“…Some of these articles (43%) describe how society and the care network tend to impose the views of normal, nondisabled bodies on care users, which leads to deeply rooted assumptions about the capabilities and skills of care users and to the exclusion of care users from life domains. For example, assumptions about the capacity (skills, emotional resources, and resilience) of older people to become a budget holder or to manage a budget [41,53,63,70,77,80,102,112,114], assumptions about the capacity of people with intellectual disabilities to have a job [49,61,87,92,107], or failing taking into account the transportation needs that people with disabilities have if they are to participate in society [49,104,120,121]. Moreover, one-third of the articles (37%) mention that informal and professional caregivers can restrict access to cash-for-care schemes or take over decision-making processes based on such ideas of the care user's incapability and need for protection.…”