Quick Question May 2026 Result:
A total of 496 people responded. Responses showed that healthcare interactions are a regular part of life for many in the FTD community.
Read MoreWhat “Deidentified Data” Really Means
We often talk about deidentified data provided to researchers., but what does “deidentified data” really mean, and how can it help advance FTD research while protecting your privacy?
Read MoreThe Future of Collaborative Research in Frontotemporal Degeneration
Frontotemporal degeneration research is becoming more collaborative, offering real momentum toward faster trials and more meaningful progress for families impacted by the disease.
Read MoreQuick Question April 2026 Result:
A total of 533 community members shared their experiences, offering valuable insight into the diagnostic journey. These responses help deepen our understanding of the challenges individuals and families face and highlight opportunities to improve earlier recognition and access to care.
Read MoreStay Research Ready: Four Simple Ways to Support FTD Research
When you stay research ready, you help researchers understand that there is a strong, engaged, community eager to accelerate progress.
Read MoreQuick Question March 2026 Result:
A total of 533 community members shared their experiences, offering valuable insight into the diagnostic journey. These responses help deepen our understanding of the challenges individuals and families face and highlight opportunities to improve earlier recognition and access to care.
Read MoreHow to Find Clinical Trials for FTD
Learn how to find FTD clinical trials and stay informed as new research opportunities emerge.
Read MoreASPIRE-FTD Trial Expands to Fourth Cohort
AviadoBio has expanded its ASPIRE-FTD clinical trial, creating new opportunities for people with GRN mutations to participate in gene therapy research.
Read MoreQuick Question February 2026 Result:
534 individuals responded, providing insight into how symptoms of FTD can sometimes intersect with law enforcement
Read MoreWhat Care Partners Teach Researchers
Care partners play a vital role in helping researchers understand how the impact of FTD unfolds in daily life. Through their observations, experiences, and participation in the FTD Disorders Registry, care partners provide insights that shape future studies and ensure research reflects the real challenges families face.
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