Research on Fetal Alcohol Spectrum Disorder (FASD) has focused on the identification and evaluation of interventions for the physical, cognitive, emotional, and behavioural manifestations of prenatal alcohol exposure on affected children and youth. Although a stable family environment and high quality care-giving have been found to improve academic, social, and life outcomes for children with FASD, limited attention has been paid to the experiences of parents raising children with this complex condition. Existing research suggests that the majority of parents raising children with FASD are adoptive or foster parents. This paper reviews recent research on the experiences of non-biological caregivers of children with FASD and outlines interventions that can be used to facilitate positive childrearing experiences and prevent caregiver burnout. [ABSTRACT FROM AUTHOR]