Fun Thing at Work

Excuse me but why in the year of our lord 2022 does our annual school registration form still force us to choose between M and F, not only for each student but for each parent and each sibling and each emergency contact?? In an emergency, when my chosen emergency contact arrives at the school, does the school office intend to VERIFY IF THAT CONTACT IS M OR F and if so BY WHAT METHOD DO THEY INTEND TO MAKE THAT VERIFICATION. This is a question I asked in a letter sent to the superintendent and cc’d to the principal and the person who handles Title IX issues. I don’t know if this quite qualifies as a Title IX issue, but I was willing to invest the additional envelope and stamp just in case. Additionally annoying: I sent this same letter two years ago AND had to talk on the phone to the principal about it, and the form STILL ISN’T CHANGED.

(If this were a paper form, I would just leave that question blank and let them come at me if they felt up to it. But this is an online form, and it’s a required field, and there is no available option other than M or F.)

Also, I was complaining and asking for advice on Twitter, and Slim had the idea to contact IT using a “technical problem with the form”-type link, which strikes me as brilliant and tailored. No need to go in with banners and Reasons, talking about Inclusive Education and so forth, when you can just get the IT person to go in and edit the HTML or whatever!

Anyway. I have been feeling a little cranky at work recently (underpaid, and some days the tasks are almost unbearably repetitive and tedious), but wanted to tell you about a real perk (I wish that to be spelled “perq,” but it just isn’t) that happened today. I follow Jeanna Kadlec on Twitter, almost certainly because of seeing some of her tweets retweeted. And she has a book coming out, called Heretic (Target link, Amazon link), and it’s a memoir, and she’s an ex-evangelical like I am, so I am very interested in reading it! But I looked it up in our library system, and it’s another library that has it (or rather WILL have it, when it comes out in October), and when I tried to place a request for it, I got an error notification about that title not being available for holds.

So I went to our reference librarian, and I’ll bet you imagined an older lady in a cardigan and glasses, but actually she’s in her mid-20s and wears fashionable clothes and also contact lenses (and a cardigan, they seriously all do wear cardigans). And I asked her why I was getting this message, and she said some of the libraries in our system have a policy that the new-release books can’t go out on interlibrary loan, which is fair enough: if that particular library ordered the book, they want their particular patrons to have first crack at it. She said usually that restriction is from 1-6 months.

Then she said, “Let me see if our library has ordered a copy; they probably have, it’s probably just not in the system yet.” And then she said, “Oh! No, we haven’t. Well, I’ll just order one right now.” And she went typey-typey-typey, and then it was in the library’s to-order cart. And then she went typey-typey-typey again and put me on hold for the not-even-ordered-yet copy, so I’ll be the first one to get it when it’s published/processed. And I am underpaid and my work is getting a little boring, but that was FUN.

Also, I feel I should mention that even though I personally went from “mentioning book” to “being on hold for a copy that was ordered because I mentioned it” in about 60 seconds, and that is definitely because I work there, it’s worth noting that the reference librarians frequently do this for non-co-worker patrons too! Our library has a form, and probably your library does too, for a patron to use if they can’t find a book within the system; the librarians will first check our wider network of libraries (there are some libraries OUR LIBRARY can borrow from, even if OUR PATRONS cannot) (we sometimes need to wheedle) and, if they can’t find the book, they will evaluate it and see if we want to purchase it, and we have a budget for doing that. Sometimes the book is out of print and too expensive, but if it’s just one that has escaped our notice, the librarian will often think, “Sure, let’s give it a whirl!” and order it.

Friends: Highly Recommended; Boarding a Cat; Firefighters

Nothing dramatic has happened since we last spoke, but I still have this feeling of not knowing where to START! I’ve had more social stuff crammed into this week than I’m used to, and it’s been great but also it is seriously cutting into my screen time.

I have seen friends, and wish to say again how WORTH IT it is if you can possibly manage it. I can’t take any credit for making it happen: it was someone else who formed the group, and chose the people, and kept arranging meetings until the habit was formed; I was fortunate to have been included. So if you can…Be Included in a Great Friend Group, I guess is what I seem to be suggesting to you, well then I heartily recommend it! We sat outside on a summer evening with our wine, and I peered a little tipsily at my friends who were so beautifully candlelit by the bug-deflecting torches, and I felt so LUCKY.

Also this week, our household went away for a few days to get together with extended family. For all previous trips, I have put out a mixing bowl of dry kibble and left the faucet dripping for the cats, and off we’ve gone, feeling lucky not to be dealing with dogs. But right now we have a cat with two daily medications who is in the middle of probably being diagnosed with lung cancer—and, most importantly of all, seems to only be able to eat wet food, which can’t be left out for days the way dry food can be. We’ve never boarded a cat before, and I was very stressed about the idea, and I wasn’t sure if we’d even be able to get a spot on such short notice; but I called the vet and they DID have an opening, and it all went well. The person in charge of the boarding program was everything you’d hope for in such a role, and she texted me photos of the cat with little messages that purported to be from the cat himself, giving me information such as “I peed and pooped and have eaten almost a whole can of food already!” and then little pawprint emojis. Everything you’d hope for.

Oh, and actually, something dramatic DID happen: at the extended-family gathering my mother lost consciousness while sitting in a chair, and we could not revive her; and we called 911 (specifically PAUL called 911, and did such a good job with it that I hope to delegate that task to him on all future occasions), and she is fine but it was a bit of a Startling Event. And it turns out they sometimes send firefighters to help the EMTs bring someone down stairs to an ambulance, and many firefighters are–oh what would be a good way to describe it?–“calendar-worthy.” Well! Some excitement all around. And in case you have a place to file such information: if someone faints / loses consciousness while seated (that is, they have not been in an accident or hit their heads, and there is no worry about broken neck/bones), 911 will tell you to lay them down on the floor if possible, to help get blood/oxygen to their brain. Perhaps you already knew this; I did not. Also: it turns out none of us really knew how to move an unconscious person from a chair to the floor. We managed it, but I was glad EMTs/firefighters were not watching us do it, and I am motivated to look for videos showing me how to do it right.

One of my favorite moments was when the EMTs had brought my mom back to consciousness and they were asking her some routine questions about medications and substances; and, after the EMTs asked if she’d been drinking plenty of fluids and she said yes, one of the firefighters (tattooed muscled arms in fitted firefighter t-shirt, shaved head) turned to me and said quietly “That true about the fluids?,” and let me tell you I IMMEDIATELY betrayed my mother (she is NOTORIOUS for leaving her water glass completely untouched at meals), and they hooked up an IV. Lie to the police if necessary, but tell THE WHOLE TRUTH to the EMTs. Even if they’re NOT cute, and crossing their tattooed arms, and looking down with warm eyes and a head tilted as if to invite confidences—as this one may or may not have been.

Cat Lung Cancer

Well, I have a sad update on the cat laryngitis. When we looked up cat laryngitis online, it said it’s nothing to be concerned about—but that if you notice the cat panting, or breathing through its mouth, a vet visit is warranted. And the cat breathed through his mouth a couple of times, and so I called the vet, feeling like a Right Fool who was about to pay $500 to find out her cat had a cold. But instead it seems to be lung cancer.

This does not mean you should panic if your cat temporarily loses its meow! And in fact, the one thing bothering the vet is that the Area of Concern on the x-ray is not in an area that explains the cat laryngitis. She says the most likely explanation by far is that there is an additional Area of Concern in/near his larynx, and that it just didn’t show up on the x-ray, as many such things do not; but she says there is a Slim Hope that this could instead be a lung parasite, which WOULD account for the Area of Concern AND the laryngitis. So she has given him a course of anti-parasite medicine Just To Make Sure before we start having Hard Discussions. But her entire manner told me she thinks this will not work and that we will be having the Hard Discussion.

One of the things I love about this vet is how easy she makes those hard discussions. She always acts as if she would be 100% Here For It if I were to tell her I wanted to do everything in our expensive power to save the cat—but she also acts as if she personally thinks it makes absolute sense to instead choose NOT to do those things.

I am sad, of course: he’s a good cat; and he’s Elizabeth’s baby, and so I also feel sad for her. But—this is a 12-14-year-old cat with Cat IBD; and one of his kidneys shut down for no apparent reason; and he had kidney stone surgery recently, and the lab analysis of the stones shows they are the kind that will almost certainly recur and can’t really be prevented. The wheels are coming off this cat, is what I’m saying. And although I was willing to pay for the original kidney-stone surgery, and also pay for the expensive food just in case it DID work and he never needed more surgeries, my feeling was that with Elizabeth leaving for college in a year…and a cat who is not happy when Elizabeth is not home…well, perhaps we could consider the cat to be in his Final Year. And if the stones didn’t recur, well, lovely! We’d be happy to continue having him with us! But…if they DID recur…well, I mean, the timing seemed about right. Lung cancer may change the timing, but not by MUCH.

I wish I had asked the vet what kind of timeframe we were looking at. She mentioned that we can keep him comfortable for awhile / until it’s Time by switching from the IBD Dose of his steroid to the Cancer Dose, but I don’t know if we’re talking about weeks? months? It seems like if he DOES have something in/near his larynx, and it is already messing with his breathing, that it won’t be very long before there are Quality of Life issues. Well, we are giving him lots of skritches and cuddles, and we are taking lots of photos.

Bourbon

Hello! Do we have any BOURBON aficionados in our midst? (I had THREE spelling errors in my first attempt at spelling the word “aficionado” AND had to look up the definition to make sure I was using it right. I was using it right: it means KNOWLEDGEABLE AND ENTHUSIASTIC about something.)

My brother had a fun idea for his birthday this year—oh, but first I should tell you that we are a WISH LIST family. I think that’s important to know, since otherwise you might be thinking, “Wait, your brother is TELLING YOU what to give him for his birthday??”—and no, he would never, this is an idea on his wish list, and wish lists are only for family members who WANT to use wish lists: that is, there is no feeling that anyone MUST or SHOULD choose from the wish list, and plenty of feeling that it is EVEN BETTER to go off-list; but SOME members of our extended family (NOT ME, it may surprise you to learn) are TOO ANXIOUS to buy anything that isn’t explicitly listed and linked to. Plus, most of us find wish lists fun, and a good way to get an idea of what SORTS of things the person might be interested in this year: some years someone might have a lot of novelty t-shirts and jewelry; other years they might have a bunch of books and mugs and treats; other years they might have mostly postcards and Etsy art. (Those are all me.)

Back to where I was. My brother had a fun idea for his birthday this year, because his wish list is very sparse right now, and he knows this will lead to some hand-wringing. He suggested that, since bourbon is perpetually on his list and he loves to try new kinds, anyone who wanted a wish list idea should choose a bottle of bourbon and then he’d have a bouquet of birthday bourbons to try, which he would find very fun.

I am NOT a bourbon aficionado (one misspelling this time, and that was WHILE LOOKING AT THE CORRECT SPELLING), but I AM an aficionado of OTHER things, so I know how sometimes an aficionado can look at someone’s likes/dislikes in their aficionado category and immediately get excited and start making suggestions. So I am hoping some of you are bourbon aficionados or perhaps you have a sibling/spouse/friend/co-worker who is a bourbon aficionado, and that you/they would find it fun to look at my brother’s list/chart and make some suggestions:

I could, of course, just buy a bottle from Old Favorites, or from Liked and Want More (ignore Looking For: it’s a standing category that happens to be empty this year), but it would be more fun to buy something he hasn’t tried yet, so what I am hoping is that someone is looking at that list right now and saying “OOOOOoooooo you know what I think he’d like??” and then going to the comments section to answer their own question.

Ignore PRICE: not only am I INTERESTED in hearing even about bourbons outside whatever my price range might be, but also there are other people buying gifts for my brother who might have different price ranges, and also-also I might want to buy a more expensive bourbon for a milestone birthday later on.

Oh, and I am familiar with the idea of a gift box / advent calendar of small bottles of various bourbons, but he’s had that gift at least once, and I think at least twice, so I am less inclined to go that route unless you are thinking “Well okay but THIS PARTICULAR GIFT BOX is especially great!”

College Visits; Kidney Stones; Cat Laryngitis; Bake Sale Ideas

I have taken the twins on some college visits! We went on an overnight trip and saw three colleges, though one of them was a self-guided tour because we couldn’t find a regular tour that worked with our schedule. We all felt that the self-guided tour was almost useless. We had THOUGHT that a self-guided tour, where we walk around and read little paragraphs the Admissions office has composed, would be as good as a tour led by a perky student the Admissions office has hired to say things the Admissions office has composed, but for some reason it absolutely was not. We came away with almost no impression of the college at all. Well, now we know not to bother with self-guided tours—and we can go back another time for a regular tour.

I think the biggest accomplishment was just DOING ANY TOURS AT ALL. It is so hard to get started! With each kid after the first one, I resolved to get started on tours EARLIER—like, spring of junior year. Yet each time, here I am in late summer, barely begun. And very soon it will be fall of their senior year, and they will be too busy to take days off for college visits! I wring the hands.

Part of the issue is that Paul usually does quite a few of the college tours (he has most Fridays off during the summer, so that’s when he took Rob/William on tours), but he has been significantly affected by his kidney-stone issues for over a month now. Which reminds me to update you: he has had his second kidney-stone surgery, which went SO MUCH BETTER than the first one. Just for starters, this time we knew what to expect from the whole process, so this time his blood pressure at the hospital was at reasonable “nervous about impending medical procedure / feel uncomfortable in hospital smock and leg-squeezing things” levels rather than “so um do you take anything for high blood pressure? are you feeling okay right now? let’s just leave that cuff on and try again in a few minutes, okay?” levels. Also, the first procedure removed the stone that was hurting him, so this time he went into it well-rested, well-fed, etc. And finally: THIS time he didn’t come out of anesthesia to hear that it was NOT all over and there would have to be ANOTHER SURGERY. That was not good for morale.

Another medical update: the cat with kidney issues has lost his meow. We looked it up online and found that cats can and do get Cat Laryngitis. Let’s see if I can post this little video of me asking the cat in my Talking To Cats voice if he has cat laryngitis:


 

Oh! and I wanted to ask you about your favorite things to bake for bake sales. Henry’s theater group is going to have a concession stand at each performance, and they’d like contributions from the families. I’m curious to know what you personally like to make for bake sales, but I am also hugely hoping that we have in our midst people who have volunteered at bake-sale tables and KNOW WHAT SELLS WELL. I am also planning to donate some pre-packaged manufactured items (snack-packs of Oreos, snack-size bags of chips, that kind of thing), since I know it can be difficult/impossible for people with food allergies to buy things from bake sales.

One important thing to know is that the concessions stand will be OUTDOORS in SUMMER HEAT, so I don’t want to make anything TOO MELTY. I’m going to go right ahead and make things with chocolate chips in them; but for example I have a recipe for yummy bars that have a thick layer of chocolate/butterscotch on top, and those would just be a MESS, so I will not make those.

Things To Discuss When We Have the Time and Energy

Things to discuss when we have the time and energy:

1. Postcards to Voters. Is it a great way to manage those evenings when one’s mental health is not what it should be? (I recently managed a very bad brain day by alternating doom-scrolling and postcard-writing.) Or is it a giant waste of time and money, and a way to FEEL like one is Doing Something when one is Not?

2. Follow-up biopsy feelings. I still have a bruise, and in fact it’s a little larger now. I also still have irritation from the adhesive. It’s been nine days.

3. Follow-up cat kidney issues. The vet got back to us and said that the kidney stone analysis shows they are the kind that can’t really be prevented, so Repeat Issues are very likely. The STARTING recommendations (prescription food, regular x-rays, regular urinalysis) are $$$ per year; each surgery is several thousand dollars; I don’t know yet if there are procedures between prevention and surgery, or what they cost. At what financial point does a person decide that a 12-year-old pet should not be…er, sustained? What if that particular cat’s Support Person is leaving for college in a year and we were all already kind of worried about how he would survive that, considering how weird and clingy and yowly he was when she went to camp for two weeks? Well. Prescription cat food for thought.

4. Follow-up Paul kidney issues. He has a second procedure a week from now. Maybe let’s wait for the follow-up until after that.

5. I have been panicking. I wish to re-tell you the story about the time I was seeing a psychiatrist, and I was explaining in a fraught, breacking voice the weird side effects I was having from a medication (for example, seeing pedestrians and feeling certain that Something Bad was going to happen to them) and she listened carefully, and then said in a very calm, almost bored, diagnostic tone, “Panic.” She wrote it down. She prescribed some short-term medication. I have been once again having a rather extended session of panicky feelings. Also: I got together with friends, and it seemed to snap the panic streak. I recommend having friends, if that’s an option where you are.

6. Henry has been doing a summer youth theater thing, and I am so happy he is Finding His People/Interests and so forth, but also I am so exhausted by this. The transportation alone!! IT CONSUMES MY LIFE. And it is nowhere NEAR what parents manage for a kid in sports!! This reminds me of high school and college, where we as students would complain that every teacher/professor acted as if their class was your ONLY CLASS. Every kid activity acts like it thinks they are the ONLY ACTIVITY for your ONLY KID.

7. Henry has a rash spreading over his face/torso/arms/legs. Trying to get this looked at has been such a surprising hassle. Our (Catholic) pediatric clinic has switched to a (Catholic) health management system that has RUINED EVERYTHING. It used to be that if one of the kids was sick I would call the pediatrician phone number, and I would say “Oh, good morning, may I please speak to a nurse?,” and then I would tell the nurse what was going on, and either they would make me an appointment or else they would tell me what to do instead. NOW, I call an automated phone tree, which gradually allows me to select the numbers that indicate I wish to make a Sick Child appointment for an Established Patient—but then I talk to the same receptionist who answers allllll the calls ANYway, and she LEAVES A MESSAGE for the nurse, who calls me back HOURS LATER, and if I can’t answer the phone at that moment (driving; at an appointment with another child; in the bathroom; at work) they leave a message and I have to call back and LEAVE ANOTHER MESSAGE and WAIT MORE HOURS. HOW IS THIS BETTER. Anyway, the nurse told me it sounded fine and he didn’t need to be seen, and to give him benadryl and use hydrocortisone cream. And the rash continued to spread over the next couple of days, so I had to call back and do the entire system again, and the second nurse was quite alarmed that the rash was also on his face (“It’s not on his FACE or anything, right?,” she asked, despite me having told the first nurse that it was on his face and around his eyes); and eventually I got an appointment for him for this morning, and the doctor thinks it’s a result of contact with some kind of poisonous plant—BUT HERE IS THE THING: HE HAS NOT ENCOUNTERED ANY PLANTS. So. I mean. I will give him the steroid. And maybe it will work! But why did NEITHER the nurses NOR the doctor think my REPEATED “No, he has not been in nature” answer was relevant for the diagnosis of “contact with poisonous plant”???

8. One reason I emphasize “(Catholic)” in the previous item is that the medical center itself is emphasizing it. I used to give NO THOUGHT AT ALL to the “St.” part of the medical center’s name. But now there is a new, large poster in the pediatric waiting room, explaining that this is a CATHOLIC medical center, and as such they must HONOR their CORE VALUES above ALL ELSE. Isn’t that ominous, in the current climate? My loose plan is to MOVE US ELSEWHERE. Religious institutions can KEEP IT.

9. Some summers feel kind of languid, with lots of time for fun—or possibly I am misremembering, and they ALWAYS feel as if they OUGHT to feel languid with lots of time for fun, but ACTUALLY they are SO BUSY and we have NO TIME FOR ANYTHING? In any case, this is a summer when we have not even had time to discuss what we want to do this summer—and now it is almost August.

10. Rob got a job in Seattle! It is…fully remote. I am concerned he is going to LOSE HIS MIND if he is living AND working in a one-room studio apartment in an expensive big city where he has NO NEED TO LIVE for a fully-remote job. But he is a grown-up and this is up to him to figure out.

11. Next week I am taking the twins on a two-day road trip to visit a couple of colleges, including the one Rob went to. I am REALLY LOOKING FORWARD TO THIS. Hotel room! (I got one for the twins, and another for just me.) Car snacks! A couple of days away from home!

Benign

The radiologist called me today and I answered the phone even though I was at work where I am not supposed to use my phone (if my supervisor had been in, I would have explained the situation after taking the call, but she was not in), and she said the sample from the breast biopsy was benign. So that is a relief, and how nice to get the news before the weekend.

In what might seem like a surprisingly fast pivot from relief/gratitude to carping/complaining, one of my co-workers has been out with Covid. She had not been wearing a mask. The co-worker who sits within a few feet of her, who also does not wear a mask at work, was today coughing steadily. Meanwhile, another of my co-workers came back to work five days after his positive test, saying it doesn’t matter that he’s still positive on rapid tests, because “those only measure antigens.” I DON’T FULLY KNOW WHAT EXACTLY AN ANTIGEN IS OR WHAT EXACTLY THE RULES ARE EITHER, BUT I DON’T WANT HIM BREATHING HIS POSITIVE BREATH NEAR ME

I feel as if I am losing my mind. I am still wearing KN95s to work, and that is NOT AT ALL COMFORTABLE TO DO in an active job, but I am doing it because it still seems to me like a very sensible thing to do. My supervisor and our library director are also wearing masks, but cloth ones, which I have been seeing FOR QUITE A WHILE NOW are no longer recommended (cloth is reportedly better than nothing, but not great at protecting against the new variants, and much less useful overall in a pandemic stage when most people are no longer masking nor distancing nor working from home nor limiting travel nor limiting the number of people in a space nor etc. etc.), and they take them off frequently to talk or eat/drink. My co-worker who used to make companionable remarks to me about how she and I were the only ones still wearing masks, has now stopped wearing a mask, because she got Long Covid, and now when she wears a mask she starts gasping and coughing and feeling like she can’t get enough air. When she stopped wearing a mask, so did the two people who work under her—even though she is a VIVID EXAMPLE OF WHY WE WANT TO DO WHAT WE CAN TO AVOID LONG COVID (THE RISKS OF WHICH MULTIPLY EACH TIME YOU ARE INFECTED). I feel increasingly embarrassed and stubborn to still be wearing one, but again: IT STILL SEEMS TO ME LIKE A VERY SENSIBLE THING TO DO.

Back to the topic of the biopsy. The biopsy site is still sore two days later, but not VERY sore—more like, I do notice it, and I try not to bump it against anything. Now and then I do a move that quickly registers as Unwise, such as pushing myself up off the floor with that arm, or snugging an armload of books against that side. I have worn a bra to bed two nights in a row, and I like that it keeps me from dragging the biopsy site against the mattress when I turn over. I haven’t had any trouble sleeping on that side, though I start out each night avoiding it. The steristrips are still on snugly, and I don’t feel inclined to remove them. I have an undramatic yellow-and-pale-purple bruise about the size of smallish cookie—an Oreo, or a Chips Ahoy.

I have been feeling a little MORTAL about this whole experience. It felt like a little test-run.

What It Was Like To Get a Breast Biopsy (Stereotactic Needle Biopsy)

As you will likely remember but let’s have a link anyway, I don’t want to act like I assume you are hanging on my every word, I was scheduled for a biopsy today to investigate some microcalcifications. I loved the radiologist, who explained excitedly to me that the biopsy involved using TRIGONOMETRY. I have such a crush on women in STEM who love their jobs (I am similarly smitten with our oral surgeon, who wears a headlamp at all times); I hung on her every word, even though I myself would not remember how to use trigonometry even if you dangled me off the side of a cliff and threatened to let go unless I could find a cosine. (I got an A in Trigonometry in high school, but it is because I am very good at test-taking and at figuring out which problems to plug into which formulas, and not because I ever remotely understood what I was doing.)

Where was I? Oh, yes: so today was the day of the biopsy. I was a little nervous. The instructions said I could wear deodorant if I wanted to, which was nice. I was not supposed to take any blood-thinners of any kind (including ibuprofen) for 72 hours beforehand. It was suggested that I have a meal before the appointment, to avoid getting faint/shaky. I did not like the sound of “getting faint/shaky.”

As with a mammogram, I was instructed to undress down to the waist and put on the hospital smock “like a bathrobe” (opening in front). Unlike during a mammogram, I had to climb up onto a high table (as in, I had a two-step stepstool to help me, and I used both steps). The table had a hole in the middle of it. I am always anxious about positioning myself on tables for medical purposes (I feel clumsy, and when I’m nervous it’s harder to understand/follow the instructions), and I would say this particular positioning was one I was glad to have had a chance to gear up for (the radiologist gave me an overview when she was telling me I needed a biopsy). I talked myself through it by telling myself that I am HARDLY the only person who does not have experience in how to correctly lie down on a breast biopsy table, and that I am DEFINITELY NOT the only person who needs to be adjusted after the first attempt.

Anyway. The basic idea is this: one lies down on the table on one’s stomach so that The Breast in Question is down through the hole in the table, but the Breast Not in Question as well as The Ribcage Below the Breast in Question are well-supported by the surrounding table, so you don’t feel as if you will fall through. They give you a couple of thin soft pads to position under your head as you prefer; I found it most comfy to use both pads and also put my hand under the pads for a little extra lift—but this is how I sleep, with a hand under my pillow, so maybe that’s just what felt Right to me, and not what would feel Right to others. In my case, The Breast in Question was the left one, so I was supposed to turn my head to my right, and it was my right arm that was up under my head; I wanted my left arm up like that too, in a sort of Sunbather’s Pose, but they did not let me do that: my left arm had to be down by my side, palm up. It felt okay once I got used to it, but still a little awkward.

The most difficult part is RELAXING. You don’t have to hold yourself up! You are lying down, and well-supported! But it FELT like I had to hold myself up. I kept having to remind myself that I could just lie there and rest and be as comfy as possible, considering the circumstances.

Both the radiologist and the nurse were good about telling me what was going to happen next. It feels pretty weird, because you are lying there on your stomach and someone is messing with your boob FROM BELOW. It is hard to wrap one’s mind around it. And one ear is squashed, which makes it a little hard to hear, or makes it feel like it’s a little hard to hear.

There is a sort of mini mammogram machine underneath the table, so they arrange the breast into that, and then the machine squeezes—not as hard as during a mammogram, just a sort of firm grasp. The machine does imaging to make sure the breast is positioned correctly; they had to ungrasp and regrasp a few times to get things right.

I am hoping I am remembering to mention all the steps. They raised the table at some point, even higher than when I had to use a two-step stepstool to climb up onto it. It’s so the radiologist can sit UNDER the table to do the biopsy. This table-raising might have happened before the grasping/ungrasping/regrasping. (By the way: the radiologist mentioned that for people who CANNOT climb up onto the table or who would PREFER NOT TO, this procedure CAN be done with the patient seated. She said but most patients find it easier not to have to hold still in an upright position, and not to have to see the radiologist RIGHT THERE, and WITH THE NEEDLE, and so forth.)

Then the radiologist warned me she was going to clean the area, and there was a cold wet wiping sensation. Then she said she was going to do the numbing medication, and that there would be a pinch, and that I should NOT “rise up” but should instead “wiggle my feet.” Feet-wiggling was so distracting, I almost don’t remember how much the pinch hurt, but my memory is that it was less than a vaccination, but in that general range of pain: a little stab, but nothing that made me want to jump or gasp. Then she said she was going to do a second dose of numbing medication, but that I would probably feel it less than the first one, and that was correct: I still did feel something, but not much. A mosquito bite, a tiny sting.

Then the procedure itself began, and she warned me that the machine was going to make funny noises, and it did; I suggested it was the sound of trigonometry being done, because I was trying to impress her, but she said “What?” and then I had to repeat it. The noises were like…low-volume vacuuming noises, intermittent machine-running noises, cycling motor noises, that kind of thing. Nothing gross or scary, but I was glad she mentioned them. I could not FEEL much while this was happening. Sometimes I thought I felt Something, but nothing upsetting or painful—just, I could feel something happening in the breast region. At one point I felt a burning sensation inside the breast, but not painful, if that makes sense combined with the word “burning”: you know how if you take a perfectly-too-hot sip of tea/coffee/cocoa, there is a “burning” feeling in your throat but not ACTUALLY burning the way there is when you burn your tongue and you hate it? or if you get in a slightly-too-hot shower when you are chilly, it is a “burning” feeling but you are not actually yelping and turning it down? It was like that kind of burning: definitely I would use the word “burning,” but it did not hurt-hurt, it just caught my notice, like “Oh there is a burning sensation.”

Then it was done, and I don’t think this doctor and nurse had worked together much in the past, because there was a little bit of a dance about getting me out of the machine / up off the table. I am not certain, but I think the issue was that someone needed to apply pressure to the biopsy area the entire time I was (1) being extricated (i.e., as the mammogram machine was releasing its grip) and (2) extricating myself (i.e., as I was moving from lying on my stomach to sitting up), but there were not enough hands to do all the things, or rather not a coordinated/understood allocation of hands; and there was some concern that I would be pinched by part of the machine, but I was not. Anyway, it was managed: I was sitting up on the table, and the nurse was “applying compression”—that is, squeezing my breast hard between her hands, with a wad of gauze over the biopsy site. It’s not an everyday sort of thing to have happen, but she was so normal about it and that helped.

She had to keep squeezing for Quite Some Time. Five minutes? Something like that, possibly longer. Periodically she would peek under the gauze to check the bleeding. I don’t mind blood, so I looked too. There was more blood than I was expecting. When they said “needle biopsy,” I was picturing a needle like a vaccination needle, where sometimes there is a teensy little pinprick dot of blood. In this case I estimate there was half a teaspoon of blood involved total (and that’s only counting the times AFTER I was able to start looking); and the first two times she checked it, there was a sudden welling of blood about the diameter of a pea, maybe a little smaller. The diameter of a petite pea. It made me grateful I did not know beforehand (or afterhand) how big a biopsy needle is.

When the bleeding had mostly stopped, the radiologist applied two pieces of tape, and there was a word for the kind of tape but I have forgotten it. Steri-strips? Steri-tape? Something like that. [Update: I see the paperwork says “steristrips.”] She put them in an X shape over the area. The nurse then took me to have a “gentle” mammogram to make sure the little piece of titanium they put in there was in the right spot. (The radiologist called the titanium “internal breast bling,” and I could not love her more.) It was like a regular mammogram but much less squeezy, and they said the little piece of titanium was where it should be. (If it had NOT been where it should have been, there was no way to adjust it, but they would have noted the situation in my record to avoid confusion later on.)

The breast/skin area around the needle site looked a little deflated to me, but maybe I was imagining it. (I don’t think I’m imagining it. It looks a tiny bit caved in. Puckered.)

The nurse gave me a little (pink, everything breast-related is always pink) ice pack to put in my bra. It felt soothing and nice, but also it was a very hot day so I think it would have felt soothing/nice regardless. I may put ice packs in my bra every summer going forward. (The ice pack had adhesive to hold it in place, and I often get pink/itchy from adhesive, and it didn’t NEED adhesive because it could be tucked into the bra, and I DID get pink/itchy from the adhesive—so if there is a next time, next time I would ask them to skip the adhesive.

She asked me to rate the pain of the procedure on a scale of 1 to 10. I HAAAAATE those scales, and can’t believe how unscientific/subjective they are: dramatic people will say 10, it’s 10, MY SUFFERING IS ALWAYS A 10!! MAYBE A 12!! Careful anxious hand-wringing overthinkers will say “Well, 10 is supposed to be the worst pain I can possibly imagine, and I can imagine some really terrible pain like if I were shot multiple times or if I were being chewed on by an alligator or maybe I mean crocodile or maybe a shark would be worse, so I guess this excruciating, about-to-pass-out pain is probably a 4 or 5 compared to THAT.” Anyway, I told her the pain of the procedure was less than 1, about 1/2, and I feel good and non-hand-wringing about that assessment. Mayyyybe it was 1 at the worst, but I don’t think so. I think it was 1/2. Maybe less.

On the way home from the hospital, the numbing stuff started to wear off. I don’t know if everyone is like this, but when I get novocaine at the dentist office, as it wears off I get a fair amount of pain that seems to be THE PAIN OF THE NOVOCAINE DEPARTING, rather than THE PAIN THE NOVOCAINE WAS CLOAKING, if you see what I mean. That is, once the novocaine has fully worn off, I am not feeling that pain; it’s more like when a limb falls asleep and is waking up again, and you feel pain as it wakes up, but not after it is awakened. It’s one of the reasons I dread novocaine. Anyway it was like that: I felt an ache like novocaine wearing off. It was not VERY painful, but it was enough to make me want to stick my lower lip out and make a small self-pitying whining sound but not a SERIOUS one. I listened to soothing classical music, which I rarely do, but neither NPR nor my usual pop stations seemed right for the situation.

The ice-pack was small, and by the time I arrived home about 40 minutes later it was not cold. They’d mentioned it was reusable—but what to do while it is re-chilling? I am definitely saving it in case I ever have to have this done again, so that I can have one ice-pack in the bra and the other recharging. [Update: I put some frozen corn into a snack-sized ziplock baggie and tucked that into my bra, and swapped it with another snack-sized ziplock baggie of frozen corn each time it got uncold, and it was as good as or better than the ice pack they gave me, so I will just do that instead of indefinitely saving a used breast-care-center ice pack Just In Case.] I put the single ice-pack I had into the freezer, and I would say the sensation at the site of the biopsy could best be described as “stinging/aching.” Again, not terrible, not VERY painful—but stinging/aching. Putting the ice-pack back on awhile later was pleasant. The whole area feels Kind Of Sore—not agonizing, and I’m not flinching much if I accidentally touch/bump it, but I’m aware of it and it’s uncomfortable, and I am enjoying the cold of each fresh ice-pack.

There was a little bit of blood on my bra. They instructed me to wear a bra to the appointment, but I’d add that you should wear one you don’t mind getting a little bit of blood on. OLD bra. Old COMFY bra. They said I might want to wear the bra to bed tonight, to snug the owie part in and keep it from getting unexpectedly jostled. And I might. But I am someone who does not mind my bra, as opposed to someone who can’t wait to take it off each day, so your experience may vary.

I’m allowed to shower/bathe normally, but I am supposed to avoid washing the area of the biopsy, and I’m supposed to gently pat the area dry afterward. I am supposed to leave the special medical tape on until it falls off, or for four days, whichever comes first. (They said it will probably fall off after three days.) I am supposed to let them know if the area of the biopsy becomes hot/pink (infection). There is apparently a small chance of internal bleeding, which would leave a big swollen bruise but would be fine, and it would go away, it would just be icky/uncomfortable for a little while.

The radiologist will call me when she gets the results; she expects that to take two days, but says because today is Wednesday there’s a possibility the results won’t come in until after work Friday, in which case I wouldn’t hear from her until Monday.

College Search Starting All Over Again

When we were doing the college-search for Rob and then for William, I am not even sure how we chose which colleges to consider. I feel like we’re completely starting over with the twins. Did we just…go to places we’d heard of? or something? It all seems so willy-nilly in retrospect.

Since then, I’ve skimmed a book about how some colleges/universities have spent a lot of money marketing their brands, and that this is part of the reason for the huge increases in costs and in application competition, and that essentially it’s better to AVOID the colleges/universities you’ve Heard Of, because they tend to be over-priced and not a good value.

This is why I feel At Sea, I think: how does one find the colleges/universities one has NOT HEARD OF? I wondered if this would be a good use of Group Input. Because it isn’t really that we want to find the ones literally no one has heard of; we’re looking for the ones people might not have heard of, but that we know of for reasons other than Good Marketing. Maybe our friend’s kid went there, and we’d never heard of it before then, but our friend and their kid were both really happy with the value. Maybe we’ve heard of the place but it has a super boring/unmemorable name.

For example, Paul’s cousin’s kid is going to University of Chicago, which is a boring-named place I would not have remembered Hearing Of. But it’s apparently a terrific school?? and he’s going there almost for free, because they have a fabulous financial-aid situation??

Anyway, I would love to hear of any school you think it would be a good idea to look into. With TWINS (and another kid probably going to college two years later, so we’ll have THREE in school at the same time), I am definitely more inclined toward the less-expensive Good Value types of schools. (I am familiar with the idea of saving money by going to a community college for the first two years, so I have tucked that idea away as one option, but right now I am looking for the usual 4-or-5-year living-in-a-dorm type colleges.)

Oh, and this is going to rule out a lot of places, but we are not interested in religious schools. I had a long paragraph here about how I went to a religious school and it was a good fit for me at that time for various reasons that don’t apply now etc. etc., and about how what I mean by Religious is probably Christian but at this point I am not really feeling favorable toward ANY religion etc. etc.—but let’s just say Not Interested in Religious Schools (including Oh But It’s Not REALLY Religious! schools) and leave it at that. If the kids want to seek out a religious school, that’s not hard to do and it’ll likely save us some money, but I’m not going to do the seeking on this one.

Second Mammography Update

When last we chatted, I’d just had a call about my mammogram: they wanted me to make a follow-up appointment so they could get a better look at some microcalcifications that were new since my scan a year ago. I had those scans today. If you’re curious, it was almost exactly like getting a normal mammogram, but they only did one side, and the technician said “I’m sorry, but it’s going to squeeze harder”; I don’t think I would have noticed, but it was good to be warned. And afterward, instead of getting dressed, I was sent back to the waiting room in my hospital smock (just in case the radiologist wanted more images) while the radiologist took a look at the scans.

I was glad no one asked about or remarked upon the little patch of sunburn in my cleavage. I had a fun afternoon outside with friends yesterday, and I did pretty well with the sunscreen application, but apparently missed a small portion down the front of my swimsuit. I am a little surprised the sunshine managed to get in there: I am not amply bosomed, and even the word “cleavage” is a stretch. Well, the sunshine managed, and it is a good lesson about how well sunscreen works, because the rest of me is nearly as pinkly pale as ever.

After I’d been in the waiting room for ten or fifteen minutes, the technician came back for me and brought me to the radiologist. The radiologist showed me the scans, which were pretty neat to see. First she showed me last year’s scan compared to this year’s, and sure enough: little tiny white specks on this year’s but not on last year’s. Then she showed me the close-up they did today, and mentioned some positives: the general shape of the cluster is oval, which is good; and also some other things which I have already forgotten.

She said she is 90% sure these are just calcium deposits and not cancer, but the close-up did not give her the information she would want to see in order to be completely sure, so she would like to do a biopsy. She says when she does the biopsy, she will leave behind a tiny little smidgen of titanium to mark the place, in case they need to go back in (like if the biopsy DOES show cancer or pre-cancer), or in case later they want to remember where those little microcalcifications were. It all sounded pretty cool, though of course 10% does not sound like a small chance to me. But the radiologist said if it IS cancer, we have caught it at absolutely the earliest possible stage, and she gave a little laugh that I found reassuring—like, we’d have caught it so early our timing would almost be comical. Ha ha. Ha ha.

I am trying to think of another update. OH. So, I mentioned a fun afternoon in the sun. Friends and I lounged in THESE in the water, with beverages in the cupholders:

(image from Target.com)

It’s a SwimWays Spring Float (Target link) (Amazon link). (One friend had the very similar Kelsyus one, if that’s easier to obtain where you are.) Once in a while we would paddle lazily inland and holler for one of the husbands to bring us a fresh drink. It was BLISS. I have ordered three of the loungers and may order more: I got overwhelmed by the Exactly How Many decision, but didn’t want to miss the Target sale, and knew I wanted AT LEAST three for an upcoming family vacation, so I got the sale price on THOSE anyway, and will order more after I’ve had some time to think.