PRESS & NEWS
The FTD Disorders Registry was featured at CTAD in San Diego, where a poster presented by Dr. Shana Dodge highlighted how the Registry is helping accelerate clinical trial recruitment in frontotemporal degeneration.
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353 people responded, sharing insights on the physical challenges that can come with FTD.
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Every biosample holds valuable information that brings us closer to earlier diagnosis and effective treatments for FTD.
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About 33% reported that they are actively exploring care options …
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The Fall Research Roundup highlights new studies now enrolling people living with FTD, care partners, and biological family members.
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.