PRESS & NEWS
Life with FTD is about so much more than medical symptoms. To better understand the impact of FTD disorders, our September Quick Question asked …
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Progress is possible. See how Registry data can unlock breakthroughs in FTD research just as new treatments are showing progress in other neurological disorders.
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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.
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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.
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Every survey response in the Registry Research Study helps turn lived experience into research data that drives discovery.
more >Together we can find a cure for ftd
The FTD Disorders Registry is a powerful tool in the movement to create therapies and find a cure. Together we can help change the course of the disease and put an end to FTD.
Your privacy is important! We promise to protect it. We will not share your contact information.