Living with FTD 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,

Our Minds. Our Lives. Our Choices This is the Voices of Alzheimer’s Member Newsletter. This edition of the Voices of Alzheimer’s newsletter features an interview with Debra and Chris Tann, and we look into Frontotemporal Dementia and its relationship to Alzheimer’s. Debra was watching her

The clinical trial, hosted by Reminiscent came to Valdosta and it was a major participant success! K2 Medical and Wanda, the mobile clinic were incredible. Read this amazing testimonial