Yesterday, I went out into the world—to dinner and to a tiki bar, where I could not, alas, have any delicious tiki drinks. But it was nice to be out in civilization for a bit. I laughed so much, my cheeks ached.

Today, my bones ache instead. I am angry and cranky. I have two raised, red bumps that look like blood clots.

Oh, I’m sorry: phlebitis. I have been corrected.

I called the doctor on call about the bumps to see if they wanted to schedule an ultrasound to confirm. He doesn’t think they’re clots and told me that he’d pass along the information to my regular doctor tomorrow.

I had to go in today to have my blood checked. The doctors don’t want my platelets to drop below 20, but today they were down from Friday’s 35 to 8, so I got a yellow bag full of platelets.

I wasn’t going to bring up my superficial clots to the nurse, but my boyfriend said I should. I asked her if the platelets would affect my clots. I wish I hadn’t. She asked me why I thought they were clots, and I said because they were exactly like the clots I had in my other arm. She asked me if I’d had an ultrasound. No. She shook her head at me. I showed my new painful, red, raised bumps to her, and my old clotted arm that still feels like I have straws embedded in my arm but is no longer swollen.

“That was phlebitis?” she asked.

Yes. I guess. All I know is that it made me miserable for weeks. I couldn’t move my arm. Sometimes, it felt like a tiny fire was inside. It hurt. A lot. Almost the time.

“It’s not the same thing as a clot,” she said.

That’s fine. Phebitis. I was being nice, despite my pain, and she went out of her way to try to make me feel stupid. I’m not sure what she perceived about my attitude. I has asked a simple question.

Still, my usual response would be to tell someone to phlebite me, but I don’t like to mess with people who have access to my bloodstream, even if they’re being condescending. That didn’t improve my mood. I feel like no one’s taking me seriously and that I’m being dismissed.

I’m not saying I know everything…or anything, for that matter. I’m saying that whatever happened to in my right arm that caused it to hurt and swell for weeks is happening in my other arm on my belly and I would prefer that it not.

I’d hoped my new platelets would make me happier, but I’m still a big jerk today. My boyfriend is out exchanging some Henley shirts for me, so I can wear them tomorrow for my stem cell collection. (Another alarming thing: one of my catheter lumens isn’t working. The nurse just said they “would do what they had to do” tomorrow and didn’t say any more.)

I am trying to get nicer in the meantime. I am wearing some pain patches. I’ve rubbed the cat’s soft belly. I might nap.

I am not taking my oxycodone. I would sell it for extra cash if I had no scruples, but I’ve recently seen a lot of news pieces on the heroin epidemic, so I’m not going to turn into a small-time Walter White. I’m also terrified to take it now, on top of my usual wariness of pain meds.

My big comfort today is the cheesefest that’s going to occur, since I have to eat a lot of dairy before my stem cell collection. For lunch, I had saag paneer, with cheese and spinach, both high calcium. For dinner, we’re having an assortment of cheeses. Cheese, at least, makes me happy.

Today’s just one of those bad days, when I want this to be over. Naptime, then hopefully I awake a new woman.

My bones hurt. Finally.

We’ve been doing two Neuopogen injections daily since Sunday. I brought my old syringes to the doctor yesterday, so they could safely be discarded,  and then I almost left them in the cab. (I’m usually not a fancy person who takes cars to the doctor, but my appointment would have put me on the train at rush hour with germy people who would all be out to knock my catheter out of my chest.) So that’s one way containers of syringes get left in cabs, I suppose.

I was told that my bones might hurt as they produce more stem cells, so I hope this is a good sign. I have pain medication, but the pain isn’t that bad, and I hate taking stuff.

I’m really looking forward to eating a lot of dairy. I see a lot of cheese in my future.

My doctor visit yesterday was pretty uneventful. I got the dressing changed on my catheter and had some bloodwork done. My red blood cell count is pretty good, because of the transfusion I had before I left the hospital. My white blood cells are low, as expected.

My platelets are also low, at 35, so I have to go in tomorrow for another blood check to make sure they don’t drop below 20. I’m at risk for bruising and bleeding more easily. So, no brawling. The catheter had ruled that out anyway. Sigh…

Until then, I’m allowed to go out and be in the world a little. I’m going to go to dinner tonight and go out on Monday with some friends for a big, cheesy dinner. If all goes well, I’ll be in the hospital soon, so I’m lobbying for a pizza party at home so I can see people before the hospital stay and my hermitage begins.

The topic of what I would do if I became a ghost arose the other day — certainly not because I plan on leaving this mortal coil anytime soon, but it just came up as ridiculous hypothetical questions often do.

I had been reading about the recent measles outbreak in New York City and the outcry against the anti-vaxxers, a growing number of parents who don’t vaccinate their children against childhood diseases like measles and mumps because they think the vaccines can possibly cause autism. There’s a mumps outbreak at my old alma mater, and I’ve heard that whooping cough, which killed my grandpa’s sister more than a century ago, is also making a comeback.

I’m a live-and-let-live type. I may rail on about my silly pet peeves like that Subway Fritos sandwich, flip-flops on the train and some truly bad Hollywood movies, but, for the most part, I don’t give a lot of thought to the personal choices of others. If you want to ditch your self-respect, rub city filth all over your feet and waste two hours of your life, it doesn’t bother me.

I felt the same about the anti-vaxxers, until I realized it could affect me, too. After this high-dose chemo, I’m pretty susceptible to just about everything with my low white blood cell counts. The whole reason for this upcoming stem cell transplant is because the chemo really does a number on your bone marrow. I think of it as being broken down and then rebuilt, like Iron Man (speaking of bad movies, Iron Man 2, I’m looking at you) or Robocop.

After the transplant (presumably before I get superpowers), I’m told I’ll have the immune system of a newborn. I’ll have to stay away from crowds and children. I’ll have to get revaccinated again. (I’ve already been vaccinated once as a baby, then again as a 12-or 13-year-old after there was some recall.) I have to take anti-shingles medicine every day, twice a day, for a year and a half after the transplant.

But I’m a little alarmed that there’s this extra risk for things like measles, mumps and whooping cough out there. I understand where the anti-vaxxers are coming from; no parent would put their child at risk for a disorder we know so little about. But that choice is having more widespread affects than I think we anticipated. I realize the term “outbreak” is being used pretty liberally. And I have a lot of real things to face, versus hypotheticals.

Yet this could affect me, whereas people who believe gluten is toxic don’t. I want everyone to be happy, so if I personally think the solution is more research into autism so we can figure out the causes. We need some real science behind this, so people can make educated, informed and safe decisions. Easier said than done. I bet no one’s ever thought of this before!

Well wishes aside, after I read about the measles, I announced that if get a turn-of-the-last century disease and perish, I will haunt the crap out of anti-vaxxers. We’re talking Amityville Horror-style. I am going to be one pissed-off ghost. I would have trouble haunting Jenny McCarthy, because I really enjoyed that Singled Out show. I always preferred Lauren Conrad to Kristin Cavallari, but if I could haunt celebs, I’d prefer to haunt someone more exciting. My hypothetical ghost has already become shallow and sidetracked from its afterlife mission.

The thing is, I don’t think you can select where you’ll end up and who you’ll haunt.

I suppose this begs the question: Do I believe in ghosts? Absolutely. I’m not sure if I believe that people’s spirits stay behind and haunt the earth, but I love stories of unexplained phenomena. So this might totally discount my reasonable stance on vaccines. I get that. I’m no expert. I’m just some lady. And I would rather talk about ghosts any day. I love a good ghost story.

Years ago, I wrote an article about ghosts of Columbus, Ohio. I spoke to a few ghost experts and enthusiasts, but maybe my favorite part was speaking to people who had just happened to see a ghost. Talking to people who had just seen something they couldn’t explain made me a believer in something—if not ghosts, then something ghost-like.

Some of the ghosts seemed cognizant of the outside world; one guy saw the ghost actually wave at him in a mirror. Most of the ghosts that people saw seemed to be intently doing the same thing—and in most cases, it’s leading up to an important moment. I can’t say why one ghost always makes his way to the same movie theater seat or why one ghost is constantly running up the service stairs of a hotel.

In that story, I also wrote about author and cartoonist James Thurber, who wrote The Secret Life of Walter Mitty and documented his ghost experience in his story, The Night the Ghost Got In. One night, Thurber heard heavy footsteps around his dining room table, then the sound of someone running up the stairs. When he asked about it, he’d heard a few people had moved out because of the ghost, belonging to a man who had lived at the house. According to Thurber’s research, the man had received information that if he went home in the morning, he’d catch his wife and her lover. Supposedly, he did catch the pair, then ran around his kitchen in despair before running upstairs and shooting himself. From what I heard, the ghost continues to haunt resident authors from time-to-time.

Most ghosts seem stuck in a loop. I imagine you can’t choose the place you’d like to haunt, as you choose your favorite haunts in life. Otherwise, places like bars, restaurants and amusement parks would be packed with fun-loving ghosts. Ghosts don’t seem very mobile. Or fun-loving, for that matter.

And you probably can’t choose who you’d haunt either, which is a big bummer. And kind of a relief. Imagine if people you’d wronged in life could suddenly show up in phantom form and seek vengeance for a past wrong. I bet we’d treat one another a little differently.

I can’t think anyone who would haunt me, but I can think of at least six people I would enjoy scaring the crap out of, if given the opportunity. I don’t know that I’d want to haunt them long-term, though.

If I ever became a ghost, haunting my current place of residence would be most likely. I wonder if I’d spook the cats.

My boyfriend and I discussed what I would do if I returned as a ghost, and I realized I would continue to pester him about the things I do now. It’s in his best interest to keep me alive.

First of all, I would rattle around the unwashed dishes in the sink. When I do the dishes, I do all of them, but he always leaves some at the bottom. He never does them all, and it drives me crazy. Also, he leaves the silverware, so that we regularly run out of all spoons. I would use my ghostly powers to make a ruckus in the kitchen.

Then I would sweep all of the papers off the dining room table. When I met my boyfriend, his dining room table was full of stacks of papers and CDs, and I had a nice empty dining room table. Since he moved in with me, my table has never been clean. I used to clear it off, but I was told I was messing things up. It doesn’t matter whether we live in a small apartment or had a house with a room that served as an office, everything ends up on the table. I’ve given up. Sweeping everything off every night as a phantom would give me great satisfaction. I would almost live an unsatisfying afterlife as a ghost so I could finally do that.

Also, no matter where I haunted, I’d probably turn up the heat. I’m always cold and waging a heat battle. I’m not sure if ghosts get cold. They’re sometimes responsible for cold spots, so maybe it’s moot. Maybe I’d just mess with the thermostat to be a jerk.

So, I suppose after careful consideration, I’d prefer not to be a ghost. It’s not the same as being invisible and acting without consequence, which would be awesome. And my boyfriend has been so nice to me during my illness, he doesn’t deserve to be nagged about the spoons and the table. (I’m just saying, though, if I lingered on this earth, I might.)

In the meantime, I’ll keep in mind that the chances of being taken out by an old virus is very small. Probably smaller, in fact, than my chances of becoming a ghost.

About a week ago, I experienced the day every girl dreams about: The day her boyfriend tells her she looks like Ian MacKaye. My new black hat creeps towards the back of my head, in the style worn by the Fugazi frontman.

memackaye

Also, this happened today: A surprise package arrived from my boot camp friends, including this Pollos Hermanos T-shirt that pairs nicely with my porkpie and sunglasses! I just might wear my shirt and hat when I have to do laps around the hospital halls to keep my strength up.

mepolloshermanos

Much to report, but I’m taking today off from blogging to blog professionally. Thank you again so much for the notes, care packages and kind words!

Pro: I think I found T-shirts to wear during my hospital stay. Con: My head looks like an old crone’s chin.

I’ll start, I suppose, with my bad news. Instead of the smooth Telly Savalas or the majestic Yul Brenner, my head is closer to Gollum’s from Lord of the Rings. My dome does not resemble a shiny apple, nor a smooth peach. It’s a kiwi gone bad, an old forgotten coconut.

My hair is almost all gone from the first round of ICE chemo, but a few stubborn hairs remain. And it’s not pretty. I expect these stragglers to fall out after this second round of ICE chemo. If not, I’ll take a razor to them.

On the bright side, the online education session about my autologous stem cell transplant put my mind at ease. A lot. And one of my fashion questions was answered; I’m pretty sure Henley T-shirts are the best option for me during my hospital stay.

Even better news, my old standby Uniqlo, where I buy almost all my clothes, has a new spring line of Henleys, so I’m going to buy some tomorrow. People sometimes ask me why I love Uniqlo so much, and it’s simple: It has the clothes I expected to wear when I thought of the present day as the future.

I was promised this future—now—in the ‘70s. The prediction then was that we were going to wear lots of white and monochromatic unitards and tunics. What about the fashion of Logan’s Run? Where are the magic amulets that I saw from other worlds in Wonder Woman, as I made myself dizzy spinning around in the living room, perfecting the change from Diana Prince to superhero and wearing bulletproof star bracelets made of paper? (Seriously, I’d wear those bracelets, bulletproof or not.) I’d even take Erin Gray’s shiny Buck Rogers suits from the 25th century all these years early.

I think of the ‘70s as a dark time for most fashion, but future ‘70s fashion—the era of tunics and unitards and shiny clothing of the 2000s and beyond—was going to be awesome.

You can only imagine how unspeakably disappointed I am.

I waited for this century only to be offered worse versions of what I wore in junior high and high school.

I am most disappointed in American Apparel. I had high hopes when I first heard about the American-made clothes and array of basics, before I realized the sizing is weird and, as Jezebel pointed out, everything makes you look like fat hooker. And why do the ads all look like young Dov Charney/Terry Richardson/Joe Francis-types took them in dorm rooms?

Things have changed a little. This week, after years away, I managed to buy an American Apparel sweatshirt in my size that fit. But I also took note of some of the “new” fashions on display, and a lot of them were straight from my junior high days. We’re not even talking the mall items you HAD to have, otherwise you would surely be expelled from society forever: The oversized ESPRIT bag, the Benetton sweatshirt, the big Express shirt with French writing on it, a long Limited sweater paired with colorful leggings.

We’re talking DEB offerings. Basics. A loose-sitting floral-print dress. A velvet tunic. Cropped sweaters. Acid-washed jeans and light denims that are begging to be French-cuffed. (I have been told that most people called it pegging, but we referred to them as French cuffs in my school.) They do have shiny skirts and clothes. But it’s not right somehow.

So I turn to Uniqlo, which feels like it’s from the future, with their mannequins in basics, long escalators and robot-voice announcements. A friend who lived in Japan doesn’t understand my fascination; she thinks they’re the Old Navy of Japan. But they promise me clothing technology, if not from the future, then from Japan, which is pretty close in my mind. They have clothes that magically stay warm and clothes that stay cool! This is what I need and what I deserve in this present-future. Otherwise I may as well go around draped in animal skins.

The thought of racks of fairly plain basics appeals to me, not only from my lady-of-the-future perspective, but also from my present wardrobe as someone in her mid-30s. At American Apparel, as I took in some of the crazier fashions from my youth and the youth of today, I realized why you pay attention less to trends as you get older, even as you keep an eye to fashion. Trends often look pretty ridiculous. And they often (but not always) expire after the first time around.

I think of my wardrobe as pretty basic and tame, especially after my last year of cancer. But then I just sent a sequin peacock dress from New Year’s Eve to the dry cleaners.

For a very brief insight into my psyche, life story and wardrobe: My mom and I dressed alike until I was in fourth grade or so. She made all our clothes, and all of them were identical mother-daughter outfits. (We were pretty darn adorable when I was little.) I eventually picked out some of my own stuff from fifth to seventh grades, during my personally most awkward phase, then transferred at the height of everyone’s most awkward of phases to public junior high in eighth grade and no longer had a uniform.

After a metal phase late freshman and sophomore years, “alternative” hit. (I’m talking about clothing here. Metal is still awesome.) So I had the Docs and the overalls and my grandpa’s flannel shirts and the band T-shirts, but I was goth-tinged. And so I’ve gone from a teen who wore black a lot to a New Yorker who wears black a lot, and I feel like I’ve really come to my fashion home.

All of this means that my fashion choices are at odds—a mix of blending in and hiding and standing out. Hence the neutrals and black and my usual uniform of black shirt and jeans, with a closet full of well worn craziness, from the Union Jack dress to the shiny pants to the sequined peacock dress.

I keep remnants of these past trends and phases in my closet, though I winnow things down as time passes. I never part with everything. It’s hard for me to part with anything, frankly, and I have a crowded closet to prove it. I delightedly broke out my Doc Martens when they came back this fall. Is it time to revive my ESPRIT bag? Because I still have it.

Tomorrow, I have an online education session about my autologous stem cell transplant. I’ve been reading the giant preparation binder, but I haven’t thought of any questions. Considering that’s what I do for a living, I’m a little disappointed in myself, but I haven’t gotten through much of the material.

Part of me is honestly scared of what’s ahead. All I can think of are frivolous and fantastical concerns. For now, I will blame my procrastination on the plastic-loving cat, who runs her sandpaper tongue over the edges of the binder whenever I try to read. Here are a few of the concerns I won’t talk about tomorrow:

Do vampires roam the hospital floors? My most immediate cause for alarm yesterday was when I read that you smell like garlic for a few days after the transplant. With all this blood, are they keeping us from turning into vampires? Is a stem cell transplant really taking someone to the edge of vampirism, and then giving us stem cells to prevent the change? Is that why some patients in the hospital have “sitters” with them all night? It’s not to help guide them to the bathroom—it’s to prevent them from draining other patients while they sleep.

I’ve seen several Blade movies. Also, I was goth for awhile and have read all the Anne Rice vampire novels, so I can be considered somewhat of a vampire expert.

According to the binder, it’s a preservative that causes the garlic smell, not your body fighting off vampirism. I prefer to turn cutting-edge science into terms I can understand: medieval villager talk.

I also read that the nurses can give you lemons to alleviate the garlic smell. That sounds…sort of delicious, if paired with a delicate fish and a nice white wine. But if I see anyone with a chef’s hat lurking around those few days, I’m leaving that hospital. At least my garlic smell will keep away those on the verge of turning.

Whatever will I wear?  After I Googled “stem cell transplant shirts” or “catheter shirts,” only a few results come up—including my own blog. Am I the only person with sartorial concerns during my stem cell transplant? I really don’t think I’ll care what I’ll look like—after all I’m supposed to feel horrible, and I’ve looked better.

But hospital gowns are drafty. After the leukapheresis catheter placement, I could wear my lounge pants, but I had to wear a gown on top to provide access to the catheter. I thought a lot about my gown when I was in the hospital after so recently seeing all the Oscar fashions. My gown could be said to have a plunging and an open back, worn off-the shoulder. Most gowns, though, whether they’re ball gowns or hospital gowns, aren’t that comfortable for long-term wear.

My booklet says that if you wear you own clothes to the hospital, to wear shirts that allow catheter access. So does that mean Henleys? Baseball jerseys? I have a few button-top tees and thermals. I’ve done some tentative internet searches and all I know is that L.L.Bean probably has whatever I need (or great Google analytics).

What do I do with my head? Right now, my head smells like a Strawberry Shortcake doll and her cat, Custard. If you were a little girl in the early ’80s, you know what I’m talking about. I should wear a big muffin hat to keep my head warm and get some striped stockings.

One of the best things about Strawberry Shortcake dolls was that they smelled like the desserts—the namesake character, Lemon Meringue, and her other friends. (Also, why do they keep updating dolls? This is not how they looked before. Strawberry Shortcake lives in a land of desserts; she doesn’t text and go shopping at the mall with her tween friends.)

In an effort to ease my scalp dryness since the hospital, I’ve taken to oiling my head with some of The Body Shop’s Beautifying Oils I got at a press event. I remember at the event, the PR person said you could put it your hair, so I did. This happened a lot at beauty events. I would put face cream on my face instead of on the back of my hand. PR people always seemed taken aback, so I kept doing it. I gave most of the oils away, but I can now choose between strawberry and Satsuma.

If I’m bald, then do I have dandruff? I’m still trying to figure out what I should use. I’m afraid to use moisturizer, although I guess I can opt for a natural brand.

So these are my concerns today. I’m sure I’ll have some legitimate ones tomorrow. Until then, I will think about how to ask delicately about vampires in the halls and hospital fashion.

When I began Thursday in the arms of a surprised nurse, I knew I wasn’t going to go home that morning, as I’d hoped. The nurse who had last come to take my blood pressure told me it was very low and she reminded me to call for help if I felt dizzy.

There are signs posted in each hospital room that glow in the dark with the image of a stick person taking a tumble and the message, “Call! Don’t Fall!” When I don’t have my glasses on, it just looks like a faintly glowing cube, but it should be ingrained in my head. In my last room, the bottom of the sign was cut off by a lampshade, and I would imagine it was a misspelled invitation to go back to “Calli” and catch a wave.

It might have been this whimsical thinking that got me in trouble. When I got up to go to the restroom Thursday morning, I didn’t feel dizzy. Going to the bathroom in the hospital is so much of a production, with the urine hat and output measurement. I think I managed to scrawl 500 cc on the piece of tape I where I was recording, but when I got to the sink, I was dizzy and started to see spots. I broke out into a cold sweat.

Luckily for me, when I opened the door, a nurse was standing right there. “Help,” I mumbled. “Help me. Help, help, help.” Then she was holding me upright and calling for backup.

I’m not sure that I could have made it the four feet to the bed without the nurse. Maybe. But as soon as I saw her, I knew I wouldn’t make it back, not without her help. And I knew I wouldn’t go home in the morning. They did some sort of test with things taped to me—I kept finding those 3M stickers all over me yesterday, like I was a dorm room wall. My near-fall was due to my low blood pressure and my lack of calling to avoid falling.

Of course, if the doctors wanted to raise my blood pressure, my boyfriend pointed out, they could have sent me down at rush hour to hail a cab to Brooklyn. “After you banged on the hoods of a few cabs, you’d probably be OK,” he told me yesterday, as we stood at the crosswalk and I threatened to make citizens’ arrests of the drivers halfway in the intersection.

In the end, the doctors decided to give me my very first blood transfusion, because my hemoglobin was low. So my transformation to Nosferatu progressed, as I impatiently waited for my blood to arrive. (I finally found out what kind I am: A+. The nerd in me loves that. A-plus!)

If the past day and a half had been a blur of sleep—I keep forgetting that an entire day happened—then the last few hours waiting for blood so I could leave made up for it. Time went from slipping by, hours at a time, undetected, to ticking down minute by minute. I longed to turn into a bat, fly out the window, drain a victim of my necessary blood and then wing my way home.

The blood transfusion itself was actually without much fanfare—they just hang a bag and there you are. I got my blood through my brand-new leukapherisis catheter, so that means no more IVs. Just in time, because I’m pretty sure I’m fresh out of veins. My right arm, with its painful clots, was out of the running this time, and they got one into my left for the beginning of the chemo.

For the procedure, they put in a neck IV and used lidocaine to numb me up first. As much as I worried about it, the catheter placement was actually pretty easy. I was wheeled down on Wednesday, sooner than I thought, and kept in a waiting room for a short time. Someone asked me if there was anything I was nervous about. “Mostly if I’ll say anything weird,” I admitted. She assured me I would probably sleep.

When I was wheeled to the procedure room, someone called being put out a “four-martini breakfast.” This alarmed me. I never have four martinis. I never go beyond two. I live by the Dorothy Parker quote. (“I like a martini, two at the very most. After three, I’m under the table. After four, I’m under my host.”)

I figured out this martini thing even before I heard the wise words of Ms. Parker, the first time I had three martinis. Why was it so easy to tell everyone what I really thought? Even when martinis were $3 each at happy hour within walking distance of my apartment in the Midwest in the late ’90s, I spent $8 (including tip) and called it a night. Or, more likely, I opted for a less potent cocktail after one cheap martini.

Not long after my pronouncement of a two-martini limit, I broke my rule, because someone bought me a third. That was a terrible mistake. I spent the night blithely telling people what I really thought. It’s really a mixed blessing that I remember what I said. Thought it felt briefly liberating, that kind of stuff should be bottled up, never to be loosened by a bottle of gin or vodka.

So you can imagine my reservations when  a member of catheter team announced, “OK, here comes five martinis!” Five? I think I would pass out. In fact, I hope that’s what happened. I don’t remember saying anything, not even my usual farewell to the doctors and nurses or alerting someone that I feel funny. I woke up later, bewildered that anything had even happened. (So if you have the equivalent of five martinis, there’s your urban legend: You’ll wake up in the hospital with a tube sticking out of your chest. It happened to me.)

So the catheter in my chest, and my old IV is gone. I also have Steri-Strips where the IV was and something there. A tube I think? Five martinis. Did I dance too? I wonder if the team saw me as a fast-forwarded version of myself drinking five martinis. Was I happy, then suddenly tipsy before deciding to tell everyone the operating room the truth? Did I then decide to dance or do karaoke before becoming surly, announcing I was going to lead a revolution and then passing out?

I slept all day Wednesday. Sometimes, I would wake up and think, Oh, my phone is in my hand, I should put it on the table. This happened about four or five times before I stayed awake long enough to do it. I am, essentially, being poisoned, and sleep isn’t so unusual…or so bad. I will take it over any other side effects.

I also lost my mind. Briefly. Being in the hospital is tough. I’ve tried to be cheerful through all of this, to look at the bright side, to remember this is just temporary. But everyone has a breaking point, and it’s a straw that breaks the camel’s back. Something insignificant.

After I was moved to a new room, my chemo pump/constant companion started beeping. Sometimes it’s like being moored to the Looney Toons Road Runner and you understand why Wile E. Coyote had so many anvils.

I try to do everything I can to avoid pressing the nurse call button. I’m among the more able-bodied (during my recent stays, at least) and there’s no point taking up people’s time with stuff I can do myself—especially when I have so little I have to do. (This last time, I saved all my urine for 12 hours in a container, so I finally have something to fill on those job applications that ask you for a fun fact about yourself in 140 characters or less.)

I empty my own urine hat and record everything on my door. This also saves me the small humiliation of calling someone on a sketchy intercom to say, “My urine hat is full!”—or worse, if they don’t hear, “I PEED IN MY HAT!” Plus, I’m a little afraid of the intercom people.

Part of is it that you never see them. And the other part is that you sometimes can’t hear them—or worse, they can’t hear you. So, after pressing your button, you wait. Sometimes, you just hear a click and say something uncertain, “My machine is beeping?” Sometimes, someone says, “Hello, how can I help you?” and you tell them your machine is beeping and he or she says a nurse will be alerted. That’s the best case, and thankfully, that’s usually what happens.

Sometimes, though, no one hears you. “Hello? HELLO?” you hear clearly. But they can’t hear you until you raise your voice. Then you feel like a jerk.

Also, I’m not as quick to shout when something’s wrong. (Unless I see a cockroach—then I will drop everything I’m doing and scream at the top of my lungs.) I’m more of a mutterer-and-repeater, as my early morning near-fall shows. That was also my reaction when one of my extra tubes (I’m not sure what it was, it was to keep my other machine from beeping) came undone while I was trying to untangle my machine’s electric cord and blood started coming out. I’m not good in those situations. When I see blood, I’m kind of like that kid from The Shining. As blood pooled from the tube into my hand, I thought, It’s going the wrong way. Again, a nurse was close by so my, “Um, help, help, help can you help me?” was answered promptly.

So obviously I’m not a great communicator. But once you press the button, where do you speak? I sometimes speak into what looks like an intercom, or a shout to the air.

Once I pressed my button, someone said they’d let someone know about the beeping. Then I waited for 20 minutes. I made sure it was 20 minutes, because I was scared to press again. Sometimes, during my second stay, I’d get mixed up like it was a walkie-talkie and press again as if I were signing out. They were not amused, and I was embarrassed.

When people are pressing the button because they’re thirsty or have to use the restroom, they’re often pretty weak. My first roommate would have to call two or three times. Sometimes, they hear her, I think, but other times, I could hear her and they wouldn’t understand and no one would come. She had a bit of an accent, but I’m not sure why so many of her calls went unanswered. Sometimes, I called for her.

So I developed an early fear of the intercom. And when I called again, 20 minutes later, they couldn’t hear me. “Yes? Hello?” “MY MACHINE IS BEEPING.”

Someone shut off the machine, but something inside me had loosened. I started to cry and I couldn’t stop.

In kindergarten, I almost got my finger stuck in the paper towel dispenser. Almost. It barely scraped my finger, but I started to cry and couldn’t stop. I wouldn’t stop. The teachers had to call my mom and grandparents, who threatened not to take me to Sea World later as we’d planned. I finally pulled it together after that.

I couldn’t tell anyone why I was crying though. Was it the horror of the gaping maw of the paper towel dispenser? The sadness of the world on my 4-year-old shoulders? A future premonition of Blackfish? I remember this, but I still can’t say why I was so sad that day.

When the nurse practitioner came in on Tuesday, I was still blubbering. I felt like that crying kindergartner. I was four again as I tried to explain to her and to the social worker and to a nurse why I couldn’t stop crying. They asked if I felt forgotten, slighted?

Yes, I was upset. I finally explained that I tried so hard to not be a pain and I just felt like I was, having to call and having to yell. I felt like a burden.

That, of course, goes deeper. I don’t like feeling like a burden on anyone, but it’s hard to not feel that way when you’re not 100 percent. Tuesday felt like the reaction to everything sad that had happened to me since I heard I had cancer a year ago.

The social worker helpfully started in on several theories to help me. “Being in the hospital can be hard…” she said, as I blubbered and nodded in agreement.

It’s hard. I’m going in for 26 days, and I can’t imagine it. I’ve been in a total of eight days or so—and feeling relatively well.

You’re not in control in the hospital. Sure, you can wheel yourself to the bathroom when you don’t feel like falling over and you can choose what you want to order when you’re allowed to eat or not throwing up or sleepy. But you also have to keep track of your urine and you have to call people for things like helping you to stop beeping.

Even in the best hospital environments, when everyone is trying to help you, you’re still alone with your thoughts just enough to drive you insane. Even if it’s for a minute. Or, in my case, an hour or so.

The hospital is hard—and surprisingly dry, somehow devoid of all moisture, despite my waterworks. After only three days there, my face is peeling, my lips are chapped and the inside of my nose will bleed spontaneously. My scalp is dry and flaking. I have to drink at least two liters of water daily, but I’m always thirsty anyway. No wonder they give you so many fluids while you’re there; it feels as if you might evaporate.  I feel like most of my houseplants must have felt before the cat finished them off. I am a husk.

The hospital smells weird, because it’s so devoid of smells. When I came home, the normal cooking smells coming from my apartment hall were almost too much. In the hospital, there’s the orange cleaning smell and food sometimes and then kind of this funk. It’s different from dorm room funk, but it’s a human funk. To me, it smells a little like popcorn, or like popcorn in its saddest form. I awoke from a three-hour nap Friday enveloped in the funk at home, and I can’t find its source.

For most of Friday, I would wake up for a few minutes and see the cat looking at me across the bed. We would blink at each other slowly, like two sun-drowsy alligators, and then go back to sleep. I napped with the covers pulled up to my chin so the cat wouldn’t bother my new plastic attachments. She loves eating plastic. I hope to give her enough credit that she won’t try to steal my new equipment from my chest cavity. She seems to walk gingerly around me these days. (It’s far more likely the other, clumsy cat will accidentally pull out my line.)

For emergencies, I have clips, in case my line gets compromised and I start losing my blood. It’s hard not to think everything’s out to kill me. I keep my clip close at hand, but mostly it’s the area at the root of my spine—the center of squeamishness—that suffers.

In the meantime, I am feeling good and energetic. I’m happy to be home and am hoping to avoid a hospital stay before my next scheduled one in April.

I was supposed to be in the hospital right now, receiving my second round of augmented ICE. Instead, I am lounging in bed and catching up on work—and, of course, this blog. I have mixed feelings about this—obviously, I’d rather not be in the hospital, but it’s just a three-day respite from the inevitable. Instead, I’m going in tomorrow, just in time for the snowstorm. (One of the many snowstorms of this winter.)

I have mixed feelings about the weather too—on one hand, it makes going to the hospital and doctors’ appointments, of which there will be many, less pleasant, but on the other hand, I have to be a hermit through May, and hermitlike through mid July, when the weather is beautiful. (I expect the winter to be done by then, at least.) This is when I wished I’d skipped the Brentuximab and gotten all this unpleasantness over with in the winter. Ah, well.

Friday, I packed up my hospital suitcase full of loungewear and my blanket and headed to my doctor’s appointment before the scheduled leukapheresis catheter placement. When the doctors saw the arm with the two clots, however, they decided to delay catheter placement and my hospital stay. My arm at that point looked better than it did on Thursday, when it swelled to giant proportions. I was worried it would burst open like a piñata filled with blood, but I realized this is probably not possible.

After a night of a heating pad and menthol pain patches, my arm was still red and hot to the touch. And it hurts. Sometimes, it feels like a tiny flame is in my arm. I rated the pain a five or six, but my boyfriend told the doctor it’s an eight. He corrects me a lot at the doctor, and I always wonder if they write down what I’ve said or his opinions. I think I have to agree with him in order for them to take his into account. An eight is pretty serious though. I maintain this is a six.

In case my arm is infected, I’m on antibiotics, and I went for another ultrasound. Apparently, the clots are the same size. They’re just inexplicably more painful and annoying. So I got some more Lovenox to inject daily to try to clear them up.

I start chemo on Monday and then I have my catheter placement on Tuesday. In the meantime, they might use a PICC line for the chemo, since my veins have been less than cooperative.

On Friday,  I did meet with the transplant doctor, who gave me an idea of what’s in store in the coming months. Spoiler alert: Not much in the way of fun.

The saddest news came when she asked me if I have pets. When she found out, I have two cats, she had a list of don’ts. I can’t change the litter, but that’s my boyfriend’s job anyway. Also, she said I have to keep them away from my face until mid-July. What? How am I supposed to resist burying my face in their fuzzy bellies?

Also, one of the cats is extremely proactive about touching our faces. Just the other night, she was curled up by my boyfriend’s face, rubbing her wet nose against his cheek while he tried to sleep. I wake up with her paw on my shoulder or her face buried in my neck, or sometimes I wake up because she’s pressing her nose against mine.

The doctor is very knowledgeable about stem cell transplants and medicine, for which I am grateful, but I suspect she knows very little about cats when she suggested we break the cat of her habits. There’s no teaching a cat anything. It’s going to be a long, sad three months.

I didn’t cry when I pulled my hair out or applied duct tape to my head. I didn’t cry when I heard about my upcoming “hell week.” But I did cry about this. Sometimes, I’ll just look at the cats and tear up. It’s not even like I won’t be able to pet them. I guess it’s just a symbol of how things are going to change in the coming months. Also, I love kitty-cats.

I have to make sure all their shots are up-to-date, so luckily we just took them to the vet. They are senior cats, but in far better shape than I am right now. In fact, the female cat is in the shape of a cat one-third her age. I wish she could understand the vet, because she is vain and would enjoy this news.

Aside from the cats, I’ll have to avoid alcohol, something I had assumed was a given. Once your fast-growing cells are poisoned and you have to take anti-nausea drugs, drinking isn’t something you feel like doing. Also, after the last ICE, the nurse advised drinking at least two liters of water a day so the drugs don’t irritate the bladder and cause bleeding. So I stayed extremely hydrated, although I’d have a little coffee with milk during the second week. Of course, I’d love to hit happy hour instead of giving myself blood thinner injections. I think I could do an excellent job of thinning my blood on my own. Alas.

I’m also supposed to walk to help with recovery. Vigorous exercise is out—I haven’t done my workout DVDs since the first round of ICE and I managed to do yoga only four times since, after being thwarted by my fever, hospital stay and the arm I can’t move because of the clots. The thing is, I don’t want to walk outside when it’s cold, and there’s no sign of spring in sight. I’ve thought of getting an elliptical, but I have a small Brooklyn apartment. I do have a Leslie Sansone walking DVD that I got when I worked at a women’s magazine and edited the fitness section of the blog. The magazine shut down before I had a chance to watch it, and I’m intrigued. It could be a nice indoor walking solution that doesn’t take up much space.

I can do gentle yoga, but I’ll have that chest catheter so I’m wary of stretching. The doctor advises stretching a little bit once it’s in, but in addition to the heebie-jeebies, I can’t move my right arm much because the clots hurt.

At some point, I’m also going to get a blood transfusion.

I got a thick binder full of information from the doctor all about the transplant with fun topics like hair loss, catheter care and giving Neupogen injections twice a day. I haven’t even scratched the surface. For those asking what’s in store and my schedule, here’s an idea:

March 3–5: Second round of augmented ICE, catheter placement. I am not looking forward to having tubes sticking out of my chest. This gives me the heebie-jeebies. There will be two for the stem cell collection—one to take my blood out and the other to put it back in once the stem cells are removed and my blood spins around in a machine.

March 7–16: Neopogen injections, a catheter dressing change. We’ll do the former, but I’m glad we don’t have to do the latter. The shots to increase stem cells might cause bone pain, I’m told. They’re going to give me pain medication, but I hate taking pain medication. I don’t even like to take aspirin. I do hate pain, though, so we’ll see.

March 17–19: Stem cell collection. This involves sitting around for four hours, while your blood is taken out and put back in. It doesn’t sound so bad. During these days, I also have a flurry of tests and appointments, including an echocardiogram and a pulmonary function test, as well as an appointment with a social worker to mentally prepare me for the transplant. The best part of this process is that I have to eat a high-dairy diet these days. Bring on the milkshakes and cheese. (Greens also have a lot of calcium, so I’ll be sure to eat those as well.)

Stem cell collection might take longer than three days. They need 5 million. The record to beat is 32 million, but the doctor said that person had a lot of bone pain, so I’m OK if it takes longer. I’d like it to take only two to three days, if possible. I hope my bone marrow cooperates.

March 24: PET scan. I need a clear one to go on to the transplant, so I hope I pass! It would be nice to finally get a clear PET scan, something I’ve been hoping for since October. And I think I start outpatient radiation this week.

April: If everything goes well, five days of inpatient radiation and three weeks in the hospital for the transplant. The radiation is supposed to have unpleasant side effects, so I’m just in the hospital so they can keep an eye on me. Then the first week, when they do the chemo, is supposed to be OK. They keep referring to the second week as the bad one. Someone called it “hell week.” I’m scheduled to speak with a volunteer who has been through this to answer any questions. Also, someone left a comment on my last blog about a friend of hers who did a stem cell transplant for refractory Hodgkin’s lymphoma and is doing well. It’s always nice to hear tales from the other side.

In the third week, I start a long recovery—about three months of rest and isolation from crowds and six months until I’m 100 percent. I’m a little disappointed to hear that the first month of recovery is so intense and that I’ll need 24-hour supervision. Of course, I didn’t expect to emerge from the hospital feeling great. But I’ll have the immune system of a newborn.

So that’s what’s in store! The next steps start tomorrow, and as much as I’m wary of what’s in store for the next few months, I’m also eager to move towards the end.