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aftd-logo
  • WHAT IS FTD?
    • Disease Overview
      • Behavioral Variant FTD
      • Primary Progressive Aphasia (PPA)
      • FTD-ALS
      • Progressive Supranuclear Palsy
      • Corticobasal Syndrome
    • FTD & Genetics
    • Find a Medical Center
    • FAQs
    • Glossary of FTD Terms
  • FIND SUPPORT
    • AFTD HelpLine
    • Find Support Near You
    • Newly Diagnosed
    • Managing FTD
      • Coordinating Care
      • Support for People with FTD
      • Support for Kids and Teens
    • Planning for Legal, Financial, and Health Insurance Issues
    • Resources
  • RESEARCH
    • Ways to Participate
    • Studies Seeking Participants
    • FTD Disorders Registry
    • For Researchers
  • GET INVOLVED
    • Ways to Give
    • Host an Event
    • Volunteer With Us
    • Be an Advocate
    • Calendar of Events
  • HEALTH PROFESSIONALS
    • Diagnosing FTD
    • Treating FTD
    • Partners in FTD Care
    • Healthcare Webinars
  • ABOUT US
    • Mission, Vision & Values
    • AFTD is Hiring
    • Our History
    • Staff
    • Board of Directors
    • Medical Advisory Council
    • Persons With FTD Advisory Council
    • AFTD Ambassadors
    • Strategic Plan
    • Financial and Impact Reports
  • NEWSROOM
    • News
      • FTD in the News
      • Events
      • Press Releases
      • Videos
      • Webinars
    • Publications
      • AFTD Insights
      • Help & Hope
      • Partners in FTD Care
    • Media
      • Contact our Newsroom
  • Search

Thanks to Generosity of AFTD Ambassador, Californians Receive Crucial Financial Help

By Julie Sullivan | November 21, 2024 | 0
AFTD Ambassador Terry Walter, of California, smiles in front of a red AFTD banner that says Every FTD Story Counts.

Terry Walter, an AFTD Ambassador in California and Nevada, has been a force for positive change and support since 2008, when she began volunteering for AFTD. Over the years she…

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AFTD Care Partner Learning Series Webinar: Navigating the Holidays with an FTD Diagnosis

By Matt Ozga | November 20, 2024 | 0

The changes brought on by an FTD diagnosis can make navigating the holidays difficult. The routine changes of travel, large crowds, and busy days can lead to unsuccessful holiday experiences.…

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AFTD Advocacy: State Resolution Training

By Matt Ozga | November 20, 2024 | 0

This training will cover the process of how to obtain a resolution — from identifying your legislators to receiving your approved resolution. It will also cover press strategies to maximize…

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Young Caregiver Talks About Finding Support Amid FTD Journey on Dementia UK Podcast

By Julie Sullivan | November 20, 2024 | 0
Young Caregiver Talks About Finding Support Amid FTD Journey on Dementia UK Podcast

A young FTD caregiver named Lizzie discussed the grief, uncertainty, and unexpected responsibilities she faced as she cared for her father — all while navigating the natural changes of young…

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Perspectives in FTD Webinar: FTD Research 2024 — Where We’ve Come From and Where We’re Headed

By Matt Ozga | November 18, 2024 | 0

The science of FTD is evolving at a rapid pace and it can be difficult to interpret the scientific advancements and how they may impact families facing an FTD diagnosis.…

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AFTD Webinar: Care Partner Learning Series — Navigating the Holidays with an FTD Diagnosis

By Matt Ozga | November 18, 2024 | 0

The changes brought on by an FTD diagnosis can make navigating the holidays difficult. The routine changes of travel, large crowds, and busy days can lead to unsuccessful holiday experiences.…

Read More

Advancing Hope: AFTD Staff Attend NORD Breakthrough Summit in Washington, DC

By Mike Mooney | November 15, 2024 | 0
Graphic: Advancing Hope - AFTD Staff Attend NORD Breakthrough Summit in Washington DC

Shana Dodge, PhD, AFTD’s Director of Research Engagement and Meghan Buzby, MBA, AFTD’s Director of Advocacy and Volunteer Engagement attended the National Organization for Rare Disorders (NORD) Breakthrough Summit, held…

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GemVax & KAEL Announces Results from Phase 2a Clinical Trial for PSP

By Mike Mooney | November 13, 2024 | 0
Title: GemVax & KAEL Announces Results from Phase 2a Clinical Trial for PSP Background: A woman looks through a microscope

South Korean biopharmaceutical company GemVax & Kael announced in late October the results from its phase 2a clinical trial evaluating a drug for PSP. While the drug failed to show…

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Dear HelpLine: Navigating Travel During the Holidays

By Mike Mooney | November 8, 2024 | 0
Text: Dear HelpLine - Navigating Travel During the Holidays Background: A woman fastens straps inside of a packed suitcase.

Dear HelpLine, I am thinking of traveling to see family this year for the holidays, but this would be the first time taking my wife since she was diagnosed with…

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A Conversation with Alector’s Vice President of Clinical Development

By Mike Mooney | November 6, 2024 | 0
Text: A conversation with alector's vice president of clinical development. Background: Photo of Lawrence Carter, AFTD and Alector logos

Earlier this year, the biopharmaceutical company Alector announced that the U.S. Food and Drug Administration (FDA) had granted a “breakthrough therapy designation” to latozinemab, the company’s investigational drug designed to…

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