“…The caregiver experience within families raising children with autism has been well documented in high-income areas around the world (Corcoran, Berry, & Hill, 2015; DePape & Lindsay, 2014; Ooi, Ong, Jacob, & Khan, 2016), but has been less studied in low- and middle-income countries. Caregiver studies in these regions can be particularly beneficial in areas lacking other types of ASD research, as their insights can reveal (1) a variety of elements within the family and community environment that may affect ASD detection and care (DuBay, Watson, & Zhang, 2017; Liao, Dillenburger, & Buchanan, 2017), (2) unmet family needs (Gomes, Lima, Bueno, Araújo, & Souza, 2015; Sitimin, Fikry, Ismail, & Hussein, 2017; Tilahun et al., 2016), (3) underlying elements such as cultural, lingual, and religious factors (Hampton, Rabagliati, Sorace, & Fletcher-Watson, 2017; Jegatheesan, Miller, & Fowler, 2010; Kheir et al., 2012), (4) local knowledge and awareness of ASD (Heys et al., 2016; Wetherston et al., 2017), and (5) accessibility of resources and services (Daniels et al., 2017; Minhas et al., 2015; Zeleke, Hughes, & Chitiyo, 2018). Adjustment information, such as emotional states and socio-relational changes, may speak to local needs for mental health education as well as emotional and social support for families (Hobart, 2008; Koydemir & Tosun, 2010; Rayan & Ahmad, 2018).…”