PRESS & NEWS
673 participants responded to the FTD Disorders Registry’s May Quick Question on their diagnosis journey.
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The FTD Disorders Registry joined FTD community advocates for a behind-the-scenes tour of the Penn FTD Center,
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The FTD Disorders Registry is a powerful resource for scientists studying FTD disorders. Learn more about how your de-identified data is used.
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When people hear “ALS,” they often think of Lou Gehrig, ice bucket challenges, and the devastating loss of motor function that…
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The Association for Frontotemporal Degeneration (AFTD) has shared that two drugs have been selected for evaluation in a new platform trial aimed at accelerating the development of treatments for progressive supranuclear palsy (PSP).
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.
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