Remember Me

Meg & Gary: Life After Loss

For our Season 12 finale, we’re bringing you a conversation especially close to home. Maria and Rachael sit down with Maria’s dad, Gary, and his wife, Meg, for a deeply

Bob V.

Today’s episode is one of deep love, steadfast care, and the kind of devotion that quietly changes you. This week, we sit with Meg as she shares the story of her husband

With love, from Seattle: Community Caregiver Tips

This episode is made up of your voices—listener-submitted advice, caregiving hacks, and the real-life tips that have helped you get through the days (and the nights). The

Ike

This week, we sit with Kim as she shares the story of her life with Ike—the love at the center of it all, and the long, complicated road of FTD they’ve walked together. Y

Jeff

This week, we sit with Amy as she shares the quiet, enduring love she built with Jeff—before, during, and beyond his diagnosis of Frontotemporal Dementia (FTD). It’s a st

Bob B.

We're back from our mid-season break with a story of a young couple - Erin and Bob. Erin shares the journey to an FTD diagnosis after many misdiagnosis including young-on

Faye

In our last episode before the mid-season break, Shane, takes to the mic , and both of us were eager to hear his story with his late wife, Faye. This episode was extrem

Barbara

Today you'll meet Susan and her late wife, Barbara. Susan joined us all the way from Mexico, where we saw her beautiful Milagro wall as she spoke so vulnerably about her

Doug

Karen sits down with us for this week's episode and the conversation took right off. Karen spoke openly, albeit delicately, about the changes she noted in her husband, Do

Maureen

Today we welcome Michael as he shares his journey with his wife Maureen. Maureen was diagnosed with FTD after a misdiagnosis of psychiatric disorders and Lewy body Dement

Larry

We are excited to share this weeks guest, Elin with all of you. During our conversation, Elin openly shared her feelings and her confusion as her husband, Larry’s, FTD be

Al

Welcome to Season 12. We are so happy you’re back and if you’re joining us for the first time, welcome in. This season, our stories are all being shared from the spouse

"This is what it's all about"

Our season 11 finale - a chat with just us - reflecting on the season, our journey of building RM + our latest project: The Remember Me Foundation. We talk about the nitt

FTD Real Talk with Kelsey Cook

Get ready—comedian Kelsey Cook joins us for a powerful Real Talk episode all about Frontotemporal Dementia (FTD), caregiving, grief, and finding a way forward when life f

Managing FTD Behaviors & Caregiver Expectations with Allison Lindauer, PhD, APRN

Allison Lindauer, PhD, APRN joins us to tackle the challenges of navigating behavioral changes caused by Frontotemporal Degeneration (FTD). We talk about some behavior ma

The Unexpected Journey with Emma Heming Willis

Emma Heming Willis is here! Powerhouse FTD advocate, loving wife and care partner to her husband Bruce, devoted mama to her two young daughters - entrepreneur and co-foun

Should I get genetic testing?

We’re tackling the question - Should I get genetic testing? We have the incredible return guest - Erynn Gordon, CGC, program manager at Progranulin Information Navigator

The end isn't always scary

Today we talk about 'the end' - our experiences, our fears + how peaceful it ended up being. We call in our friend Katie Duncan, nurse practitioner, educator and founder

Anticipatory grief is brutal

We talk about the type of grief we feel like people don't understand: Anticipatory Grief. Losing someone bit by bit, and always waiting for the next change, the next disa

FTD changed my family

One of the hardest parts of the wreckage that FTD leaves in its wake is the effect it has on families. In today's episode, we open up about the dynamics that have shifted