The blind person who tries to make an online purchase. The young girl who cannot speak due to a cognitive disability. The man confined to his home due to permanent injury. The single mother with a long-term illness who struggles to feed her family.

With one in seven people worldwide currently living with a disability, the term "outcast" covers numerous scenarios. Digital outcasts rely on technology for everyday services that many people take for granted. However, poorly designed products risk alienating this important (and growing) population.

Through a "grass roots" approach to innovation, digital outcasts are gradually taking action to transform their lives and communities. This emerging trend provides exciting learning opportunities for all of us. Citing real-world case studies from healthcare to social science, this book examines the emerging legal and cultural impact of inclusive design.
Gain a better understanding of how people with disabilities use technology

Discover pitfalls and approaches to help you stay current in your UX practices

Anticipate a future in which ambient benefit can be achieved for people of all abilities and backgrounds

This book follows a physically disabled researcher's journey from stigmatized embodiment on her way to creating accessible storytelling performances. These unique performances function not only as traditional, peer-reviewed forms of critical qualitative research, but also as 'narrative teaching productions' that guide students and their audiences in the pursuit of social justice and equality. The book begins by developing the author's personal standpoint, and provides an evocative discussion of the multiple perceptions and identities experienced by those with disabled bodies. It negotiates how performance research can be created and conducted within the confines of course learning objectives, moves through complications encountered in research design and data collection, and explores a range of insightful responses from community members, social activists, and performance critics, as well as more traditional academic audiences. Critical autoethnographic personal narratives, performance scripts, and poetry are used to illuminate struggles over legitimate methodological practice and storytelling performance pedagogy. Each chapter confronts the fear of mortality that presses us to stigmatize those who remind us of our inescapably vulnerable embodiments and offers hope for an inclusive, adaptable culture. The book will be compelling reading for scholars in Performance Studies, Disability Studies, Cultural Studies, Narrative Methodology, Ethnography, Higher Education, Autoethnography, Creative Nonfiction and everyone interested embodiment and/or storytelling for social change. Please visit www.uncwstorytelling.org/chapter-summaries-1 to access supplementary material for the book.

I speak candidly about radiation sickness in a poignant manner, because of not only the fact concerning myself succumbing to it, but I wanted to create a memorable impact as well as there exist people scattered about this world as these same people are suffering and dying from this copiously sad disease, or affliction, or mans' desires to alter the enviornment as he is now doing more harm than aiding it. ...But as this story that is heart touching as it is revealing, the young victim still maintained a sense of gentleness and patience in the direction of his unprovoked enemies, which were those at the very nuclear power plant, in his eyes, gave him life; a chance at hope for a brighter future in a rural place, but still candidly holding onto the past in which he has grown. Becomming completely ravaged from the terrible effects of the high level of nuclear radiation and from the industrial accident in which he fell prey, this toxic waste worker still manages to keep himself peacefully aware of not only the ultimate consequences of their mistake, or inexcusable blunder that should never be forgotten or done again.

Rochefort updates his classic comprehensive review of mental health policy issues in American society, beginning with early practices that predate the formal "mental health system" and ending with current debates about parity insurance coverage for mental illnesses, managed care, and Medicaid reform. At the same time, he provides a perspective on mental health policy analysis that draws on diverse work in the policy sciences, looks to both applied and theoretical concerns, and gives full recognition to the distinctive nature of mental health care problems. This new edition will be of enhanced value to policymakers in the mental health field as well as to students of American social welfare policy and public administration in general.

Contends that disability is a central but misunderstood element of global austerity politics. Broadly attentive to the political and economic shifts of the last several decades, Robert McRuer asks how disability activists, artists and social movements generate change and resist the dominant forms of globalization in an age of austerity, or "crip times." Throughout Crip Times, McRuer considers how transnational queer disability theory and culture-activism, blogs, art, photography, literature, and performance-provide important and generative sites for both contesting austerity politics and imagining alternatives. The book engages various cultural flashpoints, including the spectacle surrounding the London 2012 Olympic and Paralympic Games; the murder trial of South African Paralympian Oscar Pistorius; the photography of Brazilian artist Livia Radwanski which documents the gentrification of Colonia Roma in Mexico City; the defiance of Chilean students demanding a free and accessible education for all; the sculpture and performance of UK artist Liz Crow; and the problematic rhetoric of "aspiration" dependent upon both able-bodied and disabled figurations that emerged in Thatcher's England. Crip Times asserts that disabled people themselves are demanding that disability be central to our understanding of political economy and uneven development and suggests that, in some locations, their demand for disability justice is starting to register. Ultimately, McRuer argues that a politics of austerity will always generate the compulsion to fortify borders and to separate a narrowly defined "us" in need of protection from "them."

This is the first book-length study of Helen Keller's public speaking. It contains rhetorical analysis about how a person who was "sightless but seen, deaf but heard" learned to communicate, and how she gave public speeches for nearly 80 years inspiring others with her "vision for a better tomorrow." The analysis, texts of various speeches on a broad range of subjects, a chronology of her speeches, and bibliography will be helpful to students and teachers of speech and all those interested in Helen Keller.

How have disabled Americans been portrayed by the media through the years and how are images and the role of the handicapped changing? Jack Nelson and a series of experts in communication and the disabled offer an easy-to-read overview of key issues, continuing problems, new opportunities, and new technological tools. Professionals and teachers in communication, along with experts and general readers interested in public policy and social issues, will find this short study, with its illustrations, descriptions and lists of organizations and its bibliographical materials, a handy reference.

The first major anthology by parents with disabilities. 'Being a disabled parent is a rebellious act. Disabled people should have the same right to parent as anyone else, but often when we decide to start a family we are met with judgement and discrimination. We are questioned rather than supported. We have to push up against the medical system. And we have to confront society's model of parenting. Yet, despite all this, we still choose to parent. And we are damn good at it too!' When writer and musician Eliza Hull was pregnant with her first child, like most like most parents-to-be she felt a mix of nerves and excitement. But as a disabled person, she faced added complexities. She wondered: Will the pregnancy be too hard? Will people judge me? Will I cope with the demands of parenting? In We've Got This, thirty parents who identify as Deaf, disabled, neurodiverse, or chronically ill discuss the highs and lows of their parenting journeys and show that the greatest obstacles lie in other people's attitudes. The result is a moving, revelatory, and empowering anthology that celebrates the richness of disabled parenting in the twenty-first century. 'Such an important book. Joyous, eye-opening, and deeply moving, these powerful stories will challenge long-held assumptions and hopefully shift societal attitudes towards disabled parents. Everyone should read this.' Francesca Martinez, author of What the **** Is Normal?!

Historically, the diagnosis of deafness in a child has been closely associated with profound disability, including such typical outcomes as unmet potential and a life of isolation. A major shift away from this negative view has led to improved prospects for deaf children.

"Resilience in Deaf Children" emphasizes not only the capability of deaf individuals to withstand adversity, but also their positive adaptation through interactions with parents, peers, school, and community. In this engaging volume, leading researchers and professionals pay particular attention to such issues as attachment, self-concept, and social competence, which are crucial to the development of all young people. In addition, the volume offers strategies for family members, professionals, and others for promoting the well-being of deaf children and youth.

Coverage includes: Attachment formation among deaf infants and their primary caregivers.Deaf parents as sources of positive development and resilience for deaf infants.Enhancing resilience to mental health disorders in deaf school children.Strength-based guidelines for improving the developmental environments of deaf children and youth.Community cultural wealth and deaf adolescents' resilience.Self-efficacy in the management of anticipated work-family conflict as a resilience factor among young deaf adults.

"Resilience in Deaf Children" is essential reading for researchers, clinicians, and graduate students in clinical child, school, and developmental psychology as well as for allied researchers and professionals in such disciplines as school counseling, occupational therapy, and social work.

The Americans With Disabilities Act (ADA) is grounded in the human rights perspective. Like other civil rights legislation, the ADA is aimed at an oppressed group, persons with disabilities, who have been denied equal opportunities to participate in the larger society. As Pardeck makes clear, the goal of ADA, ending discrimination against people with disabilities in all facets of American life, is aligned with the philosophies and traditions of the social work profession. Pardeck provides a detailed overview and analysis of the ADA that will help professional social workers as well as students entering the field realize the full significance of the new rights and protections extended to people with disabilities. He also provides specific case studies and examples to illustrate the range of opportunities afforded the disabled and their advocates.

This book provides insight into the globally interlinked disability rights community and its political efforts today. By analysing what disability rights activism contributes to a global power apparatus of disability-related knowledge, it demonstrates how disability advocacy influences the way we categorise, classify, distribute, manipulate, and therefore transform knowledge. By unpacking the mutually constitutive relations between (practical) moral knowledge of international disability advocates and (formal) disability rights norms that are codified in international treaties such as the UN Convention on the Rights of Persons with Disabilities (CRPD), the author shows that the disability rights movement is largely critical of statements that attempt to streamline it. At the same time, cross-cultural disability rights advocacy requires images of uniformity to stabilise its global legitimacy among international stakeholders and retain a common meta-code that visibly identifies its means and aims. As an epistemic community, disability rights advocates simultaneously rely on and contest the authority of international human rights infrastructure and its language. Proving that disability rights advocates contribute immensely to a global culture that standardises what is considered morally and legally 'right' and 'wrong', thereby shaping the human body and the body politic, this book will be of interest to all scholars and students of critical disability studies, sociology of knowledge, legal and linguistic anthropology, social inequality, and social movements.

This volume points out how the increasing need for scientists in this country can be lessened by utilizing a long overlooked pool of scientific talent in those persons who are scientifically oriented but who happen to have physical or sensory disabilities. Robert A. Weisgerber argues that the main obstacle to the mainstreaming of the disabled is the reluctance of the nondisabled to offer opportunities and support. By speaking positively to the disabled concerning current recruitment efforts within the educational and the professional scientific communities, and to the public regarding the capability, energy, and competence of many disabled persons, this discussion aims to break down barriers.

An important part of the text is comprised of 21 success stories of college students and career scientists, all disabled yet highly motivated and excelling in their field. Together they can encourage other disabled persons to consider careers in the sciences, provide support for their families and teachers, and remind the caring public to view disabilities in their proper perspective. The technical results of the research conducted appear in the appendix, and suggestions for increasing opportunities for the disabled, educating the scientific profession about their qualifications, and improving relevant information services conclude the study.

Philosophy as Disability and Exclusion examines the history of ideas on arts in the education of people who are blind in England, from 1688 to 2010. This book also examines a number of the earlier influences on the enlightenment, and the international context of this topic. The two hypotheses on which this study is based are: (1) Our understanding of blindness in English intellectual culture is less to do with homologous physical characteristics. Instead it is more to do with an ethical philosophy of human capacity. (2) The arts education of people who are blind through touch tells us much about our psychology of mythologies and the intellectual construction of human thought. Furthermore, the myth that people who are blind are incapable of visual arts and have an enhanced capacity for the musical arts is one of the most engrained modern folklores. It is part of our cultural, intellectual and philosophical conscience. In the process of investigating these hypotheses, this book argues that philosophies have linked immorality, intelligence and physical ability. These have become connected in ways that are unrelated to eyesight in order to fulfill broader cultural processes of developing social theory. In this book, the process of knowledge creation is termed passive exclusion and is analyzed through an epistemological model of examining disability and exclusion.

More than a century of research has sought to identify the causes of stuttering, describe its nature, and enhance its clinical treatment. By contrast, studies directly focused upon public and professional attitudes toward stuttering began in the 1970s. Recent work has taken this research to new levels, including the development of standard attitude measures; ad dressing the widely reported phenomena of teasing, bullying, and discrimination against people who stutter; and attempting to change public opinion toward stuttering to more accepting and sensitive levels. Stuttering Meets Stereotype, Stigma, and Discrimination: An Overview of Attitude Research is the only reference work to date devoted entirely to the topic of stuttering attitudes. It features comprehensive review chapters by St. Louis, Boyle and Blood, Gabel, Langevin, and Abdalla; an annotated bibliography by Hughes; and experimental studies by other seasoned and new researchers. The book leads the reader through a maze of research efforts, emerging with a clear understanding of the important issues involved and ideas of where to go next. Importantly, the evidence base for stuttering attitude research extends beyond research in this fluency disorder to such areas as mental illness, obesity, and race. Thus, although of interest primarily to those who work, interact, or oth erwise deal with stuttering, the book has potential for increasing under standing, ameliorating negative attitudes, and informing research on any of a host of other stigmatized conditions.

Caring for people with disabilities often becomes an all-encompassing responsibility for one or more family members. To manage the multifaceted demands, caregivers must possess strong multitasking skills, including the ability to assist with daily life tasks; provide emotional support; help with financial affairs; mediate and advocate with health care providers. Maintaining balance within their own lives can become incredibly challenging for caregivers. More often than not, providing care for family members or loved ones occurs at the expense of the caregivers' well-being. And for caregivers who themselves have disabilities, it further complicates matters.

"Multiple Dimensions of Caregiving and Disability" addresses concerns that have been long familiar to the caregiver population and examines the current state of family care for individuals with disabilities. With a lifespan perspective, this concise reference reviews the literature on specific problems of caregivers and explores which care strategies are effective, promising, or lacking in available resources and support interventions. Contributors also explore the more fluid and subjective aspects of caregiving, such as feelings, spirituality, and family roles. Suggestions for future policy improvements, particularly within the public health sector, are discussed as well.

Topics covered include:

Family dynamics and caregiving for people with disabilities.
Parent caregiving of children with disabilities.
Race, ethnicity, socioeconomic status, and caregiving.
Educational, training, and support programs for caregivers.
Emerging technologies to aid caregivers.
Developing partnerships between caregivers and health care providers.

"Multiple Dimensions of Caregiving and Disability" is a must-have resource for researchers, scientist-practitioners, policy makers, and graduate students across such disciplines as clinical psychology, nursing, social work, public health, medicine, and social and education policy."

The growing prominence of ecological and social systems perspectives in the child development and family studies fields is having a significant impact on the conceptualization and delivery of early intervention services. The exclusive focus on the handicapped or developmentally delayed child is gradually giving way to a much broader focus on the family as a system. The parent-child relationship is increasingly becoming a major intervention target. At the same time, the need to fine-tune intervention programs to respond to the unique needs of different etiological groups is being emphasized. This book brings together the conceptual and empirical work of a number of scholars whose current research is at the leading edge of these shifts.

The volume consists of an introductory overview of transitions occurring in the early intervention field, a six-chapter section dealing with current themes and conceptualizations of early intervention, and a four-chapter section focusing on international perspectives that describes influences on and noticeable trends in early intervention programming and research in several countries. This book by its nature has an international appeal--but perhaps more significantly it affords American researchers a unique opportunity to learn about the field of intervention as practiced in other lands. The volume is intended for researchers, graduate and senior undergraduate students, program developers and administrators in the early intervention field, and other human service professionals.

Written for health care administrators with little accounting or finance background, this book provides a readable, easily understood overview of health care finance. Hy fully discusses accounting concepts, working capital, rate setting, cost analysis, accounts receivable, revenue sources, and inventory management. The abundant use of figures facilitates the understanding of complex financial concepts such as the financial functions involved with implementing operational and capital budgets, managing different types of accounts, determining costs, and setting prices. The aim throughout is to acquaint readers with the concepts involved and enable them to communicate effectively with finance officials.

In addition to thorough coverage of health care finance issues, the book also deals with some functions not normally covered in texts on the subject. These include both a thorough exploration of various types of revenue sources and an explanation of techniques used to cut costs associated with inventories, thereby saving organizations money. Especially valuable are appendices which illustrate two different procedures for estimating volume--the heart of financial forecasting. Practicing health care administrators whose job requires financial proficiency as well as students with no financial training will find this book an indispensable resource.

This international handbook is the first to analyze mental health policies systematically across a variety of both developed and developing countries. Mental health and public policy experts survey current policies, the public policy process, and critical issues in twenty countries that are representative of different problems. The work considers the treatment of the mentally ill and mentally retarded, mentally disordered offenses, questions of substance abuse, deinstitutionalization, funding, and consumer rights. This major reference, with its comprehensive and comparative survey, is designed for scholars, students, and professionals who deal with mental health and public policy issues.