The Wisconsin Alzheimer’s Institute (WAI) is committed to helping people living with Alzheimer’s disease or other dementia, their caregivers, and the health professionals working to support them.
Our mission is to advance health equity through research, education, clinical care and community engagement for all people impacted by Alzheimer’s disease and related disorders.
Our purpose is to increase dementia awareness, provide education on Alzheimer’s disease and related disorders, identify and disseminate strategies to reduce dementia risk, convene stakeholders across the state, improve access to quality dementia care services, and to develop and support culturally tailored, effective clinical and community-based models of care.
Our commitment is to advancing health equity. In 2021, we pledged to strengthen this commitment and announced our WAI Diversity, Equity and Inclusion Statement:
“We believe that racism is a public health crisis affecting the communities we serve and society as a whole and have signed on to the Racism is a Public Health Crisis in Wisconsin declaration. The Wisconsin Alzheimer’s Institute is committed to health equity and inclusive excellence that embraces diversity among its faculty, staff, students, research participants, stakeholders, and constituents. We embrace a definition of diversity that acknowledges the richness of all races and ethnicities, identities, ages, abilities, experiences, and opinions. We embrace a definition of inclusion that acknowledges the unique contributions of all and prioritizes people just as much as the desired outcomes of our organization. We embrace a definition of health equity where everyone has a fair and just opportunity to be as healthy as possible with resources that are accessible to all.”
In the spirit of the Wisconsin Idea to share knowledge, WAI collaborates with both rural communities and urban centers, the Wisconsin Alzheimer’s Disease Research Center (ADRC), and various University of Wisconsin academic and research departments.
WAI receives core funding from the state of Wisconsin, research funding from the National Institutes of Health (NIH), and program funding from Bader Philanthropies.
The WAI is home to the Wisconsin Registry for Alzheimer’s Prevention (WRAP), the largest family history study of Alzheimer’s disease in the world.
In 2016, WAI partnered with the Wisconsin ADRC to launch the UW Initiative to End Alzheimer’s (IEA). Through IEA, we are working together across the spectrum of Alzheimer’s disease – from research to community outreach to improved patient care – committed to developing the next breakthroughs in Alzheimer’s disease research, prevention and care.
WAI History
WAI was established in 1998 by a coalition of service providers, community-based organizations, educational institutions and advocates organized by the Wisconsin Bureau on Aging and Long-Term Care Resources and Bader Philanthropies. WAI received pioneering guidance and support under the leadership of our founding director Dr. Mark Sager.
In 2008, the WAI Regional Milwaukee Office was established in Milwaukee, WI with the goals of empowering the local community, improving access to quality care, and increasing African-American research participation by building culturally-tailored programs.
Alzheimer’s by the numbers
There are more than 110,900 people living with Alzheimer’s disease in Wisconsin. That represents more than ten percent of the adults over age 65 in the state.
In Wisconsin, there are more than 205,000 caregivers providing unpaid care for a loved one with Alzheimer’s disease
Alzheimer’s disease is the 7th leading cause of death in the United States. The lifetime risk for Alzheimer’s at age 45 is one in five for women and one in ten for men.
More than 7 million Americans are living with Alzheimer’s. The cost of caring for those with Alzheimer’s and other dementias is estimated to total $360 billion in 2024,
increasing to nearly $1 trillion by 2050. Dementia caregivers today are providing 20% more care than in 2009.