As dementia rates rise nationwide, health plans, public health agencies, and community organizations have an opportunity to improve outcomes, reduce costs, and strengthen communities by investing in caregiver education, resource navigation, and support services.

Family caregivers are the backbone of dementia care in the United States. They coordinate appointments, manage medications, navigate healthcare systems, provide emotional support, and often serve as the primary advocate for a loved one living with dementia. Yet despite their critical role, millions of caregivers remain disconnected from the education, resources, and support systems that could help them succeed.