Gæstefunktion: Skab muligheder for befrielse og håb på FTD-rejsen
The FTD journey is difficult for families due to its distressing symptoms and the sweeping life changes that are often required to adapt to them. Families often find that there is little support for those affected by FTD because not enough people know about it. Chris Tann, who is currently living with FTD, and Debra,…
Læs mereUK Man diskuterer FTD Caregiving med BBC og Yahoo! Liv
An FTD caregiver in the United Kingdom spoke about the disease’s emotional and financial impact in recent interviews with the BBC and Yahoo! Life. Gareth Heslop, of Sheffield, UK, said that being a care partner for his long-time partner and fiancée, Sarah Frith, has put a “huge strain on the family.” And like so many…
Læs mere“50 & Better” Senior Health Fair
Join Robert Meddaugh, a member of AFTD’s Persons with FTD Advisory Council, will host an information table with AFTD resources you can take with you at the Des Moines University’s annual “50 & Better” Senior Health Fair. The fair combines complimentary health screenings and informational booths with a friendly, social atmosphere.
Læs mereTil minde om George F. Sidoris: A Siblings' Labor of Love
More than 20 years ago, siblings Christine and George J. Sidoris first noticed troubling changes in their father’s behavior during a family gathering. “Normally, when my brother and his family visited, my father was gregarious and the life of the party. This time, we noticed he wasn’t socializing,” shared Christine. Their father also started to…
Læs mereAdvancing Hope: AFTD deltager i AAIC 2024.
Debra Niehoff, Kim Jenny, and Shana Dodge from AFTD and Sweatha Reddy from the FTD Disorders Registry attended the Alzheimer’s Association International Conference (AAIC), which took place in Philadelphia starting July 26, 2024. AAIC welcomed more than 9,000 attendees from 93 countries and included sessions and posters on the science of Alzheimer’s Disease and related…
Læs mereDen levede oplevelse af FTD: At lære personerne med FTD at kende: Deb Jobe
Formally chartered in 2020, the Persons with FTD Advisory Council works to ensure that the insights and perspectives of people living with FTD are included in the development of AFTD’s policies, programs, and services. The stories of members like Deb Jobe, who joined the council recently, help illustrate what FTD is truly like to challenge…
Læs mereAviado Bio CMO diskuterer ASPIRE-FTD klinisk forsøg med Neurology Live
In a recent interview with Neurology Live, Aviado Bio chief medical officer David Cooper, MD, discussed the company’s Phase 1/2 ASPIRE-FTD trial. Dr. Cooper shared how the company’s AVB-101 gene therapy worked, and he outlined what criteria the study would need to meet to be successful. The ASPIRE-FTD trial is focused on treating a specific…
Læs mereAdvocacy Update: FTD Awareness Week
With FTD Awareness Week quickly approaching, we asked AFTD advocates to help us obtain a resolution or proclamation in every state, and the community has definitely risen to the occasion. Thanks to our advocates, we have a proclamation and/or resolution recognizing FTD Awareness Week in 9 states, with another 18 states not far behind. FTD…
Læs mere2024 Fundraiser for AFTD, arrangeret af Garys FUB Team
Join Gary’s FUB Team on September 23, 2024 from 5:00pm-8:30pm at the Hutton House in Medicine Lake, MN for the 2024 Fundraiser for AFTD! The evening promises to be filled with inspiring moments, including guest speaker Dr. David Knopman, a leading dementia researcher from the Mayo Clinic, and heartfelt testimonies from local caregivers. Enjoy live…
Læs mereAFTD Brand Influencer diskuterer forpligtelse til omsorg
AFTD Brand Influencer Nicole Petrie shared her family’s FTD journey with host Lisa Opie on the podcast Miss Represented earlier this year. Petrie is a model, activist, and entrepreneur, and while she is proud of all her roles, the one she takes most seriously is being a care partner for her mother, Cheryl, who was…
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