Some of you have asked about visiting, and as Greta Garbo was famously misquoted as saying, “I want to be alone.” I think.

That’s not to say I don’t want to communicate via Internet and phone. I had a few visitors during my most cognizant stay, when I felt the most well, and that was nice. But this isn’t going to be any fun. I wouldn’t be there if I didn’t have to.

The worst way to put this is that I’m going to get burned from the inside out the first five days, followed by seven days of being continuously poisoned intravenously. Then I’m going to be sick and sleeping — and, according to what I’ve heard, in a zombie-like state. Someone who’s been through a stem cell transplant said people came to see her, and she didn’t remember. The last week, I’ll be recovering, but I still expect to be in a haze.

I hate to be one of those people who inspires a Dear Abby letter. If you really want to come visit, you can. I think it’s nice that people want to, and I don’t want to hurt anyone’s feelings. But honestly, I’d rather see people when I don’t feel the worst I’ve ever felt. Everyone’s been so supportive and nice, so I do feel bad. But again, that same person who had been through this said that there came a point when she had to ask people to leave and she had to learn how not to feel bad about it.

If you happen to be around and want to drop by, that’s OK. But if you plan to come to New York specifically to see me in the hospital, please don’t. Unless you’ve always dreamed of coming to New York without the obligation of seeing me very much.

I just honestly believe I really won’t be up for visitors. Like I said, that could change. I won’t have a roommate this time, so I won’t feel pressured to win a popularity contest. (Because you know I’d feel a little rivalry.)

If you’re worried I’ll be bored, I don’t think I will be. I grew up as an only child on a cul-de-sac with no other kids. I’m used to entertaining myself. And I really do think I’ll be sleeping a lot, if augmented ICE was any indication of how I’ll feel.

It’s possible I might change my mind, at least for that chemo week, before I enter the zombie part or “hell week” as it’s sometimes called. (I’ve thrown up on most of the people I’ve gone to college with, so this might be your big chance to join that exclusive club.) You can check with my boyfriend for the latest!

Here are the rules for visitors.

Visitors have to have received flu shots for this season. My boyfriend is going to get his first flu shot ever. I can’t say anything to its efficacy. I’ve had flu shots and I’ve not had flu shots, and I’ve never gotten the flu. (Well, not ever. I had it once in second grade and I had the worst flu ever—nicknamed the Thanksgiving Disease by my group of friends who survived that terrible 1996 plague—in college.) That said, I’m really bummed that this whole procedure is going to obliterate my immune system. My old immune system was pretty great, and I rarely got sick. Except for the cancer. So I guess it’s back to square one.

Visitors must wear face masks, gloves and sometimes gowns. I hope most people wear formal gowns and tuxes when they come to see me anyway, but the hospital will provide gowns. (I don’t think they’re hospital gowns and I don’t think you have to get naked under them, but if you do, that’s your choice.) If you wear a face mask, I’d like you to pretend you’re in the band Clinic.

Visitors can’t have any germs. Well, they can’t be sick at least. No cooties!

No kids younger than 7. As much as I complain about missing my cats as a cat lady, this must be a very sad rule for parents of young children undergoing stem cell transplants.

No live animals or plants. The last time I was in the hospital, a bed bug-sniffing beagle came around as a precaution. I had a scheme to dress the cats as beagles, but I decided not to compromise their dignity by disguising them as dogs.

After the transplant, I want to see everyone, but that’s not going to happen right away, sadly. I’ll be back to square one with my immune system, so I have to stay away from crowded places for three months. I realize New York City is a pretty crowded place. But it’s advised to stay away from places like grocery stores at peak times, something I try to do anyway because I work at home and don’t need to rub elbows with the hoi-polloi. (I assume this also means the train, which is supposedly “filthy” and officially plagued by “schmutz.”) I have to avoid people with colds and viruses and such, especially for the first three months.

Post-transplant, I’ll also probably have trouble concentrating or remembering things. (I know some of your will say I had trouble with that before — insert comedy rimshot here.) It’s something referred to as “chemo brain,” a lingering mental fog.

So far, I’ve noticed this only a few times, after emerging from ICE. In one case, someone sent me an email about one thing and I kept responding to the subject we’d discussed in another email. It’s been hard concentrating during chemo, when the fatigue sets in, and afterwards, when I awake from my days of sleep. After that, it’s a bit like Lazarus rising from the dead or Sleeping Beauty awakening from her spell—or at least how I imagine it would be—it takes a little bit of time for me to remember everything that was going on before I went into chemo-induced hibernation. If I feel as if I’ve been asleep for a thousand years after a few days, I think a week or two will be harder to recover from.

In any case, please bear with my forgetfulness and general confusion—as you always have. I will remember an anecdote in detail from 1999, but I can’t remember my keys. And I get some very different things mixed up as it is. I sometimes get Gary Numan and Randy Newman mixed up. Oh, and Billy Bragg and Billy Squier. I also get Tinder and Grindr confused, so it’s a good thing I don’t online date. Mostly it is confusing to me. If you’ve talked about one of these subjects and I’ve looked puzzled, I’m just working this stuff out.

So in short, it sounds like, for at least three months, I’ll be easily tired and worn out, but I can slowly start to get back into the swing of things. And visit—or don’t. I’m just going to be exhausted, and I might smell like garlic.

Hopefully I’ll be almost back to my old self by my birthday in October!

I now have more than 6 million stem cells ready for my transplant. It turns out my guess was pretty accurate on Monday—I had 3 million and change—and I had to go back Tuesday to have more stem cells collected.

So I had some grilled cheese and set off for Manhattan, but not without completely forgetting the Neupogen injections. I came home, took my shots and then rushed to the stem cell collection room. It was a full house, with all the beds taken, so I had to wait to get hooked up. Then my platelets were low, so I couldn’t get a heparin injection, which apparently moves things along. So this collection took a little more than five hours, and I was given heparin at the end.

I also got some yogurt to keep my calcium levels up, and the nurses shared some of their candy with me. It’s a pretty happy place, considering your blood is being drawn out, spun around and put back in for hours. The only painful part is waiting, and the nurses do their best to make that painless.

I plugged my laptop in and did some work, but I felt as if I was moving at a snail’s pace. A nurse explained that the Neopogen boosts white blood cell production, and the bone marrow is so focused on that that it lets other stuff slide — like platelets for clotting and red blood cells.

That explains why I’d been so sleepy. On Monday, I came home took a nap, and then went to bed early and slept for 10 hours. I woke up Tuesday refreshed but by hour three, I couldn’t work anymore and decided to read, and then I slept for at least an hour.

A social worker from the hospital also came by to see if I had any questions and to make sure I would have adequate care after the transplant. I was a little sleepy, so I feel as if I didn’t have any good questions. Also, my appointment list just had a name on Monday, and I didn’t check to see who I’d be seeing. So I’d gone to my dental appointment ready to discuss my feelings. (I know my regular dentist, so I guess I can discuss my concerns with her if I would like both a check-up and to talk about my well-being.) Most of my questions were answered by the online session last week with a transplant doctor and a volunteer who talked about going through an autologous stem cell transplant for Hodgkin’s lymphoma.

TMI alert: Whenever I blow my nose, my right nostril often produces blood. It’s happened after both ICE treatments and the doctors said since my platelets are low, I’m prone to bleeding. To add injury to this insult, while I was wiping up the dried blood from under my nose, it must have cut my skin, so I now have a very visible cut under my right nostril. It now beats my most stupid injury surpassing the time I chipped my tooth while drinking a fancy Bloody Mary. (Felled by an olive pit.)

I still have a giant, swollen monster arm. I’m worried that once my platelet counts go up, it might just burst open. I assume that’s never happened. In the meantime, I will continue to smell like menthol patches and not bend my arm.

phlebitis

I am in the second hour of my stem cell collection. Currently, a bag of my stem cells is filling up behind me. One lumen of my leukapheresis catheter is feeding blood to what appears to be some sort of Rube Goldberg machine, with a bunch of spinning dials, and the other is returning blood back to me.

They covered the lines for me with a blanket, because I’m a little squeamish. I accidentally took a look as the nurse drew a big vial of blood from my chest catheter and it really gave me the heebie-jeebies. Apparently, the blood is being taken out, spun around and then returned.

My stem cell bag is filling up, but I don’t know what 5 million stem cells look like. If I had to guess, like those jellybean contests at stores, I’d say I have about 3 million. We’ll see if I’m right. I have to come back every day until I reach 5 million. I’d like to be done soon, since I’m running out of places for the Neuopogen injections.

I’ve been here since a little after 8 am for a marathon of tests. They slated one after the other so I could get them out of the way before my stem cell collection at noon. Everything has gone smoothly so far, aside from my decision to take the train instead of taking a car. I thought I’d miss rush hour, but I forgot how crazy the 4, 5 and 6 trains are in the mornings.

I started with a pulmonary function test. I think this is my third or fourth one, so I’m an old pro. I wonder if my scores are worsening—not from potential lung damage, but because I haven’t been to Bikram yoga in a year, so I haven’t been doing any pranayama breathing. The test is a bit like that, without the head and arm motions. You blow into an apparatus as hard as you can and take a sharp inhale a few times, and there are a few other exercises where you completely empty and fill your lungs.

My finger also gets hooked up to a machine and I step up and down some stairs while it records my heart rate. Sometimes, I’m tempted to think of something that makes me angry to see if I can make my heart rate go up, but I never do.

Then I had an EKG. It’s the test, where they put those 3M poster-hanger things on you, followed by an echocardiogram. More breath-holding, this time with ultrasound goo and heart images.

After yesterday’s unsympathetic nurse, I finally got the reaction I wanted from the person who did my echocardiogram. “Phlebitis? Oh, I’m sorry,” she said. “That really hurts.”

Yes. Thank you. That’s all I wanted. Some sympathy and acknowledgement of pain.

My arm is even more swollen that yesterday. I have two giant, swollen bumps, one in the crook of my arm so I can’t bend it. My arm feels like it weighs 50 pounds. I usually use my other arm to move it around.

The good news is that the doctors had me pop by to take a look at it. The bad news is that they can’t do much. Since my platelets and counts are low, I can’t do blood thinners right now. (Alas! If I could celebrate St. Patrick’s Day, I could thin my blood on my own with some festive drinks!) In the meantime, I’m on antibiotics. Once my counts go up, they will consider the Lovenox again.

As for the painful bump on my belly, where we’ve been doing injections, it’s just a little bit of bleeding from the shots. It feels like a mini-phebitis. It hurts. Like a broken heart, it just needs time to heal. Sigh…

I also got a dressing change while I was there. It’s a piece of protective plastic around the chest catheter with a tape edge. The nurse has to write the date on it, and the nurse practitioner drew a shamrock on it, so I feel decidedly more festive.

The nurses at the stem cell collection room are decked out for St. Patrick’s Day. I think I have about 45 minutes left before I can go home. Since I usually spend my afternoons in bed with my laptop, not much is different aside from the big blood machine and the noticeable lack of cats.

I also had an appointment at the dental office here, so they can check to make sure I don’t have any tooth issues before my stem cell transplant and radiation. My teeth look good! I feel as if it’s the one area of me that’s not falling apart in some way.

On the way to the office, I got lost and spent some time wandering the back halls of this massive complex. When I found the elevators to leave, I realized I’d been steps from where I started, after a very long detour. I have no sense of direction, so this was not very much of a surprise.

In a few hours, I expect to get the call about my stem cell count. I hope it’s good news and that this big bag of stem cells hits the 5 million mark. I was worried I’d be a few short, but the nurse says if it’s close, it should be good enough.

We’re having pizza for dinner—just in case I need the calcium. I didn’t have lunch because I don’t want to have to get unhooked to use the restroom. I’m looking forward to sitting in front of the space heater with some food and cats.

I salute all those who have been going outside all winter. I’ve been outside a total of 10 or 15 minutes, and I can’t deal with one more second of winter. I’m ready to retreat to my hermitage until the weather improves.

Note: I feel conspicuous taking a photo here, so here is another photo of my cats.

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.

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.

I got my blood drawn this afternoon and 15 minutes later, my room phone rang. It was the doctor. My blood count reached the magic number of 500 and I would be released! After the general consensus had been a Sunday discharge, this was an unexpected bit of good news.

As nice as Memorial Sloan-Kettering Cancer Center is, I was packed and ready to go in 20 minutes. After this morning’s breakfast Nutella and banana crepes and my jambalaya lunch, I was looking forward to tonight’s stir-fry shrimp, but I’ll be back at the hospital in a week. I also didn’t have time to check out the recreation center again and I was going to avail myself of the free board games tomorrow.

Also, I discovered there’s a pool table. How do you navigate a pool table with an IV in your arm?  I also discovered that there’s an afternoon tea service. If the hospital had a happy hour and I could get a beer to go with my pool game, I might have found it harder to leave.

But I was tired of wheeling around an IV stand and I’d gotten away without peeing in a hat until today. I did figure out how to take a hot shower. I don’t know what it is about dials, but I constantly misinterpret them. I’m terrible at math, don’t know my left from my right and I can’t figure out dials. I think there’s some kind of diagnosis for that, other than being dimwitted. (I repeatedly burned things in the oven our landlord brought up to replace our broken one until I realized I had been misreading the dial. I had been turning things up to 400 or 500 degrees.) So in this unfamiliar shower, I had the dial pointed toward lukewarm instead of hot.

Today I found myself packed and waiting for my IV removal, two days before expected.  I didn’t even have to change my pants, as I was wearing my brand-new dignity pants, suitable for public viewing. I threw on my boots and sweatshirt and was ready to go.

The only hitch was the car service I called to come pick me up. Since my boyfriend was working, I wasn’t being released to anyone and the nurse had to witness me getting into a cab or car. When I called right before 5 pm, the operator said 15 minutes, so the nurse escorted me to downstairs. At 5:18, I called to check. At 5:25 I had to call back after being on hold and forgotten about. “Two minutes,” snapped the person who answered the phone. Seven minutes later, I called to check again and was told the car was outside. After walking through the rain and asking several cars if they were for me, I had to call back because he’s hung up on me. By this time, I couldn’t get through. At 5:38, I called and was told to wait five more minutes.  At 5:41, I called to cancel. At least I gave them the courtesy of an update. The front desk called me a car service that arrived in three minutes.

By this time, I was in tears, upset and having to have someone else waste her time, even though she so kindly waited with me and eventually ended up comforting me.

It’s always the little things that push you over the edge. Or push me over the edge, at least. Being back in the hospital was disappointing, but I had been OK up until the point where I couldn’t leave because of a car service. That was my breaking point. The car service just acted like they were doing me a favor. They had obviously lied about when they would arrive and even being there and then didn’t seem to understand why I was upset that they were almost an hour late. Once I even got into a car, finally, from another service, I couldn’t stop the tears. It wasn’t about the car anymore. The dam had broken and I just let things flow out. Quietly. Maybe a dam isn’t the right analogy. It was more like a slow leak.

I had been so angry, I worried my blood boiled and threw off my counts again.

But all is well, once again. As I type this, a cat is weighing down my right arm with her paw over my hand. I have a week at home, and all is right with the world.

Yesterday, I felt great. I woke up early, got a bunch of stuff done and felt ready to conquer the world, albeit from my bed. I even did yoga for a few days this week. In the afternoon, I felt a little sleepy, so I took a nap. Then I took another nap. By the time I woke up at 6, I had the chills and felt a little achey.

I took my temperature and it was 100, then 101, so I called the doctor. I had hoped he would just tell me to take more of the antibiotics I had on hand, but the doctor wanted me to come in to urgent care with the possibility of being admitted to the hospital since my white blood cell count is low and I’m at high risk for infection. So I packed up my bags and we headed to the hospital, about a week and a half sooner than I wanted to return.

My white blood cell count was 1 on Monday and now it’s hovering around 0, meaning I am neutropenic and have no immune system to speak of. It’s what they had expected after the augmented ICE, and the shot I was given on Friday hasn’t kicked my white blood cell count back up for some reason.

The good news is that they didn’t detect any virus activity, though I’ve been sniffly the past few days. After waiting in Urgent Care, I finally got an X-ray and got to my room around 1:30 am. I tried to keep in mind it’s always better to wait in Urgent Care than being rushed in as an emergency. My boyfriend offered to stay, but sleeping on an uncomfortable pull-out chair among all-night beeping machines is no way to get proper rest. I sent him home.

This morning, I got the verdict: I probably won’t go home until Sunday, or at least until my blood counts are back up. They don’t want to send me home just to have me return. This is a pretty common thing after augmented ICE chemotherapy, so I just have to bide my time until I can return home. Although I’ll be turning around and coming back here next Friday if everything goes as planned for my second round of augmented ICE.

The hospital is full of surprises. When I took a shower, I came back to find my bed made. It was nice, like going to the bathroom at a restaurant and finding your napkin folded upon your return. Later on, the nurse came in with a Lovenox blood thinner shot and I remembered that it stings a little bit, so that was a less fun surprise.

I like this room better — the bathroom is probably one square foot bigger and it makes all the difference. Also, I’m at a slightly different angle than before — the A side of the room versus the B side, so I have a nice view of the Queensboro bridge. But as I told a friend who stopped by earlier, I think I’m on a less fun floor. My last floor when I was here for the ICE had an activity center with movies, crafts and live entertainment. This floor is quieter, and I don’t think they’re as enthused to have me walk around, since I’m at risk for catching everything. That’s OK — I like my quieter bit of real estate.

The good news is that I will have the opportunity to try the Maryland crabcake and the Nutella and banana crepes during my stay. There’s also a make-your-own sandwich option, and I was going to try to get three fillings and four cheeses on one sandwich or see if the kitchen would make a giant Dagwood, but now I can space out my sandwiches.

I’m on a low microbial diet to avoid any potential pathogens, because of my suppressed immune system. It’s pretty much what I’ve been following while eating outside of my home during chemo: No deli meats or cold cuts, no raw fish and no raw fruits and vegetables (except for self-contained bananas and oranges).

I’m also not supposed to have mold-ripened cheeses, and while I haven’t had any raw cheeses for months, I think I’ve been living dangerously and eating Brie, goat and blue cheese. (Oops.) I’m also apparently not supposed to have frozen yogurt, but it’s not the ’90s, so I should be OK. (People keep telling me that frozen yogurt is making a comeback but I don’t believe it.)

For now, I bide my time and hope for an uneventful stay. I still feel a little sniffly. The internet connection here has been a little spotty, and this prevented me from taking an important Zimbio quiz on which ’90s boyfriend I would have. I will do my best to make it to Sunday in such conditions.

Well, that cat nap inspiration must have worked, because I slept all day yesterday. After a somewhat miserable hour or so the night before, with violent hiccups and nausea, I fell into a deep sleep that would have lasted until about now unless I hadn’t been woken up to eat, for tests and to go home this morning.

It’s an appropriate day return home from my first round of augmented ICE, on a day when the typical misery of a horrible snowy winter day is augmented with icy rain. Since my treatment had started late on Monday, they wanted to keep me through the morning. I got the impression the C part of the regimen — the last medication — is the harshest, so they want to keep an eye on your fluids and nausea. I slept right through everything, so the doctors seemed pleased.

My view yesterday, as a comparison.

My view yesterday, as a comparison.

Yesterday evening, the nurse woke me up around 6 to make sure I slept through the night. I managed to eat my dinner, type a few things and then talk to my boyfriend before drifting off to sleep again. (I am bummed that I slept through eating my breakfast burrito yesterday, but did get to enjoy a dinner of stir-fried vegetables last night. And if you ever find yourself at MSKCC on a day when the wonton soup is a special, order it for the tender shrimp-filled wontons and fresh cabbage and ginger.)

This morning, I woke up before 8 and tried to get as ready as I could. I must have looked impatient as I felt, as I slurped down my breakfast and asked, “Can I go?” Or had my IV tubes unhooked and asked, “Can I go?” I looked like a desperate movie character about to rip out her own IVs and scale down the wall by the time they removed those and said that yes, I could go.

Bedheaded and ready to head home.

Bedheaded and ready to head home.

Now I’m at home with my little NYC family, our two-cat, two-person republic. TMI alert, but I am extremely happy about being able to shower and not having to pee in a hat. I haven’t been this excited to get back to my own bathroom since spending a few months in Mexico using a latrine and taking lukewarm showers. There’s nothing like a hitch in your toiletry schedule to really mess you up.

Years ago, a friend had free tickets to see Urinetown, a musical based on the premise that the residents of the entire town had to pay to pee. Afterwards, my friend, who is prone to body-shaking moments of pure merriment when he thinks something is particularly funny, turned to us. Laughing, red-faced and gasping for air, he asked, “Did we just spend the last few hours watching people singing about not being able to pee?”

Yet, as I regarded my urine hat this week, I found myself thinking about that musical and how I longed for less complicated days.

And on a completely different note of gratitude: Thank you all again for your kind words and notes. If I haven’t answered in the past few days, it’s because I’ve been asleep but I have been cognizant of your thoughts. Being in the hospital can be lonely, but I never felt alone. I would only have to look at my fleece cat blanket — which was a big hit and very warm compared to the thinner hospital blankets — and my cat totem to know that I wasn’t alone. Or I would think of my friend across the Atlantic who shaved her head in solidarity — and looks amazing! Or read some poetry from a friend-of-a-friend in remission from cancer. Or I could read a nice Facebook note or text, even though I couldn’t write much back.

Thank you for helping me remember that even though I have a long road to recovery ahead — one that won’t be pleasant — I’m still one of the luckiest people in the world.