PRESS & NEWS

Quick Question June 2022: Have you tried to get genetic testing for FTD over the last 3 years?

RESULTS The following charts and lists are based on 852 submissions. Question results: 48% No, I have not tried to get…

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FTD Registry Launches Quick Questions Campaign: June 2022

The FTD Disorders Registry invites you to answer our monthly Quick Questions!

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Remember Me Podcast Discusses ALLFTD Study – June 2022

Rachel and Maria, founders of the Remember Me Podcast, joined the ALLFTD Study and produced eight podcast episodes in June 2022…

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Clinical Trials and Beyond Webinar: June 24, 2022

Clinical Trials and Beyond: What Do I Need to Know About Types of FTD Research? will be presented Friday, June 24, 2022, beginning at 3:00 p.m.

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CurePSP Ask the Expert Webinar with Julie Hicks: June 27, 2022

Julie Hicks, MA, CCC-SLP, a speech-language pathologist, will discuss swallowing issues during a CurePSP Ask the Expert webinar on Monday, June…

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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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