I hope this doesn’t come across as preachy, but I was feeling sorry for myself and thinking about how much all this sucks, when I took a moment to reflect on my first cancer experience. Like many others with cancer on their resume, I gained perspective the hard way. Perhaps there’s a nugget here that will resonate with you.
The year was 1999. I was 43 years old. I had outpatient surgery in March – an attempt to figure out what was wrong with me. That’s when they discovered I had an unusual form of ovarian cancer that forms in the lining of the abdomen.
Lots of doctor appointments, lots of tests, lots of unknowns and lots of fear. The big surgery was in April. I learned it was Stage 3, Grade 3. The survival statistics were terrible – about a 30 percent chance of living five years.
I went home to recover and prepare for chemotherapy.
The treatment was basically six months of intravenous chemotherapy, which I think I finished toward the end of August. I fared pretty well through the ordeal, but it was no pleasure cruise. Then I had to recover enough from the chemotherapy to face another surgery in October. Although all signs indicated the cancer was gone, it has a high recurrence rate, and the doctor wanted to do what is called a second-look.
They go in and biopsy the crap out of everything. If all is clear, you’re done with chemo. If they find microscopic cancer, you get more chemo. I had no evidence of disease and have been fine ever since, except for breast cancer in 2015.
For the first two years after treatment in 1999, I went to the doctor every two months for a check-up. That included a pelvic exam, blood tests and sometimes a CT scan of the abdomen. After two years, I graduated to every six months, and that went on for three years. After five years, I started going once a year, which I still do, although now it’s just a blood test and a howdy-do.
After every appointment ending with an all-clear, I’d think, another two months to live! Another six months to live! Another year to live! It was kind of a joke, but life was what happened between appointments.
I wanted to share this because it made me feel better about life’s most recent curve balls. We’re what? Six months in? I know it’s not the same. My illness didn’t impact the world or the economy or anyone’s job. As I was recovering, I could go to restaurants and parties and otherwise lead a normal life. I was lucky.
Still, statistically speaking, the odds were against me. I could cocoon myself in a bubble, but the very real threat of getting sick and dying was with me for years, no matter what I did. I learned to live with ambiguity, and I just kept going. I’m certainly not alone. Somebody reading this or someone you know is living with a life-threatening illness or a deep personal tragedy, and yet they just keep going.
Maybe that’s it in terms of the message here. Just keep going. And this might be a cop-out, but I try not to think too much about the big picture. It’s too big. There are smarter and stronger people who can take on the world, but when the shit hits the fan, I do better by focusing on small things that make me happy.
It’s like I’ve been saying all along. Simple pleasures. I don’t know any other way to get through this.