(Title image: Photo by 光术 山影 on Unsplash)
Nine years after my initial breast cancer diagnosis, I was still finding things to complain about. Yes, it’s 100% true that cancer treatments (surgery, chemo, radiation, endocrine therapy, etc.) are kind of like taking a 2-by-4 between the eyes. You do your best to keep yourself afloat but, with the exception of the effectiveness of the treatments on the tumor cells, you could argue that they are a net negative for the rest of your body.
Once treatments are done, side effects can linger. Some of them may linger for quite a long time, years even. And that’s where I got caught up in all of this.
The problem is that along with cancer treatment, other things are happening in parallel. Because I was pre-/peri-menopausal at the time of diagnosis, the onset of chemotherapy also resulted in a hard stop to my menstruation. This brought with it effects, although luckily mild, that aligned with a menopausal transition.
But there was more. At one point I was so panicked about memory issues that my oncologist decided to do a brain MRI, which found nothing (well, it found my brain…but no brain tumor. I’ll take it). But this was also during a particularly anxiety-driven point in my life, and that’s something that can also affect memory and basic mental functioning.

(Photo by Patrick Robert Doyle on Unsplash)
And so it went, on and on. I saw a cardiologist because I was experiencing heartbeat irregularities—probably anxiety-related also—but even after a stint wearing a Holter monitor (which reminded me of my chemo port, ugh), nothing serious was identified. In fact, the cardiologist remarked that I had a very strong heart. Not what I had feared, but good news.
I was frustrated with the effects of endocrine therapy on muscle wasting, something that I perceived as a huge loss, but when I finished up physical therapy for my shoulder a month ago, the therapists pointed out my strength and flexibility.
I was focused on how much I had lost, somehow ignoring the fact that I just turned 60. I was comparing myself to my abilities in my 40s, which—no big surprise—isn’t reasonable.
It really hit me when I attended an online event with other cancer patients and survivors. I wasn’t experiencing the level of impairment that others described.
This made me think hard about how I perceived myself. I finished my main treatments over eight years ago. That’s a long time, so why was I attributing anything that went “wrong” to cancer? I was doing very well. Still exercising. Still working my job. Still trying new things. Still not feeling my age.
I have nothing to complain about and a lot to be grateful for. The fact is, I left my post-cancer struggles behind some time ago. The “side effects” I thought I was still experiencing are miniscule compared what others, particularly those my age, are dealing with.
So I’m going to do my best to shut up about them.