PRESS & NEWS
CurePSP will host an “Ask the Scientist” webinar on Friday, July 10, 2020, from 12:00 to 1:00 p.m. EDT (9:00 to 10:00 a.m. PDT).
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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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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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Have a question about living with progressive supranuclear palsy (PSP), multiple system atrophy (MSA), or corticobasal degeneration (CBD)?
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The Penn FTD Center has taken its annual 2020 caregiver conference online and produced six video presentations to aid and educate…
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.