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The AFTD
@AFTDHope
AFTD offers support, education, and research updates about frontotemporal degeneration (FTD) for families, caregivers, and healthcare professionals.
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Did you know approximately one in five people diagnosed with FTD has a genetic cause, regardless of family history?
That鈥檚 why community providers play a critical role in connecting families affected by FTD to genetic services.
馃憠 Learn more in April鈥檚 edition of Partners in FTD Care: bit.ly/47CD82e
That鈥檚 why community providers play a critical role in connecting families affected by FTD to genetic services.
馃憠 Learn more in April鈥檚 edition of Partners in FTD Care: bit.ly/47CD82e
A study published in Molecular Neurodegeneration sets out to find clues that could help detect or better understand #CTE, which shares some features with other disorders like #FTD.
鉃★笍 Learn more: bit.ly/3NQDnzZ
鉃★笍 Learn more: bit.ly/3NQDnzZ
Healthcare professionals and researchers play a vital role in improving recognition and care for people affected by FTD.
The AFTD 2026 Education Conference offers opportunities to learn from leading experts, hear perspectives from people with lived experience, and connect with colleagues working across FTD research.
Register today: bit.ly/4rZBY8u
The AFTD 2026 Education Conference offers opportunities to learn from leading experts, hear perspectives from people with lived experience, and connect with colleagues working across FTD research.
Register today: bit.ly/4rZBY8u
Understanding genetic FTD can feel complex, but you don鈥檛 have to navigate it alone. 鉂わ笍
Join AFTD on April 14 at 4 pm for an open-format webinar with genetic counselor Krista Savage. Bring your questions about genetic testing, family risk, and available resources.
馃敶 Sponsored by @Passage_Bio
馃憠 Sign up today: bit.ly/47YenO3
Join AFTD on April 14 at 4 pm for an open-format webinar with genetic counselor Krista Savage. Bring your questions about genetic testing, family risk, and available resources.
馃敶 Sponsored by @Passage_Bio
馃憠 Sign up today: bit.ly/47YenO3