This thesis examines the fissures and intersections between feminist digital media, queer theory, and Mad and disability studies. Moving across social media platforms, hashtag data, and digital gaming, this project argues for the subversive and creative potential within Mad/crip/queer digital identity performances. My theorizing of the avatar as an automedial figure in this project is attentive to the politics of the face as a site of encounter, to digital bodies and movement, to identification and community-building, and to embodiment and affects that move between on- and off-screen lives. This thesis follows the “bad avatar,” a collection of Mad digital identity practices that interrupt, disrupt, and transgress normalizing and normative digital spaces of North American settler capitalist culture. Claiming the bad avatar as a deliberate identity position is an act of claiming the label of “bad,” which here has multiple meanings: Mad queer bodies—physical and digital—are bad citizens because we break the heteronormative patriarchal rules. We’re troublemakers—we make trouble for power systems and those who embody power. We can be bad workers, unproductive and fatigued. We can be bad for capitalism and bad for nationalist morale. We also experience feelings that become pathologized and policed. As despair, panic, melancholy, and angst stick to our bodies our bodies themselves become framed as bad: sick, broken, wrong, a problem in need of fixing or eradication. Reclaiming “bad” is both a celebration of the willful subject (Ahmed 2014) and a challenge to the binary of “good/bad” that is used to oppress Mad and disabled bodies. / Thesis / Doctor of Philosophy (PhD) / This thesis theorizes the digital avatar as an automedial figure, a mode of virtual embodiment and a site of encounter. I use “avatar” to draw a connecting line between widely varied digital identity acts that occur across social media platforms and video games. This thesis examines the “bad avatar,” a collection of Mad/crip/disabled faces, bodies, and identity practices that interrupt, disrupt, and transgress the normalizing and normative digital spaces of North American settler capitalist culture. Mad/crip digital identity play offers avenues for enacting modes of resistance through the politics of representation and the processes of identity performance and community-building.

z & s charts the story of Sophreen and Zehra, ostensibly two girls in love, who experience transnational migration together. Through the lens of their relationship, I explore themes of embodiment, survival, complicity, cultural erasure, and the complexity of abuse and trauma for multiply marginalized people. I use poems and visual art to portray the colliding worlds of feminized people as they navigate madness, psychosis, disability, and illness in the frame of desire.

Students attending charter schools, including those with learning disabilities, are subject to policies set by individual charter management organizations. One practice used within some charter schools is grade-level retention, or having students repeat a grade level. Literature overwhelmingly indicates that retention is associated with negative outcomes, yet the practice continues to be used. One particular charter school that uses a strict retention policy and retains students with learning disabilities was studied to understand how the process unfolds. Using the conceptual frameworks of critical disability theory and critical pedagogy, the study draws inferences regarding how this phenomenon blends with ableism and power imbalances. Six teachers (four general education and two special education teachers) participated in interviews for this qualitative case study. Through triangulation of findings from individual and group interviews, trends were identified. A major finding showed that although retention is conceptualized as beneficial for the school to threat unmotivated students, for students with learning disabilities, retention is still regarded as highly ineffective and harmful. Decision making factors used with students with disabilities include particular individual characteristics, such as abilities and parental support. Discussion into participants’ perception of students with disabilities as inferior, and how retention as punishment asserts the school’s power, follows a review of concepts, effectiveness, and decision-making factors related to retention. Implications for educators to improve inclusive and fair school policies, in addition to rethinking traditional methods of analyzing school practices are discussed. Further research in various educational initiatives and areas of study are summarized.

The freak played a significant role in late-nineteenth- and early-twentieth-century entertainment, but its significance extended beyond such venues as sideshows and minstrel shows. This dissertation examines the freak as an avatar emblematic of several issues, such as class and race, traditionally focused on in studies of Turn-of-the Century American literature and culture. Disability and freakishness are explored as central to late-nineteenth- and early twentieth- century Americans’ identity. Freakishness is applied to a series of ways in which Americans in this period constructed their identity, including race, gender, and socioeconomic class, showing the dual role that the freak played for many white, able-bodied, upper-class American men. Freaks threatened such men’s sense of their own disability, triggering such complexes as Wounded Southernness or white masculinity. But contrasting themselves with freaks also solidified their visions of themselves as models of American normalcy. Besides freak shows, they encountered freakishness in a variety of arenas, including lynchings, slums, and early horror films. The late nineteenth and early twentieth century’s fascination with freakishness is situated as an outgrowth of that period’s eugenics movement, showing how the entwined concepts of eugenics and normalcy traversed ground that went much further than studies of physical aberration and chronic illness. This extended notion of the freak is discussed by analyzing various literary texts, especially the novels of William Dean Howells and Jack London. The autobiographies of Booker T. Washington and Helen Keller exemplify how double consciousness can serve as a means of enfreakment. Further, all these texts are situated culturally by medicalizing a series of historical events, including specific lynchings, as well as laws that reconfigured urban landscapes. The final chapter focuses on early horror film, arguing that film became the new American sideshow and in the process changed the definition of freak to something far more monstrous. In short, this dissertation demonstrates how the freak show pervaded America at the turn of the twentieth century and turned the country into one large dime museum.

In Canada mental health related concerns are estimated to cost the economy $20-$50 billion annually. 500,000 Canadian each week have to take time off of work because of a mental health disability. This study explores the experiences of people living with a mental health disability in the workplace. The goal is to provide an opportunity to highlight many of the obstacles they face every day. This study relies on qualitative methodologies, using semi-structured interviews to get a more detailed understanding of their experiences. This study not only highlights the perceptions, experience and challenges of people living with a mental health disability, it highlights coping strategies and suggestions for building mentally health workplaces. The participant’s personal narratives can help by providing a chance for a community to build and be used to challenge the stigma and discrimination associated with mental health. / October 2016

Submitted for the degree of Masters of Arts in the University of the Witwatersrand, Johannesburg. / Andrew Chakane 2019

This study explored the level of involvement of school social workers in the 504-Plan process as it relates to the administrative culture of school administrators, collaboration with school personnel, training on the 504-Plan process, and finally knowledge of Section 504. Attention-deficit hyperactivity disorder affects over six-million children in the world today that may benefit from the use of a 504-Plan. A total of 147 school social workers participated in this study. A self-administered survey was used, and data analysis was conducted on two levels: descriptive which employed frequency and percent distributions of respondents and analytical procedures. The Kruskal-Wallis H test utilized for this study which indicated a statistically significant relationship which rejected the null hypotheses of all four research questions. A second test was then performed, Mann Whitney U test, to determine where the significance of the hypotheses lied. Findings revealed that overall there is a low level of involvement of school social workers in the 504-Plan process of 64.8%. Twenty-nine and a third percent reported a moderate level of involvement. There was a low to moderate level of administrative culture, moderate level of collaboration, training and knowledge among the school social workers.

Submitted by Eunice Novais (enovais@uepg.br) on 2018-06-07T18:46:22Z No. of bitstreams: 2 license_rdf: 811 bytes, checksum: e39d27027a6cc9cb039ad269a5db8e34 (MD5) Francieli Lunelli Santos.pdf: 3446624 bytes, checksum: 5ad34862c214466eddc84acb539bd624 (MD5) / Made available in DSpace on 2018-06-07T18:46:22Z (GMT). No. of bitstreams: 2 license_rdf: 811 bytes, checksum: e39d27027a6cc9cb039ad269a5db8e34 (MD5) Francieli Lunelli Santos.pdf: 3446624 bytes, checksum: 5ad34862c214466eddc84acb539bd624 (MD5) Previous issue date: 2018-03-21 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Esta pesquisa analisa aspectos da trajetória de luta por direitos para as pessoas com deficiência atingidas pela síndrome da talidomida no Brasil, discutindo os eventos ao redor do que se convencionou chamar de “primeira geração da talidomida”. A tese aqui defendida é a da invisibilidade e da cidadania ausente: os nascidos nessa primeira geração, entre 1959 e 1964, vivenciaram uma ausência quase que total de direitos e de assistência por quase duas décadas. São apontados como causas para isso tanto fatores políticos como fatores culturais: os eventos “trágicos” da iatrogenia medicamentosa transcorreram às vésperas da ditadura militar, que findou apenas em 1984; e o entendimento biomédico sobre deficiência que permeou todo o período foi hegemônico e fez do corpo com impedimentos apenas alvo de intervenção física para efeitos de reabilitação. Realizou-se uma pesquisa documental, de natureza empírica e qualitativa, baseada em fontes variadas, sobretudo em jornais impressos e também em documentos jurídicos, além de documentos do poder legislativo federal e entrevistas. A partir do aporte teórico dos Disability Studies, das reflexões sobre sociedade de risco e de ponderações sobre direitos, conclui-se que, no Brasil, a cidadania dos atingidos pela síndrome da talidomida tendo sido limitada, pois fora respaldada essencialmente pelos valores da biomedicina, e como consequência, seus direitos terem sido insuficientes. De tal forma, novas demandas mobilizaram as próprias pessoas com síndrome da talidomida pela luta por reconhecimento e por mais direitos, uma luta que parece não ter fim. / This research analyzes aspects of the fight for rights path for people with disabilities affected by the thalidomide syndrome in Brazil, discussing the events around what is known as the "first generation of thalidomide". The thesis defended here is that of invisibility and absent citizenship: those born in this first generation, between 1959 and 1964, experienced an almost total absence of rights and assistance for nearly two decades. Both political and cultural factors are cited as causes for this: the "tragic" events of drug iatrogeny occurred on the eve of the military dictatorship, which ended only in 1984; and the biomedical understanding of disability that permeated the whole period was hegemonic and made the body with impairments only the target of physical intervention for the purpose of rehabilitation. Documentary research was carried out, of an empirical and qualitative nature, based on a variety of sources, mainly in print and legal documents, as well as federal legislative documents and interviews. From the theoretical contribution of Disability Studies, reflections on risk society and rights considerations, it is concluded that, in Brazil, the citizenship of those affected by the thalidomide syndrome was limited because it was supported essentially by the values of biomedicine, and as a consequence, their rights have been insufficient. Thus, new demands mobilized the people with the thalidomide syndrome themselves for the struggle for recognition and for more rights, a struggle that seems to have no end.

This thesis aims to explore the theme of isolation in the dramatic works of Tennessee Williams using his essay “The Catastrophe of Success” as the base theory text. The essay attacks the American idea of success though an in-depth examination of the “Cinderella myth” that Williams claims is so prevalent in both Hollywood and American Democracy. Williams’ deconstruction of this myth reveals that America’s love for stories like it results the isolation of three groups: homosexuals, women and the physically disabled and terminally ill. Williams passes no judgment on his characters, instead showing their lives as they truly are. Through The Glass Menagerie (1945), A Streetcar Named Desire (1947), Orpheus Descending (1957) and Vieux Carre (1977), Williams gives readers and audiences a glimpse into the lives of isolated individuals, and the struggles each group faces.

The primary question for this dissertation was: Does online professional development increase novice itinerant Teachers of Students with Visual impairments' (TVI) efficacy for assessing learning and literacy media for students with multiple disabilities including visual impairments? The literature suggested novice TVIs might experience low efficacy when implementing strategies unique to their job after leaving teacher-training programs. Working in an itinerant position can intensify perceptions of low efficacy. One area of low efficacy was conducting and reporting on the assessment of learning and literacy media (ALLM). Using a quasi-experimental pre/post-design, data were collected from pre/postintervention knowledge questionnaires about the assessment process and pre/postintervention written ALLM reports. Eleven participants with 1-5 years of experience as TVIs were divided into control and intervention groups. Four online modules were delivered to the intervention group. The data were analyzed using two dependent and two independent sample t tests. The results indicated the change scores between the control groups pre- and post-submissions did not improve. The change scores between the intervention groups pre- and post-submissions did significantly improve after participation in the online modules. The change scores overall between the intervention and control groups' pre/post submissions were statistically significant. The intervention group completed an acceptability rating scale regarding the feasibility of the modules and the results had an average score of 3.5 (4 = strongly agree). The primary limitation of this study was the small sample size and, therefore, did not allow for generalization.