I am a cat.

Natsume of the Funky Ear

In the weeks following Michael’s death, the house seemed oddly empty. So after a time we decided to start searching for a new pet.  One of our counselors even suggested getting a pet as part of the healing process, especially for Caitlin.

We started looking at the local shelters and animal rescue centers to see what they had to offer. Initially we looked for a dog, but weren’t able to find a suitable one. Regulations for adopting a dog can be very rigid in this area, and misunderstandings seemed to be common.

So we expanded our search to include cats. I have always considered myself a dog person, but I have no real issues with cats. Especially since my cat allergy reduced. For me it really depends on the character of the cat. Some cats are insufferably aloof, even snooty. But others are great company. Both of the cats I have lived with had good personalities. Catfael was a very reserved girl, and was often suspicious of people.  She and I had a rocky start, but eventually became good friends. Nigel was a very outgoing cat to most everyone he met. He was very fond of Caitlin, and enjoyed hanging out with people.

So for me, the primary criteria for a cat was the character of the animal. That and it had to be a short hair. I still have a cat allergy, but it only seems to come out around the long hair varieties, like Himalayans or Persians. I suspect living with Catfael and Nigel gave me some resistance.

There was another criteria we had: Caitlin wanted a calico (if possible). One of her favorite programs is an anime called Bungo Stray Dogs, which is a metahuman adventure serial with a decidedly art deco appearance and film noir story style. It’s actually quite good, though it takes time to get into, given the complex backstory. Anyway, there is a calico cat that figures prominently in the setting, and his name is Natsume. Most of the characters in the show are named for writers, including Natsume.

In early December we learned of three calico cats that were up for adoption in nearby Orange county. So Lisa and I went to look at them. All three of them had good personalities and could have worked out. But one in particular stood out. Remember how I said I have always considered myself a dog person? Well one petite girl just mobbed me! She was purring like a motorboat and snuggling like she had never been petted in her entire life. I actually had to work at keeping her tail away from my eyes (the allergy thing again). Then she went over to Lisa and started doing the same stuff. I’ve been told that the pet chooses the master just as much as the master chooses the pet. As with Watson, it was clear that this petite calico had made her choice.

Just to be sure, we went back later that day with Caitlin. Not surprisingly, the cat approved of Caitlin with the same gusto she had shown Lisa and I earlier. We adopted her then and there, and by late afternoon she was at her new home, and sporting her new name, Natsume.

She was reported to be four years old, which we doubted given her small size. However, after a steady diet she put on weight and now falls into the normal weight range for an American short-hair. She lived with other cats, and we think she was bullied by larger ones (including, apparently, her own brother). According to the shelter report, she was surrendered because her owner could no longer care for her. We suspect an older person who moved into a nursing home and couldn’t bring their cats.

We sometimes call her Natsume of the Funky Ear, because one her ears sports an odd curl. We understand this is the result of a sunburn from when she was a kitten.  One of her favorite activities is attacking piles of laundry, and batting at my boot laces when I get ready for work in the morning.

When we adopted her, we weren’t thinking in terms of a therapy animal. But in many ways she has become one. Her cheerful sounding meow, frequent purring, and regular snuggling have had a very positive impact on the atmosphere of the house. She will never replace Michael, obviously. But her calm, quiet yet cheerful presence has eased some of the pain of loss.  I am very glad we adopted her, and I hope she is able to live with us for many years to come.

Regarding the writer for whom she is named, Natsume Sōseki, he was a novelist who was active in the late 19th and early 20th century. He spent two years in England, and many of his works were inspired from his time there. Which is strange, because he absolutely hated the place.

One of his most famous works, if not his most famous, is a satire called I am a cat. In this, he made comments on the behavior of certain high society types of 1905-era Japan, but from the perspective of a house cat. I understand it can be dark and biting, but also very funny. It has been compared to a political cartoon, biting newspaper editorial, or even a sarcastic monologue from late night television. I have not yet read his material, and I understand that it doesn’t translate very well. Satire often doesn’t. But even so, I am a cat is on my to-read list.

Natsume sleeping

Everyday associations

August 31, 2019. This is the last clear photograph we ever took of him.

This article is related to the tragic and unexpected death of my son, Michael.

The days immediately after Michael’s death were very difficult. I had been warned that certain objects, sights, sounds, and even scents could trigger any number of strong emotional responses. I certainly experienced those.  Some were centered on physical objects, like the jar of peanut butter on the kitchen counter, the boxes of apple juice in the refrigerator, and the articles of clothing I pulled from the dryer. Others were connected to specific words that came up in conversation. Words like pillow, tent, phone, and blanket were among his most frequently used.

I was especially aware of sounds, or rather the lack of them. Michael would frequently take a smart phone or other handheld device and use it to play some of the worst “music” I have ever heard. A lot of the stuff he liked on YouTube, for example, sounded more like white noise than music. (For someone with his sensory issues it may have sounded just fine, but I hated it.) Whatever the case, for months there had been a constant, muffled stream of sound leaking from Michael’s bedroom. In the evenings following his death, I was very aware of its absence.

I also found some associations that I didn’t expect. Lisa and I like to watch Animal Planet together. Some of the shows we watch involve the operation of zoos and wildlife sanctuaries, where all kinds of animals are featured and discussed. Some of the other shows we watch involve game wardens and other types of law enforcement officers dealing with animal control issues. Sometimes these officers deal with the search, rescue, and recovery of missing people. On the night of Michael’s accident, I saw the real thing. A group of policeman and other first respondents were combing a wooded area looking for my missing child.  When I looked at the TV screen and saw those game wardens searching a wooded area, it was like a sledgehammer to the head. Knowing that those wardens were looking for evidence of illegal hunting, and not a lost child, didn’t matter. It was the visual image that set me off. In my contorted mind, all I could see was a man in a police uniform running out of the forest carrying the wet, lifeless form of my son. The images on the television were too similar, so I reluctantly told Lisa that I couldn’t watch any more. The TV was turned off, and the disturbing silence returned to our home.

It has been four months since that horrible day. The emotional associations with everyday objects and events are starting to fade, but they still occur. I suspect some will continue for some time to come. Perhaps for the rest of my life.

Goodnight, sweet prince.

Michael Vincent Pugh, 2012-2019

“Tears are the silent language of grief.” —Voltaire

It has been said that the worst pain a parent can feel is the loss of a child. I now understand, and agree with, that statement. Thursday, November 21, 2019, would have been my son Michael’s seventh birthday. Tuesday, September 24, 2019, was the day he suffered an accident that ultimately ended his short life.

The events of that day are hard to keep straight, even after several weeks, but I will try. Caitlin, Michael and I had arrived home around 6:30 in the evening after a very routine trip to the grocery store. We had also spent a little time at a local playground and took care of a few quick errands. When we arrived home, Caitlin went into the house while I unloaded some of the groceries. Michael climbed out of the car and started walking toward the front door, like he had done dozens of times prior. At that moment I received a phone call.

Somewhere within the next few minutes, catastrophe struck. I had been on the phone for roughly five minutes, when Caitlin asked me, in alarm, where Michael was. The last time I had seen him, he was walking toward the front door. But apparently, at the last minute, he changed direction and went somewhere else.

Michael had wandered off before, so this wasn’t without precedent. He wore a signal device on his ankle for just such an emergency. Caitlin called 9-1-1 while I quickly ran around the property to see if I could find him. After a few minutes, emergency services had started scanning for his signal device, and help was on the way. In the mean time, I continued to search the area around the house while Caitlin spoke on the phone with Lisa, who was still in town on other business. Within ten minutes, people from throughout the neighborhood were searching for Michael. A few minutes after that, two sheriff’s office patrol cars arrived and joined in the search.

At roughly 7:00pm his signal was located, and he wasn’t far from the house. But the signal wasn’t moving, so the policemen were getting anxious. A few minutes later he was found floating face down in a pond, not a tenth of a mile from our house. He was cold, wasn’t breathing, was unresponsive, and his heartbeat was erratic. He was immediately rushed to Culpeper hospital.  By this time, Lisa had returned home, so we quickly loaded into the car and started for town.

Upon arriving at Culpeper hospital, Lisa ran to the emergency room to see Michael, while I stayed with Caitlin. For close to 80 minutes they worked to necessitate him and stabilize his pulse. They eventually succeeded in stabilizing his heartbeat, but he was still unresponsive. A doctor informed us that he was being airlifted to the University of Virginia’s pediatric hospital in Charlottesville where further treatment could be performed. But the doctor feared that Michael was already brain dead.

We collected ourselves and left. The plan was to make a quick stop at home for a change of clothing, medications, and the like. On the way home we hit a deer. The crazy animal literally appeared out of nowhere and destroyed the car windshield! Fortunately, the car could still be driven, so I turned on the hazard lights and slowly drove the rest of the way home. We picked up what we needed, loaded into our other car, and headed for Charlottesville.

We arrived there around 11:30pm, and found Michael in a ward room connected to various tubes and monitoring devices. We was receiving a steady supply of medication to keep his heart running, and a respirator was helping him to breathe.

By this time Lisa, Caitlin and I were expecting the worst. The hospital chaplain on duty was an Episcopal vicar from the University. He was very helpful in helping us to focus and remain calm. He did not perform last rites on Michael, because we weren’t at that point yet, but he did recite a special prayer for seriously ill patients.

The next several hours were long and surreal. The real concern was that there was no sign of neural activity. Over the course of the night, nine different doctors, all with different specialties, examined Michael. Unfortunately, all of them said the same basic thing. Namely, Michael wasn’t going to survive.

We had one last cause for hope. If Michael had slipped into some sort of coma, he could potentially wake up. If such a thing is going to happen, it almost always happens within 24 hours. Also, an EEG test would determine weather or not his brain was still functioning. But to be reliable, we would have to wait for the appropriate specialists to arrive in the morning.

We made a few phone calls to workplaces and schools to let people know where we were, and why we wouldn’t be showing up that day. Then we started calling family members, some of whom were out of the country at the time.

The neural specialists arrived around 10:00am on September 25, and started testing. There was still no neural activity. Michael didn’t even show a blink response when his eyes were subjected to bright light. The EEG rating was so low that the technicians weren’t sure they were picking up background electrical activity from the instruments themselves.

The prognosis was simple, and tragic: Michael’s brain was gone. It was only a matter of time before his heart and lungs stopped working. Now we had to make the most difficult decision that anyone can ever make. But before we did, there was one more expert we needed to consult.

We contacted the hospital chapel and requested a Roman Catholic priest. The church is notoriously strict about certain things, including when to take a person off of life support, so we wanted to speak with a priest before proceeding.

The Newman center at the University of Virginia hosts a small Dominican friary, and one of the friars came to see us at about 1:00pm. I wish I could remember his name (it is written down in our papers somewhere), but he was a very understanding man. He also knew the vicar who spoke with us the night before, and may have already spoken with him. We explained the events of the previous several hours, including the assessments of all the medical personnel who had examined Michael.

The priest informed us that whenever there is a reasonable chance of improvement, medical treatment should continue. That is, if there is still a chance of the patient recovering, we – the family – are morally obligated to continue treatment. But for Michael, this was not the case. After considering everything he knew, the priest concluded that continuing medical treatment on Michael was not going to bring any useful results. After some discussion, we decided to meet Michael “half way.” We would reduce the medication to a minimum, and allow Michael to leave on his own. 

But a new development appeared. A social worker asked us if we wanted to donate any of Michael’s organs for transplant, or if we wanted any of his tissue samples to be used for scientific study. This was a surprisingly easy decision to make.

We easily agreed to organ and tissue donations. After all, Michael wasn’t going to need them for much longer. This required him to remain on life support for a few more hours while the necessary surgical equipment was prepared and the needed personnel were gathered. Everything would be ready shortly after 8:00pm that night.

While completing the paperwork for the donations, I asked if a brain tissue sample would be taken. When I was informed that one would be, I stipulated that it include a portion of his corpus callosum membrane. That is the membrane that coordinates communication between the two hemispheres of the cerebral cortex – the left and right brain. In Michael’s case, it was always thin and inefficient. The two halves of his brain literally didn’t communicate well. This was arguably the root cause of his disability, and I wanted to make sure it was examined. Perhaps something could be learned that would help future patients. The social worker noted my concern, and told me that it would be followed.

The priest performed the anointing of the sick, followed by last rites. The equipment was re-configured to keep him stable for several more hours, and that was pretty much that. The priest returned to the friary around 2:30pm, while the three of us went to the hospital cafeteria for a much needed meal. We were beyond exhausted, and our emotions were all over the map. All in all though, it was a welcome break.

Shortly after 8:00pm that night, we were informed that the surgery rooms were in the final stages of preparation, and that everyone who needed to be present was on site. The medication drip was reduced to minimum, and he was disconnected from the respirator. Then something very beautiful happened.

The hospital has a ritual they perform when a terminal patient is being taken to donor surgery. As the patient is wheeled through the hospital, staff members in whatever rooms are passed go into the corridor and watch them roll past. It is their show of respect to the patient and the grieving family. Michael was wheeled through the hospital, flanked by several doctors and nurses, while Lisa, Caitlin and I followed behind. Along the way, his favorite song was playing on my smart phone. As difficult as it was, it did provide some comfort.

Michael’s heart and breathing stopped shortly after 9:00pm on September 25. We started for home about thirty minutes later, to whatever future awaited us.

Michael was entrusted to the Clore-English funeral home in Culpeper. His funeral mass took place a week later, on October 4, and his ashes were interred on October 21.

I will add to this story when I am able. But for the moment, this is as far as I can go.

“Tears are words that need to be written.” ―Paulo Coelho

Farewell, Dr. Watson.

Tonight, we had to say goodbye to a very dear friend. Doctor Watson, our 10-year old Border Collie / Australian Sheppard mix, had to be put to sleep. For the past few months he had been suffering from a variety of digestive issues. One of the vets we spoke with suspected a canine variant of Crohn’s disease. Whatever the case, none of the treatments he received had any lasting effect. Having to euthanize a pet is an agonizing decision, but it’s one that most pet owners eventually have to face.

At some point last weekend, Lisa and I realized that the inevitable was within sight. I wanted to take him to one of his favorite walking and running places, for a final runabout, but he had been too weak to do much moving. I then considered getting him one of his favorite treats, as a parting gift, but he hadn’t been eating consistently for a few weeks. It was painful to see.

He spent most of his last day sleeping in his favorite spot on the living room floor, right below the skylight.

Such images stir up memories. When we first moved into our house, we promised Caitlin that we would get a dog. When I was young, I had a very good experience with a Border Collie mix, so we started searching for one. We acquired Watson from the Atlantic Region Central Border Collie Rescue, based near Richmond, back in 2009. He was roughly a year old at the time. When we went to the rescue farm to pick out a dog, we were greeted by several bouncy, rambunctious Border Collies. Some were entirely too rambunctious, and one was downright pushy.

Watson was different. Granted, like the others he came into the meeting pen and vied for attention; such behavior is common for Borders. But once he finished that, he settled down on the stairs and leaned his head against Lisa’s shoulder. A short time later, he sauntered over to Caitlin and did the same. Finally he came over to me, gave me several licks on the hand, then sat down next to me. It’s been said that dogs often choose their owner. Watson certainly choose us, and we were very lucky for it.

We couldn’t have asked for a better dog. He was as friendly and good-natured a dog as one could ever find, and he was always great company. His table manners were never the best, and he tended to flop down in the most inconvenient places possible. But at the same time he rarely begged, wasn’t an incessant barker, and he never got on the furniture (unless he was invited).

In many ways, Doctor Watson was the first one to realize that Michael had a life-threatening cyst on his left lung. When Michael came home as a baby, we had some extended family milling around, and some expressed concern over Watson’s aggressive sniffing at Michael’s left chest. When we learned that Michael had the cyst, we concluded that Watson must have sensed that something was wrong. (Perhaps he could smell the corrupted tissue?) Apparently he was trying to inform us.

The decision to put him to sleep was heartbreaking. But again, the various treatments we tried were not working. It was as if his entire digestive system just gradually stopped functioning. Given that he wasn’t eating at all consistently, there was a real chance that he would starve right in front of us. We had simply run out of options and time.

As I write this, I realize how much I’m going to miss the furry goofball.

After taking care of things at the vet’s office, Lisa started for home, while I took care of some errands in town. When it came time for me to grab a quick dinner, another strange memory surfaced.

A few years back, I brought home take out from Burger King, because we were all too tired for much else. Before I could distribute the food, however, Watson’s muzzle had descended into one of the bags. He managed to snarf up a double whopper with cheese, some chicken tenders, and an order of onion rings. He didn’t even have the decency to get a stomach ache later! I wasn’t happy with him. Neither was Lisa, because it was her sandwich that he had stolen!

Earlier this evening, I went into Burger King and ordered a double whopper with cheese, with onion rings. Such fare is unwise for a type-ii diabetic, and I suspect I will be reminded of that when I check my sugar before going to bed. But Watson would have loved it.

I looked at that big, greasy sandwich, and couldn’t help but smile before biting into it. This one is for you, Watson.

Sleep well.

Lisa featured Watson in an article connected to her blog.