BC Becky

Never thought I'd want to be a breast cancer survivor

Category: Second Memoir

  • The end of breast self-exams

    The end of breast self-exams

    This is a story written base on reflections my initial year after diagnosis (2016), with added comments about what I’m thinking after my second diagnosis (2024).

    The feature image is from Wikimedia Commons.

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    Introduction

    Before my first diagnosis, I was obsessive about breast self-exams. Every time I showered, I would check, feeling each part carefully. It was just part of my routine—not because I had any family history of cancer, but because of a high school health class. The nurse had brought in these dummy breasts with a “lump” we were supposed to find. I remember how I could never feel it, no matter how hard I tried. That really stuck with me. I was afraid that when it mattered, I wouldn’t feel anything.

    I missed the lesson on looking for changes, not just lumps. Now I can tell you everything you should be looking for in a breast self-exam – changes, not lumps. However, only days after seeing initial changes, I felt a lump. I thought it was a muscle strain at first, but it didn’t hurt and it didn’t go away. It wasn’t a muscle strain, it was a 4.5cm tumour in my left breast. 

    ~~~~ 2016 ~~~~

    It has been a year since my diagnosis and treatment for bilateral breast cancer. I no longer have breasts. I have fat tissue that was transplanted from my stomach to make forms that look like breasts. The breast-self exams I did before don’t make sense anymore. I have no breast tissue. But I also have no sensation, which comes with new risks. 

    One of my new risks is the cold. I have body parts now—my reconstructed breasts, my belly—that I can’t feel. They’re living flesh, warm to the touch, but numb. I have to relearn what “normal” feels like, but also how to check myself to make sure I’m not getting frostbite.

    I’m still exploring what a breast self-exam means for me now. This was how I found my cancer. I used to check every time I showered, and I saw the change almost immediately—a lump, and a strange discharge. But now, I don’t have breasts with breast tissue. My nipples are still there, but they don’t leak anymore. They’re unfeeling and unresponsive, but they’re warm to the touch.

    I still examine my chest, but I’m looking for something else. No lumps—just damage. I’m scanning my skin for signs of anything that could have happened without me noticing, because I can’t feel it.

    Part of my new normal is this constant exploration of my changed body. I trace the areas with no feeling, trying to find the boundaries—where sensation fades from something to nothing. I want to see if these boundaries shift. I’ve been told there’s a chance I might regain some feeling, but nerves can take up to three years to grow back. For now, I’m grateful it’s not winter. I’ll have at least a year or two, maybe more, before I need to think about what snow and freezing temperatures mean for my body.

    ~~~~ 2024 ~~~~

    I am used to my body. My urge to inspect it so closely fades. I stop any form of breast exam in the winter. Now, it’s during the warmer months that I need to check. Instead of worrying about frostbite, I’m prone to heat rash, especially under my breasts. I don’t feel it when it starts; I only notice it later, after it’s become severe. By the time I see it, it needs days of treatment—creams and patience—to calm down. I can’t always tell if the creams are working; I just wait for the rash to fade.

    I stopped looking for cancer years ago. Then came a regional recurrence, in my lymph nodes. They found it on a scan. I couldn’t feel the swollen nodes, even with a 2.5 cm tumour growing in the largest of the five cancerous nodes. My family doctor also could not feel it. That experience stripped away any faith I had in self-exams to detect recurrence. The familiar routine I once had, washing and inspecting my new breasts, has fallen by the wayside, offering no comfort now. All I can rely on are blood tests and scans.

    My new normal feels like my old normal. After a shower, I give myself a quick glance in the mirror, just to check if anything looks wrong. That’s it. I don’t dwell on it. There’s nothing left for me to find. A self-exam in the shower isn’t going to catch cancer if it comes back. So, unconsciously, and now consciously, I’ve moved on from that practice.

  • Avoiding Scanxiety

    Avoiding Scanxiety

    I am working on a new memoir related to my cancer experience. As I create, I had been sharing stories over on substack, but I have decide to close my substack blog and move my stories back over here. In addition to writing about my ongoing survivorship experiences, I will be sharing stories that are a mix of old and new – that may one day be included in my future memoir. Stories related to the memoir which are historical but written in present tense, will begin with a declaimer like this and a rough date so you know it isn’t a new report on my health.

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    October 2024

    I have a scan coming up next week, and everything feels like it hinges on the results. Will I live, or will I die? My brain is constantly fighting with itself, stuck between logic and fear, spiralling into worst-case—or at least bad-case—scenarios. Every little symptom sets off alarm bells. When my headache returns, or my head feels spacey, I immediately think, the cancer has spread to my brain. If my side aches, I worry about my liver. If there’s a twinge in my mid-back, I fear for my spine. The big question is always lurking: Has the cancer spread?

    It’s hard to explain this constant state of fear to people who haven’t lived it. In a casual conversation this week, Jane asks me, “Do you think eating meat caused your cancer?” I pause, a little stunned by the simplicity of her question. “Uh, no,” I reply, keeping my tone as calm as I can. “I know vegans and vegetarians who also have cancer.” I can tell Jane, like so many others, is searching for something—an explanation that makes cancer feel more understandable, less random. But cancer doesn’t work like that. It doesn’t follow simple rules or offer easy answers.

    Jane isn’t done. She follows up with, “If I had cancer, I wouldn’t do chemotherapy.” Her words hang in the air, and I find myself at a loss for how to respond. I’ve heard this kind of remark more often than I’d like. The problem is how generic it is. There are so many types of cancer, and not all of them are treated with chemotherapy. Even among breast cancers, treatment varies widely. The truth is, until you’ve been there, you have no idea what you would actually do.

    Before my diagnosis, I thought I knew. I always believed that if I ever got cancer, I’d want the tumour removed immediately. But when the time came, surgery was the last thing I wanted. I delayed it as long as I could because I needed time to process. You can’t prepare for something like this—you don’t know how you’ll respond until you’re living it.

    Now, as I wait for the scan, that same uncertainty looms over me. I’m a planner by nature, and my mind is already mapping out what I’ll do if the worst happens, if the scan shows the cancer has spread. I wonder what my treatment options will be. I question whether I’ll go back to work. My brain keeps spinning, planning for endless possibilities, because that’s how I cope with the unknown.

    The fear is legitimate. I’m experiencing symptoms that could very well mean the cancer has spread, and that’s why we’re doing the scan. But letting the fear control me isn’t productive. The scan is booked. I have a follow-up call with my oncologist scheduled. There’s nothing more I can do right now, and I remind myself of that every time my mind drifts toward the dark, uncertain path ahead.

    For now, I wait.

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