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Award Recognizes Organizations That Provide Enrichment, Care and Non-Medical Therapies for Families Impacted by Dementia Dementia Society Team Recognizes James A Michener Museum Team in Front of Edward Redfield Paintings DOYLESTOWN, PA – February 12, 2026 – The Dementia Society of America ®  (DSA) announces its annual Ginny Gives ® Awards, celebrating extraordinary organizations on the forefront of dementia care in the country. Named in honor of Ginny Jameson, the late wife of Dementia Society of America’s founder, CEO, and volunteer Chairman, Kevin Jameson, the award recognizes programs that have benefited thousands of individuals and their care partners.   “Dementia takes many forms and requires a variety of approaches to care,” said Kevin Jameson. “For more than a decade, the Ginny Gives Awards have recognized some of the many non-profit organizations that are addressing the growing needs of individuals and their care partners who face dementia challenges, through non-medical programs like music, the arts, movement, and tactile stimulation including touch.” Kevin Jameson and Dementia Society of America Announced Annual 2025 Awards at Ceremony Jameson, along with the volunteer Board of Directors and Advisory Council , recently hosted a ceremony for award recipients. Thanking and commending all of the non-medical programs, Jameson applauded the diversity of work occurring in the field saying, “when cures and meaningful treatments are still around the corner to address the causes of dementia, supporting community engagement programs focused on uplifting those living with dementia and their care partners is integral to Dementia Society of America’s mission to serve others—wherever they happen to be in their journey.” National Support for Non-Medical Programming Dementia Society of America awarded funds and a certificate of appreciation to more than two dozen organizations for their programming. Examples of the programming include a community support in Ohio (Carolyn L. Farrell Foundation for Brain Health); an intergenerational art creative in California (Creative HeARTS Art Therapy); art discovery conversations in Pennsylvania (James A. Michener Art Museum), modeled after the “ Meet Me at the Museum ” initiative of The Metropolitan Museum of Art in New York City, and an anxiety-support program in Texas (The Grand Baby Project).   In addition, and more broadly, Dementia Society of America funds seed grants to researchers across the spectrum of dementia and to further advances in brain health. To learn more visit GinnyGives.org . About the Dementia Society of America Dementia Society of America ®  (DSA) is a volunteer-driven 501(c)(3) nonprofit organization dedicated to creating Dementia and brain health awareness, advancing research, and enriching the lives of those facing Dementia in all its forms. DSA supports individuals, families, and caregivers through education, advocacy, and non-medical life enrichment programs such as art, music, touch, and movement. Learn more at DementiaSociety.org . Media Inquiries Dementia Society of America info@dementiasociety.org Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

In Chris Hemsworth's A Road Trip to Remember , the man best known as Marvel’s hammer-wielding Thor trades CGI battles for something far more human: a motorcycle ride across Australia with his dad, Craig, who is living with a form of Dementia (in his case, caused by Alzheimer’s disease). It’s a one-hour National Geographic® special, produced with Darren Aronofsky’s Protozoa and streaming on Disney+® and Hulu®. Still, it feels more like a lovingly shot home movie than a blockbuster event. Set against the vast landscapes of Melbourne, the Northern Territory, and the outback communities that shaped the Hemsworth family, the documentary follows father and son as they retrace the routes of Chris’s childhood. They visit places like Bulman (also known as Gulin Gulin), the remote Aboriginal community where Craig once worked as a social-services counsellor and Chris’s mother, Leonie, taught English. These aren’t just scenic backdrops; they’re memory prompts, anchors to a life Craig sometimes struggles to recall fully. A road trip built on memory science At the heart of A Road Trip to Remember  is a simple but powerful idea: social connection and reminiscence can help spark memories and support brain health. The film weaves in the science of reminiscence therapy and social engagement, highlighting research that shows strong social ties can significantly reduce the risk of Dementia and improve well-being for people already living with cognitive decline. Guided by Dr. Suraj Samtani from the University of New South Wales’ Centre for Healthy Brain Ageing, Chris designs the trip as a kind of “therapeutic road trip back in time.” Old photos, familiar roads, and reunions with people from their past become active tools, not just nostalgia. We see the way Craig’s face lights up when an old story surfaces, or when a shared joke suddenly returns to him. The documentary isn’t promising a cure—because there isn’t one—but it gently shows how thoughtful connection can offer moments of clarity, dignity, and joy for families living with all causes of Dementia. For anyone who has watched a loved one fade in and out of recognition, those moments matter more than almost anything. Chris Hemsworth: from outback kid to global advocate Part of what makes this documentary so compelling is how closely it’s tied to Chris Hemsworth’s own life story. Born on August 11, 1983, in Melbourne, Hemsworth grew up bouncing between city life and the rugged Outback. His parents moved the family back and forth between Melbourne, the Northern Territory community of Bulman, and later Phillip Island. He has often described his childhood in the bush—surrounded by cattle stations, crocodiles, and buffalo—as an “adventure,” and credits that period with shaping his love of the outdoors and his grounded, no-nonsense personality. That kid from Bulman eventually became one of the world’s highest-profile actors, breaking through in Australian television ( Home and Away ) before leaping into global stardom as Thor in the Marvel Cinematic Universe. But away from the red carpets, Hemsworth has slowly turned his public platform toward something deeply personal: brain health and aging. While filming his earlier National Geographic series Limitless , Chris learned that he carries two copies of the APOE-e4 gene variant—one from each parent—placing him at a significantly higher-than-average risk for developing Alzheimer’s disease later in life. The revelation was jarring enough that he publicly announced he would step back from acting to spend more time with his family and rethink his priorities. That genetic news sits quietly in the background of A Road Trip to Remember , but it’s there. Chris isn’t just walking beside a father living with Alzheimer’s; he’s a son who knows his own risk is elevated. The documentary becomes, in a sense, a rehearsal for a future he hopes never fully arrives—and an act of defiance against fatalism. A family story that loops back on itself The trip Chris and Craig take in the film isn’t random. Years ago, father and son dreamed of riding motorcycles from Melbourne back up to the Northern Territory, revisiting the places that meant so much to their family when the three Hemsworth boys were young. Life, as it tends to do, got in the way. Now, as Craig faces early-stage Alzheimer’s, the promise finally becomes urgent. Along the way, the film revisits the Hemsworths’ time living and working in Bulman: Craig counselling in the community, Leonie teaching in the local school, and the boys racing around in a childhood that had more to do with red dirt and open sky than screens. When Chris stands in those same places decades later—sometimes in tears, sometimes laughing—it’s hard not to feel how memory, place, and identity are all tangled up together. In recent years, Hemsworth has also physically returned to Gulin Gulin outside of filming, sharing on social media that some of his “earliest and happiest memories” came from that remote community. That personal loop—childhood to fame to homecoming—adds emotional weight to every frame of the documentary. More than Thor: the creator behind the camera Although A Road Trip to Remember  is directed by Tom Barbor-Might and produced alongside heavyweights like Darren Aronofsky and Jane Root, Chris is not just the on-screen star. He’s also a creator and producer through his company, Wild State, continuing a partnership with National Geographic that began with Limitless . You can feel that creative fingerprint. The film blends the polished visual language of adventure travel—big skies, long roads, sweeping drone shots—with intimate, unguarded family moments: Craig’s pauses as he searches for a word, Chris’s voice cracking as he reads an old photo. This casual ribbing only happens between a father and son who genuinely like each other. Hemsworth’s previous work in Limitless  explored topics like stress, cold exposure, and longevity with an almost superheroic bravado. A Road Trip to Remember  keeps the curiosity and the science, but dials down the bravado. Here, Chris isn’t trying to push his body to its extremes; he’s trying to hold onto his dad, one story at a time. Why this documentary matters now Globally, more than 57 million people are living with some type/cause of Dementia (Alzheimer's, Vascular, Lewy Body, Frontotemporal & over 200 more) , a number expected to rise sharply in the coming decades. Families like the Hemsworths are far from alone in navigating the daily realities of memory loss, grief, and uncertainty. What makes this film important is not that a celebrity family is affected—it’s that they’re choosing to show the messy, hopeful, funny, painful parts of that journey in detail. The documentary also helps correct a narrative about Dementia that can feel overwhelmingly bleak. Yes, it is a progressive, currently incurable disease. But embedded in the science the film showcases is a quieter message: there are things we can do, right now, to support brain health and quality of life. Social connection. Community engagement. Physical activity. Emotional closeness. For Chris Hemsworth, those aren’t abstract recommendations. Having learned that his own genetic risk is higher, he’s been candid about reshaping his life—leaning into family, prioritizing balance, and using his platform to talk openly about brain health rather than hiding it in the shadows. A love letter to dads, memories, and showing up Ultimately, A Road Trip to Remember  lands as a love letter: from a son to his father, from a family to the places that formed them, and from a global movie star to anyone whose life has been touched by dementia. It reminds us that while we wait for better treatments and cures, there is profound power in the ordinary things: a shared ride, a familiar song on the radio, a dusty road you’ve driven a hundred times before. For people living with Dementia, these echoes of the past can sometimes open a door. For the rest of us, they’re a nudge to make the memories now, while we still can. And that might be Chris Hemsworth’s most heroic role yet—not as a god of thunder, but as a son on a motorcycle, riding beside his dad into a future none of us can fully predict, determined to fill the road with as much love and connection as possible. Chris Hemsworth, National Geographic, Disney+, and Hulu do not endorse the Dementia Society or underwrite our content. Their trademarks are the property of their respective owners. Sources: Business  Wire The Courier-Mail Celebrity Business  Wire Encyclopedia Britannica FinancialContent Daily Telegraph StarsUnfolded FinancialContent Sky  News Sohu Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

chicagotribune.com/2025/12/01/opinion-dementia-education-memory-loss   Chicago Tribune Dateline: Dec. 1, 2025 Opinion Contributors: Kevin Jameson and Dr. Jeannine Forrest A terrible irony of Dementia — which can result in the inability to recognize people and places — is that the condition itself does not get the worldwide recognition it deserves. Until now. The United Nations Announces Dementia Plan The United Nations (U.N.) recently announced a plan to address major neurological disorders, such as Dementia. This is particularly significant because many countries do not always understand or treat the condition, which affects more than 57 million people worldwide. The U.N. action, though overdue, is welcome news for those of us working to raise awareness and improve the lives of people living with Dementia and their care partners. Families are Often Overwhelmed by Dementia Unfortunately, too many people and families are struggling with the condition and need more assistance. As a condition, Dementia is not a single disease. Instead, it is an umbrella term — a syndrome with a wide array of symptoms caused by one or more underlying pathologies affecting the brain. Just as the term “cancer” refers to numerous forms of the disease, Dementia encompasses wide-ranging impacts to cognition, including memory loss, difficulty with language, motor skill deterioration, behavioral changes, and impacts to decision-making and problem-solving. The syndrome of Dementia is one of the most critical health care challenges of our time. The Centers for Disease Control and Prevention calculates that more than 11 million adults provide unpaid care for someone living with Dementia. The annual cost of Dementia in the U.S., inclusive of medical care and foregone earnings of care partners, is $781 billion. As our population ages, we can expect that the condition will become more prevalent and the emotional and economic burdens on families will grow. Dementia Society Brings Help to Those Living with Dementia While there are currently no cures or ways to reverse Dementia permanently, there are three vital ways families and communities can plan for and work to address the syndrome that can make a real difference. Increase Dementia Awareness Knowledge fights fear. Facilitating education about Dementia by using nonmedical, jargon-free language helps families understand what they are facing and reduces the stigma that makes isolation worse. Organizations such as the Dementia Society offer crucial resources that help people navigate this journey and support their loved ones living with Dementia. Fund Dementia research We need more research into what triggers cognitive decline and how to protect brain health. To advance cures, interventions, and meaningful therapies, it is critical to support early-stage research aimed at a better understanding of possible upstream triggers of cognitive impairment, as well as underappreciated approaches to enhance brain health. Enrich life, and Help Those Living with Dementia Living with Dementia does not mean that life stops — it means that life changes. Communities across America are pioneering compassionate approaches that preserve dignity and create moments of joy: memory cafes where people gather without judgment, music therapy programs that unlock memories through familiar melodies, art classes adapted for changing abilities, and Dementia-friendly businesses training staff to offer patient, respectful service. These efforts prove a fundamental truth: While we cannot yet cure Dementia, we can radically improve how people live with it. When we invest in quality of life, we honor the humanity of every person facing cognitive decline. Global Dementia Awareness Matters The U.N.’s announcement matters because it elevates Dementia from a private family burden to a global public health priority. Yet, the response to this crisis will be measured not in international resolutions but in local action. For the estimated 57 million people globally currently living with Dementia, the syndrome is now our shared responsibility to work together to address. Kevin Jameson is CEO of Dementia Society of America (DSA), a volunteer-driven nonprofit based in the Philadelphia area. Jeannine Forrest, Ph.D., directs the Dementia Horizons Academy, an educational program at the DSA, and lives in Chicago. Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

How proactive planning and biometrics can make a difference. App Developer, My Family ID ™, Interviews Kevin Jameson, CEO of the National Nonprofit Charity, Dementia Society of America®. Dementia is a long, emotion-filled journey, not just for those experiencing cognitive decline but also for their families and care partners. This “road” traverses the shifting tectonics of altered realities, profound emotional and physical changes, and, critically, a heightened risk of elopement, putting vulnerable adults at risk. The fear of a loved one going missing is a constant concern for many families, highlighting the importance of compassionate support and proactive safety measures. This is where organizations like the Dementia Society of America (DSA), become beacons of hope and practical assistance. My Family ID™ aligns itself with organizations like DSA, which are making a difference in caring for the vulnerable. We interviewed Kevin Jameson, the Founder and CEO of this immeasurably important organization, about the work being done to protect our aging adults with cognitive issues. Dementia Society of America stands as a leading national nonprofit dedicated to providing essential support, education, and resources to families and individuals impacted by Dementia, with the goal of improving the quality of life for all affected. My Family ID proudly recommends organizations that do amazing, life-changing work. Through their tireless efforts, DSA works to enhance understanding, promote well-being, and advocate for the dignity and safety of every person living with and impacted by Dementia. "When a loved one with cognitive impairment goes missing, words cannot describe the panic and dread that their loved ones feel," said Detective Chuck Still (Ret.), Founder of My Family ID. “Silver alerts or missing adult cases are worked firsthand as a detective. That's why I deeply admire organizations like Dementia Society of America. Their dedication to supporting families and providing crucial resources aligns perfectly with My Family ID's mission to empower caregivers with the tools for immediate identification." Protecting Those Living with Dementia It’s not uncommon, the Dementia Society states, for a person living with Dementia, at some point, to experience one or more “critical wandering” events. These events, in law enforcement, are technically called elopement, the physical act of an individual leaving a safe environment undetected. Unfortunately, many simply call it “wandering,” but this is a mistake. Wandering, which may include rummaging, are common behaviors for all of us, and they may even be enjoyable, for example: wandering in a garden to enjoy the sights, smells and sounds, or rummaging through old knick-knacks to spark memories of good times from the past. However, wandering becomes a critical event when someone puts themselves in harm’s way, becoming confused about their location, how old they are, and while seeking out a safe place (childhood home, vacation spot, or long-time workplace) which may not exist or, their parents who are no longer are living. In these cases, the urgency of proactive safety measures, like having a recent photo and a record of a loved one's fingerprints to provide to first responders, cannot be overstated. “I know the heart-wrenching panic firsthand. I remember vividly one incident many years ago when my wife moved into the driver’s seat while I was in a store and drove off. I did ultimately find her much further away in the parking lot, but you can imagine the distance someone can cover in a short amount of time; they may end up hours away before you know it. Fortunately, law enforcement understands the gravity of this. They deal with difficult situations every day, but they never take a missing person call lightly because they know the stakes. The challenge, then, becomes ensuring that you can alert law enforcement agencies and get them to respond fast enough”, added Jameson. Why Did Kevin Jameson Start the Dementia Society of America? Dementia Society of America was born not from corporate strategy, but from profound personal experience. Jameson established the organization after his first wife developed Dementia, a journey that brought the realities of the syndrome all too close to home. Through his experience, Jameson recognized a huge need for accessible, practical education for all those navigating this difficult path. He also realized he wasn't alone. “At DSA presentations, when audiences are asked who has been impacted by Dementia, nearly 90% of the hands go up. It is a challenge that touches virtually everyone, directly or indirectly,” explained Jameson. Today, DSA serves as a vital 'on-ramp' to understanding, helping thousands of families annually turn fear into preparedness and ensuring those facing the risks of critical wandering never have to do so alone. Who Does the Dementia Society of America Serve? Dementia Society of America is the nation’s leading volunteer-driven all-Dementia awareness organization with a board of directors and advisory council composed entirely of volunteers, supported by a small paid staff. “Unlike other nonprofits, our organization has more volunteers than paid employees. This is really a testament to just how many lives Dementia touches. As the leading all-Dementia awareness organization, our focus right now is on broad awareness rather than specific diseases and disorders which can cause Dementia. We have been seen and heard on TV , radio, taxis, and billboards over 3 billion times in the last four years through public outreach in the U.S. and Canada,” reflected Jameson with pride. Through their information and support services, DSA helps thousands of families annually. This support is becoming increasingly vital as the "Baby Boomer" generation lives longer due to medical advances in other areas, leaving Dementia as one of the last remaining significant health challenges. The impact, Jameson says, is universal. Dementia Society of America’s education and information programs aim to reach a broad audience through multimedia efforts and, ultimately, improve the quality of life for those who are facing Dementia, including those: Living with a form of Dementia Acting as caregivers/care partners Who are isolated from friends and family Who have spent down their life savings Who are now on medical subsidies Who are beginning to observe early signs of cognitive impairment Who are educators and safety partners seeking practical safety tools DSA also provides materials and resources to small businesses, larger corporations, civic organizations, and communities-at-large. “Any resources, tools, or even available apps that can help reduce the risks or increase the likelihood of better outcomes go a long way to providing what can be so elusive – peace of mind. When my wife was living with Dementia, I would do anything to reduce that risk. We know caregivers can’t do this alone, so we’re here for them. Protecting those living with Dementia provides peace of mind and relief to those who are always carrying this immense burden of worry,” said Jameson. The Vital Role of Dementia Society of America Dementia Society of America’s comprehensive approach encompasses a variety of programs and resources designed to empower and inform: Education and Awareness: Knowledge is the first step toward effectively addressing and managing Dementia. DSA offers a wealth of non-medical, easy-to-understand educational materials, workshops, and online resources that have been well-received and help families and the public understand the different types of Dementia, their progression, and effective care strategies. “Education is probably the most important component of equipping people to face the issues that arise with Dementia. For example, critical wandering can happen anywhere, from a grocery store to a park, and often stems from a sudden feeling of being unsafe. Understanding this frame of mind is important to getting ahead of and preventing elopement events. When you hear an elder say, ‘I have to get home because my mother is expecting me,’ that is a critical warning sign that an elopement event may be about to occur,” explained Jameson. Caregiver Tools and Support: Recognizing the immense burden often placed on caregivers, DSA provides practical tools and emotional support. While they do not offer direct services, their support includes providing access to helplines, support groups, and local resources that offer guidance on managing challenging behaviors, promoting self-care, and navigating legal and financial considerations. Research & Program Funding: Their funding and research are forward-facing while addressing critical present issues. Their work shapes a future where better treatments and prevention methods are within reach. “On the medical side, our Medical Advisory Council guides us in awarding seed grants to researchers, typically in teaching hospitals. But we are equally committed to the ‘now,’ which is why we champion non-medical programming centered on art, music, movement, and touch. Each year, we recognize the care communities and nonprofits that are using these four modalities to improve the quality of life for those living with Dementia,” said Jameson. For those who have questions about Dementia or the resources DSA offers, they encourage you to call them at 1-800-DEMENTIA® or email them at info@dementiasociety.org . Guest Writer: My Family ID My Family ID is a smartphone app designed to store secure biometric data (fingerprints and photos) to safeguard vulnerable populations at risk for critical wandering or go missing, like those living with Dementia. When every second counts, My Family ID ensures caregivers have actionable identifying information to alert first responders. Because of our commitment to safety, we are thrilled to endorse and partner with nonprofit organizations that share our goals to amplify their impact. Disclaimer:  Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

Comprehensive Program Takes Holistic Approach to Dementia Education, Moving Beyond Awareness to Actionable Learning Dementia Horizons Encourages Music as Meaningful Caregiver Tool DOYLESTOWN, PA – January 21, 2026 – Today, Dementia Society of America's mission-driven Care Partner Academy™ announces its new and comprehensive educational caregiver support program, Dementia Horizons ™. Designed to equip care partners, friends, community members, and professionals with the practical skills needed to address the most common challenges of Dementia, the program is gaining momentum with rapid enrollment following its launch.   “The syndrome of Dementia is one of the most critical healthcare challenges of our time. Far too many care partners face the challenges of Dementia, feeling isolated and unprepared," said Kevin Jameson, CEO of Dementia Society of America. “Dementia Horizons addresses this critical need by providing comprehensive, accessible education that transforms uncertainty into confidence. In transforming care partner skills and support, we teach about Dementia in its various forms and build a community where caregivers gain insight, find connection, and discover they're not alone on this journey.” Dementia Horizons takes a comprehensive approach   Unlike many programs that focus solely on Alzheimer's disease, Dementia Horizons takes a comprehensive approach, covering a broad spectrum of Dementia-related conditions—including Alzheimer's and its subtypes, Lewy Body Dementia, Frontotemporal Degeneration, Vascular Dementia , and many more. The program's goal is to move beyond awareness into actionable learning, helping participants develop practical strategies for a deeper understanding of the needs of those living with Dementia, while providing educational support to anticipate future care in real-world settings.   “Dementia Horizons stands out as a practical and inclusive educational program that equips care partners with the tools, knowledge, and confidence to better support individuals living with Dementia and themselves,” said Dr. Jeannine Forrest, Program Director of the Care Partner Academy. “Designed to meet care partners exactly where they are in their journey, Dementia Horizons delivers accessible and flexible programming helping participants develop actionable strategies for connection, and compassionate care.”   Customized Care Partner Skills and Support The Dementia Horizons course consists of 16 interactive workshops available both online and in person. When delivered in person, the sessions are highly customizable. They can be taken individually or as a complete series, organized as two eight-week programs or adapted to meet the specific needs of different groups. To encourage meaningful discussion, peer support, and engagement, in-person workshops are intentionally kept small—with a maximum of 16 participants.   The workshops can be hosted in a variety of venues, including libraries, community centers, senior centers, houses of worship, civic organizations, and long-term care facilities, making them accessible to a broad audience. To expand access to the program, the Care Partners Academy plans to train empathetic facilitators through its “Train the Trainer” program, offered in various formats depending on facilitator experience. This initiative ensures that the Academy's supportive, evidence-based approach will reach communities nationwide.   Online, courses are delivered through a web-based Learning Management System (LMS), which uses a multimedia approach to accommodate various learning styles while reinforcing the educational experience through videos, quizzes, and written transcripts. Whether in person or online, learners who successfully meet the course requirements can obtain a personalized Certificate of Completion.   About the Dementia Society of America Dementia Society of America ®  (DSA) is a volunteer-driven 501(c)(3) nonprofit organization dedicated to creating Dementia and brain health awareness, advancing research, and enriching the lives of those facing Dementia in all its forms. DSA supports individuals, families, and caregivers through education, advocacy, and non-medical life enrichment programs such as art, music, touch, and movement. Learn more at DementiaSociety.org . Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

Dementia Society of America Cares www.dementiasociety.org/donate   What is Dementia? Dementia is a collection of symptoms, a syndrome, that includes Alzheimer’s, Vascular, Lewy Body, Frontotemporal, Mixed Dementia, and over 200 other underlying causes. Our mission is simple yet profound: Providing Hope by Raising Awareness, Funding Research, and Enriching Lives. Thanks to you Thanks to you, we’ve been able to touch the lives of hundreds of thousands of individuals this year who are seeking trusted, accessible Dementia education online. Every one of those visits represents a family looking for clarity… a spouse trying to understand what is Dementia, and how might it change a loved one… an adult child seeking guidance in the middle of the night… a person newly diagnosed searching for hope. Thanks to you, we have directly served thousands of families this year with information, support, and compassion when they needed it most. These are real people—neighbors, friends, parents, grandparents—leaning on us during some of the hardest chapters of their lives. You can continue making a difference One family, one resource, one act of generosity at a time. Click here to donate www.DSAdonate.org Thank you, thank you, thank you! PS: Read online or request a free copy of our popular guide to be sent to your home at www.dementiasociety.org/the-big-umbrella Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

The realities of Dementia are not lost on the caregiver. | Copyright: Dementia Society, Inc. Dementia changes everything—not just for the person diagnosed, but for everyone who loves and cares for them. When you give to the Dementia Society of America® (DSA), you become part of a support system that helps families feel less alone, less overwhelmed, and more hopeful. How Your Financial Support Helps Your gift brings hope and an immediate impact because DSA is a volunteer-driven, grassroots nonprofit. Instead of mountains of red tape and multiple layers of bureaucratic administration, we are nimble and target $0.70 of every $1.00 to be spent directly on mission-related programs that make a difference: Caregiver Support : Many caregivers are family members who never expected to become full-time helpers. Your donation funds education, awareness , online support programs , and easy-to-understand resources that guide them through challenging moments—like how to communicate kindly or manage stress. Monthly eNews : concise, helpful information selected especially for overwhelmed caregivers and busy care professionals. Trusted Information : Families often search online late at night, scared and confused. Your support keeps DSA’s website accurate and up-to-date, replacing fear with clarity. Operation KeepSafe ®: A wearable identification program designed to address the risks associated with critical wandering and elopement (leaving one's home undetected), as well as increase safety in the home and caregiver peace of mind. Community Programs : Initiatives such as  Dementia ENRICH, Dementia SMART®, and Dementia CARER®  awards recognize and fund creative, non-medical efforts, such as music, art, movement, and touch, that improve daily life, stimulate engagement, and promote the dignity of those living with Dementia, and their care partners. Research Through Dementia QUEST ®: Your gift helps fund seed grants at leading teaching hospitals—small investments that can spark big discoveries for better care and future breakthroughs. Helpful Brain Health Information:  Our popular magazine,  Better Brain Nation ® , supports families, professionals, and communities with cognitively-engaging ideas and activities to foster a brain-healthy lifestyle, along with links to the latest noteworthy brain research. Why It Matters: Your Gift Brings Hope Every donation helps someone feel seen, supported, and stronger. It helps a caregiver keep going. It helps a family find answers. It helps progress begin. Candid GuideStar Platinum Rating https://www.guidestar.org/profile/46-3401769 Charity Navigator 4-Star Rating https://www.charitynavigator.org/ein/463401769 Charity Ninja's Best Dementia Nonprofits https://impactful.ninja/best-charities-that-fight-dementia/ Join Us Today Make a gift that brings hope and change—one person, one family, one moment at a time. Click Here to Donate . Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

Click here for Spanish Click here for French Video Transcript [Answer 1023] Welcome and thank you for joining me. Today, we're talking about how to handle the holidays when someone you care for is living with Dementia. Some holidays are joyful, and some are meant to be times of reflection and somberness, but they can also feel confusing or stressful. For someone with cognitive challenges, with some planning, you can help make the season more peaceful and meaningful for everyone. First, Keep Holidays Simple A calm and quiet holiday is better than a busy one. Choose a few special traditions that feel familiar. Avoid loud music, large crowds, or too many decorations that can cause confusion. Try to keep a routine. People with Dementia feel more secure when their day is predictable. Fatigue and over-planning can cause anxiety, so plan meals and visits around their best time of day, usually in the morning or early afternoon. Involve Your Loved One In Small Ways Let them help with safe and simple tasks like folding napkins, stirring batter, or looking through old photos. These activities can bring comfort and help them feel included. Prepare guests ahead of time. Let family and friends know how the person is doing, and remind them to speak slowly, smile, and be patient. If you notice signs of anxiety or distress, be prepared to roll back activities or bring the person into a quieter room. Consider having everyone wear large name tag labels, even if they've been together for years. It lowers stress levels when trying to remember names. Focus on Joy Most importantly, focus on moments of joy and connectedness rather than perfection. Even small smiles or shared memories can mean a lot. On behalf of the Dementia Society of America ® , thank you again for joining me today. Stay informed, stay healthy, and take care of yourself. Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

usatoday.com/story/opinion/voices/2025/12/20/warning-signs-dementia-symptoms-memory/87778893007   USA TODAY Opinion Contributor: Kevin Jameson Dateline: Dec. 20, 2025 For individuals who suspect friends and loved ones are exhibiting signs of cognitive decline, the holidays are a particularly important time to gauge differences in behavior and help address signs. Ginny and Kevin, 2006, Maple Sugar House, Shelbourne Falls, MA | Courtesy of Kevin Jameson Dementia can sneak up on you. I know, because it happened to my family. Back in the early 2000s, my first wife, Ginny, began demonstrating some unusual behavior. She was not her usual bubbly self. Instead, she became caustic, somewhat aggressive, got lost driving , and was unable to follow written directions. At times, these episodes frustrated me, but I assumed they were caused by stress or marital difficulties. Then, one day, we went to dinner at a favorite Indian restaurant near our home in Bucks County, Pennsylvania. The hostess met us at the front door, and I greeted her by name. As we sat down, Ginny asked how I knew her. I responded by saying that we knew her from the last time we were there. Ginny insisted she had never been to the restaurant before and accused me of having been there with another woman. For some time, I had been thinking strongly about a divorce. But after that night, I realized I had missed the signs of what might be a severe cognitive disorder ; so, the journey began. Fast-forward nearly 10 years, and I left my corporate career to care for Ginny in the last year of her life while in hospice and started the Dementia Society of America to help those who were facing similar circumstances. Early signs of Dementia: What to look for and what to do Today, for individuals who suspect friends and loved ones are exhibiting early signs of Dementia or cognitive decline, the holidays are a particularly important time. The traditional gatherings enable people to interact with each other, gauge differences in behavior from the last holiday get-together, and compare perspectives on what steps might be taken to help address signs of possible Dementia. In our work, we urge families during the holidays to look for " 22 Clues " of potential impairment and to take several key actions. Is your family member or friend: Forgetting important recent information, not just the occasional memory lapse? Having trouble completing familiar routines, like cooking or driving? Fumbling with words, substituting words, or struggling to follow conversations? Putting items in odd places (e.g., keys in the freezer, bedsheets with the china)? Becoming confused, suspicious, aggressive, anxious, or exhibiting any behaviors or movement disorders that are not normal for them? If something seems highly unusual, you should consider the following steps: If difficulties over memory or ability crop up, don't argue or challenge their reality in the moment; instead, step back and focus on lowering their anxiety by redirecting conversations to less complex discussions, speaking more slowly and a bit louder, and asking yes/no questions. Ask others about what you’re seeing and hearing; be especially prepared for close family to be the first ones to deny anything is amiss. Make written notes about what you’re observing and keep them organized by time and date. If changes persist, firmly but gently push to involve health care professionals. These signs and clues warrant evaluation, as severe cognitive impairments are not considered a normal part of aging and aren’t limited to adults over 65. Most important, seek to better understand Dementia Dementia is not a specific disease but a syndrome, an umbrella term for a collection of symptoms (which can include impaired memory, trouble with following directions, inappropriate mood swings, physical instability, as well as abnormal movements) caused by various brain diseases and disorders. Some of these causes are treatable, and all can benefit from intervention. Eventually, we got my wife, Ginny, the help she needed – though I always wish I had acted sooner. This holiday season, make sure to take care of your loved ones, too. Dementia Society of America (DSA), a volunteer-driven 501(c)(3) nonprofit organization dedicated to creating awareness, advancing research, and enriching the lives of those facing Dementia in all its forms. Source: usatoday.com/story/opinion/voices/2025/12/20/warning-signs-dementia-symptoms-memory/87778893007   Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

Click here for Spanish Click here for French Video Transcript [Answer 1088] Welcome, and thank you for joining me. Today we're talking about Traumatic Brain Injury, often called TBI. A traumatic brain injury happens when a sudden hard bump, blow, or jolt to the head causes the brain to move inside the skull. Brain surgeons tell us that your brain has the same consistency and firmness as bean curd, also known as tofu. So you can imagine that the soft structure of the brain knocking against the hard skull that surrounds it might lead to some unpleasant outcomes. Also, without advanced testing, and unlike a broken leg in a cast, this type of injury is nearly impossible to see in the traditional sense. So for many people, it's a hidden condition that is not easily understood. TBI may lead to neuroinflammation of the brain tissue, damage brain cells, and affect how a person thinks, feels, behaves, or moves. TBI can happen from falls, car accidents, sports injuries, or being hit in the head. Some injuries are mild, like a concussion, and others can be more serious, leading to long-term problems. In addition, some TBIs are severe one-time events, while others are mild but repeated over time. Signs of a TBI can include confusion, headaches, memory loss, dizziness, mood changes, or trouble speaking. Some symptoms show up right away, but others might appear days or weeks later. For older adults, a TBI can be especially risky. Falls are the most common cause. Even a mild injury can affect thinking, balance, and daily life. It may also increase the risk of developing conditions that express themselves as Dementia later on. If someone has a head injury, it's essential to see a doctor right away, even if they seem okay at first. Rest, follow-up care, and sometimes physical or speech therapy may be needed to help heal the brain. To help prevent TBI, make the home safer by removing tripping hazards, using grab bars in the bathroom, and wearing shoes with a good grip. Looking both ways at intersections when driving, wearing seat belts and helmets when participating in sports or biking, also helps protect the brain. On behalf of the Dementia Society of America ® , thank you again for joining me today. Stay informed, stay healthy, and take care of yourself. Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

Melora Hardin | Public Service Announcement |Dementia Society of America Video Transcript Hi, yes, it's me, Melora Hardin . You probably know me from a lot of roles I've played, like when I played Jan on The Office . That was funny, but this is not today. I'm here to talk to you about Dementia. You might be surprised by this, but Dementia is not a disease. It's actually a syndrome with many underlying causes. And as of today, no medical cures. The loss of memories and cognitive functions that occur over time is very serious and not something to be ashamed of or hide from your doctor. If you had chest pain or dizziness that wouldn't go away. You'd get it checked out, right? Interestingly, some cognitive impairments that aren't Dementia may be reversible or manageable, and not all cognitive impairments lead to Dementia. You should know resources are available, and knowledge is power. If you or someone you love is experiencing unusual behavior, repeating themselves has trouble finding words, not recognizing others, or getting lost, it's time to seek professional help. Talk to a doctor. Learn more about Dementia and brain health. Call the Dementia Society of America ® at 1-800-DEMENTIA ® , or go online to DementiaSociety.org . Take it from me, Melora Hardin, your brain is more than important. It's essential. Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.

Did you know that moving your body in slow, thoughtful ways can make your brain healthier? It’s true! Activities like yoga, tai chi, and other meditative exercises help you stretch, relax, and boost your brainpower. Let’s examine how these special movements can help your mind feel calmer, sharper, and more focused. What Are Meditative Exercises? Meditative exercises are gentle activities that combine movement, breathing, and focus. You might have heard of some of them: Yoga is a mix of stretching, balance, and deep breathing. Tai Chi is a slow-moving martial art that looks like a dance. Qi Gong is another ancient practice that uses breathing, movement, and meditation. Mindfulness is sitting quietly and paying attention to your thoughts and breath. All of these activities help your body feel strong and relaxed. But even more, they help your brain work better, too. How Do These Activities Help Your Brain? Our brains are like muscles—they need exercise, rest, and good fuel. Yoga, tai chi, and similar exercises give your brain all three. Less Stress, More Calm When we feel worried or upset, our brain releases stress chemicals like cortisol. A little stress is okay, but too much can make it hard to think clearly. Meditative movement helps lower those stress chemicals. It also tells the brain to release “feel-good” chemicals like dopamine and serotonin. That’s why you feel more relaxed after yoga or tai chi. Better Focus and Memory When you practice slow, mindful movement, you train your brain to pay attention. You learn to focus on your breath, body, and feelings. Over time, this can help improve your memory and make it easier to concentrate, whether studying for a test or playing sports. Stronger Brain Connections Scientists have used brain scans to study people who do yoga and tai chi. They found that these people had stronger connections in brain parts that control memory, attention, and emotions. This finding means their brains were “talking” better between different areas, like having faster Wi-Fi in your head. Improved Sleep Getting enough sleep is super important for brain health. Yoga and mindfulness can help you fall asleep faster and sleep more deeply, giving your brain more time to rest and grow. What Does Science Say? Many scientists have studied how yoga, tai chi, and meditation affect the brain. Here are some cool facts: People who practice yoga regularly show more brain activity in areas related to attention and decision-making. A study found that older adults who did tai chi for 12 weeks had better memory and felt less tired. Kids who practiced mindfulness in school showed better focus, less stress, and even did better in their classes. Even a little practice—10 to 15 minutes daily—can make a big difference. Who Can Try These Exercises? The best part? Anyone can do them! You don’t need to be super flexible or have fancy clothes. These activities can be done by: Kids and teens Adults and older people People with disabilities or injuries There are even special classes made just for beginners. And many of them are free online. How to Get Started Ready to try it out? Here are some easy ways that the Dementia Society of America ® suggests to begin: Look up a beginner yoga or tai chi video on YouTube. Try a guided meditation app like Calm or Headspace. Practice mindful breathing: Close your eyes, breathe in slowly, and count to four. Then, breathe out and count to four again. Ask your school or local community center if they offer yoga or meditation classes. You don’t have to do everything at once. Five minutes of quiet breathing or stretching can help your brain feel better. Final Thoughts: A Healthy Brain for Life Taking care of your brain isn’t just about doing puzzles or eating healthy food. Moving your body in mindful, gentle ways helps too. Yoga, tai chi, and meditation are fun and powerful tools that help your mind stay calm, focused, and happy. So the next time you feel stressed or tired, take a deep breath, stretch your arms, and move slowly. Your brain will thank you! Author:  AI-Assisted Human-Edited Staff Writer Additional Reading: Streeter, C. C., et al. (2012). Meditative Movement Reduces Stress and Boosts Mood. Journal of Alternative and Complementary Medicine , 16(11), 1145–1152. Pascoe, M. C., Thompson, D. R., & Ski, C. F. (2017). Yoga, mindfulness-based stress reduction, and stress-related physiological measures: A meta-analysis. Psychoneuroendocrinology , 86, 152–168. Tang, Y. Y., Ma, Y., Wang, J., et al. (2007). Short-term meditation training improves attention and self-regulation. Proceedings of the National Academy of Sciences , 104(43), 17152–17156. Gothe, N. P., Pontifex, M. B., Hillman, C. H., & McAuley, E. (2013). The acute effects of yoga on executive function. Journal of Physical Activity and Health , 10(4), 488–495. Villemure, C., & Bushnell, M. C. (2012). Yoga-based interventions decrease pain and increase gray matter density in brain regions involved in pain modulation. The Journal of Neuroscience , 32(15), 5242–5248. Gard, T., Hölzel, B. K., & Lazar, S. W. (2014). The potential effects of meditation on age-related cognitive decline: A systematic review. Annals of the New York Academy of Sciences , 1307(1), 89–103. Wayne, P. M., Walsh, J. N., Taylor-Piliae, R. E., et al. (2014). Effect of tai chi on cognitive performance in older adults: Systematic review and meta-analysis. Journal of the American Geriatrics Society , 62(1), 25–39. Lam, L. C. W., Chau, R. C. M., Wong, B. M. L., et al. (2012). A 1-year randomized controlled trial comparing mind-body exercise (Tai Chi) with stretching and toning exercise on cognitive function in older Chinese adults at risk of cognitive decline. Journal of the American Medical Directors Association , 13(6), 568.e15–568.e20. Zenner, C., Herrnleben-Kurz, S., & Walach, H. (2014). Mindfulness-based interventions in schools—a systematic review and meta-analysis. Frontiers in Psychology , 5, 603. Flook, L., Smalley, S. L., Kitil, M. J., et al. (2010). Effects of mindful awareness practices on executive functions in elementary school children. Journal of Applied School Psychology , 26(1), 70–95. Disclaimer: Dementia Society of America (DSA) provides educational content only and does not offer medical advice. Always consult a qualified healthcare professional before making changes to your medical care. DSA content is created by both human and computer-generated means and is reviewed for accuracy; however, errors may occur. Views expressed by third-party contributors do not necessarily reflect those of DSA. Unless expressly stated, DSA does not endorse or guarantee any third-party products, services, organizations, or external content. All DSA content is copyrighted and/or trademarked and may not be used without written permission.