I had the CT scan on Monday. No one weighed me. I went back
to the foreign halls of IVs, nurses and scrubs where they poked me with a
needle, taped me up and gave me a big-gulp size apple juice with barium contrast
inside it. In case you’re wondering, it’s not a tasty après ski drink. I nursed
it for the requisite hour and a half. Then they called me back again. I changed
into blues and got flat on a hard table. They tested the IV with a speed-racer
injection of saline. All systems go. The giant white donut whirled to life and
the next bits of information began to cascade into the computers. It was
cataloging the progression or regression of my cancer.
Deb and I ate steak and had a nice glass of wine that night
to run-off the memories of the testing and the fears of finding out the results
with Dr. Javle.
The next morning, Tuesday, Deb and I found ourselves again
in the waiting room for Dr. Javle. We sat for an hour, two hours, waiting for
him to show. Someone weighed me. I broke the 150 mark and my weight has fallen
to 147. This is the lowest I have gone in a long, long time, and is really
worrisome for me. I will have to start eating more and more and more. Looks
like it’s time for some Ben and Jerry’s!
Dr. Javle showed up in a good mood. My treatments have
shrunk my tumors in all cases. I look good for a cancer guy. The past 10-12
weeks of constrained life have indeed accomplished something positive. He was
so late because he had already called the liver transplant board at Methodist
Hospital to see if they could interview me this week. We’re waiting to see if
that happens. We were with Dr. Javle for thirty minutes asking questions about
liver transplants and next steps. In short, liver transplants are hard to get, but we are at least on the next stage of the journey.
He also told me I can start working out again. This is, as
you know, bitter sweet since I have loved lying around watching Sports Center
while others stay fit. Of course that is not true. I will be out there doing
something physical now – it’s about time.
Finally, we go to get the stent replaced this morning. I am
fasting in preparation; losing more weight. We hope to get the stent in so that
we can go into the Holidays with a brand new piece of plastic stuck in my
liver. We find out today.
Because it is so present in my thoughts, I have to say that while we have been here one of our close
friends who has been so thoughtful to me during my bout with cancer is struggling in his own fight. He is here with his wife and some of their friends and family. They
live close to us. They have kids at our school. He loves to fly-fish. They have
brought us Howdy Donuts on Saturdays. They are friends.
Deb and I have been
with them several times here and it is devastating. The
fiction of the situation has become so real. It sits in a strange “other” zone
that comes and goes with distraction; when you engage in a conversation, when
you read, when you walk through a crowd, the hospital room with your loved one lying in bed fades. But when you snap back to
reality, all the undeniable presence, sadness, and inevitability are still
there, demanding engagement.
We are heartbroken to see our friends in this place. Life brings a shocking reality upon which all of us teeter. It
helps to remember that loss is not so far away. Hugging a kid, helping with
dinner, making the bed, doing a date night, building a fire, wetting a line,
taking a hike, having lunch with a friend—these are all extravagant luxuries to
be appreciated.
Your words provoke me to number my luxuries. Thank you. We are keeping updates via pres and di but most importantly walking with you and deb and having numerous conversations with Father
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