Showing posts with label caregivers. Show all posts
Showing posts with label caregivers. Show all posts

Tuesday, July 18, 2017

Choose Your Battles

In Missouri, 2017 should be put on the calendar as the year of the Japanese beetles. Sure, we had some last year and they were a nuisance, but this year they are a plague of biblical proportions.

These voracious bugs started on our grapevine—just like last year—then they moved on to the wild roses, blackberry bush, returned to destroy the apple tree and all the apples on it, attacked the yard trees making them look like autumn instead of summer.

It’s a dilemma how to battle beetles. The traps attract more, and it certainly was tedious to pick them off and throw them in soapy water. That might work if you had a scattering of beetles, but when they congregate in huge clusters and there are thousands of them, picking seems like an exercise in futility.

So we sprayed a little Seven on them, but mostly we hoped they would move along like they did last year. But oh, no! They were way cockier than last year. One morning while relaxing with my cup of coffee on the deck, I was horrified to see our rose of Sharon bush covered with the foliage eating monsters. “Okay, they have gone too far!” I told Harold.

I used the remainder of the spray he had mixed, and although it killed hundreds, it seemed that a legion was moving along the front line of the battle to kill the bush. Harold got serious and bombarded the tree with spray. That seemed to do the trick. We had chosen our battle and although they haven’t left entirely, the remaining beetles lost interest in the bush.

As a person who is often out of sync with the opinions of those who surround me, I’ve found that choosing battles has become more important than ever. It isn’t always easy for an outspoken, opinionated woman to do that, especially when so many have lost their sense of civility and respect for their fellow humans.

Choosing battles became an integral part of caregiving. When Jim was in long-term care, I could count on some residents’ family members charging into the memory unit just spoiling for battle. Nothing was ever done to their satisfaction. Complain, complain, complain. I might mention that the biggest complainers were the ones who seldom visited their family member. Too often, it seemed that since they felt guilty, they wanted to belittle the aides and nurses that tended to the residents.

When these same people saw me feeding, bathing, or providing extra care for Jim,  they would say, “You shouldn’t be doing that!You are paying to have that done.” In the first place (a) it really wasn’t any of their concern what I wanted to do for my husband, and (b) I saw how overworked and unappreciated the aides were.

There were two kinds of aides: the ones that needed a job so desperately they were willing to try anything, and the majority who had a caring nature and whose job was less of a job and more a “calling.” The people who stayed were not working solely for a paycheck.

Abuse and neglect of  your loved one should not be tolerated. Show up for care planning and provide helpful input. Rather than ranting at the unfortunate person who happens to be nearby, rational conversation with the person in charge is much more effective.

In life, we need to choose our battles. Instead of waging war against fellow human beings, negotiation may be the key to settling problems.

On the other hand, an all-out battle against Japanese beetles is not only totally acceptable, it may be the only way to save your yard.

Copyright © July 2017 by L.S. Fisher
http://earlyonset.blogspot.com

Monday, October 26, 2015

Once In a Lifetime

On Sunday, I was working at the Sedalia Business Women’s Chicken Dinner when I saw an elderly lady sitting all alone at a table. Unlike everyone else, she did not have a plate of chicken and trimmings in front of her.

She had a lost look, and instinctively I knew she had dementia. Concerned that she had wandered in and didn’t have a ticket, I walked over to her and asked, “Are you hungry for chicken?” I had already decided that if she didn’t have a ticket, I’d buy her lunch.

She smiled at me, tilted her hand back and forth, and murmured some indiscernible words. I smiled at her and walked to the ticket table.

“Do you know who that lady is?” I asked.

“No, but I think she has Alzheimer’s. Her husband is fixing her plate.”

I milled around, refilling drinks, cleaning trays and tables. Eventually, a lady walked up to me, read my nametag and asked, “Are you the Linda Fisher I saw in the paper that’s involved with the Alzheimer’s Association.” I told her I was. With tears in her eyes, she told me her husband had Alzheimer’s, and she had always wanted to meet me.

Later, another woman introduced herself to me to let me know a mutual friend had steered her toward my blog. Her husband, only in his sixties, had Alzheimer’s.

Eventually, I worked my way back to the table where the lady sat with her husband eating her chicken dinner. She spotted me and reached out to give me a hug. “I love you,” she said as she kissed me on the cheek. I hugged her back. When the hug ended, she kissed my hand.

Her husband smiled and said, “She thinks everyone is the Pope.”

I introduced myself and told him my husband had passed away at fifty-nine from dementia.

“Then, you understand what we are going through,” he said.

“Yes, I do,” I said. We chatted for a while about caregivers. He had just hired a new one. He was dismayed with the lack of help and support he had found. He told me he didn’t have a computer, I took his name and phone number to pass on to the Alzheimer’s Association.

It doesn’t matter where we are or what we are doing, the chances are good we will run into someone who has a personal connection with Alzheimer’s—people filled with questions and looking for answers. Caregivers muddle through the disease doing the best they can based on trial and error.

Unfortunately, when I look into the face of someone with Alzheimer’s or the faces of caregivers, I don’t have all the answers to their questions. All I can really do is offer hugs or hug back when I’m being hugged. Offer support and caring. Listen. Accept human flaws. Know that the worst response is indifference.

I’m thankful that these people shared their personal stories, and thankful for the opportunity to share a hug with a lovely lady who happens to have Alzheimer’s. I’m grateful for a glimpse into her life—learn she was once a teacher, know she has a life beyond the scope of the disease, and grateful she has a husband who fixes her plate and looks out for her well-being.

Alzheimer’s disease is as unpredictable as life itself. Each day is a new adventure and a new experience. Yesterday, I met a lovely lady named Alice, and just like in Lisa Genova’s book, she is still Alice. Thanks to her, a chicken dinner turned into a once in a lifetime experience of being mistaken for the Pope, and to share a few unforgettable moments with a loving, good-hearted woman named Alice.   

Copyright © October 2015 by L.S. Fisher
http://earlyonset.blogspot