Three Years After Chemo: A Look Back at the Toughest 6 Months of my Life

It’s almost the third anniversary of the day I started chemotherapy. It has been three years since chemo went from being something that my grandfather did when he was losing his life to lung cancer…to being something that I had to do to save my own.

It lasted for six months.

When I think about the enormity of that experience and its defining effect on my biography, it’s hard to believe that it can be fully encapsulated in a short hyphen between January 2015 and July 2015. That’s only half a year. That’s shorter than a pregnancy.

But when you’re pumping poison into your veins on a bi-weekly basis, you start to measure time differently.

You’re measuring the time between lying on the floor on a mattress in the living room and going back to lie down in your bed. (Healthy folks call that a “day.”) You’re measuring the time between weekly oncologist visits. You’re measuring the time between meals you’re forcing yourself to eat. You’re measuring the time between when you start to feel a little bit better and when you have to go back for more poison.

I was dealt the cruel hand of starting out with a treatment plan calling for three months of chemo that suddenly evolved into six months somewhere around the middle of the first three. Time seems to move a lot slower when you think you’re halfway done with something and it turns out that you’re further back than where you were when you started.

When other people find out you had chemo, you get instant credibility. You must be so strong. So resilient. It’s unimaginable having to go through that. They can’t believe you actually did it.

Chemo 10 of 12. No eyebrows is a great look.

The distance from the chemo experience and the relative lack of reoccurence scares in its wake has led me to sometimes rewrite the narrative in my mind. I think back to how it “wasn’t really that bad” and that maybe I don’t even deserve to claim the vaunted title of cancer survivor, with all its rights and privileges and instant respect. There are so many others who have it so much worse and are fighting so much harder. But that’s no way to honor my own struggle or the struggle of anyone who battles cancer. Chemo is chemo. We were all worthy opponents and we are now blessed and thankful survivors.

But heroism and strength aren’t exhibited simply by doing something that you’re forced to do. It’s the way you endure it that defines you, and there’s something about cancer — for all its wickedness — that seems to bring out the best in its victims.

You are a cancer survivor long before you can actually claim to have survived cancer. Chemo puts you in survival mode.

No matter how much time has passed, there are things about chemo that I will never forget. Dreading the appointment all morning. My wife coming home early from work to join me for the treatment. Putting the chemo parking pass on our dashboard so we could park right by the hospital door. The distinct smell of the waiting room, where insipid daytime television droned on, oblivious to all the sick and worried people watching there. Being the youngest person — by a mile — in that waiting room.

Accessing my port for my first chemo treatment.

Unbuttoning the first few buttons of my shirt so the nurse could access my port for the day. The smell of the disinfectant solution applied to my port before they inserted the needle. The unpleasant pressure and pinch of the needle entering the foreign lump on my chest just above my heart. Watching the vial of blood fill up and knowing I wouldn’t get woozy like I did when they drew from my arm. Getting my port flushed and cramming animal crackers into my mouth to hide the taste of the saline.

Settling into our chemo room and putting the pink pillow behind my head on the less-than-comfortable recliner. Debating whether we would get the nice nurse or the cranky nurse. Getting the cranky nurse. The first round of painkillers and anti-nausea medication that sometimes had weird side effects that almost made me nauseous. The impossible-to-fight feeling of drowsiness that would overtake me. Drifting in and out of a weird sleep to the sounds of the “Arrested Development” episode that we watched on my laptop as a distraction.

Awaking more fully when it was time for the nurse to switch out the IV bag. Getting up to pee and dragging the IV stand behind me. The nauseating metallic taste of the “red devil” component of chemo that the nurse had to manually and all-too-slowly push into my IV line. Desperately munching more animal crackers and wondering how I got to this point and how I could possibly keep doing this.

Enduring the short drive home in a semi-nauseated, completely exhausted state. Collapsing into bed without knowing what time it was or what time it would be when I awoke. Finally waking up and feeling a tad more human. Hearing my wife making dinner in the kitchen, but knowing I wouldn’t really want to eat any of it.

I did that 12 times. I’m not sure if that sounds like a lot or a little, but it certainly felt like enough.

Now that I’m healthy, it’s easy to sometimes feel a disconnect from the person who went through all of that, even though it changed me forever in so many ways. I see the fading scar on my neck from my surgery and on my chest from my port, and I feel like someone who was abducted by aliens. In this case, the bodysnatcher was cancer. The scars help me know it wasn’t just a dream.

There was undeniably so much good that came out of this experience, and I think of that often. But when I reach the anniversary of various stages of my cancer fight, it’s important for me to remind myself of these grittier details and memories.

“Remission” too often means being remiss in my pledge to never take my good health for granted again.

And neither should you.

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