PRESS & NEWS

Share Your FTD Experiences with the FDA Through FTD Insights Survey

In March 2021, the Association for Frontotemporal Degeneration (AFTD) will host a Patient-Focused Drug Discovery (PFDD) meeting with representatives of the…

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World FTD Awareness Week 2020 Marathon

On Saturday, October 3, 2020, presenters from around the globe will mark World FTD Awareness Week by sharing information, resources, and…

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Genetic Counseling & Testing During the Coronavirus Pandemic 2020

The coronavirus pandemic due to COVID-19 has changed the process of genetic counseling and testing.

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Genetic Testing and Counseling in FTD

The importance of genetics in the search for FTD treatments and a cure.

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CurePSP Ask the Doctor: September 22, 2020

A conversation with Dr. Sonja W. Scholz, M.D., Ph.D.

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Together we can find a cure for ftd

The FTD Disorders Registry is a powerful tool in the movement to create therapies and find a cure. Together we can help change the course of the disease and put an end to FTD.

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