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Help & Hope
Finding Your Way Through the Holidays with FTD
The holidays can magnify everything about living with FTD, but can also become opportunities to adapt and…
Dear Helpline: Look For the Helpers
Dear HelpLine, I’m caring for my husband who was diagnosed with FTD two years ago. Some days…
New Recommendation: Expanding Genetic Counseling and Testing for People Diagnosed with FTD
The FTD genetic research landscape is evolving at an unprecedented pace. Although most FTD cases do not…
When “I’m Fine” Isn’t Fine – Understanding Anosognosia in FTD
“I’m not going back to that doctor. I don’t have FTD. I’m fine.” This type of response…
Advancing Hope: AFTD Convenes 3rd Annual FTD Research Roundtable Meeting
AFTD’s 2025 FTD Research Roundtable, in-person meeting, was held September 15-17 in Arlington, Virginia. Approximately 100 scientific…
Advancing Hope – AFTD Staff Attend 2025 ALS Nexus in Dallas
Amanda Gleixner, PhD, attended the Amyotrophic Lateral Sclerosis (ALS) Nexus, held in Dallas, TX in August. The…
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