PRESS & NEWS

CurePSP Ask the Expert Webinar – July 20, 2023

Legacy and Science: Understanding Brain Donation for Neurodegenerative Diseases – July 20, 2023 @ 1:30 pm – 2:30 pm

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Quick Question June 2023 Results: What types of insurance does/did the FTD-diagnosed person have?

Thank you for taking the time to answer our Quick Questions.

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Quick Question May 2023 Results: What question would you like us to ask as a Quick Question?

Thank you for taking the time to answer our Quick Questions.

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CurePSP Ask The Expert: Webinar June 20, 2023

Do you have questions about urinary symptoms related to PSP, CBD and MSA? Join this CurePSP webinar and get your questions answered.

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Quick Question April 2023 Results: Do You Participate in an FTD Support Group?

Of the 809 people who responded to our April 2023 Quick Question, 65% do not participate in an FTD Support Group.

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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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