................."I started out with nothing, and I still have most of it left.".................

Friday, December 21, 2012

Thanksgiving and Veteran’s Day


Today, December 21st, is my Thanksgiving and Veteran’s Day.

Many of my friends have urged me to write about my cancer experience, and I certainly have enough material to make it book-length.  I will take this occasion to pen my first public comments by way of a short and to-the-point blog post.  Maybe someday that book will come, too.

On October 30, 2007 I discovered blood in my urine.  After an emergency room visit, a CT scan, and an ambulance ride to a downtown Seattle hospital, on Friday, November 2nd I underwent a procedure called a TURB (Trans-Urethral Resection of the Bladder) to remove a tumor.

On November 5th, 2007 I was diagnosed with advanced bladder cancer.

When the urologist had first looked at the results of the CT scan, he told me to expect the worst.  While he was very clear that he could not give an actual diagnosis until he removed and analyzed the tumor, he said that from the size and location of the growth, in his experience it was most likely T3 disease, which is cancer that has spread beyond the bladder. The 3-year survival rate for T3 bladder cancer is 5%.

Following the TURB, the official diagnosis was not as bad as he expected.  He and a second-opinion doctor both recommended bio-therapies and a second TURB to look for any other tumors.  The experience gained in four years of volunteer work with the Lance Armstrong Foundation kicked in, and I sought a third opinion as well as reading everything I could find on and off line about bladder cancer.  I soon learned that there are two opposed schools of thought: the “bladder sparing” proponents, also known as the Sloane-Kettering or east coast school, and the “radical surgery” proponents, known as the USC or west coast school. Realizing that all three opinions were solidly from the bladder sparing side, I asked my urologist to recommend a doctor from the opposing school for a fourth opinion.  This turned out to be Dr. Sia Daneshmand at OHSU (Oregon Health and Science University) in Portland, OR, considered among the finest bladder cancer surgeons in the world and a veteran of the USC Norris bladder cancer program.  I met with him on Monday, November 12, 2007, and after a day of tests and consultations he recommended immediate surgery to remove the bladder.

I will never forget his words. “This thing only exists for one reason,” he said. “It exists only to kill you. You must play offense.  If you play defense it will always win, and you will die.”

On December 21st, 2007 I underwent a Radical Cystoprostatectomy with Lymph Node Dissection and Orthotopic Ileal Neo-bladder Diversion, performed at OHSU by a surgical team led by Dr. Daneshmand.  The surgery took almost eight hours, and involved creating a new bladder (neo-bladder) from a one-meter section of living small intestine (Ilium) and installing it where my original bladder had been removed.  The recovery was hard.  From a urological standpoint, I was like an infant when I came home from the hospital six days later.

My recovery was slow at first but gained speed quickly after the first three weeks.  I was walking a mile a day after week four, and I took my first wobbly one-mile bike ride around the neighborhood in week eight.  Today I am fit and healthy.  Of course if I had a choice I would never had gotten sick, but we don’t get to make that choice, and cancer for me has been a great blessing in my life.  I can honestly say that the last five years have been the happiest of my life, by far.  Over that time I have watched my youngest two children graduate from college, and three weeks ago I held my first granddaughter.  Tomorrow I will turn 60 years old.  I never thought I would see any of these things on November 5th, 2007.  I feel I am a better friend, a better father, and a better husband because of what I have experienced and what I have learned.

I have been cancer-free for five years today.

Dr. Sia Daneshmand and the author


That explains why today is my Thanksgiving pretty easily, but what about Veteran’s Day?

Through my work with the Lance Armstrong Foundation, dealing with cancer in my immediate family, and of course my own cancer experience, I have talked to a great many people who have dealt with this disease.  Here are three of the most significant things I’ve found:

There is still stigma attached to cancer.  Yes, we’ve come a long way in our country, thanks to the Pink Ribbons, the Foundation, and many other well-meaning organizations.  In rural Africa, those afflicted with cancer are routinely driven out of their village and left to suffer and die alone.  But major stigma still exists even in first-world post-industrial countries like Italy, where it is taboo to talk about cancer, and cancer in a family is considered a deep dishonor.  It exists here too, if in a lesser form.  Exactly 100% of the people I’ve spoken to who are living with and through cancer and its aftermath have told of friends who have simply vanished permanently from their life, apparently unable to deal with the reality of cancer so close at hand.  Regrettably, I have experienced this myself.

Hold the battle metaphors, please.  The vocabulary of those writing about cancer is dripping with comparisons to war.  Nobody dies from cancer; they “lost their courageous battle,” etc.  Almost everyone I have spoken with in the cancer community hates this.  As one of my favorite cancer wits put it: “When someone dies in a car accident, you never hear about how they lost their brave battle with a Subaru.”

Survivor, or surviving?  Many of the folks I have spoken with are deeply uncomfortable with the whole “survivor” terminology.  To many, it demeans those who die from cancer, and let’s face it, more people die from cancer than are cured.  It seems like you are self-identifying as somehow superior, when all of us know how fortunate we are to be among the minority group whose treatment has worked, if only for now.  We’re surviving, I suppose, but does that make us survivors?  One of my favorite writers, Mary Elizabeth Williams (Salon.com) was diagnosed with malignant melanoma a few years back, and we have had some interesting discussions on these issues, including the survivor thing.  If we’re not survivors, then what do we call ourselves?   We’ve not yet come up with the perfect name, and I don’t think there really is one, but she likes to call us “veterans.”  I must say I like all of the connotations of that word in relation to cancer, even though it does suggest the old war analogies.  I’ve run this one by many cancer – ahem – veterans, and most seem more comfortable with this one than others.

So, please join me in wishing a very happy Thanksgiving and Veteran’s Day to, well….me.

Now where’s that corkscrew…