Part 5 - My Prostate Cancer Story
The Operation and Recuperation
I had to starve myself for three whole days prior to the operation. I could consume only clear liquids, like water, weak tea, Gatorade, and popsicles. No beer or alcohol, either. I was starving when I reported for surgery at some ungodly hour like 5:30 in the morning on June 16th. Everybody was very nice. I think surgery started around 7:00 or 8:00 a.m. Once they stuck the needle in the back of my hand, the next thing I knew was I was waking up in the recovery room in mid-afternoon. They told me the surgery lasted for three hours. My wife was there once I started coming around from the stupor. They wheeled me up to the ninth floor into a semi-private room. The other guy in the room was making all sorts of noises all night long and I couldn’t get much rest. I was pretty worn out.
I felt pretty good, though. I was desperately hungry. I was allowed to eat almost anything, so what did they bring me? Weak broth and Jell-O cubes. Ugh!!!! I hit the call button. The nurse came in. “How about a grilled cheese sandwich?” I asked. “No problem” she said. About twenty minutes later the angel of culinary excellence brought me the sandwich. Finally, some food!!! I was starving and now I was feeling a lot better.
I had IVs in my harm and a catheter running up into my bladder. During the operation, they cut away a portion of the urethra that is inside the prostate gland. They run a catheter into your bladder; then they stretch the remaining part of the urethra up to the bladder and sew it to the part just below the bladder sphincter. This has to heal up over time and is the reason for the catheter and the incontinence that will follow removal of the catheter. In the early evening, they got me up to walk around the corridors, to get some exercise. I had to take my urine bag off the bed and hood it onto that IV stand on wheels. I was now mobile as long as I kept a good grip on the IV stand. During the night, I would do some laps in the corridors. I think I did a half mile or so. I liked joking around with the nurses on duty. “How many laps in a mile?” I asked.
They released me the next day around noon. My wife brought me home for the recovery period. I had prescriptions for pain medications, which I didn’t take. I was uncomfortable with that damn catheter in me, but there was no pain. I couldn’t go to work for a week because of the catheter. There is actually a leg bag you wear. I took walks down the street and tried to avoid inquisitive neighbors. I hadn’t told any of them what I was up to either. My abdomen turned all sorts of shades of red, blue, black and purple. Apparently, those robot arms do the trick inside, but as they move around, they bruise all of your abdominal wall muscles and skin and it looked like someone held my arms while someone else walloped the tar out of me. Blood and fluids would sink inside of me. Eventually, it would be absorbed and dissipate.
I went back a week later to have the catheter removed. It was only a little uncomfortable. This is a job they assign to residents. I was glad to be free of this thing. They tested it for leakage and found none. I was good to go. I could almost walk normal now. I was to do no lifting over 5 lbs. for the next few weeks, as I might tear apart the stitches that held the urethra to the bladder. They threatened me with a fate worse than death (wearing a catheter for six weeks) if that thing ever came apart. I was scared straight. I was off work for two more days. I was off work for a total of seven days.
My surgeon, Dr. Abaza, has since told me that in the old style surgery, the most vexing problem for patients was the healing of the big long scar. With robotic surgery, that nearly ceases to be an issue and the focus is now on the nuisance and the discomfort of the catheter, a testament to the advantages of the less invasive robotic surgery.
I had to wear pads now to catch the leakage. We stopped once on the 90 minute trip home to change. There is more leakage in the beginning and it lessens as the bladder sphincter muscle heals. Leakage is supposed to last from six weeks to three months for most men. In the first day after removal of the catheter, my bladder was holding more urine. I went through the first night with no leaks, maybe because I slept on my back and there wasn’t much pressure on the bladder sphincter. In any case, over the next few days, leakage was down to a few drops a day. On July 4, I declared independence from pads. I was leak-proof. Today, I can sometimes go the whole night without getting up. I go to bed around 11:00 or 11:30 p.m. and don’t have to get up until about 5:30 a.m. My usual getting up time is 6:00 a.m. It helps not to drink anything after 9:00 p.m. I still can’t consume great quantities of liquids and hold it for a few hours, but I never could. With practice and time, maybe I can.
The potency restoration strategy.
The potency restoration strategy revolves around two things. First, take 50 mg. of Viagra (or Cialis or Levitra) every evening before bed. Don’t expect anything to happen for at least six months. The medication is supposed to improve the healing process for the damaged nerves. It is supposed to be long and slow. The second thing they want you to do is use a vacuum constriction device once or twice a day on the penis. This is the gizmo that Austin Powers brought with home from the 1960’s in his first movie. It is supposed to be funny. Laugh if you like. The idea here is that there have been reports by researchers that if you don’t use your penis for the real deal, then it will shrink. Just the thought of that scenario strikes fear into the hearts of most men. These are sort of penis calisthenics, to get the blood into it and make it big, even if only artificially so. If, after some practice, you actually want to use it for sex, you can use a rubber band-type constriction device. It rolls onto the base of the penis after you engorge it. It stays on until you release it. Don’t leave it on too long or your penis will turn blue and fall off. Imagine putting a rubber band about your wrist and watching your hand turn blue. You get the picture.
Five weeks after surgery I regained potency. I was stunned. I couldn’t believe it. The folks at Ohio State Medical Center, where I go for follow-up checks, said that I was the earliest person on their records to regain potency. I am now an official outlier, at least statistically speaking
My follow-up PSA numbers are in the non-detect range, essentially zero. The biopsy from my prostate showed that no cancer had reached the margins of the prostate. The lymph nodes adjacent to the prostate looked good and functional. (prostate cancer often affects these lymph nodes) It appears no cancer cells escaped and that, at least for now, I am cancer free.
A word about Viagra (and the others). When you depart the hospital after having the catheter removed, they will hand you a prescription for Viagra for 100 mgs/day for three months supply, along with a letter of medical necessity. Once you get this you are supposed to cut the pills in half, because the real dose is 50 mg. and they cost just the same (or similar) as the 100s. They sort of tell you “good luck with getting your prescription filled”. Your prescription provider usually only allows you to buy six pills per month. Apparently, the folks at the insurance company haven’t heard of this treatment modality and they think you are just some sort of party guy, or you’re selling to your best buds. Plan on a bit of a fight with your insurance company. Or you can go avoid the hassle and go on-line to Canada, but I’m not supposed to tell you that.
A final word of my Swedish daughter. She told me that her Swedish father had prostate cancer the year before and had his removed the old fashioned way. They have robots in Sweden, but he would have had to travel to Stockholm, a distance of some five hours away. He preferred having the procedure done closer to their home in Nässjo, so he opted for a local community hospital. She said he was doing just fine.
If anybody wants to contact me with questions about prostate cancer, its treatment or the side effects of treatment, you can contact me at jluken@miamicountyhealth,net.
A Final Word
I have to give tremendous credit to my wife, Ellen. She has been the most understanding and helpful person through this entire ordeal. She had to put up with my mood swings (in fairness, I had to put up with hers during her recent “change of life” status), my anxieties and a guy who lays around watching TV for a week.
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