“…Barriers included a persistent lack of willingness on the part of organizations to share their information databases in order to ease the stress on YADD and their families (Clement, & Obar, 2016 ; Desai, 2013 ; Dyke et al, 2016 ; Gagnon et al, 2016 ; Larivie’re-Bastien, & Racine, 2011 ; Peekhaus, 2008 ; Mills, et al, 2003 ; Ministry of Health and Long-Term care (MHLTC), 2006 ; Lacobucci, 2014 ; Urowitz et al, 2008 ) and lack of commitment to use of technological advances to protect information privacy rights (Mills, et al, 2003 ; Siegel et al, 2009 ; Urowitz et al, 2008 ). Throughout the review, YADD needs were found to be unrepresented in organizational processes (Austin, 2006 ; CACL, 2011 ; Clement, & Obar, 2016 ; Siegel et al, 2009 ).…”