...
首页> 外文期刊>Interactive Journal of Medical Research >Views of People With Epilepsy About Web-Based Self-Presentation: A Qualitative Study
【24h】

Views of People With Epilepsy About Web-Based Self-Presentation: A Qualitative Study

机译:癫痫患者对基于Web的自我介绍的观点:定性研究

获取原文

摘要

Background Web-based media, particularly social networking sites (SNSs), are a source of support for people with long-term conditions, like epilepsy. Living with epilepsy can reduce opportunities for accessing information and social support owing to transportation difficulties and stigma leading to self-isolation. However, some people with epilepsy (PWE) overcome these barriers using SNSs and other Web-based media. At present, little is known about Web-based identity and self-presentation of PWE; this study aims to address this gap. Objective This study aims to describe how the use of digital technologies, such as SNSs, impacts sense of identity in PWE. Methods We used qualitative research methods to examine Web-based media use and self-presentation in a group of 14 PWE (age range: 33-73 years; 7 men and 7 women). The median diagnosis duration was 25 years. Semistructured interviews ranged from 40 to 120 minutes, held at participants’ homes or in a public place of their choice, in the United Kingdom. QSR Nvivo 11 software was used to perform an inductive thematic analysis. Results In this study, 9 participants used Web-based media to “silently” learn from other PWE by reading user posts on SNSs and epilepsy-related forums. When asked about self-presentation, 7 participants described feeling cautious about disclosing their epilepsy to others online. Six participants presented themselves in the same manner irrespective of the situation and described their identity as being presented in the same way both online and offline. Conclusions PWE can deploy SNSs and Web-based media to manage aspects of their condition by learning from others and obtaining social support that may otherwise be difficult to access. Some PWE share openly, whereas others silently observe, without posting. Both benefit from the shared experiences of others. Privacy concerns and stigma can act as a barrier to sharing using Web-based media and SNSs. For some, Web-based media offers a chance to experiment with identity and change self-presentation, leading to gradually “coming out” and feeling more comfortable discussing epilepsy with others.
机译:基于背景的基于Web的媒体,尤其是社交网站(SNS),是对患有癫痫病等长期病的人的支持来源。由于交通困难和导致自我隔离的污名,患有癫痫病的人可以减少获得信息和社会支持的机会。但是,某些癫痫病患者(PWE)使用SNS和其他基于Web的媒体克服了这些障碍。目前,关于PWE的基于Web的身份和自我表示知之甚少。这项研究旨在解决这一差距。目的本研究旨在描述SNS等数字技术的使用如何影响PWE中的身份感。方法我们采用定性研究方法,对14名PWE(年龄范围:33-73岁; 7名男性和7名女性)中的基于Web的媒体使用和自我展示进行了研究。中位诊断持续时间为25年。在英国参与者的家中或他们选择的公共场所中进行的半结构化访谈时间从40分钟到120分钟不等。使用QSR Nvivo 11软件进行归纳主题分析。结果在这项研究中,有9名参与者使用基于Web的媒体通过阅读SNS和癫痫相关论坛上的用户帖子来“静默地”从其他PWE中学习。当被问及自我介绍时,有7位参与者表示对在网上向其他人透露自己的癫痫病感到谨慎。六名参与者不论情况如何都以相同的方式展示自己,并以在线和离线两种方式展示自己的身份。结论PWE可以通过向他人学习并获得原本难以获得的社会支持,来部署SNS和基于Web的媒体来管理其状况的各个方面。一些PWE公开共享,而另一些PWE默默地观察,没有发布。两者都受益于他人的共同经验。隐私问题和污名化可能成为使用基于Web的媒体和SNS进行共享的障碍。对于某些人而言,基于Web的媒体提供了一个尝试身份认同和改变自我表现的机会,从而逐渐“脱颖而出”并使与他人讨论癫痫病更加自在。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号