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Facing My Mother’s Dementia
Kimberly Williams-Paisley describes the effects of PPA on her once eloquent mother.
AFTD zwoła spotkanie rodzin dotkniętych rzadką chorobą mózgu
Stowarzyszenie na rzecz Degeneracji Czołowo-skroniowej (AFTD), ogólnokrajowa organizacja non-profit z siedzibą w Filadelfii, zorganizuje w 2014 roku swoje wydarzenie edukacyjne…
Kiedy nie wiedzą, że są chorzy
Reporter Judith Graham writes about frontotemporal degeneration in this New York Times blog entry.
Żona autora badań medycznych dotknięta FTD
Dan Browning, a medical research writer for the Star Tribune in Minneapolis, writes about his wife’s change…
Artykuł FTD w Internecie na Atlantyku
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…
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