FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous Survey

Fetal Alcohol Spectrum Disorder (FASD) is considered a lifelong disability that has been framed with neurobiological descriptions focused on the brain. These are important features but fail to tell the story of living with FASD. By surveying those with FASD, this work expanded upon prior survey work...

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Main Authors: Emily Hargrove, C. J. Lutke, Katrina Griffin, Myles Himmelreich, Justin Mitchell, Anique Lutke, Peter Choate
格式: Article
語言:English
出版: MDPI AG 2024-05-01
叢編:Disabilities
主題:
在線閱讀:https://www.mdpi.com/2673-7272/4/2/22
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author Emily Hargrove
C. J. Lutke
Katrina Griffin
Myles Himmelreich
Justin Mitchell
Anique Lutke
Peter Choate
author_facet Emily Hargrove
C. J. Lutke
Katrina Griffin
Myles Himmelreich
Justin Mitchell
Anique Lutke
Peter Choate
author_sort Emily Hargrove
collection DOAJ
description Fetal Alcohol Spectrum Disorder (FASD) is considered a lifelong disability that has been framed with neurobiological descriptions focused on the brain. These are important features but fail to tell the story of living with FASD. By surveying those with FASD, this work expanded upon prior survey work which illustrated a multitude of early-onset physiological issues occurring at rates much higher than is typical of the general population. The current project, again using an anonymous survey methodology, sought to open up other direct experiences to better understand the complexity of living with FASD. An anonymous online survey was used to gather data on adversity in childhood, schooling, employment, housing and finances, and involvement with the criminal justice system, as well as relationships and parenting. Results indicate high levels of adversity throughout the life span; vulnerability to manipulation, which is connected to involvement in the criminal justice system; struggles with housing; economic instability; and struggles maintaining employment, as well as difficulties with social and familial relationships. Systemic stigma was also identified. Suggestions are offered to inform others on how support can be enhanced and targeted with a goal of improving quality of life, as well as dealing with self-imposed stigma. The survey was developed by adults living with FASD who have served as a long-standing advocacy and educational group influencing policy and practice in the field.
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spelling doaj.art-e901b692366e45a09481b5e4ba411a6e2024-06-26T14:19:55ZengMDPI AGDisabilities2673-72722024-05-014233234710.3390/disabilities4020022FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous SurveyEmily Hargrove0C. J. Lutke1Katrina Griffin2Myles Himmelreich3Justin Mitchell4Anique Lutke5Peter Choate6Faculty of Graduate Studies, Walden University, Minneapolis, MN 55401, USAThe Adult Leadership Committee on FASD, Vancouver, BC, CanadaThe Adult Leadership Committee on FASD, Vancouver, BC, CanadaThe Adult Leadership Committee on FASD, Vancouver, BC, CanadaThe Adult Leadership Committee on FASD, Vancouver, BC, CanadaThe Adult Leadership Committee on FASD, Vancouver, BC, CanadaDepartment of Child Studies and Social Work, Mount Royal University, Calgary, AB T3E 6K6, CanadaFetal Alcohol Spectrum Disorder (FASD) is considered a lifelong disability that has been framed with neurobiological descriptions focused on the brain. These are important features but fail to tell the story of living with FASD. By surveying those with FASD, this work expanded upon prior survey work which illustrated a multitude of early-onset physiological issues occurring at rates much higher than is typical of the general population. The current project, again using an anonymous survey methodology, sought to open up other direct experiences to better understand the complexity of living with FASD. An anonymous online survey was used to gather data on adversity in childhood, schooling, employment, housing and finances, and involvement with the criminal justice system, as well as relationships and parenting. Results indicate high levels of adversity throughout the life span; vulnerability to manipulation, which is connected to involvement in the criminal justice system; struggles with housing; economic instability; and struggles maintaining employment, as well as difficulties with social and familial relationships. Systemic stigma was also identified. Suggestions are offered to inform others on how support can be enhanced and targeted with a goal of improving quality of life, as well as dealing with self-imposed stigma. The survey was developed by adults living with FASD who have served as a long-standing advocacy and educational group influencing policy and practice in the field.https://www.mdpi.com/2673-7272/4/2/22Fetal Alcohol Spectrum DisorderFASDFASD living experiencesanonymous surveystigma and FASDself-stigma and FASD
spellingShingle Emily Hargrove
C. J. Lutke
Katrina Griffin
Myles Himmelreich
Justin Mitchell
Anique Lutke
Peter Choate
FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous Survey
Disabilities
Fetal Alcohol Spectrum Disorder
FASD
FASD living experiences
anonymous survey
stigma and FASD
self-stigma and FASD
title FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous Survey
title_full FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous Survey
title_fullStr FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous Survey
title_full_unstemmed FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous Survey
title_short FASD: The Living Experience of People with Fetal Alcohol Spectrum Disorder—Results of an Anonymous Survey
title_sort fasd the living experience of people with fetal alcohol spectrum disorder results of an anonymous survey
topic Fetal Alcohol Spectrum Disorder
FASD
FASD living experiences
anonymous survey
stigma and FASD
self-stigma and FASD
url https://www.mdpi.com/2673-7272/4/2/22
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