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Transition From Adolescence to Adulthood, Disability and

The Individuals with Disabilities Education Act (IDEA), the federal law requiring that all students with disabilities receive free and appropriate public education, has since 1990 required that the educational programs for adolescents receiving special education services also include a focus on services and instruction that enable students with disabilities to “transition” from secondary to post-secondary education and adult life. The term transition generally refers to the movement from adolescence and school to adulthood, independent living, and work. This transition from adolescence to adulthood is a universal experience, but by the mid-1980s, it was evident that for students with disabilities, it was an experience that was too frequently unsuccessful. National studies over the past 2 decades have shown that although the situation has improved over time, students with disabilities lag behind their nondisabled peers in attainment of important transition outcomes. Namely, students with disabilities have more limited involvement in postsecondary education, lower rates of employment, lower wages earned if employed, and limited independent living and community inclusion.

Factors That Influence Transition Outcomes

When considering issues of diversity in education, it is self-evident that disability itself is a source of diversity. However, there are other factors, some co-occurring with disability, that warrant consideration when considering issues of diversity and transition. Two of the most widely researched are gender and type of disability. The following section examines these factors that influence transition outcomes for students with disabilities.

Gender and Disability

Research shows that girls and young women with disabilities achieve less positive transition-related outcomes than do their male peers with disabilities. Prior to examining this issue further, it is important to make several points. First, girls and young women with disabilities are not a homogenous group. Disability determinations vary from country to country and even within countries. For this entry, the World Health Organization's (WHO) International Classification of Functioning, Disability, and Health serves as the point of reference for defining disability. The WHO defines disability as an outcome of the interaction between a person's health condition and contextual factors that result in an impairment of body function or structure, capacity limitations, and/or performance or participation restrictions. This is a broad definition that acknowledges the role of biological limitations and societal barriers.

Second, there is a reciprocal relationship among gender, disability, and several other factors impacting equity in education, including socioeconomic status and poverty level as well as race and ethnicity. For example, there is a reciprocal relationship between poverty and disability. Poverty can cause disability, particularly in women and girls who, in the face of limited resources, are more likely than their male counterparts to be deprived of basic necessities such as food and medicine. Disability, in turn, can contribute to poverty because of the additional expenses that it can entail or its impact on employment. Thus, girls with disabilities are disproportionately likely to grow up in poor families, a reality that, in itself, places them at an educational disadvantage. Race and ethnicity can also be a compounding factor. For instance, in the United States, there is a disproportionate number of African American students receiving special education services, which, in part, reflects the intersection of race and disability bias, and thus affects educational equity.

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