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The Lived Experience: Brain Donation
By Cindy Odell I was diagnosed with bvFTD more than ten years ago. My immediate reaction was…
Guest Feature: “Until We Knew, Twice: Life With MND/ALS and FTD” Shares a Story of Love and Grief on the FTD Journey
The FTD journey can be an isolating experience; it can often feel like nobody knows what you…
Perspectives in FTD Research Webinar: Brain Donations — Who, What, Where, When, and Why?
In this Perspectives in Research Webinar, presented jointly by AFTD and the FTD Disorders Registry, Dr. David…
March’s Athlete of the Month: Lynne Lewis
Our Charity Miles Athlete of the Month for March is Lynne Lewis from Pennsylvania. Lynne uses the…
Advocacy Update: AFTD Ambassador Corey Esannason Meets with Staff from State Senator Andrea Stewart-Cousins’ Office
On March 3 AFTD Ambassador Corey Esannason met with staff from New York State Senator Andrea Stewart-Cousins’ office….
Annual AFTD Hope Rising Benefit Raises Crucial Funds for Fight Against FTD
(L-R: Hope Rising Benefit Co-Chair David Zaslav, AFTD CEO Susan L-J Dickinson, AFTD Board member Kristin Holloway,…
