Many people want to keep their brains sharp, especially as they age. In the United States, over-the-counter (OTC) supplements for brain health have gained popularity. These products claim to improve memory, focus, and brain function. But do they work? The Dementia Society of America® explains what these supplements are, what’s in them, and whether they help your brain. What Are Brain Health Supplements? Brain health supplements are pills, powders, or drinks that people buy without a doctor’s prescription. They are sold in stores and online, often labeled as “memory boosters” or “focus enhancers.” These supplements contain ingredients like: Omega-3 fatty acids – found in fish oil – may support brain function. B Vitamins – contribute to energy levels and brain cell health. Ginkgo Biloba – a plant extract that some believe enhances memory. Caffeine – present in coffee and tea, it can increase alertness. Herbs such as ashwagandha – thought to reduce stress. Do Brain Health Supplements Actually Work? Scientists are still unsure if these supplements improve brain function. Some studies suggest that certain ingredients, like omega-3s and B vitamins, may support brain health, especially for people who don’t get enough from food. However, many other ingredients lack scientific evidence to support their effectiveness. There Is No Magic Pill – The U.S. Food and Drug Administration (FDA) does not test supplements for effectiveness before they are sold. This means companies can claim their products help the brain, even without strong evidence. Not a Cure for Memory Loss – Some supplements say they prevent the diseases that cause Dementia or Alzheimer’s disease, but no supplement has been proven to do this. The Dementia Society of America® reminds the public to be cautious of products that make these claims. Are There Any Risks? While most brain supplements are generally safe, some may have side effects or interact with certain medications. Too Much of a Good Thing – High doses of specific vitamins, like B6 or B12, can cause nerve problems. Blood Thinners – Ingredients like Ginkgo Biloba may thin the blood and increase the risk of bleeding problems. Fake or Unregulated Products—Some supplements do not contain what they promise since the U.S. supplement industry is little regulated. Better Ways to Support Brain Health Instead of relying on supplements, scientists recommend proven methods to keep your brain healthy: Eat a Brain-Boosting Diet – Foods like fish, nuts, berries, and leafy greens help brain function. Exercise Regularly – Physical activity improves blood flow to the brain. Get Enough Sleep – The brain needs rest to function correctly. Stay Mentally Active – Reading, puzzles, and learning new things help keep your brain sharp. Stay Social – Talking to friends and family helps memory and mental well-being. Conclusion While brain health supplements are popular in the United States, there is limited evidence that they enhance memory or focus. Some ingredients may have mild benefits, but they do not cure memory loss or brain diseases. Instead of relying on supplements, people can maintain a strong brain by eating a balanced diet, exercising regularly, and engaging in mentally stimulating activities. A healthy lifestyle is the best way to support brain health for life! Author: AI-Assisted Human-Edited Staff Writer Additional Reading: National Institutes of Health (NIH) – Office of Dietary Supplements. Dietary Supplements for Cognitive Function, Dementia, and Brain Health. https://ods.od.nih.gov/ U.S. Food and Drug Administration (FDA). Caution on Dietary Supplements for Brain Health and Memory Claims. https://www.fda.gov/ National Center for Complementary and Integrative Health (NCCIH). Can Supplements Help with Memory and Thinking? https://www.nccih.nih.gov/ Harvard Medical School. Brain Supplements: What Works and What Doesn’t? https://www.health.harvard.edu/ American Academy of Neurology (AAN). The Truth About Over-the-Counter Memory Supplements. https://www.aan.com/ 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.

Supporting loved ones with Behavioral Variant Frontotemporal Dementia (bVFTD). Caring for a loved one with behavioral variant Frontotemporal Dementia (bvFTD) can be a challenging and demanding experience. The behavioral changes that are often associated with bvFTD can make it difficult to provide care, and the emotional toll of caregiving can be significant. However, there are a number of things that caregivers can do to cope with the challenges of caregiving and to provide their loved ones with the best possible care. In this blog post, we will discuss some of the unique challenges of caregiving for someone with bvFTD, as well as some strategies that can help caregivers to manage these challenges. We will also discuss the importance of self-care for caregivers, and we will provide some resources that can help caregivers to find support and information. Understanding bvFTD Behavioral variant Frontotemporal Dementia (bvFTD) is a type of Dementia that affects the frontal and temporal lobes of the brain. These are the areas of the brain that control personality, behavior, language, and executive function. Symptoms The symptoms of bvFTD can vary from person to person, but they often include: Changes in Personality and Behavior: People with bvFTD may become more impulsive, aggressive, or apathetic. They may also lose their inhibitions and engage in socially inappropriate behavior. Language Problems: People with bvFTD may have difficulty understanding or using language. They may also have difficulty finding the right words to express themselves. Executive Dysfunction: People with bvFTD may have difficulty planning, organizing, and carrying out tasks. They may also have difficulty making decisions. Cognitive Changes The cognitive changes associated with bvFTD are often less pronounced than the behavioral changes. However, people with bvFTD may experience some difficulty with memory, attention, and problem-solving. Behavioral Changes The behavioral changes associated with bvFTD can be disruptive and challenging to manage. Caregivers may need to deal with aggression, apathy, and other difficult behaviors. Some of the most common behavioral changes associated with bvFTD include: Loss of Inhibitions: People with bvFTD may lose their inhibitions and engage in socially inappropriate behavior, such as making inappropriate comments or gestures, or behaving in a sexually suggestive way. Apathy: People with bvFTD may become apathetic, losing interest in activities that they used to enjoy. They may also become withdrawn and socially isolated. Impulsivity: People with bvFTD may become more impulsive, making decisions without thinking through the consequences. They may also engage in risky or dangerous behaviors, such as gambling or driving recklessly. Repetition: People with bvFTD may repeat themselves, saying the same thing over and over again. They may also become fixated on certain topics or activities. Language problems The language problems associated with bvFTD can make it difficult to communicate with people with the condition. Some of the most common language problems associated with bvFTD include: Word-Finding Difficulty: People with bvFTD may have difficulty finding the right words to express themselves. They may also use the wrong words or coin new ones. Reduced Fluency: People with bvFTD may speak less fluently, pausing frequently or leaving sentences unfinished. Changes in Tone and Prosody: People with bvFTD may change the tone or rhythm of their voices, making it difficult to understand what they say. Executive Dysfunction The executive dysfunction associated with bvFTD can make it difficult to plan, organize, and carry out tasks. People with bvFTD may also have difficulty making decisions. Some of the most common executive dysfunction problems associated with bvFTD include: Planning: People with bvFTD may have difficulty planning ahead or deciding how to accomplish tasks. Organizing: People with bvFTD may have difficulty organizing their thoughts or belongings. Executing Tasks: People with bvFTD may have difficulty carrying out tasks, even if they are able to plan and organize them. Decision-Making: People with bvFTD may have difficulty making decisions, even simple ones. The Unique Challenges of Caregiving The challenges of caring for someone with bvFTD can be significant. These challenges include: Behavioral Changes: The behavioral changes associated with bvFTD can be disruptive and challenging to manage. Caregivers may need to deal with aggression, apathy, and other difficult behaviors. Communication Difficulties: Language problems associated with bvFTD can make communication challenging. Caregivers may need to find creative ways to communicate with their loved one. Caregiver Stress and Burnout: Caring for someone with bvFTD can be emotionally and physically demanding. Caregivers are at risk for stress, burnout, and depression. Strategies For Effective Caregiving in Frontotemporal Dementia There are a number of strategies that can help caregivers to cope with the challenges of caring for someone with bvFTD. These strategies include: Building a Support Network: Caregivers should reach out to friends, family, and support groups for assistance. Having a strong support network can help to reduce stress and burnout. Creating a Structured Environment: Caregivers can establish routines and minimize potential triggers. This can help to reduce anxiety and agitation. Enhancing Communication: Caregivers can improve communication by using clear, simple language, avoiding jargon, and repeating information as needed. They can also use visual aids and gestures to help their loved one understand. Seeking Professional Help: Caregivers should consult healthcare professionals, therapists, and Dementia care specialists. These professionals can provide guidance and support and help develop a personalized care plan. Resources And Support There are a number of resources available to support caregivers of people with bvFTD. These resources include: National And Local Organizations: There are numerous national and local organizations that provide information, support, and resources for caregivers. These organizations can provide information about bvFTD, connect caregivers with other caregivers, and offer educational programs and support groups. Online Communities and Forums: There are a number of online communities and forums where caregivers can connect with other caregivers, share experiences, and find support. These online platforms can provide a sense of community and can help caregivers to feel less alone. Caregiver Education: There are a number of workshops, webinars, and educational materials available to help caregivers learn more about Dementia and caregiving. These educational resources can help caregivers to develop the skills and knowledge they need to provide effective care. Conclusion Caring for someone with bvFTD can be a challenging but rewarding experience. By building a support network, creating a structured environment, enhancing communication, and seeking professional help, caregivers can cope with the challenges of caregiving and provide their loved ones with the best possible care. For more information on bvFTD and treatment, visit Dementia Society of America today! 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.

Memorizing names can be a serious challenge for some people. The world is rife with all kinds of tricks for putting faces with names and the like. Most of them have various degrees of success. In a certain light, saying someone’s name three times during your first meeting can essentially be a type of brain game. Most brain games are simple exercises to help your brain work better. Saying someone’s name three times is as much about memorization as it is about developing conversational skills and working on associations. I must admit that I’m not the best when it comes to remembering names. I’ve tried a lot of different tips and tricks over the years and very few of them ever really helped. Saying someone’s name three times is a simple brain game you can do when you meet people (and they will never know it). The goal is to be subtle about it. You don’t want to shake someone’s hand and simply rattle off their name three times. Repeat Names to Enhance Your Memory of a New Person What you want to do when you first meet somebody: at the first handshake, you want to repeat their name. For example, if I was meeting someone named Jason for the first time, I would say, “Hello Jason, how are you doing?” As the introduction and conversation flow naturally, I follow up with opportunities. “So tell me, Jason, where do you live?” So, at this point, I’ve already said his name twice. My brain is getting used to that, and it’s associating that person’s face, his demeanor, and everything in that environment at that particular time. Within the next minute or so, create another opportunity to use their name again. Something along the lines of “So Jason, how many kids do you have?” Not only are you repeating their name to help it stick in your memory, but you’re also creating associations relevant to them (e.g., where they live and how many kids they have). Of course, there are many different topics you could touch on. Family, hobbies, where they live, or what they do for a living are all common topics that help you learn more about them and create memorable associations that will stick in your mind the next time you meet them. With regular practice, I think you’ll find that you can get to know a lot about people in a relatively short period of time. This is especially helpful if you’re involved in any kind of networking or social group, where you’re trying to learn as much as you can about someone in a short period of time. The key is to drop their name into the conversation. As you say the name, really try to emphasize your focus on their face or their demeanor. This could also include finding a similarity to someone you know who has the same name. Contributor Author: Dr. Michael Trayford is a Board Certified Chiropractic Neurologist and Founder of APEX Brain Centers in Asheville, NC. For more information, please visit our Author's page. 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.

When it comes to sleep, establishing a routine is critical. Sleep-wake cycles are for the brain what your transmission is for your car. Further, sleep issues are often associated with Dementia and may very well be a catalyst for Dementia onset and severity. In this day and age, a lot of people are simply going to bed whenever they crash, or whenever their kids or life demands allow. When they wake up, it’s rarely of their own accord. Instead, they tend to wake up to loud alarm clocks blaring, someone else waking them, or something like the dog jumping on the bed. Sleep routines are critically important for brain function, and it can be as simple as setting a time to go to bed and a time to wake up, then sticking with it to make it a part of your regular routine. Establishing a routine helps your body achieve homeostasis in hormone production, regulate blood pressure, and support the glymphatic system, which removes toxins from the brain while you sleep. This is often easier said than done. Family life, career demands, pets, and many other distractions can make it challenging to establish a consistent sleep routine. Getting Your Sleep There’s no magic number for the number of hours you need to get each night, although 7-9 hours is a good rule of thumb. The brain needs a good, solid two to three deep sleep cycles per night, and you can’t do that if you’re only getting three or four hours of sleep per night. The key is to listen to your body. Ideally, you want to establish a sleep routine where you fall asleep easily at a set time and wake up in the morning feeling energized, alert, and ready to face the day. Some people might only need six hours of sleep, while others might need eight or even ten hours! Some people meditate quite regularly, and the deep-state training involved in the process means they may only require five or so hours of sleep each night. Sleep science is constantly evolving as research reveals more about the benefits of sleep and how to incorporate a healthy sleep routine into your daily life. What it boils down to is the routine that is best for you, your body, and what makes you feel the most rested. Contributor Author: Dr. Michael Trayford is a Board Certified Chiropractic Neurologist and Founder of APEX Brain Centers in Asheville, NC. For more information, please visit our Author's page. 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.

Some people find the loved one in their care almost seems like a stranger - perhaps morphing from a kind and helpful person to a combative and vulgar one. Other times, Dementia seems to magnify personality traits. When this happens, people often say, it’s my father only “more so.” Though difficult, do try to remember that it is the disease, not the person, who is responsible for these worrisome and sometimes embarrassing changes in his or her temperament. The diseases causing Dementia alter and destroy brain structures. The consequences of the damage include loss of the ability to accurately process and relay information. Another outcome is the inability to control emotions such as anger and censor impolite and socially inappropriate behaviors. Because of the progressive nature of Dementia, behavioral changes tend to worsen with time. Understanding why behaviors occur can help one deal with them. Emotional blunting, or the inability to express verbal and non-verbal feelings, is another characteristic of having Dementia. The inability to express needs and feelings can make people who have Dementia angry, combative, and sometimes violent. Many people who have Dementia experience depression. Dementia can also affect sexual behaviors in ways that are often unpredictable. Some people who have Dementia cannot understand that it is impolite to touch or expose their private areas in public or make unwanted or inappropriate sexual advances. There are many simple ways to reduce the incidents and intensity of these difficult-to-manage behaviors. However, first, consider other reasons for your loved one’s difficult behaviors. Drug interactions and side effects may intensify Dementia symptoms, cause hallucinations, and intensify agitation and combativeness. Other explanations for uncharacteristic behaviors and emotions can include pain, fatigue, overstimulation, as well as other medical problems such as a bladder infection. Understanding and Managing Difficult Behaviors There are many strategies you can use to prevent or diffuse your loved one’s outbursts. Perhaps the most important one is communication. Do not argue with your loved ones, remind them of what they have forgotten, or ask probing questions to assess their memory. Use supportive language to affirm that you are listening, respecting his or her concerns, and responding appropriately. For example, it is better to respond to fear, but the unlikely true incident is to say, “I’ll look into it” rather than “Don’t be silly.” Sometimes all it takes is a calming hug or a kind and supportive touch. Distraction and redirection are useful ways to diffuse anger or sexually aggressive behaviors. Give your loved one a snack, go for a walk, point out a pretty flower, or talk about the weather. Sometimes your loved one’s behavior is more than you can handle. When this happens, call the Crisis Intervention Team, rather than 911, maybe the best option. The Crisis Intervention Team (CIT) refers to the police officers in your community who have special training in how to manage a variety of behavioral, drug-related, and mental health crises. Having the CIT present to address unmanageable or threatening behavior can prevent a difficult situation from escalating into something worse. The CIT can also accompany you and your loved one to the medical facility. Be sure to include your local CIT's phone number in your list of emergency phone numbers. Content Contributor: Janet Yagoda Shagam, Ph.D., is a freelance medical and science writer and the author of "An Unintended Journey: A Caregiver's Guide to Dementia", available through Amazon. Please visit our Author's page to learn more and find this title. 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.

Put simply, neuroplasticity is the brain’s ability to change and grow throughout time, dependent on its environment. The brain is a sensory-driven organism. This means it thrives, survives, and functions based on the input it receives. The brain essentially is a relay station; the information coming in influences the information going out. So we want to make sure our brain is wired in the best way possible. There is a brilliant quote from neuroscientist Santiago Ramón y Cajal: “Any man can, if he so desires, become the sculptor of his own brain.” Cajal said that at the turn of the last century, when most everything we knew about the brain came from head-to-toe physical examination. In fact, Cajal was one of the first people to really study brain cells under a microscope. The conventional wisdom at that time was that your brain was hardwired and what you had at birth was how your brain would be the rest of your life. In recent years, we have learned that the brain is capable of change. Neuroplasticity is the key concept for everything we talk about regarding brain training. How Can I Increase My Brain's Neuroplasticity? The picnic game exercise is just one of many examples. The game is played with two or more people. It starts out with the first person saying something like “I’m going on a picnic, and I’m bringing an apple,” or something that starts with the letter A. The second person says they’re going on a picnic and will bring an apple and something else that starts with the letter B. The game continues on with each person reciting the items in the list and then adding an item that starts with the next letter of the alphabet. When you expand it out through the alphabet, and you get to the letter Z, it can actually be rather complicated. There are two points to this game – improving working memory and short-term memory, which are closely connected. Short-term memory is where you hold onto a piece of information for a brief period. If that information is worth committing to long-term memory, it will be based on repetition or importance. Repetition is somewhat obvious, where you do something over and over again until it becomes learned (e.g., playing the guitar). Importance is related to something happening that has a significant impact. For example, if someone was hit by a car in a hit-and-run accident and they got the license plate number as the car drove off. The picnic game primarily exercises working memory and, secondarily, short-term memory. Working memory helps you hold onto small amounts of information while you are attending to something else, and is often the first aspect of memory impairment in certain types of Dementia. Contributor Author: Dr. Michael Trayford is a Board Certified Chiropractic Neurologist and Founder of APEX Brain Centers in Asheville, NC. For more information, please visit our Author's page. 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 phrase “Get moving!” can mean something different for each of us. For some people, it means getting up, walking on the treadmill, going for a bike ride, or walking the dog. Unfortunately, for other people it means getting up, going to the bathroom, and going back to the couch. So there is certainly a need to put this concept in perspective. When it comes to proper brain function, movement is absolutely critical. Think about somebody you know that isn’t very mobile. They might be sedentary because they are bedridden, have mobility issues, or it might just be that they are plain lazy. Do their brains work as well as someone who is active, getting out and about all the time? The bottom line is that movement is essential for appropriate brain function. Chances are that you’ve heard the term “If you don’t use it, you lose it.” The brain essentially is a relay station for sensory information. When we don’t have appropriate sensory information going into the brain from our muscles, joints, balance system, and more, it starts to wear away and degenerate more rapidly than it should. Over time, it can cause the brain not to perform at its highest potential, as you can imagine. The brain is stimulated by nerve fibers from several different sources. This includes senses like vision and hearing, as well as other sources. The nerve fibers that carry information from muscles and joints are by far the largest nerve fibers that supply the brain with the greatest amount of information. If you are inactive, you are cutting out your greatest amount of input to the brain. This will, in turn, reduce the efficiency of the brain's output. This can manifest itself as physical problems, mental and emotional problems, cognitive and thinking problems, and memory decline. Get Yourself Moving! To stimulate the brain, you don’t need particularly intense activity. You can start out small. It might be going to the gym, taking a walk in the woods, or on your streets. Just so long as you’re getting out there and getting moving. Developing the habit of regular activity starts you building a foundation to explore other exercises and more intense activities that can have an even more significant positive impact on brain health. Contributor Author: Dr. Michael Trayford is a Board Certified Chiropractic Neurologist and Founder of APEX Brain Centers in Asheville, NC. For additional information, and to learn more, please visit our Author's page. 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.

2026 Candid Platinum Transparency recognition. Computer-Generated Image (CGI). National recognition of the Dementia Society of America reinforces our commitment to accountability, measurable impact, and the responsible stewardship of every donor dollar. The Dementia Society of America® (DSA) is proud to announce that we have once again earned the Platinum Seal of Transparency for 2026 from Candid (formerly GuideStar)—the highest level of recognition awarded to nonprofit organizations for transparency, accountability, and measurable impact. (Candid) For our supporters, this distinction represents much more than a badge displayed on our website. It is an independent affirmation that DSA is committed to operating openly and responsibly, with a clear focus on results. It reflects our belief that every donor deserves to know how their charitable investment is being used and what difference it is making in the lives of individuals and families affected by Dementia. Today's donors are more informed than ever before. Before making a charitable gift, many people research organizations to better understand their mission, leadership, finances, and effectiveness. They want confidence that their donation will be used wisely and that the organization they support is achieving meaningful outcomes. That is exactly what the Platinum Seal represents. Publicly Sharing Comprehensive Information To earn this recognition, organizations must publicly share comprehensive information about their mission, programs, financial information, leadership, strategic goals, and measurable impact. Unlike lower levels of recognition, the Platinum Seal requires nonprofits to report meaningful performance metrics that demonstrate progress toward their mission. (Candid) For the Dementia Society of America, transparency has never been simply about meeting a requirement. It has always been part of who we are. Since our founding, DSA has worked to become one of the nation's leading nonprofit organizations dedicated to supporting everyone affected by the many disorders that can cause Dementia. We believe families deserve reliable information, compassionate guidance, practical educational resources, opportunities for meaningful engagement in life, and hope at every stage of the journey. Every contribution entrusted to DSA helps make that mission possible. Reaching Families Across the Country Donor support enables us to provide educational resources that reach families across the country, develop innovative caregiver education programs, expand awareness about brain health and Dementia, seed-fund promising research, and recognize life-enriching engagement programs that improve quality of life for those living with cognitive impairment and those who care for them. The Platinum Seal assures donors that these efforts are supported by an organization willing to openly share its goals, strategies, and measurable accomplishments. Transparency also creates accountability When organizations publicly report their objectives and outcomes, they invite supporters to evaluate their progress. Rather than asking donors to simply trust our intentions, DSA believes it is better to demonstrate our performance through measurable results and continual improvement. That approach strengthens confidence while encouraging us to remain focused on delivering the greatest possible benefit for the communities we serve. Independent Recognition Matters The Candid Platinum Seal is not a self-awarded honor. It is earned by providing detailed organizational information through Candid's nationally recognized nonprofit profile system, which millions of donors, foundations, corporations, and grantmakers use to evaluate charitable organizations. Candid profiles are also distributed across more than 200 charitable giving platforms, increasing visibility and helping donors make informed decisions. (Candid) For many prospective donors, this independent validation provides valuable peace of mind. It confirms that DSA willingly shares information about their leadership, finances, governance, organizational strategy, and measurable impact, rather than keeping it hidden. Transparency Reduces Uncertainty Transparency helps donors feel confident that their generosity is supporting a well-managed organization committed to responsible stewardship. Research published by Candid further underscores why transparency matters. According to Candid, nonprofits that earn a Seal of Transparency receive, on average, 62% more donor contributions than organizations without a Seal. While every donor makes giving decisions differently, the findings suggest that openness and accountability inspire greater confidence among charitable supporters. (Candid) Increased confidence ultimately benefits those we serve Greater donor trust leads to stronger financial support. Stronger support allows us to expand educational outreach, invest in innovative programs, strengthen caregiver resources, increase awareness campaigns, and continue supporting promising Dementia research initiatives that may improve lives today while contributing to better outcomes tomorrow. Our commitment to transparency extends beyond financial reporting. We recognize that families facing Dementia want honesty, compassion, and practical guidance. Likewise, our donors deserve clear communication about how their generosity is making a difference. Whether someone contributes $5 or $50,000, every donor becomes a partner in our mission, and every partner deserves openness and respect. As we look toward the future, DSA remains committed to continually improving our programs, expanding our national reach, measuring our impact more effectively, and sharing those results openly with our supporters. The 2026 Platinum Seal of Transparency represents an important milestone, but it is not our destination. It is another step in our ongoing promise to earn, and keep, the trust placed in us by thousands of generous individuals, families, foundations, and organizations across America. We are grateful for everyone who makes our work possible When you choose to support the Dementia Society of America, you are partnering with an organization that has demonstrated its commitment to transparency, accountability, and measurable impact. Your gift helps educate families, empower caregivers, fund innovative research, increase public awareness, and improve the lives of those affected by all forms of Dementia. Together, we are building a future where every family facing Dementia has access to knowledge, hope, compassionate support, and opportunities to live life with dignity and purpose. That is the true value of transparency—and the lasting impact of your generosity. www.dementiasociety.org/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.

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.

Medical professional reading brain scans. At Dementia Society of America, families often ask us: Are scientists getting closer to better treatments? Is there anything new on the horizon? The answer is yes — and in many different ways. Researchers around the world are working to develop medications that do more than manage symptoms. The goal is to slow, stop, or even prevent the brain changes that cause Dementia. Because Dementia is not just one disease, scientists are pursuing different strategies for Alzheimer’s disease, vascular Dementia, Lewy body Dementia, and frontotemporal Dementia (FTD). Here’s a look at where research stands today. Alzheimer’s Disease: Moving Beyond One Target For many years, Alzheimer’s research focused on a protein called amyloid, which builds up in sticky plaques in the brain. Recently approved treatments that remove amyloid have shown that slowing decline is possible — at least in early stages of the disease. But scientists now believe Alzheimer’s is more complex than amyloid alone. Current research includes: Improved amyloid treatments are designed to work earlier or more safely. Tau-targeting therapies, aimed at another protein that forms tangles inside brain cells and spreads through brain networks. Anti-inflammatory treatments, because immune cells in the brain may contribute to damage when they become overactive. Synapse-protecting drugs are designed to protect the connections between brain cells. Earlier detection tools, including blood tests that may identify Alzheimer’s-related changes years before major symptoms appear. The big shift? Researchers increasingly believe future treatment may require combination approaches, similar to how we treat heart disease or cancer. Vascular Dementia: Protecting the Brain’s Blood Supply Vascular Dementia is caused by problems with blood flow in the brain, often due to strokes or damage to very small blood vessels (called small vessel disease). Instead of targeting one specific protein, research here focuses on protecting the brain’s “plumbing.” Current directions include: Strengthening small blood vessels and improving blood flow. Protecting the blood–brain barrier, which acts like a filter to keep harmful substances out of the brain. Reducing inflammation that damages vessels. Repurposing heart and stroke medications to see if they can also protect cognition. Improving clinical trial design, since vascular brain damage looks different from person to person. Researchers also emphasize prevention: managing blood pressure, cholesterol, and diabetes, as well as stroke risk, remains critical. Lewy Body Dementia: Targeting Alpha-Synuclein Lewy body Dementia (which includes Dementia with Lewy bodies and Parkinson’s disease Dementia) is strongly linked to a protein called alpha-synuclein. This protein forms clumps inside brain cells, disrupting how they function. Research efforts focus on: Preventing alpha-synuclein clumping. Immunotherapy approaches, such as antibodies that help the body clear abnormal proteins. Reducing inflammation in the brain. Addressing mixed disease, since many people with Lewy body Dementia also have Alzheimer’s-related changes. Scientists are also working to improve symptom treatments — especially for hallucinations, sleep disorders, and movement problems — while minimizing medication side effects. Frontotemporal Dementia (FTD): Precision and Gene-Based Therapies FTD often affects people at a younger age and can sometimes be linked to specific genetic changes. That makes it a promising area for precision medicine — treatments tailored to a person’s genetic makeup. Key research areas include: Gene therapies to boost levels of important brain proteins, such as progranulin, in certain genetic forms of FTD. Antisense oligonucleotides (ASOs) — small pieces of genetic material designed to change how harmful proteins are made. Targeting tau or TDP-43 proteins, which accumulate in different types of FTD. Because some FTD cases are linked to known gene mutations, researchers can test therapies in highly specific patient groups, increasing the likelihood of meaningful results. A Common Theme: Earlier Is Better Across all types of Dementia, one idea is becoming clearer: the earlier we treat, the better the chances of success. New blood tests and imaging tools are helping researchers identify people at earlier stages of disease. That allows clinical trials to test medications before extensive brain damage occurs. Many scientists believe the future of Dementia treatment will involve: Earlier diagnosis More personalized treatment Combination therapies Continued focus on brain health and prevention While there is still much work to do, progress is real — and accelerating. If you would like to know how you can get involved in Dementia research, we'll have a future post on this topic. Sources National Institute on Aging (NIA). NIH Alzheimer’s Disease and Related Dementias Research Progress Report. Alzheimer’s & Dementia: Translational Research & Clinical Interventions. Alzheimer’s disease drug development pipeline. Nature. Reporting on advances in Alzheimer’s drug development. Aging and Disease. Review on cerebral small vessel disease therapies. Neurology International (MDPI). Clinical trial design in vascular cognitive impairment. The Lancet Neurology. Review on Dementia with Lewy bodies therapeutic landscape. BJPsych Open (Cambridge Core). Disease-modifying therapies for synucleinopathies. ClinicalTrials.gov. Ongoing frontotemporal Dementia gene therapy trials. MDPI. Updates on disease-modifying treatments for frontotemporal Dementia. Dementia Society of America is committed to sharing trustworthy, research-based information to support individuals and families living with Dementia. 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 words we use reflect our values and help shape how people around us are treated. Person-centered approaches focus on respect, dignity, and partnership. At the Dementia Society of America, we value this approach to describing the experience of Dementia. Here are some examples of this language, and why this shift is so important in the context of Dementia. 1. Care Partner (vs. Caregiver) Meaning: A “care partner” is someone who works with a person, not just for them. Why it matters: This term shows that care is a relationship. It recognizes that both people give and receive support, even in situations like Dementia care. 2. Person Living With (vs. Patient, Victim, or Sufferer) Examples: “Person living with Dementia” “Person living with diabetes” Why it matters: This is called person-first language. It puts the individual before the condition. It reduces stigma and reminds others that a diagnosis does not define the whole person. 3. Elder (vs. Resident or Patient) Meaning: Refers to older adults with respect for their life experience and wisdom. Why it matters: Words like “resident” can feel clinical or impersonal. “Elder” honors identity, history, and value. 4. Person-Directed Care (vs. Patient Care) Meaning: The individual’s preferences, choices, and goals guide medical care. Why it matters: This term shifts power back to the person receiving care. It encourages independence and respects autonomy. 5. Support (vs. Assistance or Help) Meaning: Working alongside someone to enable them to do as much as they can. Why it matters: “Support” feels empowering, while “help” can sometimes feel limiting or one-sided. 6. Strengths-Based Language (vs. Deficit-Based Language) Examples: “Has strong communication skills” instead of “struggles less with speaking.” Why it matters: Focuses on what a person can do, not what they cannot. This approach builds confidence and encourages growth. 7. Behavior as Communication (vs. Problem Behavior) Meaning: Actions are seen as a way of expressing needs or feelings. Why it matters: Especially in Dementia care, this reduces blame and encourages understanding. It leads to more compassionate responses. 8. Engagement (vs. Activities or Tasks) Meaning: Meaningful involvement based on a person’s interests and preferences. Why it matters: Emphasizes purpose and enjoyment, not just filling time. 9. Community (vs. Facility or Institution) Meaning: A place where people belong and connect. Why it matters: Promotes inclusion, relationships, and a sense of home. Why Language Is So Important in Dementia Care 1. Shapes Attitudes The words we use influence how we think. For example, calling someone a “patient” may lead to a more clinical mindset, while “person” or “Elder” encourages respect and empathy. 2. Affects Relationships Language can create either distance or connection. Terms like “care partner” promote teamwork and mutual respect. 3. Supports Dignity and Identity Person-centered language helps protect a person’s sense of self. This approach is especially important in Dementia care, where identity can feel at risk. 4. Reduces Stigma Words like “sufferer” or “victim” can carry negative meanings. Person-first language helps reduce stereotypes and bias. 5. Encourages Better Outcomes When people feel respected and heard, they are more likely to engage in care or learning. This approach can lead to improved well-being and quality of life. Final Thought Person-centered language is more than just choosing “nicer” words. It reflects a deeper shift in values—from doing things to people, to working with them. Across education, healthcare, and elder care, these words help create environments where people feel seen, heard, and valued. 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 Horizons™ | Workshop 11 | Home Safety Video Module [11] Transcript Home. What does that mean to you? Are you surrounded by pictures and mementos that have a story or bring you joy? Does home mean safety, peace, and familiarity? When you come home, do you love a particular scent or smell? Our job today is to learn how to adapt a home for someone whose brain and senses are changing over time, due to progressive cognitive impairments that we call Dementia. That way, you can better understand why modifications to create a safer home environment are necessary in the first place. It is also essential to know how the underlying diseases or disorders that can cause Dementia may impact the senses. Let's start with vision or eyesight. Peripheral vision narrows, meaning that the person sees primarily what is directly in front of them, like looking through a tunnel, with less ability to see what is happening on the sides. Because of this, people living with Dementia may then bump into objects if pathways are narrow or cluttered. Also, identifying shapes and objects can be difficult if the lighting is dim. For example, the vacuum can look like a small child in the distance. Shadows can be misinterpreted, especially at night, looking like strangers entering the room. The shape, purpose, or function of an object can be misconstrued, so a TV remote control and a cell phone can look the same. Because of changes in the brain, which keeps track of what does what and how, managing devices can become overwhelming. Depth perception changes over time. It may be more difficult to safely walk up or down stairs, or know how to step into or out of a bathtub. As you can anticipate, there is a higher risk of slips, falls, and injuries. The brain also controls our ability to move our legs and maintain balance while walking. As Dementia progresses, steps shorten, people may shuffle their feet; and reflexes slow, creating another reason why the risk of trips and falls is a common concern. The sense of smell may diminish, making it problematic to identify smoke, foul odors, or spoiled food. It is also common for hearing to become impaired with age. Therefore, older people living with Dementia can have more difficulty deciphering sounds and voices. This is especially true when there is too much background noise or people are talking simultaneously. Although this may not happen to everyone with Dementia, hallucinations can occur. Hallucinations are perceptions of having touched, heard, seen, tasted, or smelled something that does not exist. Given this wide range of potential changes, I hope you can see why creating a home environment that supports safety and thriving is wise and loving. Hearing all of this may be overwhelming to absorb. Take four deep breaths. Creating Greater Safety at Home By anticipating challenges and making proactive adjustments inside and outside the home, care partners and caregivers can significantly enhance the quality of life for those living with Dementia and provide reassurance for themselves. You can do hard things, and I am here to help you get started. Let's start by imagining yourself walking into the kitchen. Objects might look different to a person living with Dementia. Now, scan the room. Take inventory of what is inside the cabinets and drawers, and consider the following recommendations. Remove knives and other sharp utensils. Purchase kitchen appliances, such as coffee makers, with automatic shut-off. Disconnect the garbage disposal, or make it very difficult to turn on. If possible, remove the knobs from the stove. Lock up cleaning supplies. People may misinterpret cleaning solutions for juice. Be especially sure to secure dishwasher soap pods. They are poisonous and commonly mistaken for candy. Remove anything mistaken for food, such as fake fruit in a bowl. Clear the refrigerator of expired food regularly. Some cabinets may require safety locks to keep items hidden and secure. Keep the fire extinguisher or fire blanket within easy reach. Label cabinets so that things are easier to find. This will also help support a sense of independence. Use chairs that are sturdy, with armrests that make it easier to get in and out of. As you walk through the hallways, clear the pathways. Remove throw rugs that can be tripping hazards, and add additional lighting where necessary. Consider using non-skid wax on floors. If not, be sure the person wears non-skid shoes or slippers when walking on wooden or tile surfaces. Some people with Dementia find it easier to locate rooms in the house if way-finding signs are in place. These signs usually have the room's name in large print and a picture. Use brightly colored tape or paint to mark the edges of steps, or changes in the flooring. Install or secure handrails on stairs. If steps become too challenging, the person may need to remain on one main floor. If clear glass doors or partitions are present in your home, use decals to prevent people from bumping into them. Now, let's imagine going into the bedroom or bedrooms. I would encourage you to decorate the bed with a color that contrasts with the rug or floor so that it can be easily identified. For example, a blue bedspread and a cream colored carpet. Install motion detector nightlights for times when someone wakes up and needs to find the restroom. Again, be sure to remove throw rugs. Listen for low battery chirps from smoke alarms, and don't wait to change them. Supervise the use of heating pads or electric blankets. Remove clutter, and label drawers and cabinets. Moving into the bathroom. This is an area that requires particular attention: Remove or secure prescription or over-the-counter medications from cabinets, and place mouthwash and colognes where they can be supervised during use. Replace door locks with non-locking levers. Install grab bars in shower and bathtubs. Use a non-slip bath mat. Install non-slip toilet seats that contrast with the color of the floor, making them easier to see. Set water temperature to avoid scalding. Use overflow valves or flood sensors to avoid or detect flooding. Find yourself now in the living room: Remove throw rugs, and use non-slip surfaces if possible. Do your best to declutter. It's easier to pay attention when there is less overstimulation. Remove long cords to avoid tripping. Perhaps in the living room or somewhere else, create a calm and inviting space for the person living with Dementia to relax and have access to meaningful activities such as books, magazines, simple puzzles, paper and pencils for drawing, and music for listening. If guns or a knife collection exists, secure and disable them. Safety, autonomy, and comfort also apply to the backyard and garage: Secure the keys to the snowblower or lawnmower and car. Place power tools out of reach. Disconnect the gas or electric source for the grill. Adjust uneven pathways. Create a space for gardening, walking, sitting and spending time in the fresh air and sunshine. Consider adding a bird feeder or gentle wind chime. Now, you may be wondering, how do I make these changes when the person with Dementia may resist? Start gradually, one slight modification at a time. Have a friend or family member take the person out for a meal or for the day, while the remodeling happens. Do not say anything in advance. Wait to see if the person recognizes the changes. Be matter of fact. Avoid saying you needed this "because...". Instead, say "We needed to make a slight improvement." Creating a safe home environment for individuals living with Dementia requires a combination of understanding, empathy, creativity, and practical adjustments. It's a journey, but ultimately, it can significantly improve the quality of life for both the individuals living with Dementia and their loved ones. Consider these adaptations as a way of loving your spouse, parent, or sibling differently. There we have it: home sweet home. Thank you for joining me today. There was a lot to take in, but use our support material to review and help you implement changes over time. Thank you again. Be well. 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.