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Children with Disabilities in South Africa: Policies for Early Identification and Education

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Social Justice and Education in the 21st Century

Part of the book series: Diversity and Inclusion Research ((DIRE))

Abstract

The majority of people with disabilities reside in developing countries, which have a high number of people living in poverty. Disability exacerbates poverty due to reduced employment and increased medical costs, while poverty exacerbates the incidence and effect of disability due to lack of access to care. Studies have shown that disability results in a reduced chance of attaining appropriate levels of education, higher rates of unemployment, limited/no access to health facilities, or services and schools with no resources. Although equality and educational rights for disabled students are documented under the South African Constitution (1994), catering for the needs of students with disability in a developing country is challenging. In South Africa literature on the incidence of disability, availability of health services, schooling provision and outcomes, and impact of interventions is scarce.

This chapter focuses on childhood disability and the importance of early identification and intervention, from a human rights and social justice perspective, for providing quality education for disabled children. South African policies pertaining to education are discussed, with a focus on policy related specifically to children with disabilities.

South Africa has a number of comprehensive policies with reference to the education and rights of children with disabilities. However, the implementation of policies is weak. For the evaluation and adequate implementation of policies standardised measures for early disability screening and intervention are needed. National statistics will increase awareness of disability and feed into the cycle of screening, early identification and early intervention.

The establishment of a common non-medical definition of disability, including accurate and consistent categorisation of the different components of disability, will improve the awareness and allow for increased advocacy for the rights of children with disabilities. Acknowledging the role of parent advocacy and community involvement in the equitable education of children with disabilities is essential.

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Notes

  1. 1.

    Deaf with a capital “D” refers to the cultural recognition of deafness, with Deaf people embracing Deaf culture and generally using Sign Language as a communication modality. Deaf with a small “d” (deaf) refers to individuals who consider themselves to have a hearing loss and choose to be part of the hearing world through the use of amplification technology (hearing aids/cochlear implants), and use spoken language to communicate.

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Moodley, S. (2021). Children with Disabilities in South Africa: Policies for Early Identification and Education. In: Pearson Jr., W., Reddy, V. (eds) Social Justice and Education in the 21st Century. Diversity and Inclusion Research. Springer, Cham. https://doi.org/10.1007/978-3-030-65417-7_6

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