“…For example, studies on MS have utilized generic health and well-being scales (e.g., Short Form Health Survey [SF-36]; Ware & Sherbourne, 1992; Sickness Impact Profile; Bergner, Bobbitt, Carter, & Gilson, 1981), and/or condition-specific instruments (e.g., MS Quality of Life Scale; Vickrey, Hays, Harooni, Myers, & Ellison, 1995) to measure social participation. Furthermore, these measures do not necessarily map across the broader ICF domain of activity and participation (Kwiatkowski et al, 2014; Mpofu et al, 2016).…”