What's New

FDA Grants Breakthrough Therapy Designation to Experimental FTD Therapy

The U.S. Food and Drug Administration (FDA) has granted a “breakthrough therapy designation” to latozinemab, an experimental treatment for FTD caused by a GRN genetic mutation. The drug is being…

Read More about FDA Grants Breakthrough Therapy Designation to Experimental FTD Therapy

UK Researchers Discover How to Block Toxic Protein Associated with FTD and ALS

Researchers at the University of Sheffield have discovered how to prevent the production of toxic repeat proteins that cause the death of nerve cells in neurodegenerative diseases like FTD and…

Read More about UK Researchers Discover How to Block Toxic Protein Associated with FTD and ALS

Dear HelpLine: What to Look for When Considering Facility Care for a Person with FTD

Dear HelpLine, We have reached the difficult decision to look for long-term facility care for my sister, and I feel overwhelmed because I don’t know what to look for or…

Read More about Dear HelpLine: What to Look for When Considering Facility Care for a Person with FTD

“The Longest Goodbye”: Montana Woman Shares Family’s FTD Journey in Interview

Krista Payzant of Montana characterized FTD as a thief that “strips the person of who they are” in an interview published in November by the news station KRTV3. Sharing the…

Read More about “The Longest Goodbye”: Montana Woman Shares Family’s FTD Journey in Interview

February 26, 2024: In-Person Meet & Greet in Fresno, Calif.

Join and learn from others who understand the FTD journey at this AFTD Meet & Greet event, taking place in Fresno, California on Monday, February 26, starting at 6:00 p.m.…

Read More about February 26, 2024: In-Person Meet & Greet in Fresno, Calif.

NY State Senator Michelle Hinchey Introduces Bill to Create State FTD Registry

New York State Senator Michelle Hinchey introduced a bill on January 3 to create a statewide FTD registry that would document diagnoses. Senate Bill S7874 would require healthcare providers in…

Read More about NY State Senator Michelle Hinchey Introduces Bill to Create State FTD Registry

Guest Feature: Capturing Voices – Considerations When Writing YOUR Book

The grief caused by FTD is persistent, lasting well beyond the end of the FTD journey for family and friends. However, as author and support group volunteer Scott Rose shares in the…

Read More about Guest Feature: Capturing Voices – Considerations When Writing YOUR Book

Researcher Discusses Integrating Genetic Testing Into Routine FTD/ALS Care in Podcast Interview

Offering genetic testing to persons diagnosed with FTD/ALS disorders should be a routine part of clinical care, Laynie Dratch, ScM, CGC, of Penn Medicine, said in a December 2023 interview…

Read More about Researcher Discusses Integrating Genetic Testing Into Routine FTD/ALS Care in Podcast Interview

Perspectives in FTD Research Webinar: Gene Therapy for FTD — What Do I Need to Know?

In the last several years, new clinical trials have begun for drugs that can potentially slow or stop the progression of FTD caused by specific genes. Gene therapy and gene…

Read More about Perspectives in FTD Research Webinar: Gene Therapy for FTD — What Do I Need to Know?

February 24, 2024: Virtual Meet & Greet for Delray Beach, Fla. Area

Join and learn from others who understand the FTD journey at this virtual AFTD Meet & Greet event for people in and around Delray Beach, Florida on Saturday, February 24,…

Read More about February 24, 2024: Virtual Meet & Greet for Delray Beach, Fla. Area