PRESS & NEWS
During the 2023 World FTD Awareness Week, the Registry used communication channels to ask participants: 1 “What webinar content would you…
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Are you a current or former caregiver for someone with FTD?
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Understanding the experiences of people living with Frontotemporal degeneration (FTD) disorders and those supporting them is essential to developing clinical tools…
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“Have you ever served in the military?” The purpose of this quick question was to assess the military status of individuals diagnosed with FTD.
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Are you interested in knowing your genetic risk for developing FTD?
more >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.
Your privacy is important! We promise to protect it. We will not share your contact information.