Understanding Disability

Learning Objectives

In this session, you will engage with colleagues to:

  • Define disability and accessibility
  • Distinguish models of disability
  • Uncover disabling environments in higher education

Definitions of Disability

Before we explore accessibility, it is important to clarify our understanding of “disability.” According to the United Nations Convention on the Rights of Persons with Disabilities (2006), “Persons with disabilities include those who have long-term physical, mental, intellectual or sensory impairments which in interaction with various barriers may hinder their full and effective participation in society on an equal basis with others.” The CDC defines disability as “any condition of the body or mind (impairment) that makes it more difficult for the person with the condition to do certain activities (activity limitation) and interact with the world around them (participation restrictions).” The Americans with Disabilities Act (ADA) defines an individual with a disability as one who has “a physical or mental impairment that substantially limits one or more major life activities, a person who has a history or record of such an impairment, or a person who is perceived by others as having such an impairment.”

Over time, different conceptual models of disability have arisen, affecting not only our definition of “disability” but also the creation of laws, policies, and practices-including those in educational contexts. This section presents three models of disability; for a more thorough discussion, see Models of Disability.

→ As you read the next section, think about which of these models is apparent in higher ed contexts. What effect might that have on the academic success and well-being of students living with disabilities?

The Medical Model

The medical model (or individual model) considers disability as a problem of the individual that is directly caused by a disease, an injury, or other health conditions, and requires prevention interventions or medical care in the form of treatment and rehabilitation. People are disabled on the basis of being unable to function as a ‘normal’ person does. So this model is strongly normative. In the medical model, disability refers to impairment, health condition, or an ability to perform an activity in a normal way. It restricts disability to an individual phenomenon. Medical rehabilitation then has an important role to play in bringing the person back or close to the norm. The major concern of the medical model at the political level is to provide healthcare and rehabilitation services. The medical model leads to ‘paternalism, pathologisation and benevolence’ (Goodley 2016).

The Social Model

In contrast, the social model would be focused on a person’s environment, for instance the physical environment (can he access his school?) or the social/attitudinal environment (does he get discriminated against by his teachers and classmates?). The social model sees disability as a social creation. Within this framing, disability is not the attribute of the individual, but is instead created by the social environment and thus requires social change. The terms ‘impairment’ and ‘disability’ have very different meanings, with impairment referring to an individual’s condition and disability referring to social disadvantage, discrimination, and exclusion.

The minority model is another version of the social model. It was developed in North America by activists and scholars. This version says that persons with disabilities face discrimination and segregation through sensory, attitudinal, cognitive, physical, and economic barriers, and their experiences are therefore perceived as similar to those of an oppressed minority group. Social inequalities by disability status are considered as similar to those encountered by other minorities based on race/ethnicity such as ‘extraordinary high rates of unemployment, poverty and welfare dependency; school segregation; inadequate housing and transportation; and exclusion from many public facilities…’ (Hahn 2002; p. 171).

The social model has been very influential in policy. To some extent, it has grounded human rights advances, such as the United Nations CRPD, which has guided disability laws worldwide. In recent years, it has certainly dominated as a conceptual framework in research at the intersection of disability and development (Coleridge 1993; Stone 1999; Turmusani 2003). For instance, using the social model, Turmusani (2003) advocates a move away from the medical model toward the social model. Disadvantages are viewed as a result of social neglect, oppression, and discrimination, and thus unsurprisingly, it considers the environment as the ‘focal point of action’ for a policy agenda on disability (p. 146). Similarly, Amerena and Barron (2007) argue that change is needed to stop ‘the exclusion of disabled people from social, economic, political and community life’ (p. 19).

The ICF Model

There are many other models of disability, including several interactional models. One of the most influential interactional models is the International Classification of Functioning, Disability and Health (ICF) developed by the World Health Organization (WHO).
The ICF model was developed as a synthesis of the medical and social models to model and classify the consequences of health conditions (WHO 2001). It is a revision of the International Classification of Impairments, Disabilities and Handicaps (ICIDH) (WHO 1980). It was developed by WHO as part of its mandate to collect information about the health of populations worldwide. Briefly, under the ICF, disability is the result of the interaction of the environment and the person with a health condition. This model starts with a health condition (disorder or disease) that within contextual factors gives rise to impairments, activity limitations, and/or participation restrictions. An impairment, using WHO’s (2001) definition, is defined as a ‘problem in bodily function or structure as a significant deviation or loss.’ An activity is the execution of a task or action by an individual. Participation is understood in terms of an involvement in a life situation. Activity and participation domains include among others, learning and applying knowledge, mobility, self-care, education, remunerative employment, and economic self-sufficiency.
Functioning and disability are umbrella terms, one the mirror image of the other. Functioning covers body functions and structures, activities, and participation, while disability refers to impairments, activity limitations, and participation restrictions. Contextual factors refer to the entire background of an individual’s life. It includes personal factors: gender, age, coping styles, social background, education, profession, and behavioral patterns character. Contextual factors also include structural factors. They make up the ‘physical, social and attitudinal environment in which people live and conduct their lives’ (WHO 2001). They include the physical environment (terrain, climate, and architecture), social attitudes, laws and institutions (e.g., home, school and work, services, systems, and policies (e.g., transportation, health, social services)), products and technology. Structural factors may be barriers or facilitators when it comes to the individual’s functioning.

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Creating Inclusive and Accessible Learning Copyright © 2023 by Emily Scida is licensed under a Creative Commons Attribution 4.0 International License, except where otherwise noted.

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