What's New

Emma Heming Willis Shares Family Updates on The Oprah Podcast

Emma Heming Willis, Bruce Willis’s wife and caregiver, was interviewed by Oprah Winfrey on “The Oprah Podcast” yesterday about her family’s journey with FTD. Mrs. Willis is currently making a…

Read More about Emma Heming Willis Shares Family Updates on The Oprah Podcast

AFTD Grantee Discusses Use of Proteins for Diagnosing FTD and Tracking Severity in Interview

Rowan Saloner, PhD, recipient of AFTD’s 2024 Clinical Research Training Scholarship in FTD, discusses how measuring protein levels in cerebrospinal fluid (CSF) can help diagnose FTD in a recent interview with…

Read More about AFTD Grantee Discusses Use of Proteins for Diagnosing FTD and Tracking Severity in Interview

Guest Feature: Learning to live with familial FTD

The following Guest Feature was written by Brooke Teweles, who lost her mother and aunt this year to a form of FTD-ALS with genetic roots. Brooke is a proud advocate…

Read More about Guest Feature: Learning to live with familial FTD

AFTD Advocates Visit California Capitol for Passage of FTD Awareness Week Resolution

AFTD staff and advocates, including Emma Heming Willis, traveled to Sacramento on August 18 to celebrate California’s official recognition of FTD Awareness Week 2025. This is California’s second consecutive year…

Read More about AFTD Advocates Visit California Capitol for Passage of FTD Awareness Week Resolution

Emma Heming Willis Interviewed by Diane Sawyer in Prime-Time Special

Emma Heming Willis was interviewed Tuesday night, August 26, on “Emma and Bruce Willis: The Unexpected Journey – A Diane Sawyer Special,” sharing her family’s experience of living with FTD.…

Read More about Emma Heming Willis Interviewed by Diane Sawyer in Prime-Time Special

Book About Family’s FTD Journey Helps Raise Funds for AFTD’s Mission

“No Fault of His Own,” a novel released this summer, was the focus of a recent AFTD fundraiser organized by its author Gina Biskupic, a speech and language pathologist and…

Read More about Book About Family’s FTD Journey Helps Raise Funds for AFTD’s Mission

The Lived Experience of FTD: Talk Therapy in FTD – Risks and Benefits

The following article was written by Anne Fargusson, RN, a member of AFTD Persons with FTD Advisory Council. You can learn more about Anne and her colleagues by visiting the…

Read More about The Lived Experience of FTD: Talk Therapy in FTD – Risks and Benefits

Ferrer PSP Drug Receives Fast Track Designation from U.S. FDA

Spanish pharmaceutical company Ferrer announced that its experimental drug for progressive supranuclear palsy (PSP) has received a Fast Track designation from the United States Food and Drug Administration (FDA).  …

Read More about Ferrer PSP Drug Receives Fast Track Designation from U.S. FDA

Leading FTD Expert Dr. Bruce Miller Interviewed on “Big Brains” Podcast

Bruce Miller, MD, was a recent guest of the University of Chicago podcast “Big Brains,” sharing his experiences observing people with FTD. He discussed the need for a new way…

Read More about Leading FTD Expert Dr. Bruce Miller Interviewed on “Big Brains” Podcast

AFTD Joins Lawmakers to Advance Dementia Awareness in California

Above, L-R: Emma Heming Willis, AFTD Ambassador Terry Walter, Calif. State Senator Roger Niello, and AFTD volunteers Jeanine Walter Misirli, MD, and Kristine Golden, PA-C   SACRAMENTO, CA – The…

Read More about AFTD Joins Lawmakers to Advance Dementia Awareness in California