Linde Jacobs and Tanya Steel are guest editors of an upcoming collection in npj dementia - The Human Connection. Submissions due by Aug 7, 2026.
Welcoming Dr. Sally Temple, a valued member of our and the Scientific Director at the Neural Stem Cell Institute. Our last meeting of 2025!
Her mother gave her the genes for a rare form of dementia, but a Minnesota woman is fighting back. Read the full story in CBS News Minnesota
Read our co-founder Linde Jacobs's story featured in the New York Times by author Virginia Hughes about her experience with MAPT FTD.
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We offer educational resources, explain options for genetic testing, support group options, and information on FTD resources around the world.
We want YOU to study MAPT FTD! We seek to foster collaboration, share breakthroughs, and accelerate discoveries that will lead to treatments, and ultimately a cure, for MAPT FTD.
¿Le interesan las pruebas genéticas? ¿Ensayos con MAPT? ¿Apoyo y recursos para la FTD? Póngase en contacto con nosotros y nos pondremos en contacto con usted lo antes posible.
hello@curemaptftd.org
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