News & Events

Dear HelpLine – Support for Veterans

Dear HelpLine, My loved one is a veteran. Do we qualify for any support?  Navigating the Department of Veterans Affairs, and the benefits you or your loved one might be…

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Provide Help and Bring Hope with a Year-End Gift

AFTD was founded more than 20 years ago with a single donation. Since then, the dedication and generosity of our volunteers, donors, and partners have enabled us to better meet…

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AFTD Ambassador Shares Challenges of Being a Long-Distance Care Partner in Interview

AFTD Ambassador Melissa Fisher shared the realities of being a long-distance care partner in an interview published by GoodRx Health. Fisher joined two other long-distance care partners who have loved…

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FDA Clears Way for Clinical Trial for AviadoBio Therapy That Could Halt FTD Progression

AviadoBio will soon open U.S. clinical trial sites for an experimental gene therapy that could halt the progression of FTD when caused by a variant in the GRN gene, the…

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AFTD Update: Updated Digital Resources for FTD & Genetics 

The FTD & Genetics section of AFTD’s website has been newly updated to help families better understand FTD’s genetic risk and the options available for addressing it. Approximately 40% of…

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Landmark Trial Evaluating Potential FTD-GRN Therapeutic Completes Enrollment

Biotechnology company Alector Therapeutics announced on October 27 that it has completed enrollment for INFRONT-3, a Phase 3 clinical trial testing the safety and efficacy of the drug latozinemab as…

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The Lived Experience of FTD: Anosognosia

The following article was written by Kevin Rhodes, a member of AFTD’s Persons with FTD Advisory Council. Council members like Kevin and Anne Fargusson, who contributed to this article, work…

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AFTD Webinar: Grief, Loss, and Hope — Helping Families Living with FTD

FTD is the most common dementia for people under 60, and often occurs when there are teens or young adults still at home. An FTD diagnosis can bring feelings of…

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