The first time Dad left the Margate Rehabilitation Facility in West Jefferson, NC was to get his staples out at the orthopedic office. The plan was staff from Margate would get him to the office and mom and I would meet him there. Mom and I arrived at the office before dad. The waiting room was pretty large–it probably seated around forty people–and it was L-shaped so that when you went up to the window where people were being checked in, it was hard to see the whole room. I went to the window to talk to the receptionist about how patients usually arrived from skilled nursing facilities. The nurse said sometimes there were multiple drop offs for the bus driver to make at different locations and they could work Dad in even if he got there late.
I went back to sit with mom and a few minutes passed. I absentmindedly scanned the room and saw Dad sitting in a wheelchair near the door. His face was blank as he stared ahead. I’m sure he didn’t know where he was or what he was doing here, and I thought about Dad’s life. These days, he mostly lay in bed. It used to be he’d watch any basketball game that was on, and he’d watch a lot of cable news including Fox and CNN. He stopped watching sports first; he just couldn’t follow what was going on anymore. Dad had coached sports his whole working life–including basketball, baseball, and golf–but now sports on television didn’t hold his interest. For nearly ten years, watching the news had really riled him up, and I’d say hadn’t been very healthy for him. He worried about my sister living in LA. He worried about terrorists taking out the power grid. He worried the banks would be unable to function or that the grocery stores would cease to have food. Of course all of these things could happen, and it’s probably not a bad idea to prepare by degree for those contingencies, but Dad was in his eighties with advanced Parkinson’s, and I wished for him that he could have let all of that go. If I’m blessed enough to make it to eighty, we’ll see what I pay attention to.
I thought maybe one reason that Dad stopped watching sports and the news was that he couldn’t see very well. As a part of Parkinson’s, his eyes were really sensitive to light. One day at Margate, I turned on Dad’s television. “Wolf Blitzer,” Dad cried out, as if seeing an old friend. Dad’s life was mostly something that happened to him–as opposed to his making choices to make things happen. Dad lay in bed. Food arrived. People came to change his diaper. People came to give him a sponge bath or a haircut or to shave him. Two big dudes came to take him down the hall to, as he said about his therapy, rough him up.
I walked over to Dad at the orthopedic office. “Well hello, Dad!” I said.
“Bill!” Dad exclaimed with surprise. “Boy am I glad to see you.” I wondered if anyone told him why he was here, and if they had, if he had been able to understand them. I explained he was going to get his stitches out from his hip surgery. When it was Dad’s turn to go back to an examination room, Mom, Dad, and I all crammed into a little room with a nurse. Dad was taken away for an x-ray and eventually we were told that his hip looked good. The staple removal was tough for a couple of reasons. We had to get Dad’s pants down, and I had to hold him at a certain angle for the doctor–or maybe she was a physician’s assistant or a nurse practitioner–to clip the staples and pull them out. “It might feel like a bee sting,” she said as she worked her way through the staples. She had some trouble with several of them. Dad groaned as she took some of them out.
Through no fault of the staff or conditions at the skilled nursing facility, I could see Dad give up while he was there. I tried to show Dad how to work the television remote and the buttons on the side of his bed, but he didn’t show any interest. Maybe he couldn’t comprehend any longer how those things worked, or maybe he just wanted to sit halfway up and stare at the wall in front of him. He had what seemed like daily hallucinations to me in which he’d think he was talking to one of his golf buddies or coaching a basketball game from decades before. His enthusiasm for my visits began to wane too. “Hey Bill,” he’d say when I’d walk into his room. Then, he’d just go back to staring ahead at the wall. Even though insurance would pay for dad to stay longer, I thought it might be time for him to come home.
The main pro of having Dad at the facility was that mom was able to get a pretty good night’s sleep and the staff at the facility changed dad and kept him clean. It was summer, I wasn’t teaching a class, and the high school basketball team I coached wasn’t playing games. For now, I’d be able to be around the house most of the time. The cons of keeping him in the facility were that dad didn’t want to be there and the forty-five minute drive each way that mom had been doing most ways. She probably didn’t need to be driving that much, and it was a lot for me to get out there and it might be less to just have dad conveniently located in the same house as the rest of the family. I thought Dad’s life would be better–I don’t think I could go so far as to say happier–if he came back home to live with us.
Could we just take Dad out of the facility whenever we wanted? It turned out the answer was mostly yes. I remember some light pushback related to the therapists thinking that in another week or two Dad might be able to stand with the assistance of only one, but when I called the woman I’d first talked to when considering the facility, the woman I knew had recently lost her own mom, she told me there’s no place like home. It was decided. We would bring dad home in two days, on Thursday, September 5, 2024.

