The Alzheimer’s Teacher Friday, Mar 10 2023 

Loving a spouse with dementia for decades comes with tremendous heartache. The treacherous path that must be tread requires steady, patient, and unstoppable footing as well as a thick skin. But through this journey, I also gained some wisdom.

Here are a few things I learned from loving a spouse with Alzheimer’s:

  • Faith, family, and friends can get us through everything.
  • Looking back with regret is pointless. 
  • Get as much rest as you can when you can.
  • Some days neither our spouse with dementia or we spousal caregivers make sense.
  • We don’t need the correct words to get our point across.
  • We’re all a little “off.”
  • Remain in the present moment. The past is over and whatever future we have will be our present. 
  • Slow down. What we are doing at a given time deserves our attention.
  • Skip the little worries and place the big ones in God’s hands.
  • Appreciate everything as if experiencing it for the first time.
  • No matter how far away someone is mentally, they can feel the love.
  • If this moment is troubling, believe there will be others that are better.
  • You can’t take care of anyone else if you don’t take care of yourself.
  • Forget the to-do list. Just do the next right thing.
  • There’s always something to cry about.
  • There’s always hope. New medicines, new therapies, and a new peace are ahead.
  • There’s always joy. Even in the worst of times something good is happening.
  • Don’t ignore all your blessings.

*I wrote a few books just for you. These books offer answers to your questions and comfort–Navigating Alzheimer’s, The Alzheimer’s Spouse, and Inspired Caregiving. (These books are also available on Amazon)

Love Them Where They Are Tuesday, Jan 3 2023 

Like sunshine

on an overcast day

rays of the man I knew

peek through the clouds

leaving me longing for more.

This poem sums up how we feel while living with a loved one with Alzheimer’s disease. Like a tease, we are shown moments of lucidity that briefly allow us to think all is well. Periodically, our loved one knows us, remembers our many adventures and shared life. Such moments quickly vanish and become less frequent as the disease progresses.

I wrote this poem for the opening page of my book, Navigating Alzheimer’s. My husband, Marshall, showed symptoms of Alzheimer’s during the last 15 years of our marriage. The heartache of witnessing the decline of his health and memories of our lives together continuously diminishing, in addition to the demands of around-the-clock caregiving, took its toll on my own mental and physical health. However, I learned while caring for him that loving and accepting him where he was at each point in time in the illness was important. Since, as of this writing, there is no way to reverse the disease, symptoms are progressive. Although today may be sad and difficult, tomorrow will likely be worse.

Live in the moment, enjoy the moment, alongside your loved one, wherever that takes you.

***Learn more about managing symptoms of Alzheimer’s and other dementias, as well as my experience, in the books The Alzheimer’s Spouse and Navigating Alzheimer’s. And please, if you have read either of these books, write a short review on Amazon.

Modified Holidays for Loved Ones with Dementia Monday, Nov 14 2022 

With the holidays approaching, all the fun and memorable events ahead present increased challenges for people with dementia. In addition, the darker days of fall and winter present other issues related to less sunshine. As many as 66% of people with dementia are thought to be affected by the setting of the sun. Beginning in the late afternoon, these people may show symptoms of confusion, anxiety, and aggression.

Families long for the traditions that mark the holidays. Special foods, music, colors, clothing, and decor shared with family and friends trigger emotions and tie memories of the past with the ones we make today. Sadly, our meaningful traditions are likely to be too much for our loved one with dementia. Including them can be more harmful and upsetting for them than enjoyable.

Brain power continues to diminish with dementias such as Alzheimer’s disease. Every level of stimulation we present to someone with this disease requires them to manage it with less and less ability. Think of all the stimulation we have this time of year–holiday lights; aromas from the kitchen; rich foods; and music, laughter, and multiple simultaneous conversations. This stimulation overload is exhausting for the healthiest people much less those already fatigued from daily living.

Maintaining a predictable routine with limited, controlled stimulation, and periodic rest periods is the key to keeping a person with mid-to-late-stage Alzheimer’s and other dementias calm. Parties that include our loved one with dementia are best limited to a handful of people at a time, close to or at home, in a quiet location, and for no more than two to three hours including travel time. Small group visits throughout the season rather than everyone at one time may be the best alternative.

Family members who do not spend much time with our loved one are not likely able to understand the change in traditions, or that our loved one may not be able to attend their festivities at all. However, celebrations with a loved one with Alzheimer’s is often more difficult for them than memorable or meaningful and therefore, need to be modified or completely abandoned. If we truly love them, the impact of our festivities on them and how we may include them in a way that is good for them rather than appeasing our emotional needs will be our priority.

**For additional guidance on living with loved ones with Alzheimer’s disease and other dementias, see Navigating Alzheimer’s, The Alzheimer’s Spouse, and Inspired Caregiving.

The Book of Which I’m Most Proud Tuesday, Jun 14 2022 

A question I’ve been asked over the years is which of the books that I’ve written is my favorite. This is a question that is as impossible to answer as which child is my favorite. Each book is special to me. I’m proud of all of all of them for different reasons.

Each was written with an intent to fill a need. Each book was sent out into the world with a mission to offer information and consolation to a particular audience. Most have won awards and sold consistently well over the years. And now I’m very excited about a new book coming out this year, which I will tell you about at the end of this post.

Mentoring Heroes was my first book. Published in 2000, this book centered on my recognition through newspaper articles I’d written that successful people attributed their progress to the mentors who helped them along the way. I also recognized that women’s lives are complicated and multi-layered with family, household, and work responsibilities, and therefore, more challenging in finding ways in which to be mentored. Mentoring Heroes was widely used in university Women Studies programs and by clubs and groups. Today, I know that the book is dated in the way that it was printed–with copper plates and blue-line editing as opposed to today’s digital print method–and due to men participating more in household responsibilities and technology offering more ways in which to be mentored. Yet, the overall benefits and need for mentoring remains relevant.

The Rosary Prayer by Prayer, Grieving with Mary, and Fatima at 100. Fatima Today were inspired by a devotion to the Virgin Mary. These were the types of books I wanted to write since childhood. Praying with Mary should always lead to a greater devotion to her son, Jesus. Mary is our heavenly mother, and like a good mother, she loves us dearly, promotes peace among all creation, and encourages us to care for one another as Jesus does. Praying with her offers a sense of calm in a world where this type of alliance is greatly needed.

With the The Rosary Prayer by Prayer readers can pray along simply by following pages showing the placement on the rosary, the prayer to be prayed, illustrations by Joseph Cannella, and a reflection. Grieving with Mary is a best-seller that aligns praying with Mary in a wide variety of ways during times of loss. And Fatima at 100. Fatima Today is a little booklet that reviews Mary’s messages in Fatima, Portugal in 1917 and how those messages remain vital in attaining peace.

Seven Principles of Sainthood Following Saint Mother Theodore Guerin and Saint Theodora and Her Promise to God are books about a woman who immigrated to the United States to teach children and young woman. Saint Mother Theodore Guerin, also known as Saint Theodora, and a small group of sisters opened schools throughout rural Indiana and Illinois in the mid to late 1800s, a time when Catholic schools were greatly needed and in which this band of women faced great obstacles. The sisters also opened a school for the higher education of women when women had little-to-no choice for such an opportunity. Seven Principles was written for adults and Saint Theodora and Her Promise to God was written for children. I was inspired to write these books after attending Saint Mary of the Woods College, the school Saint Mother Theodore founded, as well as her canonization in Rome, Italy.

Young in the Spirit was published in 2013 when I was closing in on one of those big decade birthdays (I was 60 in 2014-Yikes!). Big birthdays spark contemplation on where we came from, how we arrived at a particular point in time, and where we anticipate the future to bring us. One of the areas of contemplation for me was in regard to my faith—how it changed through the years and what I could offer the Church now. Those thoughts are at the heart of Young in the Spirit.

Hans Christian Andersen Illuminated by The Message was part of a series initiated by my publisher, Greg Pierce. The series offers a unique way to promote prayer by pairing Scripture verses with passages from classic writings. I chose Hans Christian Andersen in remembrance of my mother and her childhood book, a 1936 edition of Anderson’s Fairy Tales, the same book from which my mother read to me.

Navigating Alzheimer’s, The Alzheimer’s Spouse, and Inspired Caregiving was born from a need recognized by Pam Sebern, the director of a memory care home where my husband resided in his last years. Pam asked for books to help families understand dementia and better care for their loved ones while caring for themselves along the way. She felt that the books available at that time were too medical and needed a perspective from one who lived the experience. As my husband suffered from symptoms from Alzheimer’s disease for more than 15 years, and I was an author with substantial writing experience, Pam believed I could fulfill that need.

Navigating Alzheimer’s covers the basics of Alzheimer’s and ways in which we can work with our loved one. It offers family members and caregivers a clear overall of the changes they’re likely to notice. The Alzheimer’s Spouse also covers the basics of the disease but from the perspective of the spouse. Alzheimer’s touches every aspect of both spouses in devastating ways. Inspired Caregiving provides readers with a daily/weekly boost of inspiration. Each weekly reflection follows a rotation that includes a photo, prayer, thought, activity, stretch, affirmation, quote, and bit of humor to offer guidance, encouragement, improved self-talk, and maybe a smile. All three of these books are recommended by memory care facilities across the country.  

My next book, which currently is in publication, is less serious. I believe readers and I are in need of opportunities that promote peace, beauty, love, and inspiration. For this reason, my newest book, tentatively called The Gifts of Public Gardens, showcases vivid photos of nature that I have taken at public gardens paired with short, thoughtful poems. My intent is for readers to escape into the positive, wonderous gifts around us. I will keep you posted on when this book will be available.

If you’ve read any of my books, please post a review on Amazon. Readers rely on these comments to find books best suited to their needs.

The Battle of the Bath Thursday, Apr 7 2022 

Getting a loved one with later stages of dementia into the shower is like setting them up for torture. They can put up quite a fight over things we commonly do. We need a hefty dose of patience and compassion to move our loved one through the process.

Bathing is a necessary, albeit challenging, component of Alzheimer’s care. Not only do the people around us appreciate cleanliness, bathing aides in the prevention of rashes, skin disease, and urinary tract infections. We can reduce frequency to three times a week because skin tends to thin with age and illness. However, hands, face, and private parts should be kept clean throughout each day.

The reasons people with Alzheimer’s detest bathing are many. 

  • They no longer understand why they need to bathe.
  • The concept of time is lost, so it can feel as if they just took a bath.
  • The cleansing process is confusing and forgotten.
  • People with dementia cannot regulate body temperate very well, which makes them feel cold.
  • The sensation of the water on their body is uncomfortable.
  • And they may be embarrassed about being naked and needing assistance.

Reasoning with someone with Alzheimer’s is not possible. An argument is sure to develop if we try to explain why a bath is necessary. But there are a few things that can be done to make it a little easier and safer for both the caregiver and bather.

  • If your loved one is emphatically resisting stepping into the shower, let it go for an hour or so. Our loved one may be more agreeable if we try again at a later time.
  • Engage them in a story, perhaps with a topic they still like to talk about or sing a song while you undress them and escort them into the shower.
  • Offer a treat, such as potato chips, a cookie, or ice cream as a reward once the shower is over.
  • Provide a safe shower with a hand-held shower head, safety bars, non-slip flooring, and a seat or bench.
  • Ensure that the room and the water temperature is comfortable.
  • Offer a washcloth, toy, or fidget item for them to hold.
  • Speak softly, respectfully, and directly to help move things along.

My recommendation for everything we do while caring for our loved one is to consider health and safety for both our loved one and ourselves. When that health or safety is compromised for either of us, it’s time to think about additional or different support. I know the challenges and 24/7 responsibilities you’re experiencing. I’ve been through it myself, and I hold you close in prayer.

**You’ll find many helpful hints in books written with you in mind: Navigating Alzheimer’s, The Alzheimer’s Spouse and Inspired Caregiving.

Dreaming of the Dead Monday, Jan 27 2020 

The theory is that we can learn much about ourselves by analyzing our dreams. And although there are many suggestions as to what images mean, only we can know the true significance. What can be a terrifying symbol to one person can be reassuring to another.

Recurring dreams and topics are common. I often dream of babies. People give me their babies to hold, rock, feed, care for.

I also dream of the dead. I believe the “dreams” offer important messages from loved ones who have passed away. Sometimes, souls simply show up to say “Hello.” They are often smiling or even laughing, and I’m reassured to see them this way.

Lately, some of my dreams have a different twist. The dead truly are just that. In every appearance friends and relatives who are no longer physically walking this earth are dead in the dream. They tredge zombie-like, or not at all. They do not speak or react.

As I’ve written about in other posts, my husband, Marshall, passed away last March. I also speak and write about a fatal illness, hear stories of those who have the disease and are fading from this life, and learn of residents in memory care homes who are no longer with us. Perhaps, all of these factors contribute to my morbid dreams.

Or mayber there’s a deaper meaning. A typical interpretation of death is change, rebirth, or the need to get rid of dead weight. There have been many changes in my life over the past year, so perhaps this is the gist of these nigh visions.

Here are some of my latest ones.

  • I was walking up and down stairways in apartment buildings with Marshall. Dead Marshall. He walked but was silent, grey, and stumbled along. I had to guide and hold him up. – I believe I understand the significance of this dream as it occurred during a time I was considering a permanent home for his remains and where I would eventually join him.
  • I sat at a dinner table with the living and the dead, many dead. Most I recognized, and those who were deceased in my dream truly are gone. I was disturbed because when I’ve dreamed of them in the past, they looked alive and spoke to me but did not on this occasion.
  • In this dream, everyone was “alive.” My family was in a large home that was under massive renovation and we were selling. My parents, who passed away 20 years ago were there, and my cousin, Cathy, who also is deceased, walked in with another cousin. Cathy was beautiful, happy, and it was wonderful to see her.
  • My mother suggested that I drive her turquoise car around the corner to go to school. After class, I returned to the parking lot to discover that her car was missing. I was so upset that I borrowed her car when I could have walked and now it was gone. But my mother didn’t care at all since she never used it. In fact, my mother never did drive when she was alive. — Maybe my mother is encouraging me to get rid of more things that no longer have a use.

If you like analyzing dreams, I’m interested in your thoughts. What do you think they indicate, and what are some of your recurring dreams? I’d love to hear from you.

***

Did you see my last post on my other blog, Sacred Water?

You can see all my posts, random thoughts, and presentation dates on my author Facebook page.

Looking Behind to Look Ahead Monday, Dec 30 2019 

Last year my resolution was to be healthy. I ended up in the hospital right off the bat the second week of January. So, I hesitate to try this resolution thing again.

Statistics say that about half of all adults make New Year’s resolutions. The new year, and new decade, offers us an opportunity to assess where we are and where we want to go, as well as the person we want to be. However, fewer than 10% keep these goals for more than a few months.

The most common resolutions in 2019 were to diet, exercise, lose weight, and save money. Most said that keeping those resolutions, especially in relation to dieting, were difficult to keep.

Psychologists note that the best way to honor a resolution is to make a realistic goal. A small step is more likely to be reached than aiming far beyond what is possible. Their guideline is to be SMART: specific, measurable, achievable, realistic, and time-bound.

2019 certainly was not the most difficult year I’ve ever experienced, but it certainly was intense. After 15 years of watching Alzheimer’s disease devour my husband, Marshall, he passed away in March. Although still greatly saddened by what was robbed from us, I’m at peace holding on to the love he showed me and my children and knowing that he is playing tricks in heaven with way too many other loved ones. This year alone, another dozen friends and family members in addition to Marshall crossed the threshold into eternal life.

No matter how difficult or sad life can be, it also offers us occasions to celebrate. 2019 was no different. I attended three joyful weddings, including Disney’s Rapunzel and Flint at Blackberry Farm, and a 50th and a 40th wedding anniversary.

Work was fabulous. I had the privilege of meeting with other family members dealing with Alzheimer’s disease through 19 presentations across the country. In addition, my 10th book, The Alzheimer’s Spouse, was published, and is selling phenomenally well.

Updating on my townhouse continued, and I’m loving living here. Thanks to my son, Joe, the laundry room and guest bathroom had complete makeovers; stairway railings, powder room cabinets, my bedroom and bedroom furniture, and guest bedroom were painted; and major work was done on my garage.

Frequent Flyer miles built up this year, and the travel wasn’t only for business. My daughter, Lisa, and I went on a memorable pilgrimage with her church. We traveled through Israel and Italy sparking our faith to new heights.

And our timing was perfect. Soon after our return, Israel saw some unrest and Venice flooded. The places and people challenged by these troubles touch our hearts so much more now since connecting with them. We hold all of them close in prayer.

My personal life also took an unexpected turn when a friend become more than a friend this year. Paul and I met when our spouses resided in the same memory care home. We supported each other through some of the agony Alzheimer’s presents spouses and are now enjoying making new, loving memories together.

I can’t imagine the new year will have as many changes as this past one. All I know is that it’s ending significantly happier and more peacefully than it began. And that is my goal, rather than resolution, for 2020 and beyond.

Here’s to a peaceful, happy 2020!

***

Please join me at my next presentations in New Jersey:

Tuesday, January 21, 2020, “The Alzheimer’s Spouse,” 5:30 p.m. – 6:00 p.m. Registration and Dinner, 6:00 p.m. – 7:00 p.m. Seminar, Arden Courts of West Orange, 510 Prospect Avenue, West Orange, NJ  07052, 973.736.3100

Wednesday, January 22, 2020, “Navigating Alzheimer’s as the Family Caregiver, 5:30 p.m. – 6:00 p.m. Registration, 6:00 p.m. – 7:00 p.m. Seminar
Arden Courts of Whippany, 18 Eden Lane, Whippany, NJ 07981, 973.581.1800

Thursday, January 23, 2020, “Navigating Alzheimer’s as the Family Caregiver,” 5:30 p.m. – 6:00 p.m. Registration, 6:00 p.m. – 7:00 p.m. Seminar, Arden Courts of Wayne, 800 Hamburg Turnpike, Wayne, NJ  07470, 973.942.5600

Singing the Holiday Blues Monday, Dec 2 2019 

I thought it would be easier this year. Yes, my husband, Marshall, only passed away less than nine months ago, but this was my fifth year without him at Thanksgiving dinner, and I am at peace knowing that Alzheimer’s has released him into the hands of the Lord. Yet, at the end of Thanksgiving Day, I was still depressed.

As my friend, David, who just lost his wife to Alzheimer’s, said to me, no matter how we fill our days, the evenings are sad and lonely. I’ve noticed that the last few years have been like that. I’m more depressed after being with loved ones and returning home.

Keeping busy and social are important elements in preventing getting stuck in the muck of holiday depression. We need to do things that bring us joy. And at the end of the day, especially the most difficult ones, ease the loneliness with uplifting music, movies/tv/reading, and friends.

I’m fortunate to have people who help me through. My friend, Paul, insisted on coming over on Friday to watch a silly Christmas movie. He knew a cure for loss was company and humor. And then, my son and his girlfriend visited yesterday.

Remember, that although missing our loved ones, especially around the holidays never fully disappears, it does get easier. As my psychologist friend, Sue, says, it becomes a different kind of, more bearable mourning. My mother passed away in 1999, and I especially long for her while baking during the holidays. It’s not the heart-wrenching type of pain of the past, but more like a missing part of the puzzle of tradition and a gratitude for having those experiences at all.

May all your memories of passed loved ones bring a smile to your face and a warmth to your heart this holiday season.

***

If you’re in the area, please join me for my last presentation of the year. “The Alzheimer’s Spouse,” will be from 1:00 p.m. – 2:30 p.m. on Thursday, December 5, 2019 at The Inter-Faith Chapel at Leisure World, 3680 S. Leisure World Boulevard, Silver Spring, MD 20906. For reservations, please call Julie Boone Roth, 301.847.3051.

***

The Alzheimer’s Spouse is available from Amazon.com and ACTA Publications.comNavigating Alzheimer’s is also available from Amazon and ACTA.

***

Do you follow my other blog, Midwest Mary, or my author Facebook page?

Now Appearing in Heaven Saturday, Mar 9 2019 

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We who believe in a loving God and the gift of everlasting life, rejoice in death. In our hearts, we know our loved one is at peace in the midst of the Light. We mourn the passing of one we’d prefer with us in this world but this belief does bring comfort in our loss.

My husband, Marshall Brodien (84) of Geneva, passed away peacefully early morning on March 8, 2019. He was surrounded by family in his last days, and I only left his side to shower (which the rest of the family appreciated.) Most of the week, I held his hand. In his last hours I sat beside him with my head on his pillow, holding both of his hands, and listening to his last breaths.

Hospice educated me on the signs of passing which became increasingly more evident with every minute. As his hands grew colder, I prayed the rosary and spoke to God and to Marshall. His breaths gently faded, he squeezed my hands, and I felt his spirit leave the body.

Twenty five years ago when I first told my mother about Marshall she was concerned about the 20 years age difference between us. I assured my mom that Marshall was a gentleman, and she soon realized his kindness for herself.

Marshall’s public persona meant that he belonged to the public. Loved ones had to share him with fans everywhere we went. His attention often was elsewhere.

However, Marshall made me feel loved every day of our marriage. He called me “My Mary” and “The love of his life.” He didn’t hesitate to publicly say, “I love that girl.” I never doubted I was in his heart and greatly appreciated the joy he brought to me and my children.

Marshall may be best known for creating the Marshall Brodien Magic sets and TV magic cards with his famous tagline, “Magic is easy, once you know the Secret.” He’s also fondly remembered as the magical, wacky character Wizzo on Chicago’s Bozo Show for 26 years. Marshall, aka Wizzo, would wave his stone of Zanzibar and say the magic words, “Do-dee-do-dee-do.”

Marshall’s rich life began in Chicago with his loving mother, Mildred, Father Arthur, and brother, Charles. At the age of eight, a female magician entertained at his school. He soon became hooked and put on his own shows for family and friends. He later became a side-show barker at Riverview Park.

He was drafted into the army in 1957 and commissioned to the Special Services Entertainment Division at Fort Carson, Colorado. He performed more than 700 shows at hospitals, officer clubs, and private parties over his two years in the military.

Marshall continued entertaining by performing magic and stage hypnosis at lounges, clubs, and county fairs as well working as a trade show spokesperson for corporations such as Owens-Corning Fiberglass, Bethlehem Steel, Reynolds Aluminum, and the American Gas Association.

Marshall showed symptoms of Alzheimer’s disease disruptive to daily life since 2004. I cared for him at home for ten years and he lived in managed care for almost another five.

In addition to me, Marshall is survived by his three children, three step-children, nine grandchildren, four step-grandchildren, and one great-grandchild. There also is one more on the way. He was preceded in death by his daughter, Christine, who passed away in 2016, and his brother, Charles.

Donations can be made in his name to Arden Courts of Geneva (2388 Bricher Road, Geneva, IL 60134), Heartland Hospice (1010 Executive Drive, Suite 200, Westmont, IL 60559), or the Alzheimer’s Association (225 Michigan Ave, Fl 17, Chicago, IL 60601).

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Marshall Brodien Day Tuesday, Jul 10 2018 

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