School of Population Health, University of Queensland, Herston, Australia.
J Intellect Disabil Res. 2012 Nov;56(11):1087-97. doi: 10.1111/j.1365-2788.2012.01637.x.
People with intellectual disability (ID) experience health inequity compared with the general population, a key contributing factor being disparities in social determinants of health. The enactment of the United Nations Convention on the Rights of Persons with Disabilities (CRPD) provides a platform for the progression and promotion of health and other interconnected rights to address barriers to the highest attainable standard of health for this populace. Rights can be brought to life through advocacy efforts. This paper explores the meaning, perceptions and experiences of advocacy by family members and paid support workers of adults with ID and locates the findings within a health and human rights discourse.
As part of a larger randomised controlled trial, 113 parents and 84 support workers of adults with ID completed a telephone interview that included open-ended questions about their understanding and experiences of advocacy. Thematic analysis was used to identify relevant themes.
Five key themes were identified. The first underscored how advocacy to 'speak up' for the person with ID is integral to both parent and support worker roles. The second and third themes considered the contexts for advocacy efforts. Access to quality health care was a core concern, along with advocacy across other areas and sectors to address the person's wider psychosocial needs. The remaining themes highlighted the many dimensions to advocacy, including differences between parent and support worker views, with parental advocacy being an expression of 'caring' and support workers motivated by a 'duty of care' to protect the individual's 'rights'.
Parent and support worker advocacy provides one means to address the social determinants of health and fulfilment of health rights of and for people with ID. Policy and practice in the context of governmental obligation under the CRPD should support advocacy and make health rights the reality not rhetoric for this group of men and women.
与普通人群相比,智力障碍者(ID)经历着健康不平等,其中一个关键的促成因素是健康社会决定因素方面的差异。《联合国残疾人权利公约》(CRPD)的颁布为促进和增进健康以及其他相互关联的权利提供了一个平台,以解决这一人群实现最高可达健康标准的障碍。权利可以通过倡导努力来实现。本文探讨了成年 ID 患者的家庭成员和付费支持工作者对倡导的理解、看法和体验,并将这些发现置于健康和人权话语中。
作为一项更大的随机对照试验的一部分,113 名成年 ID 患者的父母和 84 名支持工作者完成了电话访谈,其中包括关于他们对倡导的理解和经验的开放式问题。使用主题分析来确定相关主题。
确定了五个关键主题。第一个主题强调了为 ID 患者“发声”的倡导对于父母和支持工作者的角色都是不可或缺的。第二个和第三个主题考虑了倡导努力的背景。获得高质量的医疗保健是一个核心关注点,同时还需要在其他领域和部门进行倡导,以满足个人的广泛心理社会需求。其余主题强调了倡导的许多方面,包括父母和支持工作者观点之间的差异,父母的倡导是“关爱”的表达,而支持工作者则是出于“关爱”的责任,以保护个人的“权利”。
父母和支持工作者的倡导提供了一种解决健康社会决定因素和实现 ID 患者健康权利的手段。在 CRPD 规定的政府义务背景下的政策和实践应支持倡导,并使健康权利成为这一群体的现实,而不是空话。