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AFTD - Full Color Logo 2025
  • 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
      • Create Your Care Team
      • 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
      • FTD Research Spotlight
      • FTD Science Digest
    • Media
      • Contact our Newsroom
  • Search

Words of Encouragement: Coloring Book Collages

By Lauren Gauthier | September 1, 2022 | 0
Collages created by Cathey Merrill to honor and remember her late husband Ron, who was diagnosed with bvFTD

Coloring Book Collages by Cathey Merrill Ron and I married when I was 17 and he was 18, and our only child arrived during our first year of marriage. Life…

Read More

How to Support AFTD’s Mission through Your Workplace 

By Mike Mooney | September 1, 2022 | 0

AFTD’s volunteers and donors are essential to advancing our mission. Each contribution of time and funds provides help and brings hope to all affected by FTD, and we are grateful…

Read More

Blood Pressure Medication Could Protect Against Motor Neuron Death in ALS 

By Mike Mooney | August 31, 2022 | 0
Researchers at the Universities of Edinburgh and Oxford have found evidence that the drug terasozin could help prevent motor neuron death in people with ALS

A joint study by the University of Edinburgh and University of Oxford has found that the drug terasozin shows potential as a treatment for ALS and other forms of motor…

Read More

Study Finds Abnormal Protein that Could Be Common Link Between Forms of Motor Neuron Disease 

By Mike Mooney | August 30, 2022 | 0
Researchers at the University of Sydney have discovered that an abnormal protein could be a common link between forms of motor neuron disease

A new study by researchers at the University of Sydney has uncovered an abnormal protein that could be a common link between the different forms of motor neuron disease (MND).…

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Messages of Hope

By Lauren Gauthier | August 29, 2022 | 0
Read More

Community Connection: Open Office Hours for Support Group Volunteers

By Lauren Gauthier | August 25, 2022 | 0
Support Services Coordinator Erin Ficca at her desk holding Open Office Hours for Support Group Volunteers

AFTD Support Services Coordinator Erin Ficca has started hosting Open Office Hours for Support Group Volunteers twice a month. One of these monthly meetings is assigned a theme, based on…

Read More
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The Association for Frontotemporal Degeneration
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