Pro: I think I found T-shirts to wear during my hospital stay. Con: My head looks like an old crone’s chin.

I’ll start, I suppose, with my bad news. Instead of the smooth Telly Savalas or the majestic Yul Brenner, my head is closer to Gollum’s from Lord of the Rings. My dome does not resemble a shiny apple, nor a smooth peach. It’s a kiwi gone bad, an old forgotten coconut.

My hair is almost all gone from the first round of ICE chemo, but a few stubborn hairs remain. And it’s not pretty. I expect these stragglers to fall out after this second round of ICE chemo. If not, I’ll take a razor to them.

On the bright side, the online education session about my autologous stem cell transplant put my mind at ease. A lot. And one of my fashion questions was answered; I’m pretty sure Henley T-shirts are the best option for me during my hospital stay.

Even better news, my old standby Uniqlo, where I buy almost all my clothes, has a new spring line of Henleys, so I’m going to buy some tomorrow. People sometimes ask me why I love Uniqlo so much, and it’s simple: It has the clothes I expected to wear when I thought of the present day as the future.

I was promised this future—now—in the ‘70s. The prediction then was that we were going to wear lots of white and monochromatic unitards and tunics. What about the fashion of Logan’s Run? Where are the magic amulets that I saw from other worlds in Wonder Woman, as I made myself dizzy spinning around in the living room, perfecting the change from Diana Prince to superhero and wearing bulletproof star bracelets made of paper? (Seriously, I’d wear those bracelets, bulletproof or not.) I’d even take Erin Gray’s shiny Buck Rogers suits from the 25th century all these years early.

I think of the ‘70s as a dark time for most fashion, but future ‘70s fashion—the era of tunics and unitards and shiny clothing of the 2000s and beyond—was going to be awesome.

You can only imagine how unspeakably disappointed I am.

I waited for this century only to be offered worse versions of what I wore in junior high and high school.

I am most disappointed in American Apparel. I had high hopes when I first heard about the American-made clothes and array of basics, before I realized the sizing is weird and, as Jezebel pointed out, everything makes you look like fat hooker. And why do the ads all look like young Dov Charney/Terry Richardson/Joe Francis-types took them in dorm rooms?

Things have changed a little. This week, after years away, I managed to buy an American Apparel sweatshirt in my size that fit. But I also took note of some of the “new” fashions on display, and a lot of them were straight from my junior high days. We’re not even talking the mall items you HAD to have, otherwise you would surely be expelled from society forever: The oversized ESPRIT bag, the Benetton sweatshirt, the big Express shirt with French writing on it, a long Limited sweater paired with colorful leggings.

We’re talking DEB offerings. Basics. A loose-sitting floral-print dress. A velvet tunic. Cropped sweaters. Acid-washed jeans and light denims that are begging to be French-cuffed. (I have been told that most people called it pegging, but we referred to them as French cuffs in my school.) They do have shiny skirts and clothes. But it’s not right somehow.

So I turn to Uniqlo, which feels like it’s from the future, with their mannequins in basics, long escalators and robot-voice announcements. A friend who lived in Japan doesn’t understand my fascination; she thinks they’re the Old Navy of Japan. But they promise me clothing technology, if not from the future, then from Japan, which is pretty close in my mind. They have clothes that magically stay warm and clothes that stay cool! This is what I need and what I deserve in this present-future. Otherwise I may as well go around draped in animal skins.

The thought of racks of fairly plain basics appeals to me, not only from my lady-of-the-future perspective, but also from my present wardrobe as someone in her mid-30s. At American Apparel, as I took in some of the crazier fashions from my youth and the youth of today, I realized why you pay attention less to trends as you get older, even as you keep an eye to fashion. Trends often look pretty ridiculous. And they often (but not always) expire after the first time around.

I think of my wardrobe as pretty basic and tame, especially after my last year of cancer. But then I just sent a sequin peacock dress from New Year’s Eve to the dry cleaners.

For a very brief insight into my psyche, life story and wardrobe: My mom and I dressed alike until I was in fourth grade or so. She made all our clothes, and all of them were identical mother-daughter outfits. (We were pretty darn adorable when I was little.) I eventually picked out some of my own stuff from fifth to seventh grades, during my personally most awkward phase, then transferred at the height of everyone’s most awkward of phases to public junior high in eighth grade and no longer had a uniform.

After a metal phase late freshman and sophomore years, “alternative” hit. (I’m talking about clothing here. Metal is still awesome.) So I had the Docs and the overalls and my grandpa’s flannel shirts and the band T-shirts, but I was goth-tinged. And so I’ve gone from a teen who wore black a lot to a New Yorker who wears black a lot, and I feel like I’ve really come to my fashion home.

All of this means that my fashion choices are at odds—a mix of blending in and hiding and standing out. Hence the neutrals and black and my usual uniform of black shirt and jeans, with a closet full of well worn craziness, from the Union Jack dress to the shiny pants to the sequined peacock dress.

I keep remnants of these past trends and phases in my closet, though I winnow things down as time passes. I never part with everything. It’s hard for me to part with anything, frankly, and I have a crowded closet to prove it. I delightedly broke out my Doc Martens when they came back this fall. Is it time to revive my ESPRIT bag? Because I still have it.

Tomorrow, I have an online education session about my autologous stem cell transplant. I’ve been reading the giant preparation binder, but I haven’t thought of any questions. Considering that’s what I do for a living, I’m a little disappointed in myself, but I haven’t gotten through much of the material.

Part of me is honestly scared of what’s ahead. All I can think of are frivolous and fantastical concerns. For now, I will blame my procrastination on the plastic-loving cat, who runs her sandpaper tongue over the edges of the binder whenever I try to read. Here are a few of the concerns I won’t talk about tomorrow:

Do vampires roam the hospital floors? My most immediate cause for alarm yesterday was when I read that you smell like garlic for a few days after the transplant. With all this blood, are they keeping us from turning into vampires? Is a stem cell transplant really taking someone to the edge of vampirism, and then giving us stem cells to prevent the change? Is that why some patients in the hospital have “sitters” with them all night? It’s not to help guide them to the bathroom—it’s to prevent them from draining other patients while they sleep.

I’ve seen several Blade movies. Also, I was goth for awhile and have read all the Anne Rice vampire novels, so I can be considered somewhat of a vampire expert.

According to the binder, it’s a preservative that causes the garlic smell, not your body fighting off vampirism. I prefer to turn cutting-edge science into terms I can understand: medieval villager talk.

I also read that the nurses can give you lemons to alleviate the garlic smell. That sounds…sort of delicious, if paired with a delicate fish and a nice white wine. But if I see anyone with a chef’s hat lurking around those few days, I’m leaving that hospital. At least my garlic smell will keep away those on the verge of turning.

Whatever will I wear?  After I Googled “stem cell transplant shirts” or “catheter shirts,” only a few results come up—including my own blog. Am I the only person with sartorial concerns during my stem cell transplant? I really don’t think I’ll care what I’ll look like—after all I’m supposed to feel horrible, and I’ve looked better.

But hospital gowns are drafty. After the leukapheresis catheter placement, I could wear my lounge pants, but I had to wear a gown on top to provide access to the catheter. I thought a lot about my gown when I was in the hospital after so recently seeing all the Oscar fashions. My gown could be said to have a plunging and an open back, worn off-the shoulder. Most gowns, though, whether they’re ball gowns or hospital gowns, aren’t that comfortable for long-term wear.

My booklet says that if you wear you own clothes to the hospital, to wear shirts that allow catheter access. So does that mean Henleys? Baseball jerseys? I have a few button-top tees and thermals. I’ve done some tentative internet searches and all I know is that L.L.Bean probably has whatever I need (or great Google analytics).

What do I do with my head? Right now, my head smells like a Strawberry Shortcake doll and her cat, Custard. If you were a little girl in the early ’80s, you know what I’m talking about. I should wear a big muffin hat to keep my head warm and get some striped stockings.

One of the best things about Strawberry Shortcake dolls was that they smelled like the desserts—the namesake character, Lemon Meringue, and her other friends. (Also, why do they keep updating dolls? This is not how they looked before. Strawberry Shortcake lives in a land of desserts; she doesn’t text and go shopping at the mall with her tween friends.)

In an effort to ease my scalp dryness since the hospital, I’ve taken to oiling my head with some of The Body Shop’s Beautifying Oils I got at a press event. I remember at the event, the PR person said you could put it your hair, so I did. This happened a lot at beauty events. I would put face cream on my face instead of on the back of my hand. PR people always seemed taken aback, so I kept doing it. I gave most of the oils away, but I can now choose between strawberry and Satsuma.

If I’m bald, then do I have dandruff? I’m still trying to figure out what I should use. I’m afraid to use moisturizer, although I guess I can opt for a natural brand.

So these are my concerns today. I’m sure I’ll have some legitimate ones tomorrow. Until then, I will think about how to ask delicately about vampires in the halls and hospital fashion.

I was supposed to be in the hospital right now, receiving my second round of augmented ICE. Instead, I am lounging in bed and catching up on work—and, of course, this blog. I have mixed feelings about this—obviously, I’d rather not be in the hospital, but it’s just a three-day respite from the inevitable. Instead, I’m going in tomorrow, just in time for the snowstorm. (One of the many snowstorms of this winter.)

I have mixed feelings about the weather too—on one hand, it makes going to the hospital and doctors’ appointments, of which there will be many, less pleasant, but on the other hand, I have to be a hermit through May, and hermitlike through mid July, when the weather is beautiful. (I expect the winter to be done by then, at least.) This is when I wished I’d skipped the Brentuximab and gotten all this unpleasantness over with in the winter. Ah, well.

Friday, I packed up my hospital suitcase full of loungewear and my blanket and headed to my doctor’s appointment before the scheduled leukapheresis catheter placement. When the doctors saw the arm with the two clots, however, they decided to delay catheter placement and my hospital stay. My arm at that point looked better than it did on Thursday, when it swelled to giant proportions. I was worried it would burst open like a piñata filled with blood, but I realized this is probably not possible.

After a night of a heating pad and menthol pain patches, my arm was still red and hot to the touch. And it hurts. Sometimes, it feels like a tiny flame is in my arm. I rated the pain a five or six, but my boyfriend told the doctor it’s an eight. He corrects me a lot at the doctor, and I always wonder if they write down what I’ve said or his opinions. I think I have to agree with him in order for them to take his into account. An eight is pretty serious though. I maintain this is a six.

In case my arm is infected, I’m on antibiotics, and I went for another ultrasound. Apparently, the clots are the same size. They’re just inexplicably more painful and annoying. So I got some more Lovenox to inject daily to try to clear them up.

I start chemo on Monday and then I have my catheter placement on Tuesday. In the meantime, they might use a PICC line for the chemo, since my veins have been less than cooperative.

On Friday,  I did meet with the transplant doctor, who gave me an idea of what’s in store in the coming months. Spoiler alert: Not much in the way of fun.

The saddest news came when she asked me if I have pets. When she found out, I have two cats, she had a list of don’ts. I can’t change the litter, but that’s my boyfriend’s job anyway. Also, she said I have to keep them away from my face until mid-July. What? How am I supposed to resist burying my face in their fuzzy bellies?

Also, one of the cats is extremely proactive about touching our faces. Just the other night, she was curled up by my boyfriend’s face, rubbing her wet nose against his cheek while he tried to sleep. I wake up with her paw on my shoulder or her face buried in my neck, or sometimes I wake up because she’s pressing her nose against mine.

The doctor is very knowledgeable about stem cell transplants and medicine, for which I am grateful, but I suspect she knows very little about cats when she suggested we break the cat of her habits. There’s no teaching a cat anything. It’s going to be a long, sad three months.

I didn’t cry when I pulled my hair out or applied duct tape to my head. I didn’t cry when I heard about my upcoming “hell week.” But I did cry about this. Sometimes, I’ll just look at the cats and tear up. It’s not even like I won’t be able to pet them. I guess it’s just a symbol of how things are going to change in the coming months. Also, I love kitty-cats.

I have to make sure all their shots are up-to-date, so luckily we just took them to the vet. They are senior cats, but in far better shape than I am right now. In fact, the female cat is in the shape of a cat one-third her age. I wish she could understand the vet, because she is vain and would enjoy this news.

Aside from the cats, I’ll have to avoid alcohol, something I had assumed was a given. Once your fast-growing cells are poisoned and you have to take anti-nausea drugs, drinking isn’t something you feel like doing. Also, after the last ICE, the nurse advised drinking at least two liters of water a day so the drugs don’t irritate the bladder and cause bleeding. So I stayed extremely hydrated, although I’d have a little coffee with milk during the second week. Of course, I’d love to hit happy hour instead of giving myself blood thinner injections. I think I could do an excellent job of thinning my blood on my own. Alas.

I’m also supposed to walk to help with recovery. Vigorous exercise is out—I haven’t done my workout DVDs since the first round of ICE and I managed to do yoga only four times since, after being thwarted by my fever, hospital stay and the arm I can’t move because of the clots. The thing is, I don’t want to walk outside when it’s cold, and there’s no sign of spring in sight. I’ve thought of getting an elliptical, but I have a small Brooklyn apartment. I do have a Leslie Sansone walking DVD that I got when I worked at a women’s magazine and edited the fitness section of the blog. The magazine shut down before I had a chance to watch it, and I’m intrigued. It could be a nice indoor walking solution that doesn’t take up much space.

I can do gentle yoga, but I’ll have that chest catheter so I’m wary of stretching. The doctor advises stretching a little bit once it’s in, but in addition to the heebie-jeebies, I can’t move my right arm much because the clots hurt.

At some point, I’m also going to get a blood transfusion.

I got a thick binder full of information from the doctor all about the transplant with fun topics like hair loss, catheter care and giving Neupogen injections twice a day. I haven’t even scratched the surface. For those asking what’s in store and my schedule, here’s an idea:

March 3–5: Second round of augmented ICE, catheter placement. I am not looking forward to having tubes sticking out of my chest. This gives me the heebie-jeebies. There will be two for the stem cell collection—one to take my blood out and the other to put it back in once the stem cells are removed and my blood spins around in a machine.

March 7–16: Neopogen injections, a catheter dressing change. We’ll do the former, but I’m glad we don’t have to do the latter. The shots to increase stem cells might cause bone pain, I’m told. They’re going to give me pain medication, but I hate taking pain medication. I don’t even like to take aspirin. I do hate pain, though, so we’ll see.

March 17–19: Stem cell collection. This involves sitting around for four hours, while your blood is taken out and put back in. It doesn’t sound so bad. During these days, I also have a flurry of tests and appointments, including an echocardiogram and a pulmonary function test, as well as an appointment with a social worker to mentally prepare me for the transplant. The best part of this process is that I have to eat a high-dairy diet these days. Bring on the milkshakes and cheese. (Greens also have a lot of calcium, so I’ll be sure to eat those as well.)

Stem cell collection might take longer than three days. They need 5 million. The record to beat is 32 million, but the doctor said that person had a lot of bone pain, so I’m OK if it takes longer. I’d like it to take only two to three days, if possible. I hope my bone marrow cooperates.

March 24: PET scan. I need a clear one to go on to the transplant, so I hope I pass! It would be nice to finally get a clear PET scan, something I’ve been hoping for since October. And I think I start outpatient radiation this week.

April: If everything goes well, five days of inpatient radiation and three weeks in the hospital for the transplant. The radiation is supposed to have unpleasant side effects, so I’m just in the hospital so they can keep an eye on me. Then the first week, when they do the chemo, is supposed to be OK. They keep referring to the second week as the bad one. Someone called it “hell week.” I’m scheduled to speak with a volunteer who has been through this to answer any questions. Also, someone left a comment on my last blog about a friend of hers who did a stem cell transplant for refractory Hodgkin’s lymphoma and is doing well. It’s always nice to hear tales from the other side.

In the third week, I start a long recovery—about three months of rest and isolation from crowds and six months until I’m 100 percent. I’m a little disappointed to hear that the first month of recovery is so intense and that I’ll need 24-hour supervision. Of course, I didn’t expect to emerge from the hospital feeling great. But I’ll have the immune system of a newborn.

So that’s what’s in store! The next steps start tomorrow, and as much as I’m wary of what’s in store for the next few months, I’m also eager to move towards the end.