Guest Feature: Learning to live with familial FTD

Graphic Text: Guest Feature - Learning to live with familial FTD | Background: A photo of Brooke Teweles as a child being held by her mother.

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 for FTD and ALS research. On her blog, Both Things Are True, and her Instagram, she writes about grief, joy, and hope. The summer before…

Read More

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 passing a resolution to mark FTD Awareness Week. It joins 19 other states that have passed FTD Awareness Week resolutions and/or proclamations. Last year, a…

Read More

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. In a moving discussion, Mrs. Willis talked about the onset of symptoms in her husband, the difficulty of getting a diagnosis, explaining the disease to…

Read More

An Evening for Caregivers

AFTD is attending An Evening for Caregivers, a special event for caregivers featuring Emma Heming Willis in conversation with Anderson Cooper. Panel discussions featuring caregiving experts will kick off the event, providing attendees with resources and information that can make a positive difference at all steps of the caregiving journey. AFTD will have an information…

Read More