This thesis draws on the experiences of 21 young people transitioning from a special school for students with labels of moderate learning difficulty, to further education college. Taking a disability studies approach, that is, viewing disability as a social and political response to human diversity, I examine some social processes through which student identity and agency meanings may be negotiated during transition. Times of change offer circumstances of opportunity in which new identity and agency meanings may be improvised and tested in various forms. Some students found emergent ways to subvert and transgress expectations, given the different labels applied to them. Transition, with its focus on future change, offers limbic moments which appear to support situations for such opportunistic transgression. Of particular interest are the environments and circumstances that support or promote broadening of identity and agency options, because an understanding of these may enable the engineering of such situations. Whilst the students were transitioning to college, my own researcher subjectivities and understandings of ‘knowledge’ were also in flux. I describe the considerable influence these changes had on the research processes and my understandings of identity and agency. I propose that identity and agency meanings, whilst fluid and ever-changing, are linked with particular people and situated in particular social sites. With this in mind, and as a provocation to new ways of thinking I discuss foundation level further education as an ethical project, envisaging circumstances that may support and promote broader, more positive opportunities for identity and agency negotiations amongst young people with labels of learning disability. In this context, further education is re-imagined as an opportunity for potential empowerment, repositioning learning disabled students as agents of social change.

The grotesque has long been utilized in literature as a means for subverting societal constraints and inverting constructions of normalcy. Unfortunately, in many instances, it has been constructed at the expense of disabled characters using their embodiment as metaphorical plot devices rather than social and political agents. Criticism of the grotesque’s use of bodily difference has prompted this analytical project in order to rethink disability as socially and politically positioned within texts, rather than simply aesthetics for symbolic means. The aim of this paper is to explore the ways the literary grotesque can be reread using queer theory and crip theory as frameworks for constructing agential disabled embodiments in Katherine Dunn’s Geek Love. Ultimately, the potential of queer and crip interventions necessitates an examination of the systems of power disabled subjects operate within in these narratives.

This dissertation explores the effects disability had on the aesthetics of American modernist writers like Langston Hughes, William Faulkner, Amy Lowell, and Ezra Pound at a time when eugenics' insistence on a superior and uniform humanity dominated social thought and how their writings complicate generalized conclusions espousing ablist tendencies in modernist literature, demonstrating that such generalizations can be complicated with careful attention to a broad range of modernist texts. The introduction highlights important ideas and events in the development of disability studies and applies the theory to Emily Dickinson’s “Safe in their Alabaster Chambers” to demonstrate how scholars have largely overlooked even well-known authors’ engagement with disability. The first chapter interrogates Faulkner's The Sound and the Fury to demonstrate that, rather than reify disability, Faulkner questions the idea of norms that imply a stable identity by alluding to and investigating ideas relevant to important events and conceptions of the time such as Henry H. Goddard’s The Kallikak Family and the U.S. Supreme court case of Buck v. Bell. Chapter two’s analysis of Langston Hughes's Fine Clothes to the Jew identifies a tendency in the poetry to enact Tobin Sieber’s concept of disability masquerade to assume but play against the intellectually disabled identity forced on Blacks at the time, rather than attempting to distance himself from the label as disability theorists such as Douglas Baynton posit generally occurs when racialized groups are associated with disability. In the third chapter, Robert McRuer’s concept of compulsory able-bodiedness is identified as a source for Amy Lowell’s fall from popularity and she is considered alongside conceptions of the freak to identify a source for her creativity most evident in the "polyphonic prose" of Can Grande's Castle, her invention to free poets of the restrictions of traditional cadenced verse. The final chapter offers a reading of Pound's Drafts & Fragments that, while highlighting this often neglected collection's importance because of the social awareness brought to it through Pound's twelve and a half years in a mental institution, also explores the limitations of readings that assume that his disabled status guided this poetry. Concluding the dissertation is an analysis of Sherman Alexie's Pulitzer prize winning young adult novel, The Absolutely True Diary of a Part-Time Indian, that demonstrates disability’s continued applicability after eugenics’ fall from grace and highlights Alexie’s use of humor to get readers to stare as a part of considering the serious topics he writes into the novel, instigating what Rosemarie Garland-Thomson calls the "good stare" that welcomes identification between staree and starer. Together, these chapters attempt to further expand the inclusivity of discussions of modernism and complicate long-standing understandings of disability.

abstract: This study re-frames learning disabilities (LD) through the emotion-laden talk of four Latina/o students with LD. The research questions included: 1) What are the emotion-laden talk of Latina/o students about being labeled with LD? 2) What are Latina/o students' emotion-laden talk of the idea of LD? I identified master narratives, the "pre-existent sociocultural forms of interpretation. They are meant to delineate and confine the local interpretation strategies and agency constellations in individual subjects as well as in social institutions," (Bamberg, 2004, p. 287) within the following literatures to inform my research questions and conceptual framework: a) historiography and interdisciplinary literature on LD; b) policy (i.e., Individuals with Disabilities Education Act (IDEA)), c) the academic and d) social and emotional dimensions of LD; and e) student voice research with students with LD. Interdisciplinary, critical ethnographic and qualitative research methods such as taking into account issues of power, etic and emic perspectives, in-depth interviewing, field notes were used. Total participants included: four students, three parents and three teachers. More specifically, descriptive coding, identification of emotion-laden talk, a thematic analysis, memoing and intersectional and cultural-historical developmental constructs were used to analyze students’ emotion-laden talk. Emotion-laden talk about being labeled with LD included the hegemony of smartness, disability microaggressions, on the trinity of LD: help + teachers + literacy troubles, on being bullied, embarrassment to ask for assistance from others and help as hope. The emotion-laden talk about the idea of LD included LD as double-edge sword, LDness as X, the meaning of LD as resource, trouble with information processing, speech, and silence, the salience of the intersection of disability, ethnicity and language and other markers of difference, struggles due to lack of understanding and LD myths. This study provides a discussion and implications for theory, research, policy, and practice. / Dissertation/Thesis / Doctoral Dissertation Curriculum and Instruction 2016

abstract: From Impossible Angles Towards Strategic Ones: Narratives of Death, Life, and Disability in La Muerte me Da and El Huesped The glamour of single-handedly overcoming adversity, sidestepping obstacles, or defying the odds makes for great mystery or adventure fiction, but fails to do justice (poetic or otherwise) to lives that are both physically and conceptually "marked" by more complex challenges. From a theoretical view, a similar desire to escape or maintain the perceived "dividing line" between fact and fiction, nature and nurture, mind and body, is confronted by a diverse set of human experiences, all of which have come to be defined, and continue to define themselves, along both sides of such a divide. Disability, typically viewed as an "emerging" branch of literary and cultural critique, is perhaps the most pervasive. Hidden under the covert language of the "grotesque", "monstrous", "doppelgänger", "freak", "eccentric" or "queer", disability has historically represented something other than itself. Two texts that attest to both the real and imagined possibilities of resignification and new modes of articulation surrounding disability are La muerte me da (2007) by Cristina Rivera Garza and El huésped (2006) by Guadalupe Nettel. From different points of departure, both texts offer a narrative approximation towards the disabled mind, body, and perceptual experience. In ways that are both similar and different, these narratives question one's perceived access to that which is otherwise understood to be the physically and conceptually "inaccessible" or "illegible" space of disability. Such approximations towards, and articulations of, the disability experience are processes that move, largely unnoticed, both within and beyond texts. As this construct continues to transform itself from both within and outside itself, disability acquires intellectual and practical value while requiring the "experts" in fields beyond the narrow scope of medicine, education, and rehabilitation to (re)consider their own approaches to, and apprehensions of, disability in order to redefine what or who is accessible or viable for literary and cultural debate. / Dissertation/Thesis / M.A. Spanish 2014

<p> The purpose of this study was to examine the effectiveness of a group art therapy intervention on psychological well-being of Korean mothers of children with disabilities. This study employed a quasi-experimental pre- and post-test research design with non-random assignment of participants to either the art therapy intervention group (AG) or the control group (CG). The present study quantitatively examined the effectiveness of the group art therapy intervention using four standardized measurements (Parental Distress sub-scale from Parenting Stress Index-Short Form, Perceived Stress Scale, Beck Depression Inventory-II, &amp; The Multidimensional Scale for Social Support) assessing parenting stress, perceived stress, depression, and perceived social support. In addition, the Draw-a-Person-in-the-Rain (the DAPR) assessment with numerical scoring system was used to assess the mothers&rsquo; stress. </p><p> A total of 44 participants from multiple regions across Korea were included, and mothers in AG (<i>n</i> = 22) participated in 6 sessions of 100 minutes in length. The results of the statistical analysis showed significant differences between the two groups in parenting stress, perceived stress, and depression with those in the AG reporting a greater decrease in parenting stress, perceived stress, and depression than those in the CG. In terms of perceived social support, no significant difference was found between the AG and the CG. The results of the DAPR-Stress scale showed that stress indicators on the post-drawing assessment decreased significantly compared to the pre-drawing assessment after participating in the art therapy intervention. Thus, the art-based projective drawing assessment (the DAPR) supported the quantitative results of the art therapy intervention on decreasing stress. Overall findings support the effectiveness of the group art therapy intervention in enhancing psychological well-being of Korean mothers of children with disabilities.</p><p>

The purpose of this thesis was to explore socially constructed discursive barriers to physical activity for people with physical disabilities. This research was informed by a critical disability studies framework. Eight interviews were conducted, split between end-users and stakeholders. The end-user article discusses their perspectives with regard to their own PA participation, their use of PA resources, and their views of how disability is constructed. The stakeholder article deals with their views with regard to Canada’s progress in creating inclusive PA guidelines, the research process as it effects people with physical disabilities, and how disability is constructed. The results showed awareness among both groups of the social model of disability, but that the medical model is still firmly rooted. Work is needed to create inclusive promotional materials and disseminate them effectively. An effective advocacy and lobbying effort was suggested as one avenue towards a possible solution to this issue.

This dissertation investigates discourses of anti-violence strategies in the context of international development. While violence against women is, of course, an urgent problem, this dissertation explores how the urgency to end violence against women is socially, culturally, economically, and politically constructed. I consider the manufacturing of urgency in three case studies of contemporary anti-violence initiatives: i) American foreign policy including what has been branded as “The Hillary Doctrine” and proposed International Violence Against Women Act; ii) the World Bank’s report entitled The Cost of Violence; and iii) the United Nation’s UNiTE To End Violence Against Women and Say NO campaigns. In doing so, I argue that World Bank, the United Nations, and American foreign policies are too often technocratic, narrow, depoliticized, and are executed in an urgent manner in the interest of neoliberal economic growth, security concerns, and “feel good” aid at the expense of more holistic, effective and accountable responses to global violence against women.

Although more students with learning disabilities (LDs) are attending postsecondary institutions, faculty lacks the necessary training to educate students with LDs. A need exists to ensure that their college experiences include resources or support services to help students meet their academic requirements. Without support services, students may encounter poor outcomes in postsecondary education. This bounded, qualitative case study was designed to explore perspectives and experiences of students with LDs related to student services and accommodations at a postsecondary institution. Knowles's theory of andragogy formed the study's conceptual framework. A purposeful sample of 6 students, who were medically diagnosed as having a learning disability and who were, at the time of the study, receiving support services from the office of student support services, participated in the semistructured interviews. Qualitative data were analyzed using open and axial coding to search for patterns and emerging themes. Key results included that even though students were satisfied overall with the services and accommodations provided by the university, they lacked adequate support from some of the faculty on the importance of accommodations and services and how they influence academic success in postsecondary education. Based on the findings, a 3-day professional development training was developed to educate faculty in learning disabilities, understanding accommodations, and enhancing their abilities to provide support in working with students with LDs. These endeavors may promote positive faculty-student relationships and increased academic success of students with LDs in postsecondary education.

There has been a heightened effort to research the overwhelming prevalence of sexual assault on college campuses. Female undergraduates are the most common victims, with rates of one in five experiencing nonconsensual sexual contact during their college years. However, there is very little research that has examined sexual assault among students with disabilities. Students with intellectual disability are sexually assaulted at rates more than seven times higher than students with no disabilities. Thus, students with disabilities are hidden victims who experience sexual violence at extremely high rates. The current study used an online survey to assess the prevalence of sexual assault among students with disabilities at a large southern university. Findings may help inform future prevention efforts to help the high rates of sexual violence rates among students with disabilities on college campuses.