Posts by Mary Krause

Every biosample holds valuable information that brings us closer to earlier diagnosis and effective treatments for FTD.

The Fall Research Roundup highlights new studies now enrolling people living with FTD, care partners, and biological family members.

Registry data is helping to bridge the gap between the FTD and ALS research communities and to accelerate recruitment for future clinical trials.

Registry data reveal which FTD subtypes and genes have the highest representation of research-ready participants, helping scientists design stronger, more focused studies.

Alector has announced topline results from its Phase 3 INFRONT-3 trial of latozinemab for FTD-GRN.

Progress is possible. See how Registry data can unlock breakthroughs in FTD research just as new treatments are showing progress in other neurological disorders.

Only a fraction of people with FTD and their relatives pursue genetic testing. This World FTD Awareness Week, discover how genetic counseling can guide the way.

Caring for a loved one with FTD can make research participation feel impossible. Learn more about the barriers caregivers face and how researchers can make studies more accessible.

Every survey response in the Registry Research Study helps turn lived experience into research data that drives discovery.

World FTD Awareness Week is September 21-27, 2025.