My mother’s sister, Thea Maria, died the other day. She was 101 years old and was the oldest of six children, Maria, Thespina, Eleni, Sophia, Efrosini, and George. Yes, five girls and finally a boy.
As their mother died very young, when my mother was only three years old or so, Maria took on helping to raise the other children. My mom told me stories about how hard she worked and how she was often strict with them. She also told me about how, while still a girl, Maria broke her ankle badly. In the hills of the Peloponese back in the 1920’s, there was not great medical care. The villagers set it as best they could and let it heal. But she was considered crippled after that. How crippled? I’m not really sure. What I do know is that she didn’t work in the fields after that, and she didn’t attract a mate. When she died this week, she had been living with her sister Thespina for the better part of 70 years.
They lived together in Thea Thespina’s house in Athens. Uncle George, the baby of the family, had lived around the corner and looked after the sisters. He bought groceries. He fixed things. He drove them to the doctor. He did a lot. He drove them from Athens to the village every summer, and back in the fall. The sisters spent summers in the village of Arbouna, in the family home, the home in which they were all born, until fairly recently. But Uncle George had been too ill to drive everyone around the last few years, and he finally passed away last spring. Neither George nor Thespina had children. As they aged, it fell to their nephew Taki, Thea Eleni’s son, to look after them all. Thea Eleni herself died more than 40 years ago.
Thea Sophia died in 2002. So now it is just Thespina, and my mother, Efrosini. Both have dementia, and my mom is a little worse, I think, though at 91 she is a good five years younger. My mom had a tough year last year, real tough. But she is bouncing back and doing surprising well right now. Who knows, she might have another 10 years in her.
All I know is that I wish I had gone to Greece more, paid closer attention, and knew more about my blood than I do. I suppose there is still time to learn a little more before the last two of the people that connect me to a different world and a different time are gone.
A couple of weeks ago I got a call from the board and care facility where my mom lives. It was late morning. They said she simply woke up complaining of intense pain and couldn’t move her left leg. She had been in bed all morning. I went over as soon as I could. She was clearly not able to move her leg much and certainly could not stand. But as she lay there in bed, she said she would be okay, that she just needed to rest her leg because she had been overdoing it. Then a little later, she said she had fallen down a couple days before and now it was sore. I had seen her a couple days ago. And the day before. This didn’t really quite add up. That’s not really a big surprise considering she has worsening dementia. Nonetheless, I worried that she had indeed fallen and that I wasn’t getting the whole story from the nursing home. They claimed she just woke up with pain in her leg.
She was actually in pretty good spirits and insisted she would be fine with some bed rest. I already had a lot on my mind that day, so I didn’t push it. I decided I would go back home to finish a couple errands and call the Kaiser advice nurse from there. I described the situation as best I could. The advice was to get to the ER as soon as possible. Which we did.
I started to assume the worst, which was that she had fallen and destroyed the hip replacement she had just had done in May, and from which that she had only just fully recovered. In fact, just two days before when I had seen her she was really getting around great with her walker, and taking a few steps here and there without it. This was part of the reason for my increased worry. She has always been incredibly stubborn. I plead with her to be safe and always use her walker. Which she doesn’t.
We spent all day and evening in the ER. They x-rayed her hip. It looked fine. That was a huge relief. She is so small that the x-ray image got about down to her knee, and the ER doctor saw something down there. So eventually they got another set of shots of the left knee. There they saw a bone chip. The location and lack of bruising suggested that she had not fallen. The doctor opined that something like a sudden muscle contraction could have pulled off a bit of her fragile bone. Perhaps she was catching herself from falling. It also appeared that there was not much to be done about it. After finally hearing back from the orthopedic doctors about her x-rays, the ER doc declared that they would put a brace on her leg and that we could leave. But it was now midnight. Everyone would be asleep at her facility. I would have to get her into my car here, and out at the other end—or pay a few hundred bucks for an ambulance. And she was pretty loopy from the morphine, not to mention tired and in pain when she moved. Moving her at the moment didn’t see like a good idea. So, I talked the doc into keeping her there in the ER overnight so that I could come and get her in the morning. Which I did.
We had an appointment with the orthopedists the following week. We sat in the waiting room. I took some pictures. Eventually we saw the doctor. The doctor agreed that surgical intervention was not worth it. But she cautioned that it would be painful for a while. Which it has been.
Ever since I was laid off from my job in February, life has been exceptionally hectic. This seems completely counter-intuitive. This is because I obviously have much more free time than I did when I was working full time. Nonetheless, the free time seems to fill up fast with things that I either wish to do or that come up that I must do.
One huge thing that has come up is caring for my mother. This started the very day I was laid off when she fell and broke her wrist. About three weeks later, her left hip, which had been painful for months as the prosthesis from a much earlier hip replacement was rattling around loose in her femur, finally just broke. That is, her femur just started disintegrating. It was time to attempt a total revision of the hip replacement. This was a major undertaking that just a couple months before was seen as not worth the risks by an orthopedist at Kaiser Richmond. But now the risk of a failed surgery, becoming wheelchair bound, was already a reality.
The first orthopedic surgeon to look at her new situation, basically thought he could not do anything for her, but offered to refer us for a second opinion. The referral was to Dr. Bini, director of orthopedics for Kaiser East Bay. Dr. Bini was very confident he could fix her. “I can cut this and replace that; and if that doesn’t work, I have some other toys I can play with.” But he was very upfront about the risks: “For a 91-year-old, the anesthesia is dangerous. Or afterwards, she gets a clot and it goes to her lungs, that’s it. Or she gets pneumonia, which it’s unlikely she’ll recover from.”
We decide to move forward with it, and he schedules her for April 29th, at the end of an already full day of surgery for him. He just adds her in. So, there were three days of appointments for tests, including blood, urine, ekg, and biggest of all, a heart stress test with nuclear imaging.
Finally, she has the surgery. Dr. Bini calls me 5 or 6 hours after I left her with the pre-surgery team to say that the surgery went great, and that she came through it well. By Friday, she was recovering really well and they were planning on discharge to a rehab home the next day.
But the next day, Saturday, she started having terrible trouble breathing, and a chest x-ray showed patchy fluid throughout her lungs. It looked like pneumonia. By Sunday, she was moved to ICU, on an oxygen machine that helped keep her lungs inflated (bipapp?) and the doctors there were mostly talking to me about her health directive and “do not resuscitate” (DNR) status. We were all preparing for the end game. But I know these old Greeks, and her in particular. She’s too stubborn. Monday morning, the doc on watch suggested that she could be on the breathing machine indefinitely and that if she goes a couple days without change it might be time to think about pulling tubes out of her and just keeping her comfortable till the end. I said let’s see what we can pull back in terms of intervention and see how she does. So, over the course of a couple hours, we took her off the back-pressure oxygen, and got her down to just a little oxygen through a nose tube, not even a mask. And there started the big rally. The ICU docs were surprised.
She continued to improve through the week in terms of her infection and ability to breathe. However, she refused to eat, take her meds or otherwise cooperate in any way. Her lack of English, baseline dementia, and combination of lack of sleep and regular morphine all had her totally delusional. I was having to come in everyday to try to get her to eat and take some meds. By Friday, the ICU docs were again concerned that this was going to send her into decline again. And they felt like the hospital environment was a big factor in her disposition. They wanted to discharge her to a skilled nursing facility for rehab and focus on getting her on a normal routine. Saturday they did that, and sent her to Kaiser Post-Acute. Of course, that didn’t change her attitude much. They called me this morning to talk to her about eating, letting them take her vitals, and starting physical therapy on her hip. I tried. Later in the morning, we (Sarah, Theo, and my friend David) all went there for a mother’s day visit, and to see what the situation is. I actually got her to eat several bites of pureed food (can’t blame her for not liking it), and let them get her vitals. It looks like that is going to be the drill for the coming days, until she gets oriented. Assuming she ever does.
A portrait of my father taken when he was a young man, probably about 1918 or so. Here it is up in my mom’s apartment in Albany CA. 2009.
It hung on the wall in the living room, in the corner, next to the door, over the couch, when we lived at 1210 Griffith Way. When I was really little, up until at least seven or eight years old or so, I was scared to be alone in the room with it at night–i felt like the eyes followed me. I surely loved my father, and i was not scared during the day, but somehow, at night everything changes.
I can’t quite bring myself to put it up in my mom’s room at the rest home. I’ll have to scan it and print a copy for her to have there.
i was holding it in my hand today, and really looking closely at it, noticing the various imperfections, damaged corners and so on. I also really noticed what a fine looking young man my father was. He was 63 when I was born, so my concept of him is, of course, of an older man. I wondered too, about his motivation for having such a portrait made of himself, at 18 or 20 years old, fresh off the boat in New York and not speaking much English at the time. Was it a simply convention to do so? Was it vanity? Was it for family?
I’ll never know.
This print of the last supper had always hung near the breakfast table in my parents’ home. It was no different here at my mother’s last apartment, although it had fallen off the wall and sat around for a few months. I set it back here the other day, and it seemed a fine place for photo. A detail shot would reveal drops of this and that, and a spattering of tomato sauce.
It is a bit of an odd assortment off things on the cupboard, most sitting for weeks without notice from mom. Tomato sauce, orzo, salt, vanilla flavoring, the Greek coffee pot (the briki), and assorted trivets. A couple times in recent months my mom had cooked food with some odd flavorings, like baked chicken with a heavy dose of cinnamon or ground cloves. Eventually she gave up on seasonings and then finally on cooking much of anything besides boiled eggs, green beans, or broccoli.
Today, we went to Kaiser for an eye check-up and to start the process of getting a new pair of glasses. She had misplaced her only pair. It turns out that her right eye needs just about the strongest lens available. The doctor could not determine a prescription for the left eye at all because she is nearly blind from a cataract. So, we’ll be going back for cataract removal, and then eventually for a prescription for the left eye. Shit, no wonder the apartment was a mess. And no wonder the chicken was seasoned with salt and clove instead of salt and pepper.
I’m slowly making my way through photographing the items in my mother’s apartment. I only vaguely remember the suitcase. It was not used very often. In fact, the only time I remember it being used was when my mom visited Greece once. When we moved my mother up here we just packed it full of curtains she had made for her house. She would not let me throw them away.
The chair and end table are part of a set purchased when we moved into a new house my dad had built on Griffith Way in Fresno, back in 1967. There are two chairs and couch which, unfortunately, were reupholstered around 1980. The sofa was cobalt blue and I’ll never forget that thing. But I can’t quite picture the original color of the chairs.
The furniture all has to be gotten rid of soon. I was all ready for that. But now I feel more sad about seeing it all go. I had a fantasy while I was going through stuff the other day that I could move my mom back into her house in Fresno and find a wonderful, reliable, relatively inexpensive 24/7 live-in caretaker for her. Then all the power objects could stay together for another couple years. But these childish dreams must be left behind…
My mother, Efrosini Serafimidis, will be 90 years old this month. For the last five years she has been living down the street from us in a little one bedroom apartment. We moved her up here to Albany from Fresno and the home in which she had lived for over 30 years. I was resistant to moving her at the time, but my cousins insisted it was necessary. It is not easy for a person in their 80’s to switch gears like that. She still complains bitterly everyday about this place, and I think she still is a little resentful towards me on that count. But she did okay for two or three years.
The last couple years have been increasingly challenging. She has had a hip replacement and big surgery on a broken elbow. Also, she has been pretty lonely during the days when we are at work, and the lack of interaction and stimulation has taken a toll on her.
The next move is now necessary. This month, Effie will be going to a board and care facility somewhere nearby. It is going to be hard to do, and the transition is going to be a struggle, I’m sure. But her hips are not holding her up very well, and she is suffering from some dementia. She has wandered off a couple times, but her incredible luck with coming across non-Greek-speaking people who are charmed by her old-country, head-scarved, four-foot-ten-inch figure has held up. Each time we got her back none the worse for the wear.
Of course, Sarah and I both work full time, and have a five-year-old to attend to. And living in the Bay Area has its own challenges. So, I would not say I have been an overly conscientious caregiver, but nonetheless, I see her and give her her meds almost every day, try to keep her reasonably safe and fed, bring her back and forth to my home, clean her apartment, pay her bills, take care of her legal and financial matters, manage the renting of the family home in Fresno, and so on.
Chief among the challenges of moving her to a care facility is going to be the dissolving of her apartment home and figuring out what to do with all the things in it. We got rid of a lot of stuff when we moved her to Albany. But a lot of stuff is still packed away in her apartment. I am very nostalgic about these things and have a tough time just trashing them even though they are otherwise pretty worthless.
In response to all this I am planning a photo series. Right now the idea is simple snapshot-like photos of, basically, every object in her apartment. Where possible, descriptions will accompany the photos. Eventually, the series will include photos of each and every object I still have from my parents. I may be an old man myself by the time I finish.
My earliest memories go back to the house my parents lived in when I was born, at 818 “S” St. in Fresno CA. We were Greeks on the edge of Armenian Town. I don’t quite remember living there, since we moved when I was about two years old. But I almost do. I remember being at the house, although I think it was when my parents were going back and fixing it up to sell when I was about three and half years old.
I remember the look of the old wooden house, the wood floors, the old door knobs, the pulley clothes line that stretched from a window to the far reaches of the back yard. I remember the feel of the hot, powdery dirt in the Fresno summer, and the way it smelled when the water from the bib fell onto it, making dusty explosions that turned to mud. I vividly recall, even now, the smell of the cellar we retreated to for lunch once the sun was high and hot. We sat at a card table and ate in near darkness, the only light streaming in from the cellar door at the top of the stairs. There was a certain musty smell of damp concrete that I encounter every few years, and when I do I am transported back to that cellar more fully than any sci-fi invention could ever achieve.
I toddled around the front yard and wandered into the yard next door. There I encountered the old Armenian woman who lived there. She was very old and bent over, wrinkled and gray. In my memory, she was wandering around her garden tending to her plantings, she wore nothing above the waist and her breasts hung low and flat. She spoke to me in Armenian and I understood nothing of what she said to me. I stood and stared up at her, a little afraid, but not too much, perplexed by the sound of this language. She smiled as she spoke and chuckled around the edges. My mother called and I turned to go, running through the powdery dirt that burned my feet. The smell of Sycamores wafted by as I scrambled up the front steps.
A bit tragic. The stove was in mom’s house in Fresno. The renters swapped it out with the Wedgewood that I had stored in the garage there, and left it out in the elements for a couple months. When I found out, I brought it up to the Bay Area and stored it at my work place for a couple years. I fretted about it and wondered where I could move it. I called some old stove restorers to see about having it serviced and cleaned up. They didn’t want to work on it, but said they would take it off my hands for parts, for free. I said “no”. I eventually had to it move out back of the shop wrapped in plastic for several months. But eventually the wrapping failed, and it got wet and started to rust. The other day, a couple scavengers from the neighborhood came by in an old Datsun pickup and asked if we wanted to get rid of it and a crappy old refrigerator that was sitting with it. At this point, I was no longer able to justify spending a lot of money trying to fix it up, and I had no place to install it, or to store it. I gave it to them. Another little piece of my life lost in the mists of time.
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