Season Seven
This season, we focus the stories on the genetics of FTD. We will discuss the importance of gene mutations in FTD and the importance of genetic testing. Genetic testing not only helps current families affected by FTD but can also help future generations to come.
Episode 1
In episode 1, this season is all about genetics. We dive into recent FTD news and what to expect .
Episode 2
In episode 2, Wanda chronicles her mother Sarah's dementia journey in the 1980s , receiving the (mis)diagnosis of Alzheimer's at the age of 52.
Episode 3
In episode 3, Rachael shares her mother Mary's journey with FTD -Primary Progressive Aphasia. She also shares her journey with genetic testing.
Episode 4
In episode 4, Peggy shares her experience of learning she is positive for FTD- the GRN mutation.
Episode 5
In episode 5, we discuss Sarah’s mother Julie’s journey with FTD and her own path to genetic testing.
Episode 6
In episode 6, Laynie Dratch of Penn Medicine answers all the questions on working with a genetic counselor.
Episode 7
In episode 7, Linde bravely shares her mother Allison's journey with FTD and her own journey with genetic testing.
Episode 8
In episode 8, Linde returns this week to dive into her journey with genetic testing following her mother Allison's passing.
Episode 9
In episode 9, Lauren shares the search for answers to her mother's behavior changes and what made it hard to decipher what the culprit was.
Episode 10
In episode 10, a physician shares his family's journey with FTD clinical trials.
Episode 11
In episode 11, our very own Rachael asks herself the question, "Do I want to know my genetic status?"
Episode 12
In episode 12, we close out season 7 with an update on FTD research from world renowned neurologist Dr. Bradley Boeve.