News & Events

British/Dutch Study Discovers Role of ANG Gene Mutations in ALS-FTD

Researchers at the University of Bath in the United Kingdom and the University Medical Center Utrecht in the Netherlands have uncovered an association between an inherited genetic variant of the…

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AFTD and ALLFTD Collaborate on Brain Donation Video

AFTD and ALLFTD have partnered to create a brief animated video that explains the brain donation process, as well as how it helps FTD researchers and families affected by FTD.…

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Dear HelpLine: Support for Familial and Genetic FTD

Dear HelpLine, My mom was recently diagnosed with FTD; my late uncle and grandmother had dementia, and I’m concerned that this may be genetic. Is there support for people facing…

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Vesper Bio Completes Single Ascending Dose Stage of Its Clinical Trial for Potential Disease Modifying Treatment for FTD-GRN

Biotechnology company Vesper Bio announces it has completed the single ascending dose stage in its clinical trial of its potentially disease-modifying treatment for FTD-GRN. The recently completed trial evaluated the…

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Delaware Passes Resolution Recognizing FTD Awareness Week 2024

Delaware became the third state to officially recognize FTD Awareness Week 2024 (September 22-29) after its Senate unanimously passed the resolution SR23 on June 27. State Senator Kyra Hoffner sponsored…

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Advocacy Update: Join AFTD in Advocating for FTD Awareness Week in All 50 States

This past May, AFTD staff and other FTD advocates traveled to New York and California to celebrate the successful passing of their respective resolutions that commemorate September 22-29 as FTD…

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Study Explores Racial Differences in Clinical Presentation of FTD Symptoms, Disease Severity

A study published in JAMA Neurology explores whether FTD symptoms present differently based on the race of the person diagnosed. Previous studies have sought to compare neuropsychiatric symptoms in Black/African…

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AFTD Webinar: FTD and ALS — A Collaborative Approach to Diagnosis and Care

We know of several genes that can cause hereditary FTD, ALS, and ALS with FTD, with C9orf72 the most common. Yet genetics is not the complete story, as these conditions…

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