Disability studies in education

Disability studies in education is a field of academic study concerned with education research and practice related to disability. DSE scholars promote an understanding of disability from a social model of disability perspective to "challenge social, medical, and psychological models of disability as they relate to education". A DSE perspective situates disability within social and political context and is concerned with the civil and human rights of students with disabilities, including issues of equity, access, and inclusion in educational settings, curricula, and activities.
DSE emerged as a part of the broader, interdisciplinary field of disability studies and as a critique of special education, which aims to enhance individuals with disabilities' performance by focusing on changing their given educational environments and the limitations placed on them to foster growth and opportunities. SPED focuses on improving outcomes for individuals with disabilities without stigmatizing them with hopes of building a society that is more accepting of individuals with disabilities. By contrast, DSE proponents argue that education should be inclusive of students with and without disabilities to best foster awareness and understanding of disabilities. SPED lacks the challenge of the social model of disability, which is seen in DSE.
DSE is one manifestation of the disability rights movement. Its roots are in the United States, but its effects may be felt globally. With the entry into force of the UN's Convention on the Rights of Persons with Disabilities, issues underpinning DSE can extend to efforts to hold states accountable for failure to serve a range of disability communities.

History

DSE became more prominent around the 1990s when educators became leaders within the Society for Disability Studies and research became more visible in the United States disability studies community. The SDS became a place in the U.S. that was labelled as the "clearinghouse of disability studies", and also held conferences and had a journal named, Disability Studies Quarterly. At the forefront of the SDS was three members in the Disability Studies in Education, Phil Ferguson, Susan Gabel, and Susan Peters. In the 1990s, these three individuals were highly active in the disability studies realm, keeping the connection between educational research visible within the disability studies community in the United States. In the late 1990s, DSE became more popular in Europe, Australia, and New Zealand.
Some recognize the expansion and formalization of Disability Studies in education were caused by a small international conference funded by the Spencer Foundation and hosted by Linda Ware. This 1999 conference challenged the way the current ideology had decreased inclusive education and criticized the special education system. Also in 1999, Scot Danforth submitted a proposal titled Ways of Constructing Lives and Disabilities: The Case for Open Inquiry to the national conference of The Association for Persons With Severe Handicaps. This led to questions being asked about why research is important and then the expansion of what is considered legitimate research in special education journals, conferences, etc. It also led to new ways that ideate a different way of educating students with disabilities. Susan Gabel and Linda Ware insisted on affiliating special education with the academic discipline, Disability Studies. From there, Disability Studies in education strengthened as its own discipline.

Foundations

DSE scholarship is based on a social conception of disability that identifies barriers, attitudes, and actions that serve to systematically exclude individuals with disabilities society. These may include lack of resources for students and knowledge on how to effectively teach individuals with disabilities. It is a reaction to the dominant medical model of disability which positions people with disabilities as having limitations outside of the "normal" or typical boundaries that require remediation and intervention. Examples of the medical model may look like professionals in an individualized education plan being the authority. Their goal is to fix the disability or "normalize" the individual. DSE has its origins in sociological theories of deviance, social stigma and labeling theory as social construction. By 1970, there emerged critiques of labeling in special education, now referred to as ableism. Ableism is combated in schools through educators recognizing and challenging the idea of normalcy, as well as integrating individualizing programs that both recognize disability while creating learning opportunities in order to foster participation in the classroom with peers.
The social model of disability positions physical, intellectual, psychological, sensory, and emotional variations as natural and therefore requires societal changes in the response to those variations. The problem therefore resides not within the individual with impairments, but in the attitudes toward and treatment of people with disabilities. A DSE perspective is grounded in the belief that a collective social response to disability has resulted in systematic inequality, marginalization, discrimination, and oppression. There is also the recognition that disability is both a form of individuation and group identification. Because individual identities are complex and intersect with other identity categories, there are varied ways that individuals may identify themselves as disabled. DSE can be supported by laws that make discrimination against people with disabilities illegal.

Issues

DSE is concerned with critical issues concerning the education of people identified as disabled. Central questions of concern to DSE scholars are:

What is an appropriate education for students with disabilities?
What are criticisms of the medical model of disability in education?
What counts as research and inquiry?
What is inclusion and who is included?
Appropriate education for students with disabilities

DSE scholars promote academic activism in that they seek to counter the dominant discourse of the disabled student as deficient and abnormal. They criticize special education as an inadequate response to disability which seeks to remediate the individual in order for them to fit in with the norm. They promote a social justice perspective in which the purpose of education is to accept and care for all students. When putting a label on what is appropriate versus what is not can be hard to navigate without knowing the definition. An appropriate education for students with disabilities can be defined under the Individuals with Disabilities Education Act as Free Appropriate Public Education. This includes education services that meet the individual's needs on the same level as non-disabled students. Keeping the needs of the child at the forefront of the educational plan is essential in creating an appropriate education. It also includes being in the least restrictive environment possible. Creating an appropriate education plan for students with disabilities, services should be designed in order to meet the individual's education needs while also not being physically excluded from a mainstream focus. This also mean that a student with disabilities should receive the same quality of education services as a non-disabled student would. There also needs to be periodic Individualized Education Program meetings with the IEP team where reevaluation takes place. The parents or guardians have legal rights to be involved, review records, and challenge placement or other IEP decisions. Lastly, a student with disabilities should be able to participate or experience nonacademic services and extracurricular activities, like P.E., transportation, and groups or clubs sponsored by the school.

Criticisms of the medical model in education

Using the medical model of disability in education is heavily criticized by DSE scholars. The medical model of disability assumes that someone's disability limits their autonomy and therefore needs to be fixed/cured. In education, it is the responsibility of the student to work hard to fix/cure their disability and not society's responsibility to remove barriers. Although it is the responsibility of the student to work towards "normalcy", they are not the authority. The professionals take the authoritative role over the caregivers/student and if the professionals believe that they cannot be "fixed", it may lead to social and/or educational exclusion. Exclusion is a consequence of the medical model because it emphasizes the "sick role" that perpetuates stigmatizing attitudes towards students with disabilities. In actuality, these same attitudes are misguided because many learning disabilities are not caused by biological factors and most do not need constant medical services.

Research and inquiry

DSE scholars challenge research methodologies that serve to objectify, marginalize, and oppress disabled people. They promote research that is created by and accountable to disabled people, rather than portraying them as subjects. They recognize the value of interdisciplinary approaches within and outside the educational field and promote interaction among researchers from a variety of disciplinary perspectives. Research on DSE depends on who is telling their story, and who is being recorded in the research. The research is not intended to exclude some voices of the disability community, but to amplify all voices to share their stories. Research in DSE holds power because it can be used as a tool for others in society who deserve equity, inclusion, and dignity. In DSE research there is no evidence to claim the research is scientific. Most of the research is made up of beliefs and assumptions. This is because researches are not free from theory free observation, thus causing observations to be influenced. Scientific research procedures can objectify people with disabilities because they are looked at as subjects instead of people.