After reading through Monday’s post that I wrote while falling asleep in a chair, I realized it had some egregious typos and a final paragraph that stopped in mid-sentence. I went back to fix them, and so had my boyfriend. It’s good to have the love of great editor.  (Actually, it’s nice when places that work with “content” have actual editors, but that’s another argument for another day.)

But here’s some breaking news:  The doctors agree that I’m getting better!

That’s the good, long-term news. My counts are going to start going up, so I’m just starting my recovery. And this doesn’t necessarily mean I’ll be in remission. I’ll find that out in August. But I’ll be out of here probably in the coming weeks.

Right now, my throat still feels like it’s on fire and my tongue is swollen. The inside of my mouth is covered in blisters, and I can’t swallow. I had to take some Vitamin K, and I opted for the shot to avoid the pain of choking down three tiny pills. Just a few sips of water or tea send me into a choking or nausea fit.

But this is it. This is about the worst I should feel as things turn around.  It’s “The Final Countdown.” One of the instructors at the fitness bootcamp I attended would remind us of the Europe song as we suffered through the last seconds of plank. “Doo-DOO-DOO-DOO, Doo-DA-DOO-DOO-DOO. It’s the final countdown!”

Since Monday (well Saturday, really), I’ve been mostly asleep, because of my fatigue, morphine and occasional Ativan. (I prefer Compazine when I can get it.)

A side effect of the mucositis is thick, clear saliva. Because there’s often blood in my saliva, I often get little blood stains on my lips, so I look like a baby vampire, a wee Nosferatu. And the excess mucus makes me feel like an infant, able to blow spit bubbles and gurgle at people who try to talk to me. Yesterday, a nurse who came in to draw blood in the early morning said, “Hi, I remember you.”

Me, as I put on my glasses to see: Spit bubble. Happy noises. Nodding.

Once I could use my tissues, tiny spittoon and mouth vacuum taped to the side of by bed, I could try to pack all my greetings into a few seconds. This mouth vacuum is a tiny version of the dentist vacs and helps clear up my drool overflow. The first moments of waking, however, require a lot of gargling.

If you were looking into my room most of this week, you would have seen me carrying on happy conversations with myself and answering questions that had been posed to me. In one dream, I talked to my boyfriend about horse pregnancy, while in another, I helped the pope pick out a new watercolor for the Vatican. The latter’s a little far-fetched, especially when I don’t know much about impressionism; my own collection includes mainly anthropomorphic art (squirrels with martinis, crocodiles with bananas, etc.). Mostly, I’ll wake up as I’m saying something profound, like “OK,” or “I’m not sure.”

When my boyfriend visits, I’ll suddenly look at him and announce things like, “OK, but we’ll have to go by plane,” much to his amusement. I also know I’ve said things to the night nurses, who I’m sure hear a lot of morphine talk. I think I must look sometimes like I’m meditating.

Every time I hit the morphine button, I think of Kraftwerk’s “Pocket Calculator.”

My boyfriend’s parents came by today. Because of the no-travel rule, I haven’t seen them for almost a year-and-a-half. His mom’s cat quilt that she made has been receiving high praise throughout the hospital. Next time they visit, I’d like to join in on the NYC fun, but it was comforting to have them here.

Though I’ve turned a corner, I’m still not taking most visitors or people I don’t consider immediate family. I’m still too gooey for public consumption.

I texted my boyfriend the good news about being on upswing, since he was out and about. Perhaps one of the best things about today was telling my mom that I’m getting better. Almost every day, she’s been saying, “But you’re getting better, right?” or “Does this mean you’re getting better?” I mean, eventually, but I was just holding steady there for awhile, and that’s what they expected me to do. This wasn’t fast enough for my mom. (By the way, if you DO know my mom, don’t tell her about my blog. She doesn’t understand blogs, which she pronounces as blags.]

So I could finally pass along this news from the doctors: I’m getting better. She was so giddy that, at the end of a conversation she had with me about some vegetables she bought, my announcement that I need to go so I could pack didn’t even phase her. (I nodded off for a second and thought I needed to hitch a ride with a truck on a rainy interstate.) “No, nevermind,” I sighed. “I think I just need to get to sleep.”

And on that note, after falling asleep about a dozen times while writing this, good night!

 

 

 

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

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.

After finishing up with chemo in late September, I shaved my head once more to be Walter White for Halloween, and my hair has grown in once more, thick and lustrous. It’s finally to a point where it looks like a haircut on purpose, like a cute pixie cut.

And now it’s time for it to fall out again. I was told I would lose my hair about two weeks after the augmented ICE chemotherapy, and sure enough, it’s time. I just realized I won’t have to pack shampoo for my next hospital stay.

My scalp aches. It’s as if I can feel each follicle letting go of its hair. This happened with the ABVD chemo as well. Although with the lower dose chemo, the hair loss was gradual—until one day I noticed my hair was too thin to keep.

I had wondered if my hair loss would happen all at once with the high-dose chemo, and it pretty much is. If I reach up and tug at the back of my scalp, I can pull out a handful of hair. It’s been perversely tempting to do so, but I don’t need to develop any more nervous habits. (Or maybe I do need a new one to break me of biting my nails.) I’m pretty sure I could just wash my hair away in a few days. But I’m worried I’ll end up looking like Smigel.

So I’ll probably have to shave my head for the third time tomorrow or Monday.

What makes me a little nervous is that when it does come back, some time in April or May, it’s probably going to be a different color or texture. I hope it doesn’t turn white, like Moses after talking to the burning bush. (Actually, I just looked that up and it’s not a Bible fact, but I saw that Charlton Heston movie a lot as a kid.) I guess I’ll just have to wait and see what happens.

I do know I’m going to keep it short once it comes back in. I don’t even have any interest in wearing my long wig. All these years I’ve based my hairstyle on what I thought would look best and be easiest to take care of, and i thought that was long and straight. Now that I’ve found a hairstyle with even less maintenance is available to me, I can’t go back to anything else.

So long, hair, it’s been fun. See you again in the spring!

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.