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AFTD Hope Rising Benefit Convenes Hundreds in NYC
(L-R: AFTD CEO Susan L-J Dickinson, Hope Rising Benefit Chairs David Zaslav and Anna Wintour, AFTD Board…
From a Caregiver’s Perspective: Deciding to Learn One’s Genetic Status
Partners in FTD Care, Winter 2022 Download the full issue (pdf) by A. Parker FTD runs in…
The Role of Genetics in FTD: An Overview
Partners in FTD Care, Winter 2022 Download the full issue (pdf) Frontotemporal degeneration (FTD) is a group…
Watch the Global Conversation on FTD this Saturday!
To mark World FTD Awareness Week, World FTD United worked in partnership with FTD to convene voices…
Communicating with Persons Living with PPA: Tips and Strategies
Compiled by Stacey Moeller, MSc, AFTD-affiliated PPA Support Group Volunteer Primary progressive aphasia (PPA) is characterized by…
The AFTD HelpLine: A Vital Source of Support and Information
The FTD journey can be filled with many questions. Having a place to turn to for answers…
Driving and FTD
Following an FTD diagnosis, determining whether the person diagnosed can and should still drive becomes increasingly urgent….
Ask an Expert: “Corticobasal Degeneration” Or “Corticobasal Syndrome”?
Partners in FTD Care, Winter 2021 Download the full issue (pdf) by Ece Bayram, MD, PhD Corticobasal degeneration…
Living Alone with CBD: Balancing Autonomy and Risk
Partners in FTD Care, Winter 2021 Download the full issue (pdf) by Mary O’Hara, LCSW While living alone…
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