Hostname: page-component-586b7cd67f-rcrh6 Total loading time: 0 Render date: 2024-11-28T23:15:23.906Z Has data issue: false hasContentIssue false

Services to Children with Intellectual Disability in New South Wales Government Schools: Parental Perceptions

Published online by Cambridge University Press:  26 February 2016

Philip J Foreman*
Affiliation:
Special Education Centre, University of Newcastle
*
Correspondence concerning this article should be addressed to: Assoc. Prof. P J Foreman, Director, Special Education Centre, University of Newcastle, Callaglian, NSW, 2308, Australia

Abstract

Parents of 1003 children with moderate or severe intellectual disability attending state schools in New South Wales responded to a survey about provision of services from the time of suspicion or identification of their child’s disability. The survey sought to obtain information about the types of services the parents were offered, the services they used and were still using, and the extent to which they found the services beneficial. Another aim was to see if there were differences between responses of parents of older and younger children which might suggest changes over time or for children of different ages. Parents of younger children were more likely to have received helpful information and to have been referred to support services. Some children were found to be receiving up to eight separate services, while others were receiving nil. Special schools were rated as very useful by the highest number of parents, with parents of younger children showing a slight preference for an integrated placement. Work-related training or activity was mentioned by more than half of the parents as being required in their child’s future.

Type
Research Article
Copyright
Copyright © The Australian Association of Special Education 1992

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Ashman, A. (1990). Intellectual disability. In Ashman, A. and Elkins, J. (Eds) Educating children with special needs. Sydney: Prentice Hall.Google Scholar
Biklen, D. (1988). The myth of clinical judgement. Journal of Social Issues, 44, 127140.CrossRefGoogle Scholar
Cunningham, C.C. (1987). Early intervention with families of children with Down syndrome. Paper presented at the International Convention on Down syndrome. Rome, March.Google Scholar
Cunningham, C.C., Morgan, P.A. & McGucken, R.B. (1985). Down’s syndrome: is dissatisfaction with diagnosis inevitable? Developmental Medicine and Child Neurology, 26, 3339.CrossRefGoogle Scholar
Foreman, P.J. & Neilands, J. (1991). Parental perceptions of services to children with intellectual disability. Australia and New Zealand Journal of Developmental Disabilities, 17, 249258.CrossRefGoogle Scholar
Gallagher, J., Beekman, P. & Cross, A. (1983). Families of handicapped children: sources of stress and its amelioration. Exceptional Children, 50, 6370.CrossRefGoogle ScholarPubMed
Gath, A. (1985). Parental reactions to loss and disappointment: the diagnosis of Down’s syndrome. Developmental Medicine and Child Neurology, 27, 392–400.CrossRefGoogle ScholarPubMed
Giangreco, M.F., Cloninger, C. J., Mueller, P.H., Yuan, S. & Ashworth, S. (1991). Perspectives of parents whose children have dual sensory impairments. Journal of the Association for Persons With Severe Handicaps, 16, 1424.CrossRefGoogle Scholar
McKay, M. & Hensey, O. (1990). From the other side: parents’ views of their early contact with health professionals. Child: care, health and development, 16, 373381.CrossRefGoogle ScholarPubMed
New South Wales Department of School Education (1989). Age grade distribution of students in NSW Government Schools.Google Scholar
Rogers, R.C. & Simensen, R.J. (1987). Fragile X syndrome: a common etiology of mental retardation. American Journal of Mental Deficiency, 91, 445449.Google ScholarPubMed
Turner, G. & Turner, B. (1974). X-linked mental retardation. Journal of Medical Genetics, 11, 83112.CrossRefGoogle ScholarPubMed
Waisbren, S.E. (1980). Parents’ reactions after the birth of a developmentally disabled child. American Journal of Mental Deficiency, 84, 345351.Google ScholarPubMed
Wilgosh, L., Waggoner, K. & Adams, B. (1988). Parent views on education and daily living concerns for children with mental handicaps. Australia and New Zealand Journal of Developmental Disabilities, 14, 255–259.CrossRefGoogle Scholar