“I hope for nothing. I fear nothing. I am free.” Nikos Kazantzakis’ epitaph.
Those words from the Greek Author and philosopher, Nikos Kazantzakis, have both inspired and haunted me since I was first introduced to them as a twenty-something seminary student 53 years ago. Kazantzakis, most famous for his novel, “Zorba the Greek,” wrote many volumes full of such deep and baffling sayings. Many of them have stuck with me my entire adult life, and I was reminded of again of them when my wife and I had a chance to visit Crete on a cruise to several Greek Islands last spring. Crete is both the birthplace of Kazantzakis and where he is buried.
The epitaph in particular has been on my mind recently as my awful, terrible, no good, horrible summer of 2024 has continued right into the fall. [Please read my posts from August 4th and 12th if you want all the details.]. Quite frankly I do know that my little problems the last 4 months can’t hold a candle to hurricane destruction, people living in war zones, people starving from famine and climate change, people suffering from chronic pain, grief, persecution, broken relationships, addiction, homelessness, and so many more. Is it possible for any of us to truly hope for nothing and fear nothing?
My most recent personal challenge is undergoing chemotherapy for a rare form of lymphoma in my blood. I’ve known this day was coming sooner or later since my oncologist has been tracking the slow increase of a monoclonal glutamate in my blood for over a decade. I was personally hoping for later, like much later. But of course this was the great summer of my discontent, and what better time for my IgM antibodies to set off a siren alerting my doctor that something was wrong. This alarm was as loud as our home security system when I accidentally set if off. When the IgM jumped from around 2000 in January to 6500 in July it was such a loud warning that even my denial mechanisms were overpowered.
Technically I have been a “cancer patient” for about 13 years now because I was diagnosed with a mild prostate cancer in 2011. But that cancer has never needed any kind of treatment. Being told I needed to start getting chemotherapy ASAP for this lymphoma was a whole different ball game. One of my first challenges after this diagnosis was a debate within about how I wanted to think about myself going forward. Naming something helps give us some agency over it.
I knew I didn’t want to think of myself as a “cancer patient” because I am so much more than any diagnosis or label or title can convey. We are complex and complicated beings who defy narrow definitions of ourselves. In other words, I have cancer; it doesn’t have me. But knowing what I didn’t want to identify as didn’t answer the harder question of finding a name for this new, added dimension of my being. I toyed with “victor” (maybe too ambiguous depending on how one defines what victory even looks like. Jesus certainly didn’t look like a victor on the cross, but how our ideas of victory change on Easter morning! Don’t like “survivor” either. I want more from life than just surviving. As an aside, it has taken me 6 weeks or so to reach sporadic bouts of peace where I can live into the words above. In fact I hadn’t been able to express those thoughts and feelings like this until I started writing them. One of the many reasons writing is so therapeutic for me.
At those many other times when I don’t feel good at all about my new blood brother, I have caught myself recalling the title of a 1995 movie, “Dead Man Walking.” As time goes on I have had fewer of those DMW moments and more of the positive ones. After writing this, I’m pretty sure that ratio will continue to improve. Because as I wrote this post I realized that I have a simple and maybe fun way to embrace and integrate my cancer into my “Stevenness.” You see, my cancer has a pretty cool name. It’s Waldenstrom, named after a 20th Swedish Doctor who first described it. But Waldenstrom is a very heavy handle for my little cancer. It sounds like a cousin to Frankenstein. So I have decided to christen my cancer with the nickname, “Waldy,” and that seems like a name I get arms around.
One final thought (or two): Throughout this naming/identity dialogue with myself there was a biblical scene that kept coming to my mind. All three synoptic Gospels (Matt. 16:15, Mark 8:29, Luke 9:20) recount the time Jesus gave his disciples a pop quiz. Like all good teachers Jesus starts with a safe, impersonal question. He asks, “Who do people say that I am?” After the disciples respond with several Hebrew heroes from the past, Jesus stops them and asks the zinger: “and who do you say that I am?’ Jesus went from preaching to meddling in a hurry.
Simon Peter as usual jumps in with the answer: “You are the Christ, the Messiah.” Peter knows the right words, he just doesn’t yet understand what those words really mean or will mean to him. Far too many of us today know “who” Jesus is, but that’s only half the equation. It’s one thing to answer the catechism, or recite the Apostles’ Creed, but quite another to know what those words require of us who claim the identity of Jesus’ followers.
It occurs to me that the unspoken question that Jesus leaves hanging in the air for his disciples to discover for themselves is this: “Who do You say that you are?” Have you wrestled with that question recently? Who do you identify with/as? What name do you give to the totality of the amazing God-created being you are? We humans are more than the sum of our parts. Be gentle with your being. But remember to ask yourself occasionally: “Who do You say that you are?”
The answer to that question is never final; it is dynamic and ever-changing. But the closer we get to an answer we can live with, the closer we are to fearing nothing—not even my new friend Waldy or whatever other demons with which we have wrestle.
Sorry to hear about Waldy and the need to start chemo, Steve. You have had quite a summer and now Fall. I hope that “who you are” includes being a person who tolerates the chemo well.
This post was personally helpful to me as almost 2 years ago, my routine blood work for an annual wellness visit with my doc got me sent to the Zangmeister Center, where an oncologist confirmed that I have CLL, chronic lymphocytic leukemia, a slow growing malignancy. So far the only “symptom” is the ever rising number of lymphocytes in my blood. “Some day” I will have to begin chemo. So I read your post with interest, as I have wrestled with “who I say that I am” now. I have always identified as a very healthy person. Now I have joked that I am “very healthy for a person with an incurable disease”!
I appreciate your sharing about your lymphoma and your thoughts about identity.
All the best to both of us as we navigate this!
Phyllis