It is 3:22 am, on a Sunday night. The undertoad keeps me from sleep.
Last week I went to see my urologist, to get what I thought was routine information on the composition of the 6mm stone that was removed 5 weeks ago. Boy, was I looking forward to unearthing the culprits: splenda? cottage cheese? diet cola? all dairy? All disposable, anything to never go through this again.
This is what happened: the doctor tells me I have a 12mm lesion on my kidney. It showed up during the cat scan from 5 weeks ago, the one they made me hold still for during the worst pain my life, the day my kidney shut down from the stone.
He also tells me I have a greatly enlarged prostate, and that there are palpable abnormalities in it.
So he sent me for lab work, and in a week I will know if it's kidney cancer, or prostate cancer, or hey, maybe both!
He outlines 4 procedures I will go thru over the next 8 weeks. One involves a kit they gave me, to be used over a 48 hr period, 3 weeks before the second procedure. A box with instructions and disturbing vials and tubes in it. But that's the easy one.
The other things are worse. One of them is like the shunt removal, involving a penis clamp and some guy inserting an instrument into my urethra in order to root around my prostate. Another is an intra-anal sonogram. Both of these, he concedes, are "extremely uncomfortable". Both of these are prep for the 4th procedure: a "heat reduction" of my prostate. Relatively new, this is now the preferable alternative to a lifetime of pharmacology. And fewer side effects.
Except the two weeks of pain after the procedure.
Unless the blood screen shows cancer. It seems I have a 1 in 3 chance of that. Hard to tell, exactly. I did the inevitable Google on it. But if it is, then this is what is next, this is why I am here and not asleep: they remove my kidney, perhaps part of my prostate. If it is already in both then hasta la vista, baby, no one comes back from that, multiple organ involvement, ya da ya da, better take that vacation now before the chemo makes it no fun at all, get your house in order kee-do.
Wait, there's more: my landlord -- I have one of those for a year now; we sold my only home to avoid bankruptcy when my wife got cancer 18 months ago -- has decided to sell his house, to fend off his own woes. So this will also be the summer of the 2nd move in 15 months.
I have two daughters in high school. Tonight the four of us, including my words-fail-me Good Wife Deborah, went to see The Soloist. Perfect, right? Just the thing. Silly me, I thought it would be uplifting: a Disney ending, concert with the philharmonic, life-back-on-track fable. No such luck. It was, unfortunately, a better, more realistic movie than that.
So now here I sit, alone, after hours of thrashing, trying to sleep. I wasn't going to write about this. How boring. Plus: write what? what MIGHT be?
I am thinking about what I will miss. I am wondering if I will get to take, finally, my 2nd vacation, in 25 years, with my wife, the pity vacation if it is C, or none at all, deferred again if it is not. Bittersweet, that.
I am thinking about my middle daughter's prom last month, my youngest's, coming up, in two years. I am thinking about all three of my girls being without me, at some bat mitzvah or wedding someday, unseen by me. Merely remembered. I have to stop this maudlin shit.
My Shi Tzu has padded over to me, looks at me with that empty-headed intensity, cocked head, bulging eyes, whines a little, like what are doing up? what is that noise? and I say, like I never do, in baby talk that I loathe, to a phony infant in fur, I say: Shh. Sad sack Daddy is crying.
Jesus.


Salon.com
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thinking of you...
My wife and I will pray for You. My best friend, a cyber-buddy in the mainland is in His sixth month of winning a battle with stage IIIA non-small cell lung cancer, through conventional (chemo/radiation) means, thank G-d.
I have been monitoring this site for months since the discovery. Maybe You'll find it helpful:
https://www.inspire.com/member-home.pl
You probably already know of these two, the latest in robotic surgery and the least invasive treatments:
http://www.intuitivesurgical.com/index.aspx
http://www.accuray.com/
Please do NOT hesitate to contact me if I can be of assistance in ANY way.
You went in to see the doctor for what you thought was a fairly routine situation, and then …, BOOM! … the hammer drops on top of you and you realize that your whole life just changed. I know that feeling. Your visceral expression here of your feelings is something truly shared. As Sandra says, you’ll be in our thoughts.
I wish you the best.
FUCK!
But these wonderful comments. Sandra, in a page of moving and heartfelt encouragement your voice is unique, poetry and compassion and believable. You tapped the intrinsic thing, and I am deeply touched, and admiring of how the heck you did this, writerlyissimo-speaking: made prayer pertinent, with supernaturalism beside the point. And so warm.
Thanks, everybody.
I was thinking today, that life is somewhat like war. You never know who's going to get called next. Your post reminds all of us of how fleeting this all is, and it humbles me and reminds me of how close I came. I'll be thinking of you and wishing you and your family the best.
One more thing. I did ask myself when I was waiting for those tests if those 29 years I had lived were long enough. I realized that I had been pretty lucky to experience those 29 years and all the times I'd had and friends I'd met. Suddenly, that seemed like a long time. Maybe it was just a way to cope.
Keep us informed.
face the fear, feel it, let it wash through you and do its worst, then you can put it behind you knowing exactly what it is
embrace the grief, it's just another face of love, weep when you have to, kiss your kids, love your wife, scratch your dog's ears
know that you have a community that cares, and that will refuse to give up hope
and you haven't got the diagnosis yet, I'm gonna keep believing in the best outcome
After surgery, in the convalescent home among the old men crying for their mothers, and the silent roommates waiting for death she called me over to see her wound, stapled and stitched, fourteen raw inches from below her breasts to below her navel. And when I said, "Mom, I don't want to see it," she said, "Johnny, don't be such a baby."
Six months later, at the end of her chemo, my mother knows why the old men cry. A few wiry strands of hair on head, her hands so weak she couldn't hold a cup, her legs swollen and blotched with blue lesions, she says, "I'll get better. After his chemo, Pauline's second husband had ten more years. He was playing golf and breaking down doors when he died of a heart attack at ninety."
Then my mom's eyes lock on mine, and she says, "You know, optimism is a crazy man's mother."
And she laughs.
--- hsl
low PSA numbers. No cancer.
and breathe...
and breathe...