“…Despite the theoretical change toward a family-centered health care service delivery approach, parents of children with CP continue to experience dissatisfaction with their child’s care (Darrah, Magill-Evans, & Adkins, 2002; Irochu-Omare, 2004; McKay & Hensey, 1990; Reid et al, 2011). In addition, the guidelines and standards of care for this population have been developed without the input of children and their parents (Bakheit et al, 2001; Berker & Yalçin, 2010; Koops, Burdo-Hartman, & Dodge, 2008; Nickel & Desch, 2000; Ohio Department of Health, 1995; Seattle Children’s Hospital, 2011; Wilson & Cooley, 2000). This is at variance with the principles of family-centered care.…”