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AFTD to Convene Families Affected by Rare Brain Disease
The Association for Frontotemporal Degeneration (AFTD), a national nonprofit based in Philadelphia, will hold its 2014 Education…
When They Don’t Know They Are Ill
Reporter Judith Graham writes about frontotemporal degeneration in this New York Times blog entry.
Medical Research Writer’s Wife Affected with FTD
Dan Browning, a medical research writer for the Star Tribune in Minneapolis, writes about his wife’s change…
FTD Article Online in The Atlantic
Writer Erika Hayasaki spoke with Nicole Savini, member of AFTD’s Awareness Committee, about her mother’s struggle with…
Progressive Aphasia: When Words Get Stuck Between Mind and Mouth
The Las Vegas Review-Journal published a story about 65-year-old Jacob Sobotka, a man affected with primary progressive…
Denise’s Decision: When to Put Husband in Nursing Home
Randy Thomas has FTD. He is 63. His wife Denise faces the difficult decision of figuring out…
UCSF Neurologist Develops Brain Imaging Strategies for Mapping Disease
Dr. William Seeley’s research about mapping the course of bvFTD is discussed in an article posted to the…
International Conferences Spotlight FTD
AFTD helped support two important research conferences this November. The 8th Brain Research Conference: RNA Metabolism in…
CA Woman with FTD Calls for More Attention to Disease
A 50-year-old woman diagnosed with FTD in San Rafael, CA spoke with the Marin Independent Journal about being…
Howard Glick’s Blog Surpasses 100,000 Visitors
Howard Glick, who is affected with FTD, began a blog in 2011 about his journey with FTD. …