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Journal articles on the topic 'Drawing disability'

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1

Conti, Adam. "Drawing the Line: Disability, Genetic Intervention and Bioethics." Laws 6, no. 3 (July 17, 2017): 9. http://dx.doi.org/10.3390/laws6030009.

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2

Tiszai, Luca, Katalin Sándor, and Veronika Kálló. "Visual Narratives of Disability in Projective Drawing Test." Pro&Contra 3, no. 2 (2021): 47–67. http://dx.doi.org/10.33033/pc.2019.2.47.

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3

Celik Kayapinar, Fatma, and Behsat Savas. "Determining elementary teacher candidates cognitive structure on the concept of ‘disabled people’ through the drawing technique." New Trends and Issues Proceedings on Humanities and Social Sciences 6, no. 1 (May 10, 2019): 78–84. http://dx.doi.org/10.18844/prosoc.v6i1.4157.

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Currently, around 10% of the world's population, or roughly 650 million people, live with a disability. According to the results of the in Turkey 2011 Population and Housing Survey, the proportion of the population with at least one disability is 6.9%. The aim of the study is to investigate primary teacher candidates cognitive structures related to ‘disabled people’ through the drawing technique. The data were collected from 89 teacher candidates participated in this study in the 2018–2019 academic year in Mehmet Akif Ersoy University. Each student was asked to draw a picture about disabled people. The students were encouraged if they want to write their own interpretation of the drawing ‘in a couple of sentences. Of the drawings, 89 were subjected to the content analysis. Half of the drawings are multicoloured and black is second. Most of the teacher candidates (88%) handed wheelchairs to people with disabilities. Keywords: Disabled people, drawing technique, teacher candidate.
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4

Barnes, Colin, and Geof Mercer. "Disability, work, and welfare." Work, Employment and Society 19, no. 3 (September 2005): 527–45. http://dx.doi.org/10.1177/0950017005055669.

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This article engages with debates relating to social policy and disabled people’s exclusion from the British labour market. Drawing on recent developments from within the disabled people’s movement, in particular, the concept of independent living and the social model of disability, and the associated disability studies literature, a critical evaluation of orthodox sociological theories of work, unemployment, and under-employment in relation to disabled people’s exclusion from the workplace is provided. It is argued that hitherto, analyses of work and disability have failed to address in sufficient depth or breadth the various social and environmental barriers that confront disabled people. It is suggested therefore that a reconfiguration of the meaning of work for disabled people - drawing on and commensurate with disabled people’s perspectives as expressed by the philosophy of independent living - and a social model analysis of their oppression is needed and long overdue.
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5

Förstl, H., A. Burns, R. Levy, and N. Cairns. "Neuropathological basis for drawing disability (constructional apraxia) in Alzheimer's disease." Psychological Medicine 23, no. 3 (August 1993): 623–29. http://dx.doi.org/10.1017/s003329170002540x.

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SynopsisThe performance on four drawing tasks was studied in a sample of patients with verified Alzheimer's disease in order to examine the relationship of ‘constructional apraxia’ to neuropathological changes in the parietal lobe and in other brain areas. Twenty-three patients were able to attempt to copy pentagons, a spiral and a three-dimensional drawing of a house, 22 patients were able to draw a clock-face spontaneously. The results were rank-ordered by two independent raters. The values obtained in the different drawing tasks were correlated significantly with each other, with global estimates of cognitive performance (CAMCOG, Mini-Mental State), with a shorter duration of illness, higher brain weight (in the subsample of female patients), higher counts of large neurons in the parahippocampal gyrus and hippocampus, but not in the parietal lobe. This suggests that there is no specific relationship between ‘constructional apraxia’ and neuropathological changes in the parietal lobes of patients with advanced Alzheimer's disease, but that there is a correlation between widespread brain changes and several neuropsychological deficits, one of them being drawing disability.
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6

Prince, Michael J. "Drawing hidden figures of disability: youth and adults with disabilities in Canada." Evidence & Policy: A Journal of Research, Debate and Practice 17, no. 2 (May 1, 2021): 227–41. http://dx.doi.org/10.1332/174426421x16146827140135.

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Background: While governments draw on survey data to inform policy choices, the design, application, and interpretation of surveys can generate certain images of disability and ignore many others.Aims and objectives: This article draws attention to social circumstances of people with disabilities often unacknowledged in research evidence: hidden figures of disability.Methods: Selected results from the Canadian Survey on Disability are examined with a focus on working-age youth and adults (aged 15 to 64) with a range of disabilities.Findings: Five figures of disability and corresponding conceptual models are identified. These hidden figures of disability are the uncounted, those with needs unsupported, youth in multiple transitions, potential workers, and what may be called ‘the fearful’. Several models of disability are identified intersecting with the evidence. These are the absent citizen, biomedical model and charitable model, social and economic integration model, human rights and full citizenship, and psycho-emotional model of affective disablism and ableism.Discussion: Hidden figures of disability are more than statistical tests and texts; more than calculations derived from quantitative research where people become a data point. The function of drawing hidden figures is to disclose and describe the bodily experiences of people with disabilities in their social positions and structural contexts.Conclusion: We need to see the production of evidence for policy not as painting a portrait but as portraits in the plural, and appreciate not only what is in the frame but also what faces and forms of knowledge get glossed over or brushed aside.
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7

Shaw, Susan A. "Drawing on three discursive modes in learning disability nurse education." Nurse Education Today 29, no. 2 (February 2009): 188–95. http://dx.doi.org/10.1016/j.nedt.2008.08.007.

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8

Virdi, Jaipreet. "Material Traces of Disability." Nuncius 35, no. 3 (December 14, 2020): 606–31. http://dx.doi.org/10.1163/18253911-03503008.

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Abstract This paper examines the lived experiences of Canadian machinist and double-amputee Andrew A. Gawley (1895–1961), whose prosthetic “steel hands” rose him to fame during the mid-twentieth century, to analyze how disability objects can illuminate complex tensions of unruliness to represent a fraught epistemological materiality. Drawing on Williamson and Guffey’s “design model of disability,” I argue that Gawley’s prostheses are physical and tangible representations of his need to achieve functional normalcy. His self-reliance and identity was not only premised on ability, but dependent upon the complex unruliness ascribed within the prostheses, such that the sensationalized freakery of the “steel hands” become as crucial to Gawley’s identity as his performances of normative masculinity.
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9

Belser. "Drawing Torah from Troubling Texts: Gender, Disability, and Jewish Feminist Ethics." Journal of Jewish Ethics 6, no. 2 (2021): 140. http://dx.doi.org/10.5325/jjewiethi.6.2.0140.

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10

Crossley, Mary. "Normalizing Disability in Families." Journal of Law, Medicine & Ethics 43, no. 2 (2015): 224–27. http://dx.doi.org/10.1111/jlme.12236.

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In “Selection against Disability: Abortion, ART, and Access,” Alicia Ouellette probes a particularly vexing point of intersection between ART and abortion: how negative assumptions about the capacities of disabled persons and the value of life with disability infect both prospective parents’ prenatal decisions about what pregnancies to pursue and fertility doctors’ decisions about providing services to disabled adults. This commentary first briefly describes what I view as Ouellette’s key points and her article’s most valuable contributions. It then suggests further expanding the frame of reference for Ouellette’s discussion. Viewing decisions about who can reproduce and what children will be born as fundamentally decisions about family suggests ways of drawing on intersectional approaches and growing public acceptance of nontraditional families to promote acceptance of people with disabilities as valued family members — without limiting reproductive liberties.
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11

Simpson, Hannah. "Samuel Beckett and Disability Performance." Journal of Beckett Studies 30, no. 1 (April 2021): 26–44. http://dx.doi.org/10.3366/jobs.2021.0327.

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Beckett's plays have attracted a striking range of disability performances, in part because of their insistent attention on embodied existence and the impaired body. Here, I examine four recent disability performances of Beckett's plays, exploring how these productions prompt re-evaluation of the previously undetected indicators of disability in the scripts, including mobility impairment, automatic speech, stuttering, and memory deficiency. Drawing on a series of original interviews with the practitioners in question, I examine the intersection between textual aesthetics and disability ethics in these contemporary productions, emphasising how these performances illuminate crucial corporeal, social, and ontological concerns in Beckett's original scripts, in newly embodied terms.
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Morris, Zachary A., and Asghar Zaidi. "Estimating the extra costs of disability in European countries: Implications for poverty measurement and disability-related decommodification." Journal of European Social Policy 30, no. 3 (January 20, 2020): 339–54. http://dx.doi.org/10.1177/0958928719891317.

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It is widely accepted that people with disabilities incur additional expenditures on transport, heating, equipment and other items. In this article, we estimate the magnitude of these extra costs of living for adults with disabilities aged 50–65 across 15 countries of Europe using the Survey of Health, Aging, and Retirement in Europe (SHARE) data. Drawing on the standard of living approach of Zaidi and Burchardt, we compare the incomes required by households with and without adults with disabilities to obtain an equivalent standard of living. We advance upon this research by drawing on the cross-nationally harmonized data of adults aged 50+ from the SHARE. The results suggest that there are substantial extra costs of disability in these countries: around 44 percent of income for a household with an adult reporting a work-related disability and somewhat less than 30 percent of income for a household with an adult who receives disability benefits. Applying an equivalization scale based on these figures increases the overall poverty incidence rate, especially for households with disabled adult members. These findings thus have implications for analysing the entitlement and benefit levels for disability support programmes and for devising accurate poverty estimates concerning persons with disabilities.
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Pande, Ketan C., Ketan Khurjekar, and Vilas Kanikdaley. "Correlation of Low Back Pain to a High-Intensity Zone of the Lumbar Disc in Indian Patients." Journal of Orthopaedic Surgery 17, no. 2 (August 2009): 190–93. http://dx.doi.org/10.1177/230949900901700214.

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Purpose. To assess the correlation between low back pain and a high-intensity zone (HIZ) of the lumbar disc in Indian patients. Methods. 200 patients with low back and/or leg pain underwent magnetic resonance imaging of the lumbosacral spine. The location and severity of pain and disability were assessed using the pain drawing, visual analogue scale, and Oswestry Disability Index, respectively. The inter-observer reliability was assessed using the kappa statistic. Results. The prevalence of an HIZ was 13% and 17% according to observers A and B, respectively. The inter-observer reliability was fair (κ=0.64, p<0.005). The presence of an HIZ did not correlate with low back pain according to the pain drawing, visual analogue scale, and Oswestry Disability Index. According to the pain drawing data, the sensitivity, specificity, and positive predictive values of an HIZ to low back pain were 11%, 82%, and 62%, respectively. Conclusion. The presence of an HIZ is not diagnostic of a disrupted and painful disc, and should be interpreted together with other prevailing symptoms and clinical findings.
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14

Arshad, Rowena, and Sheila Riddell. "Managing Disability Equality in Scotland: Tensions between Social Audit and Disability Equality." Social Policy and Society 10, no. 2 (February 24, 2011): 229–38. http://dx.doi.org/10.1017/s1474746410000576.

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This paper focuses on the implications of adopting social audit approaches in order to implement equality policies in Scotland, exploring the tension between surface compliance and deep institutional engagement. Drawing on data from an evaluation of pubic sector bodies’ disability equality schemes, the paper provides examples of different levels of engagement, ranging from surface compliance (some education authorities) to institutional permeation of an equalities ethos (the Scottish Arts Council). The paper concludes by considering the future potential of single equality schemes to promote equality across Scottish society. It is argued that unless there is stronger support and challenge from Scottish government, there is a danger that equality schemes may become paper exercises rather than opportunities for institutional reflection and planning. At the same time, it would be a mistake to dismiss equality planning as merely an exercise in managerialism, since measuring the extent of inequality over time is an essential first step in the long process of achieving institutional change.
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Nicki, Andrea. "The Abused Mind: Feminist Theory, Psychiatric Disability, and Trauma." Hypatia 16, no. 4 (2001): 80–104. http://dx.doi.org/10.1111/j.1527-2001.2001.tb00754.x.

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I show how much psychiatric disability is informed by trauma, marginalization, sexist norms, social inequalities, concepts of irrationality and normalcy, oppositional mind-body dualism, and mainstream moral values. Drawing on feminist discussion of physical disability, I present a feminist theory of psychiatric disability that serves to liberate not only those who are psychiatrically disabled but also the mind and moral consciousness restricted in their ranges of rational possibilities.
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16

McCausland, Ruth, and Eileen Baldry. "‘I feel like I failed him by ringing the police’: Criminalising disability in Australia." Punishment & Society 19, no. 3 (March 3, 2017): 290–309. http://dx.doi.org/10.1177/1462474517696126.

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The stigmatisation, control, criminalisation and incarceration of people with disability have a long history. While in recent decades there has been increasing commitment to the rights of people with disabilities by governments in western nations, the over-representation of people with mental and cognitive disability in criminal justice systems has continued. Although there are similarities amongst Western jurisdictions in regard to the treatment of people with disability in justice systems, there are particularities in Australia that will be drawn out in this article. We argue that disadvantaged people with mental and cognitive disability are being managed by and entrenched in criminal justice systems across Australia’s six states and two territories, including so-called diversionary and therapeutic measures that appear to accommodate their disability. In the absence of early and appropriate diagnosis, intervention and support in the community, some disadvantaged and poor persons with mental and cognitive disability, in particular Indigenous Australians, are being systematically criminalised. Criminal justice agencies and especially youth and adult prisons have become normalised as places of disability management and control. Drawing on research that focuses in detail on the jurisdictions of the Northern Territory and New South Wales, we argue for a reconstruction of the understanding of and response to people with these disabilities in the criminal justice system.
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Shakespeare, Tom, Harriet Cooper, Dikmen Bezmez, and Fiona Poland. "Rehabilitation as a Disability Equality Issue: A Conceptual Shift for Disability Studies?" Social Inclusion 6, no. 1 (March 26, 2018): 61–72. http://dx.doi.org/10.17645/si.v6i1.1175.

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Rehabilitation is a controversial subject in disability studies, often discussed in terms of oppression, normalisation, and unwanted intrusion. While there may be good reasons for positioning rehabilitation in this way, this has also meant that, as a lived experience, it is under-researched and neglected in disabilities literature, as we show by surveying leading disability studies journals. With some notable exceptions, rehabilitation research has remained the preserve of the rehabilitation sciences, and such studies have rarely included the voices of disabled people themselves, as we also demonstrate by surveying a cross-section of rehabilitation science literature. Next, drawing on new research, we argue for reframing access to rehabilitation as a disability equality issue. Through in-depth discussion of two case studies, we demonstrate that rehabilitation can be a tool for inclusion and for supporting an equal life. Indeed, we contend that rehabilitation merits disability researchers’ sustained engagement, precisely to ensure that a ‘right-based rehabilitation’ policy and practice can be developed, which is <em>not</em> oppressive, but reflects the views and experiences of the disabled people who rehabilitation should serve.
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Nadai, Eva, Anna Gonon, and Fabienne Rotzetter. "Costs, Risks and Responsibility. Negotiating the Value of Disabled Workers Between Disability Insurance and Employers." Swiss Journal of Sociology 44, no. 3 (November 1, 2018): 405–22. http://dx.doi.org/10.1515/sjs-2018-0018.

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Abstract Drawing on the theoretical framework of the Economics of Convention this paper analyses the employment of people with disabilities as a valuation process. Based on case studies and interviews in business companies and disability insurance offices, it explores how employers and disability insurance determine the value of disabled workers. Inasmuch as employers are not willing to adapt performance standards, job design and work organisation, disability insurance attains individual exceptions for its clients at best, while disabling standards remain intact.
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Ware, Linda P. "A Moral Conversation on Disability: Risking the Personal in Educational Contexts." Hypatia 17, no. 3 (2002): 143–72. http://dx.doi.org/10.1111/j.1527-2001.2002.tb00945.x.

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The author explores disability in K-12 schools where attitudes, beliefs, and practices shape the school culture and influence enduring perceptions about disability among school professionals, students, and their families. Drawing on recent conversations among moral philosophers who view disability as a central feature of human life that has yet to enrich understanding of ourselves and others, the author encourages the practice of reform grounded in a process that begins with a “suspicion of the self” and a willingness to risk the personal.
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Ferrucci, Fabio. "Disability and work inclusion in Italy: between unfulfilled promises and new disability culture." Modern Italy 19, no. 2 (May 2014): 183–97. http://dx.doi.org/10.1080/13532944.2014.910507.

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This article outlines the existing provisions in Italy for inclusion in workplaces for persons with disabilities. It reports available statistics on the numbers of persons with disabilities in paid employment by sector, those seeking work and drawing pensions and those employed according to educational qualification. It considers the different channels, both formal and informal, through which persons with disabilities are able to gain access to paid employment and the concrete effects of Law 68/1999 on access to work and collocamento mirato (targeted work placement). One of the problems with the Italian legislation on compulsory work placement of disabled persons is that it applies only to employers who have at least 15 employees, whereas the vast majority of employers in Italy have fewer than 10. Lastly, the article reflects on the current situation and the challenges posed by new ways of conceiving of disability and of work. Work needs to be understood not simply as an occupation or position for which one receives payment but as a set of social relations between people, which has value in itself.
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WOODHAMS, CAROL, and SUSAN CORBY. "Defining Disability in Theory and Practice: A Critique of the British Disability Discrimination Act 1995." Journal of Social Policy 32, no. 2 (April 2003): 159–78. http://dx.doi.org/10.1017/s0047279402006979.

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This article presents a theoretical critique of the employment provisions of the Disability Discrimination Act (DDA) (1995), focusing on the definition of disability. It argues that the underpinning medical assumption of the statutory definition of disability is detrimental to the achievement of disability equality in the workplace and is problematic for practitioners and Employment Tribunals. In particular there are four areas of significant confusion arising from the need for medical evidence, the lack of congruence between managerial and legal definitions, the focus on the negative aspects of disability and the fact that disability is often hidden. By exploring these four themes and drawing on comparisons with the other equality laws, the article concludes that the definition of disability contained in the DDA (1995) contradicts many of the principles of the liberal equality framework that underpins it. Finally the article considers the public policy implications and suggests a new statutory approach.
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Huskin, Patricia R., Christine Reiser-Robbins, and Soyoung Kwon. "Attitudes of Undergraduate Students Toward Persons With Disabilities: Exploring Effects of Contact Experience on Social Distance Across Ten Disability Types." Rehabilitation Counseling Bulletin 62, no. 1 (September 6, 2017): 53–63. http://dx.doi.org/10.1177/0034355217727600.

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Attitudes toward individuals with disabilities have been one of the most important and focal topics in disability studies. However, most studies have either treated disability in a broad sense without distinguishing disability type or have been limited to one specific disability type. Drawing upon a social distance scale, the study was designed to examine undergraduate students’ perceptions toward 10 different disability types and across a range of social contexts. Utilizing intergroup contact theory, an analysis was performed to determine how these responses were affected by contact experience with persons with disability. Results show that contact experience was statistically significant for six of 10 disability types. Specifically, across all disabilities, regular contact was related to decreased social distance, with the notable exception of autism. Attendant conclusions about stigma hierarchies and implications for research and practice are discussed.
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Saltes, Natasha. "‘Abnormal’ Bodies on the Borders of Inclusion: Biopolitics and the Paradox of Disability Surveillance." Surveillance & Society 11, no. 1/2 (May 27, 2013): 55–73. http://dx.doi.org/10.24908/ss.v11i1/2.4460.

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When conducted according to the biomedical definition of disability, ‘disability surveillance’ involves monitoring bodies against normative ontological standards, classifying ‘abnormality’ and problematizing ‘abnormal bodies’ as risky. While disability surveillance that operates within a biomedical perspective contributes to the exclusion of disabled people, the counting and classifying of disabled people is necessary to achieve the aims and objectives of the disability rights movement. In examining this paradox, this paper looks at the ways in which the Canadian government defines and measures disability and the implication of discriminatory immigration policies and ableist biometric technologies. A theoretical framework with which to situate and examine disability surveillance is proposed. Drawing from the work of Foucault on normality/abnormality and subsequent literature on biopolitics, this paper contextualizes the paradoxical implications of surveillance practices that target disabled people.
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Jones, Chelsea Temple, and Kim Collins. "Ordinary Extraordinary Activism: Student-led filmmaking in disability studies." International Journal of Education Through Art 16, no. 1 (March 1, 2020): 29–41. http://dx.doi.org/10.1386/eta_00015_1.

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Abstract In this article, we, as disability studies educators in Toronto, Canada, reflect on our interpretations of a student group's call to 'people' disability culture. This request tasked us with mapping disability culture in Canada, and representing it through the arts-based approach of new disability documentary. We produced five student-directed films, Ordinary Extraordinary Activism, that bridge theory with lived experience by profiling activists whose lives involve participating in disability culture. Here, we describe how our work supported and transcended the affirmative model by drawing on intersectionality and Disability Justice. We critically consider the aesthetic and representational tensions of producing films under crip time. Through this writing, we reflect on the three-year process of filmmaking as a gesture of online pedagogy and analyse three out of five films.
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Jacobson, Jessica, Phillip Sabuni, and Jenny Talbot. "Disability and the criminal justice system in Zambia." Journal of Intellectual Disabilities and Offending Behaviour 8, no. 2 (June 12, 2017): 59–69. http://dx.doi.org/10.1108/jidob-12-2016-0023.

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Purpose Drawing on multi-method research conducted in 2013-2014, the purpose of this paper is to consider the extent and nature of disadvantage experienced by individuals with psychosocial and intellectual disabilities (PID) who come into contact with the criminal justice system in Zambia. The research was conducted as part of a wider project aiming to bring about improvements in how people with PID are dealt with by the criminal justice services. Design/methodology/approach The research activities included interviews with 29 individuals with PID who had experienced the criminal justice system as suspects, defendants or prisoners (“self-advocates”). A focus group and interviews were also conducted with the family members of people with PID who had criminal justice experience. Findings People with PID in contact with the criminal justice services in Zambia are disadvantaged and discriminated against routinely and systematically. Like all detainees, they experience harsh and at times brutal conditions of detention. However, because of their disabilities, such experiences can be more keenly felt: their disabilities may be exacerbated by detention or by limited or non-existent health care; and they are likely to be less resourceful than other detainees and, therefore, less able to cope with the privations of detention. Originality/value In drawing on the self-advocate interviews, this paper presents direct, vivid accounts of what it means to be a suspect, defendant or prisoner with disabilities in Zambia. These are extremely marginalised and multiply disadvantaged individuals whose voices are rarely heard.
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Powell, Lisa D. "Disability and Resurrection: Eschatological Bodies, Identity, and Continuity." Journal of the Society of Christian Ethics 41, no. 1 (2021): 89–106. http://dx.doi.org/10.5840/jsce20216141.

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This article engages the debate around embodiment in the resurrected life, drawing from sources in disability theology, black theology, and womanist ethics. Do we retain “body marks,” as M. Shawn Copeland calls them in her consideration of the scars and wounds on black bodies? Or, as Nancy Eiesland and Amos Yong discuss it: do we retain our impairments as Christ did after his resurrection? I will describe the debate, highlight concern over continuity of identity, and use J. Kameron Carter’s work on theology and race to propose an alternative approach.
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Snounu, Yasmin. "Disability and Higher Education in Palestine." Journal of Culture and Values in Education 2, no. 3 (December 10, 2019): 61–78. http://dx.doi.org/10.46303/jcve.03.02.4.

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Disability in Palestine and the experiences and practices of professors and administrators on accommodating disabled students in Palestinian higher education institutions are captured through critical ethnography mode. Disability in Palestine is discussed within the context of what I, as the researcher, call “segregating democracy.” The term segregating democracy refers to the political bonds between Israel and the United States of America that often lead to exclusion of the indigenous Palestinian community from the rest of the world. Segregating democracy and its consequences on disability in Palestine are the context in which the experiences of the Palestinian faculty and administrators are analyzed. Using critical disability studies, while also drawing from elements of teacher development theories, this paper identifies transformational ways of thinking about disability as well as the unique role of educators in promoting/adopting inclusive pedagogical practices towards accommodating disabled students in higher education.
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Swartz, Leslie. "Representing disability and development in the global south." Medical Humanities 44, no. 4 (November 27, 2018): 281–84. http://dx.doi.org/10.1136/medhum-2018-011484.

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I reflect on two aesthetics which are at play in the presentation of critical disability and development work in the global south. On the one hand, authors of critical texts commonly use very complex and abstruse language, which may make such texts relatively inaccessible to some disabled people in the global south. On the other hand, the ways in which development work in the south is portrayed sometimes emphasises methods of engagement which may seen to be infantilising. Drawing on my own experience in such engagement activities, I suggest that it is important to understand, and to subvert, dominant forms of representation.
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Van Aswegen, Jennifer, David Hyatt, and Dan Goodley. "A critical discourse problematization framework for (disability) policy analysis." Qualitative Research Journal 19, no. 2 (May 7, 2019): 185–98. http://dx.doi.org/10.1108/qrj-12-2018-0004.

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Purpose The purpose of this paper is to present a composite framework for critical policy analysis drawing from discourse analysis and post-structuralist analysis. Drawing on an interpretive paradigm (Yanow, 2014), this paper provides a thick description (Geertz, 1973) of the processes involved in the application of these tools in a critical policy analysis project, focusing on disability policy within the Irish context. Methodologically, this is a resourceful cross-fertilization of analytical tools to interrogate policy, highlighting its potential within critical disability policy analysis and beyond. Design/methodology/approach Merging a critical discourse analysis framework and a policy problematization approach, the combination of tools presented here, along with their associated processes, is referred to as the critical discourse problematization framework. Findings Potentially, the framework can also be employed across a number of cognate social policy fields including education, welfare and social justice. Practical implications The value of this paper lies in its potential to be used within analytical practice in the field of critical (disability) policy work by offering an evaluation of the analytical tools and theoretical framework deployed and modeled across an entire research process. Social implications The framework has the potential and has been used successfully as a tool for disability activism to influence policy development. Originality/value The analytical framework presented here is a methodically innovative approach to the study of policy analysis, marrying two distinct analytical tools to form a composite framework for the study of policy text.
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Vinck, Julie, and Wim Van Lancker. "An Intersectional Approach towards Parental Employment in Families with a Child with a Disability: The Case of Belgium." Work, Employment and Society 34, no. 2 (October 30, 2019): 228–61. http://dx.doi.org/10.1177/0950017019872648.

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For parents with disabled children labour market participation is difficult since these children require care that exceeds typical parental care. At the same time, disabled children often live in families who belong to social categories that are associated with lower employment probabilities. However, the intersection between disability and social categories is hitherto overlooked in the literature. Drawing on a case study of Belgium, this article empirically examines to what extent parental employment is explained by the child’s disability and/or the family’s social disadvantages. For this, unique and large-scale register data are used. The results show that (1) childhood disability overlapped with social disadvantages; (2) childhood disability inhibited parental employment; but (3) the relationship differed by social category: for single parents, parents with low educational qualifications, and parents having multiple disabled children, disability and social disadvantage reinforced each other.
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Simpson, Murray K. "Power, Ideology and Structure: The Legacy of Normalization for Intellectual Disability." Social Inclusion 6, no. 2 (May 17, 2018): 12–21. http://dx.doi.org/10.17645/si.v6i2.1264.

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Since its first formulation in English, the ‘principle of normalization’ has had a profound impact on policy and practice in the field of intellectual disability. Over the past fifty years, normalization, and Social Role Valorization, have drawn on liberal humanist philosophy, adopting varied and complex positions in relation to it. This article will consider an apparent structural correspondence between a discourse of ‘liberal equality’ with versions of normalization that emphasised conformity to social norms, and those drawing primarily on ‘liberal autonomy’, emphasising independence and self-determination of people with intellectual disabilities. Despite this seeming correspondence, the article eschews a structuralist account in favour of a discursive and rhizomatic model, in which the philosophical elements are seen as tactical forces deployed in the pursuit of wider strategic ends. The article concludes by highlighting paradoxes in contemporary thinking that can be traced to the legacy of normalization, specifically, the tensions between sameness, difference, equality and independence.
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Fritsch, Kelly, and Anne McGuire. "Risk and the Spectral Politics of Disability." Body & Society 25, no. 4 (June 19, 2019): 29–54. http://dx.doi.org/10.1177/1357034x19857138.

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Drawing on the institutional history of the sperm bank and legacies of eugenics, we consider how spectrums of risk simultaneously constrain and expand possibilities for disability justice. We do so by examining the discourses surrounding US-based Xytex Corporation sperm bank Donor 9623, described as the ‘perfect’ donor but later discovered to have a criminal record and a diagnosis of schizophrenia. Haunted by the dread of disability, we examine how parents mark the fate of their donor-conceived child on a graded spectrum of genetic and psychiatric risk, in need of perpetual monitoring and intervention. Using this case to understand the contemporary reorganization of disability via spectral risk, we advocate for a critical engagement with how disability haunting can enable us to better attend to the effects of the past and present in such a way that provokes a more collectively just future.
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Polvinen, Anu, Mikko Laaksonen, Juha Rantala, Marjukka Hietaniemi, Jari Kannisto, and Susan Kuivalainen. "Working while on a disability pension in Finland: Association of diagnosis and financial factors to employment." Scandinavian Journal of Public Health 46, no. 19_suppl (February 2018): 74–81. http://dx.doi.org/10.1177/1403494817738460.

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Aims: The aim of this study was to find out whether health and financial factors are associated with engagement in paid work during a disability pension. Methods: The data included a 10 per cent sample of Finns aged 20–62 years who were drawing earnings-related full or partial disability pension in 2012 ( n = 14,418). Logistic regression analysis was used to estimate odds ratios for working while on a full or partial disability pension. Results: Fourteen per cent of full disability pensioners and 76 per cent of partial disability pensioners were engaged in paid work. Full disability pensioners due to mental disorders were working less often than full disability pensioners due to other diseases. Partial disability pensioners due to cardiovascular diseases were working more than partial disability pensioners due to other diseases. More recent timing of disability pension was associated with working for both partial and full disability pensioners. Working while on disability pension was more common among those with higher education. Partial disability pensioners with average pension worked more often than those with high pension. Conclusions: By knowing the factors associated with working while on a disability pension, policies could be more efficiently allocated to encourage disability pensioners to take up work. One way would be to support disability pensioners with low education to work more. Another way to increase work among disability pensioners is to support the recently retired in working longer.
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Goodley, Dan. "Challenging Transhumanism." Balkan Journal of Philosophy 12, no. 1 (2020): 5–16. http://dx.doi.org/10.5840/bjp20201212.

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This paper cautiously ponders the offerings of transhumanism. We begin the paper by introducing the transhumanist movement and related transdisciplinary thinking before giving space to the emergence of critical disability studies. We argue that the latter field has the potential to ground a critical and reflexive analysis of transhumanism– not least through a consideration of the contributions of posthuman and green disability studies. Drawing on these two perspectives, two specific areas of transhuman contemplation are offered. First, we consider (in the section titled, ‘The Ban on Straws: Disability prosthetics and the complication of eco-politics’) the relationship between disability advocacy politics and the potential ableism present in popular eco-political discourse. Second, we explore mainstreaming assistive technologies and e-waste collateral. These analytical thematics highlight the complexities of a critical transhuman disability studies, not least, in relation to the clash of disability and green politics. We conclude the paper with some considerations for future theory and research that trouble an uncritical acceptance of transhumanism in the area of critical disability studies.
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Sterne, Jonathan. "Ballad of the dork-o-phone: Towards a crip vocal technoscience." Journal of Interdisciplinary Voice Studies 4, no. 2 (October 1, 2019): 179–89. http://dx.doi.org/10.1386/jivs_00004_1.

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Abstract This piece elucidates the related politics of vocal impairment and vocal prosthesis through a close analysis of the Spokeman Personal Voice Amplifier, a.k.a., the dork-o-phone. Drawing from voice theory, disability studies and phenomenology, I present an analysis of the dork-o-phone in use and challenge the boundaries between disability and impairment. In the process, I also show how vocal impairments and protheses ultimately give the lie to the idea that voices are self-sufficient and can exist without supplementation.
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Pifer, Natalie A. "The Scientific and the Social in Implementing Atkins v. Virginia." Law & Social Inquiry 41, no. 04 (2016): 1036–60. http://dx.doi.org/10.1111/lsi.12156.

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Atkins v. Virginia (2002) categorically exempts intellectually disabled defendants from execution, yet some constitutionally suspect punishments suggest a gap between law and practice. This article moves beyond critiquing Atkins' formal implementation to provide a decentered analysis of the Atkins gap focused on the category of intellectual disability. It explores how drawing boundaries around intellectual disability in capital cases requires law to grapple with fluid scientific and social constructs through a study of how courts operationalize intellectual disability in capital cases. It draws from literatures considering the construction of intellectual disability and law's relationship to the scientific and the social and finds that this intersection first enables a conceptual disconnect between scientific and legal constructions of intellectual disability and, second, invites the use of stereotypes to inform the category. These processes undermine Atkins'—and other categorical exemptions'—ability to functionally limit extreme punishments and also reveal law as mutually constitutive.
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Hladki, Janice. "Hazardous Futures and Damned Embodiments: Disability and White Masculinization in Science Fiction Film." Journal of Literary & Cultural Disability Studies: Volume 14, Issue 4 14, no. 4 (October 1, 2020): 453–67. http://dx.doi.org/10.3828/jlcds.2020.30.

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Drawing on critical disability interrogations of the “human,” this article explores how frameworks of normalization shape conceptions of human qualification and disqualification in two science fiction films. It examines how representations of the contaminated, injured, unstable, and mutated body produce discourses of, and social anxieties about, abnormalization and monstrosity. The films The Thing (1982) and Deadpool (2016), both characterized by science fiction cult popularity, are linked through multiple concerns for human futurity, including the dangers of monstrous disability and the need to redeem damaged and infected bodies. Bringing disability together with gender and race, the article argues that white able-bodied masculinization in the films, including aspects of militarism and colonialism, focuses on human qualification and on securing a future made non-hazardous by a masculinity recuperated from vulnerability and disability.
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Price, Margaret. "The Bodymind Problem and the Possibilities of Pain." Hypatia 30, no. 1 (2015): 268–84. http://dx.doi.org/10.1111/hypa.12127.

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What is a crip politics of bodymind? Drawing upon Rosemarie Garland‐Thomson's theory of the misfit, I explain my understanding of crip and bodymind within a feminist materialist framework, and argue that careful investigation of a crip politics of bodymind must involve accounting for two key, but under‐explored, disability studies (DS) concepts: desire and pain. I trace the turn toward desire that has characterized DS theory for the last decade, and argue that while acknowledging disability desire, we must also attend to the aspects of disability, including pain, that are sometimes bad. Although I don't argue that pain is always and only bad, I call for recognition of the ways pain complicates disability desire, as well as the possibilities it opens for specifically located, collective forms of care.
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Skarstad, Kjersti. "Human rights through the lens of disability." Netherlands Quarterly of Human Rights 36, no. 1 (January 9, 2018): 24–42. http://dx.doi.org/10.1177/0924051917753251.

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Notions discriminatory to persons with disabilities commonly underpin political theories of rights. While persons without disabilities are considered “normal” and independent, persons with disabilities are commonly seen as “deviant” and dependent. Persons with intellectual disabilities are also seen as lacking the autonomy required to have human rights. Acknowledging the equal human rights of all human beings, the United Nations Convention on the Rights of Persons with Disabilities (CRPD) refutes such notions. Drawing upon relational theory, this Article provides a theoretical basis to some of the novel features of the CRPD. In contrast to many dominant theories of rights, the author argues that 1) disability constitutes a natural part of human diversity, 2) human beings are interdependent, 3) rights are achieved through supportive relations, and 4) human rights are ideals that inform how we should treat each other. The Article shows that a human rights theory fully inclusive of persons with intellectual disabilities also strengthens the human rights of others.
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Yun, Ilhong, Sejong Jung, and Jusung Yoo. "Disability and Violent Victimization in a National Sample of Adolescents: A Longitudinal Study." Violence and Victims 30, no. 6 (2015): 1099–116. http://dx.doi.org/10.1891/0886-6708.vv-d-14-00008.

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In the victimization literature, a significant association has been consistently observed between disability and the victimization of children and adolescents. It is largely unknown, however, whether individuals with disabilities continue to suffer from a heightened risk of violent victimization when they reach young adulthood and adulthood. In addition, despite the close nexus between victimization and perpetration, prior studies have generally failed to control for violent acts perpetrated by individuals with disabilities. This study addresses these issues by drawing on the panel design nature of the National Longitudinal Study of Adolescent Health. The results show that although physical disability is not linked to victimization risk, learning disability is significantly associated with an elevated risk of violent victimization.
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MacEachen, Ellen, Sharanya Varatharajan, Bronson Du, Emma Bartel, and Kerstin Ekberg. "The Uneven Foci of Work Disability Research Across Cause-based and Comprehensive Social Security Systems." International Journal of Health Services 49, no. 1 (November 14, 2018): 142–64. http://dx.doi.org/10.1177/0020731418809857.

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This scoping review identified what kinds of work disability policy issues are critiqued in articles published in countries with cause-based versus comprehensive welfare systems. Drawing on a review of work disability policy research, we identified 74 English-language, peer-reviewed articles that focused on program adequacy and design. Articles on cause-based systems dwelled on system fairness and policies of proof of entitlement, while those on comprehensive systems focused more on system design complexities relating to worker inclusion and scope of medical certificates. Overall, we observed a clear difference in the nature of problems examined in the different systems. Gaps in work disability policy literature are identified, and challenges for comparative policy research are discussed.
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Pickard, Beth. "A critical reflection on the Health and Care Professions Council Standards of Proficiency for music therapists: A critical disability studies perspective." British Journal of Music Therapy 34, no. 2 (November 2020): 82–94. http://dx.doi.org/10.1177/1359457520971812.

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This article takes the theoretical and philosophical lens of critical disability studies to critically reflect on the Health and Care Professions Council Standards of Proficiency for Arts Therapists. The discipline of critical disability studies, evolving from disability studies and the disability rights movement, is initially defined before multiple paradigms of disability are introduced as central tenets of these disciplines. The relationship between critical disability studies and music therapy is explored, with reference to seminal publications and the perceptions of music therapy within them. The Health and Care Professions Council Standards of Proficiency are then taken as a source of reflection to attempt to understand the perpetuation of medicalised perspectives in the profession and the potential friction between critical disability studies and music therapy. A selection of the Standards of Proficiency are analysed according to distinct paradigms of disability. Questions are posed to interrogate and contextualise the standards in relation to critical disability studies philosophy. From this critical reflection, a discussion emerges which reflects on the reach of these professional standards and how they might contribute to a continuing, outdated expert-model of music therapy in the United Kingdom. The article concludes by drawing these threads together in a series of recommendations to educators, practitioners and the wider profession.
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Scales, Rebecca. "Radio Broadcasting, Disability Activism, and the Remaking of the Postwar Welfare State." French Politics, Culture & Society 37, no. 3 (December 1, 2019): 53–78. http://dx.doi.org/10.3167/fpcs.2019.370303.

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Through the history of the short-lived 1947 radio show La Tribune de l’Invalide, this article examines how the social and political context of the Liberation offered disability activists a unique opportunity to demand pensions, medical care, and social services hitherto denied to them by the French state. Drawing on transcripts of the broadcasts and correspondence between listeners and the show’s host Maurice Didier, the article demonstrates how disability activists played a pivotal, if little acknowledged, role in the construction of the postwar welfare state by highlighting French society’s historic neglect of disabled civilians.
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Baumohl, Jim, Richard Speiglman, James A. Swartz, and Roland Stahl. "Substance Abuse and Welfare Policy at the New Century." Contemporary Drug Problems 30, no. 1-2 (March 2003): 501–37. http://dx.doi.org/10.1177/00914509030301-218.

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Drawing on findings from the SSI Study and other research, this paper takes up various policy questions fundamental to any welfare program for substance abusers. The paper considers the place of disability benefits in the U.S. system of categorical aid and the problems raised by substance abuse for the disability category. It discusses the desirable objectives of a welfare program for substance abusers and the various mechanisms by which they might be achieved. And finally, it considers how any new program might be positioned in the context of categorical aid and American federalism.
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Francis, Leslie J., and Susan H. Jones. "Preparing for Disability Awareness Sunday: An educational exercise drawing on psychological perspectives for biblical hermeneutics." International Journal of Christianity & Education 19, no. 3 (September 25, 2015): 197–214. http://dx.doi.org/10.1177/2056997115602485.

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Saltychev, Mikhail, and Katri Laimi. "Predicting self-reported disability level by a number of pain sites marked on pain drawing." International Journal of Rehabilitation Research 41, no. 3 (September 2018): 276–79. http://dx.doi.org/10.1097/mrr.0000000000000293.

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Meagher, Timothy. "COVID-19 and Mental Health: Should We Expect an Increase in Disability?" Journal of Insurance Medicine 49, no. 1 (January 1, 2021): 24–31. http://dx.doi.org/10.17849/insm-49-1-1-8.1.

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Disability due to mental health disorders has been increasing in many countries over the past years. The COVID-19 pandemic may worsen this trend because of 3 different, and at times overlapping, pathways. This article describes each pathway, and by drawing on the experience of previous coronavirus epidemics and recent recessions, attempts to estimate the likelihood that claims due to mental health disorders will increase.
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Staples, James. "Doing disability through charity and philanthropy in contemporary South India." Contributions to Indian Sociology 52, no. 2 (April 23, 2018): 129–55. http://dx.doi.org/10.1177/0069966718761228.

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Drawing on multi-sited ethnographic fieldwork in Hyderabad, South India, this article explores the relationship between charity and disability. Despite a stereotype of philanthropic aid as reproductive of existing power structures or symptomatic of state failures to eliminate poverty, closer investigation exposes a more multi-layered picture. Disjunctures in donor and recipient perspectives on charity are shown to create spaces in which recipients might challenge the very characterisations that allow them access to aid in the first place, revealing both the potential and the limitations of charitable aid to bring about social change for disabled people.
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Rogers, Amanda. "Transforming the national body: choreopolitics and disability in contemporary Cambodian dance." cultural geographies 27, no. 4 (December 5, 2019): 527–43. http://dx.doi.org/10.1177/1474474019892000.

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This article analyses how dance traces geographies of nation and national identity. Focusing on contemporary dance in Cambodia, particularly in relation to disability, it examines how some dancers are shifting the constitution of the national ‘body’. The article extends geographical exchanges with dance studies by drawing upon the concept of choreopolitics and analysing how it produces variegated enactments of nationality. In the process, the article works across different approaches to the study of nations and extends our understanding of how the nation is a performed entity.
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Merid, Beza, and Tamara Kneese. "Illness Narratives, Networked Subjects, and Intimate Publics." Catalyst: Feminism, Theory, Technoscience 4, no. 1 (May 7, 2018): 1–6. http://dx.doi.org/10.28968/cftt.v4i1.293.

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This introduction provides an overview of the themes of this Special Section on Illness Narratives, Networked Subjects, and Intimate Publics. Drawing on the intersection of illness narratives and human-technological assemblages, the introduction frames this section’s consideration of how illness, disability, dying, and death are mediated within emerging digital spaces.
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