Note: I know that when I started this business, I promised to include health-related info first, so as not to make you dig for any REAL updates about my situation before I start endlessly rambling about all the other things; but as I write this, I’ve already written several paragraphs of rambling, and I’m in the FLOW, yo, so I’m taking a moment to append this message to the top of the post, just to say that although I’ll be sharing a few slightly personal and wholly unnecessary physical weirdnesses with you in this blog post, things are pretty much the same: I have 15 treatments done, and ONE TO GO. As I write this (6 days past treatment), I’m still feeling somewhat puny—still largely in the applesauce and rice phase, although I’m planning chicken enchiladas for dinner tonight—but have gotten past the part where I hate everyone. That’s it. Carry on.
So, I’m down to ONE chemo treatment left.
The most recent one happened two days after Christmas, and hit me a little harder than usual, because of the cumulative effects of these drugs over time, I’m sure—but also because I’m a ding dong and forgot to take my nausea meds.
But I’m getting ahead of myself.
So on the Tuesday after Christmas, I went in for not only my penultimate chemo treatment, but also the lab work that I typically do on the Monday prior to each Tuesday treatment (but couldn’t on the Monday following Christmas, as it was a holiday). That meant a two-hour wait between my arrival for my appointment and my actual visit with Dr. Cool-and-Calm, because ain’t NOTHIN’ happening until the lab work comes back.
Following the blood draw, I was ushered back to the chemo treatment area to wait for the lab results. I was delighted to find that my favorite treatment “pod” (as you may recall, there are three treatment areas, each with anywhere from 3-5 recliners—and my favorite one is the one nearest the bathrooms) was sparsely populated (only one other guy, accompanied by, presumably, his wife) AND that the “good” recliner (one of two close to the windows, but NOT the one folx call “the catapult” due to it’s rather violent foot rest spring action) was free!
I happily settled in to await my doctor consult—and to nap because, in anticipation of the coming week plus of “chemo blues,” I decided to do ALLLLLLL THE THINGS on the Monday before treatment: coffee with a new friend; a day of post-Christmas shopping with Love Tank in cusstastically frigid weather (you couldn’t walk a block with out spitting an f-bomb through clenched teeth, but it was WORTH IT, because I got new Trina Turk PJs, and Love Tank got a leather jacket, both on super-sale); and dinner (plus baby-squeezing!) with my Mother in Law and other beloved family people I haven’t seen in far too long.
And you know how this exhaustion is doing me lately, so Mama was WIPED TF OUUUUUUUT, people.
Yet and still, the nap didn’t come. The nurse brought me a heated blanket (they don’t even have to ask me anymore if I want one), and I snugged down into the recliner with my pillow . . .
. . . but as I swirled down into dreamland, my brain began to process noises coming from the television in the pod, and be like, “WTF is this fresh RV shitter full of bad burrito aftermath?”
I opened one eye.
The other occupant of the pod had turned on Fox News.
And I tried to live with it; I screwed my eyes shut again, breathed deeply, and willed sleep to set me free from this bullshit. Failing that, I sat back up and tried to occupy myself on my phone (mostly by sending “FML” texts to Love Tank and my friends to complain about my current situation). Still the swill infiltrated.
So I got up, stretched, and took an ever-so-casual stroll past the other two treatment pods—you know, just to stretch the old gams—and found, to my dismay, that they were all FULL.
I trudged back to the Fox hole (which was STILLLLL 50% empty) and sat back down.
I considered asking the couple (who otherwise seemed lovely; upbeat, friendly, and genuinely fond of one another) if we could change channels (thinking maybe they just had it on for company, or to coax the dude getting treatment to sleep), but alas, they were actively watching—and at some points, discussing—the broadcast. To their immense credit, they did NOT discuss any of the typical fuckery that comes out of Fox News faces; rather, they only discussed the one or two unbiased, fact-based aspects of the broadcast—for example, they discussed how horrible it was that so many people had died in the winter storm that hit Buffalo (which I, too, found horrible—who wouldn’t?), and refrained from discussing any of the subsequent Fux Nooz Vyooz about how this was somehow all the fault of the Democrats.
But I still couldn’t take it.
So when my nurse came to tell me my lab results were in (NORMAL ranges across the board, baby, EVEN for my once-tanking hemoglobin and potassium!), and asked if I’d like the doctor to come to me where I was, or if I’d like a private room for the consult, I asked for the private room and, once she’d ushered me inside, nearly yanked her off her feet to get her inside the room with me so that I could ask to be relocated. I told her I couldn’t take one more minute of Fox News.
She responded, with a meaningful “tone” (if you catch my drift) that she respected that, and seemed to be pickin’ up what I was layin’ down . . .
. . . but then she launched into something about how things were depressing enough without having to watch the news, so now I’m not sure if she caught my ball at all. But she did find me a vacancy in the pod furthest away from the bathroom, which may well have saved my blood pressure.
Insurance can kiss my ass.
What nearly wrecked my blood pressure all over again, however, was meeting another patient in the second treatment pod. Lovely woman, accompanied by her son, who was equally friendly. I don’t recall how we started talking, but once I’d settled into my new treatment digs to start the poison drip, we shared some stories.
And hers broke my heart, y’all.
In a nutshell: she was diagnosed with breast cancer in 2021. Although her cancer was at Stage 3 (whereas mine was Stage 2), her treatment plan was otherwise pretty much lock-step with mine: chemo, then surgery, then radiation.
Remember the echocardiogram I had back at the beginning of this ride, to ensure that my heart was going to be able to withstand treatment? Well, my new friend was unable to get hers, because INSURANCE DENIED IT. She fought, the doctors fought . . . and eventually, she said, she “just got tired.”
And as a result, she went A YEAR without treatment.
Of her STAGE THREE breast cancer.
Finally, her son (the one who was with her for treatment, although she has other kids) found her SEIZING one day, and got her to the ER—and lo and behold! She was finally deemed sick enough by her insurance company to do ALL the things necessary to start chemo treatments for her cancer.
Now, though, the plan has changed. The cancer has spread to her spine (although she can stand for brief periods, she now relies heavily on a wheelchair) and brain (hence the seizures), and though she says radiation took care of the brain lesions, surgery is now off the table, and she has been told she’ll never be cancer-free.
There are so many things to say, here, but y’all know. Y’ALL KNOW. So I’ll refrain.
Instead, I’ll wrap this up by saying that at one point, when the woman and her son had wheeled away so that she could visit the restroom, my kind nurse (having witnessed chunks of the lengthy conversation between me and my new friends as she came back and forth to change out meds for both of us) lightly joked, “So much for your nap, huh?”
But I told her I’d rather stay up for THREE DAYS STRAIGHT talking to that woman and her son (as enraging and sad as it was) than watch three more minutes of Fox News.
Ding dong, the bitch forgot her meds
So on the Thursday following treatment, I woke up my sleepy head, rubbed my eyes . . . and TRIED to get out of bed, but was knocked right back down by worse nausea than I’ve become accustomed to. There was no THOUGHT of eating or drinking; rather, I just burrowed and hoped it would subside.
By the early afternoon, when things didn’t seem to be getting better, it hit me: I hadn’t taken any of my anti-nausea pills since leaving treatment.
(Sorry; I’ve been watching Emily in Paris—mainly for the clothes and the scenery, because the story line is getting way too Three’s Company for me.)
Of course I took some immediately, stayed up later than usual that evening just to take the next dose (which couldn’t be taken until 8 hours later), and from then on, popped those bad boys like like (kinda literal) clockwork . . .
. . . but now I get why from the beginning, the nurses have always said, “Don’t wait until you feel sick to take your nausea meds—stay ahead of it!” because once I got behind, I never quite caught up; I continued to feel worse than usual for the rest of the week.
For example, by the Sunday following treatment, while food still does not taste good, I’m typically able to participate in our weekly Breakfast with Grandma (wherein the boys and I pop over to her place on Sunday morning, bearing something brekky (usually pastries of some sort) and fancy coffee shop drinks), because the mere idea of food no longer grosses me out. This past Sunday, Grandma requested McDonald’s for breakfast, and I happily obliged, because even though I felt a little punier than usual, I’m accustomed to Sunday being the day I’m able to move beyond the rice and applesauce diet (not TOO far beyond, as I don’t eat much—and sometimes applesauce is included—but I can usually do a croissant or something).
However, I took one bite of my sausage, egg & cheese biscuit, and everything in me said, “Aw, HELLLLLLLLLL naw; we not doin’ this today.”
Not one to shy away from a challenge, I took another bite, and then everything in me said, “Oh, you think we’re here to PLAY? Well, let me tell you something—”
So I decided to try a bite of the hashbrowns instead.
“WHAT. DID. I. SAYYYYYYYY, MUHFUGGAH???” my body replied.
So I gave up on my breakfast, apologized to my body, and eventually it forgave me enough to let me drink the orange juice that came with my meal. (“You eat that sandwich! You NEED food!” my mother chastised, when she saw me gingerly wrapping the biscuit back up, because my body had told me not to even LOOK at it. But I kept wrapping. I’m no fool.) But I digress.
The point is, this time it was a FULLLLLLL week before my body stopped carrying nunchucks around in case of any more encounters with *actual* food.
Therefore I will depart unkissed.
Here’s the thing about the nausea, though: I described it at length in a previous blog post, in terms of all the things my gut does. But I haven’t told y’all how my mouth participates in this party. And truly, I shouldn’t because it is DISGUSTING—perhaps most of all to me, because you know I have a thing about mouths, right?
I mean, first of all, I can’t handle excess saliva. Ask anyone who knows me, and they’ll tell you that seeing someone drool sends me straight to Gag City. (Y’all remember all the drama I had surrounding the idea of doing a spit test to see if I had the BRCA gene mutation, right?)
Second of all, I can’t handle the sight of someone puking. Or the thought of someone puking. With a great deal of intestinal fortitude, a buttload of love, and the help of Jesus, I have been able, on most occasions, to deal with puking children (ONLY my own; NOBODY else’s) without contributing to the barf-o-rama myself, but anyone else’s puke is OUT OF THE QUESTION (and quite frankly, I haven’t had to deal with the older one’s puke in years, so it may be that I’m only equipped to deal with my kids’ puke when the face it comes out of is little and cute, and not when it’s hairy and manly).
Needless to say, I can’t even WATCH that scene in The Big Easy when Ellen Barkin kisses Dennis Quaid (a) with a mouthful of toothpaste, and (b) AFTER SHE JUST BARFED. (But if you’re feeling brave, be my guest. Don’t say I didn’t warn you.)
Anyway. You get the idea.
So imagine my revulsion to discover that this second line of chemo treatments does horrible things to my mouth. (Warning: this is WAYYYY TMI, y’all.)
During the first few days following treatment (the days when food is disgusting), the inside of my mouth becomes irrevocably slimy. In addition to having a horrible, metallic taste in my mouth, I get this gag-worthy, thick, slick coating over my tongue. I guzzle blistering hot tea in an effort to melt it away . . . chew strong, minty gum in the hope of generating enough saliva to wash it away . . . scrub the shit out of my tongue with my toothbrush . . . and still the slime prevails.
But what’s even worse is that during Slime Time, the inside of my mouth LOOKS different, which I accidentally discovered on a Facetime call with my sister; every time I caught a glimpse of myself talking, I noticed that the inside of my mouth looked weirdly . . . white.
Once we hung up, I went to the bathroom mirror to get a better look . . . and—hand to God—my tongue looked like a flokati rug, y’all. It wasn’t just white, it was covered in this thick, furry-looking grossness that shocked and horrified me.
Meanwhile, my gums had their OWN party going on: whereas my tongue was slimy, white, and furry, my gums were dark and sandpaper-y.
I mean, WTF is going ON??? SO GROSS.
Fortunately, it goes away after about a week (and THEN, for another week, food is completely flavorless, but it’s not entirely disgusting), but when it’s happening, I have the absolute grossest maw on the planet. And in MY book, that’s saying something.
And if thy right shoe offend thee
The other weird thing that’s been happening with the Red Devil treatments is that I’ve developed this sort of . . . associative nausea. When I visualize the treatment area in the hospital, for example (which I do naturally, as I’m sharing treatment stories here and in other conversations with friends), I start to feel nauseated.
Similarly, there is one particular pair of shoes, and one particular pair of yoga pants I no longer wear—and don’t like to look at—because they’re part of my “treatment outfit.” When I first got diagnosed, I’d been eyeing this cute pair of bootleg Adidas yoga pants that I couldn’t justify buying because they were, like, 70 bucks, and who needs to spend 70 bucks for yoga pants?
Once I got diagnosed, however, I started justifying ALL THE THINGS, so I bought the yoga pants. Then I rationalized that I couldn’t wear my Asics sneakers with very obviously Adidas pants, so I bought a pair of Adidas sneakers to go with them, and determined that I’d wear this little get-up to treatment, thinking they’d give me a little boost of happy in the midst of all the shit.
So I did—and THEY did—for awhile. But now, I find I can’t even look at the pants or the shoes—let alone WEAR them—without feeling mildly nauseated and squicky.
The good news is that the awesome bag Love Tank got for me to take to my treatments has NOT lost its charm—largely, I’d imagine, because I stopped using it VERY early on, once I realized I was just going to sleep through my treatments, and therefore didn’t need to bring a bunch of stuff to keep me entertained.
But needless to say, I’m being kind of careful about what I do (and by “do,” I mean wear, eat, cook, watch, read, love, etc.) these days, lest it become something I start to associate with chemo (and the concomitant sickness), and therefore start to hate.
At what price beauty?
One of the things I’m ever-so-cautiously growing to love, however, makes NO kinda sense at all, because it is—of all things—a friggin’ BEAUTY product.
First of all, I’m not much of a beauty products gal; I mean, sure, I like to try stuff here and there (fun masks and stuff), but unlike some other women, I don’t have a set beauty regimen I started honing at age 13, or invest in a lot of different products. Heck, I don’t even wear makeup, so my skincare routine doesn’t go much beyond washing, exfoliating, moisturizing, and cussing about the fact that I still get pimples at my age.
Second of all, I HAVE NO EYELASHES OR EYEBROWS (hell, there’s more hair on my TONGUE than on my face these days), so why I’d choose NOW to start buying fancy face products is anyone’s guess.
Well, OK. ONE reason I chose now was because, after months of spending the $80 monthly “wellness” stipend I get from my employer on (automatic) membership payments to Hotworx—even though I stopped going in the middle of last summer—I finally canceled my membership . . . which meant I had to find something else to do with that 80 bucks in December. And it’s a “use it or lose it” situation, so I had to spend it IN December, giving me little time to waffle about what to buy. Plus, with two treatments in December, and all the Christmas fruffle in between, I was afraid I’d forget to buy something if I didn’t just do it while I was thinking about it.
Now, if you know me, you KNOW that I am a marketer’s DREAM. I’d say fully 73.78% of the items I buy for myself or others are items that I discovered via Facebook ads.
Thazz right. I’m the “OooooOOOOOooooh” Girl. No joke; I literally HEAR myself saying, “OooooOOOOOoooooh!” when I scroll past an ad for something intriguing I’ve never seen before. But I digress.
The point is, I got sucked into checking out Ursa Major products by a Facebook ad. However, while I stand by the aforementioned 73.78% statistic, my ratio of “stuff I check out because of an ad” vs. “stuff I actually buy because of an ad” is like 94:1. (These are extremely accurate numbers.) So I didn’t actually have any intention of BUYING anything from Ursa Major, due to all the reasons listed above—and also because the product I found most intriguing was the Mountain Glow serum, which cost $84. (Just for comparison, the serum I typically use costs $12.)
But of course, the ads kept coming. And I kept “window shopping.”
And finally, one day, with my $80 bucks of “use it or lose it” funds burning a hole in my pocket, I thought, “What the heck?” and bought the serum.
Which actually came with a “first-time buyer” discount (so I didn’t even have to spend the whole 80 bucks, let alone the extra four + tax I thought I’d spend), AND a free sample of another product of my choosing (I picked the Golden Hour Recovery cream).
Been using the serum and the sample for two weeks, and Y’ALL. My skin is SO SOFT. I’m kind of obsessed with it, and I can’t stop touching my face (although with the Triple-demic raging, and a weakened immune system, I should probably stop that shit). I don’t know that I LOOK any different—but I will say that (a) it’s the middle of winter and my shit is all glow, zero flake, and (b) I may have already spent my January stipend on the Golden Hour Recovery cream (with a free sample of the Forest Alchemy eye cream this time).
WHAT IS HAPPENING TO ME???
I know this sounds like a paid testimonial (or one done in exchange for free product), but I assure you it’s not; that’s not how I roll (and if I did, I would pick a different free product, because I can’t tell you how long I’ll be obsessed with my face, but I can promise you I will ALWAYS be obsessed with FOOD . . . except when I have slimy flokati mouth). I do not care about your skin care routine. I do not urge you to try Ursa Major anything. I think you’re fine the way you are.
I will say, though, that for a gal with no eyebrows, I sure feel pretty.
And that perhaps the reason I was drawn to this particular product line (and the reason I’m less afraid I’ll start associating it with chemo sickness) was that I once had a rat named Ursa Major—and I tend to associate rats with cuteness and love.
Anyone want to adopt a rat?
And speaking of rats and love . . .
Y’all. It happened. Hot Jack is knocked up.
Philly Roll’s surprise balls were, in fact, balls (after such a long time with no evidence of pregnancy, we had begun to think maybe they weren’t b’doobies after all)—and working ones at that.
We made the discovery this evening, when my elder dude managed to catch Hot Jack by grabbing the entire structure in which she was snuggled (sister is FAST; he’s had a hard time socializing her, because all you have to do is glance in the direction of the cage, and no matter where she is (even if it’s in one of the little hidey cubbies where you can’t even reach her) she darts away like she grew a rocket launcher out of her ass, and wedges herself behind the litter box on the bottom level of the cage). He brought her, structure and all, over to me to say hello (weirdly, once she’s caught, she’s totally chill about being handled), and commented about how easy it had been to catch her this time. I said I’d noticed, as I cleaned the cage out the last couple of times, that she seemed less determined to dart away—and slower when she did.
There was a moment of silent reflection for both of us, and then, suddenly, we both had the same thought.
The boy reached into the structure to try to pull her out—and he didn’t succeed (once she was in his hand, he couldn’t get it back through the entrance), but he thrust the structure at me with raised eyebrows and said, “Mom . . . reach in there and wrap your hand around her body.”
“Oh, shit,” I said, once my hand made contact with her.
Love Tank, who’d been in the living room listening to this conversation (which took place in my dining-room-turned-office, where the rats live) requested that Hot Jack be brought to him to check out. He managed to coax her out of the little house (he’s her favorite), and when we SAW her, we were all like, “OHHHHHHHH.”
My girl was PLUMP-a-DUMP.
Now, keep in mind that I clean the cage EVERY OTHER DAY (really, I should do it DAILY, but since the previous rats did not poop NEARLY as much, and only required alternate-day cleanings, the habit’s been hard to break), and I lay eyes on her EVERY TIME . . . but not until TODAY did she become the chunk of cheese she is now.
Thing is, although I know rat gestation periods are about a month, I have NO idea when she started gestating; my guess, based on the looks of her, is that we finna have babies SOOOOOOON (like TOMORROW, even), but maybe I still have time to plan a shower . . . ?
And HAPPY NEW YEAR!