I just spent a few hours cleaning. Mostly this was filing papers and dusting. With my bum phlebitis-inflamed arm and my chest catheter, I can’t do things like dust under the bed, or move things around so I can vacuum and mop.

I’ve had several last-cleaning-before-the-hospital-stay situations—before both rounds of augmented ICE, for instance. But this feels particularly final, since I’ll be away for my stem cell transplant and radiation for a month and I won’t be allowed to clean for three months. Specifically, I won’t be allowed to vacuum or clean the bathroom.

There’s a chance my hospital stay will be delayed a week or two. (The worst case scenario would be longer, if the PET scan still shows cancerous activity.) So I may be able to clean next weekend. Yippee.

People have asked why I don’t hire a cleaning person. I’ve suggested getting a cleaning person during my convalescence, but my boyfriend shot down that idea. Truthfully, I’m relieved.

I’m not comfortable hiring someone to clean for me. That’s not to say I’m against having things done for me. My boyfriend does most of the cooking, because I don’t have time. And he would do the driving when we had a car. I liked pretending that I was a fancy NYC person with a driver.

I love having my laundry done. I might live here forever specifically for that reason. When I heard that you could just take your laundry to the laundromat and it would be returned to you neatly folded and clean, I nearly wept for joy. It’s like being in college and going home for the weekend and having your mom do your laundry, without the guilt.

The thought of doing my own laundry again leaves me deeply depressed. It’s not just the laundromat, which is an inconvenience. When I had my own washer and dryer in Ohio, I still wasn’t big on doing laundry. Or doing laundry correctly, I’m told. I just put all my clothes in together, without sorting. My laundry all has something in common—it’s dirty. So in it goes, and out it comes, clean, if maybe grayer or smaller.

I was taught to read labels when buying things to avoid buying dry-clean-only items and things with complicated instructions. Sometimes I forget. With dry-clean-only items, I often leave them in a pile and then wear them again a few times, my own version of dry-cleaning, before actually taking them in to be cleaned professionally.

If I have my way, I will never do my own laundry again. But I’d probably hire an assassin before I hired a cleaning person.

Growing up, somewhere along the way, it was instilled in me that having a cleaning person is for lazy people. Frivolous people. People who can’t clean up after themselves.

I know this isn’t true. Friends who are highly respectable, responsible people have cleaning people or cleaning services. So I don’t judge others, but I would judge myself harshly on this point.

I’m not sure where I got this idea. I don’t think it was ever overtly stated. But it was implied.

My grandmother did all her own cleaning. I’m not sure how she would feel about my laundry situation, but I know she hated ironing, so I feel as if she’d approve of my current choices. (Ironing depressed her. I think it made her dwell on disappointments. I feel the same way about cleaning the bathtub. I can’t clean the tub without feeling angry and depressed, so I get it. We all have a household chore that gives us too much time to think and inevitably and inexplicably stirs up all of life’s disappointments.)

I think when the subject of someone with a cleaning person was brought up, there wasn’t quite an eye-roll. But it was said with a hint of disapproval and a slight pursing of the lips.

So, with my last bit of strength, I will be dusting or mopping, reluctantly and with an air of martyrdom and grim determination. Though now that I physically can’t do some chores, I will channel my energy into bugging my boyfriend. He might change his mind about hiring a cleaning person after all.

 

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.

I’m extremely late to the party on this. Most days, I’ve been working from about 9 am to 9 pm, and by the time I’m done, I can’t look at a computer screen anymore.

But I still think about the weeks-old controversy surrounding the Emma Keller column in The Guardian, in which she asks: “Forget funeral selfies. What are the ethics of tweeting a terminal illness?” It’s a opinion piece about Lisa Boncheck Adams’ Twitter account, in which she tweets about dealing with stage 4 breast cancer.

I didn’t get a chance to read the post before it was taken down, but according to snippets I’ve seen on the Internet, it wasn’t the questions about the morbid curiosity that got people upset — it was Keller’s diagnosing of Adams with a case of TMI. In response to the backlash, Emma Keller’s husband, Bill Keller, also responded with his own column in The New York Times.

The whole thing seems to be fraught with misunderstandings and misinterpretations of other people’s words and intentions. It played out in major convention and social media outlets, but I’m sure people with opinions like the Kellers whisper similar criticisms to friends about cancer patients’ choices on how much they divulge. Since I didn’t read Emma Keller’s piece, I can’t respond much to that, but this got me thinking about cancer blogging.

What I took away from this recent controversy is something that everyone already knows: Everybody deals with cancer differently. And most people have opinions on the way you should deal with it or they way her or she would deal with it. I’m not sure there’s a wrong way to cope. Well, I guess Walter White probably could have handled things better in Breaking Bad. I hope we can all learn from his mistakes and have disassembled our meth labs.

Also, you shouldn’t piss a bunch of people with cancer off. And it’s fine to offer advice, but leave self-righteousness at the door.

At some point, you get tired of absolutely everything to do with cancer, including being told what to do. I almost had a meltdown this weekend after a museum employee told me that my bag was too big to carry through. She did it nicely, but I’d spent the whole time there trying not to get reprimanded, because it seemed like everyone was getting in trouble for something. I almost burst into tears, and when my boyfriend asked me what was wrong, I said, “I’m so tired of people telling me what to do.” (Yeah, I had a rough couple days there.)

Today, I think TMI depends on what you want to know. Twitter is, by nature, full of TMI. Lunch photos. Tweets from companies trying to get you to buy their products. Selfies of so many duck faces. Politicians’ private parts.

My own Twitter is mainly promotions of sites I’ve been working on (check out the article I wrote about fitness/bands/healthy eating/insurance/travel, etc.), followed by cat photos (Facebook is my cats’ main social medium). There are also tweets of inside jokes to two of my former cubicle neighbors, one of whom isn’t on Facebook. And the last category is angry tweets. (The fancy dress I bought on sale is poorly made! This venue is overbooked! Fandango ruined Christmas!)

It doesn’t reflect this blog or even retweet anything from my Pain in the Neck Twitter account. My mom discovered my Twitter feed, linked to a story that I wrote, and she asked me if I was writing about having cancer. So, like a teenager whose diary had been discovered, I just denied everything. She might be reading this right now for all I know.

She doesn’t think I should tell anyone about having cancer. She’s in the cancer-should-be-kept-to-yourself camp. My family wasn’t big on talking about stuff like this. I wouldn’t say it’s a bad thing; it’s just how we are. In fact, I don’t really talk about cancer much in person. That’s why it’s nice to have a blog.

I’m an introvert. Just borderline, if you believe the Briggs-Meyers test; it’s as if I want to be an extrovert, but I can never shake my introvert ways. I stay in one place at a party and wait for people to come to me, often in a nice cocoon of people I already know. Most often, this position is by the snack table or in a comfy chair, but that’s because I love snacking and sitting.

And lately, at parties, sometimes I’ll talk about cancer, but really only if someone asks. Mostly, it’s just a rundown of what’s going to happen. A lot of people think I’m done with treatment, so I feel bad telling them that the worst part is yet to come. I finish up the Brentuximab trial, followed by a hospital stay for at least 26 days, including inpatient and outpatient radiation and a stem cell transplant. Plus there’s possibly an additional month of treatment with augmented ICE.  The blog has been a nice outlet for me to deal with things and keep people updated.

When people find out that I still have several more months of treatment, they seem apologetic. A lot of them say, “Oh, I didn’t know!” That’s because I haven’t really talked about it much. I mostly keep it to the blog. As someone who personally falls somewhere on the spectrum between the Kellers and Adams as far as information-sharing, I keep my cancer news mostly here, in this public forum that feels strangely private.

I find other people’s cancer blogs informative and helpful. I don’t delve too much into them, mostly because I just don’t want to freak myself out. But I know other people’s stories are there, and if I want to read about their experiences, I can. As one blogger wrote in Gawker in a much more timely response to all this, blogging is therapeutic and cancer is nothing to be ashamed about.

If Emma Keller calls into question people’s morbid curiosity, including her own, we’re all guilty. Who hasn’t found themselves reading someone’s blog for that very reason? Every now and then, I click on something friends with children share on Facebook and find myself reading a parenting blog, fascinated at something I know nothing about that sounds truly terrifying. I’ll read about all the ways you might physically or mentally damage offspring by not strapping them in properly or by not watching them every single second of the day and night or teaching them the wrong thing. Just a little bit of scary reading to sate my curiosity.

But I think Adams’ tweets serve to inspire more people than it might upset. I’m glad to see she’s gotten so much support.

It doesn’t seem like the Kellers are saying you shouldn’t be able to blog or tweet, unless I totally misread Bill Keller’s column. And they have a choice as to whether they read it or not. I would like to not have cancer. You can’t always get what you want.

Last night, I had a dream in which two women were making fun of my haircut and I said, “Hey, I have cancer!” Predictably, only one looked shamed, and the other seemed nonplussed. You’d think my own subconscious would be nicer to me.

But then, in my dream, I headed to a Mexican restaurant for margaritas and appetizers, so perhaps it was a form of apology from my REM sleep cycle. Sorry this lady conjured up was so inconsiderate; have some fried food that doesn’t count because you’re not actually eating it.

Sometimes, though, I do want to go around saying, “Hey, I have cancer! Be nice to me!” Yes, I would like to pull the cancer card to bully and shame people into being nice to me.

But then again, isn’t everybody going through something? Who am I to demand special consideration? Should I be allowed to lash out because things aren’t going the way I planned?

A few months ago, someone shared an article on Facebook titled “Let’s be gentle with each other. Let’s read each other’s signs.” The post was written by a woman whose husband suffered a traumatic brain injury that took six years to recover from, and during that time, she wanted to walk around with a sign telling people to be gentle with her because of what she was going through. She posited that we would treat one another differently if we all wore signs about what we were going through. (Hopefully.)

I do hate pulling the cancer card, so I try not to. Unless it’s because I want a seat on public transit. It’s often because I want to have a temper tantrum. Don’t we all have those days when we want to vent about life’s unfairness to then hypocritically demand special treatment? Maybe it’s just me.

On days like today, I do sink to lows, and something today made me want to throw a fit and let everything out in a flood of tears and angry words. (The type of angry words, by the way, that I think are stuck below my trachea and causing the abnormal PET scans.) So that’s why I’m writing it down here.

Today, someone told me that I wouldn’t be able to get the questions I needed answered for a story because the person was too busy. I was upset because it’s a day after my deadline and I sent the questions more than a week ago. Mostly, however, I was upset because I had cancelled by first post-chemo date with an oyster happy hour to finish this story tonight. Woe to the person who is responsible for coming between me and an icy platter of delicious $1 bivalves after months of separation.

This stuff happens all the time, so my personal reaction to this isn’t warranted. It’s unreasonable to think that this person thinks my time is less valuable. Yet I wanted to announce, “I rushed home after hearing that I might still have cancer and might have to spend three weeks in the hospital to interview the director of this program when I wanted to go home and cry.” I suppose that might have been a good thing, in retrospect, to have something constructive to do instead of wallow in self-pity and fear.  I also wanted to say, “I spent hours working on this, already, and I just need five minutes from you.” But what I really wanted to say was, “I haven’t eaten oysters in months, and tonight was the only chance I had to eat them for $1 each this week, and I might need to have more chemo so my time to enjoy them is limited, and I am holding you personally responsible for this, though it is not your fault.”

But honestly, I don’t know what the person who can’t answer my questions is going through. I do know she’s extremely busy. And, after all, I’m the one with the cancer and the chemo restrictions and the hankering for oysters and the bad mood. While I haven’t actively thought about the disappointing PET scan results and the need for another biopsy, I’m extremely sensitive to the smallest disappointments.

I tried to cling to the positive after the news on Friday. It might not be cancer; it could just be inflammation. Also, I met with the doctor yesterday, and I found out the surgery isn’t very invasive at all and I don’t have to spend the night at the hospital. And it’s after Halloween, so my plans to be Heisenberg will not be foiled.

The surgery takes only an hour, so the chances of a full zombie outbreak while I’m out are very slim. My boyfriend told his dad about my fears, and his dad pragmatically responded, “That probably won’t happen.” For his recent birthday, my boyfriend’s dad got some sort of chainsaw on a stick, though, so that’s easy for him to say, since he has the perfect zombie-killing tool.

Also, I can get back to working out again, and hopefully I can lose the 10 or so pounds I’ve gained while being somewhat sedentary. But the surgery and the possibility of remaining cancer—not to mention some pretty intense-sounding treatments—have me a little down. The thought of heading out for $1 oysters like things were almost normal again made me smile, and so that’s why I was so disappointed today. It’s what they symbolized. I want to slip into a pool of self-pity and think, “Well, it’s not like I have good scan results to celebrate anyway, so I may as well spend the evening writing this.”

Although what’s more normal than having to cancel plans because someone didn’t meet a deadline? I guess that’s not the kind of normalcy I was seeking, but there it is.

I suppose if I had a sign right now, it could be summed up, “I’m sad and feeling sorry for myself and prone to irrational feelings. Please send oysters.”

When I watched the first of the final eight Breaking Bad episodes on AMC last night, I had something in common with Walter White. We’re both bald.

Well, I guess we have two things in common, as I learned in the middle of the show (spoiler alert): It turns out Walt is going through chemotherapy too. I feel as if Walt and I have been through a lot together in the past few months, as he’s become somewhat of my cancer hero—or antihero. (Though I’m no Gale. W.W. is far from a shining star in my eyes. And perhaps Gale is the most obvious example of the dangers of loving Walter White.)

As everyone turned against him as the show progressed—from his wife to his former business partner to viewers of the show—I still felt somewhat of a cancer kinship with him. He was beginning to lose me in season five—but as we see so often with Jesse Pinkman or with Skyler—just when I thought I might be done with him, Walt pulled me back in.

In February, I was diagnosed with Hodgkin’s lymphoma, and I’ve been undergoing chemotherapy at Memorial Sloan-Kettering Cancer Center since April. In June, I started watching Breaking Bad, after hearing hype about the show for years. The show’s premise—a high-school teacher who makes crystal meth after a fatal lung cancer diagnosis—seemed timely.

Just as everyone predicted, I became addicted. In fact, when I watched all of season four at Lincoln Center during a recent Breaking Bad marathon, a fellow fan confessed he would sometimes skip work or lie to his friends about having plans when he wanted to stay home and watch multiple episodes.

As I feverishly caught up on the show in time for the new episodes, Walt became a cancer companion of sorts. There are the physical effects of the chemotherapy—the nightstand full of medications, the red urine, the PET scans—but it’s the psychological effects on Walt to which I could relate.

Anyone who has ever received a bill for cancer treatment has probably thought that they need to make more money—fast. Even with insurance—something that I may be losing at the end of the month—the bills for a biopsy, medications, scans and chemotherapy add up.

Obviously, making and selling drugs is no joke. But if you could do something to make enough money—even if it were illegal—to not worry about medical bills, would you?

I might. As I’ve mentioned before, it’s as if, from time to time, the snakes from the medical caduceus symbol slither from their post and curl up in bed with me and hiss into my ear, reminding me of the expense.

Fortunately, for society’s sake, I have no illegal talents. I’m also a terrible liar and a goodie-goodie at heart, so I’m not cut out for a life of crime.

The thing that resonates with me the most about Walter White, however, is his anger, always bubbling near the surface, and his need for control, which drives him as much as—if not more than—his love for his family.

Walt’s anger is always present, constantly bubbling near the surface. After his diagnosis, he tells off his boss at the car wash and beats up a teenager for making fun of Walter Jr.’s cerebral palsy. Most of us can relate to wanting to do these things—and a cancer diagnosis is just the thing to push you to actually do it. You often want to have a tempter tantrum over how this isn’t fair. The smallest things can set you off, because you find yourself thinking, “This happened and I have cancer.”

Sometimes, I find myself walking around daring the world to piss me off—just for the release of pent-up anger. While I haven’t blown up a drug den or even thrown a pizza on a roof, I did find myself hanging on to a cab’s door handle and screaming at a startled driver when he refused to take me to Brooklyn after my biopsy surgery in Manhattan. It was during the change in shifts for cab drivers, when they decide whether you’re on their way home or not. After being turned down by one cab, I vowed to not let it happen again. “I just had surgery and you won’t take me to Brooklyn!” I screamed, pounding on his window. If I had been close enough to the open part of the window, I would have tried to force my upper body into the cab, new stitches along my neck or not.

Most of my anger is reserved for insurance companies and bureaucratic entities that are out of the grasp of my wrath. It make me feel helpless and as if I don’t have control—which brings me back to Walt.

But pride and a need for control are what really drives Walter, more than anything, and that’s when he started to lose my sympathy. Had he accepted the offer of his former business partners, he could have avoided this meth mess completely. We finally learned this season that he’s always been haunted by his decision to sell his share of a company now worth billions for $5,000, and that’s when his reluctance to quit the meth business comes into focus.

Yet I relate to his need for control in the face of cancer. To me, cancer has felt like a betrayal of the body. Your own cells are going renegade. When you have so little control over your own body, then what do you have?

You want to be tough. I’ve assured people over and over again that I’m fine, that this is no big deal. You put on your badass black hat or your wig and you become Heisenberg, your alter ego who is always strong and in control and unfazed. Who doesn’t want to assert, “I am the danger,” and “I am the one who knocks” when you feel as if you have very little control?

As Walt sits in a hospital gown and socks for his PET scan—a test that determines the state of your cancer, whether the treatment is working or whether you’re in remission—he’s still struggling for control. As a fellow patient spouts clichés and grapples with his diagnosis aloud, Walt goes off—again there’s the anger—and asserts to this poor stranger that he’s in control.

During one of several Breaking Bad discussions this past weekend, someone observed Walt has become the cancer. He’s the danger, but as the body count piles up and the consequences of his actions become increasingly dire, he still doesn’t have the control that he wants.

In spite of all of Walt’s transgressions, I still wanted him to be happy. I often find myself defending unlikeable characters. So I was disappointed when Hank found that copy of Leaves of Grass, after it seems that poor Walt had only a month of what he finally wanted. And now his cancer is back—as is Heisenberg.

I am now bald. I have a black hat, though it’s more Holly Hobbie than Heisenberg. Am I the danger? Inadvertently. I almost set my kitchen on fire while baking cookies and two of my lab partners in high school science classes almost set our stations on fire. (I wasn’t responsible, but I still feel as if I was an accomplice.)

Before the premiere of the new episode last night, my boyfriend shaved my head. A lot of people shave their heads early in the chemo process, but my hair was so thick that the thinning wasn’t noticeable until this week. Within the course of a week and half, my hair suddenly looked really thin. It was time. And what better time than before the return of Walter White?

I didn’t cry, though I’ve done my share of it over the past several months. But I’ve never been one of those people who cry when they get their hair cut. It will grow back—though in this case it will take longer.

Right now, I’m waiting for the results of my most recent PET scan. If everything is on track, my last chemotherapy appointment will be September 27—two days before Breaking Bad comes to an end. Walter White’s story and my cancer journey will end together. I know better than to expect a happy ending for Walt, though I hope for one for the end of my own story.

 

Charles Dickens began A Tale of Two Cities with, “It was the best of times, it was the worst of times…” I couldn’t tell you anything else about the rest of the novel. So I guess it’s fortunate that he put the best part right at the beginning like that, so I wouldn’t have to continue reading.

I’m a bookworm and goodie-goodie who always did my homework and the assigned reading. But when that book was required for 10th grade English, I just couldn’t get through it. It was my mom’s copy of the book, and I don’t think she read it either. Maybe I had a cursed volume. Judging from her high school copy of Much Ado About Nothing, in which she scribbled out the word “ado” to show her sentiments about the play, I would say I inherited her aversion to Shakespeare as well.

But the other day I found myself thinking about this opening phrase. While Dickens is talking about the time around the French Revolution, those lines can refer to almost any time. High school, for example.

There have been some good things that have come from this cancer diagnosis—the outpouring of support from friends and family, my realization that I need to be more confident and fearless.

But this will obviously not be the best of times. With the cancer diagnosis in February and the job loss this summer, 2013 really hasn’t been my year so far. Irrationally, I hope that this double dose of bad luck means only good things ahead, though I know there’s not a finite amount of sad things that can happen.

I wondered aloud if I’d appreciated what I had before the cancer diagnosis. I think so. I knew things were good and was grateful for what I had. I appreciated my good health and my great job.

In Everything Changes: The Insider’s Guide to Cancer in Your 20s and 30s, one of the young people with cancer notes that she felt she appreciated life. She didn’t need cancer to teach her a life lesson.

But then again, cancer is a cell aberration, not something you get because you need to learn something. Not that I’m saying you shouldn’t try to learn something from every experience.  Still, before cancer, I lived for the moment and mindfully and experienced daily gratitude, all the things that you’re supposed to learn in yoga. Now, I feel that is less so, but that’s temporary.

In fact, everything is temporary. I can’t even remember where I heard that the bad doesn’t stay forever, but neither does the good. Was it a yoga class? Something I read? The last part haunted me—even good things are fleeting. But we know that.

This weekend has been particularly hard for me, and I’m not sure why. Maybe because, as of Friday, I’m two-thirds done—eight treatments down, four to go. It didn’t bring with it the jubilation the halfway mark did. With the possible end in sight, I’m getting impatient. Only two more months to go, yet two more months to go. I’ve become a full-time worrier, when I know it doesn’t help. I worry about Wednesday’s PET scan. What if it turns out I need more treatment?

Physically, I’m starting to feel the effects of the chemotherapy a bit more, since it’s cumulative. I have an appointment tomorrow with a podiatrist to get my toenails lopped off to avoid infection. They’ve been separating from the nail bed and turning various colors, and it’s best that they go, for now. I’m also on some new medications to keep me from getting infections: Bactrim, Acyclovir (an anti-viral) and Fluconozole.

My hair is still falling out, and it’s noticeably thinner.  I was hoping it could hang on for the next few months. Knowing my deep love of pop culture and my current obsession with Breaking Bad, my boyfriend suggested I could time the shaving of my head with the premiere of the show’s final eight episodes next Sunday. I have to admit, that prospect cheers me up immensely. Shaving my head to be a Walter White superfan? I’m in!

I have a weird mark that looks like a bruise from one of my bra straps, and my doctor says that’s common with ABVD—a scratch or skin irritation becomes a brown mark on your skin. I have another on my arm from carrying a plastic bag yesterday.

I bruise like an overripe peach, yet inside, I feel myself getting bitter. Plus, I’m actually physically hardening inside. My veins are hardening from the chemotherapy drugs. The good news is that my left arm hurts a bit less, but now my right arm feels bruised, and it looks red and irritated. So I am getting physically tougher in some ways while falling apart. I’d like to get through these next four treatments intravenously without needing a chemo port installed.

Then the bargaining begins. OK, I’ll shave my head if it means I don’t have to get a port. Who, exactly, am I bargaining with? Life doesn’t work that way.

But it’s the bitterness that makes me feel the worst. My temper has been unbearably short. I know better than to act like this. I hate that I sometimes have to struggle to focus on the good now.

I will get better. This is temporary. Happy events have happened this week, including the birth of my best friend’s baby. If I focus on the bad, I’ll miss out on the good.

So this won’t be my best summer. I’ve never really had a bad summer, since it’s my favorite season. Even the summer of 1993, when I spent the summer painting all my furniture black, was OK.

I have some amazing things left to do and experience in the next few months. Maybe that’s my lesson, for today, at least—not letting the negative cloud the good.

This is hard for me to admit, especially after so many people have told me how tough I am and have complimented me on my positive attitude. But I’ll let you in a little secret: I’ve been bursting into tears recently.

Most of the time, I can’t even tell you why. Usually, it’s not even real crying—it’s more of a passing wave of sadness that results in 10 seconds of tearing up or a single whimper.

Usually, I’m kind of a goofball, joking around and making light of situations. So it’s been really hard for me, personally, to deal with the seriousness of this cancer situation.

I’ve seen a lot of articles with titles like “10 Things Not to Say to People with Cancer” or “Things to Never Say to Cancer Patients.” Those definitely apply to some people, but I’m pretty hard to offend. In Are You My Guru? How Medicine, Meditation & Madonna Saved My Life, author Wendy Shanker, who has a rare autoimmune disorder, has a great chapter on things not to say to people who are ill—and she has an amazing sense of humor, which I appreciate.

I myself am horribly awkward in these situations—including the present one. I don’t know what I would say to myself. And I generally clam up when someone tells me something awful, or stick with the honest, “I don’t know what to say.”

With a few exceptions, no one has said anything wrong or shocking. When people talk to me about my own cancer, I’m still often the awkward party.

I suppose the compliments I get now are different. “Your hair looks full.” If someone commented about my hairiness pre-chemo, I don’t know how I’d feel. But it’s currently a good thing.

Some people have expressed worry that complaining about other things when I have cancer seems selfish or trivializes my situation somehow. I don’t think so. I don’t expect the world to stop for my health concerns. There will be heat waves and heartbreaks, and I will still be here to listen.

I sometimes wish I could stop other aspects of my life, but then I think having less to do might be part of the current crying situation. I’ve kept myself busy with work and social obligations. Now that work has stopped, I continue to book 9 to 5 and beyond with job search, applications and freelance pitches and work.

I’ve been working really hard at working really hard. I’m not sure if I’m avoiding dealing with cancer or this is my way of dealing with it.

So why the crying? I feel a little helpless and scared. So many things seem out of my control right now—including my own body.

Whenever I’ve been sick with even something trivial, I feel so betrayed. I’ve done yoga since the late ’90s, when Madonna made it trendy. There’s a lot of talk about the mind-body connection, but I still feel as if they’re at odds. Even my preferred form of yoga—Bikram yoga, a series of 26 postures in a room heated to 105 degrees—doesn’t focus on harmony. You’re often pushing your body to a limit, very carefully.

This isn’t the first time I feel as if there’s been a struggle for control. Nine years ago, I had panic disorder. It started while I was in a waiting room while getting a tire changed. Suddenly, I felt dizzy, and my extremities started to go numb. I was a little nauseated and started to sweat, then I couldn’t breathe. I also felt like my brain was trying to escape my head. The best way to describe a panic attack is that you feel as if you’re dying and losing your mind at the same time.

Panic disorder happens when you’re so worried about having another panic attack that you keep inducing panic attacks. It’s a fear of fear itself.

A panic attack itself is your body’s fight-or-flight response at the wrong time. A rapidly beating heart might help if you’re being chased by a predator, but when you’re waiting for a tire to be changed or driving, it’s extremely inconvenient. It’s a physical thing—something a lot of people don’t understand. People often tell you to calm down, but it’s not an emotion. It’s a physical reaction that’s happening for seemingly no reason, and that’s why you also feel crazy.

When you end up in the emergency room a few times because you feel like you’re dying but the doctors don’t find anything wrong with you, it’s really hard to not feel like you’re losing your mind. You’re often not taken seriously. Doctors openly scoffed at me and mocked me. At one urgent care, a sympathetic nurse who suffered from panic attacks after the birth of her first child listened to me and made me feel somewhat sane. I’m not saying panic disorder is worse than cancer, but the latter is taken seriously by the medical community.

Panic disorder makes you feel so alone. And you often alienate yourself, compounding the problem. A lot of people become agoraphobic or self-medicate with alcohol with panic disorder. I feel as if I lost about a year to a year and a half of my life to it. I was able to overcome panic disorder through a mixture of medication, cognitive therapy and educating myself about it. Writing an article about panic disorder and learning so much about it really helped more than medication. (If you want to read a great book about someone overcoming panic disorder, I highly recommend Priscilla Warner’s Learning to Breathe: My Yearlong Quest to Bring Calm to My Life.)

I found myself talking a lot about panic disorder, but I haven’t talked as much about the cancer. But I talk about the panic attacks more openly because they’re in my rearview mirror. They’re in the past tense.

I haven’t told everyone about my diagnosis. There was no Facebook announcement. I don’t link to my blog on my own social media. I’ve been telling people on a case-by-case basis. And even when I tell people, I follow up with a quick, “But I’m going to be fine!” and reassure them that things are going well. (Both are true.)

In fact, my boyfriend goes with me to my doctor’s appointments not only for support but to also make sure that I don’t downplay my symptoms and side effects. I want to reassure the doctors that I am fine, but he keeps reminding me that they really need to know about any symptoms.

So a lot of people don’t see the dark side—only my boyfriend in many cases, and that’s because he’s around. And my two cats, who sometimes hear me announce, to no one in particular, “I’m sad.” Though sometimes I address the nearest feline with, “Oh, kitty. I’m so sad.” Just a sad cat lady talking to her cats.

I generally find it difficult to talk about my Hodgkin’s lymphoma. That’s why I write about it. Maybe I’ll feel more comfortable discussing it in the past tense. I certainly hope that’s the case by the end of the year. I tell myself if I got through panic disorder, then surely I can get through this, with support and some of the best medical treatment around, even though my instinct is to try to deal with this alone. Like I’m some sort of wild animal who will be left behind or eaten if I show weakness.

But doubt lingers, like the sore throat I’m experiencing. (Not another cold and eye infection! Please!) This is irrational thinking, but that last time I randomly burst into fits of tears was at the very beginning of my diagnosis, so I wonder if the treatment’s stopped working. It was, of course, also a time of great uncertainty.

At that time, right after my diagnosis, I was also experiencing night sweats. At night, I would lay down a yoga or beach towel on my bed and put on my moisture-wicking workout clothes, with extra clothes by the bed for the nights I would wake up drenched and have to change. I felt as if the night sweats were my body’s way of grieving for itself and what was happening—as were the bouts of crying. It was like my body was a sponge full of sadness that couldn’t escape through my tear ducts and had to seep out my pores at night, when I couldn’t be on guard.

My next PET scan, which will show the chemo’s progress, is in a few weeks. Even if I need longer treatment or stronger treatment, I’m expected to get better.

For now, I will let myself cry and will move forward, until I can say, “I had cancer.”

For the first time since I was about 10 years old, I found myself looking for a four-leaf clover this week. As I weeded the brick path of the community garden, I examined the few patches of clover I found for any lucky ones.

I’ve never found a four-leaf clover, outside of the plastic or paper shamrocks at St. Patrick’s Day celebrations. But I figured I could use some luck. I’ve had two job interviews and sent out countless resumes. I have a PET scan in about three weeks to see how the chemotherapy is working. When you’re waiting and hoping for good news, you’ll take anything as a good sign.

About four weeks ago, the evening before the company I worked for shut down, I was weeding the paths in the community garden. I thought that if I had some time off, I would completely conquer the paths and free the bricks from the weeds, at least temporarily. The paths are never weed-free all at once, because once I weed the path, they’re back in a few weeks.

Now that I finally had time this week, finally over my cold and eye infection, temperatures outside soared over the 90-degree mark all week. That’s not good luck. So I stopped by early in the morning, to beat the heat. There’s something therapeutic about weeding the paths. Almost all the plants growing in between the bricks aren’t supposed to be there. A landscape architect I interviewed once told me an old garden adage: “A weed is just a plant out of place.”

So I don’t have to think much, except for the occasional pressing matter: “Why are all these ants crawling on me?” and “I hope that’s not poison ivy.” With my mind freed up, I can reflect on the random information that collects in the junk drawer of my brain. “Whatever happened to Tom Green? I really think his show was a precursor to Jackass and other shows I didn’t like, when MTV started to lose me.” Or, “I really liked that Jesus Jones album in 1991, but I think if I went back and listened to it, it wouldn’t hold up.”

I don’t think about cancer all the time—I don’t think anyone does. The other day, my boyfriend noticed I was pensive and looked upset as we were walking home from a comedy show, so he asked me what I was thinking about. “The first Sex and the City movie was on the other night, so I watched it, and it’s even worse than I remembered,” I replied. “It’s so bad that, for me, it even ruined the TV show, which I used to love.” Some people seem relieved that I still have the energy to reserve such ire for trivial matters.

Sometimes, however, I get a strange chorus in my head that’s just, “Cancer, cancer, cancer, cancer.” Just that word, over and over again, like Jan Brady’s jealous proclamation of “Marcia! Marcia! Marcia!” on The Brady Bunch. More alarmingly, I suppose it’s also like the phrase “All work and no play makes Jack a dull boy” typed over and over again in Stanley Kubrick’s film version of The Shining. So either my subconscious is jealous of all the attention the Hodgkin’s lymphoma thoughts are getting, or I’m losing my mind. Probably a little bit of both.

As I weeded that morning, I didn’t find any four-leaf clovers. But my search sparked a childhood memory I hadn’t thought about in a long time.

When I was little—maybe from the ages of 4­ to 6—my grandma would get out sheet music and we’d sing songs together. This is notable because no one on my mom’s side of the family can sing. In my 20s, a friend and I stayed with my mom and my grandma to see a Peter Murphy concert in Cleveland for her birthday. My grandma baked her a cake. She was an amazing baker. I explained that we meant well, but we’d all be off key. To anyone who celebrates birthdays with us, I assure you, the song is mercifully short and the homemade cakes are delicious.

I’m not sure if my grandma could sing at one time, but age made her voice a little creaky. My mom always sings high and off-key. I don’t sing. In fact, even when I’m required or expected to sing, I usually would just lip sync in high school choir, church and birthday parties.

But in those days, my grandma and I would get out the sheet music and sing a few songs, joyously and loudly. One of these was “I’m Looking Over a Four Leaf Clover,” the 1948 version by Art Mooney. (Apparently Willie Nelson also has a version of this song, but c’mon—do we really think he was looking for clover on purpose or he happened upon some while looking for a different type of harvest?)

The other was “You Are My Sunshine.” The line, “So I hung my head and cried,” always sent me into fits of laughter. Not because I enjoyed dark lyrics—that would come later, during my goth years in high school and college. At 4, I wasn’t familiar with the term hanging your head, so I pictured this poor guy taking off his head and hanging it on a coat rack to cry and dry off. And that image is hilarious to a 4-year-old.

Since then, I don’t think I’ve ever really sang a song without some degree of self-consciousness or self-awareness. I got the picture when I was never picked for singing or dancing parts in grade school productions.

My grandma died in 2006, so I can’t ask her why we sang songs together, other than it seemed to be a lot of fun. That must have been the point. Just doing something fun even if you weren’t very good at it. I’m not sure that lesson stayed with me, as I stress out over everything from how I do on these interviews and tests to whether or not I’m doing all I should to beat cancer.

I wish my grandma could have seen me move to New York City, by far one of her favorite places in the world. She took me here first when I was 10 years old. She thought the city was so exciting and enjoyed interacting with so many people.

So I didn’t find a four-leaf clover the other day. But the next day, as I boarded the A train, a man was playing the guitar and singing. He was playing “You Are My Sunshine.”

I know in my last post I said I wasn’t going to cook meth Breaking Bad-style, but that was before I realized how much my COBRA payment was going to be. I’m baking cookies for tomorrow’s community garden meeting, so I’ll see how that cooking experiment goes before I set up my lab.

Still, I’m grateful to have COBRA to carry on with my health insurance while I look for a new job. The opthamologist I saw the other day asked me what COBRA stood for, as I gave him the abbreviated story of my Hodgkin’s lymphoma, my job loss and my insurance situation. I later discovered it stands for the Consolidated Omnibus Budget Reconciliation Act. But it’s aptly named because it poisons your soul and sinks its fangs into your unemployment check.

I had made an appointment with this new doctor after nearly three weeks of a lingering eye infection. My boyfriend suggested him from the list of opthamologists within my insurance network because, according to this doctor’s credentials, he also has a degree in philosophy from Yale. Perhaps he would understand my existential crisis and anguish brought on by wearing my glasses. Also, he had an appointment open right away.

I knew I made the right selection when, after hearing my health tale, he made the following analogy: “I think the eye infection may be the least of your concerns,” he said. “It’s like World War II is going on, and the eye infection is a battle for a small island.”

He’s right, of course. I have been focusing on my eye problems, though I could argue that my nearsightedness makes it even harder to see the big picture.

Things are still going pretty well, all things considered, but this past week I’ve been plagued with random pain twinges more than usual. It’s not that they’re even that painful, just puzzling. And slightly alarming. Like someone’s playing Operation and hitting the sides. Stop dropping the spare rib already!

Right now for instance, I have a slight twinge in my abdomen. What’s in there? My liver? Then the worries begin.

One of my favorite funny writers, Laurie Notaro, describes the random pain pangs of being in her thirties in I Love Everybody (and Other Atrocious Lies), as being located in areas devoid of major organs, “places I thought were used for extra storage, for things like extra bile, a couple of feet of rolled-up intestine, balls of hair that may come in handy in the future, maybe some additional vein parts, or bits of corn.” In the book, Notaro worries she has cancer, and I don’t mean to alarm you, hypochondriacs, but that’s exactly what it feels like. Or at least that’s what my chemotherapy side effects feel like.

The other side of my chest has twinges too. And my arm socket is sore, as is the back of my neck on my less cancerous side. My doctors, at least, aren’t alarmed. When I bring these things up, the answer is, “Well, you have Hodgkin’s lymphoma and are undergoing chemo.” So I try not to worry, even when it feels like someone’s been messing with the wishbone again and my nose lights up.

I also haven’t been able to shake this funk for the past several weeks, since losing my job and having the eye infection. After applying for several positions and taking a test for a job, all of my worries and insecurities caught up to me in the middle of the night. I couldn’t sleep and sunk into despair about my ability to land a new job, my hair loss and, yes, my glasses.

Not working out on a regular basis because of everything that’s been going on is also catching up to me. I feel bad when I’m a little winded after reaching the top of a long flight of subway stairs.

I feel squishier than I used to. I’ve had to wear my glasses. My hair’s thinner. I feel diminished. Whether it’s at a job interview or walking down the street, sometimes I want to put up a sign that says, “Please Excuse Our Appearance While We’re Under Construction.” Or reconstruction, I suppose.

I realize that I’m very lucky as far as cancer patients go. And lately, I’ve realized that the thing that’s making me unhappy isn’t even the cancer so much—it’s my insecurities. I’ve spent the past few weeks obsessing about how I look or grappling with self-doubt about my career.

I’ve had these insecurities a lot longer than this cancer, and they’ve probably affected my life much more negatively over the years than this disease, a relative newcomer. They’re so ingrained, they may even be harder to find and treat. But now that I’ve diagnosed some of these nagging self-doubts and insecurities, I can hopefully shed those along with the cancerous cells.