Dementia is a slow, persistent, odd mixture of impaired undoing and living.

Doug and coffee were synonymous! There was even a time he momentarily romanticized he could be a coffee connoisseur. He took his coffee seriously and took people to enjoy a cup before going to coffee was a thing. Doug even worked a very short stent at Starbucks, but that’s a different story for another day. 

We had a fancy coffee maker, a bean grinder, and a French Press. Doug loved his morning brew routine, enjoyed a coffee break in the afternoon, and always looked forward to sharing a cup with a friend at the newest up-and-coming (or hole-in-the-wall) coffee shop.

He insisted that making a good cup of coffee is a delicate, sophisticated process. First, he would say, it involved grinding the beans to the ideal texture for the expert smooth taste. Then it required using the correct amount of water (filtered if possible) at the appropriate temperature. And finally, after completing the brewing process to perfection, which I guess is a thing all by itself (Doug would say this is when you can ruin all deliciousness), a good morning aromatic sip necessitated the right coffee mug. So, Doug collected assorted mugs from his many travels, each with its own story.

Dementia has undone Doug’s ability to make coffee and care about it. This reversing wasn’t sudden or abrupt, like an epiphany or a surprise. Instead, it happened slowly, in steps, in phases, as if his coffee knowledge and passion gradually leaked out and evaporated into unlearning. 

At first, he struggled with the order of the steps he used, but he muddled through, sometimes remembering and making coffee seamlessly, and other times baffled by the clunkiness of his ability. Then grinding the beans all by itself became problematic, so he occasionally purchased ground coffee beans to have in case the bean grinder was impossibly uncooperative. He eventually scrapped the fancy coffee maker and the bean grinder altogether and used the French Press exclusively. It was more straightforward, especially when using pre-ground beans and a hot water tap. But even that became unworkable eventually.

Doug is, most of the time, entirely apathetic about coffee now. The preparation has become too complicated, so he no longer makes it; I do. I use a simplistic coffee maker with pre-ground coffee beans, water, and a basic push-button start. I set his coffee at the breakfast table in what I think is a favorite mug. He doesn’t seem to care, sometimes he drinks it, and sometimes he doesn’t, but he always says thank you.

The early signs of Doug’s coffee confusion eluded me due to patchy inconsistencies. I would justify the confusion as tiredness or stress, not realizing brain change was well underway. I didn’t catch on until much later in the dementia process when the confusion became consistent and prominent enough that I could not miss it.

Since then, I have learned. I now know the dementia digression of any task always starts the same way. The slow, awkward undoing with a light bulb of coherency here and there is classic – two steps forward, one back, two steps forward, two back, two steps backward, one forward until backward eventually wins the war.

Doug’s executive functioning (step-by-step cognition) was where his early hiccups of dementia were first noticed, like in brewing coffee, keeping his golf score, driving a car, and playing cards. He is now in the later stage of the disease, meaning brain change is more global and simultaneously affects numerous regions. For example, the information his brain catches from his eyesight is progressively changing. I took him to an Ophthalmologist, thinking he needed glasses, but his vision was fine according to the eye tests; he did not need glasses. Still, he struggles with depth perception, peripheral vision, and even sometimes seeing what’s directly in front of him, like the spaghetti on his plate or the pillow on his bed. The parts of his brain that interpret his visual world are weakening, affecting many things like making the bed, eating a meal, buckling his seatbelt, or navigating up or down a curb.

Think about how you respond to what you see, trusting that your visual interpretation is accurate. Now consider how you would navigate your world if your brain did not accurately interpret what you see. It’s crazy confusing to consider Doug’s reality this way. Even crazier is his unawareness of the misinterpretations.

Dementia is a long slow road of persistent defeating brain change with intermittent coherent periods woven in, making much of it confusing and exhausting for both the person and the one helping. It is not like Doug does something without mistake one day, and the next day he is completely incapable. It’s more like this. Last year at this time, Doug made his bed religiously as he always did, every morning without a wrinkle; you could bounce a coin on it. But now, a year later, his bed-making skills are mostly absent. He still recognizes that the blanket goes on the bed, but the order – sheet, blanket, comforter, is a mystery, and smoothing one out over the other is abstract. Wrinkles and sometimes wads of bed covers are the best he can do, but every morning he still attempts to make his bed.

It’s strange what he does and what he no longer does, proficiently or even at all. He still laughs at a joke, whistles a little tune, and swings a golf club, but he struggles with most ADLs (Activities of Daily Living). I help him shower, brush his teeth, and get dressed. I hold his hand to cross the street, unbuckle and buckle his belt before and after the bathroom, drive him around, and serve him a plate of food at meals. Doug always used a handheld razor and shaving cream to shave. Then, a year ago, he started using an electric razor at my prompting. I figured it would be less risky for him and less complicated for me to manage. He has always been clean-shaven, never much for facial hair, but now he misses large splotchy spots and doesn’t notice. I imagine soon I will be stepping in as his shaving buddy.

Each area I assist with has gradually dissolved from competent proficiency to ineffective ability, with occasional lucidness within the disappearing. When lucidity brightens Doug, it is tempting to think he will get better and relearn, memorize, or reconstruct the details. It seduces me into believing that if I help a little more, clarify better, or ensure he gets adequate rest, exercise, broccoli, or fresh air, all will reverse and return to normal. But alas, it just isn’t so. The pain in my heart catches and stings afresh each time I realize lucidity is temporary and backward is pilfering new territory.

Cohabitating with dementia’s undoing reveals soggy and wishy-washy sentiments in me. It hovers grey and muted as my insides wrestle with loss while trying to reconcile what remains. Grieving the loss of someone who lives is painfully raw. Some days grief consumes me, but most days, joy and sorrow hold hands as we walk out fragile tension together.

Prayer helps me find my voice, and it empowers me forward. Doug and I believe life is sacred and time on earth, however short or long, is a priceless, God-given gift that includes an embedded assignment to spread love around. Doug still does that. Even with advanced dementia, he extends love to me, his family, friends, and even strangers. Indeed, his brain change is a slow, persistent undoing, and backward is taking additional territory daily. Still, Doug’s spirit is strong, and his display of love inspires me repeatedly, reminding me one day at a time that grief and love are intertwined.

Karen

I have always loved the Christmas holiday. 

As a child, there was believing in Santa Claus, the reindeer hoof beats on the roof (I still swear it happened), and the year we got a sled and a toboggan under the tree.

As a young adult, there was tension between what I liked about my childhood family traditions and what I wanted to skip or redo and the internal pressure I put on myself to be home on Christmas. 

As a young married person, there was the first Christmas tree, the first ornament, and the blending of two very different family traditions. 

As a new mom, There was the challenge of traveling, especially when sharing the grandbabies between grandparents who lived far away. There was the fear that my baby might choke on a Christmas tree ornament and there was the start of the Christmas morning cinnamon roll tradition.

As a mom of tweens, there was the gift chart, so no one had more gifts under the tree than another, there were family traditions that had become non-negotiable, and there was the hope that the Christmas bonus would be enough to cover the cost of Christmas dinner.

As a mom of young adults, there was the heartache of the empty nest, the work to gather and make it memorable, and the very true fact that Christmas presents had become more expensive.

As a grandma, there is a deep understanding that Christmas cheer is about the children, their smiles, and their new Christmas morning PJs. Of course, there is also baking Christmas cookies to share with the neighbors and watching Hallmark Christmas movies before Thanksgiving to get into the holiday spirit early. Being a grandma also means buying gifts all year round, saving them on the top shelf in the bedroom closet for December 25th, giving homemade gifts that can become keepsakes, and celebrating the season with Jesus at the center.

As a caregiver of progressing FTD, Christmas time has become complicated, especially for me – wanting, wishing, watching, and struggling with staying one day at a time.  Actually, I wasn’t sure I could write about it… Being honest about feelings as reliable as an old, rickety, wobbly suspended jungle bridge is hard. 

So far this Christmas season, I have baked cookies, made gifts, wrapped presents, and smiled at strangers (under my mask) in the grocery store. But on the inside, even while humming along to Frank Sinatra’s Christmas songs, I hurt. The grief of longing for Christmas’ gone by waves over me – the fragrance of memories shared and the absence of the physical help, often required to adorn Christmas spirit (and a tree), has left me unfairly lopsided. Doug is physically in attendance but quietly disconnected. I am deeply missing how we used to share this season, how we transitioned from Pumpkins and Scarecrows to lights and Nativities together.  

This year, responsibilities have been added to the common festivity preparations. Responsibilities like preparing and serving lots of healthy, calorie-dense meals and yummy sweet treats to add weight to Doug’s thinning frame and working in doctor visits for his new random health concerns. There is implementing and helping with consistent showering and daily (sometimes hourly, or even by the minute, depending on where we are or what we are doing) checking in with Doug to temper any anxiety or offset any apathy that may be vying for attention. There are also restless nights, feeling out of balance, checking in with myself for a bit of self-care, and so much more. I think you get the picture. 

In the past, Doug’s contribution to this favorite time of year overflowed with his flair for music, creativity, and overall merriment. He loved Rudolph and Santa, Starbucks and Costco, presents, and planning for the year ahead. Mostly, he loved the Nativity, the Christmas story, and the gathering of his family. But this year, while still physically present – occasionally whistling to a favorite Christmas carol, eating a Christmas cookie or two or three, and sometimes taking a cleansing breath while looking at the sparkle of lights and decorations – he is sadly missing. His enthusiasm is absent. His desire is vague. His sparkle is dim. My heart is heavy. 

More than any other, this year has felt hard and sad and lonely and festive and breakable.

I realize the holiday times are difficult for many people, especially this year after enduring so much loss and community fracturing because of COVID and the craziness of our national welfare. But somehow, I was caught off guard by the holiday blues I have experienced. 

There were beautiful, even sweet, moments woven into this holiday. It wasn’t all hard. We even laughed quite often, actually. But I realized that advancing into this new year will look different than many of my younger dreams and grander hopes had imagined. And at the same time, I recognize the call within, urging me to regroup and reassess. It’s funny how expectations can be both invigorating and disappointing. I am learning that a perspective fraught with unrealistic expectations often leaves me exhausted and haunted by disappointment. 

I have always been that person who plans next year during the week between Christmas and New Year’s. Typically, I get out the whiteboard, lined paper, and colored pens.   I write goals and objectives on 3×5 cards that I glance at throughout the year to keep me on track. I have not done much of that this year. I tremble to think about what 2022 will bring.  

However, I have decided what I will do in honor of the upcoming year and as a way to say goodbye to this last year.  I will focus on today.  I will make it the best day I (we) have. Not in the denial, disowning sort of way where refusal of reality takes center stage. But in the becoming pleasing way a flower blooms a little more each day, making the time it shares with us that much more beautiful and graceful. 

The seesaw of dementia continually remembers and reminds us that “Today is our very best day.”

So, to you and the world, while balancing my wobbly jungle bridge feelings and managing the intermittent collision of grief and brokenness, I pledge to be as present, honest, and loving as possible today and this year ahead, not worrying too much about the future. But instead, laugh a little more often and share in the beauty and grace of the moment, one day at a time.

Yes, I put this on a 3×5 card.

Karen

Once upon a time, about 27 years ago, in the spring, I was driving through town with a lot on my mind, nothing special really, just a lot going on.  I felt normal enough…  Then it happened.  I wasn’t prepared.  It had never happened to me before, at least not like this.  I knew life had my plate filled to overflowing but so what, that was nothing new or unusual.  Three young children, a job, a home, a busy husband, and overcommitted finances.

We’ve all been there a time or two, right?

The sun was shining, I was driving alone in the car (which was unusual, I guess, because I was most often a kid taxi), and suddenly… I had to pull over.  I couldn’t breathe.  My heart felt like it was beating out of my chest, like maybe I was having a heart attack.  My thoughts were racing, my hands were shaking, and I didn’t know what to do.  I was in trouble.

I took a couple of deep breaths and tried to relax.  Phones were not as prolific as now, so I did not have one with me.  I couldn’t call for help.  I tried to keep from panicking as I saw my life flash before my eyes.  Nothing seemed right.  Everything felt surreal, almost out of body-like.  I don’t know how long I sat in my car on the side of the road, but my breath eventually became even, my heart stopped racing, my tears dried up, and my hands steadied.  I drove home.

When I got home, I called my dad.  He was a physician and my trusted ally.  I told him what happened, and he asked me if I had a rash on my body.  I remember thinking that was an odd question, and I was stunned that he knew.  How did he know I had an angry hive-like rash all over my body?

“It was a panic attack,” Dad said.  He suggested I unload some stuff from my overfilled plate and rest more… Easier said than done.

The only other time I had a similar experience was years later following the words, “You have cancer.” After that shocking announcement, I walked out of the doctor’s office into the fresh, sunny air and lost it, totally lost it!  Couldn’t breathe, couldn’t control my erratic heartbeat, sobbed uncontrollably… You get it.  Enough said.

It’s surprising how much I am hearing about anxiety these days.  Everywhere I turn, it seems I see articles and social media posts and hear conversations about these very difficult days we are living in – These COVID days, with employment uncertainty, life relocation becoming a norm, online school still in the headlines, political dissension, health fears, Zoom meeting interruptions – These are stressful days!  Anxiety pierced days.  Even new puppies can be stressful and cause anxiety. Trust me, I have one!  People everywhere are feeling overwhelmed and fearful.

As long as I have known Doug, he has been my stable, chill, enduring comrade. Quick-witted and confident. Don’t misunderstand me, we have been married 38 years.  I have seen him mad before, sad, confused, frustrated, and overwhelmed, but I haven’t known him to be anxious or fearful.  In fact, Doug is famous for one-liners that hint at the way he does life.

The one-liner I most often repeat is, “More will be revealed.”  Patience and acceptance are all over that.  He is also known for saying, “Living the dream,” when someone asks him how he’s doing. “One-day-at-a-time” and “Keep it simple” describe how he travels through life and “This is not my home” and “God is in control”, basically sums up his spiritual convictions.

Sadly, his childhood was difficult.  Some stories he shares about his young years can bring a chill up my spine.  He told me, as a child, he was anxious.  I can imagine that to be true.  Even so, anxiousness is not a familiar behavior I attach to Doug.

Until recently.  Until FTD

Frontal Temporal Degeneration (FTD) is a dementia type that is often associated with behavior change.  I understand that the behavior variant of FTD can cause a person to become erratic, angry, and unpredictable.  Fortunately, that has not been our experience.  Doug’s behavior hasn’t changed much, at least not drastically or permanently. 

During Doug’s FTD diagnosis at Loma Linda University Neuropsychology Center, the testing was stressful, and the doctor used the word anxious to describe Doug’s behavior.  I was surprised.  I did not know Doug to be anxious, and his “anxiety” did not present like my experience with anxiety at all.  He didn’t have a full-blown dramatic panic attack where he couldn’t breathe and had heart palpitations and loud sobs amidst tears.  The anxiety that showed up in Doug during diagnosis was almost silent – he withdrew into himself.  Just stopped.  He stopped talking to me and relating to things around him.  He became apathetic and withdrawn, with bouts of nervous, fidgety, agitated energy.  He retreated, checked out, and paced.  It took about three days following this early FTD anxiety before he was back to his normal, relaxed, calm Doug. 

My reactions to this experience were scared, uncomfortable, and lonely.  I felt helpless.  I decided then, in all my puffed-up prowess, I would do all I could to try to control Doug’s environment enough to keep him out of those stressful experiences and thwart anxiety and the decline of dementia whenever possible…

Are you laughing yet at how powerful I thought I was?  You should be!

I used to try to solve and regulate dementia like a temperature control on a thermostat. I spent lots of hours reading and researching and hoping and wishing, with my guard up, that somehow, Doug was different and would not experience the unfriendly parts of this disease.   But alas, that is not the case.  I now realize we will not escape unscathed.  The dementia brain will do what the dementia brain will do, no matter how hard I work to control it. FTD brain change happens unpredictably and erratically.

We have been on this journey long enough to notice times of stability and decline.  But predicting those intervals is hopelessly hard, and preventing them is impossible.

Sadly, Doug is currently in decline, and anxiety has reared its head – quiet, internal, unsettling anxiety laced with nervous, fidgety energy.  While watching evening TV recently, he said to me, “I’m anxious.”  The announcement of his self-diagnosis was noteworthy.  Doug’s language is impaired, along with his awareness.  So, to plainly state how he was feeling gave me pause.  When I asked him a clarifying question to better understand how anxiety was affecting him, however, Doug answered with his typical muddled and confused messaging.

I let out a sigh.

Maybe I sighed because the answer was muddled and confusing, and I hoped for better.  But more likely, I sighed because anxiety in Doug reminds me that dementia doesn’t take a vacation.  It keeps pushing onward like an engine on a mission.

The truth is, I sigh and cry more often and more easily these days.  I am finally less intense about controlling the outcome (which is good for my overall well-being), and I am more connected with reality right now.  Meditatively, I frequently take deep breaths and concentrate on relaxing my shoulders, my forehead, and my jaw in a slow, intentional exhale as I say a prayer for Doug. For me. For us.

Even as dementia trudges on, this prayer practice helps remind me God is in control, I can trust Him, and more will be revealed as I keep it simple one day at a time.  

Karen

I do not like the feeling of being lost.  Being lost gives me hives.  It makes me breathe erratically and I wring my hands. Okay, that’s a bit of an exaggeration, but not by much.  When I’m lost (which isn’t very often because I have an aversion towards it) I think thoughts like: “What if I never make it back?  Do I have my affairs in order and are my wishes put where people who care can find them? Does anyone care? I really should have told him/her where I was going… or where I thought I was going.   Why didn’t I drop breadcrumbs or tie a bandana… somewhere…”

Doug used to love being lost.  He considered it a great adventure.  I considered it a waste of time, usually a waste of money, and always a waste of precious energy I could be using to save the world somehow.  I have said it many times, the invention of the GPS single-handedly saved our marriage.

When we returned from a European excursion that included a trip to Spain, England, Scotland, and a few other hotspots, we were thrilled with the photos.  The one of Doug and me on London’s Tower Bridge is a favorite.  So is the amazing sunset over the Mediterranean. But some photos we have of that trip confuse me.  They are beautiful and green, some with sheep, a sheepherder, and a barn.  One with a cobblestone street and an amazing arch.  One of a town square… I look at those pictures and I have no idea where we were.  Looking at those pictures raises my blood pressure a point or two because it reminds me how lost we were most of the time.

The truth is, traveling with Doug was traveling lost most of the time.  And the craziest thing is, he usually preferred it that way! 

We were in the middle of Spain in the middle of nowhere with no idea where we were or how to get back to our luggage that was safe in a cozy hotel room with a view.  Out on this lonely road, after aimlessly wandering for what I considered “way too long” we happened upon a road construction crew fixing a random hole in the road.  Doug decided to stop and ask for directions because he was tired of listening to me whine.

I was curious how this would go.

Doug knew not a word of Spanish.

He approached one of the construction guys, showed him a map, and shrugged his shoulders with an exaggerated hand gesture that clearly communicated he was lost.  After pointing and nodding and smiling and finally shaking hands, Doug returned to the car, made a U-turn and we were back to the hotel by dark.  He saw the whole experience as a grand adventure.  I was exhausted.

By the time we finished up the trip in London, I was leading Doug around, with map in hand, and refusing to follow him anywhere off the beaten path. To my credit, that’s when we got the great picture of us on the London Tower Bridge.

I am not wound quite as tight as I was back then, but I still don’t enjoy being lost.

Recently I took Doug to the grocery store.  It was crowded.  I felt responsible to keep him close because cluttered environments can be unsettling for him and get him easily turned around. Dementia complicates even the simplest or most common activities quickly.  In Doug’s dementia normal, he no longer enjoys being lost.  Being lost, especially in a crowded environment, can cause him penetrating anxiety.

Doug is typically calm when I am within arm’s reach.  He is okay when he can see me, but he is quickly beside himself if he loses track of where he is or where I am.    To my chagrin, Doug often follows behind me like a duckling following its mama.  I get why he does that, even though I feel a bit like the Pied Piper of one.  It makes it easier for him to see me. 

I have learned that dementia affects vision (it affects everything eventually, but vision is one of those subtle surprises that happens when you’re not watching). For Doug, his peripheral vision is affected.  I have been told that the vision can become cave-like.  It is like peering through a pair of binoculars or wearing horse blinders. Over time the vision becomes almost exclusively forward-focused. Doug doesn’t verbalize this about his eyesight, but he does say he likes things out in front so he “knows it’s there”.  He turns his head, and sometimes his body, in a formal sort of way to the right and to the left to see things you and I would see peripherally.

I prefer Doug to walk alongside me and not play follow the leader. When grocery shopping, I will sometimes hold his hand or have him help me “push the grocery cart” by holding onto the cart with at least one hand. Doing this forces him to walk beside me, where I can see him, instead of behind me, where I cannot. The caveat, however, is that he struggles to see me peripherally when he is beside me, triggering lots of head-turning and general uneasiness.

We had finished shopping and were preparing to join a checkout line. I carefully scanned, trying to determine which line would be the quickest and easiest for us. I was counting carts, analyzing their contents, and evaluating the proficiency of the checker.  If the checker is newish at the job and a cart is heaping with produce, you can forget getting out of there before your next appointment.  I know you know what I mean.  We all do it!  If the cart has a bunch of soda, cereal, chips, dog food, and no produce, then a quick checkout is a sure thing. 

My scan led me away from the hired help and to the self-checkout line.  It would be faster… I thought. I didn’t consider the produce in my cart, the eggs, and the fact I had more than 15 items – I guess there is a rule that nobody talks about, but everyone expects when using the self-checkout line, 15 items or less! 

I began by awkwardly scanning the oatmeal container.  I could not find the bar code. The scanner wouldn’t beep.  Impatiently I looked at Doug (who was oblivious to my struggle) and then at the checker who was overworked with 6 or 8 (too many) self-scanning stations in her charge.  I felt the eyes of the people in line boring into me because I was slow. I had maybe 17 items (more than 15 for sure), and Doug wasn’t helping.  I could hear the critics questioning, really loud in their heads, “why is he just standing there, he should be helping her.”

The self-checkout grocery store line peer pressure was mounting.  I used the picture lookup button to ring in the Produce because I didn’t realize it is important (when doing self-checkout) that all the Produce you pick should have a barcode sticker attached. It makes it way easier! I was slow and flustered, I admit it.  But the real issue happened when I picked up the eggs. 

Yep, the flimsy carton sagged, and three eggs fell out and broke onto the scanner. Now I had the attention of the overworked checker and the people in line!  The checker swooped over, rag in hand, and went immediately into cleaning mode.  She handed Doug the flimsy carton of eggs (I assumed to move it out of the way) and then said to him, “Why don’t you go get another carton of eggs.” My brain, at this point, was on overload, and my agitation was intensifying.  Doug, going to get eggs was not an option! He gets lost in the grocery store if his back is turned to me. Roaming through the store trying to find the egg section was an impossibility.  I boldly, probably too loudly, completely flustered, said, “No! No, he won’t get eggs. I mean, he can’t. No… I will just take the eggs.”

I grabbed the damaged carton of eggs out of Doug’s hands and shoved them into the bag.

The checker looked totally befuddled.  She had no idea why I responded as I did.  She didn’t know Doug has dementia or the difficulties involved with taking him shopping with me in an effort to break up the monotony of his days. She was completely unaware of the pressure I feel to keep Doug healthy and happy, well-fed, and entertained.  She didn’t realize that being lost anywhere, even in his own home (which is a reality), can cause penetrating anxiety.  She didn’t understand that when out and about, Doug needs an escort everywhere he goes, even to the bathroom.  She didn’t know that Doug is the best person I have ever known and that I miss him terribly every day.

No, she was just an innocent, lovely person doing her job when I lost it.  I couldn’t get out of the store fast enough.  I felt like the walls were pressing in on me, like I saw once on a Batman and Robin episode when I was ten.  I grabbed Doug’s hand and forcibly led him out of the store with the broken eggs bobbing precariously atop the bag.

Dementia affects everyone, not just the one with the diagnosis.  Days can be good, and days can be not so good.  With dementia, traveling lost is routine.  I am learning how to forgive myself for being the one who’s lost and for those uncharacteristic outbursts.  Meditation, taking a deep breath, and prayer help with that.  So does making peace with the moment.

I calmed down as I placed my arm around Doug’s waist and walked with him slowly back to the car.  “It’s okay”, I told myself. “We’re okay,” I said to him, “and right now, in this moment together, we have each other, one day at a time”.

“One day at a time,” he repeated.

Karen

Those of you who know me know I am extroverted, and I like to talk. My primary school teachers and the principal knew that fact without question. So did my high school swim coach, my best friends, and my dad. Words are, and always have been, my engine. They fuel me. They guide and direct like a compass. My career choices have leaned heavily on language – writing, public speaking, lecturing, instructing, one-on-one dialogue. I even have a master’s degree in communication and leadership!

So, words are my thing.

Some people would say music is their thing, or painting is their thing, or technology, astrology or economics, or dance is their thing. This thing is the thing that helps make your world go around. It communicates to you and through you. It has probably been your thing since day go. I like to talk and listen and dialogue back and forth. I also like to read and write (hence this blog) and expand my vocabulary. Words give me the leverage I need to solve a problem or direct the traffic of my life. 

The use of words can calm me down, like when I read a bedtime story to my grandkids or listen to meditation with headphones, or they can energize me like when I meet a friend for tea and have more to say than I have time.

Doug found pleasure in teasing me about needing to “use up my words”. When the children were young and I spent more hours serving small toddlers than I did interacting with the world, Doug would come home from work and be barraged by my daily unspoken – turned verbal – thoughts. He heard everything from what the kids did throughout the day to my opinion about world events. Doug learned very early in our relationship that it was easier to nod and give an occasional “uh-huh” now and then as I spewed the plethora of my thoughts than to have any opinion at all about any of my musings. His listening and my talking fortified me.

Doug’s opinions came later. 

He let me talk and talk and talk, and then, when the timing was right (which was often on a different day), he would revisit my words, remind me about what I said, and then give his opinion. I valued his opinions (most of the time). 

Doug would think and then speak. He was often funny, sometimes right, sometimes wrong, and commonly gentle in his interpretation of my oration. I came to appreciate his usually well-thought-out delayed feedback and conversation.

The track star, Jesse Owens, says, “If we walk long enough and talk long enough, we might come to understand one another.” I just love this quote and believe it wholeheartedly.

Doug and I used to walk the river trail. It was a beautiful long nature trail with stunning river and canyon views behind our house, where we raised our kids to be adults. The two of us would walk together and talk together and come to understand each other on this trail. We talked about everything we cared about. We discussed whatever was top of mind at the time and whatever needed to be considered. We laughed sometimes, and we cried sometimes. We decided things on those walks. Basic things like which toys went under the Christmas tree. Things that mattered more, like the best college for our graduating senior. Even the really tough things like the optimal time to sell our memory-filled family home. On that river trail, I learned, I talked, I listened, I trusted, I ached, I argued, and I grew up. Those walks and talks are now some of my most precious marriage memories. Sigh.

Dementia, more specifically Frontotemporal Dementia, more specifically still Primary Progressive Aphasia, is chipping away at Doug’s language faculties. His ability to follow and understand language, formulate words, ideas, and opinions, and his ability to express, using the limited language skill he still retains, is steadily becoming silenced. He spends much of his day quiet.

Of course, I still use up my words on his ears. It’s my thing after all. But more importantly, it is my one-dimensional way to attempt connection; to try to coax him out of his silence. My daily discourse is my genuine attempt at igniting hope; just maybe, his gaze will meet mine, and his opinion will be expressed boldly and without reservation, with no confusing words, mixed-up sentences, and halting patterns, or single-word speeches. Sadly, however, the once-upon-a-time exchange I well remember and hope for, the two-way conversation and dialogue I covet, has not happened in a long time.  

Doug and I go to Speech Therapy together. His speech therapist is good at drawing words out of him and making me quiet. She is patient and tricky. With her guidance, I am developing a notebook of words, pictures of family, places, objects, and lots of stuff that will perhaps stir recollection and unite sentences. I also use a whiteboard with erasable markers to jot down words. I ask him, “Would you like tuna or ham or veggies?” I write Tuna, Ham, and Veggies on the whiteboard. Seeing the words makes it easier for him to pick. It’s harder for me, more work, I mean. It’s easier to just give him something to eat. Being a good sport can be tiring for both of us.

I wonder what he is thinking; what he comprehends, if I talk too fast or say too many words to follow, if he wants to say something but can’t find words or finds it too cumbersome to try. The whiteboard slows me down and gives him word choices. It helps.

Undesired silence is deafening in its volume, decapitating choice. When I am craving Doug’s unique opinion – lying down next to him at bedtime, where we used to dissect the day together, or deciding on something alone, I wish he was deciding on with me or for me – the stifling clutch of silence booms and often lingers. 

Sometimes, to break the domineering silence, I turn on music, usually quiet in the background of my day. It breaks up the monotony of my thoughts and occasionally detonates Doug’s voice in song. He may sing a lick or two with little or no language deficit if the song is familiar. He has always sung beautifully. But now, hearing his voice – the tone, the unique edge of his sound – can sometimes startle me with uninvited watery eyes and a lump in my throat.  

Doug rarely appears frustrated in his silence. If I were him and had to manage all the word chaos, I assume he is navigating in his head every time he goes to say something, I would be very frustrated. It is almost as if he doesn’t recognize silence is happening. Sometimes, he participates in surface three or four-word chit-chat, usually initiated by someone else, and sometimes, he speaks sentences that have a point, albeit elusive. When I listen as he wrangles with sentences, trying to nail down a point, I get exhausted in my efforts to follow along, like how I imagine herding cats would make me feel.  

Little children like short sentences and chit-chat too. Our granddaughter mimics her mom with phone-like chit-chat and voice fluctuations that adults use when talking to friends. It is very cute.  Doug identifies with her language. He has short, sweet conversations with her using her size words. Doug also talks with an adult friend on the phone. They laugh. Bruce (his phone friend who used to be his in-person friend, but then we moved 1100 miles away) understands short, sweet, uncomplicated, dementia pacing (if that’s a thing) chit-chat. Doug smiles and feels successful after tele-talks with Bruce. I smile too. Thank you, Bruce.

Mostly, though, Doug is just peacefully quiet. His peacefulness is the beautiful hidden blessing in the brutality of his dementia. We are lucky for that.  

I am also lucky God is a good listener. He often endures my word outpourings, equal in volume to the summer monsoon rains of Arizona. I think he can handle it. God clearly understands how words are my thing. He made me that way. Graciously, he never interrupts, never chastens me for my many verbal protests about how it is hard and how I wish things were different as I bemoan the slow-motion tragedy of dementia unfolding before me, and he never tells me to quiet down or sends me to the principal’s office. Instead, he brings balance; he gives me courage fresh every morning, unconditional love, and the patience required to be a good sport. God knows I need that. God knows Doug needs that.

And deeply, I am grateful for that every day, one day at a time.

Karen