为艾滋病毒感染者建设社区:共同赋权与参与式行动研究

Patricia Miller, Brent Oliver, Ken LaPointe, Kimberley Samson, Vincenzo Sabella
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摘要

卡尔加里艾滋病病毒感染者社会协会(CHSS)自行决定并组织了几次社会娱乐月度活动,以减少和了解艾滋病病毒感染者每天面临的社会隔离和污名化的影响。研究发现,COVID-19 对艾滋病病毒感染者的生活产生了影响,因为它使那些已经因为感染艾滋病病毒而蒙受耻辱的人变得更加孤立。研究采用参与式行动研究(PAR)方法,并在活动结束时进行焦点小组讨论,展示了 COVID-19 以及与之相关的隔离是如何影响艾滋病病毒感染者的生活的。这项研究包括三次面对面的社交聚会,共有 60 名艾滋病病毒感染者参加,以及一个有 10 名参与者参加的焦点小组。阿尔伯塔省卡尔加里市周边的社交聚会表明,拥有一个安全的空间,并得到生活在类似系统障碍下的人们的支持,是如何缓冲艾滋病毒感染者的有害社会污名化及其隐秘性的。这项研究让人们更好地了解到,在 COVID-19 期间,艾滋病病毒感染者的社会联系(包括在线支持)如何增强他们的总体归属感、减少污名化,并成为他们整体心理健康的保护因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Building Community for Those Living With HIV: Co-Empowerment and Participatory Action Research
The Calgary HIV Social Society (CHSS) self-determined and organized several social-recreational monthly events to reduce and understand the effects of social isolation and stigma that people living with HIV face every day. It has been found that COVID-19 had impacted the lives of people living with HIV by creating significant isolation for those already stigmatized because of living with HIV. Using a Participatory Action Research (PAR) methodology and focus group at the end of the events, the research showed how COVID 19, and the related concurring isolation has impacted the lives of people living with HIV. The research included three in-person social gatherings with a total of 60 participants living with HIV attending and a focus group with 10 participants. The social gatherings around the city of Calgary, Alberta showed how the possibility of having a safe space and being supported by people who live with similar systematic barriers, buffers the detrimental, social stigmatization of living with HIV and its secrecy. The research brought forth a better understanding on how social connection (including on-line support) during COVID-19 for persons living with HIV increased their general sense of belonging, reduced stigma and was a protective factor for their overall mental health.
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