“…Although there is a growing body of evidence regarding the disparities in end-of-life care for minority adult patients in a variety of settings (Anderson, Mendoza, & Valero, 2000;Cleeland, Gonin, Baez, Loehrer, & Pandya, 1997;Crawley, Marshall, Lo, & Koenig, 2002;Todd, 2001), few studies have focused on the care of minority children with life-limiting illnesses and their families. An incipient body of knowledge suggests that significant barriers to children receiving optimal medical care emerge when health care providers neither understand the family's cultural background nor speak the same language (Barker & Horton, 2008;Contro, Larson, Scofield, Sourkes, & Cohen, 2002;Doty & Ives, 2001;Flores et al, 2002).…”