FTD Care Partner Shares Memories of Her Mother on TikTok

Graphic: FTD Care Partner Shares Memories of Her Mother on TikTok

In an interview with Newsweek, FTD care partner Channing Clifford shares her favorite memories with her mother, Valerie, who was diagnosed with FTD last year. Roughly 10 years ago, Valerie was struck by a car while riding her bike and suffered a traumatic brain injury. In the years since, Clifford noted that Valerie was acting…

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The Lived Experience of FTD: Driving and FTD

Graphic: The Lived Experience of FTD - Driving and FTD

The following column was written by members of the Persons with FTD Advisory Council. Members of the Council work to share the insights of persons diagnosed to help guide AFTD on its mission for an FTD-free future. We remember that exciting day when we got our driver’s license. Driving a car by ourselves, we discovered our…

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Link Between TAF15 Protein and FTD Discovered in UK Study

Graphic: Link Between TAF15 Protein and FTD Discovered in UK Study.

In a study published in the scientific journal Nature, researchers in the United Kingdom discovered that a previously known protein may play a role in the development of an FTD subtype once thought to be associated with the FUS protein. The abnormal accumulation of the proteins TDP-43 and tau have been previously identified as playing…

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AFTD Launches Social Media Campaign to #EndDementiaStigma

#EndDementiaStigma

AFTD has launched #EndDementiaStigma, a social media campaign to mark Brain Awareness Week. The campaign empowers people with FTD, along with their care partners, family members, and friends, to share stories of how they continue to find meaning and connection, and to educate those around them to end dementia stigma. The campaign is initially launching…

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“Smple Mnds” Fundraiser

HL McIntyre from the UK is holding a fundraiser for her book, “Smple Mnds” where 20% of proceeds from the book sales will be donated to AFTD’s mission for the next six months in memory of her husband, who died in 2018, shortly after his FTD diagnosis. In this book, she shares her family’s FTD…

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Dear HelpLine: Looking for Support Options

Graphic: Dear HelpLine - Looking for Support Options

Dear HelpLine, Our family is looking for ways to connect with other FTD care partners for support. What options are available? A core part of AFTD’s mission is to help FTD care partners access the support they need. One way to get support is by connecting with other care partners. These connections can be a…

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Los Angeles, Calif. Meet & Greet

Join and learn from others who understand the FTD journey at this in-person AFTD Meet & Greet event, hosted by AFTD volunteer Alma Valencia at Be Nice Have Fun, a community space and gift shop in Los Angeles, on Saturday, March 30, at 9:30 a.m. PT. Please RSVP to Alma at almav21@gmail.com or by calling…

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March 30, 2024: In-Person Meet & Greet in Los Angeles, Calif.

Join and learn from others who understand the FTD journey at this in-person AFTD Meet & Greet event in Los Angeles, hosted by AFTD volunteer Alma Valencia at Be Nice Have Fun (5011 York Boulevard), a community space and gift shop, on Saturday, March 30, from 9:30 to 10:30 a.m. PT. Please RSVP to Alma…

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Understanding Dementia with a Focus on Alzheimer’s & FTD

Alzheimer's Association Logo

Join AFTD Ambassador Dawn O’Gara and Julie McMurray, MA, LMHC, CDP, of the Alzheimer’s Association for this virtual presentation on FTD and Alzheimer’s disease. Attendees will learn about the signs and symptoms of FTD and Alzheimer’s and the resources available through AFTD and the Alzheimer’s association. View this downloadable pdf for more information. 

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