Linde Jacobs and Tanya Steel are guest editors of an upcoming collection in npj dementia - The Human Connection. Submissions due by Aug 7, 2026.
We welcome Dr. Sally Temple, a valued member of our Scientific Advisory Board, and the Scientific Director at the Neural Stem Cell Institute.
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.
Are you interested in genetic testing? MAPT trials? Support and resources for FTD? Contact us and we'll get back to you quickly.
hello@curemaptftd.org
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