Najmah Najmah, Davies Sharyn Graham, Kusnan Kusnan, Davies Tom Graham
Public Health Faculty, University of Sriwijaya, JL. Raya Palembang-Prabumulih KM 32 Indralaya, Ogan Ilir, Sumatera Selatan, Palembang 30662, Indonesia.
Monash University, Clayton, VIC, Australia.
Ther Adv Infect Dis. 2021 Dec 20;8:20499361211064191. doi: 10.1177/20499361211064191. eCollection 2021 Jan-Dec.
Women living with HIV in Indonesia encounter challenging obstacles to healthcare, which is exacerbated by COVID-19. Access is difficult as there are limited numbers of poorly supported healthcare providers. Women also face significant stigma when disclosing their HIV-status.
Our main purpose is to give a voice to disempowered women living with HIV, by normalising the discussion of HIV, to empower health professionals to better understand the issues faced by women living with HIV, and develop improved treatment practices.
Our project was guided by a Feminist Participatory Action Research (FPAR) framework. FPAR refers to 'a participatory and action-oriented approach to research that centres gender and women's experiences both theoretically and practically'. It creates meaningful participation for women throughout the research process, ensuring a collective critical consciousness that challenges oppressive attitudes, beliefs, and practices that may be deeply embedded in society.
Purposive sampling and a thematic analysis was applied to focus group discussions with 20 women living with HIV and 20 women without HIV in Palembang, South Sumatra.
When women living with HIV face a difficult decision, do they disclose their status knowing that they may face stigma and even a refusal to be treated; or do they conceal their status and face not receiving the right care? In this article, we explore the stories of women living with HIV as they seek medical treatment during the COVID-19 pandemic. We show that there is no optimal solution for women as they lose whether they disclose their HIV status or not.
Women's stories around HIV and COVID-19 intersect with conditions such as poverty and discrimination, as well as embedded gender systems, creating overlapping barriers to treatment. Government must challenge this culture by introducing a comprehensive sex and HIV education programme. This would normalise discussions of HIV-related topics, leading to improved health outcomes.
印度尼西亚感染艾滋病毒的女性在获得医疗保健方面面临诸多挑战,而新冠疫情更是加剧了这些困难。由于医疗服务提供者数量有限且支持不足,就医变得困难。女性在披露自己的艾滋病毒感染状况时还面临着巨大的耻辱感。
我们的主要目的是让无权的感染艾滋病毒的女性有发声的机会,通过使关于艾滋病毒的讨论常态化,使卫生专业人员能够更好地理解感染艾滋病毒的女性所面临的问题,并制定改进的治疗方法。
我们的项目以女权主义参与式行动研究(FPAR)框架为指导。FPAR指的是“一种以参与和行动为导向的研究方法,在理论和实践上都以性别和女性的经历为中心”。它在整个研究过程中为女性创造有意义的参与机会,确保形成一种集体批判意识,挑战可能深深植根于社会的压迫性态度、信仰和做法。
采用目的抽样和主题分析方法,对南苏门答腊巨港的20名感染艾滋病毒的女性和20名未感染艾滋病毒的女性进行焦点小组讨论。
当感染艾滋病毒的女性面临艰难抉择时,她们是在明知可能面临耻辱甚至被拒绝治疗的情况下披露自己的感染状况,还是隐瞒自己的状况并面临无法获得正确治疗的情况?在本文中我们探讨了感染艾滋病毒的女性在新冠疫情期间寻求治疗时的故事。我们发现,无论她们是否披露自己的艾滋病毒感染状况,女性都没有最优解决方案。
女性围绕艾滋病毒和新冠疫情的故事与贫困、歧视等状况以及根深蒂固的性别制度相互交织,给治疗造成了重叠障碍。政府必须通过推行全面的性与艾滋教育计划来挑战这种文化。这将使关于艾滋病毒相关话题的讨论常态化,从而改善健康结果。