Author: Rachel Harmon
Approved: Spring 2018
The purpose of the current study was to address a gap in the literature through investigating the differences in experiences of caring for a child with a disability between a developed country, the United States, and a developing country, Mexico. Participants included caregivers of children with disabilities in the US (N = 25) and Mexico (N = 45). Self-report data were collected to measure caregivers’ demographic information, knowledge of resources, positive and negative emotional response, and stress level. Additional observational data was collected regarding the physical resources, educational resources, therapy services, government policies, caregiver reactions, child behavior, and transportation services in each location. Analyses revealed that caregivers in the US reported significantly higher levels of stress compared to caregivers in Mexico. No significant differences were found in caregivers’ knowledge of government policies; however, Mexico caregivers were significantly more satisfied with the policies that they were aware of compared to US caregivers. US caregivers were more aware of support groups/organizations for themselves or their child and were more likely to participate in known support groups. There was no difference in reports of access to educational opportunities; however, US caregivers reported significantly more inclusion opportunities compared to Mexico caregivers. No significant differences were found in caregivers’ belief that their child would one day be employed. There were significant differences in the number of observations made regarding educational resources, therapy services, government policies, and transportation services between the US and Mexico. The findings of the current study provide important information about the effect of culture on the experiences of caring for a child with a disability, which could be useful for professionals who work directly with families and for the development of future resources.