“…Involving patients and families in shaping health services has potential benefits in terms of improving quality of care and health outcomes (Prior & Campbell, 2018). Communication is central to human existence and participation, so living with a chronic communication impairment has far‐reaching negative effects on health‐related quality of life, self‐identity, mental health, social networks and relationships, return to work, social and community participation, stigmatisation, disadvantage, access to digital technology and ‘third‐party disability’ for family members (FMs) (Baker, Worrall, Rose, & Ryan, 2019; Black‐Schaffer & Osberg, 1990; Grawburg, Howe, Worrall, & Scarinci, 2013; Hersh, 2017; Hilari, Needle, & Harrison, 2012; Kelly, Kennedy, Britton, McGuire, & Law, 2016; Morris, Franklin, & Menger, 2011; Northcott, Marshall, & Hilari, 2016; Northcott, Moss, Harrison, & Hilari, 2016; Parr, 1997; Shadden, 2005). Advocates have shifted focus to providing holistic support targeting personally meaningful outcomes and removal of barriers to participation in society more generally, for example using the International Classification of Functioning, Disability and Health (ICF) framework (WHO, 2001).…”