Information Needs of Albinos in the Yoruba Ethnic Group, Nigeria

T. Adenekan
{"title":"Information Needs of Albinos in the Yoruba Ethnic Group, Nigeria","authors":"T. Adenekan","doi":"10.20533/ijtie.2047.0533.2019.0169","DOIUrl":null,"url":null,"abstract":"Albinism, is a relatively common condition in many communities in Nigeria. However, there is a lingering dearth of information concerning the real cause(s), management and appropriate behavior towards people living with this condition. This paper explores the perception of Ibule-soro people about albinism and also closely considers the unanswered questions about their rejection. Existing literature was reviewed and an ethnographic approach was also adopted, using key informant interview to collect data from prominent members of the community. The paper found out that Albinos have information deficiencies on how to properly take care of their skin, to prevent them from being unhappy and unattractive and also take care of their already impaired vision. All the respondents confirmed that giving birth to or accommodating an albino is a taboo in Ibulesoro community. They equally reported that the Jooro river goddess abhors albinos because her request that an albino be sacrificed to it was declined. The paper concluded that there are no negative psychological, social or spiritual consequence associated with albinism except as initiated by stigmatization and discrimination. Information Professionals should therefore educate the general public concerning the ills of discrimination and social exclusion of albinos. This would make Albinos feel a sense of belonging in their communities and consequently make them live healthy and productive lives.","PeriodicalId":106634,"journal":{"name":"International Journal of Technology and Inclusive Education","volume":"72 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Technology and Inclusive Education","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20533/ijtie.2047.0533.2019.0169","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Albinism, is a relatively common condition in many communities in Nigeria. However, there is a lingering dearth of information concerning the real cause(s), management and appropriate behavior towards people living with this condition. This paper explores the perception of Ibule-soro people about albinism and also closely considers the unanswered questions about their rejection. Existing literature was reviewed and an ethnographic approach was also adopted, using key informant interview to collect data from prominent members of the community. The paper found out that Albinos have information deficiencies on how to properly take care of their skin, to prevent them from being unhappy and unattractive and also take care of their already impaired vision. All the respondents confirmed that giving birth to or accommodating an albino is a taboo in Ibulesoro community. They equally reported that the Jooro river goddess abhors albinos because her request that an albino be sacrificed to it was declined. The paper concluded that there are no negative psychological, social or spiritual consequence associated with albinism except as initiated by stigmatization and discrimination. Information Professionals should therefore educate the general public concerning the ills of discrimination and social exclusion of albinos. This would make Albinos feel a sense of belonging in their communities and consequently make them live healthy and productive lives.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
尼日利亚约鲁巴族白化病患者的信息需求
在尼日利亚的许多社区,白化病是一种相对常见的疾病。然而,关于真正的原因,管理和对患有这种疾病的人的适当行为的信息仍然缺乏。本文探讨了ible -soro人对白化病的看法,并密切关注他们拒绝的未解问题。对现有文献进行了回顾,并采用了民族志方法,使用关键线人访谈从社区知名成员那里收集数据。研究发现,白化病患者在如何正确护理自己的皮肤、如何防止自己不开心、不吸引人以及如何照顾自己已经受损的视力方面缺乏信息。所有受访者都确认,在伊布莱索罗社区,生育或收容白化病患者是一种禁忌。他们同样报告说,Jooro河女神憎恶白化病人,因为她要求将一名白化病人献给她的请求被拒绝了。该论文的结论是,除了由污名化和歧视引起的后果外,与白化病没有负面的心理、社会或精神后果。因此,信息专业人员应教育公众了解歧视和社会排斥白化病的弊病。这将使白化病患者在他们的社区中感到归属感,从而使他们过上健康和富有成效的生活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Interteach - A Total Investigation Study of Swedish Schools Regarding the Education of Pupils with Intellectual Disabilities Developing Inclusion: A Participatory Action Research of Primary Education for Students with Invisible Disabilities in Thailand A Systematic Approaches for People with Autism to Develop Logical Thinking Process with a Successful Case Crisis Management in Education: A Comparative Case Study of a Special School and a Standardized School in Greece Successful Inclusion of Students with Autism Spectrum Disorder
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1