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Volunteer Update: How Can a Meet & Greet Help?

Navigating FTD can be a frustrating, exhausting, and isolating ordeal for persons diagnosed, care partners, and family members. Information about the disease and how to manage its symptoms guidance can…

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AFTD announces 2023 Pathways for Hope Pilot Grant recipients

AFTD’s Pilot Grant program – our longest running funding opportunity – provides seed funding for innovative FTD research, laying the groundwork for additional follow-on support from a larger funder. Pathways…

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Tips & Advice: Dealing With the Loss of Empathy

One of the most distressing symptoms of FTD is a loss of empathy, which can cause persons diagnosed to become uncharacteristically indifferent towards other people, including loved ones. This loss…

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May 15, 2024: TEDx Miami’s “Stories of Resilience,” featuring Dr. Leila Allen

Dr. Leila Allen, a neuroscientist and the founding director of the behavioral neuroscience undergraduate program at Florida International University, will be speaking at a TEDx Miami event called “Stories of…

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U.K. Researchers to Conduct Nationwide Trial Evaluating Blood Test for Dementia

Researchers in the United Kingdom are preparing to conduct a nationwide trial evaluating blood tests for biomarkers of dementias like FTD and Alzheimer’s disease, according to a recent article by…

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Dear HelpLine: Brain Donation

Dear HelpLine, How do we learn more and start the process of arranging a brain donation for FTD research? Brain donation can be a difficult topic to consider and discuss,…

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Case Report Discusses Symptoms and Diagnosis of Progressive Supranuclear Palsy

A case report published earlier this year in the journal Radiology Case Reports discusses the symptoms and features of progressive supranuclear palsy (PSP) and explores different ways to diagnose it.…

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Perspectives in FTD Research Webinar: Navigating Social and Legal Challenges in Familial FTD

Prof. Jalayne Arias, a researcher focused on policy, ethics, and law, and genetic counselor Laynie Dratch join this Perspectives in FTD Research Webinar to discuss important considerations for families impacted by…

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Advancing Hope: AFTD and Registry Staff attend Neurology Meeting

AFTD partnered with the FTD Disorders Registry to attend the annual American Academy of Neurology meeting April 13-18 in Denver. Will Reiter, Ray Frattone, and Shana Dodge from AFTD joined…

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