Time For Celebration

[I wrote this (slightly edited) post in 2017, a couple of years before I was diagnosed with myeloma. Time is a subject that has been on my mind for a very long time. I wrote my dissertation about the work of Harold Adams Innis (1894-1952). He was very much preoccupied with time and wrote extensively about it late in his career (and life it turns out). So have been hundreds of other philosophers, social theorists, physicists, biologists, etcetera. We think about time on many levels of analysis, from cosmic time to microseconds in productive processes. We think about it in social as well as personal terms. We are especially concerned with it when it begins to run out. Read on]

How do you experience the passage of time?

Time is a big subject and has been the focus of many philosophical and scientific ponderings and is, of course, a major preoccupation of the world’s religions and cultures. There is also the individual, institutional and cultural projects around time and its importance to our lives. We mark (as distinguished from experience) time in many ways. We use clocks and calendars. (The Maya had two calendars, that’s how important time was to them.) We carefully note the passage of the seasons with special celebrations, and we celebrate our birth days every year. We don’t celebrate the day we die, of course, we let others do that in the form of wakes, funerals, and these days, celebrations of life because we are no longer in any shape to celebrate anything ourselves.  We ask: “What time is it?” and we expect to get an answer: “Why, it’s two thirty in the afternoon.” We don’t expect “the anthropocene” as an answer although it would be technically correct.

But this blog post is not about any of this. It’s about how we experience time. In many ways, time and life are synonymous. As individuals we need to be conscious to experience time. In our dreams time is irrelevant or, at least, it can take on bizarre aspects, but we aren’t aware of that until we wake up and can reflect on our dream and its bizarre depiction of time. Writers, novelists in particular, distort time as a regular practice.

We experience time as past, present, and future although we live only in the present. The past and future are cultural constructs that have only the reality we give them. Our memories and our recollections of events are highly selective. There is no such thing as an objective past. We select events, actions, people, names, places, etc. and construct a cognitive map of them into a coherent picture, a picture that is congruent with our life as we experience it and build a store of impressions by which we then judge our actions and those of others. Recall is impressionistic, not realistic. It deceives us all the time as we ‘fit’ the past into our current views of things. 

We are most often not even aware that that’s what we’re doing. We drive, we brush our teeth, we pay taxes, we get on airplanes, we go to libraries, we bank, we vote and most often we don’t question these actions or even consider them a part of a consistent set of habits of life and thought that we learn from others as we live out our lives in networks of interdependencies. As Norbert Elias argues we are less individuals than interdependencies and interweavings. Our daily thoughts and desires, as they join collectively to express themselves as consciousness, make us more Borg than anything. Magically, however, we learn to believe that we control all aspects of our lives as individuals and sadly, people who have shitty lives can only blame themselves for that. That’s the classical economic view of things. Classical economics, according to Thorstein Veblen, uses what he calls the hedonistic calculus to describe how we make decisions in our lives. For him, classical economists (and I would add more contemporary trickle-down ones like Milton Friedman) think of us as ‘globules of desire’ who everywhere seek to maximize pleasure and avoid pain. Of course, life just doesn’t work that way. We do not judge every situation or opportunity we encounter in life as a calculation of pleasure or pain. There are numerous capacities and propensities we bring to our daily lives that have everything to do with the need to delay pleasure, accept pain or make decisions clearly not in our own interests. 

We interpret the past, the present and the future based on our ideologically constructed maps of how the world works. And, boy, do we love our maps. We hang on to them for dear life. Those ideas we cherish, those beliefs we idealize are created in a cauldron of the past, a past we had no hand in making and that starts presenting itself to us the moment we drop out of the womb. Of course, the ideas we pick up early in life we often reject later as we join more and more interdependencies and interweavings, some of which will have more appeal and relevance as the world changes around and in us. 

Christians and adherents to many other religions accept time as a concept, but deny its existence after death when, for them, eternal life kicks in. How could we experience time in a state of eternity? Time is change. What would happen in a place of eternity? I’m no theologian, but I’d be curious as to how a theologian would deal with the question of time in eternity.

Merry Christmas, all, and Happy New Year. 

Life and Death: How Absurd!

[This post was first published in June 2019, about four months before my myeloma diagnosis. Lately, I’ve been re-reading my posts looking for the best ones to re-post. This one is a particular favourite of mine, so here it is for you again. I don’t think I can express the ideas presented here any better now than I did back in 2019. I’ve been trying, but with no success. So, rather than continuing to beat my head against the wall, I decided to give myself a break and re-post this piece now. I hope you find it interesting (again). Just got news that an old colleague of mine just died. It seems we’re dropping like flies these days. Pretty easy to predict.]

We are born, we live and breathe for various lengths of time, then we die. Seems rather pointless, really. For as long as we know, and from all the historical records that we have unearthed or discovered one way or another, we can only conclude that humans have not ever been terribly enamoured with this situation.

Of course, most animals are averse to death, or at least to dying. Death itself isn’t particularly scary, it’s the getting there that we have a problem with. Even an ant feeling attacked will flee or fight. Of course, once it’s dead there is no issue. Not all animals face dying in the same way. Without being too anthropomorphic, some are stoic, some are frantic. In humans, some are even self-destructive but I’m not sure that death is what suicides want. Relief from pain and suffering is probably the goal more often than not, but in many cases, death seems the only respite, the only place where there may be peace. Of course, that’s silly because there is no ‘place’ after death. Death cannot be a respite from pain and suffering because we have no way of experiencing relief from pain in death. Death is the absence of sensation, of thought, or feeling; it’s the absolute negation of consciousness. Death is no thing. Before we are conceived we are also nothing, no thing. Life as we think of it as sentience, feeling, consciousness, starts sometime in our development. It’s hard to know when. In a way, death puts an end to the whole story.  Historically and linguistically, we have wanted to contrast living with dying, but they are not opposites. Death is the only way life can happen. So, why, generally, is it so hard for us to let go of life? Well, like all other animals we have a survival instinct, or an instinct for self-preservation. With rare exceptions, there seems to be an inherent drive in all animals to continue to live. I don’t think any species would get very far without it. It does present a problem for us, however. It means we go to great lengths using our big, unfortunate brains to deny death using whatever means we can, and boy do we have lots of means! Our cat is afraid of death. She skulks around wary of a stray cat in our neighbourhood we call Mean Gene because he beats up on our Princess Pretty Paws. Still, she hasn’t managed to institutionalize death denial. She just can’t take it that one step beyond immediate, visceral run-like-hell action. And when Mean Gene is no longer in sight, Princess is just fine. She is not anxious and preoccupied with dying. She’s still interested in her food bowl, however. 

What it gets right down to is the fact that as animals we reproduce sexually and engender offspring who are themselves immediately on a trajectory to death. Living and dying are the same process. Stop dying and you’re dead. Now that seems completely unfair. We are built to die! What the hell! Well, that just can’t be, damn it!

Over the millennia, we’ve created any number of ways to convince ourselves that we don’t really die, that although our bodies may perish, our ‘souls’ do not, and that makes us immortal in a god-like way, really. For us to be immortal we must be gods and by our earthly deaths experience apotheosis. Millennia ago, when we were still in our infancy as a species, we were awed by the powers of nature and our extreme vulnerability in the face of them. We decided that there must be some sentient power that controlled the forces of nature, the floods, volcanos, fires, landslides, and other deadly phenomena. Not only were there powerful natural forces, but they were capricious and unpredictable as well as uncontrollable.

In our silly wisdom, we figured out that maybe, just maybe, we could barter with the gods so that they would leave us alone. If we presented the gods with gifts, even living gifts (as in virgins thrown into a volcano), maybe we could obviate the damage the gods inflicted on us. It was fine to kill all the people in the next village, but leave us alone, please. Well, that didn’t always work according to plan, so an explanation was necessary. So, if our village was ravaged by a fire even though we had been really good and had made lots of sacrifices to the gods, maybe those sacrifices just weren’t enough. We just had to kick up the giving a notch or two. Sadly, we are still very much controlled by this narrative. 

 

Such a Mess.

I must admit that I’m a bit depressed these days. A substantial contribution to my depression is the amount of caution I need to exercise every day in the face of the coronavirus COV-2 and the cancer that I still harbour in my bones. Even though I’m triple vaccinated, I still need to be very cautious lest I contract the virus in my compromised state. Picking up an infection, any kind of infection could be deadly for me. Carolyn is also immunocompromised because of arthritis meds she is on, so we are somewhat reclusive these days. Carolyn still does virtually all the shopping, but I do get out with her now and again. In my younger days, I was a moderately social guy. Not anymore. Among many other things, I miss having a beer at the CBC with friends. 

As far as myeloma is concerned, there seems to be just minute traces of it in my blood. Of course, I’m still on chemotherapy. Who knows what would happen if I suddenly went off chemo. I may need some dental work requiring an antibiotic. My local GP/Oncologist figures that I shouldn’t be on chemo and an antibiotic at the same time. He suggested that I think about going off chemo for a while, at least during the time I need for the dental work. He also suggested I talk to ‘my’ oncologist in Victoria about it. I had an appointment with an oncologist in Victoria this coming Monday, but he cancelled, according to his assistant, because he was called away unexpectedly. Great. I haven’t had a meeting with an oncologist in Victoria for months, and now who knows for how much longer. I haven’t had an appointment with the same oncologist in Victoria twice in a row. They are specialists, of course, so I don’t expect to have the same kind of relationship with them as with my GP, but still, I don’t know how continuity of care happens in this situation. I feel a little abandoned. 

What I find as distressing as anything as a person with cancer is the absence of predictability. Well, I guess I can always predict that I won’t be able to predict how things will go. I can usually predict that I’ll be going to the hospital every fourth Thursday of the month for an infusion of Daratumumab, but even that is a toss-up. It all depends on my bloodwork. If it’s good, then I go. If not, then I don’t go, and things change quickly. What I mean by the absence of predictability is more the idea that when I get up in the morning, I have no idea whether I’ll have any energy, will be lucid, or how much pain I’ll be in, and in which part of my body. Right now, the peripheral neuropathy in my left hand is bad, especially if I sleep on it in a particular way. As I write this, I’m feeling very tired and ‘dizzy’, even disoriented. I feel like I have a hangover. I don’t like it. I’ll go down for a nap soon. I’ll see if that helps. There’s no predicting. 

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Slip slidin’ away.

I know three people who have chosen MAID (Medical Assistance in Death). The reports from relatives (or from themselves) suggest that they went gently into the night under conditions of their own making. I know others who have either not had the time to set up MAID, or who, for whatever reason, chose to let things run their course and for whom the pain of dying was muted with the help of morphine or other pain killer.  After reading Barbara Ehrenreich, Brian Greene, Siddhartha Mukherjee, Atul Gawande, and Jason Fung, all authors I’ve discussed in this blog at times, it strikes me that slipping gracefully into death is not a fate most of us will share. I don’t know what the billions of people in the poorer parts of the world suffer as they approach death. I know that in some places where wars are still all too common, death by a bullet or a machete are a fate that await many people. Death by poverty is all too common. It’s true that death awaits us all, but the conditions of dying are not democratic. Considering all living things on this planet, dying is generally shunned. Yesterday, while shaving, I inadvertently disturbed a spider who was minding its own business in and around the vanity lights. It took off, scurrying like mad, wanting to live another day, I surmised. It did not want to die. 

As biological organisms we tend to cling to life for all it’s worth. Obviously, there are exceptions to this rule. Even for people who commit suicide, I suspect (with no hard evidence whatsoever) that it’s not life they are escaping, but unrelenting pain, physical and/or mental. I’m sure that they would gladly continue living if the pain would only go away. I think that’s true of people who choose MAID as well as those who commit suicide in any number of non-sanctioned ways. Of course, the people who I know chose MAID were older. As Barbara Ehrenreich wrote (somewhere, probably in Natural Causes) when she got to be seventy-five years old: “I’m old enough to die now.” I’ll be seventy-five next year, and I guess I’m old enough to die too, but I think I’ll endeavour to stay alive in 2022. 

18 Looking in the Mirror.

[This is a reprint of a post I wrote in January of 2020. I reproduce it here in honour of Elizabeth (Bunny) Shannon who was especially drawn to it. Bunny died of cancer last month. She was a friend and an extraordinary person. I am privileged to have known her]

When I look in the mirror I see an old man. I don’t see an old man with cancer. I just see an old man with a white beard, not much hair, and wrinkly skin. Melanoma (skin cancer) often leaves visible, sometimes unsightly and disfiguring lesions. I don’t have melanoma, although my father did. No, I have myeloma (bone marrow cancer) and its damage is all done on the inside, invisibly. So, I guess I can keep expecting people who see me say: “Wow, you’re looking good!” I guess I DO look good! Now, the last thing I want is to discourage people from telling me how good I look, so keep it up! However, the invisibility of my condition is deceiving. I remember when I was a kid my friends and I used to work on our cars. That was still possible when I was a kid. Often we’d stand around looking into the engine compartment (often of my 1956 Pontiac four-door hardtop) wondering what could possibly be wrong as if just staring at the engine would give us some kind of clue. The engine was always sparkly clean and there was nothing obviously gone awry. If I had money by some quirk of circumstance I might take the car to a mechanic. If not, we might borrow my dad’s tools and start taking things apart. That usually ended up badly. Yes, the most undesirable conditions in life are often on the inside, impossible to see or diagnose by just looking at the person or car in question. I find it best to consult mechanics when our car shows signs of disfunction. I find it best to consult medical specialists for treatment related to my body. I guess I could try to treat myself using any number of the ‘cures’ available on Dr. Google, but I would like to live a while longer, thanks. Besides, I’m not that desperate.

Speaking of medical specialists, we saw my local oncologist today. I see him every five weeks. The result of our visit is that I will carry on with a second course of chemotherapy. We’ll evaluate how well it went in five weeks. My first course of treatment seems to have gone as well as could be expected. The little excavator in my bone marrow is slowly running out of gas and my red blood cell garden is growing again. I’m still exhausted and that won’t change for some time yet, but things are certainly going in the right direction for now. I think I just might be a model patient. So, where does this all leave me?

Well, I may be on my way towards remission. If and when I do go into remission, and that’s by no means guaranteed at this point, that would buy me some time. By that I mean that I may have a few years more to live, though inevitably, either the myeloma will kill me or some other condition will. I won’t be walking away from this situation, brush the dust from my sleeves and carry on. No, I’m on a one way street. So are you, of course, but I can see that damned barrier at the end of the street. I’m hoping that you’re still far enough away from it that you can live in blissful denial for a while longer. I don’t have that luxury. So now what do I do with my life?

That question came up in a recent Facebook thread, albeit expressed in a different way, but with the same effect, I believe. The question comes down to this: If you knew that you had a given amount of time left to live (six months, two years, whatever), what would you do with your time? Would you to be seized by an overwhelming sense of urgency? Would you be determined to cram as much activity and experience into your remaining time as possible? Or would you curl up in a fetal position in a corner of your bedroom quivering and whimpering while you await your inevitable demise? If you have the money and the energy you might want to get out there and travel the world. If you have a spouse, that might complicate things more or less because they may not want the same things you do and may not want to get caught up in your sense of urgency. The last thing you need when facing terminal cancer is marital discord. I think there’s a lot to be said for just carrying on with life as before.

If you have the energy and the money then good on ya. If you travelled a lot before your diagnosis then travel after. Your eventual energy deficits will tell you when to stop. If you were fairly sedentary, more into being at home and puttering around the yard, then that would be something you might want to continue doing. The stress of travel may not be that good for you. Looking around the Cancer Centre at the North Island Hospital this morning I didn’t see a lot of people with obvious enough vigour to engage in a lot of physical activity. In any case, back to my situation.

My exhaustion prevents me from doing much in the way of physical activity. If I do go for a walk I pay for it later. Travelling is impossible. At one point I thought it might be possible, say, to take a direct flight to Puerto Vallarta back and forth from Comox, but there are a number of contingencies that make that next to impossible that have more to do with arthritis and disk degeneration than cancer. Besides, I take chemo drugs once a week orally but also by injection at the hospital. For three or four days after I take my meds I feel crappy, really crappy so the chances of enjoying myself on a beach somewhere are slim to none.

So what do I want to do, and what do I actually do? Well, I want to work on our canoe, finish some paintings, do odd jobs around the property and visit family and friends in Vancouver and further afield. What I actually do is sit and lie down a lot. As I sit and lie down, I read, and sometimes I even write. At the moment I’m reading social history around the Middle Ages and doing a bit of research on my family roots in Normandy. That’s something I would have done anyway, but I do miss working in my shop and studio and going for long walks with Carolyn and our imaginary dog. My oncologist thinks I will regain my energy, at least as much as an old man can expect. If so, that would be great. I’d love to get back to canoeing, camping and puttering.

When I get closer to dying I will know it, and I expect I will have time to think about it, but there really isn’t much thinking that is productive about dying, at least not for me. I’ll know when it’s time for palliative care. I don’t want to live as long as the oncologists might want to keep me alive. I’ll make the decision when the time comes. I don’t think it will be a really hard decision. I know that beginnings are impossible without endings. My ending is a lot closer now than my beginning! That’s fine. Frankly, I’m much more concerned with my family than I am with myself. They are the ones left behind to mourn. But both of my parents are dead and we got on with life after their deaths. My family will do the same when I’m gone. That’s what we do as humans. Like it or not, accept it or not, rage against it or cower in a dark corner, the end result is the same. Don’t sweat it.