PRESS & NEWS
More than 2,300 persons affected by frontotemporal degeneration, including more than 400 diagnosed persons, have enrolled in the FTD Disorders Registry…
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Guess who’s turning two? Yes, 2 years ago on March 28, 2017, the FTD Disorders Registry (FTDDR) was launched when our…
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Find Help. Share Hope. You are invited to the 2019 AFTD Education Conference on May 3, 2019, in Los Angeles.
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The 16th Annual CurePSP Awareness & Memorial Walk, sponsored by the SW Florida PSP Support Group, will be Saturday, March 9, 2019,…
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Thursday, February 28, 2019, is Rare Disease Day® in the United States. The main objective of this day, which is observed the last…
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.