A recent study of nearly 1,800 participants from the UK Biobank found that three dietary elements — cheese, wine, and lamb — may improve long-term cognitive outcomes in aging adults. Dr. Auriel Willette, assistant professor of food science and human nutrition at Iowa State University, joins the podcast to discuss these new findings linking diet and cognitive changes. In November 2020, Willette published a study in the Journal of Alzheimer’s Disease titled “Genetic Factors of Alzheimer’s Disease Modulate How Diet is Associated with Long-Term Cognitive Trajectories: A UK Biobank Study,” where he and his team studied the effects of particular foods on a person’s brain health over time. As well as the findings surrounding cheese, wine, and lamb, they found that limiting salt intake was good for the brain, especially for those at risk for Alzheimer’s disease. Discussing the field of nutritional research, his prior work studying diet and brain health, and how these findings impact other recommended diets, Willette provides insight into how our current diets can impact our health and cognitive abilities later in life, allowing us to make better choices for the future. Guest: Auriel Willette, PhD, associate professor of food science and human nutrition, Iowa State University. Episode topics 1:34 - What sparked your interest in studying the effects of nutrition on the brain and on cognition? 4:41 - What prompted you to broaden your study to focus on overall diet and whole foods? 8:29 - Can you tell us about your prior research? 12:46 - Can you tell us a bit about the study and what you discovered? 19:48 - What do you think the mechanism is that allows cheese and alcohol to be beneficial for people’s brain health? 24:28 - How do you reconcile these findings, especially those surrounding cheese, with diets like the MIND diet? 28:38 - What dietary changes have you made in your own life that you might recommend for protecting your brain health? Show Notes Find out more about Dr. Willette by reading his bio from Iowa State University. Learn more about Dr. Willette’s study at this article by Iowa State University. Read the full study, “Genetic Factors of Alzheimer’s Disease Modulate How Diet is Associated with Long-Term Cognitive Trajectories: A UK Biobank Study.” Find us Online - Dementia Matters Website | ADRC Facebook | ADRC Twitter

Dementia Matters

You Are What You Eat: Study of Diet and Brain Health Shows Cognitive Benefits from Cheese, Wine and Lamb

With the numerous efforts currently focused on educating the public about dementia, from clinical programs to research to podcasts (like this one), how much is stigma surrounding cognitive decline affecting public understanding? On today’s podcast, Sarah Lock, Senior Vice President for Policy for AARP, discusses just that. This year, the AARP published a report on a survey focused on how the general American population and particular subgroups perceive dementia and dementia diagnoses. The survey found that the general public and health care professionals have many misperceptions about dementia, including overestimations about their likelihood to develop dementia and the shame they might feel about a diagnosis. Describing the contrasting perceptions between clinicians and the public and the impacts of stigma on dementia policy, Lock details the ways this survey will allow the AARP to build on their existing programs about brain health to better educate the public about dementia and the ways it affects a person’s life. Guest: Sarah Lenz Lock, Senior Vice President for Policy, AARP, Executive Director of the Global Council on Brain Health Episode Topics: 1:48 - Can you share what went into making the survey and who completed them? 5:05 - What did the survey find? How do people think about their own risk? 7:14 - Can you speak about those key findings surrounding stigma and dementia? 9:43 - What do you make of the stigma's connection to the fear of not being able to drive anymore? 12:48 - What key findings did you find about the clinicians who completed the survey? 15:32 - One finding from the survey showed that healthcare providers overestimated the shame and embarrassment that a person would experience with a diagnosis. What were other perceptions that clinicians overestimated in the survey? 17:20 - From a policy perspective, does the United States need to change its recommendations surrounding dementia screenings? 20:01 - Could you share the true benefits of early diagnoses, based on the survey and what you see within the AARP? 21:21 - Did the survey find any differences in the perceptions among different racial groups? 23:28 - How do you define brain health? What is the AARP doing to spread information about brain health? Show Notes: Learn more about Sarah Lock and her work at her bio on the AARP website. For a summary of the key findings of the AARP’s report, read this article by the AARP. To access the full report and its findings, find it here on the AARP website.

AARP Study Shows Stigma Surrounding Dementia among Healthcare Professionals and General Public

When talking about dementia caregiving, researchers are often working toward new treatments and strategies for supporting people with Alzheimer’s disease and dementia. But how can we push the topic further and learn how we can better support dementia caregivers themselves? Dr. Eric Larson joins the podcast to discuss possible interventions to support patients with dementia and their caregivers and care partners. Dr. Larson chaired a National Academy of Medicine committee focused on researching dementia caregiving interventions. As part of their report titled “Meeting the Challenge of Caring for Persons Living with Dementia and Their Care Partners and Caregivers: A Way Forward,” the committee found that two models, the Collaborative Care Model and REACH (Resources for Enhancing Alzheimer’s Caregiving Health), had the most evidence of benefits for supporting people with dementia and their care partners and caregivers. Discussing this new report, the recent approval of aducanumab, and the field of geriatrics as a whole, Dr. Larson shines a light on the nuances of dementia research and dementia caregiving. Guest: Eric Larson, MD, MPH, Senior Investigator, Kaiser Permanente Washington Health Research Institute   Questions: 1:07 - What sparked your interest in becoming a geriatrician and Alzheimer’s disease/dementia researcher? 2:35 - What would you say to young medical students looking for a specialty, and even considering geriatrics? 3:33 - Why do you think the field fails to attract younger doctors? 5:13 - What is the role of the National Academy of Medicine, and why did it conduct and release this report on caregiving? 7:29 - Can you offer us a brief summary of the findings or the key things that you think our audience should know about? 10:48 - What are the current limitations of the existing research on dementia care interventions for patients and caregivers, and how can we overcome those limitations? 12:38 - What is the difference between a care partner and a caregiver as you note in the report? 14:03 - What are some community, policy, or societal interventions that really should be explored? 15:46 - Does this report mean that we stop programs with low-strength of benefits, and if not, how do we continue to evaluate these programs and expand on them? 17:12 - Given the FDA approval of aducanumab, do you worry that more attention and resources will be pulled away from care work and care partner/caregiving that’s needed in research and clinical care toward this medication? 19:42 - What would you say to someone about to become an Alzheimer’s disease caregiver or care partner?   Show Notes: Read Dr. Eric Larson’s bio on the Kaiser Permanente Washington Health Research Institute’s website. Find a free download of the National Academies’ report, “Meeting the Challenge of Caring for Persons Living with Dementia and Their Care Partners and Caregivers: A Way Forward,” here. To learn more about the National Academies, find them on their website. For information about their research, publications, and events focused on dementia and Alzheimer’s disease, visit this page from their website. Find other resources related to this report by the National Academy of Medicine here: Report Highlights Press Release Recommendations 

Caregivers, Care Partners and People with Dementia: Brainstorming New Interventions for Dementia Care

Vince Tien and Dr. Dung Trinh join the podcast to discuss the many ways Alzheimer’s disease affects the Asian Americans and Pacific Islanders (AAPI) community. Vince Tien and Dr. Trinh both work as part of 360 Clinic, a multi-specialty medical group focused on telehealth services. With their experience in healthcare and telehealth services amidst the pandemic, Tien and Dr. Trinh describe the barriers and stigma that discourage the AAPI community from seeking help for dementia and the ways that we can dismantle those barriers.  Guests: Vince Tien, co-founder, CEO, 360 Clinic, and Dung Trinh, MD, chief medical officer, 360 Clinic   Episode Topics: 1:13 Vince Tien, what is your background in healthcare? How did you get involved in Alzheimer's disease and dementia care? 3:43 Dr. Trinh, what is your experience in caring for people with Alzheimer’s disease and dementia? 6:06 What are the health-related needs of AAPI communities? And, when it comes to dementia and Alzheimer’s disease, what are these communities’ needs? 7:44 Is there a certain perception of dementia, Alzheimer’s disease, and cognition within the AAPI community?  9:22 How do you find common ground between accessibility issues of technology and the benefits of telehealth? 13:07 What role does stigma play in the Asian American or Vietnamese communities specifically when it comes to Alzheimer’s disease? How does it affect caregiving and family members? 14:18 How do we start destigmatizing Alzheimer’s disease, dementia, and cognitive change within the Asian American community? 16:06 How does healthcare address the cultural, economical, linguistic barriers that Asian Americans experience regarding public health messages and care? 17:18 How can healthcare systems and organizations provide care for underresourced and underrepresented families who are suffering from dementia-related illnesses? 19:58 What would be the one thing you’d want the Asian American community to know about Alzheimer’s disease and dementia care?   Follow Dementia Matters: Find Dementia Matters online Follow us on Facebook Follow us on Twitter   Show Notes: To learn more about 360 Clinic, find them at their website, Instagram, and Twitter. Learn more about Dr. Dung Trinh at his LinkedIn and his Facebook Page. Learn more about Vince Tien at his LinkedIn.

Tackling Stigma and Alzheimer’s Disease within the AAPI Community

What would happen if caregiving strategies were inspired by wonder rather than memory? That’s what Dr. Anne Basting, founder and president of the nonprofit TimeSlips, asked when she began her research into how the arts could be integrated into dementia caregiving. Basting joins the podcast to discuss her caregiving approach rooted in creative engagement and imagination. From storytelling to beautiful questions to performance, Basting describes a new way of caregiving that helps caregivers and families meet patients and loved ones where they’re at to have meaningful connections and spark joy in the later years of life. Guest: Anne Basting, PhD, professor of English at the University of Wisconsin-Milwaukee, founder and president of TimeSlips, author of Creative Care Episode Topics: 1:31 - What inspired you to bring the arts and humanities to dementia care? 4:51 - Why did you write Creative Care, and what do you want readers to leave with? 7:49 - What are “beautiful questions” and can you offer a few examples? 14:32 - What is in the Creative Care Imagination Kit and why is each component important to the process? 15:49 - You’ve staged theater productions in care facilities as part of this process. How do performers in these plays respond to being a part of theater and how does the audience respond to the performances? 18:43 - How can people get involved in this organization and what do you recommend to people who would like something like this in a local care facility? 19:48 - What would you say to someone about to embark on the caregiving journey with someone with dementia?   Follow Dementia Matters: Find Dementia Matters online Follow us on Facebook Follow us on Twitter   Show Notes: Read Anne Basting’s biography on her website. Learn more about Anne Basting’s book, Creative Care: A Revolutionary Approach to Dementia and Elder Care, and her Creative Care Imagination Kit on her website here. Learn about Anne Basting’s nonprofit organization, TimeSlips, at its website for information on services, resources, and ways to get involved. Also find TimeSlips on Facebook, Twitter, Instagram, and YouTube.

Creative Care: The Power of Imagination in Dementia Caregiving

Researchers have produced many studies on how smoking affects parts of the body, such as the lungs or heart, but what about the brain? In today’s podcast, Adrienne Johnson, PhD, discusses her research on cigarette smoking and risk for dementia and Alzheimer’s disease. As part of a 2021 study, she found a person’s risk for dementia and Alzheimer's disease can be affected by how recently they’ve smoked. Diving into her research, the effects of smoking on different communities, and resources to support current smokers as they quit, Dr. Johnson details the impact of smoking on the brain and her hopes to develop new interventions to motivate smokers to quit for good. Guest: Adrienne Johnson, PhD, assistant scientist at the University of Wisconsin Center for Tobacco Research and Intervention Episode Topics: 1:17 What sparked your interest in studying the effects of cigarette smoking and, particularly, how it affects cognitive decline? 3:47 What are the effects of smoking on Alzheimer’s disease risk and/or general cognitive decline? 5:28 Why do you think there’s a difference in risk levels for Alzheimer’s disease and then for dementia? 6:27 Are there other things you can share about what you have found with your preliminary studies on smoking as a risk factor for Alzheimer’s disease? 8:38 You haven’t found a quantity relationship between the amount a person smokes and their risk for Alzheimer’s disesase, but rather a relationship based on smoking recency. Could you describe that further? 11:12 You’ve also done work on how there’s more disadvantaged communities that might be suffering from tobacco use compared to others. Can you speak on that? 13:01 How can caregivers and/or family motivate or support current smokers so that they can quit? 14:25 Is there a difference in a population that already has cognitive impairment? Do you have different strategies that we might use to support those individuals? 18:16 What are you looking to study in the future? 19:21 Can you share some resources where listeners can get help to stop smoking or where they can find resources for a loved one? Find Dementia Matters online Follow us on Facebook Follow us on Twitter Show Notes: Read Dr. Adrienne Johnson’s biography on the UW Center for Tobacco Research and Intervention (UW-CTRI) website. To learn more about the UW Center for Tobacco Research and Intervention (UW-CTRI) and the work they do, find them on their website, Twitter, Facebook, YouTube, and Instagram. Find resources on how to quit smoking here: Learn more information about smoking, vaping, and how to quit at https://ctri.wisc.edu 1-800-QUIT-NOW is a national smoking cessation quitline. Though it’s resources vary from state to state, in Wisconsin they can provide callers with free evidence-based evidence-based smoking cessation medications and a free coaching session to help you quit. Smokefree.gov is a website with a variety of resources, including texting programs, quit plans, mobile apps, and information on how to quit for specialty populations. Talk to primary care providers for prescribed medication and counseling for quitting smoking 

Better Now than Never: Quit Smoking to Reduce Your Risk for Alzheimer’s Disease

Elisa Ghezzi, DDS, PhD, joins the podcast to discuss the importance of maintaining oral health throughout one’s life, and especially as one grows older. Discussing the effects of oral health on our systemic health, oral health’s connection to dysphagia, and how caregivers can help dementia patients’ care for their teeth, Dr. Ghezzi provides insight on how vital it is to care for our oral health as we age. Guest: Elisa Ghezzi, DDS, PhD, adjunct clinical assistant professor, University of Michigan School of Dentistry, provider, Voiage Portable Dentistry   Episode Topics: 1:15 - How did you get interested in oral health in older adults? 3:28 - Why isn’t there more training or education in general dentistry for an older population? 4:34 - What are oral diseases, and what are their effects on systemic health? 6:00 - Is there an association between oral disease and cognition or cognitive impairment? 8:50 - IDoes inflammation affect oral health? 10:00 - What can be done to prevent oral conditions? 13:39 - What can we do to help protect our teeth? 16:38 - What should older adults and people who are experiencing dementia do about flossing? 19:05 - For our audience members who might be caring for someone who has dementia,, what recommendations would you offer when the person they are caring for is resistant to the act of having someone brush their teeth? 22:10 - What is the relationship between oral health, oral disease, and dysphagia? 28:20 - What is the most pressing issue facing older adults and their oral health care?   Find Dementia Matters online Follow us on Facebook Follow us on Twitter Vote for Dementia Matters in the 2021 Podcast Awards! Voting closes July 31st!

Dentistry and Dementia: The Importance of Caring for Oral Health

Dementia Matters has entered into the 2021 People's Choice Podcast Awards! If you enjoy our show and want to support us, register and vote before July 31st at www.podcastawards.com, and vote for us under the Health and People's Choice categories. We, the Dementia Matters team, hope that by participating, we can continue spreading our message and educate new listeners about Alzheimer’s Disease, Dementia, and brain health. Our background music is "Cases to Rest" by Blue Dot Sessions. Find Dementia Matters online - https://www.adrc.wisc.edu/dementia-ma... Follow us on Facebook - https://www.facebook.com/wisconsinadrc Follow us on Twitter - https://twitter.com/WisconsinADRC Vote for Dementia Matters in the Podcast Awards - www.podcastawards.com

Vote for Dementia Matters in the 2021 Podcast Awards!

Neurologist and author Daniel Gibbs, PhD, joins the podcast to discuss his recent book, “A Tattoo on the Brain,” which details his journey from treating Alzheimer’s disease clinically for 25 years to being diagnosed with early-stage Alzheimer’s. Dr. Gibbs discusses early signs he experienced and daily life with the disease, as well as thoughts on the recent FDA-approved treatment aducanumab (marketed as Aduhelm). Guest: Daniel Gibbs, PhD, neurologist Episode Topics: What inspired the title of your book, “A Tattoo on the Brain”? 1:01 What were these early signs of Alzheimer's disease that you recognized in yourself? 3:42 What were your impressions of the clinic process, and where is there room for improvement? 8:08 Can you share your view on family history? 9:17 What do you say to people about direct-to-consumer genetic testing, both as a recipient and as a clinician? 10:57 Did knowing your risk of Alzheimer's disease help or harm you? 12:42 Did you find any habit difficult to incorporate into your day? 13:17 How important was it for you to be involved in research and what did you gain from being a research participant? 17:15 How do you feel about the recent FDA approval of aducanumab for clinical use? 20:25 As a patient, would you sign up for this drug, and if you were still working as a neurologist, would you prescribe this drug? 22:59 How do you find the balance between enjoying daily life and engaging proactive activities meant to improve the future? 24:49 How can we reframe the way people understand Alzheimer's disease? 28:18 Was it difficult to publicly discuss your experience, and what have you learned from this process? 29:52 What do you hope the reader takes away from your book? 31:15 Find Dementia Matters online Follow us on Facebook Follow us on Twitter

From Studying to Living with Alzheimer's Disease: A Conversation with Dr. Daniel Gibbs

For our 100th episode of Dementia Matters, Nina Silverberg, PhD, director of the Alzheimer's Disease Research Centers (ADRC) Program at the National Institute on Aging (NIA), joins the podcast to offer an overview of the ADRC Program as well as insight into the state of Alzheimer’s Disease research and its future. The NIA funds more than 30 Alzheimer’s Disease Research Centers across the country, including the Wisconsin ADRC. Guest: Nina Silverberg, PhD, National Institute of Aging   Episode Topics: How did you get involved with Alzheimer's disease? 1:32 How has Alzheimer's disease research changed over the last 15 years? 3:22 Brief history of the NIA’s ADRC Program: 4:46 What role do the centers play in the field of Alzheimer's disease research and treatment? 6:24 How do the centers collaborate with one another? 7:48 What is your vision for the future of the ADRC Program? 9:47 How does the NIA report their process and findings to the public? 12:03 How does the NIA collaborate with other groups conducting research? 13:18 Are blood-based biomarkers the future of Alzheimer's disease research? 18:23 Do you think there will be more focus on other pathologies in the future? 20:09 How can Alzheimer's disease researchers help impact clinical care? 23:37 What area of Alzheimer's disease research fascinates you the most? 24:40 How close do you think we are to solving or curing Alzheimer's disease? 26:43 Find Dementia Matters online Follow us on Facebook Follow us on Twitter  

How Close Are We to Curing Alzheimer’s Disease?

Neuropsychologist and author Michelle Braun, PhD, joins the podcast to talk about lifestyle changes that can support brain health. “We have the ability to make our brain younger than our chronological age,” she says. Braun shares how and details strategies from her new book, “High-Octane Brain: 5 Science-Based Steps to Sharpen Your Memory and Reduce Your Risk of Alzheimer’s.” Hear about common misconceptions around aging, three possible brain health trajectories, and how to maximize your brain health. Guest: Michelle Braun, PhD   Episode Topics: What are the most common complaints that can be attributed to normal aging? 1:29 What are the main misconceptions of aging? 3:25 What are the three possible brain health trajectories? 5:00 What does a high-octane brain trajectory look like? 6:55  What are the three navigational forces that influence brain health trajectories? 8:21  What is epigenetics? 10:35 What are the five lifestyle factors that make up EXCELS?  13:01 How did you come up with the order of these lifestyle changes? 14:18 What do you tell your patients about the benefits of exercise? How do you recommend they start? 16:20 What diet do you recommend to support brain health? 20:06 What have you found to be the biggest struggle in following the diet? 22:21 How should a person get started with the MIND diet and what should be avoided? 23:27 What is your response when patients ask about supplements? 24:46 What are your thoughts on alcohol consumption and brain health? 26:07   Dr. Braun will be a guest speaker at the Wisconsin Alzheimer’s Disease Research Center’s "Healthy Living with Mild Cognitive Impairment: Nutrition in Action" class on June 18, 2021. The class will be held virtually on Zoom and is free and open to the public. Register Here.   Find Dementia Matters online Follow us on Facebook Follow us on Twitter

How to Shape Your Brain Health and Reduce Your Risk for Alzheimer’s Disease

Researchers at the University of California, San Francisco found that among older adults with cognitive impairment, the greater the air pollution in their neighborhood, the higher the likelihood of the presence of amyloid plaques in their brain. Lead researcher Leonardo Iaccarino, PhD, details his work examining air pollution and brain health outcomes and discusses possible ways individuals and society can lower the impact of air pollution on Alzheimer’s disease risk. Guest: Leonardo Iaccarino, PhD, University of California San Francisco Memory and Aging Center   Episode Topics: What sparked your interest in neuroscience and Alzheimer's disease research? 1:06 Why is your research so pivotal? 2:21 What was the IDEAS Study? 4:12 What kinds of air pollution are you referring to? 6:09 What can generate PM2.5? 7:45 Are cars or factories potential sources? 8:50 How does air pollution increase risk for Alzheimer's disease? 9:15 Is there a further increased risk after long exposure? 11:00 Why is it important that there was no link to ground-level ozone? 12:04 Did you look into the APOE4 genetic risk from air pollution? 14:32 What should people do with this information? 16:19 Is there a way to find your own neighborhood value of PM2.5? 18:44 Do you see any policy or system changes in the future from your findings? 19:55 Do you believe there might be other environmental factors that increase risk? 21:03 What do you do in your life to decrease risk for neurodegeneration? 21:57 Find Dementia Matters online Follow us on Facebook Follow us on Twitter

Study Finds Air Pollution a Risk Factor for Alzheimer’s Disease

Inappropriate sexual behavior is a common yet rarely discussed symptom in individuals with dementia. Author Elizabeth Marcus writes about her personal experience with her father’s behavioral changes in her new book, “Don’t Say a Word!: A Daughter’s Two Cents.” Elizabeth shares what she learned caring for her father, as well as advice for caregivers responding to the symptoms. Neurologist Dr. Martin Samuels offers background on changes in the brain that can cause inappropriate sexual behavior and other personality shifts that are common in people with dementia. Guest: Elizabeth Marcus, author; Martin Allen Samuels, MD, Brigham and Women's Hospital Episode Topics: What is your book about? 1:09 How did you react to your father’s request? 3:08 What did you learn about the experience? 4:04 What did you learn about the relationship between sex and dementia? 5:29 What is the key message of your book? 6:50 How common are these situations? 8:33 Are there physical changes in the brain that explain these symptoms? 9:10 Why do some individuals with memory loss develop these symptoms, while others don’t? 12:44 How can family members respond to the situation once it becomes uncomfortable? 14:51 What advice do you have for family member’s going through this experience? 17:27 What types of education or resources do you provide caregivers? 19:30 How do you respond to caregivers looking into medication for the symptoms? 21:55 What is your experience with the stigma around sex and individuals with memory loss? 23:44 Any suggestions for overcoming the discomfort and respectfully addressing these symptoms? 26:33 Visit Elizabeth Marcus’ author website to learn about her new book, “Don’t Say a Word! A Daughter’s Two Cents.” Find Dementia Matters online Follow us on Facebook Follow us on Twitter

Managing Inappropriate Sexual Behavior in Alzheimer’s Disease

Being Patient is an online news source dedicated to providing research news, caregiver information and resources related to Alzheimer's disease. Being Patient founder Deborah Kan discusses how her personal experiences led her to develop the website, as well as how online resources and communities can help empower individuals affected by memory loss. Guest: Deborah Kan, journalist, founder of beingpatient.com Episode Topics: What inspired you to leave a career in journalism and launch Being Patient? 0:58 How do you decide on the topics you cover? 4:18 How does social media help build a community through connection? 9:14 Have you found a certain communication platform that has better reach? 11:25 What have you learned from caregivers through your work? 13:49 Can you offer recommendations for finding reliable online sources for health information? 18:58 Why is it important for the scientific community to have a separate organization that discusses the research? 23:34 What topics in Alzheimer's disease research have been the most impactful? 27:35 Find Dementia Matters online Follow us on Facebook Follow us on Twitter

Being Patient Translates Alzheimer’s Disease Science for the General Public

Dr. Jason Karlawish discusses society’s role in addressing care for individuals with memory loss, as well as current stigmas around Alzheimer’s disease, Wealthcare, and his cautious optimism for the future of Alzheimer’s disease research and care. This is the final episode in our four-part series with Dr. Karlawish on his new book, "The Problem of Alzheimer's: How Science, Culture, and Politics Turned a Rare Disease Into a Crisis and What We Can Do About It.” Guest: Jason Karlawish, MD, co-director, Penn Memory Center Episode Topics: How do you live a good life when you’re slowly losing your ability to live life? 0:56 How do home and work fit in your life after a mild cognitive impairment diagnosis? 2:21 What are your recommendations on home looseness and time slips? 4:34 How can we improve care facilities? 10:04 What is Wealthcare? 11:19 Why haven’t caregivers been given greater support in our system? 13:32 What do you mean by time, task and truth in caregiving? 15:13 What are steps we can take to improve the care for individuals with mild cognitive impairments? 17:34 What do you mean by stigma in Alzheimer's disease? 19:37 What worries you about the effects of this stigma? 22:00 With a new presidential administration, what should be the top priorities as a country for preparing for Alzheimer’s and improving the lives of individuals with memory loss? 24:21 Learn more about Jason Karlawish's book Find Dementia Matters online Follow us on Facebook Follow us on Twitter

How Society Can Improve Care for People with Alzheimer’s Disease and Related Dementias

Dementia Matters is brought to you by the Wisconsin Alzheimer’s Disease Research Center, located in Madison, Wisconsin. Our podcast is here to help humanize Alzheimer’s disease, by speaking with the experts in our community to keep you informed on the latest headlines, research studies, and caregiver resources.