I am still half-vaccinated. I thought I’d feel a measure of freedom after dose 1, but now that I’m so close, I find I can’t justify changing things up until I reach what the CDC has deemed full protection. Is it just me or is the wait between doses interminable?
My husband got his shot last week. We don’t have the type of marriage where I make appointments for him, but I made an exception for the vaccine. He just wasn’t anxious enough about it for my liking. He was content not only to wait his turn but for appointments to become plentiful. He was sure he would get one eventually. What I wouldn’t give for that kind of confidence and trust in the system. I wasn’t about to gamble our family’s summer plans waiting for an appointment to drop into his lap, though. I pestered him into making an account on Walgreens.com and signing in on my phone and commenced with hitting refresh until I scored him a dose last week. Johnson & Johnson. One and done.
In a few weeks, we’ll both be breathing easier. In the meantime, I’m swatting off a new threat, this one coming from down the hall of my own body. I went to the dermatologist to get a mole checked last week. I figured it was nothing–it was pretty and pink and round with smooth edges–but it sprung up practically overnight (before I got vaccinated, to be clear), and what’s the point of having a dermatologist I can’t email her about mysterious new lumps and bumps? She told me to come in and I scheduled an appointment for a few weeks out, after spring break.
I was excited about the appointment because I thought of it as crossing something annoying off my list. I thought the doctor would glance at my mole and send me on my way with a pat on the back for my hypervigilance after concluding that this thing, like all the other things I’ve worked myself up about over the years, was nothing to worry about. Instead, she peered at it closely through what I can only describe as a doctor’s version of a jeweler’s loop and told me she wanted to do a biopsy. “The risks are scarring, infection, and bleeding. There will definitely be a scar. We will tell you what to do if it gets infected. There might be bleeding. Do you have any bleeding disorders or any blood thinning medication?” My voice must have wavered when I gave my informed consent, because the doctor looked up at me and asked, “Is this what you expected to happen today?” “Um, no. Because it just looks like a normal mole? Even the internet told me not to worry.” The doctor didn’t crack a smile. “Well I’m not sure it is a mole. We need to confirm none of the cells are cancerous.” The shape of the mole was not the root of my surprise, though. I was shocked because my experiences with doctors have largely been limited to them telling me the thing I’m worried about is either all in my head or there’s nothing that can be done. There’s a reason I’ve been beating the drum of mental health for so long on this blog. I’m not accustomed to having my fears validated, much less scraped off my body and sent to the lab.
Hearing the word cancer out of a doctor’s mouth made all my invisible conditions–the dragons I’ve been keeping at bay my entire adult life–seem imaginary, like a joke. The first thing I wanted when I walked out of the dermatology office was a drink, but after a year of COVID and years of sobriety before that, I didn’t know where to go, so I went to the dispensary instead. Oh, and I should have led with this: it was a dark and rainy day.
I’m sure it’s nothing, and even if it’s not, I’m sure I’ll be fine. The biopsy is more likely than not to come back normal. If it doesn’t, they’ll go back in and cut out whatever’s bad. The challenge is living in the space where things might not be fine. We know from the last year that fine was never guaranteed. I spent the day after the biopsy reading about all the skin cancers. I texted the worst-seeming one, Merkel cell carcinoma, to my mom, because some of the pictures on the internet looked just like
mole papule on my leg, and because I knew she would indulge my worry. When she didn’t text back for a few hours, I wondered what was up and checked my phone again. Oh shit. I hadn’t sent the texts to my mom, but to a long-time friend who happens to be a doctor. She wasn’t having it. “Merkel cell is so rare!! I’ve only seen it with old men. You don’t have it.” I called my sister, who has skin like mine, and pulled a bossy older sibling move. “Go get your skin checked. We’re supposed to be doing it once a year.” Probably she already knew, but maybe not. I didn’t. I wouldn’t have if it weren’t for COVID. After I got sick last year and freaked out because I didn’t know where to go, I found a primary care doctor who took one look at my pale, freckly skin and my family history of cancer and told me to get to a dermatologist. She was so serious about it she referred me to a competing practice group in town so I could get in sooner.
The biopsy results should be back before I’m due for my second dose of the vaccine, which means I’m languishing in a wait within a wait. The four weeks between shots feels longer than the entire preceding year and the four days it’s been since my biopsy feels even longer than that. You’d think I’d be better at waiting by now. You’d think I’d be a pro at passing time, but this particular stretch is stretching me.