I’ve been bald for several weeks now, and I still love it. I’ve put a big glob of shampoo on my hairless head in the shower only twice so far.

Reactions to my new look have been mostly positive. People tell me I can pull the bald thing off. I have big facial features, and it balances out the baldness somehow. They’re strong enough to stand on their own, without a hair frame. Babies seem to like me, and I think it’s for this reason. If someone increased my facial proportions just ever so slightly, I’d look like a cartoon. I’ve never had my caricature done. I’m convinced it would look just like a regular drawing.

I recently thought back to a conversation I had in high school with a friend about my nose. I hated my nose. It’s not exactly that it’s so big, it’s just kind of weird. It’s not like other noses. I mean, I wanted to be weird when I was 15, but weird in a cool way so that counterculture peers would accept me and people who might make fun of me would leave me alone. I don’t think any 15-year-old girl wants to be known for her unique nose.

Anyway, my friend’s wise words that day put me at peace with my nose. She said that my nose fit in with all my other facial features and that if I had a smaller nose, I’d look strange. I realized she was right. I wish I could say from that day forward, I shed all my insecurities and had some epiphany about what makes you unique can make you beautiful, but that didn’t really happen then. No longer hating my nose was an important step forward, though, in a still-ongoing journey of self-acceptance.

Now that I’m bald, this is probably not even the “weirdest” I’ve ever looked. Maybe it’s the most subversive look I’ve had, but not on purpose.

In my mid-teens to early 20s, I was goth. When I lived in Columbus and walked by this sports bar with a giant patio on The Ohio State University campus, I would habitually cringe and wait for insults to fly my way from drunk guys, but in later years, I remembered I wasn’t goth anymore so I wasn’t such an easy target. (Still, really drunk guys will yell for lots of reasons, so groups of them in situations where they can yell at me, safe behind some kind of patio fence, still make me nervous.)

In my 20s, I wore all sorts of crazy outfits. I wasn’t exactly Lady Gaga, but I love fun clothes. Even recently, when I worked in an office (often by myself), I would still sometimes have themes to my weeks: polka dots, black-and-white, cats, gingham.

Now that crisp fall weather has arrived, however, my head has been getting cold. I have my Kangol hat, a purple floppy hat from a friend, a purple cap knitted by another friend and my Heisenberg fedora, of course. And I have plenty of hoodies.

Unless I’m going to an office or a business thing, I don’t usually wear my wig. It’s partially out of the same laziness I’ve always shown toward my hair situation. My wig doesn’t look very realistic either, particularly because I keep fiddling with it—shifting it, touching the back to make sure it’s not puffing out, snapping at its band.

In those situations, I wear the wig for other people. I don’t want to be too distracting by being “the bald lady.” Or the “bald cancer lady” at the office. When I wear my wig, I feel a little bit less like myself, though.

In fact, I went to dinner in my neighborhood the other night after a long day at work and just left my wig on. I didn’t notice until we were almost done eating that there was a bald woman at the table of three next to us, as if we were seated in an invisible bald woman/wig area. I felt like kind of a phony wearing my wig then—I wanted to rip it off and say, “Hey, nice ‘do!”

I think we might be leading parallel, hairless lives, because I think I saw the same person at a concert on Friday. She can pull off being bald and wearing glasses, though. I’m not a huge fan of wearing my glasses, but I mind much less now. Still, I think I look a little like the Beacon’s Closet baby mascot. Oddly, I don’t mind wearing my glasses with my wig. They work together.

As long as I’m talking about wigs and glasses, an aside: Does anyone remember a TV commercial for Focus contact lenses that showed a man and a man in drag out to dinner? (It aired in 1996, so it’s OK if you don’t.) Suddenly the man in drag says, “I have to tell you something!” and he wipes off his lipstick, pulls off his wig and confesses, “I have astigmatism.” Then his date tells him about soft lenses for astigmatism. Not only did I find out I could have disposable lenses, but I loved it for some reason so much that I’ve remembered it for 17 years. So I think about this commercial when I think about pulling off my wig in a public place.

I don’t get many stares. I did get an oddly dirty look on the train that day that left me wondering if I looked like a skinhead. I don’t think so. Dirty looks on the train can be about anything.

I caught someone’s jaw drop once, but she appeared to be from out of town, because she was seated outside having dinner with a bunch of people wearing nametag stickers. She quickly composed herself, but she just didn’t have that looking-without-looking thing that New Yorkers have down, the dead-eyed subway stare—the skill of looking very intently at nothing at all.

Perhaps she wasn’t from out of town, and, like me, she wears all her emotions on her face. Maybe the look wasn’t about me. But for a moment, our eyes met, both of us confused for a second.  My look said,”Huh? Is it because you didn’t expect a bald lady when you looked up from your falafel? Or is it because I look like someone who would steal your falafel from your plate as I walked by?” I was casting an envious glance at her meal, and perhaps it was a protective feeling that made her look up at that moment. Maybe she was opening her mouth to say, “Hey, lady! Get your own food!” But she saw that I was bald and either thought I was too bad to mess with or knew that I was going through chemo and decided to be nice.

If I was worried I’d be the weirdo on the train, I quickly remembered that you have to do a lot to draw attention to yourself. On my way to a housewarming party, a man painted silver got on a few stops later. (What do people painted in silver do? Pretend to be statues? Robots?) But no one looked at him either, except for me.

I think my head sparked a discussion between two teenagers, but it wasn’t really about me. They were trying to come up with the name of the bald singer and one of them finally remembered it was Sinead O’Connor.

On a train ride home, someone stole my thunder by throwing up. I didn’t even notice, until someone warned me to watch out for my shoes, as the motion of the train caused some vomit to roll toward our area. Then, before switching train cars, the stranger and I reminisced about other times we’d seen people vomit on the train. (This was the third time for her in two years and the fourth time for me in five years, though once I was only visiting and it was New Year’s Eve so I’m not sure that incident counts. I have never thrown up on the train, but I’ve fallen asleep on a stranger, who was not at all happy about it. That’s why this is not the City of Brotherly Love, but the City That Never Sleeps, especially not on the shoulder of a public transit stranger.)

When I shaved my head, I had kind of hoped maybe I would get seats on the train. Not necessarily people standing up to offer, but at least I’d get dibs as long as no pregnant women were around. A few years ago at Upright Citizen’s Brigade, I saw comedian Pam Murphy’s one-woman show, “The C Word,” and she has a really funny, true bit where she plays two parts: the cancer patient on the train who hopes for the offer of a seat, and a seated passenger, wondering if she should give up her space.

I realize I fall into a gray area, along with pregnant women who aren’t fully showing yet. I mean, what if she’s not pregnant? In these cases, I sometimes just get up and pretend like my stop is coming up to ease my conscience. I’m also terrible at noticing pregnant women and have stared at someone’s belly for a full minute before I realize I should stand up. I saw one non-showing woman reading a pregnancy book on the train to let people know that yes, she would like to sit.

But I know all bald women don’t necessarily have cancer. And most of the time I’m fine, and I don’t even need to sit. I just like to sit.

I really just need a seat once every two weeks, right after chemo, when I’m tired and in a Benadryl haze. That day was today. I happened to get a seat on the first bus, but today everyone was in a mood. The bus stopped to pick people up and it wasn’t an official stop, so the bus driver wouldn’t let someone off. At least four people who weren’t affected by this were angry. It was just one of those days when everyone’s in a contagious bad mood and no one could break it.

I certainly couldn’t. I was just trying to stay awake and yearning to get home. I should say that today of all days, I guess I looked more like a cancer patient than ever, because I was also wearing a cancer center sweatshirt and my hand was bandaged where they had put the IV in. I was short a hospital gown and a sign, but what can you do?

The next bus was crowded. There was a group of naysayers that you sometimes find at the front of buses and by train doors who loudly assert that there’s no room. Sometimes they’re right, but often, they’re not. I tried to go past them, but got caught in a crush, and someone was yelling at my boyfriend because he was too close to her. “Let’s just leave!” I said, defeated and medicated. We finally got to the space that was behind the group, the space that they told us wasn’t there.

I was still tired and a little cranky that I had to hold on the strap with my numb, bandaged chemo hand, but my other arm hurts from blood clots (that’s another blog). Mostly I was sad—I didn’t want a seat. I just wanted people to be nicer to me, even if it’s because I’m sick.

And people are often nicer, or nice in general. It’s not always the way you think it will be. Good things happen, even on public transit. A stranger will warn you of a stream of bodily fluids heading toward your velvet flats. A comedian I recently saw said a bus driver stopped the bus and wouldn’t move again until someone gave up a seat for a really old woman. (The story was way funnier than that; I’m paraphrasing.)

Some people go beyond nice: someone I ran into this week had gone to the beach the day before and had risked his life to save a stranger who walked into the ocean and tried to commit suicide. He said that hardly anyone was there on a weekday, and he was initially annoyed that a guy had set up his beach towel pretty close to his own, but it turned out to be fortuitous, because this man also helped to save the woman. So things that might seem unfortunate sometimes turn out to be lucky. (Sometimes they’re just irritating. I don’t think the person I fell asleep on gained any good fortune from it.)

I know I’m lucky to have such good support and so many kind words from everyone. I realize it’s selfish in a way to hope to temporarily work my way into the train hierarchy of people who get seats first.

I was just looking for perks, something few and far between when it comes to cancer. Being bald, however, has quite a few benefits. Fast showers. A blank canvas on which to put temporary Cleveland Browns tattoos for football season. My impending Walter White Halloween costume. For now, I can content myself with these perks.

 

Being bald is pretty great. I’ve always wondered why one of my friends, who ordinarily would have a full head of hair, has shaved his head since college. (Though there have been a few periods where he’s had hair in that time.) But now I see the appeal.

Sometimes, I forget that I’m bald and I startle myself when I walk past a mirror. My boyfriend envisions me calling the police. “Hello? There’s a weird bald lady in my house! But I can’t find her!”

I just did yoga, and I didn’t have a ponytail in my way. My head is nice and cool—though unprotected from the sun. In fact, I have a barely noticeable tan stripe on my head from where the part in my hair was located. It’s like I’m Pepé Le Pew or wearing a Cleveland Browns helmet. (Like most of the Browns, sadly, I’m also not very good at football.)

As I mentioned, I’m not someone who cries over haircuts. When I donated my long hair earlier this year, the stylists seemed concerned and checked on me after they took off about 9 or 10 inches. (I knew then about my diagnosis and that I had more hair to lose in the coming months.)

This Sunday, as my boyfriend sheared off my hair, he asked me several times if I was OK. He also gave me a glass of whiskey.

If there’s a time for having your allotted occasional alcoholic beverage during chemo, I suggest you have it while your head is being shaved. And I recommend whiskey. It’s immediate and makes you feel warm inside.

But once my head was shaved, I realized I liked it. It’s not even the worst haircut I’ve ever had. That was probably when my mom decided to cut my hair into a short bob and perm my hair when I was in sixth grade. The result was a hairdo that someone said looked like a spaceship. A fuzzy flying saucer.

That was just the beginnings of my tress troubles. In the early 1990s, when I was in eighth grade, my hair was full of split ends, so I went to someone my mom worked with at the time, a girl who also cut hair. This girl’s hair was curled and teased on top into a heavy metal dome—a little bit like the blonde in this picture, but with a slight spiral perm to it. It was structurally magnificent, but not the look I was going for. I wanted long, beautiful completely straight hair—like Sebastian Bach of Skid Row, as long as I’m on the subject of metal hair.

Anyway, she layered my hair—a lot—to get the split ends out. And since I didn’t have enough L.A. Looks to make my hair big, I had hair like Chris Robinson of the Black Crowes in the “Hard to Handle” video. (My teenage life centered around music videos and references.) Watching the video now, his hair looks fine. But it was not OK for 13-year-old me.

I silently and constantly fretted about my hair, as only a young teenage girl can, and waited. (Like broken hearts, there’s often not much you can do for a bad haircut, except let time heal.) Once it grew out a little, I could finally spray my bangs into a big, stiff wave, keeping the lower bangs loose over my forehead. You were supposed to use a curling iron to curl the top bangs back to create this tube of hair that curled backwards, then spray it up in place. I was too lazy to use a curling iron and make it look like this, so I kind of fashioned my own side wave and sprayed it into place.

After that, I made pretty wise decisions regarding my hair. Well, for the most part. I wanted to Manic Panic my hair a crazy color, but it’s dark brown, so nothing would show up and I was too scared to bleach it. By my junior year, I had moved on from my hair metal phase. (So had the rest of the world, post-Nirvana.) After a summer of painting all my furniture black, listening to the Cure and Nine Inch Nails and buying a pair of combat boots, I had become goth.

I tried dyeing my hair black with a temporary dye, but it wasn’t black enough. (Surely not as dark as my angst!) So I used permanent dye. Over and over again. And then I didn’t want black hair anymore by that spring. But permanent dye is pretty permanent, as it turns out. The salon tried to bleach it out but it worked only at the top near the roots—not the parts that had been dyed black so many times. Until the middle of my freshman year of college, I had an orange band of the bleached part slowly growing out through my hair.

Once that finally grew out, I dyed it black again during my sophomore year of college. (What’s that definition of crazy again? Doing the same thing and expecting different results?) This time, when I wanted to go back to brown, a stylist bleached chunks of my hair to make it look more like my natural color, and this worked much better.

I sometimes dyed my hair that reddish late ’90s color. In my early twenties, I dyed it bright red and purple, but it was temporary dye that lasted only a few weeks and it didn’t show up much on my dark hair. No one seemed to notice much, except for my boss. When she walked into my cubicle, she said, “Oh. You dyed your hair.” To which I replied, “Yes, it’s Pimpin’ Purple.” (A reply that now makes me cringe and laugh. Oh, to be 21 again.)

The following year, apparently no wiser, I got gum in my hair. Not at the tips where it might make sense that a grown woman with no kids would find gum. It was at the top of my head, near my hairline. I chewed gum all the time, and sometimes, I would take it out of my mouth and just put it somewhere before falling asleep. (On my nightstand, for example.) I’m still not sure how it ended up in my hair, but it seems inevitable now. I cut it out, and just kept a hair clip in place to hold that piece down—otherwise it would stick straight up. Like that orange band in my hair, the clip moved as my hair grew.

Since my sophomore year of high school, though, my hair has pretty much been the same: Long and brown. I briefly experimented with bangs in my late twenties and that was a terrible mistake, looking back at old photos.

Until my recent hair donation, I was a huge fan of long hair, and I never wanted short hair. (Certainly not this short.) But I got a lot of compliments on my chic bob. I said thank you and I liked the bob, but vowed to return to long hair soon.

Now, I’m thinking that maybe I wasn’t into short hair because I hadn’t gone short enough. Reflecting on my hair past, I’m not sure if I should have long hair—or hair at all. I don’t use fancy shampoos or gels or sprays. I rarely used a blow dryer. It took too long, especially on my thick hair.

When I did get compliments that my hair looked nice, here’s my secret: I had brushed it that day. I sometimes didn’t bother. (If you’d seen my childhood dolls, you’d see the pattern started early.)

Often, when I found a troublesome knot or tangle, I’d just cut it out, not having to answer to anyone about it until a stylist asked me why a chunk of my hair was missing. I always felt a little sorry for my stylists, when they asked me my hair regimen. “I wash it and I sometimes brush it.”

Now that I’ve been bald, there’s no telling what I’ll do once my hair grows back and it gives me trouble. I know where the clippers are, and I’m finally free of my hair—or maybe it’s finally free of me.

I just took a nap for almost three hours. One minute, I was at the grocery store having a discussion about when mangoes are ripe and enthusiastically lobbying for the purchase of a baby watermelon, and the next minute, I was bone tired.

I knew this would happen sometimes. I napped yesterday as well. Chemo makes you tired. Mostly, I’m tired of having cancer.

I try to stay upbeat, but every now and then, I slip headlong into self-pity and a litany of complaints. I’m tired of looking for jobs. I’m tired of hustling for freelance work. My big toenails looks like this and feel like they’re about to fall off. Random stuff hurts. I can’t stay in the sun for very long before getting burnt, even with sunscreen. My fingers are numb.

I miss eating the random samples at the grocery store that everyone may or may not have sneezed upon. One of the worst parts about my compromised immune system is curbing my desire to eat food of questionable origins. And food that falls on the floor is no longer viable.

I used to invoke the five-second rule a lot. In fact, years ago, I found myself explaining the five-second rule to a member of the maintenance crew at the building where I used to work. He had witnessed me drop a French fry on the floor, then pick it up and put it in my mouth. As I rose from picking up my fallen fry, my eyes met the horrified gaze of the maintenance man. The fact that it was not even my fry, but that of an editor who I didn’t think would miss one, probably added to his confusion.

When I finished chewing (I have some manners), I explained, “Five-second rule.” I was met with a blank stare. He had never heard of it, so I had to explain how, if you eat something within five seconds of it falling on the floor, it doesn’t count. The flawed logic is that germs don’t have time to climb aboard whatever you’ve dropped. Mostly, however, the small time frame usually ensures that someone hasn’t seen you commit this questionable social behavior, so it’s like it never happened.

A few months later, when I found an article clipped from the newspaper about the 5-second rule atop my work inbox, I knew immediately who it was from and smiled. It stayed up on my cubicle bulletin board for a long time.

So you can imagine how it pains me to look at fallen comestibles, and have to throw them away.

The exception was last night, when I reached for my phone and heard something fall off my nightstand. I heard many tiny things rolling around. This was after yesterday’s nap, so I was a little groggy. I looked over the edge of the bed to see my Docusate “dolls” rolling around my (thankfully clean) bedroom floor.

The alarming part was that the cat was not only batting around the laxative/stool softeners, she was trying to eat them. And was soon joined by the other cat.

Docusate pills smell kind of like feet and fish. The cats pounced upon them like they were treats I’d neglected to share with them, impersonating Hungry Hungry Hippos.

Thankfully, the pills were too mobile and too big for the cats to easily eat, despite their best efforts. One cat just sat on them like he was going to hatch them later, hiding them under his ample belly.

I can laugh about this now, because no laxatives were ingested by the cats after all.  So there it is. A bright side. There always is, even on bad days, when I am sleepily snatching laxatives from the maws of cats. Even when it’s not a full victory, and I wonder: Would I rather lose my nails than my hair?

So chemo wiped me out this weekend. I still managed to write and apply for some jobs. I had brunch with some friends today and saw some art before slipping into afternoon exhaustion. A friend unexpectedly came into town for a bit. My cats aren’t pooping uncontrollably. Things are still good, even when I’m too tired to see clearly.

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.