Alzheimer’s disease has affected me in the most life-altering way possible. Alzheimers took away my best friend and life partner of over 35 years: my wife, Susan. I had to watch as it took simple physical coordination away from a once world-class marathon runner. It took my future retirement plans and threw them out the window. The disease took my children’s mother and best friend; it took away a friend to many people; and it took a wonderful human from this earth. The saddest thing to deal with was watching the disease progress without being able to do anything about it. It felt like we lost her twice. Susan first became a different person than we all knew, and then physically passed. The single and only positive way Alzheimers has affected my life is that I now have a much greater appreciation of life, my family and my friends. I have always said “I love you” to people, but I find myself saying it more often. Don’t wait. Say it to those that mean so much to you. We found tremendous support from Susan Frick and the Without Warning support group. Those get-togethers were so good for both my wife and myself. As a caregiver it was comforting to know I wasn’t alone with my questions, confusion, exhaustion and concern about the care we were all trying to give our loved ones. The bonding that took place between caregivers was swift, strong and comforting. We found others in similar situations that could offer advice and would understand our pain, our fears, and our frustration. An example of the bonds we created took place around Christmas. I was in my kitchen in Glen Ellyn having some melancholy moments about dealing with the holiday and trying to make sure my family stayed upbeat as it would mark one year since my wife’s passing. I got a buzz that someone was at the door, so I went down to the entry and there was a gentleman, Tom, from the Without Warning support group. He was there with a box of cookies and a hug just to let me know someone was thinking about me. I didn’t get a chance to tell him, but that one simple act carried me through the holiday with a smile in my heart. Don’t try to deal with Alzheimers alone. Get in a support group , go to therapy and lean on family and friends. I started a fundraiser with The Longest Day in honor of Susan. I organized a golf outing–which seemed like a logical thing for me as I was retired from the golf business. My original goal was to have about 100 players and try to raise about $10,000. As things got into motion I quickly realized I had many more friends and supporters in my life! First, I got a big boost from the golf club where I work part-time in the summer, Boulder Ridge Country Club. Thanks to previous owners, the Plote Family, and the current owners, The Heritage Golf Group, they afforded me a generous discount on the complete package of golf, lunch and dinner. The fantastic staff at Boulder Ridge gave me so much help and support. I cannot imagine the event running as smoothly as it did without them at my side. Many of my fellow golf professionals donated gift certificates for rounds of golf that we auctioned off. Many friends from our past and present showed up to participate, sponsor, donate or help with registration and setup at the event. My fellow Rotarians from Buffalo Grove played and donated to the fundraiser. One super generous Rotarians case donated all the signs, banners and bag tags for the day’s events. Former employees of mine came from all over. Some who had worked for me during their high school and college days flew in for the event, some who worked with me up until my retirement showed support. The members of Boulder Ridge Country Club were and continue to be such great friends–not just during the event, but in the years preceding the event when they offered their friendship, support and love. Needles to say I had my family and three of my best friends urging me on and holding me up when I would wobble a bit. When it was all said and done my event had 186 golfers and nearly 200 for dinner. The final amount raised was over $32,000 . One of my all time favorite movies is Shawshank Redemption. One of my favorites lines is, “You got to get busy living or get busy dying.” In dealing with the loss of Susan, the idea of “get busy dying” would have been to sit and feel sorry for myself, my family and Susan–to sit in my misery without doing anything. That did not seem like an option for me nor one that would make Susan or my sons proud of. I chose to “get busy living” by helping raise awareness about Alzheimer’s disease and raising funds for Alzheimer’s research so that hopefully the next generation doesn’t have to deal with this horrible disease. As the population continues to live longer, Alzheimer’s unchecked will start affecting more and more of us. If we put people on the moon and bring them back, we can do this: we can end Alzheimer’s in our lifetime. More awareness means more funds raised, and more funds raised means hope for the future. The thing I would like people to understand about Alzheimer’s disease is that it can happen to anyone. My wife Susan had no family history of Alzheimer’s. She exercised every day, she ate healthy, stayed mentally active and could have been the poster child for someone least likely to be afflicted, especially at the age of 54. It can happen to anyone and that is why it is so important to raise awareness. If it does happen to someone in your care, please do not face it alone. Join a support group, reach out to family and friends and know that you are not all by yourself. Sometimes people are a little hesitant to reach out to you first because they don’t know what to say or do. If you reach out to people first you will be amazed how much just having someone to talk to can help. I was always fortunate to have friends I could count on, but the depth and sincerity of those friendships amazed me and certainly carried me though those most difficult days.

Restituto Miranda Sr. occasionally reminisced about driving a taxicab, working in an office supplies store and riding his motorcycle. But there was one problem: To the best of his family’s knowledge, Miranda — who had worked as a meat cutter with the American Meat Packing Corp. in Chicago — never had done any of these things, says his son Resti Miranda Jr. Seeing how happy he seemed telling the stories, family members didn’t correct the elder Miranda, diagnosed in 2014 with vascular dementia after experiencing a second stroke. Dementia can affect a person’s brain in such a way that individuals may remember only fragments of something that occurred years earlier, or they may make up stories. The elder Miranda passed away in January 2020 at the age of 82. It was hard, Miranda Jr. says, to see his once-healthy, strong father fight through complications from two strokes and vascular dementia. All dementias involve changes in the brain, but symptoms vary. Alzheimer’s disease comprises 60% to 80% of dementia cases. Here are some other types: Vascular dementia Vascular dementia, which can occur after stroke or heart disease, is one of several types of dementia, says Terrianne Reynolds, director of healthcare initiatives at the Alzheimer’s Association, Illinois Chapter . This type of dementia can result from brain damage due to impaired blood flow and other conditions that damage blood vessels and reduce circulation, such as atherosclerosis, heart disease and stroke. Vascular dementia is marked by a decline in thinking skills caused by conditions that block or reduce blood flow to the brain, depriving brain cells of vital oxygen and nutrients. “These changes can sometimes occur suddenly following strokes that block major brain blood vessels,” Reynolds says. Symptoms include memory loss, confusion, language problems, difficulty paying attention and visual orientation problems. These symptoms may develop gradually or become apparent after a stroke or major surgery such as heart bypass. While tests can determine that you have dementia, there’s not a specific test that confirms vascular dementia, according to the Mayo Clinic. Your symptoms, medical history, and history of stroke or cardiovascular issues can point to vascular dementia. Lewy body dementia Lewy body dementia is an umbrella term for two related clinical diagnoses: dementia with Lewy bodies and Parkinson’s disease dementia. The most common symptoms are changes in cognition, movement, sleep and behavior. Lewy body dementia typically begins at age 50 or older, although sometimes younger people develop it. In the early stages of Lewy body dementia, symptoms can be mild, according to the National Institute on Aging (NIA). But as the disease advances, people with Lewy body dementia need more help — and eventually often depend entirely on others — because of the decline in their thinking and movement abilities. Some Lewy body dementia symptoms may respond to treatment for a period of time, but there’s not yet a cure. However, the NIA reports that research is improving scientists’ understanding of this condition. That knowledge may one day lead to earlier diagnoses, improved care and new treatments. Frontotemporal dementia Frontotemporal dementia is a group of disorders caused by progressive cell degeneration in the brain’s frontal lobes (the areas behind the forehead) or its temporal lobes (the regions behind the ears). The most common dementia for those under 60, frontotemporal dementia is misunderstood and frequently misdiagnosed as Alzheimer’s disease, Parkinson’s disease, depression or a mental health disorder, according to the Association for Frontotemporal Degeneration. It takes an average of 3.6 years to receive an accurate diagnosis, the association says. Mixed dementia When symptoms of more than one type of dementia occur simultaneously, it’s called mixed dementia. The likelihood of having mixed dementia increases with age and is highest in people age 85 and older.

The Alzheimer’s Association Illinois Chapter is hosting a research symposium. This event is dedicated to honoring National Family Caregivers Month, recognizing the vital contributions of caregivers, increasing awareness about their role, and providing valuable information and resources. Symposium Highlights: Date and Time: Friday, November 3, 2023, starting at 09:30 AM (CDT). Location: Feinberg Pavilion Conference Center, Northwestern University, 251 E Huron, 3rd Floor, Chicago, IL 60611. Purpose of the Symposium: “By hosting this annual symposium, we have the opportunity to bring together over 300 caregivers, patients, families and healthcare professionals to learn about the latest in Alzheimer’s and dementia research and the Association’s role in driving and leading global research initiatives. We are also able to provide the attendees with information, tools, and resources,” said Olivia Matongo, Vice President of Programs, Alzheimer’s Association. Key Speaker: Heather Snyder, Ph.D., Vice President, Medical & Scientific Relations at the Alzheimer’s Association, will lead a discussion on an overview of the new of era treatment which includes activities happening at the Association to advance research. The keynote discussion will also address access to the services, programs and awareness to diagnose and treat dementia, as well as support provided. Professional Track Drug Development : An overview of the drug development process to include discussion on clinical trials, the phases of trials, how to participate, and why older and diverse participants are essential in clinical research. Detection: An overview of the current Alzheimer’s and memory concerns landscape. Discussion will include the importance of early detection in the new era of treatment as it relates to medical benefits, emotional and social benefits, more time to plan for the future and cost savings. Family Track Cultural Considerations in Dementia : Discussion on the recognition of dementia across cultures including cultural specificity of screening tools, identification of differences in risk factors, incidence, onset and prevalence across cultures and culturally related issues in decision making about management. Behaviors : Identify common triggers for behaviors associated with dementia. Explaining the process for assessing and identifying challenging behaviors and strategies to address common dementia – related behaviors. New Anti-Amyloid Therapies: What do you need to know? Panel Discussion (all attendees) Discussion on current therapies that are now available and understanding the target audience for the therapies. Discussion on the process of administering the drug and the patient experience in the new journey of new treatments. The discussion will feature two early stage patients who are on Leqembi and Adulhelm. Who Should Attend: The symposium offers tracks tailored for various groups, including: Individuals with early dementia or Mild Cognitive Impairment (MCI). Family members, friends, or non-professional family care partners of individuals with dementia. Professional caregivers, direct care staff, and administrators (Please note: No continuing education credits offered in this category). Health and allied health professionals eligible for Continuing Education Units (CEU) or Continuing Medical Education (CME) credits. Continuing Education: Professional II attendees (health and allied health professionals) are eligible to earn 3.0 CEU or CME credits. Eligible professionals for continuing education credit include counselors, dietitians/nutrition counselors, marriage and family counselors, nurses, nursing home administrators, occupational therapists, physical therapists, physicians, psychologists, respiratory therapists, social workers, and others (inquire at omatongo@alz.org ). This symposium promises to be an informative and impactful event for those involved in Alzheimer’s and dementia care and research. It offers an excellent opportunity to learn, connect, and contribute to the fight against Alzheimer’s disease. To register please click here

The Alzheimer’s Association Illinois Chapter is thrilled to welcome new Board Chair, Sandy Prabhaker. Sandy is a Managing Director – Midwest Leader for the Armory Group. He works in investment banking and restructuring advisory services and specializes in Mergers and Acquisitions and Capital Advisory where he advises C-Suite management teams and Middle Market business owners as they navigate complex financial transactions.  Sandy and his wife Lynn have been event sponsors and connected with the Mission of Alzheimer’s for several years.  He continues to serve as a Planning Committee Member for the annual Memory Rock Chicago event with the Associations’ Illinois Chapter, which hosted its 17th annual event this year.   His late Father-in-law (Paul Lemire) passed away in 2007 after a 12-year fight with Frontal Temporal Dementia, which drives his and his family’s passion for helping and serving the Alzheimer’s Association, Illinois Chapter.  Sandy joined the Alzheimer’s Association, Illinois Chapter Board of Directors on July 1, 2017, and was recently appointed Chair for the Illinois Chapter Board for fiscal year 2024.

9:30 am to 2:30 pm About the Annual Symposium: The Alzheimer’s Association Illinois Chapter hosts a research symposium every year in November to honor National Family Caregivers Month – a time to celebrate the contributions of caregivers, increase their awareness and connect them with information and resources. By hosting this annual symposium, we have the opportunity to bring together over 300 caregivers, patients, families and healthcare professionals to learn about the latest in Alzheimer’s and dementia research and the Association’s role in driving and leading global research initiatives. We are also able to provide the attendees with information, tools, and resources. Who Should Attend? Clinical, research, and family tracks are designed for: Attendee with early dementia or MCI Family, friend, or family care partner* of person with dementia (*Non-Professional) Professional I (Professional caregiver, direct care staff, administrator: please note: no continuing education credits offered) Professional II (Health and allied health professionals with CEU or CME) Continuing Education 3.0 CEU, CME credits offered for attendees registered as a Professional II only. The following professionals are eligible for continuing education credit: Counselor-Professional/Clinical Dietitian/Nutrition Counselor Marriage and Family Counselor Nurse (APN, RN, LPN) Nursing Home Administrator Occupational Therapist/COTA Physical Therapist/PTA Physician Psychologist Respiratory Therapist Social Worker (LSW, LCSW) Others, please inquire at omatongo@alzweb PRINTABLE SPONSORSHIP FORM SPONSORSHIP OPPORTUNITIES EVENT SPONSORS SYMPOSIUM SCHEDULE KEYNOTE SPEAKERS MAKE A GENERAL DONATION CLICK HERE TO REGISTER NOW Location Feinberg Pavilion Conference Center Northwestern University 251 E Huron, 3rd Floor Chicago, IL 60611

Kari-Ann Ryan is a marketing executive with 30 years of experience in marketing for multi-brand and multi-location companies, the service industry, and retail management, as well as working in non profit marketing, event planning and fundraising. Kari-Ann is the Director of Marketing & Development for Mid-West Moving & Storage and Chicago Office Movers. As the master of visibility, she is responsible for all things Branding and Marketing related both internal and external. She also owns her own marketing consulting business and is a certified business partner for Constant Contact. At the end of 2022, she started her own non-profit organization called LMJ’s Lost Souls- Alzheimer’s Fund, focused on fundraising events, awareness, education, resources and support for Alzheimer’s and Dementia related Disease. She is the president of the board for this organization. Prior to starting the non-profit, her team donated over $400K to the Alzheimer’s Association over the past 9 years. Kari-Ann is also on the Board for the Schaumburg Business Association, the Elk Grove Village Chamber, and is a past long time chair and top fundraiser for the Northwest Suburban Walk To End Alzheimer’s. She serves on the Fund the Mission Committee for the Alzheimer’s Association. All the work she does as an advocate for Alzheimer’s Disease is fueled by her personal connection as her grandmother passed of the disease. She is passionate about this cause and finds purpose in all the ways she and her organization can make an impact. She is inspired by all the people who support her on this journey and she lives to always give back.

The Alzheimer’s Association Illinois Chapter is thrilled to welcome four new members of our Board of Directors for fiscal year 2024 along with a new Board Chair. Our new board members commit their talents, passion, time and connections to strengthen the fight against Alzheimer’s. We thank them for their commitment to our vision of a world without Alzheimer’s and all other dementia, and we look forward to accomplishing incredible things together in the year ahead. Sandy Prabhakar is a Managing Director – Midwest Leader the Armory Group. He works in investment banking and restructuring advisory services and specializes in Mergers and Acquisitions and Capital Advisory where he advises C-Suite management teams and Middle Market business owners as they navigate complex financial transactions. Sandy and his wife Lynn have been event sponsors and connected with the Mission of Alzheimer’s for several years. He continues to serve as a Planning Committee Member for the annual Memory Rock Chicago event with the Associations’ Illinois Chapter, which will be hosting its 17th annual event in 2023. His late Father-in-law (Paul Lemire) passed away in 2007 after a 12-year fight with Frontal Temporal Dementia, which drives his and his family’s passion for helping and serving the Alzheimer’s Association, Illinois Chapter. Sandy joined the Alzheimer’s Association, Illinois Chapter Board of Directors on July 1, 2017, and was recently appointed Chair for the Illinois Chapter Board. Kari-Ann Ryan is a marketing executive with 30 years of experience in marketing for multi-brand and multi-location companies, the service industry, and retail management, as well as working in non-profit marketing, event planning, and fundraising. Kari-Ann is the Director of Marketing & Development for Mid-West Moving & Storage and Chicago Office Movers. As the master of visibility, she is responsible for all things Branding and Marketing related both internal and external. She also owns her own marketing consulting business and is a certified business partner for Constant Contact.   At the end of 2022, she started her own non-profit organization called LMJ’s Lost Souls- Alzheimer’s Fund, focused on fundraising events, awareness, education, resources and support for Alzheimer’s and Dementia related Diseases. She is the president of the board for this organization. Prior to starting the non-profit, her team donated over $400K to the Alzheimer’s Association over the past 9 years. Kari-Ann is also on the Board for the Schaumburg Business Association, the Elk Grove Village Chamber, and is a past long time chair and top fundraiser for the Northwest Suburban Walk To End Alzheimer’s. She serves on the Fund the Mission Committee for the Alzheimer’s Association. All the work she does as an advocate for Alzheimer’s Disease is fueled by her personal connection as her grandmother passed of the disease. She is passionate about this cause and finds purpose in all the ways she and her organization can make an impact. She is inspired by all the people who support her on this journey and she lives to always give back. Rev. Frank C. Walton is a licensed and ordained minister, and affectionally, called Pastor Frank throughout the Chicagoland area and the West Coast. He is married to Pam Morris-Walton, the renowned Gospelsister of Chicago and together they have collaborated on various events including weekly radio and television broadcasts, Bud Billiken Gospel Fest in Chicago, Black Marriage Chicago, and Weekly Senior Services and have served as Ambassador for the Bernie Mac Foundation along with hosting numerous Gospel events. While on the West Coast, Frank had several business roles in both King & Pierce County of Washington State with his professional activities – The Salvation Army, Urban Ministries, Inc., Tacoma Ministerial Alliance, Tacoma Black Collective, Tacoma Sunrise Rotary and Tacoma / Pierce County Chamber of Commerce. His role in Corporate America advanced a well-rounded background in the areas of sales, customer relationships, employee morale and finance. While the positions held in the nonprofit organizations enhanced his expertise of boards with strategic planning and fund raising. Frank is humbled and honored to be a 2017 joint recipient along with his wife Pam of an Honorary Doctorate Degree from GMOR Theological Institute of America Midwest Region . He is also recognized as one of the 2017 Most Distinguished Men of Illinois . Frank is an inductee of the Broadcasters Hall of Fame in Akron, Ohio and was the GMWA/GAG 2009 Gospel Announcer of the Year . Several other notable awards include the National Jitsuo Morikawa Evangelism Award , from the American Baptist Churches of USA, numerous awards in broadcasting in honor of renowned broadcasters who exemplified commitment to the community and other acknowledgments for his effective leadership. Many know Pastor Frank as a strong, confident, and articulate leader with a passion for serving others. In addition, to having served congregations in Wheaton, LaGrange and his current intentional interim pastoral duties at Community Baptist Church of Warrenville, IL, he serves as President, of the American Baptist Churches – Metro Chicago and on several boards including the LGSSF and most recently the Alzheimer’s Association of Illinois . Bruce Hopple joined Avison Young in 2018 as a Senior Vice President on the tenant representation team. Bruce focuses on new business development and transaction advisory services for professional service firms, not-for-profits and local and national corporations. With more than 25 years of commercial real estate experience, Hopple is an expert in financial and market analysis, negotiation and commercial real estate trends. Hopple was most recently a senior director with Cushman & Wakefield in Chicago. During his career, Hopple has completed transactions for his clients valued at more than $2 billion, ranging in size from 1,000 square feet (sf) to 150,000-sf headquarters locations. A consistent top producer, his clients include American Board of Medical Specialties, Chicago Stock Exchange, CPG International; Gibbs & Soell; Landrum and Brown; Leadership Greater Chicago; March of Dimes; The Posse Foundation; SKF USA; Wonderlic, Inc.; Woolpert, Inc.; and Zurich Insurance. Prior to joining Cushman & Wakefield, Hopple was a senior vice president at Colliers International and The Staubach Company. Before his career in commercial real estate, Hopple served as in-house counsel for Chase Bank in Ohio and was a senior administrator at the University of Cincinnati. Hopple’s community service has included board positions with USO of Illinois, March of Dimes, Leadership Greater Chicago Fellows Association, the Pilsen/Rauner Family YMCA and Chicago Office Leasing Brokers Association (COLBA). He holds his juris doctorate and a bachelor’s degree in business administration from the University of Cincinnati. Hopple is a licensed real estate managing broker in the State of Illinois and is admitted to practice law in the State of Illinois. Barry Masek , former Senior Partner and now Retired Partner (Partner Emeritus) at Baker Tilly, 2006 to present. Executive VP, CFO and Treasurer at Temperature Equipment Corp, 2000 – 2005. Audit Partner at Arthur Andersen, starting as staff, 1979 – 1999. Over 40 years of experience serving middle-market and large manufacturing and distribution companies, including public and private equity owned. Held several leadership roles at Baker Tilly and served on the Baker Tilly’s Board of Partners. Prior to joining Baker Tilly, Barry was the chief financial officer for a distribution company. Prior to that, he was a partner with Arthur Andersen. Has led large engagement teams serving middle-market and large companies, including public and private equity-owned companies. Assists companies with merger, acquisition and due diligence transactions. Specializes in assisting companies with multiple entities, multiple locations and international operations. Lead advisory relationship partner on large public company projects, including restatements, internal audit and SOX service – working closely with management and audit committees. EVP and CFO, changed Banking relationship and healthcare service provider for better service and lower cost Led implementation of first-time, fully integrated ERP system. Industry specialization in manufacturing and distribution. Industry and civic involvement : American Institute of Certified Public Accountants, Illinois CPA Society, Association for Corporate Growth, Illinois Venture Capital Association, Clearbrook, Chair of the Board of Directors, Lurie Children’s Hospital of Chicago Foundation, Board of Directors member, Lurie Children’s Hospital of Chicago Medical Center, Finance Committee, formerly on Audit Committee, University of Nebraska-Lincoln, School of Accountancy, Advisory Board

We need your help to make a difference in the lives of your members People facing Alzheimer’s and dementia often turn to their faith communities for emotional and spiritual support. People who have Alzheimer’s disease or related dementia, especially those raised in religious households, are uplifted by worship services and visits. They often have the desire to continue to partake in church activities. Family members also have spiritual needs. Caring for a loved one can last for years, leaving the caregiver weary, isolated, frustrated, and depressed. At the same time, they may grieve the many losses of this journey. The Alzheimer’s Association recognizes the importance of spirituality and has developed programs to partner with congregations providing education and support to their members. The Alzheimer’s Association partners with faith-based organizations and communities to help provide resources and education, and raise awareness of the disease. We do this through collaborative action plans which are organized by the faith organization’s leadership and our Alzheimer’s Association Illinois Chapter team. If you are interested in partnering with us, please reach out to Amelia Garza at amgarza@alz.org . PURPLE SUNDAY Purple Sunday is a community event to promote awareness of Alzheimer’s disease in communities through houses of worship. By hosting a Purple Sunday event, churches can help their congregations learn more about the difference between Alzheimer’s and dementia, risk factors, warning signs, the importance of an early diagnosis, the diagnostic process, and helpful programs offered by the Alzheimer’s Association. Each faith-based group hosts Purple Sunday in different ways including: • Providing materials on a table • Devoting one sermon or bible study to issues surrounding faith, aging, and dementia • Asking members to wear purple during a Sunday service or faith event • Praying with a purpose circle for those affected by Alzheimer’s and dementia • Hosting an Alzheimer’s Association education class or awareness presentation If you live or worship in Illinois and are interested in hosting a Purple Sunday at your house of worship, contact the Alzheimer’s Association’s Illinois Chapter at 800.272.3900 or pbennett@alz.org for more information.

As temperatures rise across Illinois, extreme heat can have a significant impact on everyone’s safety, but it can be especially stressful and confusing for individuals with Alzheimer’s and other dementias. Alzheimer’s disease causes a number of changes in the brain and body that may affect their safety, including changes in sensitivity to temperatures. Today, there are more than 6 million Americans living with Alzheimer’s disease, including 233,000 in Illinois. Taking measures to plan ahead for weather changes, like extreme heat, can prevent injuries and help a person with dementia feel more relaxed and less overwhelmed. “People living with Alzheimer’s and other dementia can be vulnerable during extreme weather because their judgment may be impaired and they may be unable to communicate discomfort,” said Delia Jervier, Executive Director of Alzheimer’s Association, Illinois Chapter. “It’s really important to take extra precautions with these individuals when there is extreme heat or other excessive weather conditions.” The Illinois Chapter of the Alzheimer’s Association is offering important safety tips for caregivers and families facing Alzheimer’s and other dementias to prepare for the hot summer months: Make a plan. Family and friends should prepare accordingly and make plans to regularly check in on a person living with Alzheimer’s disease and other dementias during extreme heat. Arrange alternative plans for cooler spaces, if air conditioning is unavailable, and dress in loose, light clothing. Pay attention at night. Keep people living with Alzheimer’s disease and other dementias cool by using fans and keeping the air conditioning on. At night, low temperatures can still exceed 75 degrees with little fluctuation in humidity levels, making for difficult and exacerbating sleeping conditions, heightened anxiety and increased agitation. Prepare for behavioral challenges. Research shows that heat can increase agitation and confusion in people. Try to remove behavioral triggers by addressing the person’s physical needs related to the heat, then tending to their emotional needs. Stay hydrated. Increased water intake is essential to maintaining good hydration and health during extreme heat. Know the signs of heat exhaustion to avoid heat stroke. Dehydration may be difficult to notice in a person living with Alzheimer’s disease and other dementias, as signs like increased fatigue, dry mouth and headache may be difficult to detect. People taking diuretics, sedatives, or certain heart medications may not sweat as much as others, but this does not mean that they are not hot. Stay indoors and out of the sun. Heat stroke and heat exhaustion may occur in extreme heat conditions but symptoms may be difficult to detect in people living with Alzheimer’s and other dementias. Keep individuals cool by using air conditioning at home or moving to a public place, such as a senior center or shopping mall. If you must go outside, be sure to dress appropriately, loose, light clothing, wear a hat, and apply sunscreen with an SPF of at least 30 or higher. Stay informed. Keep an eye on local weather forecasts. High temperatures are not the only cause for concern. Humidity and air pollution indices can cause breathing difficulties. The person should be monitored regularly and seek medical attention if symptoms arise of dehydration, heat exhaustion, or heat stroke. The Alzheimer’s Association is here to help families take measures to prepare for and cope with such extraordinary circumstances. For more information, visit alz.org or call the 24/7 Helpline at 800.272.3900.

How did I get involved with the Walk to End Alzheimer’s? I first got involved in the walk when my grandfather (Dick Briel) my mom’s father was diagnosed and passed away in 2007 from Alzheimer’s. I really got involved when my mom was diagnosed in 2018. I was living in California and got a call that my mom was slipping and starting to be very forgetful. I packed up and moved in with my mom and my stepdad so I could help in whatever way. My mom has Early onset Alzheimer’s and was only 57 when she was diagnosed at the Mayo Clinic in Minnesota. I called the Alzheimer’s Association frequently to talk to someone who knew what I was going through and to ask questions, I got advice on joining a support group in my area and then I decided to join the Alzheimer’s Walk committee. It has been so amazing having the Alzheimer’s Association in my back pocket when I need to talk, get advice, or ask a question. My Committee has my back and has been a great sounding board. The committee head for the Dupage Walk Alison McEwen met me for coffee and we found out that both of our stories were very similar about our parents. How has Alzheimer’s disease impacted your life? It’s hard to put into words how much this disease has impacted me. A few words to describe my mom are Role Model, Amazing Business Women, Great Friend to all, my rock, and my best friend. My mom was diagnosed when she was at her prime and only 57. It’s just way too young and it is affecting people younger and younger every day. I did have the privilege of being my mom’s caregiver for close to 4 years. It was some of the hardest and best times that I have ever had. The hardest day was by far August 1, 2022 when we had to place my mom in a memory care facility. It was getting dangerous for her and we knew it was the best thing to do. My mom is currently living her best life in memory care in Aurora, IL we get to visit her as much as we would like and she lights up when she sees us. She still remembers the close family and it’s amazing to see her eyes look up into yours. Why should others raise funds and awareness for Alzheimer’s Disease? I think it is extremely important that we bring awareness because this disease is taking too many people too fast. Many people think it’s just an old person’s disease and that they are going to die anyway but that is not the case. It is heartbreaking for the person and the family members to watch their loved ones forget you, and everything around you. It’s so hard to watch them be confused and flustered. I do my part to speak up about it and raise awareness. This year I worked really hard with a Bowling fundraiser where the proceeds went to my Walk page. I was able to raise $2,000 just from the fundraiser and have one more in August. I work hard to advocate for my mom and for this disease. People need to know Alzheimer’s kills more people than breast cancer and prostate cancer combined. Alzheimer’s also affects Women more than it does men. Is there anything additional you would like to share to raise awareness? I just want to add that it was really hard when I was being my mom’s caregiver. I worked part-time and took shifts with my stepdad, we worked well as a team. My mom’s name is Sue Vidmar and my name is Shelbi Vidmar my stepdad is John Postlewaite. I just want people to help with raising money because we need to find a cure for this disease. We need survivors. My mom is currently 62 and is for the most part doing well. She is in a wheelchair now but can take a few steps on her own. She loves visitors, treats, and being with her family and friends.

In September 2022, Alzheimer’s Champion and country music artist Jay Allen debuted as a contestant on “The Voice,” bringing new eyes and ears to the music he created after losing his mom, Sherry, to Alzheimer’s. Jay is ready to take the stage for a live performance at Memorial Park Bandshell in Wheaton, Illinois. The event will take place on Saturday, July 15, 2023 at 6pm CT. The general cost of admission is $40 with $30 of each ticket sold going to the DuPage Co WTEA.   “When I first came to Nashville 10 years ago, my mindset was similar to every aspiring dreamer who comes to Music City. But it was not until I wrote a song out of heartbreak, “No Present Like the Time,” trying to find a sense of understanding about my mom and her Alzheimer’s experience, that I truly felt like I was doing something special,” said Allen. Allen wrote “Blank Stares” to tell his story and share the effects of this disease with the world. A video of him performing the song with his mother on stage went viral with over 500 million views on Facebook. His mother has since passed, but Jay continues to tour the country as an advocate for the Alzheimer’s Association, and the song has gone on to raise over $100 million dollars to help fight the disease. Jay has been featured on NBC’s The Voice, ABC World News, PeopleTV, Pickler & Ben, and in People & Forbes Magazine, among others. He was also presented The Caregiver Award by The National Alzheimer’s Association. Today, there are more than 6 million Americans living with Alzheimer’s, including 233,000 here in Illinois with more than 314,000 caregivers caring for them. As the size of the U.S. population age 65 and older continues to grow, so too will the number and proportion of Americans with Alzheimer’s or other dementias. By 2050, the number of seniors aged 65 and older with Alzheimer’s is projected to double to nearly 13 million. Tickets are now available online at https://www.eventbrite.com/e/jay-allen-concert-to-benefit-the-alzheimers-association-tickets-606848188267 or by calling 630-690-4880. Event Details: Memorial Park Bandshell 225 Karlskoga Avenue Wheaton, IL 60187 6PM CT – 9:30PM CT Ticket Price $40 ($30 goes to the DuPage Co WTEA) events@wheatonparks.org 630-690-4880

Story shared by: Pastor Jeanette Jordan and family On Father’s Day, Bryan, Allison, Christa, Drew, and Edilah always celebrated the day by taking their dad, Dr. Robert “Bob” Jordan, to his favorite Soul Food restaurant. Sadly, Bob is living with Alzheimer’s disease and was recently moved into a memory care facility. The children who live nearby, Allison, Christa, and Edilah continue this tradition by picking up his favorite foods and bringing the restaurant to him. This Father’s Day he can expect to dine on fried chicken, fried green tomatoes, collard greens, succotash, potato salad, cornbread and of course his favorite, a slice of German Chocolate Cake! On July 29, 1962, 20-year-old Robert Andrew Jorden married the love of his life, Pastor Jeanette Jordan. Fifty-five years later the story of love and happiness, good times and bad, ups and downs, twists and turns, from poverty to prosperity had enough guiding light that it was turned into a published book “From Suspenders to Stethoscope…The Dr. Jordan Story.” This story was released on June 30, 2017, the day which was the last day of work for Robert A. Jordan, M.D., Pediatrician, a graduate of Rush Medical College, the first African American Chief Resident at Rush Presbyterian St. Luke’s Hospital, a well-known and respected physician who was known for the quality of patient care he gave to thousands of children during his time in practice. He believed that no matter what one’s socioeconomic orientation may be, ethnicity or gender, or religious affiliation – everyone deserved the best of healthcare. Yet this dedicated clinician had been diagnosed with dementia. It was in January 2014 that the family finally came out of denial and came to terms with what was going on with their dad and husband. The news was shared with his five children as well as his mother and sisters fear of what was later confirmed – he had dementia. The family became more observant of the changes in his behavior. “He would call me from his office two or three times a day to ask how my day was going and I would share with him what I was doing or had done but a few minutes later he would call again, and ask the exact same question. When I would say you just called me and asked me that, he would laugh and say, “Oh I was just kidding,” said Jeanette Jordan. Dr. Jordan was an avid golfer and would golf at least two to three times per week with his buddies or on his off days and special occasions. However, we began to notice his buddies stopped calling to include him in their golf outings. I eventually realized it was probably because he would interrupt the game when he couldn’t find his phone or misplaced his keys, everyone would have to go on the hunt only to find that his keys were in his pocket and/or his phone in the compartment of the golf cart. He stopped being excited about golfing together. His interest in reading the bible, which he loved to do, diminished. We were a physician-pastor team and our dialogue with one another about our passions was slowly coming to a halt. I would ask him to stop by the store on his way home from the office to get a loaf of bread, or pick salad fixings and would come with everything but. Around late 2015 his staff started calling me to ask if Dr. Jordan had come home for lunch because it was way past his lunch hour and he had not returned. He once called me to say he had gone to pick up lunch for the staff but he was confused and couldn’t find his way back to the office. He seemed scared and panicky, but I was able to direct him home using landmarks and street signs after about 30 minutes. I was taking care of my 86-year-old sister who was a double amputee, and he would ask the same questions about her condition over and over. In early 2016 I finally convinced him to let me make him an appointment to see our Primary Care Physician be evaluated for possible memory loss- he wasn’t happy with the suggestion and went hesitantly. My husband was so crafty that he convinced our doctor that nothing was wrong with him, but rather he was preoccupied. When the doctor suggested that he could do a memory loss assessment just to rule out what we suspected, Bob refused. I can remember leaving the office in dismay, frustrated not knowing what to do. The family began to watch his behavior even more closely. His routine of getting up at 7 a.m., showering, getting dressed, making and drinking a cup of coffee, and stopping by McDonald’s to get some oatmeal before going to the office began to change. He started sleeping later and later. His impeccable dress was a little off and it would take him forever to complete the dressing task; he was constantly misplacing his wallet or his phone or his keys. Every morning was a search for something that he had misplaced. When I located the item, he would fuss and say “who put it there?”. I notice that his demeanor was changing and he would get irritated often. He started to get up earlier to get ready for work, sometimes as early as 6 a.m. when office hours weren’t until 9 a.m., leaving him to pace back and forth until it was time to leave. He stopped calling his mother, I would have to remind him. He forgot that our daughter’s fiancé had flown in from California to ask him for our daughter’s hand in marriage. They had a long wonderful conversation and he gave his blessing. When the day came that she called to say they were on their way to get married, he became angry and claimed he’d never met the man. He began to take longer and longer to come home. As things got progressively worse, my children and I started preparing for Dr. Jordan’s retirement. We found a psychiatrist who convinced him to do a memory loss test and diagnosed him with Alzheimer’s. A second opinion confirmed this diagnosis. He was placed on medication, which he initially refused to take. We reduced his hours at his office, and my oldest daughter immediately pitched in by becoming the office administrator to help prepare for his retirement. He was resistant to retiring but we finally convinced him it was time to enjoy life outside of medicine, he was now 75 years old and God had given him the ability to practice 10 years beyond retirement age.