Simulation Exercises in Disability Awareness Training: A Critique

This paper takes a critical look at simulation exercises. Little evidence exists that these exercises have a positive effect on either attitudes or behaviour but, despite this, they are used extensively in disability awareness training, both for children and adults. It is argued in this paper that by individualising and medicalising disability, and by focusing excessively on problems and difficulties, simulation exercises provide false and misleading information, and inculcate negative, rather than positive, attitudes towards disabled people. It is suggested that simulation exercises fail to simulate impairment correctly, and address neither the coping strategies and skills disabled people develop in living with impairment, nor the cumulative social and psychological effect of encountering social and physical barriers over a lifetime. Rather than using simulation as a means of attempting to understand the experience of disability, the paper concludes by advocating the use of disability equality training, which is devised and run by disabled people themselves.     

Understanding Men's Health and Illness: A Gender-relations Approach to Policy,Research, and Practice

Abstract

Men's health has emerged as an important public concern that may require new kinds of healthcare interventions and increased resources. Considerable uncertainty and confusion surround prevailing understandings of men's health, particularly those generated by media debate and public policy, and health research has often operated on oversimplified assumptions about men and masculinity. A more useful way of understanding men's health is to adopt a gender-relations approach. This means examining health concerns in the context of men's and women's interactions with each other, and their positions in the larger, multidimensional structure of gender relations. Such an approach raises the issue of differences among men, which is a key issue in recent research on masculinity and an important health issue. The gender-relations approach offers new ways of addressing practical issues of healthcare for men in college environments.     

Private Tragedy in Social Context? Reflections on Disability,Illness and Suffering

This article reviews aspects of the debate about the contested divide between disability and illness. It considers this divide in the context of three main themes: political efficacy; contradictions between the project of accommodation and that of cure; and Western cultural concerns with bodily control. It suggests that attempts to specify a distinction between disability and illness simply shift the boundaries of social and conceptual exclusion. Chronically sick people remain stigmatised, with their strengths unrecognised and measures to improve their lives unformulated. While acknowledging the serious difficulties involved, the article argues for a more inclusive and diverse movement, which can encompass those whose suffering is resistant to social accommodation.     

Disability Identity Formation and Affirmation: The Experiences of Persons with Severe Mental Illness

This article examines the pervasive nature and extent of the debilitating sense of shame associated with disability. It then explores the emergence of disability identity, pride, and culture to challenge such shame—illustrated in personal narrative accounts of the individual and collective journeys of people coping with severe mental illness.     

Social Citizenship Guarantee for Minorities in Japan: Present and Future

In recent years, the presence of minorities and their ways of life have become the subject of public interest in Japan. These minorities have experienced misrecognition and denial of their rights, and have been forced to live without benefiting from social redistribution. However, the lack of acceptance of minorities or their ways of life by majorities is being challenged. These aspects of recognition and redistribution are matters of universal human dignity. They are indispensable when considering issues of security in the lives of minorities. To achieve this security it is necessary to consider social citizenship. It described the way we are treated in society. In this article I examine the current state of social citizenship for minorities in Japan. An analysis of the contents and characteristics of social policy and social security systems in which social citizenship is embodied suggests that social citizenship in Japan is still strongly based on traditional social standards. This traditional orientation constitutes an obstacle to guaranteeing social citizenship for minorities. Moreover, the more serious inherent problem is that neither the concept of citizenship nor that of rights has been adequately accepted by the people. Given these points, it is unsurprising that the majority perceives minorities as deviant, and this situation has made guarantees of social citizenship for minorities much more difficult. A full guarantee of social citizenship for minorities requires further efforts to be made in human rights education and citizenship education.     

Disability and Chronic Illness Identity: Interviews with Lesbians and Bisexual Women and Their Partners

Disability rights activists and cultural workers are articulating disability identity and culture. Through interviews with lesbians and bisexual women with disabilities or chronic illnesses and their partners, the present study examined disability/chronic illness identity on the level of individual, couple, and community. Participants shared differing perspectives about how disability/chronic illness identity relates to other aspects of identity, and about whether disability/chronic illness identity is fluid or constant. They described several challenges they have encountered in developing disability/chronic illness identity. Couples talked about developing boundaries and balance in their relationships, and about how disability or chronic illness has strengthened their relationships. A number of participants spoke about identity as intimately linked with community. Implications for community building are discussed.     

Parenting with a Disability and Child Mental Health: A Propensity Score Analysis

Little research has examined the impact of having a parent with a disability on child mental health. This study used data from 7,116 families of children who participated in the 2006 National Health Interview Survey and propensity score matching (PSM) to investigate this question. Prior to PSM, differences in Child Mental Health Brief scores were significant with a moderate effect size. After PSM, differences in Child Mental Health Brief scores were still significant, but the effect size was small. Results indicate that much of the mental health risk for children of parents with disabilities is connected to related issues.     

Experiencing Stigma and Exclusion: The Influence of Neoliberal Perspectives,Practices, and Policies on Living with Chronic Illness and Disability

Neoliberal perspectives, policies, and practices increasingly affect chronically ill and disabled people's embodied experiences of stigma and exclusion. Neoliberalism emphasizes individual responsibility and self-sufficiency, a limited social safety net, and narrow governmental accountability. Examining pivotal experiences of chronically ill people shows how neoliberalism can frame their alternatives, interactions, and actions. This examination prompts reconsidering Goffman's concept of stigma to include how larger social policies and practices affect experiencing stigma and exclusion and, also, illuminates temporal features of receiving a diagnosis, disclosing illness, and dealing with disabilities and unpredictable bodies. The analysis derives from an ethnographic story and published and unpublished personal accounts from first-hand and library research over the course of my career.     

Black Jacobins in Contemporary France: On Identities on Politics,Decolonial Critique,and the Other Blackness

Formerly, issues of race were written out of the public landscape of the French Republic. Now the “black condition” is openly debated. This shift is informed by self-identified black movements and their responses to French Republican avoidance of thematizing racialized social inequalities. It is simultaneously contested by groups that experience anti-black racism as it reduces their alternate use of race and ethnicity. Does blackness lead to the homogenization of black experiences or can it initiate solidarity? This article examines current debates on blackness in Paris by drawing upon ethnographic activist research with a black activist group. I analyze how the group maneuvers through a supposedly race-blind discourse, in which the act of identifying race risks being disqualified as communitarian. I argue that a conception of blackness is introduced that provides the potential to recognize the pluralities of blackness, re-shaping notions of blackness, and the abstract Republican model itself.     

Models of Disability in the Labelling and Attitudinal Discourse in Ghana

This article considers the labelling of people with 'mental retardation' in Ghana against the background of the major underpinning models of disability. The influences of these models on individuals and on services and provisions are discussed. It is argued that traditional and religious beliefs, in addition to present day attitudes within the community, are influences on the perception of 'mental retardation' in Ghana.     

Surveying Issues That Arise in Women's Prisons: A Content Critique of Orange Is the New Black

The character Piper Chapman is presented in the Netflix original series, Orange Is the New Black (OITNB). Piper's story opens the door to the female correctional facility. With the mass incarceration of non‐violent, drug offending females comes the need for gender‐specific assessment, programming, and reentry efforts. It is the goal of this essay to briefly review several issues observed in OITNB (gender, victimization, sexuality, mental health/addiction, and race) and to raise awareness on additional issues related to women and crime. The essay will also provide a discussion on female relationships to include both outside loved ones as well as newfound friends within the facility and the accompanied policy implications. Research supports the idea that contact with prosocial loved ones reduces distress and recidivism. Policy implications suggest a need for more open visitation, assistance with welfare agencies, collaboration for reentry, and overall gender‐specific programming needs for female offenders.     

Socioeconomic Indexes for Occupations: A Review, Update, and Critique

Following a review of the history and sources of socioeconomic indexes for occupations, we estimate a new set of indexes for 1990 Census occupation lines, based on relationships between the prestige ratings obtained by Nakao and Treas in the 1989 General Social Survey and characteristics of occupational incumbents in the 1990 Census. We also investigate theoretical and empirical relationships among socioeconomic and prestige indexes, using data from the 1994 General Social Survey. Many common occupations, especially those held by women, do not fit the typical relationships among prestige, education, and earnings. The fit between prestige and socioeconomic characteristics of occupations can be improved by statistical transformation of the variables. However, in rudimentary models of occupational stratification, prestige-validated socioeconomic indexes are of limited value. They give too much weight to occupational earnings, and they ignore intergenerational relationships between occupational education and occupational earnings. Levels of occupational education appear to define the main dimension of occupational persistence across and within generations. We conclude that composite indexes of occupational socioeconomic status are scientifically obsolete.     

The International Classification of Functioning,Disability, and Health (ICF), A New Tool for Social Workers

Abstract

The World Health Organization (WHO) ratified the International Classification of Functioning, Disability and Health (ICF) in 2001. This followed a ten year period of international development which shifted emphasis from a system concerned with the consequences of disease to a system concerned with human functionality and health. Disability advocates contributed to this system which has potential as a tool for social work classification and assessment. Familiarity with the system also brings the profession in step with the disability studies movement which promotes a social model of disability.     

Democracy, Nationalism and Culture: A Social Critique of Liberal Monoculturalism

Does liberal democracy provide an ideal framework for solving nationalist disputes? Or is rather democracy more conductive to nationalism and conflict? No definitive answer can be given to this broadly formulated question. However, the trend in the scholarly literature has recently pointed towards the latter direction. This article first introduces the ‘demo‐skeptical turn’, which has emerged across disciplines in the study of democratic transitions. It then relates this to an understudied area – cultural homogenization. A social history of cultural homogenization remains yet to be written, but its historical impact is so overwhelming that its key features need to be studies on its own. This is, in turn, related to mainstream concepts of majoritarian liberal democracy.     

Disability, Religion and Health: a literature review in search of the spiritual dimensions of disability

Religious belief and practice plays an important role in the lives of millions of people worldwide, and yet little is known of the spiritual lives of people with a disability. This review explores the realm of disability, religion and health, and draws together literature from a variety of sources to illustrate the diversity of the sparse research in the field. An historical, cross-cultural and religious textual overview of attitudes toward disability throughout the centuries is presented. Studies in religious orientation, health and well-being are reviewed, highlighting the potential of religion to effect the lives of people with a disability, their families and caregivers. Finally, the spiritual dimensions of disability are explored to gain some understanding of the spiritual lives and existential challenges of people with a disability, and a discussion ensues on the importance of further research into this new field of endeavour.     

Changes in Health,Mortality, and Disability and Their Impact on Long-Term Care Needs

The need for long-term care is driven both by the growth of the elderly population and changes in the age relations of morbidity, disability, and mortality. Data show these relations changed in the U.S. elderly population from 1982 to 1989. Chronic disability prevalence declined between the 1982 and 1989 U.S. National Long Term Care Surveys. knong those impaired, many persons using personal assistance to meet their needs shifted to the use of assisted housing and special equipment. The relation of these trends to other changes-such as the increasing educational level of thc elderly population-is examined to estimate how future changes in disability and morbidity may affect the demand for long-term care. Disabilities at specific times as well as their transition rates were examined to determine how long individuals need long-term care. The analyses suggest that, while the amount of long-term care services needed will increase rapidly, the types and amounts of services used by the U.S. elderly population will undergo significant change.     

Families With Children and Adolescents: A Review,Critique, and Future Agenda

This decade's literature on families with children and adolescents can be broadly organized around the implications for youth of family statuses (e.g., family structure) and family processes (e.g., parenting). These overlapping bodies of research built on past work by emphasizing the dynamic nature of family life and the intersection of families with other ecological settings, exploring race/ethnic diversity, identifying mechanisms connecting family and child/adolescent factors, and taking steps to address the threats to causal inference that have long been a problem for family studies. Continuing these trends in the future will be valuable, as will increasing the number of international comparisons, exploring “new” kinds of family diversity, and capturing the convergence of multiple statuses and processes over time.