Disability, Stigmatization, and Children's Developing Selves


Book Description

Guided by developmental cultural psychology, this volume focuses on understandings and responses to disability and stigmatization from the perspectives of educators practicing in Japan, South Korea, Taiwan, and the United States. Synthesizing research that spanned over a decade, this volume seeks to understand disabilities in different developmental and cultural contexts. The research presented in this book found that educators from all four cultural groups expressed strikingly similar concerns about the impact of stigmatization on the emerging cultural self, both with children with disabilities and their typically developing peers, while also describing culturally nuanced socialization goals and practices pertaining to inclusive education. In providing a multicultural view of common challenges in classrooms from around the world, this book provides important lessons for the improvement of children's lives, as well as the development of theory, policy, and programs that are culturally sensitive and sustainable.




Disability, Stigmatization, and Children's Developing Selves


Book Description

Guided by developmental cultural psychology, this volume focuses on understandings and responses to disability and stigmatisation from the perspectives of educators practising in Japan, South Korea, Taiwan, and the United States. Synthesising research that spanned over a decade, this volume seeks to understand disabilities in different developmental and cultural contexts.




Ending Discrimination Against People with Mental and Substance Use Disorders


Book Description

Estimates indicate that as many as 1 in 4 Americans will experience a mental health problem or will misuse alcohol or drugs in their lifetimes. These disorders are among the most highly stigmatized health conditions in the United States, and they remain barriers to full participation in society in areas as basic as education, housing, and employment. Improving the lives of people with mental health and substance abuse disorders has been a priority in the United States for more than 50 years. The Community Mental Health Act of 1963 is considered a major turning point in America's efforts to improve behavioral healthcare. It ushered in an era of optimism and hope and laid the groundwork for the consumer movement and new models of recovery. The consumer movement gave voice to people with mental and substance use disorders and brought their perspectives and experience into national discussions about mental health. However over the same 50-year period, positive change in American public attitudes and beliefs about mental and substance use disorders has lagged behind these advances. Stigma is a complex social phenomenon based on a relationship between an attribute and a stereotype that assigns undesirable labels, qualities, and behaviors to a person with that attribute. Labeled individuals are then socially devalued, which leads to inequality and discrimination. This report contributes to national efforts to understand and change attitudes, beliefs and behaviors that can lead to stigma and discrimination. Changing stigma in a lasting way will require coordinated efforts, which are based on the best possible evidence, supported at the national level with multiyear funding, and planned and implemented by an effective coalition of representative stakeholders. Ending Discrimination Against People with Mental and Substance Use Disorders: The Evidence for Stigma Change explores stigma and discrimination faced by individuals with mental or substance use disorders and recommends effective strategies for reducing stigma and encouraging people to seek treatment and other supportive services. It offers a set of conclusions and recommendations about successful stigma change strategies and the research needed to inform and evaluate these efforts in the United States.




The Social Psychology of Childhood Disability


Book Description

‘Some years ago I read the phrase "the spontaneous revulsion to the deformed". The phrase seemed to be both potent and provocative: Was there a spontaneous revulsion to disabilities in children or did such conditions evoke a more compassionate response?’ Originally published in 1978, the problems of the disabled were no longer confined to the medical and educational professionals, but had become the concern of the community as a whole. Using terminology very much of the time, the author shows how attitudes towards different kinds of disability had developed at the time; they varied both regionally and by social class, sometimes calling into question the accepted ‘facts’ about the distribution of a particular condition. Most importantly, the author examines these attitudes together with many other social and psychological factors in relation to their impact on the social behaviour and developing self-image of the disabled child. It becomes clear that the dangers of categorization and the difficulties in overcoming stigma have a profound influence on the education and socialization of disabled children. This book will be of historical interest to students and teachers of psychology, education, social work and rehabilitation; and it will provide insight for parents and all those concerned with the care and development of the disabled child about how far we have come.




The Stigma of Disease and Disability


Book Description

The two main sections of the book comprise chapters on 10 specific illnesses and conditions and chapters relating to broader issues (stigma and family, overcoming stigma, stigma across cultures and future directions). The book concludes with observations on what has not worked in overcoming stigma as well as possible future directions. (Psychology)




Neurological, Psychiatric, and Developmental Disorders


Book Description

Brain disordersâ€"neurological, psychiatric, and developmentalâ€"now affect at least 250 million people in the developing world, and this number is expected to rise as life expectancy increases. Yet public and private health systems in developing countries have paid relatively little attention to brain disorders. The negative attitudes, prejudice, and stigma that often surround many of these disorders have contributed to this neglect. Lacking proper diagnosis and treatment, millions of individual lives are lost to disability and death. Such conditions exact both personal and economic costs on families, communities, and nations. The report describes the causes and risk factors associated with brain disorders. It focuses on six representative brain disorders that are prevalent in developing countries: developmental disabilities, epilepsy, schizophrenia, bipolar disorder, depression, and stroke. The report makes detailed recommendations of ways to reduce the toll exacted by these six disorders. In broader strokes, the report also proposes six major strategies toward reducing the overall burden of brain disorders in the developing world.




Understanding the Experience of Disability


Book Description

Rehabilitation psychologists have long argued that situational constraints (e.g., missing ramps, lack of Braille signage, nondisabled peoples' attitudes) create greater social barriers and behavioral restrictions for people with disabilities (PWDs) than do the disabilities themselves. In other words, as social psychologist Kurt Lewin argued, situational factors, including the perceptions and actions of other people, often have greater impact on the experience of disability than do the personal qualities of PWDs themselves. Thus, the experience of disability is shaped by a variety of psychosocial forces and factors, some of which enhance while others hinder daily living. For adequate understanding and to plan constructive interventions, psychological science must attend to how the disabled person and the situation interact with one another. Understanding the Experience of Disability: Perspectives from Social and Rehabilitation Psychology is an edited book containing chapters written by social and rehabilitation psychologists who study how social psychological theory can inform our understanding of the experience of disability and rehabilitation. Chapters are arranged topically into four sections: Established areas of inquiry (e.g., stigma, social biases, stereotyping), mainstream topics (e.g., women, culture and race, aging), emerging issues (e.g., implicit attitudes, family and parenting issues, positive psychology), and issues of injustice, advocacy, and social policy (e.g., perceived injustice, disability advocacy, policy implications). Besides informing advanced undergraduate and graduate students and professional (researchers, practitioners) audiences, the book will help families and caregivers of PWDs, policy makers, and PWDs themselves, understand the social psychological processes linked to disability.




Intellectual Disability and Stigma


Book Description

This book examines how intellectual disability is affected by stigma and how this stigma has developed. Around two per cent of the world's population have an intellectual disability but their low visibility in many places bears witness to their continuing exclusion from society. This prejudice has an impact on the family of those with an intellectual disability as well as the individual themselves and affects the well-being and life chances of all those involved. This book provides a framework for tackling intellectual disability stigma in institutional processes, media representations and other, less overt, settings. It also highlights the anti-stigma interventions which are already in place and the central role that self-advocacy must play.




Beyond Stigma


Book Description

This dissertation focuses on adolescent disability identity development and centers the expertise about this phenomenon in the lived experiences of students and adults with disabilities, and a larger context of disability community and culture. The purpose of understanding disability identity is twofold: first, to conceptualize adolescent disability identity development from within educational contexts, and second, to understand the impact of participatory research methods towards this development. To date, the scholarship around disability identity development and adolescents, particularly in the field of special education, has focused on development of social skills for friendships with nondisabled peers (e.g. Zambo, 2010) and negotiation (or attempted negation) of stigma, which is itself due to the overwhelmingly negative social and cultural meanings of the disability label itself (e.g. Kauffman, 2003; Shifrer, 2013). Teachers, themselves frequently nondisabled (Hart & Williams, 2009) attempt to support students academically and socially through this negotiation of stigma, from within their own training and personal experience as a nondisabled student (Linton, 1998). Changing this way of "managing" disability requires a shift in both the conceptual and methodological focus of disability from within the context of special education, and a shift from labeling disability as a feature of a person which must be remediated and normalized. Ware (2002) notes that this shift is "particularly significant in K-12 public schools, where schools reproduce an "understanding of disability warped by the shroud of shame, pity and tragedy in which the disabled students' needs, deficits, and problems are wrapped- constructing the student's institutional identity" (p. 152). Instead of assuming this institutional identity as a natural consequence of disability labeling, the study positions disabled students as knowledge holders and experts in their own identities. The first phase of the dissertation involved qualitative interviewing and reflection from disabled adults on their educational experiences and disability awareness in school, which informed and helped identified "levers" of disability identity that have an impact on growth, development, and awareness of each participant's sense of themselves as members of a disability community. Following the interviews and participation of the disabled adults, the second part of the study involved participation of adolescents with disabilities in a large public high school special education program in the Pacific Northwest. The adolescent participants engaged in both qualitative interviewing about disability identity and a photovoice project where they discussed their identity experiences in school related to disability. Following this phase, the adult participants engaged with the students' photovoice materials to identify shared experiences and identity resources (Gee, 2003) of disability identity development in school. Common shared disability identity resources included participation in self-contained special education courses and removal from general education; an initial realization of disability and difference; silence around disability in curriculum and from special and general education teachers; and attempts at participation in disability community in mostly online spaces. This study contributes to the theoretical and methodological conversations around adolescent experiences of disability in schools in a few important ways. First, it centers student meaning-making around disability as the major source for both data collection and This is the intolerable cost of special education and related disability research that treats individuals with disabilities as a subject under study and intervention, rather than meaning-makers, capable of creating community and solidarity, negotiating power and stigma, and articulating the changes that need to be made to make their communities more inclusive. Understanding these ideas about identity could potentially lead to developing schools and instructional spaces that support positive disability identity, which could have far-reaching impact on the academic and social experiences of students with disabilities in school.




Competence and Acceptance of Children with Developmental Disabilities


Book Description

The purpose of this research was to examine the relationship of the self-concepts of a sample of 248 children with developmental disabilities with demographic variables and measures of child functioning and family situational variables. In addition, responses on a measure of self-concept were compared with those of a normative sample provided by Harter. Results indicated that, using this measure and these populations, there were no differences in the self-concept of children with disabilities and those without disabilities. Canonical correlation analysis indicated that children's cognitive achievement and independent functioning skills were moderately related to their self-concepts, but demographic variables and family functioning explained very little of the variance of the self-concept constructs as measured here.