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 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.
Supporting those impacted by familial Alzheimer’s disease with community, education and advocacy
PO Box 151035
San Rafael, CA, 94915
