt to repeated dismissal and minimisation of their symptoms in healthcare settings, especially during childhood. Ultimately, self-doubt transformed not merely how they communicated their symptoms but also how they recognised, evaluated and even experienced them at a phenomenological level. While some participants developed coping strategies, others withdrew from the conventional medical system altogether.

conclusionThese findings have important implications for clinicians, who may inadvertently reinforce self-doubt through discussion of diagnostic uncertainty. Doubt need not be delegitamising. Recognising and mitigating these potential harms requires epistemic humility and attention to the psychosocial dynamics of patient-provider interaction.

Indexed as

Ehlers-Danlos SyndromeSelf ConceptAdaptation, PsychologicalAdolescentAdultEuropeFemaleHumansInterviews as TopicMaleMiddle AgedNorth AmericaPhysician-Patient RelationsQualitative ResearchYoung AdultChronic PainMEDICAL ETHICSRare Diseases

Identifiers

PMID41387006
PMCPMC12706247

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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.