PRESS & NEWS
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.
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Registry data is helping to bridge the gap between the FTD and ALS research communities and to accelerate recruitment for future clinical trials.
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Registry data reveal which FTD subtypes and genes have the highest representation of research-ready participants, helping scientists design stronger, more focused studies.
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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