Note: This blog was started about a month AFTER I had been diagnosed with MCC. This initial post is supposed to bring everyone up to speed with my current posts. For now, I'm updating this little by little until it catches up with reality. Stick with it -- it'll all make sense one day.
I just started this blog and I'm already behind.
I first heard the word Merkel on November 16, 2010 during a phone call from my dermatologist reporting the results of a recent shave biopsy. Since then I've already had surgery, consulted with a medical oncologist, a radiation oncologist, and learned that I'll probably be getting radiation and chemotherapy.
This first, very long post is an attempt to give explain and give a background for everything that's happened up until the current posts start.
My MCC was diagnosed from a skin biopsy taken around the beginning of November 2010. It was in the same spot where I had a squamous cell carcinoma (SCC) excised back in February of the same year. Why the excision of the SCC? For that, we need to go back even further.
My first kidney transplant was performed in November of 1978, back when the earth's crust was still warm. It lasted only about 6 weeks before rejection caused the graft to fail
and hemorrhage leaving me on dialysis. The rejection episode even blew
out some kind of artery in my right leg that kept me in bedridden for
nearly a week. It was a big deal. On October 15, 1979, I received my second transplant which was an qualified success. It lasted a full 24 years before it began to gradually decline because of chronic rejection. On July 8, 2005, a few weeks after it I became medically eligible to dialyze, I received my third transplant (thanks Bruce!) which continues to function beautifully to this day. I think I've finally gotten this transplant thing down.
So why am I bothering you with transplants? Because for the last 32+ years, I've had a suppressed immune system that allowed my body to host a foreign object (someone else's kidney) that kept me alive and essentially normal, but also made me more susceptible to infections and cancer. Additionally, the drugs available for transplants back in '79 were not particularly kind to the skin, making me even more susceptible to skin cancer. Oh, and since I was 18 when all this started, I was immortal and not really careful about sun exposure for the first few years of transplantation.
So from here on out, there will be minimal mention of kidney transplants except as related to immunosupression and the consequences thereof.
About 15 years into my 2nd transplant, I had my first Basal Cell Carcinoma removed. My primary doctor thought it was a wart, kept freezing it, but it wouldn't go away. I was recommended a dermatologist who naturally did a biopsy and determined that it was a BCC. To him, not a big deal, but to me, it was like boulder had dropped on my chest. Ever since the first transplant, I had been told that I was more susceptible to cancer, but like most of us, I thought it would never happen to me. Now I had been officially diagnosed with Cancer.
The BCC was excised and I made it a point to notice new lumps and bumps and
growths on my skin and take them to a doctor. I can't say I got
complacent, but I was lulled by the statistics: BCCs and SCCs are the most
common form of skin cancer, are slow growing, and are highly treatable; hardly
anyone dies of them and I'm seen pretty regularly by a doctor anyway, so I'll
catch them before they get out of hand. I figured as long as I was
vigilant and stayed out of the sun, I'd only be inconvenienced by dermatology
appointments and some pain going through the actual excisions. The thought of something like MCC screaming
in from out of the blue never occurred to me.
The BCCs and SCCs started ramping up around 2000, and later on, I was
getting at least four or five excisions done every year. Because of
changes in insurance plans, I've had several dermatologists over the years and have
lost track of how many excisions I've had, but I know for a fact that I've had
over 50 excisions done by my current dermatologist. I can't begin to count the number precancers
and suspicious stuff they've frozen off with liquid nitrogen. They have
three fat volumes on me and I'm angling for my own parking spot.
Our strategy is for me to go in every few weeks for a skin check, and freeze
the bejesus out of anything that even looks like it's thinking about
turning into a cancer. The stuff that grows back gets biopsied, the stuff
that's positive gets removed.
The frequency of my visits is what saved me. .
To be continued...
Here's what you're in for...
This is a chronicle of my experiences, observations, and feelings as I experience treatment for Merkel Cell Carcinoma (MCC). The goal is to give anyone going through chemotherapy and radiation for MCC (or any other cancer for that matter) an idea of what to expect. Of course I'm a unique individual just like everyone else, so what happens to me may or may not happen to you. Your mileage may vary.
I'm a pretty reserved guy, so most of these posts will be straightforward, just-the-facts-ma'am entries. I may occasionally get maudlin, but cut me some slack -- I could die from this.

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