Lived experience of fetal alcohol spectrum disorder: A qualitative scoping review

FASD is a lifelong disability that affects individuals, their caregivers, and families on a daily basis. Individuals with FASD are aware of their disability and can be left feeling different and isolated, while caregivers have to negotiate the daily challenge of parenting a child with FASD. Despite these challenges, individuals with FASD have talents and qualities; raising a child with FASD can bring joy to both caregivers and families. Professionals feel unprepared and overwhelmed when supporting someone with FASD because of a lack of knowledge, funding, and support for individuals living with FASD. 

Fetal alcohol spectrum disorder diagnostic clinic capacity in Canadian Provinces and territories

“…This study examined the capacity for interdisciplinary team diagnosis of FASD across selected provinces and territories in Canada. Capacity.. has either remained stable or fallen in all jurisdictions studied between 2015 and 2019..This study revealed that approximately 98% of cases of FASD are underdiagnosed or misdiagnosed, which is supported by previous publications…”

Prenatal alcohol exposure and health at midlife: Self-reported health outcomes in two cohorts

The Developmental Origins of Health and Disease Hypothesis (DOHaD) suggests prenatal alcohol exposure (PAE) should have implications for adult physical and mental health. Since the health profile of older adults with PAE and diagnoses of fetal alcohol spectrum disorder (FASD) is unknown, the current study evaluates self-reported health problems of midlife adults with and without a history of PAE to describe these outcomes.

Sensory Processing and FASD

Even though families and individuals with FASD often talk about sensory differences, researchers haven’t studied them much, especially across the lifespan. CanFASD wrote an issue paper to summarize what we do know about sensory issues in people with FASD and what still needs more research.