'Am I gonna regret this?': The experiences of diagnostic disclosure in autistic adults.

IF 5.2 2区 心理学 Q1 PSYCHOLOGY, DEVELOPMENTAL
Autism Pub Date : 2025-05-13 DOI:10.1177/13623613251337504
Sheena K Au-Yeung, Megan Freeth, Andrew R Thompson
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引用次数: 0

Abstract

An increasing number of people receive autism diagnoses in adulthood, and there are few studies investigating autistic adults' experiences of disclosing their diagnosis. This study sought to understand autistic adults' experiences of diagnostic disclosure using interpretative phenomenological analysis. Twelve autistic adults, who received their diagnosis in adulthood, participated in one-to-one semi-structured interviews exploring their experiences of diagnostic disclosure. Quality control and reflexivity procedures were used to ensure rigour. Four group experiential themes and nine subthemes emerged: (1) 'Functions of Disclosure' (subthemes: i. Accessing Support; ii. Becoming Myself; iii. Activism and its Burden); (2) 'Approaching the Conversation' (Subthemes: i. Managing Disclosure and Reactions; ii. Disclosure Started Pre-Diagnosis; iii. Impact on Others); (3) 'Negative Effects of Preconceptions' (Subthemes: i. Disbelief and Imposter Syndrome; ii. Not Having My Needs Met; iii. Caution and Avoidance), and (4) 'Acceptance, Openness and Finding Community'. Disclosure served multiple functions for the autistic participants. There was variability in the support that autistic participants received in preparation for disclosing the diagnosis. More consistent post-diagnostic support is required to engage newly diagnosed autistic adults in considering the practicalities and potential consequences of disclosure, its benefits and challenges.Lay SummaryAn increasing number of people are receiving diagnoses of autism in adulthood. However, there are few studies investigating autistic adults' experiences of 'disclosure', that is, telling others about their autism diagnosis. The aim of this study is to understand autistic adults' experiences of telling other people that they are autistic after receiving a diagnosis during adulthood. Twelve autistic adults were interviewed about their experiences of disclosure. The interviews showed that autistic people disclose to access support, be themselves and to help others. To disclose, autistic people had to make decisions about what information to share and how to handle people's reactions. Some people started telling others about their potential diagnosis before being formally diagnosed. Disclosure has an impact on people receiving the news of disclosure. Many autistic people experienced not being believed, resulting in unmet needs. This led them to be more careful about future disclosure. However, disclosure also led to some positive experiences, where autistic people felt listened to and accepted by those they disclosed to. This led to receiving support and feeling part of a community. It is recommended that clinicians and autism service providers include discussions about disclosure as part of routine post-diagnostic support.

“我会后悔吗?”:自闭症成人的诊断披露经历。
越来越多的人在成年后被诊断为自闭症,但很少有研究调查自闭症成年人透露自己诊断的经历。本研究试图利用解释现象学分析来了解自闭症成人的诊断披露经验。12名成年后接受诊断的自闭症成年人参加了一对一的半结构化访谈,探讨他们的诊断披露经历。采用质量控制和反身性程序来确保严格性。出现了4个群体体验主题和9个副主题:(1)“披露的功能”(分主题:i.获得支持;2。成为自己;3。行动主义及其负担);(2)“接近谈话”(副主题:i.管理披露和反应;2。披露开始前诊断;3。对他人的影响);(3)“先入为主的负面影响”(副主题:1 .怀疑和冒名顶替综合症;2。我的需求没有得到满足;3。注意事项和避免事项),以及(4)“接纳、开放和寻找社区”。披露对自闭症参与者有多重作用。自闭症参与者在准备披露诊断时得到的支持存在差异。需要更一致的诊断后支持,让新诊断的自闭症成年人考虑披露的实用性和潜在后果,它的好处和挑战。越来越多的人在成年后被诊断为自闭症。然而,很少有研究调查自闭症成年人的“披露”经历,即告诉别人他们的自闭症诊断。本研究的目的是了解自闭症成年人在成年后接受诊断后告诉别人自己患有自闭症的经历。12名自闭症成年人接受了采访,询问他们的自我表露经历。访谈显示,自闭症患者愿意获得支持、做自己、帮助他人。为了公开,自闭症患者必须决定分享什么信息,以及如何处理人们的反应。有些人在被正式诊断之前就开始告诉别人他们可能的诊断。信息披露对接受信息披露的人有影响。许多自闭症患者经历了不被相信的经历,导致他们的需求得不到满足。这使得他们对未来的披露更加谨慎。然而,倾诉也带来了一些积极的经历,自闭症患者感到被他们倾诉的人倾听和接受。这让我得到了支持,感觉自己是社区的一部分。建议临床医生和自闭症服务提供者将关于信息披露的讨论作为常规诊断后支持的一部分。
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来源期刊
Autism
Autism PSYCHOLOGY, DEVELOPMENTAL-
CiteScore
9.80
自引率
11.50%
发文量
160
期刊介绍: Autism is a major, peer-reviewed, international journal, published 8 times a year, publishing research of direct and practical relevance to help improve the quality of life for individuals with autism or autism-related disorders. It is interdisciplinary in nature, focusing on research in many areas, including: intervention; diagnosis; training; education; translational issues related to neuroscience, medical and genetic issues of practical import; psychological processes; evaluation of particular therapies; quality of life; family needs; and epidemiological research. Autism provides a major international forum for peer-reviewed research of direct and practical relevance to improving the quality of life for individuals with autism or autism-related disorders. The journal''s success and popularity reflect the recent worldwide growth in the research and understanding of autistic spectrum disorders, and the consequent impact on the provision of treatment and care. Autism is interdisciplinary in nature, focusing on evaluative research in all areas, including: intervention, diagnosis, training, education, neuroscience, psychological processes, evaluation of particular therapies, quality of life issues, family issues and family services, medical and genetic issues, epidemiological research.
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