Premium
A quantitative assessment of educational integration of students with D own syndrome in the N etherlands
Author(s) -
De Graaf G.,
Van Hove G.,
Haveman M.
Publication year - 2014
Publication title -
journal of intellectual disability research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.941
H-Index - 104
eISSN - 1365-2788
pISSN - 0964-2633
DOI - 10.1111/jir.12060
Subject(s) - mainstreaming , special education , psychology , inclusion (mineral) , pediatrics , medicine , developmental psychology , demography , mathematics education , sociology , social psychology
Background In the N etherlands, as in many other countries, there are indications of an inclusive school policy for children with D own syndrome. However, there is a lack of studies that evaluate to what extent this policy has actually succeeded in supporting the mainstreaming of these students. Method For the period 1984–2011, the number of children with D own syndrome entering regular education and the percentage of children still in regular education after 1–7 years were estimated on basis of samples from the database of the D utch D own S yndrome F oundation. These estimations were combined with historical demographic data on the total number of children with D own syndrome in primary school age. Validity of the model was examined by comparison of the model‐based estimations of numbers and percentages in regular education with relevant available empirical data from the D utch M inistry of E ducation and from D utch special schools. Results The percentage of all children with D own syndrome in the age range 4–13 in regular primary education has risen from 1% or 2% (at the very most about 20 children) in 1986–1987, to 10% (about 140 children) in 1991–1992, to 25% (about 400) in 1996–1997, to 35% (about 650) in 2001–2002 and to 37% (about 800) since 2005–2006. The proportional increase stopped in recent years. Conclusion During the 1980s and 1990s, clearly more and more children with D own syndrome were in regular education, being supported by the then existing ad hoc regulations aimed at providing extra support in regular education. In the N etherlands, in 2003, these temporary regulations were transformed into structural legislation for children with disabilities. With regard to the mainstreaming of students with D own syndrome, the 2003 legislation has consolidated the situation. However, as percentages in regular education stayed fairly constant after 2000, it has failed to boost the mainstreaming of children with D own syndrome. The results of this study are discussed in the context of national and international legislation and educational policy.