PRESS & NEWS
673 participants responded to the FTD 503 participants responded to the FTD Disorders Registry’s June Quick Question on how satisfied they are with the overall quality of medical care received for FTD. The results varied greatly.
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Learn what happens next after you make the decision to join the FTD Disorders Registry.
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The FTD Disorders Registry has launched a new Researcher Portal to accelerate study recruitment.
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Learn how the FTD Disorders Registry helps accelerate research by connecting willing participants with studies focused on FTD disorders.
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Understanding the genetic component of FTD can help families make informed health decisions and contribute to critical research that is paving the way toward earlier detection and better treatments.
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.