dementia

This is the first study to forecast Alzheimer's Disease by race and ethnicity and reveals disparities along both lines. It is predicted that by 2060, the burden from Alzheimer’s disease and related dementias (ADRD) will double. Therefore, the information from this study is critical in supporting the necessary public health planning and the development of appropriate support for the ADRD population and caregivers.

The purpose of these briefs is to share information for both service providers and policymakers on: Why dementia is such an important issue for the AAPI community; Barriers to dementia detection, treatment, and support for the AAPI community; Recent findings from a research study to test culturally appropriate messages to improve early identification of dementia by engaging adult children and their families; and Recommendations and resources for better reaching the AAPI community.

The University of California San Francisco published a report about dementia care coordination for duals populations with a specific look at the inadequate workforce of dementia-capable care coordinators.Currently, there are twelve states in the process of implementing demonstrations projects. This report examined three-way contracts from seven states that were selected for their expertise in care coordination.

The Kaiser Family Foundation published an issue brief of the role of Medicaid for People living with dementia. Individuals with dementia generally require a multitude of medical and behavioral health services. Medicare covers some services for this population but there are gaps where Medicaid may need to fill in for payment of long term services and supports (LTSS) for low-income people. This brief includes a fact sheet for explain the role of Medicaid for people with dementia.

Justice in Aging, in collaboration with the Alzheimer's Association, released a new survey of dementia training requirements in each state. The number of Alzheimer's and other dementia diagnoses is on the rise, but there is often little to no training for staff and professionals that work with these populations. This survey was conducted to identify the holes in state law and to find promising practices to inform improvements in the future. The findings are available in a five-paper series.

This study provides insights into higher-hour caregivers (at least 21 hours of care a week), caregivers ages 75 and older, multicultural caregivers, and the challenges facing caregivers in the workplace. While the “typical” family caregiver is a 49-year-old woman who cares for a relative, caregivers on the whole are becoming much more diverse. The study found nearly a quarter of America’s caregivers are millennials between the ages of 18 and 34 and are equally likely to be male or female.

This resource list includes key resources on the mental health needs of older adults, effective interventions, workforce issues, and more.