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My Life with Cancer

 
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I took the call on my cell phone at the Starbucks in New York's Penn Station. It was from a doctor I barely knew telling me that a CT scan—ordered after three weeks of worsening stomach pain—showed a large mass in my abdomen, with what she said was "considerable lymph node involvement." I rubbed my eyes and sensed the truth instantly: cancer, and not one that had been detected early. I was 46 years old and had not spent a night in the hospital since I was born. Nonsmoker. No junk food beyond the occasional barbecue potato chips. Jogged a couple of times a week. I was not remotely ready for this.

It was Super Tuesday, March 2, 2004, the day voters would select most of the delegates to the Democratic National Convention. Although the complete diagnosis was still several days off, the intense abdominal pain meant that my wife, Emily, and I had no time to stop, absorb and adjust to our twisted new world. We immediately began negotiating the endless round of doctors' appointments and insurance hassles that mark a cancer patient's life. With my head on fire, I quietly endured a festive lunch with political reporters and anchors, then went back to work. My job that day was to analyze the end of John Edwards's presidential campaign.

Three years later, I'm in remission and, strangely enough, thinking once more about the future of Edwards and his family. Like the 10.5 million other cancer survivors in the United States, I experienced a bit of extra stress last week. When Elizabeth Edwards's breast cancer recurred in her bones and Tony Snow's colon cancer recurred in his liver, the cold fear that many of us live with every day crept a little closer. The good news is that the candor of Edwards and Snow (who is recuperating from surgery but has been open about his situation from his perch as White House press secretary) has helped stimulate a useful national conversation about how people handle a cancer diagnosis. It has also exposed the foolishness of a few busybodies who don't have cancer, but feel free to judge the complex choices made by those who do.

My own story isn't typical, because none is. Every patient reacts a little differently, both biologically and psychologically. The only constant in cancer is inconstancy; the only certainty is a future of uncertainty, a truism for all of modern life but one made vivid by life-threatening illness. According to the latest projections, a third of all Americans will be diagnosed with cancer at some point during their lifetimes, most likely when they're old. Many will never achieve remission at all, while the lucky ones like me get to live with a sword of Damocles hanging over our heads. A friend compares his semiannual scans to visiting a parole officer. When the scans are clean, it's worth another six months of freedom, though with no guarantee of extra time for good behavior.

In my case, the news went from bad to worse. To calm my nerves before the laparoscopic surgery (they cut my colon into a semicolon and removed my appendix while they were at it), I heard some happy talk about how the bowel obstruction might be benign. As I recovered and watched the slow gait of my internist down the hospital corridor I knew otherwise. "Time is an illusion," he told me cryptically, explaining that after a certain age, a few years could seem like many, and many could seem like few. I was informed that I had non-Hodgkin's lymphoma, a blood cancer that would likely shorten my life without ending it any time soon.

But we didn't yet know the all-important cell type. The day after being discharged, I grew impatient with the slowness of the pathology report and had the hospital lab fax it to me directly. Big mistake. After Googling "mantle cell lymphoma," I learned it was a rare and nasty form of the disease with a terrifying prognosis.

 
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Member Comments
  • Posted By: heckertr @ 08/13/2008 9:53:31 PM

    Comment: A word of caution about your children's reactions. Don't let their silence fool you. Adolescence is absolutely the worst time to face a parent's mortality. I lost my father to cancer when I was twelve, and believe me, it had a lifelong effect. Of course I didn't talk about it to anyone - my mother and sisters were so overwhelmed that I couldn't add my pain to their burdens. So I soldiered on, helping my mother care for my father, and not making a fuss despite my own turmoil and pain.
    Of course your children aren't going to talk to you - they don't want to increase your burden. But make sure they have someone else to talk to, where they can let out what they feel without feeling guilty about it. Otherwise that "adolescent indifference" may turn out to have been something entirely different.

  • Posted By: dwbush@aol.com @ 06/14/2008 12:54:21 PM

    Comment: Your story sounds very similar to my own. I felt that I could really connect with so many things you experienced. My diagnosis of MCL was confirmed several weeks ago. I begin R-CHOP next week at Memorial Sloan-Kettering. Since it seems you live in the NYC area, perhaps we can connect in person at some point?

  • Posted By: sj825 @ 06/06/2008 7:39:21 AM

    Comment: I was diagnosed just last week with what they say looks like Mantel Cell. The exact type is still unknown. The doctor actually told me to check out Mantle Cell on the internet without giving me any information. I was blown away. Your article was the first I read that inspired me. It has given me hope and determination. I go to the University of Virginia for a second opinion later this month, after all the other tests have been completed. I am 53 years old and was having few symptoms other than a sinus infection and a swollen lymph node in my neck that would not go away. So the diagnosis was not at all what I was expecting.

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