Disability, Stigma, and Children's Developing Selves

Author(s):  
Misa Kayama ◽  
Wendy Haight ◽  
May-Lee Ku ◽  
Minhae Cho ◽  
Hee Yun Lee

Stigmatization is part of the everyday lives of children with disabilities, their families, and their friends. Negative social encounters, even with perfect strangers, can dampen joyful occasions, add stress to challenging situations, and lead to social isolation. This book describes a program of research spanning a decade that seeks to understand disabilities in their developmental and cultural contexts. The authors are especially interested in understanding adults’ socialization practices that promise to reduce stigmatization in the next generation. Guided by developmental cultural psychology, including the concept of “universalism without uniformity,” the authors focus on the understandings and responses to disability and associated stigmatization of elementary-school educators practicing in Japan, South Korea, Taiwan, and the U.S. Educators from all four cultural groups expressed strikingly similar concerns about the impact of stigmatization on the emerging cultural self, both of children with disabilities and their typically developing peers. Educators also described culturally nuanced socialization goals and practices pertaining to inclusive education. In Japan, for instance, educators emphasized the importance of peer group belonging and strategies to support the participation of children with disabilities. In the U.S., educators placed relatively more emphasis on individual development and discussed strategies for the equitable treatment of children with disabilities. Educators in South Korea and Taiwan emphasized the cultivation of compassion in typically developing children. The understanding gained through examination of how diverse individuals address common challenges using cultural resources available in their everyday lives provides important lessons for strengthening theory, policy, and programs.

Author(s):  
Misa Kayama ◽  
Wendy L. Haight ◽  
May-Lee Ku ◽  
Minhae Cho ◽  
Hee Yun Lee

In responding to the impact of stigmatization on children with disabilities, educators from Japan, South Korea, Taiwan, and the U.S. typically considered children’s individual self, for example, their academic progress, as well as socialization practices to help them function better in their classrooms (socially embedded self). Their responses, however, were culturally nuanced. Educators in Japan described supporting children’s sense of belonging to their classroom peer groups, while educators in South Korea described helping children become contributing members of mutually supportive classroom peer groups. Educators in Taiwan helped children to regulate their intense emotions resulting from frustration and failure to meet expectations, and educators in the U.S. worked to support children’s self-esteem. Chapter 7 also presents educators’ similar and culturally nuanced discussions of socialization practices to reduce the effect of peers’ disability and stigmatization on typically developing children’s cultural selves.


2021 ◽  
Vol 20 (2) ◽  
pp. 65-78
Author(s):  
Ivana Tomić ◽  
Milena Nikolić

Introduction. Successful implementation of inclusive education, among other things, depends on the attitudes of the participants in the process itself. Although teachers are considered a key factor in the implementation of inclusion, the role of parents should not be neglected. Objective. The main goal of the paper was to examine the attitudes of parents of typically developing children towards the inclusion of children with disabilities, and to examine the impact of gender, level of education, place of residence, and age of the child on parents' attitudes. Parents' opinions on the impact of the type of developmental disabilities on their children's education were also examined. Methods. The research sample consisted of 293 parents of typically developing children from the territory of Bosnia and Herzegovina. Parents' attitudes were examined by the Survey of Parents' Attitudes towards Inclusion (SPATI). Results. Parents of typically developing children expressed positive attitudes towards the inclusion of children with disabilities. Their attitudes were not affected by gender, level of education, place of residence, and age of the child. They expressed the most positive attitude towards the inclusion of children with sensory impairments (hearing, vision) and children with moderate or mild intellectual disabilities, while their attitude towards the inclusion of children with severe developmental disabilities (autism, severe intellectual disabilities) was less positive. Conclusion. The results of the research indicate the need for further research on this issue and planning of appropriate programs aimed at developing positive attitudes towards inclusive education of students with all kinds of disabilities.


Author(s):  
Sungho Cho ◽  
NaRi Shin ◽  
Dae Hee Kwak ◽  
Amy Chan Hyung Kim ◽  
Won Seok Jang ◽  
...  

Author(s):  
Misa Kayama ◽  
Wendy L. Haight ◽  
May-Lee Ku ◽  
Minhae Cho ◽  
Hee Yun Lee

Chapter 4 considers how educators’ perspectives and practices may be affected by the broad developmental changes experienced by the children they educate. Over the past few years, there has been an increasing interest in the importance of understanding the experiences of children with disabilities. This chapter summarizes available literature, conducted almost exclusively in Western cultural contexts, on the experiences of children with disabilities and their typically developing siblings and peers focusing on disability, stigmatization, and the cultural self. Then it considers related socialization practices by adults in East Asian countries and the U.S.


Author(s):  
Misa Kayama ◽  
Wendy L. Haight ◽  
May-Lee Ku ◽  
Minhae Cho ◽  
Hee Yun Lee

Chapter 8 describes educators’ perceptions of how stigmatization affects their relationships with parents whose children have disabilities and how they respond to these challenges in Japan, South Korea, Taiwan, and the U.S. Educators from all four cultural groups characterized the development of collaborative relationships with parents as critical to supporting the school success of children with disabilities. They also described challenges posed by stigmatization to those relationships and solutions to those challenges. The perspectives of educators from diverse contexts can help identify cultural blind spots and provide insights into the development of effective culture- and stigma-sensitive strategies to build relationships with parents to better support their children.


2019 ◽  
Vol 85 (4) ◽  
pp. 432-452 ◽  
Author(s):  
Tzu-Jung Lin ◽  
Jing Chen ◽  
Laura M. Justice ◽  
Brook Sawyer

Drawing from a social network perspective, we examined the extent to which children with and without disabilities play with each other in preschool inclusive classrooms and identified malleable child characteristics that would support children forming these cross-status play interactions. A total of 200 children with disabilities and 301 children without disabilities participated in this study ( Mage = 52.39 months, SDage = 6.13). Results showed that children with and without disabilities did not differ in the extent to which they formed cross-status play interactions after pragmatic language and self-regulation were taken into account. However, typically developing children were more likely to form same-status play interactions than children with disabilities. Children’s cross-status play interactions were predicted by self-regulation ability, which was fully mediated by their pragmatic language. The impact of pragmatic language on the formation of cross-status play interaction was greater for children with disabilities than their typically developing peers.


Author(s):  
Misa Kayama ◽  
Wendy L. Haight ◽  
May-Lee Ku ◽  
Minhae Cho ◽  
Hee Yun Lee

Interlude 2 briefly illustrates the perspectives of Japanese and South Korean parents who have children with disabilities. It also describes strategies used for approaching parents on this highly sensitive topic. Japanese parents discussed their children’s challenges, the benefits they perceived of disability services, and their preferences for how their children should be supported at school. South Korean parents described their children’s challenges including stigmatization, the impact on typically developing siblings, and the importance of the support they received from other parents raising children with disabilities. Understanding parents’ perspectives on their children’s disabilities and associated stigmatization can facilitate collaborative parent–educator relationships necessary to supporting the school functioning of children with disabilities.


2021 ◽  
Author(s):  
◽  
Nor Heu

<p>The inclusive education (IE) strategy promotes the inclusion of all children regardless of their abilities into mainstream schools. Little, however, is known about its impact on the inclusion of children with all sorts of disabilities at the primary school level. This study explores this issue. The main objective of this study is to analyse the impact of the Lao IE strategy in developing the public mainstream primary school system so as to be responsive to the needs of primary school students with impairments in Vientiane, Lao PDR. This is a qualitative research project which adopted semi-structured interviews, observations, and document analysis. Data was gathered from 45 participants from different backgrounds; notes recorded direct observations in primary schools; and documents such as reports and statistics were collected during the field work in Vientiane over the two month period of May and June 2015. The study established that many countries have experienced challenges in translating the IE concept into practice. Lao PDR also faces similar challenges.  The study suggests that despite the ongoing continuous improvement of the Lao IE, the principle of inclusion is not yet fully employed. Children with more complex disabilities, such as being blind, deaf, mute or having an intellectual impairment, are still restricted to studying in special schools. This practice appears to be in contradiction to the principles of inclusion, to the social model of disabilities, and to a rights-based approach to education. In addition, the lack of government funding allocated specifically to implement the IE strategy at both national and local levels indicates the current weakness of the Lao IE system. As a consequence, children with more complex impairments still cannot receive meaningful and quality education in almost all public mainstream primary schools.  Furthermore, it is evident that, although the Lao IE policy officially targets all children, in practice there has, as yet, been little impact on mainstream primary schools that are the focus of this research. Data regarding students with impairments is not collected by the relevant authorities in a consistent system. The IE policy has not been fully translated into mainstream primary school policies and development plans. The existing ‘IE’ schools continue to experience challenges in accessing the essential financial and technical supports they need to prepare to accept children with disabilities. Basic facilities and disabilities-related services are mostly unavailable. Importantly, the Ministry of Education and Sports (MOES) has not yet officially recognised and approved the use of braille and sign language, even though these languages have been developed by the Ministry of Health (MOH), the Centre of Medical Rehabilitation (CMR) to teach only children with disabilities who are enrolled in the Centre. Many people have criticised MOES for not taking the lead in the provision of education for children with disabilities. Although MOES has depended on the CMR’s expertise and resources to support its IE strategy, children with disabilities continuously experience obstacles in accessing and learning together with none disabled students in public mainstream primary schools that adequately meet their basic needs. This is why many people believe that children with disabilities cannot attend mainstream primary schools and the best place to learn was the CMR.  Finally, participants still retained a medical perspective regarding disabilities. The Lao government itself still translates ‘disabilities’ as medically defined health issues. An understanding of disabilities in terms of the more recent social model was not common among participants in this study. Given that many people hold the medical perspective, individual impairments continue to be blamed as barriers to accessing services such as education, which is opposed to the social model approach to disabilities. The present stage of development of Lao IE strategy still seems to reinforce the exclusion of children with disabilities from accessing the education that is their human right.</p>


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