Smith Kimberley J, Burke Jessica, Lawrence Rachel, Oputa Emily, Bailey Ruth
School of Psychology, University of Surrey, Guildford, United Kingdom.
School of Physiotherapy, Royal College of Surgeons in Ireland, Dublin, Ireland.
PLoS One. 2025 Sep 9;20(9):e0331562. doi: 10.1371/journal.pone.0331562. eCollection 2025.
There is evidence that cerebral palsy (CP) could be linked to stigma and discrimination, however current evidence is limited to small qualitative studies. The goal of this co-designed survey was to elicit information on experiences of stigma and discrimination amongst a larger sample of adults in the UK and Ireland.
Quantitative questions about sources of stigma and qualitative questions designed to elicit information on experiences of stigma were shared via an online survey.
Eighty-six people completed the qualitative survey, and 5 themes were generated that captured experiences of stigma and discrimination. Theme 1 (rigid stereotypes) captured the lack of awareness about the heterogeneity of CP. Theme 2 (impact on participation) highlighted the difficulties that participants had with participation, particularly in terms of accessibility and sexual relationships. Theme 3 (interpersonal difficulties) included the difficulties people with CP had in interactions with the public such as feel visible in some situations, invisible in others and being infantilised. Theme 4 (systematic discrimination) highlighted discrimination in the workplace, healthcare and broader environment. Theme 5 (negative emotional impact) captured the negative emotional impact that experiences of stigma and discrimination had. Quantitative responses from 48 participants indicated that stigma was a common experience (experienced by 87.5% of respondents), and the most common sources of stigma were the public, classmates and coworkers.
Results indicate that CP is linked to experiences of stigma and discrimination which arise from a lack of understanding of the heterogeneity of CP, a public lack of awareness of how to communicate with people with disabilities, inaccessible environments and negative societal attitudes towards visible impairments. Suggested ways to tackle these issues include improving understanding of CP and removing barriers to accessibility.
有证据表明脑瘫(CP)可能与耻辱感和歧视有关,然而目前的证据仅限于小型定性研究。这项共同设计的调查的目的是获取英国和爱尔兰更大样本的成年人中耻辱感和歧视经历的信息。
通过在线调查分享了关于耻辱感来源的定量问题以及旨在获取耻辱感经历信息的定性问题。
86人完成了定性调查,生成了5个主题,涵盖了耻辱感和歧视的经历。主题1(刻板印象)体现了对脑瘫异质性缺乏认识。主题2(对参与的影响)强调了参与者在参与方面遇到的困难,特别是在可达性和性关系方面。主题3(人际困难)包括脑瘫患者在与公众互动中遇到的困难,比如在某些情况下感觉被关注,在其他情况下被忽视以及被 infantilised。主题4(系统性歧视)突出了在工作场所、医疗保健和更广泛环境中的歧视。主题5(负面情绪影响)体现了耻辱感和歧视经历所带来的负面情绪影响。48名参与者的定量回答表明耻辱感是一种常见经历(87.5%的受访者有此经历),最常见的耻辱感来源是公众、同学和同事。
结果表明脑瘫与耻辱感和歧视经历有关,这些经历源于对脑瘫异质性缺乏理解、公众对如何与残疾人沟通缺乏认识、环境不便以及社会对明显残疾的负面态度。解决这些问题的建议方法包括增进对脑瘫的理解和消除可达性障碍。