“…In several studies, the individual characteristics of each child have been reported to influence hearing and deaf caregivers’ decision-making in the initial period following diagnosis, including the age of the child at diagnosis and the subsequent amount of time available for hearing caregivers to make decisions (Scarinci et al, 2017; Young & Tattersall, 2007), the extent of a child’s hearing loss (Li et al, 2003, 2004), the success of amplification devices (Crowe, Fordham, et al, 2014; Crowe, McLeod, et al, 2014), and the age that the child received the hearing devices (Watson, Archbold, & Nikolopoulos, 2006). In addition, as most caregivers of children with hearing loss do not have hearing loss themselves, caregivers’ initial choice of communication method is largely influenced by the information accessed after the diagnosis of hearing loss (Christiansen & Leigh, 2004; Eleweke & Rodda, 2000; Scarinci et al, 2017; Young, 2002). As most hearing and Deaf caregivers receive advice on choosing their child’s method of communication from early intervention professionals (Chang, 2017; Crowe, McLeod, et al, 2014; Scarinci et al, 2017), the nature and scope of the information is influenced by the attitudes and views of the professionals themselves (Elewke & Rodda, 2000; Young, 2002).…”