Tímarit um menntarannsóknir - 01.01.2011, Qupperneq 155

Tímarit um menntarannsóknir - 01.01.2011, Qupperneq 155
155 Social Policy and Social Capital: Parents and Exceptionality 1974–2007 focuses on the ex- periences of the parents of disabled chil- dren in Iceland. The emphasis is on, as the author puts it, the “waves“ of municipal and state policy that underpin services concerning disabled children and their parents over the last 30 years, but issues of medicine, education, gender and the fam- ily, among others, also receive a fair share of attention. There is food for thought to be found within these pages for academ- ics, educators and practitioners in a wide range of disciplines to be sure, but special- ists within particular fields of study may not be satisfied. From the perspective of Icelandic disability studies, there are some curious omissions in the references cited. Those who focus on the development of Icelandic disability policy may find little that has not already been covered in the Icelandic language literature. Those work- ing in education or social work in Iceland may have similar opinions. Given these factors, as well as its publication in Eng- lish, it is not entirely clear who is the in- tended audience. Yet this is offset by the fact that there is some striking material within these pages that span a long and noted research career. The 33-year span for a study that aims to analyse policy as well as present a social history is indeed ambitious. The timeframe that the work is placed within (1974–2007) seems to coincide with the author’s own research experience and personal engage- ment with disability issues. However, the author’s method of examining policy de- velopments over these three decades is intriguing and in my opinion successful. This is done though a cohort model. The parents of children born in the period of 1974–1983 are referred to as the “Explor- ers“ as they encountered a heavily medi- calised environment in which the birth of a disabled child was perceived by practitio- ners as a ‘tragedy,’ and the services on offer tended towards exclusion and segregation. The author illustrates quite well that the gains in policy advances and service pro- Exceptional waves: Parents of disabled children negotiating 30 years of Icelandic social policy Social Policy and Social Capital: Parents and Exceptionality 1974–2007 by Dóra S. Bjarnason James G. Rice, University of Iceland, Centre for Disability Studies Tímarit um menntarannsóknir / Journal of Educational Research (Iceland) 8, 2011, 155.-157.
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