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What it takes to support a loved one with Fasd

Bibliographic Data

ID21778414
AuthorsDorothy Reid (Research Network (United States)), Simon Laplante (0000-0001-6174-3287, Member of the Family Advisory Committee of the Canada FASD Research Network), Ray Marnoch (Member of the Family Advisory Committee of the Canada FASD Research Network), Tammy Roberts (Member of the Family Advisory Committee of the Canada FASD Research Network), Jennifer Noah (Member of the Family Advisory Committee of the Canada FASD Research Network), Sonja Verena Schmidt (0009-0000-3841-9067), Sonja Schmidt (Member of the Family Advisory Committee of the Canada FASD Research Network), Wanda Beland (Member of the Family Advisory Committee of the Canada FASD Research Network), Shana Mohr (Member of the Family Advisory Committee of the Canada FASD Research Network)
Year2021
Volume13
Issue2
Pages14
Publication date2021-10-26
Open AccessNo
TypeARTICLE
VenueFirst Peoples Child & Family Review An Interdisciplinary Journal Honouring the Voices Perspectives and Knowledges of First Peoples (JOURNAL)
Journal identifiersISSN: 1708-489X • E-ISSN: 2293-6610
PublisherConsortium Erudit (PUBLISHER • CA)
DOI10.7202/1082966ar
OpenAlexW2907318954
LanguageEN

This photovoice project was undertaken by the Family Advisory Committee of the Canada Fetal Alcohol Spectrum Disorder (FASD) Research Network to describe the experiences and the challenges faced by those supporting loved ones with FASD. Photovoice is a method of bringing forth the voice of those who are typically marginalized. It is a process by which people can act as recorders and potential catalysts for social action and change. The Family Advisory Committee chose the photovoice technique to communicate both their experiential knowledge and the research knowledge on both the challenges and rewards in supporting individuals with FASD. This photovoice project highlights several themes that are consistent with the results of caregiver research and provide a glimpse into the experience of those supporting loved ones with FASD. Through this type of knowledge translation the Family Advisory Committee hopes to enhance policy maker and service provider understanding of the necessity of providing support and services not only to the individual with FASD but to those who support them as well

Action research · Epistemology · Experiential knowledge · Experiential learning · Knowledge management · Knowledge translation · Medical education · Participatory action research · Pedagogy · Photovoice · Political science · Public relations · Sociology · Computer Science · Indigenous Health, Education, and Rights · Medicine · Prenatal Substance Exposure Effects · Psychology

Highly citedNo

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