Franklin Anita, Lund Patricia, Bradbury-Jones Caroline, Taylor Julie
Faculty of Health and Life Sciences, Coventry University, Priory Street, Coventry, CV1 5FB, England.
Institute of Clinical Sciences, University of Birmingham Edgbaston, Birmingham, B15 2TT, England.
BMC Int Health Hum Rights. 2018 Jan 12;18(1):2. doi: 10.1186/s12914-018-0144-8.
Albinism is an inherited condition with a relatively high prevalence in populations throughout sub-Saharan Africa. People with oculocutaneous albinism have little or no pigment in their hair, skin and eyes; thus they are visually impaired and extremely sensitive to the damaging effect of the sun on their skin. Aside from the health implications of oculocutaneous albinism, there are also significant sociocultural risks. The impacts of albinism are particularly serious in areas that associate albinism with legend and folklore, leading to stigmatisation and discrimination. In regions of Africa those with albinism may be assaulted and sometimes killed for their body parts for use in witchcraft-related rites or to make 'lucky' charms. There is a dearth of research on the psychosocial aspects of albinism and particularly on how albinism impacts on the everyday lives of people with albinism.
There is a growing recognition and acceptance in Africa that people with albinism should be considered disabled. Thomas's social-relational model of disability proposes it is essential to understand both the socio-structural barriers and restrictions that exclude disabled people (barriers to doing); and the social processes and practices which can negatively affect their psycho-emotional wellbeing (barriers to being). In this article, we combine a social model of disability with discussion on human rights to address the lacuna surrounding the psychosocial and daily experiences of people with albinism.
Through using this combined framework we conclude that the rights of people with albinism in some regions of Africa are not being enacted. Our debate highlights the need to develop a holistic concept of rights for children and young people with albinism which sees human rights as indivisible. We illuminate some of the specific ways in which the lives of children with albinism could be improved by addressing 'barriers to being' and 'barriers to doing', at the heart of which requires a shift in attitude and action to address discrimination.
白化病是一种遗传性疾病,在撒哈拉以南非洲的人群中患病率相对较高。患有眼皮肤白化病的人在头发、皮肤和眼睛中几乎没有或完全没有色素;因此,他们视力受损,并且对阳光对皮肤的损害作用极为敏感。除了眼皮肤白化病对健康的影响外,还存在重大的社会文化风险。在那些将白化病与传说和民俗联系起来的地区,白化病的影响尤为严重,导致污名化和歧视。在非洲一些地区,患有白化病的人可能会因身体部位被用于与巫术相关的仪式或制作“幸运”符咒而遭到袭击,有时甚至被杀害。关于白化病心理社会方面的研究匮乏,尤其是关于白化病如何影响白化病患者日常生活的研究。
在非洲,人们越来越认识到并接受白化病患者应被视为残疾人。托马斯的残疾社会关系模型提出,既要理解排除残疾人的社会结构障碍和限制(行为障碍),也要理解可能对其心理情感幸福产生负面影响的社会过程和做法(存在障碍),这一点至关重要。在本文中,我们将残疾社会模型与关于人权的讨论相结合,以解决围绕白化病患者心理社会和日常经历的空白。
通过使用这个综合框架,我们得出结论,非洲一些地区白化病患者的权利并未得到落实。我们的讨论强调,需要为白化病儿童和青少年制定一个整体的权利概念,将人权视为不可分割的。我们阐明了一些具体方法,通过解决“存在障碍”和“行为障碍”来改善白化病儿童的生活,而这核心在于需要转变态度和行动以应对歧视。