Lucky Number Seven

Seven years ago, my surgeon has moved my appointment ahead by two hours. Shawn booked the time off work to go to the appointment with me and this last minute change means I’ll be going alone. “It’s fine,” I tell him. “It’s not cancer.”

I’ve seen a lot of doctors and specialists over the last six months, and though there is some contradiction on how low the odds are (some say there’s a 2-5% chance and others say 5-10%) what everyone agrees on is this: the lump in my neck that has steadily grown from the size of a pea to the size of an orange is probably not cancer. In fact, one baby doctor is so sure it’s not cancer that he congratulates me, says, “you’ve had two biopsies, we’ve looked at seven samples from seven different areas of the nodule,” (it’s still a nodule at this point, not yet classified as a tumour,) “you don’t have cancer.” When his I-don’t-know-the-right-term-for-a-baby-doctor-supervisor returns and he tells her what he’s gone over with me, she speaks in a voice that is ice cold, tells him they don’t know what is growing in my neck, and shares her opinion on what my various test results mean to her. She’s the one who convinces me I should have diagnostic surgery, she’s the reason my cancer is found.

Shawn doesn’t listen to me and rearranges his schedule so he’s with me when I get my results. My surgeon is quirky, a sort of Dr. House / Sheldon Cooper hybrid. Biting and sarcastic but also awkward and a bit nerdy. He tells me I have cancer and it’s the opposite of what I expect to hear. I don’t hear anything he says after that. My brain takes a minute to fully realize what he’s said, and then I wonder if he’s joking which, yeah, in hindsight is not a reasonable response but I’m not sure there is a reasonable response to being told you have cancer.

My surgeon schedules me for another, more extensive surgery in three weeks. I have a longer wait when I book a cleaning with my dentist. Time speeds up and then slows down completely as I recover. I am thirty years old. Grady is one. I spend a lot of my time trying to mother him as deeply as I can, just in case. He’s too young to have specific memories if something goes wrong in my treatment but I want him to remember the feeling of being loved. It’s a lot to carry while I’m going to appointments and meeting new doctors and taking new meds and trying my hardest to get well.

I wish I could go back and tell thirty-year-old me that in seven short blink-and-you’ll-miss-them years, Grady will be a sensitive, creative, kind eight-year-old and he’ll have a precocious, powerful woman of a three-year-old sister. That time doesn’t erase cancer but it makes it softer. Scars lighten, memories fade, and seven years feels like a celebration. My cancerversary isn’t a celebration of being diagnosed, but of living these last seven years with as much gratitude, hope, and grit I could muster.

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Parking Woes

I had an appointment at the cancer centre today. I’ve been seeing my oncologist for six years and it hasn’t gotten easier. I’m a mess of nerves, I don’t sleep much the night before my appointment, I’m snappy and weepy, and I eat a lot of carbs.  

I say that the cancer centre has the worst parking lot I’ve ever encountered, but I’m not sure if that’s because it’s a truly crappy parking lot or if it’s so terrible because it’s the parking lot of a cancer centre. I’m not in a great headspace to begin with, I’m in no mood to forgive too-tight stalls and endless one-way lanes. 

Usually I park on the other side of the hospital in the shiny, new parkade but today I decided I had arrived early and should take the opportunity to conquer my foe. I pulled into the terrible parking lot and immediately spotted the one remaining empty space. I was stuck in a maze of one-way lanes but I dutifully followed the path of arrows until I turned the last corner just in time to see someone drive quickly the wrong way down a one-way lane and zip into my spot (MY spot). I drove slowly by, giving them the stink eye the entire time, and quickly exited the terrible parking lot. I drove around the hospital and parked in my usual lot, continued walking around the other side of the hospital, and made it to my clinic with approximately 30 seconds to spare. 

The moral of the story is: sometimes things are just terrible and you don’t have to prove you can best them. Sometimes it’s okay to just park in the easy lot, even if it means you have to walk farther to reach your destination.  

National Cancer Survivors Day

Today is National Cancer Survivors Day and you will be shocked to hear that I have some feelings about this day.

On one hand, I see the value in celebrating survivorship. I have benefited from the visibility of other survivors, and I’ve been told by others that being transparent with my story has helped them. Hope, when paired with a healthy dose of pragmatism, is a valuable tool when facing a diagnosis. I think talking about cancer openly removes some of the fear and misinformation. Cancer doesn’t always mean a death sentence.

But sometimes cancer is a death sentence and celebrating National Cancer Survivors Day feels a bit itchy and uncomfortable when I start to think about all the people who aren’t here today, who don’t get to call themselves a survivor, who receive the unfortunate label of “lost their battle with *insert type of cancer here*.”

This post by Lisa Bonchek Adams is forever etched on my heart, especially this line:

When I die don’t say I “fought a battle.” Or “lost a battle.” Or “succumbed.”

Don’t make it sound like I didn’t try hard enough, or have the right attitude, or that I simply gave up.

Today I’m thinking about my fellow members in this crappy club no one wants to be a part of, and remembering those who would give anything to be part of this club if it meant one more day with their loved ones.

Broken

When I had cancer, no one told me to just think positively and I would get over it. No one told me to use diet and exercise, to get more sleep, to focus on the good things in my life, to stop dwelling on the sad things, to change who I choose to spend time with, to meditate, and I would be healed. I was sick. I got treatment. People accepted it as what was going on in my life. 

I don't have a thyroid. I take a tiny pill every day. If I stop taking that tiny pill, I will die. No one tells me that I am weak because I need to take that tiny pill. No one rolls their eyes or judges my inability to live without taking that tiny pill. No one makes me feel unworthy for relying on that tiny pill to stay alive. My body was broken. That tiny pill fixes the brokenness and allows me to live a healthy life. 

If you are depressed or anxious, if your brain is broken, you deserve that same respect. You deserve to feel like seeking treatment, asking for help, taking that tiny pill (or talking to a therapist, or meditating, or whatever it is that makes you feel better) is a viable, valuable option. You are worthy. You are important. You deserve to feel better. 

National Suicide Prevention Lifeline: 1-800-273-8255
Kids Help Phone: 1-800-668-6868
Pacific Post Partum Support Society: 1-855-255-7999