6 research outputs found
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Who counts and who is counted? Conversations around voting, access, and divisions in the disability community
Online voting platforms have been introduced in some locations as the solution to the many barriers to political participation that disabled people continue to face. Reading the experiences of disabled student voters on university campuses alongside broader trends in electoral reform taking place in jurisdictions across Canada allows us to attend to the dangerous ways in which conversations around access have been limited through virtual solutions that encourage the physical absence of disabled voters. This article situates these absences alongside other categories of exclusion–including groups who are formally disenfranchised–and recalls many unstated values that are active in shaping citizenship cultures. Probing online voting through a critical disability angle, we present a critique of techno-fixes that builds upon broader notions of accessibility and inclusion
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Breaking the rules: Summer camping experiences and the lives of Ontario children growing up with polio in the 1940s and 1950s
This chapter presents an analysis from a critical disability studies history framework developed for a research project. It discusses how the research was conducted using an oral history method and how the analysis was produced. Oral history narratives of individuals living with polio are viewed as the most appropriate and important way to learn about and understand the meaning of polio for Canadians during the time period of 1927–1957. The chapter provides a historical backdrop to describe the development of some Ontario Society for Crippled Children (OSCC) camps, the philosophic basis for the camps, and the intended goals of the camping program. It deconstructs the philosophy of the OSCC, and presents some overarching themes. Each of the themes illustrates an aspect of the ableist dominant view of disability in relation to understandings of disabled children's lives at that time. The chapter introduces the counter narratives of the participants who attended these camps and their everyday lived experiences
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An education and negotiation of differences: the ‘schooling’ experiences of English-speaking Canadian children growing up with polio during the 1940s and 1950s
In this paper we present oral narratives focusing on schooling experiences of Canadians who lived with polio as children between 1940 and 1959. We argue that disabled students with polio received an education about the differences ascribed to them by individuals in authority (teachers, principals), by other young people, and through the dominant negative discourses of polio and normalizing, ableist practices of schooling. Using narrative accounts from participants’ interviews, we analyze their school experiences of difference: inaccessible physical and temporal spaces, bullying at school, exclusion from classes, and negotiating youth culture related to shoes, clothes and friendships. However, participants were not passive and they discussed how, along with families, they negotiated and occasionally defied normalizing processes. This research gives voice to a generation of disabled English-speaking Canadians, whose stories about school have not been heard before
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Playing with Normalcy: A Disability Material Culture Analysis
We recast a toy figure as a cultural agent of various interlocking and hegemonic discourses, and in particular, explore how normative discourses are reflected in material objects. We suggest that the Toy Gymnast represents and reinforces these discourses and therefore influences how children learn that normative bodies are desirable
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The Violent Consequences of Disclosure … and How Disabled and Mad Students Are Pushing Back
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Unlearning through Mad Studies: Disruptive pedagogical praxis
Medical discourse currently dominates as the defining framework for madness in educational praxis. Consequently, ideas rooted in a mental health/illness binary abound in higher learning, as both curriculum content and through institutional procedures that reinforce structures of normalcy. While madness, then, is included in university spaces, this inclusion proceeds in ways that continue to pathologize madness and disenfranchise mad people. This paper offers Mad Studies as an alternative entry point for engaging with madness in higher education, arguing that centring madness in pedagogical praxis has the potential to interrupt hegemonic ways of knowing, being, and learning. We illustrate how this disruption is facilitated by examining particular aspects of pedagogical praxis mobilized in Mad Studies, including building curriculum alongside mad community, centring madness in course design and student assessment, and the practice of mad positivity. Ultimately, this approach provides a metacurriculum of unlearning, challenging students to consider how their engagement with madness in the classroom, and beyond, has the potential to disrupt sanist systems of oppression and the normalcy they reconstitute