Matching Items (5)
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Description
Every day we pass people without thinking everyone has a story. If an individual looks “normal,” any struggles faced living with an invisible disability are left without words or thoughts due to the dominant norm—ableism. Conversely, a more visible disability may not be dismissed as quickly. Who

Every day we pass people without thinking everyone has a story. If an individual looks “normal,” any struggles faced living with an invisible disability are left without words or thoughts due to the dominant norm—ableism. Conversely, a more visible disability may not be dismissed as quickly. Who are unseen, ignored, and misunderstood are those who live with invisible disabilities not only in a dominant able-bodied society, but also within academic scholarship as well, because they do not fit into the dominant definition of disability. In turn, binaries form between power relations and within knowledge production that create exclusion. This thesis is an intersectional analysis on expanding the definition of disability, specifically invisible disability, in order to deconstruct, challenge, and transform the hegemonic conceptualization of disability and break binaries in order to give voice to ignored and misunderstood narratives of invisible disabilities as well as foster and create nuanced understanding within knowledge production and power itself. I particularly use an autoethnographic approach to conduct this analysis of my own everyday, lived experience as a young, mixed race woman living with an invisible disability, or chronic illness, on how ableism operates in the medical sphere and at the academy, further exploring what it means to be a “good” or “bad” chronic illness patient and categorized and labeled by the stigmas attached to the definition of disability.
ContributorsGarcia, Jordan Marie (Author) / Behl, Natasha (Thesis director) / Watrous, Lisa (Committee member) / School of Social and Behavioral Sciences (Contributor) / Barrett, The Honors College (Contributor)
Created2019-05
Description

The United States houses only five percent of the world’s population but over 20% of its prison population. There has been a dramatic increase in carceral numbers over the last several decades with much of this population being people with mental illness designations. Many scholars attribute this phenomenon to the

The United States houses only five percent of the world’s population but over 20% of its prison population. There has been a dramatic increase in carceral numbers over the last several decades with much of this population being people with mental illness designations. Many scholars attribute this phenomenon to the process of deinstitutionalization, in which mental health institutions in the U.S. were shut down in the 1950s and ‘60s. However, disability scholar Liat Ben-Moshe argues that this is a dangerous oversimplification that fails to credit the deinstitutionalization movement as an abolitionist movement and to take into account shifting demographics between institutions and prisons/jails. This study considers how mass incarceration in the U.S. stems from a trend of isolating and punishing BIPOC and people with disabilities at disproportionate rates as it explores lived experiences at the intersection of mental health and incarceration. Findings inform an abolitionist agenda by highlighting the near impossibility of rehabilitation and treatment in an inherently traumatizing space.

ContributorsKirsch-Stancliff, Willa (Author) / Gerkin, Alyssa (Co-author) / Bebout, Lee (Thesis director) / Cisneros, Milagros (Committee member) / Barrett, The Honors College (Contributor) / School of Social Transformation (Contributor) / Department of English (Contributor) / Historical, Philosophical & Religious Studies, Sch (Contributor) / School of International Letters and Cultures (Contributor)
Created2023-12
Description

The thesis represented here was for my Honors undergraduate thesis project, which explored the social stigma of disability and its representational differences between congenital and acquired disability within the user comments in an online forum of discussion. Existing literature on Critical Disability Studies and Rehabilitative Psychology has noted the nature

The thesis represented here was for my Honors undergraduate thesis project, which explored the social stigma of disability and its representational differences between congenital and acquired disability within the user comments in an online forum of discussion. Existing literature on Critical Disability Studies and Rehabilitative Psychology has noted the nature of disability stigma and lack of accurate representation in social settings as well as the ramifications that follow. (Mis)representations of disability can result in bias, inaccessibility, and other social ramifications such as microaggressions because of the long history of oppression and stigmatization that disabled individuals have experienced (Keller & Galgay, 2010). Data was collected from two online forums addressing disability stigma and analyzed using both deductive coding and inductive emergent analysis of recurrent themes, experiences, or ideas that were expressed in user comments. Analysis of user comments helped address the goal of this research which aimed to explore stigma, identity, and disability within a representational context. This thesis, then, wanted to better understand disability stigma by analyzing the representational differences (if any) of congenital and acquired disabled user’s comments.

ContributorsDavis, Kamy (Author) / Nadesan, Majia (Thesis director) / Mickelson, Kristin (Committee member) / Barrett, The Honors College (Contributor) / School of Humanities, Arts, and Cultural Studies (Contributor) / School of Social and Behavioral Sciences (Contributor)
Created2023-05
Description

The United States houses only five percent of the world’s population but over 20% of its prison population. There has been a dramatic increase in carceral numbers over the last several decades with much of this population being people with mental illness designations. Many scholars attribute this phenomenon to the

The United States houses only five percent of the world’s population but over 20% of its prison population. There has been a dramatic increase in carceral numbers over the last several decades with much of this population being people with mental illness designations. Many scholars attribute this phenomenon to the process of deinstitutionalization, in which mental health institutions in the U.S. were shut down in the 1950s and ‘60s. However, disability scholar Liat Ben-Moshe argues that this is a dangerous oversimplification that fails to credit the deinstitutionalization movement as an abolitionist movement and to take into account shifting demographics between institutions and prisons/jails. This study considers how mass incarceration in the U.S. stems from a trend of isolating and punishing BIPOC and people with disabilities at disproportionate rates as it explores lived experiences at the intersection of mental health and incarceration. Findings inform an abolitionist agenda by highlighting the near impossibility of rehabilitation and treatment in an inherently traumatizing space.

ContributorsGerkin, Alyssa (Author) / Kirsch-Stancliff, Willa (Co-author) / Henson, Abigail (Thesis director) / Bebout, Lee (Committee member) / DeMarse, Angela (Committee member) / Barrett, The Honors College (Contributor) / School of Criminology and Criminal Justice (Contributor) / School of Social Transformation (Contributor) / School of Human Evolution & Social Change (Contributor)
Created2023-05
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Description
Over thirty years after the passage of the landmark Americans with Disabilities Act (ADA), the meaning of disability accessibility and justification for accessibility measures remains unclear. Connecting work in social and political philosophy to scholarship in disability studies and disability law, this project offers an account of what access is

Over thirty years after the passage of the landmark Americans with Disabilities Act (ADA), the meaning of disability accessibility and justification for accessibility measures remains unclear. Connecting work in social and political philosophy to scholarship in disability studies and disability law, this project offers an account of what access is and why access is often owed to disabled people. This project argues that disability access is necessary both for the same reasons access is considered necessary for the non-disabled, and for counteracting harmful narratives about disability and disabled people. These narratives and stereotypes originate from a particular ideology, termed “the ideology of abledness.” This ideology informs the way policies are formed and the ways they are received; it also explains why considerations of disability are often absent in general policies, and why unique provisions for disability accessibility are necessary. In its effort to clarify disability access, the project tackles difficult questions such as the nature of accessibility, issues of cost and who is obligated to pay for accessibility measures, how all people with disabilities can be included in a social contract theory, and how disability accessibility relates to and can even expand the way non-discrimination is understood.
ContributorsLevit Ades, Rachel (Author) / McGregor, Joan (Thesis advisor) / Calhoun, Cheshire (Committee member) / de Marneffe, Peter (Committee member) / Francis, Leslie (Committee member) / Arizona State University (Publisher)
Created2023