“…However, a large proportion of those with disability who receive care do not have a formal diagnosis (Chakrabarti, 2016 ). Across different disabilities, commonly identified predictors of higher caregiver ‘burden’ or poorer mental health in these studies include female gender (Kumar and Gupta, 2014 ; Mandowara et al, 2020 ; Madavanakadu et al, 2022 ), social isolation (Jagannathan et al, 2014 ; Bapat and Shankar, 2021 ), economic disadvantage (Bapat and Shankar, 2021 ; Madavanakadu et al, 2022 ), fewer years of education (Jagannathan et al, 2014 ; Mandowara et al, 2020 ; Bapat and Shankar, 2021 ; Menon et al, 2022 ) and higher care-needs (Brinda et al, 2014 ; Mandowara et al, 2020 ). Finally, societal stigma operates towards caregivers of people with particular disabilities such as epilepsy (Bapat and Shankar, 2021 ) and psychosocial disability (Mathias et al, 2015a ; Singh et al, 2016 ; Mathias et al, 2019 ; Dijkxhoorn et al, 2022 ), as well as towards the people they provide care for.…”