Advancing Hope: AFTD hosts FTD Social at the Society for Neuroscience Annual Meeting

Graphic: Advancing Hope - AFTD hosts FTD Social at the Society for Neuroscience annual meeting.

The Society for Neuroscience (SfN), with nearly 35,000 members in 95 countries, is the world’s largest professional organization for brain researchers. SfN’s annual meeting provides a forum for scientists from around the globe to present the results of their research, discover new ideas, engage with colleagues, and learn about new tools and techniques they can…

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Volunteer Update: Hosting a Meet & Greet Event

Graphic: Volunteer Update - Hosting a Meet & Greet Event

By hosting a Meet & Greet on behalf of AFTD, volunteers can bring together people affected by FTD in their local area and neighboring communities to share resources and support for the FTD journey ahead. At a November Meet & Greet hosted by AFTD Ambassador Sandra Gonzalez-Morett and AFTD volunteer Veronica Wolfe, attendees shared their…

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Advancing Hope: AFTD Manager of Genetic Initiatives Attends National Society of Counselors Annual Education Conference

AFTD’ Manager of Genetic Initiatives Kim Jenny, MS, LCGC, attended the 2023 National Society of Genetic Counselors Annual Education Conference, which took place October 16-21. The conference kicked off with a symposium on ethical dilemmas that arise related to genetic counseling and genetic testing issues for FTD, ALS, and other neurodegenerative conditions, featuring a panel…

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January 6, 2024: In-Person Meet & Greet in Leicester, Mass.

Join and learn from others who understand the FTD journey at this in-person AFTD Meet & Greet event in Leicester, Massachusetts on Saturday, January 6, starting at 10:30 a.m. ET. Email Dawn O’Gara at dogara@theaftd.org to RSVP. The event will take place from 10:30 – 11:30 a.m. at the Leicester Public Library (1136 Main Street).…

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Leicester, Mass. Meet & Greet

Join and learn from others who understand the FTD journey at this in-person AFTD Meet & Greet event in Leicester, Massachusetts on Saturday, January 6, starting at 10:30 a.m. ET. Email Dawn O’Gara at dogara@theaftd.org to RSVP. In the case of inclement weather, this Meet & Greet will shift to Zoom; a link will be…

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AFTD Webinar: Approaching a Cure — FTD Genetics and Clinical Trials

The landscape of FTD research has evolved tremendously over the last decade. FTD-causing genetic variants, and the mechanisms they disturb, offer a window to developing disease-modifying medications that target those mechanisms. For the first time, there are clinical trials testing interventions that have the potential to slow, or even stop, the progression of FTD. While…

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Dear HelpLine: Connecting During Facility Visits

Graphic: Dear HelpLine - connecting during facility visits

Dear HelpLine, My mom has FTD and lives in a facility, and I am struggling to find ways to connect with her when I visit. How can I make our visits more meaningful? Family members and friends often wonder how to make the most of facility visits. The personality and behavioral changes caused by FTD,…

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