My relationship with the Alzheimer’s Association began in 2010. I was invited to attend the very first Reason to Hope luncheon in Chicago, honoring WGN Radio legend, Wally Phillips and his family. At the time, I was the General Manager of WGN-TV and attended as both a representative of the WGN/Tribune family and my own family – as my Dad, Cliff had already been diagnosed with Alzheimer’s. This Reason to Hope luncheon was where I first learned of the critical mission of the Alzheimer’s Association and how they were working to provide resources, education and hope to families affected by Alzheimer’s and dementia. I left that very first Reason to Hope luncheon newly inspired and hopeful for the future, for families like mine.
I was also impressed by the overall effectiveness and efficiency of the luncheon – in just one hour, Reason to Hope had changed my view of Alzheimer’s and inspired me to become a bigger part of the mission. I knew immediately that Reason To Hope was an event and an experience that I wanted to share with others in order to do my part to help raise awareness for Alzheimer’s.
In 2011, I became a Reason to Hope Table Host and invited friends and family to join me. The following year, 2012, I chaired the Reason to Hope Chicago luncheon and shared my Dad’s story with the Reason to Hope community. I have and will continue to support Reason to Hope through the years as a Table Host. Last year in 2019 and now again in 2020, I am proud to be Co-Chair of the Reason to Hope Chicago luncheon.
The first time I attended Reason to Hope it was clear that I was now a part of a bigger community through the Alzheimer’s Association. Through the years I have seen Reason to Hope grow through the dedication and expanding roster of Reason to Hope Table Hosts.
When our Table Hosts invite their friends, family, co-workers, colleagues – they help create and grow this community within Reason To Hope – a community that shares the common goal of a world without Alzheimer’s.
In addition to Reason to Hope, I have embarked on several other endeavors as a part of my fight against Alzheimer’s. I have participated in the Walk to End Alzheimer’s in Chicago with my family in honor of my Dad and his caregivers. I also participated in the Alzheimer’s Association family forum education program, and caregiver support groups. As a representative of the Illinois Broadcasters Association I have partnered with the Alzheimer’s Association to promote the Silver Search program to protect endangered missing persons through a state wide awareness campaign. I currently serve on the Silver Search Task Force and have most recently joined Illinois Women Conquer ALZ.
What gives me a reason to hope is the mission and strategy of the Alzheimer’s Association. As the world’s leading voluntary health organization, funding Alzheimer’s care, support, advocacy and research gives me HOPE!
I have benefited from the Alzheimer’s Association mission, I have embraced the mission, and will continue to participate in the mission by raising awareness and funds to help achieve the goal of a world without Alzheimer’s!
If you want to become a part of the fight against Alzheimer’s, join us at our virtual Reason to Hope event on Tuesday, November 10 at 12 p.m. CT! Learn about the mission of the Alzheimer’s Association and embrace the Reason to Hope community.
Or if you cannot join us this year, go online and donate to the Alzheimer’s Association Reason to Hope.
Jackie Marco is a Walk to End Alzheimer’s Volunteer from Sandwich, Illinois. She has raised over $4,000 in support of the Walk to End Alzheimer’s over the course of two years. She is currently employed at Financial Plus Credit Union in Ottawa, Illinois. She comes from a family of farmers, owning over 800 acres of farmland with her siblings and father. Her connections across the community make Jackie an impactful leader for the Walk to End Alzheimer’s Illinois Valley. To learn more about getting involved with Walk to End Alzheimer’s, click here.
“I am 22 years old and currently live in Sandwich, Illinois. I work in the banking industry as well as help on my family’s farms. Pictured is myself in the middle along with my parents Jeff & Patty. I have one fur baby Lizzy who is a purebred Border Collie. I got involved with the Illinois Valley Walk two years ago.
This is something that hits very close to home for me. All three of my grandparents who I grew up with have battled Alzheimer’s. I lost my grandma (my mom’s mom) in August of 2018, my grandpa (dad’s dad) in August of 2019 and most recently my other grandma (dad’s mom) in January of 2020. It had been very hard to watch all of them go through and battle this horrible disease. With the help of our families and a live-in full-time caretaker, we were able to care for all three of them and keep them in their homes. Having been through all of this and now losing all of them makes this walk mean so much more to me.
I do believe that one day there will be a cure. I am so excited to play a role in planning and putting this walk together this year and cannot wait to work with everyone!”
Claudia Amador is a volunteer support group facilitator for the Alzheimer’s Association Illinois Chapter. A support group is a regularly scheduled in-person or virtual gathering of people with Alzheimer’s disease or another dementia, family, friends or caregivers who interact around issues relating to dementia. Groups can have social, educational and/or support components and are facilitated by individuals who have received training from the Alzheimer’s Association. Find a support group near you here: Illinois Chapter Support Groups.
Claudia Amador’s connection with Alzheimer’s started with her work as a neurologist in her home country of Honduras. One day a colleague approached Claudia about starting a memory clinic in the hospital. She knew starting a memory clinic would be a good opportunity to educate herself and others, and understand memory loss. For four years she ran a memory clinic in Honduras evaluating patients with memory loss, meeting with caregivers, coordinating neurocognitive tests, and running educational seminars for the population. Through this experience, she became very familiar with Alzheimer’s and dementia and grew a passion for sharing her knowledge with others. “For that reason, it’s important to be a part of the Alzheimer’s Association because I share the same vision and mission.”
Claudia’s involvement with the Alzheimer’s Association has spread across different initiatives, allowing her to help serve the mission in many ways. She started off volunteering at the Chicago Walk to End Alzheimer’s for two years, followed by six months as a volunteer working for our 24/7 Helpline. Now Claudia serves as a support group facilitator, guiding those who are struggling to navigate the effects of Alzheimer’s and all other dementia.
Claudia values the relationships she forms with support group participants because she sees the uplifting nature of sharing experiences with others. Claudia notes that her time as a volunteer support group facilitator has shown her how many people do not have enough knowledge of the disease that drives the impetus for action. In her groups, participants have a desire to learn just as much as they do to share. The supportive, bonded nature of the groups creates a cycle of knowledge sharing and encouragement. Facilitators like Claudia are important parts of guiding such strong foundations for successful support groups.
When she’s not volunteering, Claudia enjoys spending time with her mother and son. They enjoy walks outside in the Spring and Summer, as well as good conversation over delicious meals. Her favorite movies are foreign films and comedies that she can enjoy with her family.
The health and safety of our volunteers, staff and all of our constituents are our top priority as we continue to pursue our mission. Given the evolving nature of COVID-19 and based on the guidance from the Illinois Department of Public Health and the CDC, Unforgettable Art originally planned for April 25 will be rescheduled.
Unforgettable Art is an annual event put on by the Alzheimer’s Association Illinois Chapter. A lively evening filled with creativity, artists convert blank canvases into beautiful works of art in front of your eyes. Featuring live music, appetizers and drinks, there is no shortage of entertainment making this evening truly unforgettable. The artists donate their time and talents for this event, ending with a live auction of all artwork. Proceeds benefit research, advocacy and resources for those affected by Alzheimer’s and dementia. To showcase these wonderful and dedicated creators we are featuring two Unforgettable Artist Spotlights, father-daughter duo Randy and Rhya Reed!
Randy and Rhya Reed are a father-daughter artistic duo who will be creating live work for this year’s Unforgettable Art. Randy has been with the event for all seventeen years, making him a veteran of the event. The two have crossed over many mediums in their artistic careers, including painting on wood, canvas, glass, drawing, and even tattoos.
Randy’s inspiration stemmed from watching his father draw when he was young. “Life in art started when I was a kid and would watch my dad draw horses and cars with circles. I picked up a pencil and just started creating, and drawing on everything.” Randy’s imagination was fed by his desire to create something different across mediums, a trait he passed down to his daughter Rhya.
Randy’s artwork continues to vary over the years as he draws inspiration from new and different observations. From paintings in black and white to undersea mammals with mermaids alongside them, Randy’s creative inspiration knows no limits. He has also worked in portraiture, airbrushing, caricatures, murals, and he even painted the background for Jane the Dinosaur at the Burpee Museum of Natural History in Rockford, IL. “I guess my specialty is to keep people guessing.”
Rhya’s artistic career initiated the same way her father’s did- through watching him create. She would observe as he painted or drew, every time creating something new and different. She started drawing small comics, which developed into tattoo design using markers and colored pencils. “When I was about eighteen my dad bought me my first set of brushes and canvases so I could express my creativity in a new way. I couldn’t be more thankful for having that push to continue my art.”
Randy and Rhya’s connection to Unforgettable Art emanates from their beloved Grandmother and Stepmother, Joyce Reed. Joyce was diagnosed with Alzheimer’s several years ago and the family has had to adjust to properly caring for and supporting such a beautiful and loving soul. Art has helped them to honor her- “Art has become a big part of me because it was there during dark times in my life,” says Rhya. Not only does their participation in Unforgettable Art allow them to convey their experience through creation, it also directly supports research, advocacy, and care for those affected by Alzheimer’s.
Jessica Nazario lives in St. Charles, Illinois with her husband Mark and four children- Rian, Alex, Max, and Mason. After moving around the country for Mark’s job, St. Charles finally became home. Jessica was raised in Pullman, Washington by her parents Dr. Beth Waddel and Dr. Bill Condon. Growing up, Jessica and her sister referred to their mother as “Kid Mom” due to her playful nature. She was always coming up with creative entertainment for her girls- from dance parties to Sunday Night Beauty Shop (face masks and nail painting paired with a good movie). Jessica was inspired by watching her mother conquer a PhD while having elementary aged children, and working full time as a psychologist while continuing to live up to the distinguished title of “Kid Mom”.
As a grandparent, Beth maintains the same personality and flare when spending time with her grandchildren. Beth is the master of knowing how to meet the kids where they are – both mentally and physically. As infants, she would cuddle and hold them close. When they grew into toddler age, you could find Beth lying on the ground rolling around alongside them. Once they started getting even older, she created unique clubs for each of the kids to join in on for adventures. The older grandkids titled their club “Sneaky Thieves”, while “Sneaky Ninjas” was suited for the younger ones. The goal of the clubs was to engage in their escapades without the parents knowing. For example, stealing a cake from the kitchen and escaping to the tent out back to eat it in secrecy. Once some of her grandchildren reached their teenage years, Beth downloaded Snapchat. Though it may have been to her chagrin, Beth knew it was one of the best ways to stay in communication with her grandkids.
Jessica and her sister first noted some signs of memory loss in their mother two years ago. Jessica described them as “that was weird” moments. Without much understanding behind the forgetfulness, Jessica and her sister noted the instances as being unusual but had little further explanation of what was going on. As these moments became more frequent, Beth sought medical care and was diagnosed with Mild Cognitive Impairment. Just last month, this diagnosis was advanced to Alzheimer’s disease. Jessica has since taken initiative to access all the resources and support she can get her hands on. From webinars and support programs for her father as a caregiver, to creating a Walk To End Alzheimer’s team.
Jessica’s sons have also taken matters into their own hands. Her youngest boys, Max and Mason, decided to start a fundraiser online to sell bracelets. The bracelets read “Be Strong, Be Brave” and the boys sell them to support their grandmother. “We started the fundraiser because we know people are trying to find a cure for Alzheimer’s, but need money to do it. We wanted to help, because we felt sad about Grams,” says 10-year-old Max. “I came up with the bracelet idea because I’ve seen it used for other causes. We picked purple because it’s the color for Alzheimer’s, and the quote ‘Be Strong. Be Brave.’ just came into my head.”
The boys have already raised a sizable amount of money to support Alzheimer’s care, support and research thanks to the boundless support from friends and family. “I didn’t feel like I was too young to do a fundraiser. I mean, I am only eight, but anyone can do anything,” says Mason.
Jessica, Mark and their children take on this battle with Beth’s wise words in mind. One of Beth’s favorite stories to tell Jessica growing up was about a little boy waking up on Christmas morning to horse manure under the tree in lieu of gifts. The little boy was not discouraged, instead, he began shoveling the manure exclaiming “With all this manure, there must be a pony somewhere!” With that, Jessica and her family try to live life always digging for the pony. Beth also frequently used the words “joy” and “perseverance” in day to day life, and so Jessica’s family takes on this new challenge with joyful perseverance. Getting involved with the Alzheimer’s Association is this family’s way of honoring their loving grandmother and supporting the fight to end Alzheimer’s.
I married the love of my life, Robert Andrew Jordan, on July 29, 1962. He was twenty and I was seventeen. Fifty-five years later our 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 June 30, 2017, the day which was the last day of work for my husband, Robert A. Jordan, M.D., the pediatrician, a graduate from 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, or 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 of 2014 that I finally came out of denial and came to terms with what was going on with my husband. I shared with our five children as well as Bob’smother and sisters my fear of what was later confirmed – he had dementia. I 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 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.” He 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, I 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 our 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 to 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.
I began to watch his behavior even more closely. His routine of getting up at 7 am, showering, getting dressed, making and drinking a cup of coffee, 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 am 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 fiance 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, 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.
July 3, 2017 was the first day of retirement for Dr. Jordan. On that day he got up early,got dressed in his suit and tie, put on his lab jacket, and began searching high and low for his stethoscope and car keys. On that day my duties as a caregiver began. Trying to get him to understand that he no longer had to go to work was a daily struggle. He was concerned with how we were going to survive, eat, and pay bills. This question went on all day practically every day. I eventually had to go write out our income sources and put it in his wallet so that he could visually see the numbers and understand for a short period of time that we were going to be alright. We had to move from our home which was now much to big for me to handle and seemed to be a trigger for his unhappiness. Not being able to drive the car that sat in the garage made him angry, not being able to go to the office to care for the children confused him. I was becoming frustrated, angry and confused. I hadn’t experienced or know anyone suffering from this disease and had no point of reference. I cried daily. My children insisted that I connect with a support group, so I started with the support group at South Suburban Hospital in Hazelcrest, IL, I then reached out to the Alzheimer’s Association of Illinois. After having attended an Alzheimer’s Association forum at Palos Hospital in Palos, Illinois where I shared my story I was asked if I would be interested in volunteering as a caregiver speaker for the Association and I gladly did so. I also- signed up to become a participant in the Emory University Tele-Savvy Caregiver Program which is a training program for caregivers. I needed to know all there was to know about being an informed caregiver, I knew how to be a wife but now I needed to know as a wife how to be a good caregiver for my husband. I’ve learned that I’m more than a caregiver, I am a clinician for my husband.
This journey has touched my heart so deeply that I now have a need and calling to be an advocate, not just for my husband, but for all who are affected by this disease. My husband as well as all who suffer deserve to be cared for with respect, dignity, honor and a deeper kind of love. Even though my plans were to care for him at home till death would separate us, my children and I had to make the dreaded decision in October of 2019 to place Dr. Robert A. Jordan in a long term care facility. He had begun to wander off, once having to be found by the police and brought back home. That was the most frightening day of my life. Then he was becoming aggressive toward me, my daughter and nephew; he was extremely agitated and depressed. In his new community he has become very calm and more social with the other residents. I find solace in sharing what I’m learning and experiencing every day.
One key I have learned is that self-care is most important. If I’m not healthy, I can’t see to it that my husband is cared for properly. During the time I was caring for my husband at home I was anxious, tired, short-fused, crying daily and suffering sleepless nights. I needed to share my feelings with someone who wouldn’t judge or criticize how I was feeling, so my children encouraged me to see a therapist. This was the best decision I could have made because she help me to work through my feelings of fear and frustrations by focusing on self-care. I gave myself permission to enjoy my life through spiritual disciplines, outings with friends, or enjoying free time with recreational activities. I have been blessed with an awesome support team, my daughters, my church family, my Nephew, my God Son together with his daughter and Dr Jordan’s colleagues who visit him often. My two children who live out of state come to surprise their Dad and I as often as they can, but with today’s technology we FaceTime them when we visit.
This support team allows me the flexibility to take trips to see my children and grandchildren who live out of state or to just do a getaway! I’m thankful for my support groups, the friends who have not abandoned us, my children who are the best, my colleagues, Bob’s colleagues, Bob’s agency caregiver, who still visits him, my church family and the support goes on and on. The vows we took 57 years ago have even more meaning to me now, “for better or worse, for richer or poorer, in sickness and in health we’ll be one till death parts us!”
Marisa Breese is one of the Junior Board’s newest members who worked to help put on their largest annual event, Paint the Night Purple. The evening was packed with activities- from appetizers and an open bar, live music, silent auction, raffles, and dancing! This night was a huge success and helps inform the Junior Board on ideas for next year’s event.
Marisa works in Public Relations for an agency in Chicago, has a 5-year-old Shepherd Collie mix named Harlow, and is a PADI certified open water scuba diver. When she isn’t spending time with her friends, playing volleyball, or traveling, Marisa is an active volunteer for the Junior Board.
“Hi, I’m Marisa! I first started volunteering alongside the Junior Board in February 2019 after looking up ways to get involved with advocacy and fundraising efforts related to Alzheimer’s. On my first outing with the Junior Board, we visited Sunrise Lincoln Park – a senior living community that specializes in memory care. We chatted casually with the residents, and another Junior Board member brought art supplies to create Valentine’s Day cards. Even though we were there for only a short time, I really enjoyed being able to have a positive impact on the residents.
I was inspired to find a group like this because I felt a personal connection to the cause. My maternal grandmother, Margot Gardiner (Gramma to me) is currently living with the disease. She was diagnosed with Alzheimer’s in 2017. At the time, there were only hints of the disease – she would misplace items or forget conversations. Treatment has helped keep the disease somewhat under control, but I still see a difference in her mannerisms and how she interacts with our family now. She’s always been the best grandparent – she used to be an amazing cook and seamstress, and she and my Papa (who’s taken on new roles to care for her) still try to attend every choir show, dance recital, sporting event, etc. that my cousins and I have been part of. It’s definitely been difficult for us to watch her gradually change, though, because of this awful disease. Her diagnosis is what prompted me to get involved with the Junior Board.
I’ve really enjoyed my time with the Junior Board over the past year. In the past year, I’ve had the pleasure of meeting other young professionals who all have a connection to this terrible disease, so we’re all very passionate about making an impact. So far, I’ve had the opportunity to volunteer several times at Sunrise Lincoln Park and once at Memory Rock Chicago (an annual fundraising event), and I joined the Junior Board’s Walk to End Alzheimer’s team this past October.
I was so excited to officially attend our Paint the Night Purple gala for the first time this year! I worked at the coat check as a volunteer last year, so this year was a chance to spend time with friends, family, and fellow Junior Board members at the event.”
Interested in our Junior Board? To submit an application, visit here.
Paint The Night Purple is an annual winter fundraiser hosted by the Alzheimer’s Association Junior Board. Through the dedicated efforts of our Planning Committee, the event brings together young professionals from across Chicago for an unforgettable evening featuring an open bar and lavish hors-d’oeuvres, a silent auction, raffle, and live entertainment.
More than 1,000 Chicagoans come out each year and this event has quickly become the Junior Board’s largest and longest running fundraiser. Paint the Night Purple 2020 is on the horizon, and in honor of that we are featuring one of our newest dedicated Junior Board members, Joe Barron. Joe lives in Glen Ellyn with his wife Lauren, daughter Emery and two Vizlas, Gipper and Rudy.
“Hi! I’m Joe Barron, ALZ Junior Board member since 2018. I’m truly honored to be a part of this wonderful group of people to help find a cure for Alzheimer’s. Both of my grandmothers passed away from Alzheimer’s with one of them having lived with it for over 10 years. I now fight in their honor and for a future without Alzheimer’s.
In 2017, my wife and I started a board game company, Gray Matters Games, which donates a meaningful portion of profits to Alzheimer’s research. The last two years Gray Matters has been a sponsor for Paint The Night Purple and donated our entire line of games to the silent auction. Gray Matters also holds an annual Longest Day event of playing board games! Last year the event was held at Fair Game store in La Grange and raised over $3,000 for the Alzheimer’s Association. Nothing beats having a ton of fun while raising money for an amazing cause!
My favorite memory of PTNP has been dancing the night away the past two years to The Boy Night Band. My friends and I that attended PTNP were in high school when most of that music came out, so it felt like we were back at prom!”
This will be my fourth Paint the Night Purple event I am attending as a board member. This event is so special to me because it is an opportunity to pay tribute to my loved ones who are, or were, affected by Alzheimer’s.
I got involved in this cause originally because of my grandmother on my father’s side. She passed away from Alzheimer’s when I was only 8 years old. Being so young, I was so confused by Alzheimer’s and dementia in general. I couldn’t understand how someone could not know or remember who you are, especially their own children and grandchildren. It was very traumatizing to me and extremely upsetting to our whole family. Even years later my family on my father’s side hasn’t quite been the same. I will never forget the way I felt after visiting my grandmother, we called her Nanny, shortly before she passed, and that was the main reason I vowed to one day get involved in this cause- not only to better understand it, but to help find a treatment or prevention to one day end this awful heart-wrenching disease.
Within this past year, my grandmother on my mother’s side has taken a turn for the worse. She has trouble remembering things, and it seems to be getting progressively worse. As she lives in Ohio and I’m in Chicago, I don’t get to see her as often as I’d like, but every time I go home I make sure to see her and my grandfather and help them with getting groceries, cleaning, or driving them to doctor’s appointments – whatever is needed.
I participate in the Junior Board and with this event because it’s one positive side of all this gloom and heartbreak. It’s also the biggest event the Junior Board puts on and our big night to raise funds for the Alzheimer’s Association Illinois Chapter, which goes to research and finding a cure to end Alzheimer’s once and for all.
I love PTNP because it’s a seamless event. Everyone who has a hand in this event is so impressive and so hard working, and no one is doing it for the credit, but rather because this cause means so much to them and they want to do their part. Each and every year I’m more impressed by the event and so thankful to be a part of it. I’ve convinced many friends and colleagues to attend and each and every one of them has said they look forward to attending next year’s event and that they can’t wait. It’s also a fun excuse to dress up and drink champagne, while also doing good and giving back to the community.