Connect with the FAD community
Our community programs help the familial Alzheimer’s disease (FAD) community stay connected and informed.
Events
We host expert Q&A sessions and group discussions covering topics like mental health, financial planning, caregiving, lifestyle factors, and more.
Join us for an informal virtual update from Youngtimers co-founder Lindsay covering the latest news from AAIC 2026 and the DIAD Family Conference in London last month.
What do genetic discrimination protections in the United States actually cover? Where are the gaps, and how does new blood biomarker testing fit in? Join us for a live virtual workshop with Jalayne J. Arias, JD, MA, Associate Professor at Georgia State University's School of Public Health, to learn about all this and more. This session is a MUST for anyone in the familial Alzheimer's disease (FAD) community thinking about testing or disclosure decisions.
Support groups
Connect with others who face struggles similar to yours. Our monthly support groups are free Zoom sessions facilitated by caring moderators.
More ways to connect
Peer-to-Peer Program
Connect one-on-one with someone in the FAD community who has faced similar challenges.
Online Communities
Stories from the community
Hearing from others who have gone through experiences similar to your own may offer valuable perspective.
In this interview, we speak with a member of the Youngtimers community who is a public advocate, a researcher and a strong voice for FAD. She has published a book and appeared on television in the Netherlands, sharing her own genetic story to help reduce isolation surrounding familial Alzheimer’s disease.
In this interview, we hear from a member of a family impacted by FAD. She talks about her father’s experience as an “escapee”, her own experience testing negative for an FAD genetic mutation, and what it means for her involvement in the Youngtimers community.
A Youngtimers member with multiple relatives positive for FAD discusses his expertise in legal and financial planning and supporting siblings living with familial Alzheimer’s.
In this interview, we hear from a member of the Youngtimers community about her experience navigating genetic testing for familial Alzheimer’s, facing the emotional impact of genetic test results, informing family members, and deciding when to share her truth with others.
Insights from past events
Estate planning attorney Kurt Walberg shares key steps for families facing familial Alzheimer’s, from medical powers of attorney to wills and trusts for peace of mind.
In this session, Vanessa Souza from the Alzheimer’s Association discusses how to plan for care when facing Familial Alzheimer’s Disease (FAD). Whether you’re navigating a diagnosis, supporting a loved one, or just planning ahead, this video covers everything from legal documents and financial planning, employment choices, making meaningful memories, and adjustments to stay independent for longer.
During this conversation, Dr. Tanzi teaches us about the role a person’s lifestyle can play in Alzheimer’s disease. He shares the lifestyle modifications he recommends for sporadic Alzheimer's disease, which might also help those at risk of familial Alzheimer’s disease.
During the fall of 2023, Dr. Cynthia Wilcox joined us for a 3-part Workshop Series on the topic of Mental Health. The experiential workshops focused on skills for the FAD journey, including how to process overwhelming thoughts and emotions, strategies and skills for caring for our own physical and emotional wellbeing, and learning how to make room for beauty and joy in addition to sorrow.
In this live interview, Youngtimers volunteer Susan Hiatt interviews professor and author Dr. Bonnie Hennig-Trestman about talking to children about familial Alzheimer's disease (FAD). Drawing on decades of experience studying families with Huntington’s Disease, Dr. Hennig-Trestman shares age-appropriate strategies, communication tips, and emotional support techniques to help families foster trust.
