Mon 21 Jun 2010
Last week, Nicholas Kristof wrote in the New York Times about his recent cancer scare and how it improved his outlook on life: “A brush with mortality turns out to be the best way to appreciate how blue the sky is, how sensuous grass feels underfoot, how melodious kids’ voices are.”
This has not been my experience.
Maybe it’s because Kristof’s test turned out negative, whereas I actually have cancer, but I think it’s due more to the fact that I appreciated life sufficiently before my diagnosis, thank you very much. I mean, I’m not a moron; I read books; I have an imagination; I know that even with cancer my life is more privileged than 99.99% of humanity’s. So while Kristof is fondling the grass with his insteps, I’ve just been staggering around, gobsmacked.
I should state up front that this disease, a relatively rare (I prefer “elite”) type of cancer called medullary thyroid cancer, is not immediately life-threatening. There are roughly four types of thyroid cancer. Anaplastic is a death sentence. Papillary and follicular are more or less “cancer vacations”: they are highly curable and, because treatment involves radioiodine, rendering you a biohazard to those around you, sufferers often spend a week in a hotel during recovery, ordering room service and watching round-the-clock pay-per-view.
Medullary is somewhere between the two. It metastasizes quickly to the lymph nodes around the neck, but progresses indolently from there. Thus, surgery is the standard of care, and chemo and radiation are given only in advanced cases. Radioiodine doesn’t work, because technically it’s the C cells, not the thyroid cells, that are affected. There are a few biomarkers that give an indication of how far the disease has progressed. In my case, it does not seem to have progressed very far.
It was discovered during a routine physical by my new primary care physician. I had switched doctors because of a persistent cough that homeopathic guy wasn’t helping to solve, and the new doctor found the nodule the first time she saw me. On Wednesday, I’m having a total thyroidectomy and “modified radical neck dissection” (isn’t “modified radical” an oxymoron? And will they put my neck back together after they dissect it?). After that, there’s little to do but measure the biomarkers in my blood and be on the alert for new metastases which, with any luck, could never occur.
I shared the news only with a few close friends early on. One friend, wanting to inquire discreetly about my health in front of other people who didn’t know the story, asked me, “How’s your little project going?” For some reason, that just cracks me up. My project is doing very well, thanks for asking! We’re on time, under budget, and hitting our quality targets! Just don’t use the term “deadline”!
Since then, that’s how it’s struck me: Not as a goad to more contemplative living, but as an unwanted project draining time and resources while I’m still expected to do all the rest of my work — you know, the kind I get paid for.
Or, to use another analogy: Since I got the initial diagnosis from the endocrinologist (over the phone, during a meeting with my manager and VP, after which I had to give a presentation), I’ve felt like a computer running an extra program. On my desktop are all the usual applications: commute, kids, breakfast, work, lunch, work, commute, kids, dinner, and so on. But in the background the “cancer app” is weighing all the various cancer-specific alternatives to whatever is being discussed in the foreground. Vacation plans: Will I need to reschedule them? An off-site meeting in July: Will I be able to drive by then? A new assignment: Will I be heading into a second surgery by the time it hits?
In the morning, it doesn’t bother me too much. By the time I get into the car at the end of the day, though, I feel like the cancer program has sucked up all my CPU. Every day at sundown, I crash, and I don’t know why I’m having such a hard time with this. Physically, I feel wonderful, and I expect to recover quickly. Mentally, I want to stop the world, but it just keeps going ’round in its orbit, and I’m resentful as hell. I don’t know what’s worse: being sick, or being angry at myself for not handling it all better.
You know, as a kid, I was a huge fan of all those terminal illness stories. Remember Eric? Death be Not Proud? A Summer to Die? (If every time you get a nosebleed, you think “cancer,” then you’ve probably read one or more of these books.) I always thought that if I became a tragic heroine, I’d be a lot more heroic.

June 22nd, 2010 at 12:06 pm
So glad you’re posting again. I have missed your adept prose.
June 28th, 2010 at 8:19 am
Lurker, but longtime reader here. Your physical and mental states don’t always need to match. Sometimes that disconnect makes it harder for us to give ourselves some needed space/time/breaks. Is there any way that you can take something off of your plate right now? I’ll bet you just said “cancer”.
I know that is so much easier said than done. Anyway, I’m thinking of you and sending wishes for healing and mental peace your way.
June 28th, 2010 at 1:12 pm
I just read this, and am too late to wish you good luck with the surgery, but many good wishes for a full and speedy recovery.
June 29th, 2010 at 10:00 am
I’m a long time lurker commenting for the first time because this “elite” cancer runs in my family. My father, two aunts and my brother all have been diagnosed at varying stages. One of my aunts– unfortunately, she was the first to be diagnosed at a stage when the cancer had spread to her liver– received care for about 10 years from a great endocrinologist at Mass General (who you’re probably seeing). I don’t think you should beat yourself up for feeling like you’re not handling this the “right” way. I think medullary thyroid cancer is like that for most people who are diagnosed at an early stage. It’s a big deal to have surgery and face a lifetime on synthetic thyroid hormones, but it’s not such a big deal that you take a leave of absence from work and have neighbors arranging meal schedules, etc. You’re already almost a week out from surgery, but it might cheer you up to know that my brother (22 at the time) went skiing three weeks after his surgery (which was limited to removing his thyroid). In case your doctor has not already done so, I’d caution you to be alert to your moods as you adjust to the synthroid and bring up any concerns with your doctor. They should take that into account in adjusting your dose. My father didn’t have any problems in that regard, but my brother was showing signs of depression in the first few months.
June 29th, 2010 at 3:03 pm
hope you are recovering nicely.
i assume from your links that you had an earlier project with ivf. did you find that experience good training in approaching this current project? it seemed that it would be so for me when i was contemplating the possibility of my own cancer project, but thankfully my biopsy was negative so i can go back to my existing medical projects, which are not as psychologically draining as cancer.
i know someone else who was just diagnosed with thyroid cancer, and they think it was the cause of her infertility (her normal tsh levels provided no clues).