Tennessee State Alzheimer’s Plan Overview 

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In July 2007, the Tennessee General Assembly established the Tennessee Alzheimer’s Disease Task Force to assess the current and future impact of Alzheimer’s disease in Tennessee, examine services and resources, and draft a state strategy to respond to Alzheimer’s within the state. The Task Force included representatives from long-term care organizations, adult day providers, physician groups, community organizations, state agencies, caregivers, individuals living with the disease and state legislators. In February 2009, the Task Force published the Tennessee Alzheimer’s Disease Task Force Final Report.

In May of 2019, the Tennessee General Assembly enacted Senate Bill 28 (Public Chapter No. 364) establishing the Tennessee Alzheimer’s Disease Advisory Council. In January 2020, the Advisory Council published the updated Alzheimer’s and Related Dementia State Plan.

Tennessee 2026 Policy Priorities

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Support Dementia Caregivers Through Funding for Respite Care

386,000 dementia caregivers in Tennessee provided 675 million hours of unpaid care in 2025, often enabling their loved ones with dementia to live in the community instead of moving into more costly residential long-term care. However, over half of caregivers in Tennessee are living with chronic health conditions. Respite care provides necessary relief to family caregivers, allowing the caregiver to take care of personal medical issues, complete tasks outside of the home, or simply enjoy time off from the demands of caregiving. The Alzheimer’s Association is calling on state lawmakers to appropriate recurring funding for the Alzheimer’s and Dementia Respite Care Pilot Program to ensure caregivers can continue accessing this vital support that reduces burnout, helps families stay together, and delays the need for institutional care.

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Improve Access to Biomarker Testing 

With the historic Food and Drug Administration (FDA) approval of treatments that slow the progression of Alzheimer’s in the early stages, early detection and diagnosis are even more critical to ensure individuals receive the most benefit at the earliest point possible. Biomarkers offer one of the most promising paths to improve dementia detection, diagnosis and treatment. Yet these critical tests remain out of reach for many as insurance coverage is failing to keep pace with innovations and advancements in treatments. The Alzheimer’s Association is urging state lawmakers to expand insurance coverage of comprehensive biomarker testing. Without this legislation, dementia diagnoses may take up to two years, increasing the long-term costs to the individual, family and the state.

Find My Chapter

Together, we’re making an impact. Find an Alzheimer’s Association chapter in your community for more ways to engage.

Contact Us

State Affairs Contact: Leanne Durm

Phone: 615.622.4173

Email: ledurm@alz.org

129,200

people living with Alzheimer’s in Tennessee

386,000

Tennesseans are providing unpaid care

$1.5 Billion

Medicaid cost of caring for people living with Alzheimer’s (2025)

186.4%

increase in Alzheimer’s deaths 2000-2022

19%

in hospice with a primary diagnosis of dementia

232.4%

increase of geriatricians in Tennessee needed to meet the demand in 2050