Moments shared.

A few months ago I muddled through a string of down days. Nothing specific was wrong, but nothing was right either. I sought help from family, friends, doctor, therapist. I grabbed myself by the scruff of the neck and gave myself a talking to as well. Then, I had an “aha!” moment.

Peter was watching tennis when I left him that day. He waved me off and stayed in front of the tv. He didn’t mind that I left. The next day, when I picked him up to go on a picnic with Leslie and Martin, I suddenly, aha, got it.

You see, when I collect him to go for coffee or to the car wash or lunch, I feel guilty because when I arrive the other residents are usually parked in front of the tv or tottering up and down the hall aimlessly. Many don’t seem to have visitors very often, if ever, although there are a lot of hours when I’m not there so I don’t really know.

Peter and I go out the locked door leaving them behind—it’s like picking one puppy over another, I think. Guilt swamps me because I can’t take them too, yet sometimes I can barely deal with my own husband, much less with someone else.

But Sunday when I walked in the residents—Peter included much to my surprise—were batting a balloon around and laughing hysterically. What could I do but laugh with them? Always the clown, Peter tried some of his practiced soccer maneuvers while sitting in a chair. Activities like this may happen often, but this was the first time I’d witnessed it. Aha, I thought.

No sooner had the balloon floated away than a man came in, pulled the piano to the center of the room and started playing and singing familiar old songs: You are my sunshine; Row, Row Row Your Boat; Daisy, Daisy, give me your answer, do; Shine on harvest  moon and on and on non-stop for nearly an hour. The nurses and aides clowned to the music, chair-danced with the residents, and everyone joined the singsong or tapped their feet. I even got Peter to dance with me. He remembered those moves too, although he said he wouldn’t try to “dip” me. Funny, he seemed to remember he’d dropped me once.

Two days earlier the activities personnel had organized a fall festival, complete with games and food, crafts and music, baby animals and even antique cars. Fun-filled late summer days! Moments to remember…

January to December, we’ll have moments to remember…

Excerpted lines from “Moments to Remember,” Al Stillman and Robert Allen, music and lyrics, 1955.

Header photo: Peter and Nobby walk in the mountains, 2015.

 

 

2016 National Society of Newspaper Columnists’ contest finalist. 

Seize the day!

It was more than a year after I placed my husband in memory care before I found a new normal. I’d skimmed across the days, weeks, months in a daze, I now know. Friends said I was doing well, but I knew I was barely hanging on.

But at last, mama’s got her mojo back. Carpe diem.

Almost from the start, I had concerns about certain aspects of Peter’s new life. Nearly 18 months later I realized that the route to change was for me to Do Something.

I made an appointment to talk with one person but ended up in the office of another, a nice young man who had the authority to affect change. When I sat down with him—I’ll call him Mr. L—I had two pages of notes ranging from serious matters like Peter’s refusal to take his meds or take supervised showers regularly to other, superficial items. He lay my top priorities to rest quickly. Weeks prior word had reached Mr. L’s desk that twice I’d found pills lying on my husband’s table. Steps were taken. Peter no longer gets away with his tricks to hide meds, although I’m sure he still tries.

My complaint that two showers a week aren’t enough for anyone, anywhere, anytime, much less my often “fragrant” spouse, was addressed. It’s still a battle for whoever has to convince him, but it’s happening. Who knows, maybe Peter will come to accept his new normal.

When I visited recently, an aide told me Peter had refused to shower that morning, as he had on Friday. “I’ll talk to him,” I said, thanking her for telling me. While we had our tea I told him how upset I was about his refusing showers. He looked like he’d been caught with his hand in the cookie jar, but he continued to insist he didn’t need to shower “all the time.”

I persisted. He held firm. Finally I suggested we play dominos and the best-of-seven winner would make the shower decision. Peter lost. He went to the shower room willingly. Afterwards, he came back to his room arms raised, hands clasped above his head. He looked good, he felt good and he he’d made me happy. “Domino effect” has taken on new meaning. I might have to show the aides how to play the game!

Peter always liked to garden.

Next on my list was the garden that surrounds the wing where Peter and as many as 15 others live. “The front of the facility is very nice, well maintained, welcoming,” I said to Mr L, “but that garden is pitiful. The raised bed is full of weeds and mint. The area is not inviting at all.” He agreed. I also suggested painting the ceiling of the gazebo blue. That struck a chord and Mr. L added that the porch ceilings needed paint too. Yes-s.

Then I mentioned my two occasional gardeners—they help me at home—and asked if it would be OK to contact them to see if they would be interested in a garden overhaul. Yes and yes. Before long they’ll start work on their plan that includes brilliant perennials with compelling scents—lavender, lilac, viburnum—and although fall hasn’t even started, I can’t wait until spring.

The tall black garden fence is meant to contain residents who try to escape, Peter among them! I proposed murals on some fence sections to make them less prison-like. Murals are on the radar with two potential artists lined up.

Peter ponders his next domino move.

When I asked about a table and chairs for the gazebo, snap, they appeared a few days later. I hope other residents and their families enjoy sitting there as much as we do.

How about enlisting student volunteers from local schools and the university to visit with residents or plan entertainment? I asked. Maybe youngsters could write notes to them? Would young children from day care facilities come to cheer the residents? I wondered. Worth trying, Mr. L thought, and before long he’d made some calls and ideas are flowing. Peter loves little children and I imagine other residents would enjoy little children and their antics, too.

My list grows, even as I sit here tweaking this post. At least now I’ve Done Something about things that can be remedied with the right sources and not too much money. I’ll probably make some enemies in this process, but it wouldn’t be the first time. I’m not called Mother Tough without reason!

Header photo: Peter asks if he can help when the garden rehab starts. “You can sweep up every day,” I offered.  He nodded. “I’m good at that,” he said.

 

 

 

2016 National Society of Newspaper Columnists’ contest finalist. 

‘Caregiver’ redefined?

The word “caregiver” in the tagline above bothers me because it really isn’t accurate any more. But the title, Dementia isn’t funny, still works because dementia isn’t funny. Not in the least.

The thing is, I’m no longer my husband’s caregiver per se. For the past 18 months, since he moved to a memory facility, there’ve been are nurses and aides, companions and activities personnel doing what I did at home for years. A care giver I’m not, but I do still care.

I’m no longer in charge of trying to get him to take his meds or take a shower, to change his socks, or brush his teeth. No longer do I drag him to get his hair cut, his beard trimmed, no more do I do his laundry. Still, when I visit I often try to get him to put his clothes away properly rather than stuffed in his shoes or under his pillow. To convince him to change into a clean shirt is almost  impossible. He’ll answer “Yes, dear” and continue to ignore me as he always has. I always laugh because I never could change his ingrained stubbornness and I certainly can’t now! On the other hand, the things he likes to do, sweeping for instance, he’ll do willingly, thoroughly. He leaves no leaves unswept, no blade of newly mowed grass on the pavement.

One afternoon we were sitting in the gazebo when, out of the blue, Peter said it needed a coat of paint. I agreed—that gazebo is very shabby looking. I suggested a blue ceiling, a tradition in the South said to scare “haints” away and possibly even mosquitos and wasps too. I decided to find out if painting was even possible. And it is!

The following Sunday we looked at color chips at Lowe’s and picked some blues— Playful Pool and Vintage Aqua were nice. Later I found the color at left on-line: Benjamin Moore’s Ohio Haint Blue. I favor that because, well, I grew up in Ohio. Both sets of grandparents had blue porch ceilings and none of them had ever been further south than Columbus.

The gazebo hasn’t been painted yet, but I’m confident it will be. In fact, I have it on good authority that the ceilings of the porches will also be painted “haint” blue. I’m lobbying to have the garden benches painted a matching color, and maybe find floral chair cushions shades of blue for the porch furniture.

Meanwhile, I haven’t thought of a new word to replace “caregiver” in the tagline. Peter would probably suggest “the wife”: The wife, Judith Clarke, looks for laughs every day.  He’d laugh himself silly at his joke, knowing I would not!

Haint (haunt) ain’t in my dictionary, but hain’t is.
The latter, a contraction of ain’t and have not. 

Header photo: Peter loves to sweep the porch near his room. Soon there will  be a haint blue ceiling above his head.

 

 

 

2016 National Society of Newspaper Columnists’ contest finalist.