The Registry is an online database to collect information from those affected by all types of frontotemporal degeneration (FTD). The Registry is for FTD diagnosed persons, their caregivers and family members. We work together to increase knowledge, raise awareness, and accelerate curative research for frontotemporal degeneration disorders (bvFTD, PPA, PSP, CBD, and FTD-ALS). THE REGISTRY'S MISSION IS TO FACILITATE RESEARCH AND ADVANCE RESEARCH TO ACCELERATE TREATMENT DEVELOPMENT FOR ALL TYPES OF FTD, A DEVASTATING NEURODEGENERATIVE DISEASE THAT STRIKES PEOPLE IN THE PRIME OF LIFE AND FOR WHICH, CURRENTLY, THERE IS NO CURE.