“Alzheimer’s & Dementia” Publishes Summary of AFTD’s 2022 Holloway Summit

Digital health technologies have the potential to benefit the FTD community by improving accessibility to research and clinical care. Such technologies were the focus of the 2022 Holloway Summit — a summary of which was recently published in the journal Alzheimer’s & Dementia. The article highlights several digital health technologies being developed to remotely assess…

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Leonard A. Lauder, 1933-2025

Leonard A. Lauder, a legend of the cosmetics industry who invested hundreds of millions of dollars into research seeking a cure for FTD and other dementias through his Alzheimer’s Drug Discovery Foundation (ADDF), has died at age 92. AFTD presented Mr. Lauder with the Susan Newhouse & Si Newhouse Award of Hope at our Hope…

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Advancing Hope: Blood Test for Diagnosing Alzheimer’s Disease Approved by FDA

Text: Advancing Hope: Blood Test for Diagnosing Alzheimer’s Disease Approved by FDA | Background: A scientist examines blood samples in a piece of lab equipment.

The United States Food and Drug Administration (FDA) approved the marketing of a blood test to diagnose Alzheimer’s disease. The test, known as the Lumipulse® G pTau 217/β-Amyloid 1-42 Plasma Ratio immunoassay, is intended only for specialized care settings when a person shows signs of cognitive decline. Test Measures Ratio of Alzheimer’s-Related Proteins Along with…

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