Cancer – Six months later

Six months ago, December 5, 2019, my right kidney and the associated cancerous tumor were removed.  My feelings about my kidney cancer are mixed. 

I did not have any pain or other symptoms prior to the surgery.  The surgery thus did not relieve any pain or symptoms. I know the cancer was real.  I saw the image of the tumor bisected on a table after it was removed.  I read the report confirming the tumor was cancerous.  

However, in my head, the discomfort I experienced post-surgery is associated with the surgery, not the reason for the surgery, kidney cancer.  For me, my cancer remains an almost theoretical thing more than an actual thing. 

In late June I will get another CT Scan and a couple of days later will meet with a Urologist.  I assume everything will be fine.   

Post-surgery, I slept on a recliner for a couple of weeks because my back really did not like me laying flat.  However, it got better.  We’ve since got a Sleep Number Bed and that is working great. 

On my right side of my abdomen are six small prominent, reddened surgery scars. I get tired a little more easily than I think I should.  Which is normal, I am told, until my left kidney grows larger and thus cleans my blood better.  In the meantime it is getting better but sort of annoying.

When I lift something heavy or stretch out like when I put a box on a high or low shelf, I feel a slight twinge in the area where my kidney was. The weirdest thing is when I take a drink of cold liquid, I can feel the cold as it goes down my throat into my stomach. My doctor said he had never heard of that before.  

I am on Medicare which made the cost of all of this pretty much a non-issue.  I am providing some of the details below because I imagine some are wondering how much it cost.

The removal of a kidney and cancerous tumor by a team of renowned surgeons followed by a four-day stay in a hospital is not cheap. The follow-up care by my normal doctor and my Urologist is not cheap. There was a very thorough pre-op physical.  Oh, add the ultrasound scan, CT scan, and the radiologists who interpreted them.  Did I mention the anesthesiologists?  Several lab tests and the followup calls from the nurses to make sure I was recovering properly.  The list goes on.

I only have a vague idea of what it cost to remove a kidney and a tumor.  I got numerous very confusing Explanation of Benefits forms which came over several months.  I tried to keep track in my head.  I think the amount billed was in the forty to fifty thousand dollars range. The amount actually paid by my Medicare Advantage plan was about half of that.

The important thing for me was how much I owed. When I got the news that I needed my kidney removed I called UCare, my Medicare Advantage Plan provider. I was told it would cost me a $250 copay for the hospital and $20 for each specialist visit. They were right. Now six months out, I paid the $250 copay for the hospital stay. I also paid like three or four $20 copays for specialist visits. 

Of course, each month a $329.20 premium payment ($144.20 for Medicare Part B and $185 for my UCare Classic Medicare Advantage Plan) gets deducted from my monthly Social Security.  Which is both convenient and assures the premiums will be paid even if I am physically or mentally unable to do so.   

Just a side note. For me, kidney cancer brought into focus just how important universal healthcare is.  I am now a strong supporter.  There are worse models than the Medicare model. 

Starting to get exercise was recommended by my doctor so I joined the YMCA. I  was a couple of weeks into using an elliptical machine when the  COVID-19 pandemic closed them down.  I enjoyed the Y and am looking forward to getting back at it. 

As far as COVID-19 goes, cancer and only one kidney are on my list of several “underlying conditions”.  Being reasonably careful is about the best I can do about it.   Worrying is not productive. 

I know I had a serious form of cancer and had major surgery.  Which nobody wants.  However, they are now a part of my life experience. It is like they were ingredients added to the stew which is my life. As weird as it sounds, somehow I think my life experience is richer having had this experience. 

Of course, my cancer gives me pause once in a while. There are times when I feel sorry for myself. Mostly, I am reminded life does not proceed in a predictable straight line. When the unpredictable happens, it adds more depth and breadth to my life.  Maybe I am now a slightly less boring person. 

We did several trips last year which resulted in some wonderful memories.  Between cancer and the COVID-19 Stay at Home order, our travel has stopped for the time being.  

Our life goes on.  I got a new lawnmower and mowed the lawn yesterday afternoon.  The lawn really didn’t need mowing but I really wanted to try out the mower.  Two days ago, we sat on a patio, distance talking to our grandkids.  Life is good. 

 

The closer you look, the more you see.  

www.scaleandperception.com

One thought on “Cancer – Six months later

  1. Appreciated reading about your experience . Glad you are on the mend. Sounds like you are luckier than some people I know or knew. Lots to be grateful for.

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