An Intersectionality-Based Policy Analysis of Canadian Child Advocate Reviews of Infants, Children and Youth with Prenatal Substance Exposure and Fetal Alcohol Spectrum Disorder in Child Welfare Care

Main Article Content

Dorothy Badry
Lenora Marcellus
Peter Choate

Abstract

Background and Objective
Care providers in the child welfare system often support children with Fetal Alcohol Spectrum Disorder (FASD). Women who give birth to children with FASD face many multi-dimensional socio-structural challenges, including prenatal substance use, that lead to their children being placed in care. Alcohol use disorders have strong associations to trauma histories, psychiatric problems, adverse experiences in life, and other substance use. Children with FASD experience abuse and neglect along with other forms of adversities in childhood and adolescence at higher rates than other children, and are often kept in the care of the child welfare system. Risks of harm for children and youth with FASD exist due to distinct vulnerabilities associated with the disability. Even with child welfare intervention, adverse outcomes remain for children and youth with FASD. Our objective was to examine reports generated from Child Advocate offices in Canada on deaths and serious injuries where FASD was identified to gain a deeper understanding of the experiences of this population in the child welfare system.


Material and methods
We employed an intersectionality-based policy analysis (IBPA) framework to analyze child welfare reports from 1989 to 2019 available online publicly from Child Advocate (or equivalent jurisdiction) Offices across Canada. An underpinning theoretical framework in this research was life course theory, as it is critical to rec-ognize the connection that exists between early decisions made for infants and children with FASD and later outcomes in life. Reports were included when there was evidence of FASD or prenatal substance exposure in the report. Sequential Excel spreadsheets were employed for data extraction, and individual word documents were generated for each report specific to the IBPA framework. Thematic analysis was employed to identify themes related to serious injuries or deaths in child and youth, report summaries, and recommendations.


Results
A total of 61 reports were reviewed, and deaths of 17 children or adolescents with FASD were reported. Four categories of reports existed, including investigative death reports, investigative serious injury reports, special reports, and annual reports. Key themes from these reports for this population included: (1) challenges to stability and permanency, (2) challenges to FASD-informed service provision, (3) over-representation of Indigenous children and youth, and (4) presence of concurrent mental health challenges. Recommendations within reports addressed needs of individuals, families, care providers, systems, and policies. There were many consistencies across time and jurisdictions. One notable concern was that FASD, while possible, was often not diagnosed, and therefore supports and services specific to this disability were not provided. It is critical to note that these reports served to document both a child’s history and make key policy and practice recommendations to inform a differential response in the child welfare system in the case of FASD.


Conclusion
This analysis illuminated the risks and vulnerabilities for this population in the child welfare system and has implications for assessment, diagnosis, and practice interventions in responding to the needs of this population. This analysis also identified that many opportunities exist to improve practice and service delivery for individuals with FASD and their families. It is critical to recognize that a connection exists between early decisions made for infants and children with FASD and later outcomes in life.

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How to Cite
Badry, D., Marcellus, L., & Choate, P. (2022). An Intersectionality-Based Policy Analysis of Canadian Child Advocate Reviews of Infants, Children and Youth with Prenatal Substance Exposure and Fetal Alcohol Spectrum Disorder in Child Welfare Care . Journal of Fetal Alcohol Spectrum Disorder, 4(SP1), e91-e115. https://doi.org/10.22374/jfasd.v4iSP1.11
Section
Articles
Author Biographies

Dorothy Badry, Faculty of Social Work, University of Calgary, Calgary, AB, Canada

Dorothy Badry, PhD, MSW, RSW, Professor, Faculty of Social Work, University of Calgary. Her research focuses on FASD and child welfare issues, disability, FASD prevention, homelessness, loss and grief, FASD/suicide prevention.  She is the Child Welfare Research Lead for the CanFASD Research Network and previously worked for 16 years in child protection.

Lenora Marcellus, School of Nursing, University of Victoria, Victoria, BC, Canada

Dr. Lenora Marcellus is a Professor in the School of Nursing at the University of Victoria. She has practiced as a Registered Nurse for over 30 years in a range of maternal-infant settings and roles. Her research interests include perinatal substance use, neonatal opioid withdrawal, and supporting infants in foster care. She is a member of the Canada FASD Partnership Network Action Team on FASD Prevention from a Women’s Determinants of Health Perspective.

Peter Choate, Department of Child Studies and Social Work, Mount Royal University, Calgary, AB, Canada

Dr. Peter Choate is a Registered Social Worker and Member of the Clinical Registry and Approved Clinical Supervisor for the Alberta College of Registered Social Workers. He is a Professor of Social Work and program coordinator at Mount Royal University. Peter's work is focused  is on assessing parenting capacity (with specialties in mental health, domestic violence and child abuse and addictions) as well child and adolescent mental health including maltreatment, neglect and abuse (physical, sexual, emotional) FASD and these issues within family systems. He has also appeared on over 150 occasions as an expert witness in child protection matters.

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