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This chapter explores the process through which one's moral career proceeds as one acquires a physical disability later in life. The author, who acquired a disability later in life, explores Goffman's notion of “moral career” as a process constructed from one's experience with both physical access and social access to the environment in which everyday interaction takes place. Using the extant literature and his personal experience, the author argues that one's identity as a person with a disability is always in a state of evolution. Rather than stable and fixed, it is unstable, although the rate of change is quite variable.

The concept that guides the present research is orientation toward disability. This concept is related to, but broader than, the concept of disability identity that has driven some previous research in this area (see, e.g., Gill, 1997; Putnam, 2005). The concept of identity or self suggests a person's definition of him or herself and usually includes both cognitive (“I am a person with a disability”) and evaluative (“I am proud to be a person with a disability”) components.

The number of students with disabilities pursuing a college education has increased dramatically in recent years (Hall and Belch, 2000; Hitchings et al., 2011; Horn et al., 2006; Retish and Horvath, 2005; Snyder et al., 2016; Stodden et al., 2001), yet, evidence suggests that these students continue to encounter significant challenges and barriers that may have a dramatic effect on their college experience (Madaus and Shaw, 2006; Sniatecki et al., 2015; Stodden et al., 2001). The paper aims to discuss this issue.

Positive experiences and aspects of being a college student with a disability have not garnered as much consideration and have received little attention in the professional literature to date. The current study sought to address this gap through examination of positive aspects of disability among 12 undergraduate students. Data were gathered via qualitative interviews.

Results included five distinct themes related to students’ experiences: personal growth and self-acceptance; empathy/understanding; advocacy and teaching others; unique relationship experiences and opportunities; and drive/determination/perseverance.

The implications of these themes and future directions for research on positive aspects of disability are also addressed.

The results of this study provide support for the social model of disability as a lens to view individuals with disabilities as complete people who, with their impairments, can and do go on to lead positive and meaningful lives.

We study disability duration and two aspects of disability timing (simultaneous vs. gradual onset; childhood vs. adulthood onset) for U.S. community-dwelling adults. The data set is the National Health Interview Survey Disability Supplement. Disabilities in personal care, household management, and physical tasks are analyzed. Results show that most adults with disability are older and have recent onsets. But up to a third of those whose disability started in childhood have entered middle and older ages. For most people, disabilities in a domain usually all start at the same time; gradual accumulation is less common. The mixing of simultaneous and gradual onsets, and of childhood-onset and adulthood-onset, produces great heterogeneity in the population of disabled adults. Our results give demographic support to the contemporary movement in local and state jurisdictions to combine aging services and disability services.

The purpose of this chapter is to reconsider the five principles of Elder et al.'s (2003) life course theory while centering disability status as an axis of inequality. We use existing research from the fields of the sociology of disability, disability studies, and aging and the life course to reflect on ways in which each life course principle can better attend to the experiences of disabled people. We start with the principle of time and place and discuss how cohort and period effects facilitate a deeper understanding of disabled people's experiences historically. Next, we analyze the principle of timing with an emphasis on cumulative dis/advantage to establish how disability status is an axis of inequality that contributes to the accumulation of social disadvantage and intersects with other axes of inequality (e.g., race, class, and gender). Then, we discuss the two principles of agency and linked lives and employ the concept of “bounded agency” to describe how ableism limits the agency of disabled people. Finally, we examine the principle of life-span development and discuss how adaptation and resilience are contextual and an ordinary part of human experiences. We conclude by offering recommendations for both life course and disability scholars to consider in hopes of broadening our theoretical and empirical knowledge about the lives of disabled people at every stage of the life course and the mechanisms by which resources are stratified by disability and age.

This chapter explores the challenges for the application of the concept of disability to other categories of oppression utilized in the notion of intersectionality.

The concept of intersectionality argues that oppression occurs within the contexts of class, race/ethnicity, religion, gender, and sexual orientation. We raise questions about the applicability of intersectionality to persons with disabilities. Using a Symbolic Interactionist approach to understand the matrix of domination or subordination, we examine how well disability as a category of disadvantage applies to intersectionality.

We argue that the fluid, heterogeneous, and discordant status characteristics, physicality, and diagnostic ambiguity of disability present a considerable challenge for the application of intersectionality as a useful paradigm for disability studies. While several ascribed statuses may contribute to the oppression of persons with disabilities, disability itself offers many unique challenges to understanding the intersection of these traits in the lives of these same people.

The conceptual uniqueness of disability produces rather complex methodological circumstances for understanding the social identity of persons with disabilities who are simultaneously members of additional categories of oppression. These complex and challenging methodological issues can best be met qualitatively, i.e., by approaching disability as lived experience.

For students of intersectionality, this chapter offers a comprehensive analysis and assessment of the concept of disability as a category of oppression.

Inclusive practices are supported and increasingly being implemented in Malawi. Transition to inclusion requires partnerships in which parents, educators, policymakers, and community leaders come together to build an understanding of disability which values inclusion and promotes the use of innovative, contextualized strategies to facilitate inclusive perspectives and practices. The purpose of this chapter is to highlight how one agency, the Parents of Disabled Children Association of Malawi (PODCAM), is working with parents, educators, and community members to build more inclusive schools and communities for students with disability.

In the past decade, entrepreneurship research has evolved with the contribution of different scholars, but there is a lack of studies available that focused on entrepreneurship with disabilities. The objective of the research is understanding differently abled entrepreneurs and their entrepreneurial journey. How challenges caused by disability contribute to motivate them to pursue entrepreneurship as a career. This study is based on “Underdog entrepreneurs: Challenge-based entrepreneurship model” theoretical model proposed by Miller and Breton-Miller (2017).

This qualitative research includes case study methodology to study eight differently abled entrepreneurs. All the identified cases are located in the city of Ahmedabad, Gujarat, India. In-depth interviews and multiple visits were scheduled to collect the data. Transcripts of the interview and observation notes were developed for the analysis of the content according to the adopted theoretical model.

Differently abled entrepreneurs show similar traits as the non-disabled entrepreneurs. They are also found to be more resilient and persistent while dealing with the challenges of failure, stress and uncertainty. Difficult conditions and experiences of discrimination indirectly prepare them for tackling challenges while pursuing entrepreneurship. People close to differently abled entrepreneurs play a critical role in shaping and supporting their ventures.

Owing to the lack of authentic information available on disabled entrepreneurs, the study does not include different entrepreneurs with more disabilities such as hearing impairment, speech impairment and mental illness. The study also focuses on the entrepreneurs of Ahmedabad City, Gujarat because of the similar reason.

This paper is an original submission and contributes towards understanding the differently abled entrepreneurs.

This chapter examines disability rights movement's rejection of a right to physician-assisted suicide (PAS). Supporters of PAS frame the right to enlist a physician's help in determining the nature and timing of one's death as a fundamental liberty interest and as a right to privacy. The disability opposition counters this with disparate impact and slippery slope arguments and stories of disability pride as a rhetorical rejection of a right it deems dangerous and discriminatory. In examining this clash of rights talk, this chapter analyzes the legal and political consequences of anti-rights rhetoric by a movement that is grounded in notions of autonomy and self-determination.