VoA Foundation Newsletter


February Issue:

  • Equality in Alzheimer's Care: Reflecting on African American History and the Fight Against Discrimination

  • The Importance of Early Detection in Alzheimer’s Disease

  • Additional Alzheimer’s Resources

  • About the VoA Foundation

  • Get in Touch!


About the VoA Foundation

We are proud to introduce the VoA Foundation, an educational initiative born from Voices of Alzheimer’s. Our organization, led by individuals living with Alzheimer's, is on a mission to transform the landscape of Alzheimer's care and understanding.

Through the VoA Foundation, we aspire to eradicate stigma, champion equality, and craft educational resources that shed light on cutting-edge innovations in care and treatment. Our vision? A world in which individuals grappling with Alzheimer's and other cognitive illnesses can embrace a life filled with well-being and joy.


The Importance of Early Detection in Alzheimer’s Disease

In case you missed it, the VoA Foundation launched a video on “The Importance of Early Detection in Alzheimer’s Disease,” highlighting how early detection and intervention can improve outcomes and quality of life.

We also have 15-second and 45-second versions for a quick preview. Watch, share, and help spread this vital message - let’s inspire change together!

Additional Alzheimer’s Resources

At the VoA Foundation, we are committed to providing valuable resources and support to those affected by Alzheimer's and other cognitive illnesses. We have compiled the best resources from leading Alzheimer’s organizations to provide the most comprehensive expertise for those living with the disease and their loved ones. Our subject areas include:


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Questions? Want to get in touch? Email us at voa-foundation@voicesofad.com.


Equality in Alzheimer's Care: Reflecting on African American History and the Fight Against Discrimination

As we honor African American History Month this February, we not only celebrate the rich culture, history, and contributions of African Americans but also reflect on the ongoing fight for equality and justice in all aspects of life – especially in healthcare. 

A 2023 survey by the Kaiser Family Foundation (KFF) found that African American adults are more likely than White adults to report being treated unfairly or disrespectfully by healthcare providers because of their race or ethnicity. They are also more likely to have experienced negative interactions, such as being denied necessary pain medication or having their questions or requests ignored. 

The Bill of Rights for People Living with Alzheimer’s Disease:

The Bill of Rights for People Living with Alzheimer’s Disease, introduced by Voices of Alzheimer’s (VoA) and the VoA Foundation, outlines the fundamental rights that individuals with Alzheimer’s and related disorders are entitled to. Created by those directly affected, this Bill of Rights ensures that their needs are met with the respect, dignity, and ethical consideration they deserve.  

One of its ten rights is the right to be free from all forms of discrimination. This right affirms that individuals living with Alzheimer’s should never face unfair treatment, whether based on their condition, race, ethnicity, or any other factor, and should always have access to the care and support they need without bias or prejudice. 

Resources for African Americans Affected by Alzheimer’s Disease:

We’ve compiled a list of resources dedicated to providing care and empowerment to African American families impacted by Alzheimer’s and related disorders: