Among caregivers of multiple myeloma patients, 44.1 percent and 24.4 percent report anxiety and PTSD symptoms, respectively
Caregivers with SCD more likely than caregivers without SCD to report frequent mental distress, history of depression
Risk for loss was 1.1 to 4.5 times higher among children of racial/ethnic minorities compared with non-Hispanic Whites
Receipt of informal care up, while formal care use is lower for those with dementia and disability with greater family availability
Timely anticipatory planning in early dementia is crucial to preserve autonomy over future decisions and to reduce caregiver strain
Gray market care, from an unregulated agency, often supplements unpaid or family care
Odds ratios for adverse mental health symptoms, especially suicidal ideation, highest for those in both roles