Saturday, February 22, 2020

Mary Coin

Things have been falling behind a bit here. There is a pile of White Elephant gifts wrapped in newspapers left over from Christmas when my contributions didn't get re-gifted.

You see, my Pops fell on January 11 and collapsed at home. My mom couldn't move him or get him in the bed, and I didn't hear the phone ring. I found out the next morning (a Sunday) and went the hospital where he was finally admitted from the ER for 'observation.' After a CT scan showed a spinal fracture, he was moved to the healthcare center next to my parent's duplex for rehab.

As anyone with elderly parents knows, there's a bit of wrangling about the arrangements, insurance, etc. and I'll spare further details of the other struggles (emotional and otherwise). Fortunately, my parents have good health insurance and long term care insurance. They did not want us taking care of them in our home. So off to the nursing center he goes.

Something was drilled into my head that if either of my parents ever went into a nursing home, it was my job to visit them everyday, in addition to supporting my mom when she needed me to talk to doctors, nurses, insurance people, etc.

Other than one night I sent Pat in my place, I kept my promise to myself to visit everyday or sometimes twice a day. It quickly became my job to help Dad with his upper false teeth. For some reason, he didn't think the aides could do this properly. "TTW" he repeated to me. Tablet, teeth, water (HOT water, as HOT as you can get it). At this point, he couldn't transfer, toilet, position or wheel himself , walk or stand, and is in excruciating pain every time he does have to move. Physical therapy was referred to "torture" and it was a challenge to find a medication that didn't make him nauseous.

We did take our planned trip to Florida in late January and luckily Betsy was in Illinois that weekend because Dad was admitted to the hospital again, briefly for new issues. And back to the the nursing home, which he referred to as rehab. At this point he was spelling out Plan A, B, C, then Plan A sub 1 (a) or (b). I honestly couldn't follow his thought process here. I think Plan A was 'fully' recover and go home, and C was to live in assisted living with an electric wheelchair so he could drive himself to see Mom when the weather was good.

Here I should mention what a trooper Mom was/is, and how he would get sentimental telling me about their love story. Things I never heard before. He thought he had got the greatest catch in the world.

One more ER visit and hospital admission for pneumonia February 6th. This one really scared me because one night he was making no sense, and I had to feed him the few bites he would take. He got his teeth out that night, but barely. I saw his weight on the White Board and he had lost 24 pounds from when he was home. The next day he was perfectly coherent and was discharged the day after that. Mom had also come down with a terrible cough and didn't get out of bed for days and of course you can't infect a hospital or nursing home with those germs.

Dad dragged himself, or rather they dragged him to rehab a few times over the next 8 days, but there were days he stayed in bed, too. Throughout this process I was reading him the novel "Mary Coin." It's a wonderful historical fiction piece about the picture below:



He really enjoyed the three story lines and even was reading out loud to me the last night. He repeated some when he got interrupted, but then would realize, "I read this before." It was really enjoyable for both of us, especially after he got his private room, and we didn't have to listen to Delmar grumble in the next bed about how he was trying sleep and it's supposed to be quiet after 9:00 (it was usually 7:30), and what happened to his private room?? Well, he thought he had private room until they moved a roommate (Dad) in, but he was not paying for a private room. 

The last week he told me not to remember him like this, that I didn't have to visit him everyday and should go on with my life, and made other hints that he knew time was running out. On Monday night he called Mom and I both to be there together to go over Plan A sub 1 (a) again. It still didn't make any sense but we agreed with him.

On Wednesday February 19, Mom was there in the afternoon and left about 3:00 to go take a nap, not being fully recovered from her illness, but able to visit at least. All the staff are now wearing masks all the time at this point. Dad wasn't feeling well (was in bed after rehab) and apparently had some new kind of medication. Mom got the call about 5:45 that he passed. She called us in the middle of dinner, and we had some time to be with him in the room. Mom didn't like that his mouth was open (she has a thing about that), but I told her they probably didn't want to touch him. Then the coroner came and whisked him away to be cremated. We cleaned out the room; he didn't have much since this was "temporary."

How to end this rant...know that I will write cheerier posts in the future. I feel like he went the way he wanted. He tried his best to recover but the body was worn out. He kept his mind to the end, didn't  drain his savings on a nursing home, and he wasn't a burden to anyone. I got to spend this extra time with him and be the daughter he thought I was. Praise God for this.


I think he would be happy to be remembered this way. Family vacation, the red van, and car top carrier he made from plywood. He also made sleeping benches for Betsy and me to sleep in the back. I still remember the material on those benches and the love that was sewn into them.

Monday, February 17, 2020

The Boy who would be Coach


Here's my little 8th grader leading the Mustangs onto the floor. He's first because he's the shortest.


Here he is 12 years later coaching his 8th grade team at the State quarterfinals. They led most of game, but the last two minutes didn't go their way. The team with the heart held their heads up and Coach Cal exceeded his goal of winning their Regional.

Cal wasn't the most athletically gifted player but he's taken his skills and intuition and heart to the junior high level in academics and coaching three sports. I couldn't be more happy and proud of him. He's living the dream and appreciating it everyday.

Thursday, February 06, 2020

On Surviving Four Years


I had a little dream early on 2/2/2020. It involved Adam's friend Brent whom I have been talking to. He's a big Cheif's fan so the Superbowl was coming up that day, along with the anniversary of Adam's death.

I don't remember the dream, and Adam was peripheral to it, but it felt nice, at least like he was near. Four years, and counting. Counting the days that have past, dreading some days ahead. Feeling useful in life, purposeful, as things change in my family situation. That's not my story to tell, but at some point it might come out anyway.

Saturday, February 01, 2020

Punch cards for Hope


We all have our days. Some have weeks, months or years. But healing is always possible. Sometimes we need more patience, especially with ourselves.

I choose to see the positive, skip over the negative, especially when it comes to what is happening in the world, the news, politics, social media, and in front of my face. I don't think this means I have my head in the sand. I am trying to incite change where I think I can make an impact.

I don't believe in the word "broken" as it applies to people or the world. Changing is more positive and also inevitable. Feeling broken makes room for healing and growth if one chooses to look at it this way.

Don't get me wrong, I have break downs. Things pile up sometimes and we need to take those moments to feel it. If I could give out hope in little punch cards or gift cards, wouldn't that be cool? Because true hopelessness seems to be the thing that contributes most to suicide. But hopelessness is just a feeling, too. For most of it passes eventually. Sometimes it takes work, yes.

If you are in need of a Hope infusion, please accept one punch from my heart shaped hole punch in your little card. Come back when you need another, and another. I have a little extra to share.