Many people have never heard of frontotemporal dementia (FTD) until it enters their lives. 60 Minutes once called FTD “the cruelest disease you’ve never heard of.” Greater awareness helps families receive earlier diagnosis, better guidance, and the support they need. Through the @emmabrucewillisfund, we are committed to helping bring greater understanding to this disease. To learn more about the fund, head to the link in bio.
Many people have never heard of frontotemporal dementia (FTD) until it enters their lives. 60 Minutes once called FTD “the cruelest disease you’ve never heard of.” Greater awareness helps families receive earlier diagnosis, better guidance, and the support they need. Through the @emmabrucewillisfund, we are committed to helping bring greater understanding to this disease. To learn more about the fund, head to the link in bio.
Many people have never heard of frontotemporal dementia (FTD) until it enters their lives. 60 Minutes once called FTD “the cruelest disease you’ve never heard of.” Greater awareness helps families receive earlier diagnosis, better guidance, and the support they need. Through the @emmabrucewillisfund, we are committed to helping bring greater understanding to this disease. To learn more about the fund, head to the link in bio.
Many people have never heard of frontotemporal dementia (FTD) until it enters their lives. 60 Minutes once called FTD “the cruelest disease you’ve never heard of.” Greater awareness helps families receive earlier diagnosis, better guidance, and the support they need. Through the @emmabrucewillisfund, we are committed to helping bring greater understanding to this disease. To learn more about the fund, head to the link in bio.
Many people have never heard of frontotemporal dementia (FTD) until it enters their lives. 60 Minutes once called FTD “the cruelest disease you’ve never heard of.” Greater awareness helps families receive earlier diagnosis, better guidance, and the support they need. Through the @emmabrucewillisfund, we are committed to helping bring greater understanding to this disease. To learn more about the fund, head to the link in bio.
Many people have never heard of frontotemporal dementia (FTD) until it enters their lives. 60 Minutes once called FTD “the cruelest disease you’ve never heard of.” Greater awareness helps families receive earlier diagnosis, better guidance, and the support they need. Through the @emmabrucewillisfund, we are committed to helping bring greater understanding to this disease. To learn more about the fund, head to the link in bio.
Everyone will give or receive care at some point in their life — so why aren’t we talking about it? We’re on a mission to spark 1 million conversations about care so we can build a future where care systems actually reflect and support us! Join our upcoming virtual event, Why We Talk About Care: A Conversation with Emma Heming Willis, Senator Andy Kim, and Ai-jen Poo, to kick it all off! 🗓️ Save the date: March 18 at 3:30 p.m. PT / 6:30 p.m ET live on Zoom! 🔗 RSVP now via the link in our bio.
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
Bruce and I received the Susan Newhouse & Si Newhouse Award of Hope, and I was deeply moved to be part of such a special, yet bittersweet moment. Having my mom and our two young daughters there made the evening incredibly powerful. I was also proud to announce the launch of The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support, with our first gift going to AFTD, an organization that has been supporting families affected by FTD since 2002. Being in a room filled with families living with FTD, those who have lost someone to it, and the friends, advocates, and researchers working every day to bring greater understanding and progress to this disease was deeply profound. Thank you to @theaftd for the extraordinary work you do every day for families navigating FTD, including mine, and for bringing such a beautiful evening to life. 🤍 @emmabrucewillisfund 📷: @aguinz, James Salzano, Leo Sorel
When FTD enters your life, you quickly realize how much more awareness, research, and caregiver support is needed. The Emma & Bruce Willis Fund was created to help move that work forward. Our vision is a world where frontotemporal dementia is understood and every caregiver has the support they need to thrive. Together, we can change the future for families facing this disease. To learn more, go to the link in bio 💙 @emmabrucewillisfund @eifoundation
When FTD enters your life, you quickly realize how much more awareness, research, and caregiver support is needed. The Emma & Bruce Willis Fund was created to help move that work forward. Our vision is a world where frontotemporal dementia is understood and every caregiver has the support they need to thrive. Together, we can change the future for families facing this disease. To learn more, go to the link in bio 💙 @emmabrucewillisfund @eifoundation
When FTD enters your life, you quickly realize how much more awareness, research, and caregiver support is needed. The Emma & Bruce Willis Fund was created to help move that work forward. Our vision is a world where frontotemporal dementia is understood and every caregiver has the support they need to thrive. Together, we can change the future for families facing this disease. To learn more, go to the link in bio 💙 @emmabrucewillisfund @eifoundation
When FTD enters your life, you quickly realize how much more awareness, research, and caregiver support is needed. The Emma & Bruce Willis Fund was created to help move that work forward. Our vision is a world where frontotemporal dementia is understood and every caregiver has the support they need to thrive. Together, we can change the future for families facing this disease. To learn more, go to the link in bio 💙 @emmabrucewillisfund @eifoundation
Today we’re introducing The Emma & Bruce Willis Fund for Dementia Research and Caregiver Support. Our family’s journey with frontotemporal dementia has opened my eyes to what so many families experience when someone they love is living with this disease. The uncertainty, the challenges, and the incredible strength of the caregivers who show up every day. This fund is our way of helping move things forward by raising FTD awareness, supporting promising research, and standing beside the caregivers who carry so much. I’m grateful to be partnering with @eifoundation to help bring this effort to life. To learn more about the fund, please follow @emmabrucewillisfund and also go to the link in my bio 💙
Our lean, mean @maketimewellness team took on @natprodexpo and started asking women one simple question… “When was the last time someone talked to you about your brain?” The answer? Almost never. And that’s exactly why we exist. 🧠✨ We hosted a Women’s Brain Health panel, met so many incredible people, and our Brain, Body & Beauty drink powder became a NEXTY finalist. Because at Make Time, we’re here to get the world talking seriously about women’s brain health and empower women to take care of their most valuable asset. Your brain. And trust me… we’re just getting started. 🎯
Our lean, mean @maketimewellness team took on @natprodexpo and started asking women one simple question… “When was the last time someone talked to you about your brain?” The answer? Almost never. And that’s exactly why we exist. 🧠✨ We hosted a Women’s Brain Health panel, met so many incredible people, and our Brain, Body & Beauty drink powder became a NEXTY finalist. Because at Make Time, we’re here to get the world talking seriously about women’s brain health and empower women to take care of their most valuable asset. Your brain. And trust me… we’re just getting started. 🎯
Our lean, mean @maketimewellness team took on @natprodexpo and started asking women one simple question… “When was the last time someone talked to you about your brain?” The answer? Almost never. And that’s exactly why we exist. 🧠✨ We hosted a Women’s Brain Health panel, met so many incredible people, and our Brain, Body & Beauty drink powder became a NEXTY finalist. Because at Make Time, we’re here to get the world talking seriously about women’s brain health and empower women to take care of their most valuable asset. Your brain. And trust me… we’re just getting started. 🎯
Our lean, mean @maketimewellness team took on @natprodexpo and started asking women one simple question… “When was the last time someone talked to you about your brain?” The answer? Almost never. And that’s exactly why we exist. 🧠✨ We hosted a Women’s Brain Health panel, met so many incredible people, and our Brain, Body & Beauty drink powder became a NEXTY finalist. Because at Make Time, we’re here to get the world talking seriously about women’s brain health and empower women to take care of their most valuable asset. Your brain. And trust me… we’re just getting started. 🎯
