Dad’s bachelor years and the holidays

I’m inching closer to home, and as I sit in a Starbucks writing this, watching people gathering and exchanging gifts and wishing each other “happy holidays” I feel that pang of homesickness strike even harder. That got me to thinking about all of those years when Dad was a single guy, after he immigrated to America. He could rarely afford to make trips home to Ireland. So what did he do for Christmas all of those years?

I don’t remember him ever talking about memories of Christmas spent as a bachelor. Dad was pretty good at making pals, so maybe one of them invited him over to their family’s house for a Christmas dinner. Certainly Dad was quite handsome back then, so maybe he had a girlfriend to go out on a date with on Christmas. Knowing Dad, I’m guessing a pub was involved at some point. Maybe other solitary types banded together for a night of merriment. Also, I’m sure Dad would have attended holiday mass.

ornament

Or perhaps Dad had to work, or offered to work, to let the family guys spend the holiday at home. That’s something that Dad would have done.

I’m sure the pangs of homesickness were quite strong, especially those first few years in the States. He worshipped his mother and it must have been difficult to be separated from her during the holiday season. Did he even get a chance to make a phone call home?

This is one of those moments where I wish I could call up Dad and ask him to solve this mystery I’ve just created. Instead, I am left to my own imagination of what Dad did all of those holidays before Mom and I came along.

The best gift you can give yourself this holiday season is to ask your loved ones to tell stories about their past. Ask those burning questions now. You never know when it might be too late.

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One year later, trying to return home again

Mom’s surgery was a week ago and went amazingly well, according to the doctors. She was discharged early and has been home for a few days now. She’s doing well physically, but emotionally she is down. I am desperate once again to get home to my own family, thousands of miles away, who I’ve pretty much abandoned over the last six months.

So I’ve made plans to return home for Christmas. Just like I did last year, after my father’s death.

My plans didn’t work out so well last year. A freak snowstorm hit, and I was stranded in Roswell, NM alone for the holiday. Weather shouldn’t be an issue this time, but with the way this year has gone, I won’t believe it until I actually walk into my home.

Mom is understanding but obviously depressed, just like last year. If there was ever a time to clone myself, it would be now.

I found this post called Embracing the Caregiver Role quite accurate in the guilt and mixed emotions one has in caring for an ill parent and balancing family responsibilities.

The author writes, “To be there for my Mother I had to borrow from all of those areas at a cost.” This is so true, and I’m sure other caregivers can relate to this statement.

Also, this statement is telling: “Circumstance had converted our relationship.” This is so true as well, when adult children have to assume the parent role for their own parents. It is never an easy transition to make.

So I’m giving myself the gift of guilt this holiday season, just like last year. Of course, last year, I never would have predicted how much I would be sacrificing this year in order to take care of another ill parent. Perhaps karma paid me a visit? Hopefully by now, I’ve paid back any karma debts owed.

Hopefully, I will make it home.

Hopefully, Mom will be okay.

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One year since Dad has been gone

It’s hard for me to believe that it has been one whole year since Dad died. So much has happened, with Mom being ill for most of this year. Through it all, I’ve thought about Dad each and every day.

Today I remembered Dad by walking along his favorite walking trail and visiting the local library, his favorite place. I will be making a donation to the library in his honor. It was an absolutely gorgeous day, and such a stark contrast to the hideous weather yesterday. Today, the skies were as blue as they could be, the sun was shining bright, and the winds were calm.

Dad and I at the assisted living facility, March 2011.

Dad and I at the assisted living facility, March 2011.

I started The Memories Project blog at the beginning of 2012 as my way to remember my father, to record memories and work through my grief. It has been a wonderful experience. From the NPR interview to all of the wonderful bloggers I have met that I otherwise would never have known, it has been truly rewarding and enlightening.

Today, I added an entry on Cowbird to mark this anniversary. It includes some priceless audio of my father singing to me as a baby. The recording is one of my most precious possessions.

While I haven’t been able to dedicate as much time to Alzheimer’s awareness as I would have liked this year, I hope to engage in more activities in 2013.

Thanks to all of you who take the time to read about someone you’ve never met. Dad would be so proud to know that he is making a positive difference in the world.

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Howls of Alzheimer’s

It was a brutal, ugly weather day where my mom lives. The wind howled like a banshee all through the night and into the day. The wind was sustained at 40 mph, and geared up to 60 mph gusts at times. It left me feeling unsettled and on edge all day long. I set in the living room and in the chair that Dad spent most of his time in when he still lived at home. I watched the thin trees take a beating. They bent, but did not break with the vicious wind gusts. It was a miracle of nature to me.

At one point, blowing snow whipped its way through the sky.

Even though I avoided going out in the windy weather, I felt like the wind symbolized the battering my family has taken over the last year. And the howling made me think back to my Dad’s nightmares, and the sounds I would hear at the nursing home Dad spent the last year of his life in.

Perhaps we were lucky that Dad mainly became mute as his Alzheimer’s progressed, and there were no verbal tirades or helpless cries that some families have to endure.

Those howls and moans of souls trapped by the cruel disease of Alzheimer’s. It is a sound one can never forget.

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Fleeting moments of connection

I read a moving blog post today about someone with Alzheimer’s who pleasantly surprised their family caregiver with a rare moment of lucidity. They were able to express their love verbally before Alzheimer’s moved back in and took the light out of their eyes, returning them to a glassy, blank stare.

For most of us, these lucid moments are few and far between.

This made me think about the last lucid interactions I had with my father. He was at the point where he was barely able to verbally communicate. He would sometimes be able to utter a few words that made sense, but most of the time, he carried that sad, faraway look in his eyes. But I remember that moment so clearly in the hospital room, when Dad’s eyes lit up with recognition while I was holding his hand.

“Oh, there you are,” he said, as if startled by this temporary retreat into reality.

“At first I couldn’t see you but now I can,” Dad said with a wan smile.

I knew that was the moment to say what was burning in my heart. “I love you Dad,” I said, slowly, clearly.

“I know you do,” Dad said. Then he began to drift away from me, back into the isolating world of Alzheimer’s.

But it is the moment of love that I remember the most.

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Big warm hands

Mom is recovering in an amazing fashion from her major surgery on Friday. She’s still in the hospital, but may be released back home as soon as tomorrow!

Today Dad was weighing heavily on her mind. She began to weep as she talked about how she still missed him, the way he was before Alzheimer’s took hold of him

hands

She mentioned that one of the first things that she remembered about Dad was his big, warm hands. She remembered when they were courting and holding his big, strong, warm hand and feeling comforted.

She remembers dating other guys when she was younger who had cold, rough hands and that was such a turn-off to her. But Dad was a winner because not only were his hands big and warm, but they were soft, despite decades spent as a manual laborer.

It’s interesting what we remember most of the people we love. It’s not always what one would expect, but it is sweet just the same.

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Connection between loneliness and Alzheimer’s?

I read an interesting study today that suggested there may be a connection between loneliness and Alzheimer’s. What was most interesting was that it was those who felt lonely versus those who lived alone but didn’t express feelings of loneliness that had a higher incidence of Alzheimer’s.

It was a surprising result to the researchers. I’ve read numerous studies about social isolation leading to everything from dementia to depression. I wonder if these studies have some inbuilt bias towards extroverted people. There are some people who need constant company or they feel lonely; others can interact socially with people once or twice a week and be perfectly happy.

I’m not sure if Dad felt lonely before Alzheimer’s set in. Dad certainly had a passion for “alone time” activities like reading. He also had a solitary job as a security guard for many years. So like me, he was comfortable being alone and entertaining himself. Did he yearn for more socializing? That I will never know.

But what is clear to me is that once Alzheimer’s took hold of my father, he was whisked away into an isolating world, where we really could no longer connect with him in a meaningful way. And I saw that same isolation play out on the faces of every patient in the dementia ward of the residential facility where my dad spent the last year of his life. I remember so many residents reaching out, touching my arm, trying to communicate with me, hoping to make some kind of human connection. I often felt like I let them down when they shuffled away after an awkward, confusing exchange.

I hope there are more studies investigating social isolation and dementia, and I hope they take into account that both introverts and extroverts exist, and that the definition of loneliness is different for every human being.

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The caregiver’s curse

Mom is recovering in an amazing fashion from her major surgery that was just performed yesterday. The surgeon came to check on her today and sketch out a plan for the next few days.

Mom took the opportunity to tell the doctor about how she had cared for Dad at home for 2-3 years until his dementia became too much for her to handle at home. She had been healthy for 74 years, and then all hell broke loose.

The surgeon nodded sympathetically. “I have heard so many stories just like yours. There’s a certain level of adrenaline that kicks in to handle crisis situations, and surprisingly, that level can stay quite high for long periods of time. Then once the loved one dies, the caregiver completely loses that adrenaline boost, and that’s when sickness can kick in.”

It seems particularly cruel that the reward for doing something so selfless and loving as caring for a loved one with a disease can end up causing you to get sick, but that is reality.

Even doctors are admitting that caregiving can be hazardous to your health, but what real alternatives are there? Residential facilities are extremely expensive in the U.S. and out of the financial reach of many families.

I’m an only child. My father passed away a year ago. My mother is now sick. I quit my job to take care of her. Sure, I could put her in a facility and her life savings would be gone in a few months. Home nursing options are limited to a couple of visits per week in the small, rural town Mom lives in. I live in a big, expensive city. There are no easy options here.

We must do better for our elderly, and their families. We need more support, emotionally, physically and yes, financially.

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A storm of emotions

Today was Mom’s surgery day. We had to be at the hospital before sunrise, and the air outside was swirling eerily, a rush of warm wetness with an undercurrent of bitter cold wind. A winter storm warning was in effect, but no one knew quite what Mother Nature would bring.

It was a relief just to get Mom to the hospital. Then she was taken and I was left to sit and stare at the clock in the waiting room, and try to occupy my rushing thoughts like I had done so many times before with Dad. It began to rain, with the skies dark and bruised with clouds.

hospital

Almost two hours dragged by before I receive word Mom was out of surgery. The doctor rushes out and lets me know Mom did great and everything went as planned.

The rain began to pound harder, and the wind picked up with it. Ice pellets start to pop off the ground in the hospital’s garden.

I am led back to see Mom in ICU. She is calm and peaceful, just like Dad had been when he was sedated last year while on a ventilator. There is a serenity that could almost pass for death, but the machines and Mom’s rising chest prove she is quite alive. She opens her eyes and recognizes me. With Mom, I expect this more, but I remember being caught off guard when Dad seemed to recognize me a little over a month before he died.

CNN was just beginning to report the Connecticut school shootings while I was stroking Mom’s forehead in ICU.

I walk back out to the hospital lobby to let Mom rest. People are gathered around the huge windows, staring out into a winter apocalypse. The driving rain has turned into a wet snow, which is being blown sideways by the 40 mph + winds.

The weather reminds me of the winter storm we slogged through last year to see Dad’s body at the mortuary. We barely made it back home before the roads became impassible.

And the same thing happened today. I hated to leave Mom but the nurses said she was doing quite well and I didn’t want to get stranded at the hospital overnight. There were a couple of scary slides and heart-pounding moments on the way back to Mom’s place, but I was finally able to close the door on this emotionally draining day.

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Mom’s new dream of Dad

Mom is having her second major surgery of the year tomorrow. Of course, she’s having a great deal of anxiety about it. Major surgery carries plenty of risk factors that can lead to death, and as you get older and have other complications (like Mom’s blood clots) that potential brush with death seems even more real.

This morning, Mom wanted me to wake her up so we could go for some pre-surgery blood tests. I stopped in the bathroom first, letting her get a few more minutes of sleep. Suddenly, through the door, I heard a plaintive plea:

“Pat! Pat! Pat!”

Pat was my Dad’s name.

I rushed out of the bathroom and Mom realized that she was having a dream and it was actually her daughter in front of her. She said she was having a dream about Dad, and had mistakenly called out his name instead of mine.

Perhaps Dad is sending supportive and loving energy from wherever he is now. I know he wouldn’t want Mom to suffer, and would do whatever was in his power to make her better.

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