Donnelly Leeann R, Bailey Lauren, Jessani Abbas, Postnikoff Jonathan, Kerston Paul, Brondani Mario
J Assoc Nurses AIDS Care. 2016 Nov-Dec;27(6):768-783. doi: 10.1016/j.jana.2016.07.003. Epub 2016 Jul 21.
HIV stigma may prevent people from obtaining a timely diagnosis and engaging in life-saving care. It may also prevent those who are HIV infected from seeking health and education resources, particularly if they are from marginalized communities. We inductively explored the roots of stigma and its impact on health services and resource seeking as experienced by HIV-infected members of marginalized communities in Vancouver, British Columbia, Canada, using a community-based participatory research framework. Five peer-facilitated focus groups were conducted with 33 Aboriginal, Latino, Asian, and African participants. Thematic analysis of the experiences revealed four dominant themes: beginnings of stigma, tensions related to disclosure, experiences of service seeking, and beyond HIV stigma and discrimination. Persons living with HIV from Aboriginal and refugee communities continue to experience disproportionate rates of stigma and discrimination. Fear remains a prime obstacle influencing these groups' abilities and willingness to access care in various settings.
对艾滋病病毒的污名化可能会阻碍人们及时获得诊断并接受挽救生命的治疗。这也可能会使那些感染了艾滋病病毒的人无法获取健康和教育资源,尤其是当他们来自边缘化社区时。我们采用基于社区的参与性研究框架,归纳性地探究了加拿大不列颠哥伦比亚省温哥华市边缘化社区中感染艾滋病病毒的成员所经历的污名化根源及其对医疗服务和资源寻求的影响。我们与33名原住民、拉丁裔、亚裔和非洲裔参与者进行了5次由同伴主持的焦点小组讨论。对这些经历的主题分析揭示了四个主要主题:污名化的起源、与披露相关的紧张关系、寻求服务的经历,以及超越艾滋病病毒污名化和歧视。来自原住民和难民社区的艾滋病病毒感染者仍然遭受着不成比例的污名化和歧视。恐惧仍然是影响这些群体在各种情况下获得治疗的能力和意愿的主要障碍。