“…The strain or load borne by a person who assists a chronically ill or frail older family member or other person with a disability (Knight & Sayegh, 2010; Stucki & Mulvey, 2000) and a reluctance to report such burden, to delegate tasks, or to use outside services, may increase vulnerability, exhaustion, worrying, and distress (Crist et al, 2006; Escandón, 2006; Evans et al, 2014; Neary & Mahoney, 2005). One recent study of Hispanic caregivers found that while they experience greater psychic benefits caring for older adults, they also report greater levels of sadness caring for a household member, possibly due to weaker support networks and reluctance to share burden (Kalenkoski et al, 2022). Thus, foundational beliefs about the caregiver role influence their experience, resource utilization, burden perceptions, and characterizations (Gallagher-Thompson et al, 2003).…”