Search results for ‘Subject term:"foetal alcohol syndrome"’ Sort:
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Progress in addressing FASD in Scotland
- Author:
- WATTS Margaret
- Journal article citation:
- Adoption and Fostering, 39(3), 2015, pp.256-262.
- Publisher:
- Sage
In Scotland, despite high levels of alcohol use by women, public awareness and professional knowledge of the risks of drinking while pregnant are low and there has been very little research into foetal alcohol spectrum disorders (FASD) and their effects. Recently, however, the Scottish Government has shown leadership with the commissioning of an FASD e-learning resource from NHS Education Scotland, the development of a toolkit for FASD Awareness Day and the planned institution of two two-day intensive training courses for health and social care professionals in the recognition, assessment, diagnosis and support of children affected by foetal alcohol harm. This article charts some of these developments. (Publisher abstract)
Finding answers, improving outcomes: a case study of the Canada fetal alcohol spectrum disorder research network
- Authors:
- BADRY Dorothy, et al
- Journal article citation:
- Advances in Dual Diagnosis, 12(1/2), 2019, pp.53-61.
- Publisher:
- Emerald
Purpose: The purpose of this paper is to present a profile of the Canada fetal alcohol spectrum disorder (CanFASD) research network which is descriptive in nature and profiles the work of the network and its national activities. CanFASD is a unique Canadian, non-governmental organization whose aim is to engage cross-disciplinary research and knowledge translation for stakeholders and partners including communities, policy makers and governments. Design/methodology/approach: A case study approach was undertaken to describe the network whose main focus and purpose is specifically research related to FASD. Findings: The creation of CanFASD has contributed to a strong network of researchers on key topic areas including diagnosis, prevention, intervention, justice and child welfare, with a focus on evidence-based decision making, research and knowledge exchange. A key role of the network is to provide access to research and education on FASD nationally. Research limitations/implications: A case study approach, while descriptive, does not provide the details of specific research projects. Originality/value: CanFASD has had a key role in stimulating meaningful dialogue and research in the field of FASD. The need exists to collaboratively work on a national and international basis in response to the distinct challenges posed by FASD for individuals, families and society. (Edited publisher abstract)