Perspectives in FTD Research Webinar: FTD Research '24 - Where We’ve Come From & Where We’re Headed

[@janegefell6502]

This is very interesting. My BROTHER WAS JUST DOING WITH THIS FTD 😢

[@janegefell6502]

Now I am aware ftdd

[@ybarden2491]

How can a person who exhibits many symptoms of bvFTD and needs help getting a diagnosis do this when insurance does not cover the more precise PET scans or genetic testing? Can he volunteer to participate in research ?

[@ybarden2491]

How can a person who exhibits many symptoms of bvFTD and needs help getting a diagnosis do this when insurance does not cover the more precise PET scans or genetic testing? How can he volunteer for research ?

[@TheAFTD]

Hello! We encourage you to contact AFTD’s HelpLine for guidance on navigating the diagnostic process, exploring options for accessing tests, and learning about opportunities to participate in research. You can reach the HelpLine at [e-mail] or call 1-866-507-7222.

[@janegefell6502]

His Sister has Cerebral Palsy and I WAS BORN THIS WAY