PRESS & NEWS
Knowledge gained from participation in FTD Disorders Registry research surveys helps advance science toward finding treatments and a cure for FTD.
more >Whether you have recently received a diagnosis of frontotemporal degeneration (FTD) or have been living with it or caring for a…
more >Have a question about living with progressive supranuclear palsy (PSP), multiple system atrophy (MSA), or corticobasal degeneration (CBD)?
more >The Penn FTD Center has taken its annual 2020 caregiver conference online and produced six video presentations to aid and educate…
more >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).
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.