AFTD Webinar: Talking to Family About Genetic FTD RiskStart time where you are: 08:00 pm UTC

When a family learns FTD is genetic, it’s important to find relatives and convey the potential risk to them, as well as raise awareness around the hope research progress offers for a treatment in the future. Join us for this webinar, where we’ll discuss practical approaches to navigating the sensitive topic of sharing genetic risk information with extended family.  Community members Wanda Smith and Ansel Dow will talk about their experiences, and Angela Lunde, Mayo Clinic’s Program Manager of Alzheimer’s Disease Research, will share some strategies.