PRESS & NEWS

FTD Registry Research Survey Results – Summer 2020

Knowledge gained from participation in FTD Disorders Registry research surveys helps advance science toward finding treatments and a cure for FTD.

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FTD Resources for You!

Whether you have recently received a diagnosis of frontotemporal degeneration (FTD) or have been living with it or caring for a…

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CurePSP Ask the Doctor #4 – July 7, 2020

Have a question about living with progressive supranuclear palsy (PSP), multiple system atrophy (MSA), or corticobasal degeneration (CBD)?

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Penn FTD Center 2020 Virtual Caregiver Conference Is on YouTube

The Penn FTD Center has taken its annual 2020 caregiver conference online and produced six video presentations to aid and educate…

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CurePSP: Ask the Doctor #3 – June 11, 2020

CurePSP will host its next “Ask the Doctor” webinar on Thursday, June 11, 2020, at 4:00 p.m. Eastern Daylight Time (1:00 p.m. Pacific).

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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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