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.

A year ago yesterday, I found out I had Hodgkin’s lymphoma. That day, if you would have told me I’d be putting duct tape all over my head a year later, I may not have believed you.

This past year has seen me do a lot of things I didn’t think I would or could do. I’ve been through six months of chemo. I’ve given myself blood thinner injections. Until this past month, I’d never been in the hospital overnight. I have nine radiation tattoos. I’ve shaved my head three times.

That last part brings me to the duct tape. On Saturday and Sunday, I noticed all my hair was falling out at once. I could just reach up and give it a slight pull, and it would easily come out.

I was thinking of just pulling it all out, and I started to do so Sunday morning, but got bored, so we decided to shave the rest off. I’m not sure who reads this, but if all your hair starts falling out after augmented ICE, just pull it out, no matter how long it takes. When I shaved it, I had stubble left. But it hurt. When I put my head on a pillow or touched my head, it felt like tiny needles in my scalp. The places where I’d pulled it out felt nice and smooth.

On Monday, I was desperate. I asked my boyfriend if we had duct tape. At first, he said we didn’t and he added that he thought pulling out my remaining hair with duct tape was a bad idea. He argued that you didn’t know what was on the sticky part of the tape. But since I’m regularly being injected with chemicals that kill all my rapidly-growing cells (including my hair and those is my stomach lining—and hopefully the cancer), the toxicity of duct tape is the least of my worries.

“We do have duct tape, but you’re not using it on your head,” he finally admitted. Killjoy.

I spent lots of time putting masking tape on my head.

I spent lots of time putting masking tape on my head.

I tried packing tape, but that pulled out only part of my hair. And then masking tape, which worked a little better. If you’ve ever wondered what it’s like to apply masking tape to your whole head and pull it off, it’s as tedious as it sounds. I would never try it, obviously, when your hair wants to be attached to your head. But I just needed to get these remaining hairs. I was obsessed.

After another night of prickly sleep, I begged my boyfriend to look for the duct tape. He really couldn’t find it this time. (Or so he claims.) And then he “forgot” to pick up some at the store. I applied more masking tape to my scalp.

Then, yesterday, I noticed a painful bump on my arm, near where one of the chemo IVs had been. I recognized this as signs of a superficial blood clot, which I’d had on my other arm during the ABVD chemo. I called the doctor and had to go in for an ultrasound and rescheduled a work conference call.

The results were two superficial clots — not serious (but painful) clots in my right arm. Since I am having a leukapheresis catheter put in on Friday, I can’t take blood thinners. (On a good note, this stays in for the remainder of treatment and my arm veins get a nice break. Overall, though, I’m really grossed out by having tubes sticking out of my chest for a few months.)

The doctors told me to apply warm compresses to my arms. I forgot to pick some up, so I’ve been thinking about applying the cats after they’re done sunning themselves or after the big white cat is done absorbing the heat from the space heater.

What I did pick up on my way to the ultrasound, however, was duct tape. (And a Snickers egg. Snickers are my favorite candy bar, but they lose something in egg form. I think the carmel, nougat, nut and chocolate ratio is compromised.)

Free at last!

Free at last!

Upon returning home, I triumphantly applied duct tape to my head (and ate half of my Snickers egg). And — just as I thought — it removed my hair. I am free of stubble and smooth-domed. I’m pretty sure my hair won’t grow back until May or June, so this will be my look for awhile. And, unlike last time, nothing is left of my hair.

During this time of baldness, I’m always kind of at a loss of what to do in the shower. The majority of the time is spent washing my hair and shaving. I could take up singing my bald theme song, but I don’t have a very good voice. I’ll probably just exfoliate.

Despite his reluctance to assist me in applying duct tape to my head, my boyfriend assures me that I’m not funny looking. But I had been reluctant to wear one of my usual sleep T-shirts, and I couldn’t pinpoint why. It has the logo of Cleveland goth band Lestat, with a depiction of Nosferatu. I inherited this T-shirt in high school from a friend’s older sister. Today, when I looked in the mirror while brushing my teeth, I realized that there were two bald people with prominent ears displayed in the reflection. After I emerged from the bathroom, my boyfriend looked at my shirt and then at me and said, “Hey, you kind of look like…”

That guy on my T-shirt looks familiar...

That guy on my T-shirt looks familiar…

“I know,” I said. I’d hoped if I ever looked like a vampire, it would be one of those sexy, preternaturally good-looking Anne Rice characters. I suppose this is what I get for those years of being goth, emulating that vampire look: Nosferatu. Be careful — or very specific — about what you wish for.

Speaking of vampires and blood, my blood pressure’s been very low. I’m not sure why. If I had to venture a non-medical guess, I’d say it’s because I’ve been pretty calm and haven’t been in public much. My blood pressure’s usually a little on the low side, but I wonder if my Frank Costanza-like short fuse raises my blood pressure and keeps it normal. (Serenity now!) I’m not sure what I should to do raise it, other than stew about topics that upset me, like flip flops on the train, Doritos Tacos Locos or that new Kevin Costner movie that looks so bad it makes me angry that Hollywood continually expects us to watch some of the terrible films they keep making.

Aww...

Aww…

In the meantime, I haven’t gotten around to applying a cat to my arm. But this evening, my arm clots really hurt. As I whimpered and cried as I tried to extend my arm, one of the cats came over and put her paw over my hand and licked my knuckles. (Aw.)

To his credit, the other cat is not without his own sweet gestures. A few weeks ago, I felt a little overwhelmed by everything and just put my head down, face-first on the bed. I was about to cry when I felt a sandpaper tongue on my head and a paw patting my head. I suppose it’s possible I had crumbs in my then-short hair, but I’d like to think he was comforting me. He may never understand how to get treats out of his toys and he may lack feline grace and fall off the couch a lot, but he’s a sweet cat.

Obviously, this is not where I’d like to be a year from my initial diagnosis. I wish the six months of ABVD had cleared up the cancer. I’d rather not have refractory Hodgkin’s lymphoma, The hardest part of treatment still lies ahead, in these coming months. Yet absolute ridiculousness of covering my head with duct tape and looking like Nosferatu is at least keeping me from taking myself too seriously on what could have been a very sad anniversary.

I realized when the nurse practitioner told me I needed to do the ICE high-dose chemotherapy before moving on to the stem cell transplant that it was what I’d been expecting. My PET scan looked better, but it’s not 100 percent clear. The stubborn lymphoma spots in my chest and belly have decreased in size, and they don’t show up as brightly on the scan. So that’s good. But I still have to do the ICE. Close, but no cigar, Brentuximab.

Part of the reason that the doctors were doing this trial was to find a less toxic alternative to ICE. And ICE doesn’t sound pleasant. I allowed myself one blog read of someone who has gone through it, just to prepare myself without scaring myself.

On Monday, I pack up for three days and go to the hospital for round one of augmented ICE. Then I’m home for 21 days, while going in for blood tests and such, before going back for three more days of ICE. Then it’s on to the stem cell collection, then 10 days of radiation and the 21-day stay in the hospital for the transplant.

Everything’s going to change as of Monday, even if most of it is temporary. (After the stem cell transplant, I should be back to normal in about six months with a few long-term side effects.)

I feel as if I shouldn’t be writing this. Lately, no matter what I’m doing, I feel as if I should be doing something else. I have a limited time to do everything, a looming deadline that I can’t push back. I have work I need to finish, so I feel as if I need to get as much done as possible before I go into the hospital.

I won’t be able to work out for months. I’ve finally started doing yoga at home and a 20-minute Jillian Michaels workout. (I’m up to level two on the 30-Day Shred!) After six months of working out sporadically and about two months of barely working out at all, I’m finally getting stronger. I’ve even returned to a few kickboxing and TRX classes here and there.

But, of course, I’m going to have to take a long break again. So I also feel as if I should be working out more. Sometimes, I’ll sneak in some yoga, but I’ve usually been doing just the 20 minutes—and even that’s been hard to work in. Where does my time go?

I also feel as if I should be out having fun, though all this snow and cold makes me want to stay in and hibernate. And when I am out, what constitutes enough fun when the next few months are going to be no fun at all? There isn’t enough fun to be had. Am I failing at fun?

I picture this elusive fun as something like Mötley Crüe’s “Girls, Girls, Girls” video (though I’m not particularly comfortable with strippers or motorcycles) and Bananarama’s “Cruel Summer” (filmed not far from where I live, in much warmer weather, years ago). I should be carelessly frolicking or maybe doing something debauched right now. Instead I am inside, blogging, after working all day and doing my 20-minute workout.

There’s a perverse part of me that wants to see what I can get away with before my hospital stays. Sometimes, it’s all-or-nothing with me. When the radiology oncologist told me that I’d have to eat heart-healthy for the rest of my life, I wondered, “Should I just eat a bunch of double bacon cheeseburgers until then?”

I should be dining like a medieval king, eating giant turkey legs, swilling mead and making jesters entertain me. Tonight, I have veggie chili, tea and the cats—oh, and Homeland, which I’m catching up on. I should be living like Marie Antoinette in that Sofia Coppola movie, before the beheading. Mile End deli is having a poutine week, so I might indulge in that at some point.

I feel all this pressure to work, workout and have fun before the unknown fatigue and nausea of the next few months. Aside from that, another main factor, according to the doctors and nurses, is boredom. Apparently, I’m better than I thought at hiding my lazy streak. Everyone seems to be underestimating how good I can be at doing nothing.

I’m glad that all the hard work I’ve put into appearing hard-working is working. People assume that doing nothing will bother me. I know that, since I say I’m stressed out about having fun, it doesn’t seem like I’m capable of relaxing, but that really is my natural state.

I achieve a delicate balance of hard work and utter laziness. A few weeks ago, I worked from 9 am to midnight, with the exception of a radiology appointment. (Even at the appointment, before seeing the doctor, I had my laptop out, working on a last-minute assignment.) And I did my quick 20-minute DVD, which is essentially working out really hard so you don’t have to work out as long. Later that evening, my idea of good planning was wearing a navy T-shirt because we were having pasta, and I thought there was a good chance I’d drop some on myself. So on one hand, I got a lot done, but on the other, I’m too lazy to properly feed myself.

Last week I achieved my main sloth goal, which was to not leave the apartment during the deep freeze. I also managed to see some friends who I haven’t seen during my hibernation. One of them lives just a few blocks from me and when I finally emerged from near hermitage to go to chemo on Friday, she lured me over with cookies.

That’s about as crazy as it gets around here, before my months of being somewhat of a shut-in begins. I’ll be enjoying time with my boyfriend, friends and cats (sadly banned from hospital visits) before my time of rest and recovery. However, two friends gave me a cat totem to take with me in lieu of my cats, and my boyfriend’s mom made me a blanket with a cat pattern, so I can be properly identified as a cat lady in the hospital.

This week, however, you will probably not see me cruise by on a motorcycle or dancing on rooftops or throwing bananas at cops—at least not if this snow prediction is accurate.  I’ll have to save that for after the transplant.