Remember Me

  1. May 20

    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 personal conversation about caregiving, grief, and life after loss. After both losing their spouses to Frontotemporal Dementia, Gary and Meg found love again—showing us that heartbreak and hope can somehow coexist. This episode is tender, honest, and full of heart. A conversation about honoring the people we carry with us, making room for joy again, and the quiet reminder that even after unimaginable loss, life can quietly surprise us with beautiful things again. Thank you for spending Season 12 with us. What a gift it’s been. 🕊️ --- Worried you'll miss us during the break? Unlock A TON of bonus content on our Re-Members Only Patreon → ⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠ Today’s Sponsors — Progranulin Information Navigator Learn more about genetic testing, clinical trials, and FTD resources → ⁠⁠⁠www.progranulinnavigator.org⁠⁠⁠ Psilera → ⁠⁠⁠⁠⁠⁠Psilera is a biotechnology company developing next-generation neurotherapeutics .⁠⁠https://www.psilera.com⁠⁠ Follow along: Instagram → @remembermepodcast Website → ⁠⁠⁠www.remembermeftd.com⁠⁠⁠ Our Non-Profit — The Remember Me Foundation ⁠⁠⁠www.remembermefoundation.org⁠⁠⁠ — Remember Me Podcast + Community exists to offer hope, connection, and support for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  2. May 13

    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, Bob—a laid-back soul who knew what mattered most in life. Though they had known each other since childhood, life brought them back together years later at a high school reunion, where friendship turned into a love story. Bob’s journey with FTD—from diagnosis to his passing—was heartbreakingly short, lasting just two years. And through it all, Meg cared for him with extraordinary tenderness, strength, and grace. As we near the close of this season, we want to thank you for listening, sharing, and walking alongside these stories with us. This is our second-to-last episode of the season, and next week, we’ll close things out with a very special episode you won’t want to miss. Thank you for being here. Always, always accept the good. 🤍 — Support the show + unlock bonus content: Patreon → ⁠⁠www.patreon.com/remembermecommunity⁠⁠ Today’s Sponsors — Progranulin Information Navigator Learn more about genetic testing, clinical trials, and FTD resources → ⁠⁠www.progranulinnavigator.org⁠⁠ Psilera → ⁠⁠⁠⁠Psilera is a biotechnology company developing next-generation neurotherapeutics .⁠https://www.psilera.com⁠ Follow along: Instagram → @remembermepodcast Website → ⁠⁠www.remembermeftd.com⁠⁠ Our Non-Profit — The Remember Me Foundation ⁠⁠www.remembermefoundation.org⁠⁠ — Remember Me Podcast + Community exists to offer hope, connection, and support for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  3. May 6

    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 small things, the practical things, the “why didn’t anyone tell me this sooner?” kind of things. From navigating behaviors, to finding moments of relief, to the ways you’ve learned to care—for them and for yourself—this is wisdom that only comes from lived experience. So whether you’re in it right now, or finding your footing on the other side, we hope something in here meets you where you are. Thank you for showing up, for sharing, and for continuing to build this community with us. --- FIRST - THE LINKS MENTIONED IN TODAY'S EPISODE: Searching for the Words Substack Expert Chat: How To Advocate For A Loved One Living In A Care Facility with Laurette Klier. Participate in our Ask A Genetic Counselor Episode Support the show + unlock bonus content (including a bonus episode with Amy): Patreon → ⁠⁠www.patreon.com/remembermecommunity⁠⁠ Today’s Sponsors — Progranulin Information Navigator Learn more about genetic testing, clinical trials, and FTD resources → ⁠⁠www.progranulinnavigator.org⁠⁠ Psilera → ⁠⁠⁠⁠Psilera is a biotechnology company developing next-generation neurotherapeutics .⁠https://www.psilera.com⁠ Follow along: Instagram → @remembermepodcast Website → ⁠⁠www.remembermeftd.com⁠⁠ Our Non-Profit — The Remember Me Foundation ⁠⁠www.remembermefoundation.org⁠⁠ — Remember Me Podcast + Community exists to offer hope, connection, and support for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  4. Apr 29

    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. You can feel that love in every moment of this conversation—steady, enduring, and deeply human—as Kim speaks with honesty and courage about what it means to lose someone in pieces. This episode holds so much of what Remember Me is about: the quiet and not-so-quiet challenges of care, the complexity of loving someone through delusion and change, the financial weight so many families carry, and the layered grief that weaves through it all. Kim, thank you for trusting us—and this community—with your story. — Support the show + unlock bonus content (including a bonus episode with Amy): Patreon → ⁠www.patreon.com/remembermecommunity⁠ Today’s Sponsors — Progranulin Information Navigator Learn more about genetic testing, clinical trials, and FTD resources → ⁠www.progranulinnavigator.org⁠ Psilera → ⁠⁠Psilera is a biotechnology company developing next-generation neurotherapeutics .https://www.psilera.com Follow along: Instagram → @remembermepodcast Website → ⁠www.remembermeftd.com⁠ Our Non-Profit — The Remember Me Foundation ⁠www.remembermefoundation.org⁠ — Remember Me Podcast + Community exists to offer hope, connection, and support for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  5. Mar 25

    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 extremely powerful to listen to as the love and the pain are both present. It’s a beautiful love story of self preservation, of letting go, of listening to your gut and leaning in to that love… that sweet, sweet love. Thanks for being so vulnerable, Shane. Yours and Faye's story will stay with us forever.  We'll be back April 14th to kick off the second half of Season 12. Be well. xx-R+M A big thank you to our listeners, our supporters, our Patreons and our guests.  Want to support the podcast + get more content? Join us over on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ We'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram @remembermepodcast. For more general info about the podcast, please visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. Before you go, we’d love for you to check out our new non profit foundation for the general neurodegenerative community of caregivers:  ⁠www.remembermefoundation.org⁠ ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  6. Mar 18

    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 love story with Barbara. Susan has a way of telling her story with so much tenderness and adoration that we could feel the beauty of their relationship across the miles. This story also so delicately discusses genetic FTD, and the incredible dedication Barbara and Susan had to research and clinical trials. Oh, and Ms. Susan has written a book about her experience and we HIGHLY recommend you sign up for her e-mail list + keep an eye out for the book in June here: https://www.susankoen.com Thank you, Susan, for sharing your love story with all of us. ---- A big thank you to our listeners, our supporters, our Patreons and our guests. A special thank you to ⁠⁠⁠Psilera⁠⁠⁠ for supporting this season of Remember Me. Ways to connect, get more resources + support RM: Patreon: ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Instagram: www.instagram.com/remembermepodcast Website: www.remembermeftd.com Our non-profit created to support caregivers before and after their journey: www.remembermefoundation.org ⁠⁠⁠------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good. #spouse #dementia #grieving #grief #caregiving #frontotemporaldementia #ftd #podcast #marriage

  7. Mar 11

    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, Doug and how the family roles have shifted and morphed alongside Doug’s disease. A beautiful love story that highlights love, resilience and strength. --- A big thank you to our listeners, our supporters, our Patreons and our guests. A special thank you to ⁠⁠⁠Psilera⁠⁠⁠ for supporting this season of Remember Me. Want to support the podcast + get more content? Join us over on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ We'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram @remembermepodcast. For more general info about the podcast, please visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠⁠www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. Before you go, we’d love for you to check out our new non profit foundation for the general neurodegenerative community of caregivers:  ⁠⁠⁠www.remembermefoundation.org⁠⁠⁠ ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  8. Mar 4

    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 Dementia due to her symptoms of hallucinations. Michael walks us through his experiences navigating caring for his changing wife - and the grief and love woven throughout. Thank you, Michael for sharing your story with us. --- A big thank you to our listeners, our supporters, our Patreons and our guests. A special thank you to ⁠⁠Psilera⁠⁠ for supporting this season of Remember Me. Want to support the podcast + get more content? Join us over on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ We'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram @remembermepodcast. For more general info about the podcast, please visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ⁠www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. Before you go, we’d love for you to check out our new non profit foundation for the general neurodegenerative community of caregivers:  ⁠⁠www.remembermefoundation.org⁠⁠ ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  9. Feb 25

    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 began to set in. With a child at home, Elin shares the trials she encountered, the love that persists and the beautiful grief that remains. We loved chatting with Elin and we know you will enjoy hearing her perspective. Mentioned in this episode: ⁠ALS Scribes of Strength⁠ --- A big thank you to our listeners, our supporters, our Patreons and our guests. A special thank you to ⁠Psilera⁠ for supporting this season of Remember Me. Want to support the podcast + get more content? Join us over on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ We'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram @remembermepodcast. For more general info about the podcast, please visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. Before you go, we’d love for you to check out our new non profit foundation for the general neurodegenerative community of caregivers:  ⁠www.remembermefoundation.org⁠ ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  10. Feb 18

    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 spouses perspective and we are so honored to welcome our first guest, Catherine. Listening to the story of Al, Catherine's late husband, we were able to explore aspects of aggravation, hard decisions, and vulnerable topics (we discuss what it feels like to grieve “lightly,” - powerful stuff!) This episode was told with a steady undercurrent of love and compassion. Take a listen! A big thank you to our listeners, our supporters, our Patreons and our guests.  Want to support the podcast + get more content? Join us over on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ Thank you to our friends at Psilera for their support this season! We'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram @remembermepodcast. For more general info about the podcast, please visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠. Before you go, we’d love for you to check out our new non profit foundation for the general neurodegenerative community of caregivers: ⁠www.remembermefoundation.org⁠

  11. 12/17/2025

    "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 nitty gritty of building Remember Me - while grieving, and healing, and mothering.. and our realization that "this is what it's all about." Thank you to our incredible guests this season - our SPONSORS (!) Psilera, Progranulin Information Navigator & AviadoBio. Our amazing Patreon members that give us so much love + support + JOY. We love you all. Thank you for sticking with us - 2026 is going to great, we promise. And if the holiday season feels heavy - just know you are not alone. You are a part of a community who gets it. And we hope you find ways to let some light in + accept the good. xx-R+M A VERY special thank you to today’s sponsors ⁠⁠Progranulin Information Navigator⁠⁠ and ⁠⁠Psilera⁠⁠.  Want to support the podcast + get more content? Join us on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ If you're curious about anything RM, we'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram, and visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, all the latest updates! Also checkout our new charity foundation for the FTD Community ⁠www.remembermefoundation.org⁠ ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  12. 12/03/2025

    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 management strategies and the importance of seeking support early and prioritizing your own well-being as a caregiver. Let us know what you think when you listen. - R+M Allison Lindauer is a nationally certified nurse practitioner, researcher, and Associate Director at Oregon Health & Science University’s Aging and Alzheimer’s Disease Research Center, where she leads outreach and clinical care for families affected by dementia and FTD through her National Institute on Aging–funded STELLA-FTD study. Learn more about the STELLA FTD Study here. A VERY special thank you to today’s sponsors ⁠Progranulin Information Navigator⁠ and ⁠Psilera⁠.  Want to support the podcast + get more content? Join us on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ If you're curious about anything RM, we'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram, and visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, all the latest updates! Also checkout our new charity foundation for the FTD Community www.remembermefoundation.org ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  13. 11/19/2025

    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-founder of Make Time Wellness and now a NYT bestselling author of the perfectly titled book The Unexpected Journey. Emma's here to real talk with us about this journey. Let us know what you think when you listen and a big thank you to Emma for the light she is shining on FTD. Check out all the amazing work she is doing here. xx A VERY special thank you to today’s sponsors ⁠Progranulin Information Navigator⁠ and ⁠Psilera⁠.  If you're curious about anything RM, we'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram, and visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, all the latest updates! Want to support the podcast + get more content? Join us on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  14. 11/05/2025

    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. We also brought on some incredible advocates in the FTD Community - Annika from Cure MAPT FTD, Jackie & Wanda from CureGRN and Michael from End the Legacy to share their personal experiences and thought processes around genetic testing. Let us know what you think when you listen. - R+M A VERY special thank you to today’s sponsors Progranulin Information Navigator and Psilera.  FTD Genetic Resources: Progranulin Information Navigator Cure MAPT FTD CureGRN End The Legacy - ALS & FTD FTD Disorders Registry The Penn FTD Center Genetics Resources The AFTD Genetics Overview The National Society of Genetic Counselors UCSF Memory Familial FTD Page Want to support the podcast + get more content? Join us on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠! You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ If you're curious about anything RM, we'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram, and visit ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, all the latest updates! ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  15. 07/01/2025

    Tommy

    In our Season 10 finale, Alyssa describes the FTD journey with her father, Tommy - starting from her perspective at 11 years-old. She weaves us through her memories of her father's strange behavior - and the long road to finding answers. This story covers so much about family dynamics - but also what a healing journey can look like. And the unbelievable things that happen in life that we just can't explain. Thank you, Alyssa for sharing your story with us. You are an incredible woman. Keep fighting. ---------- A VERY SPECIAL THANK YOU TO TODAY'S SPONSORS: ⁠⁠PROGRANULIN INFORMATION NAVIGATOR⁠⁠ & ⁠⁠AVIADOBIO⁠⁠⁠⁠⁠. Mentioned in this episode: Season 9, Episode 15: Grief & Genetic Testing which you can listen to ⁠⁠here⁠⁠. Gonna miss us on the break? Support our podcast and join us on ⁠⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ - You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠⁠ If you're curious about anything RM, we'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram, and visit ⁠⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, all the latest updates! ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.

  16. 06/24/2025

    Family Dynamics 101 with Dr. Adam, Professor of Interpersonal & Family Communication

    Dr. Adam a professor of Interpersonal & Family Communication (and host of one of Maria's favorite podcasts The Sister Wives Professor) is here for what may be our favorite expert chat of all time. An open + honest conversation about life, family + grief. We talk a lot about family estrangement, family roles, what it means for someone to "be the glue" and so much more. Thank you, Thank you, Thank you to Adam for all of his love and attention to our community + thank you for coming on to share your insight with us. You can learn more about Dr. Adam's Patreon he mentioned in today's episode here: https://www.patreon.com/thesisterwivesprofessor ---------- A VERY SPECIAL THANK YOU TO TODAY'S SPONSORS: ⁠PROGRANULIN INFORMATION NAVIGATOR⁠ & ⁠AVIADOBIO⁠⁠⁠⁠. Mentioned in this episode: Season 9, Episode 15: Grief & Genetic Testing which you can listen to ⁠here⁠. Support our podcast and join us on ⁠⁠⁠⁠Patreon⁠⁠⁠⁠⁠⁠⁠⁠⁠ - You get exclusive content + a space to share and connect with others. ⁠⁠⁠⁠⁠⁠⁠⁠www.patreon.com/remembermecommunity⁠⁠⁠⁠⁠⁠⁠⁠ If you're curious about anything RM, we'd love to connect with you on ⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠Instagram, and visit ⁠⁠⁠⁠⁠⁠⁠our website at⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠ www.remembermeftd.com⁠⁠⁠⁠⁠⁠⁠⁠⁠⁠, all the latest updates! ------ Remember Me Podcast + Community is here to offer hope + human connection for families, caregivers, and individuals impacted by Frontotemporal Dementia (FTD). Always, always accept the good.