Stories from the community
Some of the most valuable insights a person can receive when facing familial Alzheimer's disease (FAD) come from the stories within our community.
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.
In this interview, we hear from a member of the Youngtimers community whose son and husband were her inspiration to know whether she carried the genetic mutation that has plagued her family. Kristina talks about the decisions to pursue genetic testing, finding a genetic counselor through the VA, and what it was like to talk to family about her results.
Interested in sharing your story?
Families in the FAD community have a lot of insight to share with one another. It can also feel really good to tell your story.
