Summer Buzzies Are Out

For the (wow I’ve already lost track so fill in blank) day, the weather in London has been absolutely, positively supercalifragilisticexpialidocious. I don’t think I saw a single cloud today and that is something else considering how the wind blows things across this island.

We had a mellow day. My big event was walking to Hampstead for a polish change, a medical necessity to help strengthen my nails (sort of hard hit by the chemo drugs). Plus it gives a bald girl a lift. A little colour is always good.

I slathered on SPF 50 and put on the bare minimum of clothing, having worn my parka just last week! (Do you think that warranted an exclamation point, or what is overkill?) A black GAP body tank top, my H&M striped miniskirt, flip-flops and an apple-print headscarf (also H&M). I’d post a pic but I am in my pyjamas now and that train has left the station.

Then I hoofed it up the hill to the Beauty Boutique on Flask Walk. I love this place because it is low-key, friendly, they know who I am and act normal toward me. How nice.

With good weather comes skimpy clothing. People of all shapes and sizes partake, and there were indeed some eye-catching ensembles this afternoon.

The thing I noticed most was how everyone’s tits were out. Lots of tank tops, bustiers, revealing sundresses, you name it. A little sunshine and all hell broke loose. The women of north London were practically serving them up on a plate.

Lots and lots of cleavage. And bouncing scoops of flesh.

As I mentioned in “One to Go,” after chemo on Thursday I saw the radiation oncologist. She warned that there was a good chance the radiation would foul up the reconstruction on my right side. Nothing to be done about that but wait and hope for the best. Expect the worst.

I am not gonna lie. I ain’t thrilled about this. But it wasn’t new information. It just sort of sucked to hear it again when I am about to kick chemo’s ass and embark on the next phase. Got to hand it to the docs, though, they are on the ball. Yesterday I got my entire radiation schedule e-mailed to me, with times and everything. It’s on my iCal, waiting to be crossed off.

I just hope that at the end of the day I won’t have too many complications. Radiation has what my reconstruction surgeon calls “the bystander effect.” For every one bad cell that you are targeting, it destroys or alters about a billion healthy cells. This is too bad. But Das ist so.

Having implant-only based reconstruction surgery following (or prior to) radiation can be problematic. Your skin acts different, the blood supply is affected and you are more prone to bleeding, infections and capsular contracture. Capsular contracture is when scar tissue forms around the implant and sort of squeezes it. It can cause the implant to be hard and/or misshapen. And sometimes further surgery is required, including eventually removing the implant.

I don’t really want to be an Amazon.

I’ll tell you what, though. If that shit happens, if that is my lot, then I’ll take it over the cancer.  I’d rather be an unwitting Amazon than have a great set of reconstructed boobs for two years and then find out I have a recurrence in my chest wall.

If that shit happens, I will become Katniss (from The Hunger Games, people) and take up the bow and arrow (although it is reputed that the Amazons had their left breast removed not their right, so that they could shoot arrows and throw spears more freely, despite being depicted with both breasts in artwork).

I will admit that it is not my first choice, and it would definitely cramp my fashion style. However, sometimes you have to make a sacrifice in order to kill it. And my reconstruction surgeon has more than one trick up his sleeve. So we’ll play it by ear. And meanwhile I will continue to watch the parade of large, jiggly buzzies romping up and down the high street.

An unruly sea to which I not so long ago belonged.

My Stay Puft Marshmallow Man

The end of the school year is drawing to a close. And with it the end of chemotherapy. You may think that this is cause for celebration, and for many reasons, it is. Only somehow that isn’t entirely how I’m feeling.

It has been a remarkable year at the American School in London. What my girls have learned, how they have grown and what they have accomplished in about eight months astounds me. Living here has opened up a new world for them and allowed them to gain perspective that comes, I believe, only with the experience of living abroad. Once they transitioned to their new school, having made friends and gotten to know their teachers, they blossomed like well-tended flowers in a hot house. They are lush and gorgeous and powerful. I stand in awe of them.

One reason I’m sad the school year is almost over is that the girls must let go of this year’s teachers and classes and plunge into the great unknown of the summer. But I think I am the one who will have the most trouble letting go, really. The school has provided stability and routine but it has also served as a community of friends, teachers and other staff who poured forth so much help and support that my cup literally ran over and I started to feel guilty about all the meals I was receiving. Guilty that I wasn’t unwell enough to need or accept this help. That it should go to someone more needy, more deserving. Like I was a faker.

The other reason is that the end of school means the end of chemo. What? You say. The end of chemo is cause for celebration! Cause for champagne and party hats! Right. But the strange thing is, having focused so much of my energy on getting through chemo, it has become my routine, my life, my situation. The end will be one big boring-ass anticlimax. And it will mark the beginning of a new era.

The new era has two flaws: (1) it will be filled with the monotony of daily (or at least five days a week) trips to radiation; and (2) there will no longer by any cancer-fighting toxins coursing through my veins, seeking out and destroying any rogue cell daring to remain in my body.

On a lighter note, it will also mean the end of posts about what I will wear to chemo (see What I Wore To Chemo Today and Party in the Chemo Suite). “What I Wore to Radiation Today” and “Party in the Radiation Room” just don’t have the same ring to them. And because radiation will be five times weekly for five weeks, could get old rather fast.

Don’t get all depressed on me. I am not really sorry that chemo is almost over. I never ever want to do it again. It has been, for lack of a better word, disgusting. Still now, about six weeks after my last dose of AC (doxorubicin and cyclophosphamide), the former of which is, disturbingly, bright red, I hesitate when I reach for the mug in the cabinet with the red apple on it. I prefer its green, yellow, pink, blue or orange sibling. I’ll get over it though. And sometimes I use that red one intentionally just to show it who’s boss.

Chemo will end and then radiation will be over in the flashiest of flashes. And that will be that. There I will stand, Emily Rome, breast cancer survivor, having completed almost the whole shebang (there’s the matter of being on Tamoxifen for five years and more reconstructive surgery later this year… but I’m not too fussed over that at the moment).

And what then? What will I do with myself once these treatments are over when thoughts regarding their effectiveness begin to fester?

That’s when it hit me. Why it is so hard to have or to have had a life threatening illness.

Anyone at any time can be walking down the street and be struck by a falling branch, felled by an undiagnosed congenital heart defect, hit by the proverbial bus. And although these things can happen, normally we don’t spend a whole heap of time worrying about these theoretical unknown causes of our death (unless we are of the unusually morbid persuasion). Because they are theoretical. And unknown.

But when you have something that you can name, it becomes this thing, this presence. Even if it isn’t going to get you, it follows you around like luggage.

Did you ever see the movie Ghostbusters? If you are American and you haven’t and you are over the age of thirty then you are a loser. Anyhow whatever your excuse I don’t care — go rent it right now and watch it. Oh — I like my popcorn buttered and salted, thanks.

You know the scene, after the dumbass EPA lawyer (William Atherton) has let all of the ghosts out of containment and all hell’s breaking loose and the end of the world is nigh. The Ghostbusters (Dan Aykroyd, Bill Murray, Harold Ramis and Ernie Hudson) are on top of 55 Central Park West and have been instructed by Gozer to choose a destructor (like, of the world). So Venkman (Bill Murray) orders the Ghostbusters to clear their heads and not think of anything so that the destructor can take no form. No sooner have the words left his lips, however, than Gozer announces that the choice has been made. It seems Ray (Dan Aykroyd) didn’t clear his mind at all but rather thought of something that couldn’t possibly harm them: to wit, the Stay Puft Marshmallow Man.

Oh humour me and watch THIS.  Don’t you just love the (Chinese?) subtitles?

Well then. All that was a rather clumsy, long-winded way of trying to explain that when you have a life-threatening illness, even though you might live until you are 99 or get hit by that bus at 25, the destructor has been named. It has been named and it’s in the room with you. Somewhere. Forever.

At times you won’t think of it at all. You’ll forget about it. Other times it will rear its ugly head and be all up in your grill. Big, scary and possibly wearing a sailor outfit.

Cancer is my Stay Puft Marshmallow Man.

But just because it has been named doesn’t mean it’s going to get me. Nope.

I know just what to do after school lets out and chemo and radiation are over and I’m just chilling with my new ultra-short hair-do, maybe on a beach in Cape Cod, if all goes well.

I’m going to have me a fuckin’ marshmallow roast to end all roasts. I like mine burnt to a crisp. I like to kill ’em before I eat ’em.

Now if you’ll excuse me. I’ve got to see a man about a beach bonfire permit.

 

Party Dress and Party Hair

I was thinking back today to my thirtieth birthday party in Manhattan. It seems like ages ago. Bill and I were working as M&A associates at large NY law firms at the time and we hadn’t any kids. We decided to have a small party in our 800 (on a good day) square foot apartment on 26th Street and Sixth Avenue. Back when the Chelsea Flea Market was just across the street, now long since displaced by another high-rise apartment building.

Here I sit ten years later, faced with trying to decide what to wear to my fortieth birthday party this evening (celebrated a week late so it wouldn’t be two days after chemo). For the past couple of days I have half-heartedly shopped for dresses but for some reason I just haven’t been in a shopping mood. I ain’t feeling it.

That doesn’t mean I’m not looking forward to my party. Au contraire. I am totally in a party mood. We are dining at an Italian restaurant (Zafferano) in Knightsbridge. We’ve hired the private dining room in the wine cellar for a small group.

Anyhow, in weighing my “hair” and dress options for tonight I couldn’t help but think back ten years ago to that thirtieth birthday. To a younger, different, cancer-free me. I love any excuse to dress up, so I took the long brunette extensions I had used for my wedding up-do (you realise that those Oscar-worthy do’s involve extensions don’t you? No one has that much hair…) and had a hairdresser create a high, slicked-back ponytail for the occasion.

I wore a knee-length beige, slightly see-through, ruched Diane Von Furstenberg dress with spaghetti straps. I might still have it somewhere. That and a groovy vintage gold-tone necklace from a secondhand shop on 23rd Street. I know I still have the extensions, but that concept wouldn’t work out so well at present, would it?

So what should I wear? An old dress or a new dress (and if new time is running out… the party is in fewer than four hours)? If old what will still look good? There are a number of dresses from before but I haven’t tested them all with my “interim set.” And what about the matter of my head? Do I go bald and beautiful or scarf it or maybe try the little black hat with a flower? Or should I bring Gabriella (read Cold Cap: From Rapunzel to Rambo if you don’t know Gabriella) as my second date?

Decisions, decisions. Whatever I choose I will let you know. I really need a killer ensemble.

Because I plan to party hard tonight.

 

Why I’m Lucky

Yeah, I know. This is a loaded title. There are just too many ways and too many things I can think of. But I am going to start with a couple of ideas and maybe soon there will need to be a part deux, trois and even quatre.

I am tolerating the Taxol pretty well. For you newcomers or those who just, ahem, haven’t been keeping up to speed (tsssk tsssk), that is the chemo drug that I am currently on. Sure, I have a couple of irritating little side effects, but nothing the honey badger can’t handle. One of them is zits (or as the English like to say, “spots” which is what I thought one found on a dalmatian). Yes. I broke out. Ridiculous. Hair loss, then a break out. My young and gorgeous gal pal and fellow survivor pointed out to me at lunch the other day that it’s like going through puberty in reverse. Throw in that I had to give up my boobs and that something else (if you catch my drift) hasn’t shown up in a while and she’s really got a point.

So I decided I didn’t need to be dealing with that bullshit (the pimples, people) and went straight to the dermatologist (okay full disclosure I also had some irritating little rashies developing on my hands and head… so it was a multi-purpose visit) who promptly put me on something to curtail that unwanted effect. It’s working. Part of feeling good is looking good, right? Balk if you will, but to me this is important. To the dermatologist too. Which is why I love her.

When you think about it, it is not at all surprising that one might erupt on the outside given what’s going on on the inside of one’s bod at the moment, no? No.

So what else? Bone pain. Not bad, just a little. Not enough for me to run out and buy the cane (read Countdown if this isn’t ringing a bell) but enough to remind me I have bones and they hurt. Just the legs so far. I don’t even need Tylenol (sorry Brits — Paracetamol). Just a little homeopathic stuff and I can deal. In fact I’ll pop one right now… excuse me. There.

And for some reason it hurts under my finger nails, especially my right thumb. I took off my fingernail polish yesterday to investigate and lo and behold there was some brown discolouration under there. I had read that this could happen. In fact your entire nail can fall off. (Ew!)

Oh — sorry. I am rambling and you are confused. This is where the “why I am lucky” part comes in, in case you were wondering what the hell the title was about since all I have done thus far is bitch about insignificant side effects. I’m getting there…

Today I visited the nail salon to get a polish change on my fingernails and a pedicure. I wanted to see if there was more brown discolouration under my toenails and get new polish on all the nails to strengthen and protect them. I do a lot with my hands (cook, mow the lawn (really), give my kids a bath, you name it), so it is pretty annoying to feel weakness and vulnerability in that area.

So I was chatting to the aesthetician about all of this when I noticed a woman watching me and slowly approaching. Call her Greta. I would say she was about sixty-five. Short white hair, blue eyes, one eye completely dilated. Attractive.

Turns out she was a fellow breast cancer survivor and had heard me talking about it.

She was about six months out from treatment, having gone through a mastectomy, chemotherapy and radiotherapy. But unlike me, she did not have an easy breezy time of it. She ended up in the hospital for three weeks during chemo because her white blood cell count didn’t rise as it should have despite her having had immune booster shots (as I do) after every treatment. Her right eye was dilated because she had developed a serious infection in that eye and they were now watching it closely — the outcome unclear. She had a prosthetic breast and hadn’t had a reconstruction because her body couldn’t tolerate it after chemo. She had had a hell of a time. But there she was, out and about, standing before me. Dealing. And she was lovely.

She was also both empathetic and encouraging, without any preachiness or gloom, unlike previous “mentors” I may have unwittingly had (see Assaulted at the Global Festival: Things Not to Say to a Cancer Patient for that story). She didn’t tell me how I was going to feel or prescribe anything except courage, basically. I really liked her. I hope I see here there again.

She made me feel like I am having a cake walk. Just an inconvenience. Just a few months out of my year so that I can kill this piece of crap and get on with my life, thank you very much.

I’m not Job, sitting on that dung heap. No sir. I’ve had way too easy a time of it.

I’m lucky.

Party in the Chemo Suite

I’m coming to you live from the chemo suite, people. So inspired am I.

Today there are a lot of drawn curtains (lame — I like to spy on my fellow sufferers and make faces at them) and someone is hacking up a lung (makes you want to run out and get a big juicy steak, doesn’t it, and eat it off the floor). Unacceptable. What this place needs is a couppla disco balls. Maybe a conga line. The choreography might get a little complicated with all of us on a drip, which hangs from this metal coat rack thingy on wheels, but it’s nothing me and Paula Abdul couldn’t work around.

My blood work came back and I am — naturally — good to go.  White blood cells up from my immune booster that I jab into my stomach the day after every treatment. Actually I kind of enjoy that. I should have been a nurse (well I do share a birthday with Florence Nightingale and that’s about all we have in common) or maybe a torturer.

Now they are pumping me full of steroids and then antihistamine (like Benadryl) and anti tummy upset and lots of sodium chloride mixed in to flush the line, all to ward off any unpleasant reaction to the Taxol. A lot of people are allergic to Taxol, which is derived from the Pacific yew, by the way. Did you think that everything “natural” was good for you? Don’t be a dumbass. What about poisonous mushrooms? One bite and you’re dead.

I don’t care for the Benadryl. Although it doesn’t put me to sleep (this is because I am defective and cannot nap during the day no matter what they do to me), it makes me a little sluggish, so I am chugging a flat white (I described this in What I Wore To Chemo Today so you had better catch UP), which my awesome friend Paige brought me from Gail’s, my fave coffee shop and bakery. I am also chugging tea. It’s England so everyone drinks tea constantly — it’s really true. And water. This makes for a lot of trips to the loo wheeling my coat rack to and fro. But it’s good to take in fluids. Flush the system. Stretch the legs. Sashay around in my absurd outfit.

Ooh goody. My machine is beeping. That means the bag of sodium chloride is empty and it will soon be time for the poison. Linda, Uma, Katniss? Get ready, girls. Get your gold cuffs and your Hattori Hanzo and your bow and arrows because we’re gonna fire it up, beeyotches.  (Read Chicks I Dig Vol. 1 if this makes no sense to you).

Speaking of artillery, does anyone know where I can get me one of those long leather (nylon would do as well) belts with bullets in it so that I could incorporate that into my outfit? Can you get that shit on Amazon?

So the stuff is going in now, slowly over three hours. I thought I just had a tinge of metal mouth, which I did not experience two weeks ago. It is one of my least favourite side effects so I am plenty pissed off about it. These things can be cumulative. But I ate my lunch and that tasted fine, so maybe I am imagining it. Grr.

My bum is falling asleep. I need to do some gluteal clenches while I’m sitting here. One… two… three…….. Might as well multitask. And this really is the ideal environment for that. I mean, what else can you do? Sit here and think about cancer? Bo-ring. So I write and I talk incessantly when there is someone to listen, and I visualise the chicks I dig doing violence to any remaining cancer cell.

I imagine one trying to flee from Uma’s sword. Nowhere to run, nowhere to hide, MF. You have met your maker and she happens to be hot. Hot and lethal, that’s a great combination. Oh, sorry, she just eradicated your ass, as lickety-split as she plucked that eyeball out of Elle Driver (Daryl Hannah’s character in Kill Bill), the other eye having been plucked out by Pai Mei, who trained both Driver and Kiddo in martial arts the likes of which I could really get into. It was kind of mean when Kiddo then stepped on the eye-ball and squished it. But I respect that decision.

This is Elle Driver when she is about to try to inject a comatose Beatrix Kiddo with some red shit to kill her for good. I would pluck someone’s eyeball out too if they were standing over me with red shit. That looks just like chemo medicine numero uno, which was that same colour and some really naaaaaaaasty stuff.

On a separate note, Hannah is killing the ole one-eye look, dontcha think? Let’s hope that’s a look I don’t have to rock, but given my retina’s tendency to misbehave I have had to wear the occasional eye patch after a procedure. If it ever happens again I’m going to commission a Louis Vuitton eye patch with my initials on it. Not really, but it would be hilarious to see the salesperson’s reaction. All horrified yet awkwardly trying to be polite, as I stand there looking earnest amidst a sea of shoppers who just want the latest Neverfull. But I digress… blame it on the Benadryl or the chemo or whatever. Though Florence Nightingale did say “I attribute my success to this — I never gave or took any excuse.” So just blame ME. I don’t care.

Three hours after the Taxol drip started I’m outta there. Now I’m back home.

So do you want to see today’s outfit? Come on, do ya? I’m afraid it was not possible to top the last one but I made a valiant effort.

I know, the pic isn’t great quality but I was pretty far away from the computer so deal with it. I like to think of this look as Coco Chanel meets sixties biker chick (the boots have buckles and zip up the back). Badass from the neck down but sort of classy from the neck up. Classy badass. It’s the new thing. My fabulous new French buddy lent me the cute black hat. It has that je ne sais quoi, non? The flower is one of my recent acquisitions from H&M. You don’t have to pay Chanel prices, dear.

Well, now that I have killed it for the sixth time I have to make my meds chart so I don’t do the wrong thing. I have so many pills and fluids in me you could shake me and I’d rattle and slosh. But I am doing fine.

Because today I am one step closer to putting this puppy to bed.

I’ll leave you with one more quote from Florence Nightingale: “How very little can be done under the spirit of fear.” A lot, however, can be done under the spirit of KILLING IT.

So take that, MF.

 

Writer’s Block

It has occurred to me that at some point I may get writer’s block. In fact, it is almost a sure thing. How could I not at some point struggle with what to write on this blog or how to write it?

I was thinking about that yesterday. Then I considered that, provided I stay on schedule, only one month from today I will receive my last chemotherapy treatment. After which I will have five weeks of radiation, five days a week, which should prove anticlimactic comparatively (from what I have heard). More on that later.

I thought, dang, what if I have nothing interesting to write after chemo is over? No more interesting chemo ensembles (see What I Wore To Chemo Today)… No more entertaining other patients in the chemo suite with my antics and bad behaviour (oh I forgot to tell you that the last time I was there this one dude kept coming up to me and telling me he was really feeling my outfit and he was there with his wife, who was the patient!  Shameless!)… No more bizarre, unexpected “side effects of the week” (more on that later too)…

I mean, every time I gear up for and go to chemo I am inspired to write something. There is a ton about it I haven’t even told you yet and I still have three treatments left. It’s just excellent fodder for the blog. So it will be a real shame when it is all over. Not. Chemo sucks. But I won’t be too hard on it since it is killing the hell out of anything floating around in there that doesn’t belong.

I suppose when I do radiation I can still yell “die, motherfuckers,” and imagine my heroines (see Chicks I Dig Vol. 1) going in there with their signature weapons and obliterating any microscopic cells that dare to remain near the original site of the tumours. (That and cross my fingers that the radiation doesn’t burn my skin too badly and otherwise complicate the final stages of my reconstruction, because in the end I would really like a nice “set” out of all of this nonsense.)

I just don’t want my posts to become boring. Or predictable.

When my hair grows back I won’t be able to write about being bald anymore and all of the interesting things that go with that particular side effect. Or take anymore badass “I’m bald and I’m killing it” pictures. But I suppose I will have been there and done that, so maybe that’s not the worst thing. I mean how many times can I take a picture of my bald self looking pissed off and post it and think “I really like what I’ve done here.” (A lot actually — you should try it sometime it is pretty great.)

Who knows where all this will take me. I just hope that you’ll continue to tag along. I need you. I want you. I have to have you.

Speaking of which where are you right now? Are you in the US or the UK? Kenya or Kuwait? Why do you read this? Do you know me? Did you once? Is or was someone in your life touched by cancer? Are you a survivor? Are you just curious? Tell me… I’ll be right here. Killing it.

Why Sometimes I Let Myself Go There

For some reason whenever I ride the tube in London I get introspective. Especially if I am alone, quietly observing the other passengers as the cars clickety-clack along. There is something about sitting there without speaking that makes me wonder what other people are thinking.

Today I needed to take my younger daughter to a birthday party in Northwest London and, being at a friend’s house about an hour away in Southwest London, we had quite a journey ahead of us. For about the first nine stops there were no seats and Charlotte and I stood side by side, holding hands. When I am standing I feel more powerful and imposing, because I am relatively tall. I don’t wonder so much what anyone around me might be thinking. But when I sit down and shrink to everyone else’s size, I start to feel a little vulnerable.

When we made our switch there was one seat available and I told Charlotte to take it. The man next to her looked at me and offered me his seat. I happily accepted and thanked him. I wasn’t sure if he gave it up so that I could sit next to my young child, or because he knew I was a cancer patient.

I started to think about how I perceive myself versus how others perceive me. Do I look like a cancer patient even when I don’t feel like one? And how about when I do? When I am tired and have dark circles under my eyes do people notice? Do I make them feel sad? Or disgusted? Today, did that man look at the five-year-old child by my side and pity her? Did he wonder if she would have a mother in a year or two? Did he think that it was unfair for such a young child to have a mother like me?

These thoughts violated my mind in rapid succession as the train hurtled toward Bond Street, where we would get off and meet my husband. He had finished work for the day and had agreed to take Charlotte the rest of the way to the party, shortening my journey and enabling him to spend some time with her.

We found him on the platform. I handed her off and gave him a quick peck. Then the next train came and they were gone. I started toward the exit (“way out” we call it here). I paused. My hand felt conspicuously empty. I looked at it. Reminded myself that I was no longer holding Charlotte’s hand, that I had relinquished her and the bag containing the birthday present, card and directions to the party to Bill. She was safe. She was okay.

I walked up the short flight of stairs and rode the long escalator up. Stopped in an inexpensive store to study a collection of clip-on flowers for my head scarves. I bought three. Felt a little bit better. Then I emerged from Bond Street Station and looked up Oxford Street. A light drizzle spattered my parka, which I had hoped by now would be stored until next winter. I looked toward Selfridges department store, looming across the street with its grand facade and its flags. Glitzy retail beckoning. But I didn’t want it. Not today.

I crossed the street. H&M was right there. More my speed. Cheap. Almost disposable. I walked in and was assaulted by pop music, whatever sweet perfume they were pushing and brightly coloured sequined tops and tropical-print bikinis. I found the accessories and selected more flowers. I had now amassed a bouquet, but wasn’t ready to leave.

I surveyed the store and picked up an inappropriately short colour-blocked mini skirt and a gauzy leaf-print beach cover-up. There was a long line at the fitting room. I bought everything without trying on. Screw it.

Pure unadulterated retail therapy. Cheap retail. Maybe the best kind and the purest form.

My mood lifted. I’m killing it again, I thought, picturing myself striding out of the house in that striped miniskirt with black combat boots and a black beaded flower perched on the side of my head.

This was one of those days. When I let myself go there. I let myself think about the fact that I have a life-threatening illness. About what it could mean. About what it has meant for others before me. But then I pull myself back. I was just visiting. I won’t linger. I will not. It won’t be me.

It’s okay for me to visit. I never stay long. But then I know that I am really dealing with this and it isn’t all for show. Not just a brave facade. Not just for you. I know what could be. And have chosen to reject it.

Because I’m killing it. Fuck you, cancer.

Night Off

I decided to take the night off and not do a post.

My husband was supposed to fly to the US for a partners’ retreat in Washington DC but he got some new deal and had to cancel his trip and spend all day in the office. Bummer. Meanwhile plans were already made for the girls and me to spend the long weekend (this Monday is a bank holiday in Britain) at his law partner’s house in Southwest London.

The real reason the plan was put in place, of course, was so that his lovely wife could babysit me in case I had some unforeseen medical emergency and keeled over while Bill was away — which was clearly not going to happen. But still, a weekend in someone else’s house sounded pretty good. No cooking, no cleaning and a little adventure in a new location. Oh, and built-in entertainment for my two girls in the form of twin eight-year-old boys. Thus avoiding another grey Saturday with no plans filled with “Mommy… Mommy… Mommy!!!!!!!!!!!”

Anyhow I’m taking the night off. I thought about doing a post, since I have pretty much done one every day since I started this blog. And I feel a little bit guilty and self-indulgent about this decision, really. I don’t want to let anyone down. But the truth is that doing a post every day is quite tiring. Some days I do something short and quippy and it seems to flow out of my fingers like molten lava, taking only an hour or so. But the heavier posts, such as Breast Cancer for Dummies Part I and Part Deux, took a hell of a long time and were mentally draining to write. I’m starting to get sleep deprived and I am a cancer patient for Christ’s sake!

So, tonight we are lounging on sofas and watching The Voice UK and Britain’s Got Talent. The cheese factor is extreme on both, which really hits the spot. And I’m having a peppermint tea and some oatmeal raisin biscuits with my “cheese.”

I guess that means you get the night off too. But don’t abandon me, because I’ll be back tomorrow. Bonne nuit

 

 

 

How To Tell Your Children That You Have Breast Cancer

One of the hardest things my husband and I have had to do since all of this started, and indeed, ever in our lives, is to sit down and tell our young children that I had breast cancer.

We waited until a few days after my diagnosis before we let on that anything was going on. This was very difficult, because during those initial days leading up to and following the diagnosis I was on the phone so much that I was constantly tiptoeing around the house, shutting myself in rooms and hunching over the receiver trying to arrange doctors appointments, get my pathology slides FedExed to London from the US and other delightful logistical nonsense. All while pretending to be same ole Mommy.

The “you have cancer” call came the evening of the girls’ first day back at school after Christmas holidays, January 3. That was a Tuesday. Bill and I decided that we would tell the kids that weekend so that we could (a) have time to figure out how to do it, (b) procrastinate it for a few days for mental health reasons, and (c) keep a close eye on the girls over the weekend in case they seemed anxious or upset following the big talk.

As I think back to that time, which seems like ages ago but in fact was not so long ago at all, I can tell you right now that my thinking was not nearly as clear as it is currently. I was still reeling from the news, as was Bill, and I really wasn’t sure how to go about telling the kids. What was clear from the get-go, however, and what we both agreed, was that we would tell them. We never considered otherwise.

Let me give you some background.

Our girls, who were seven and four at the time, are no slouches. They are smart and perceptive. The first-born is fairly high-strung and a bit of a worrier, which I consider to be unsurprising for a first child. The little one is more laid back but highly sensitive and empathetic and seems to notice everything around her even when you think she is not paying attention.

Some people hinted that given their ages, the kids, particularly the “baby,” wouldn’t really “get it.” That they wouldn’t understand what was going on and the whole thing would just wash over them. Whenever I fielded a comment such as this I tried to let it slide, fighting that honey badger instinct to tell the well-meaning yet misguided person, pardon my French, that that was a load of bullshit. No one knows your own children the way you do. Trust your instincts.

So, we set the date. We would tell them on Saturday morning after breakfast so that they would be fed and comfortable and then we would have the whole rest of the day and the next day to watch them, let the news percolate and evaluate the fallout.

In preparation, I did a little bit of internet research on some cancer websites. I watched a video about a woman telling her kids she had breast cancer. That particular video involved two children with a large age gap (one was a teenager), so the mother decided to tell the kids separately because they would have different levels of understanding and different emotional needs. I thought that was an excellent point, though it didn’t apply to our children. We would be telling them together.

Then, at one of my doctors appointments, I was given a book about talking to young children about early stage breast cancer entitled Mummy’s Lump. It goes very briefly through the mother finding a lump in her breast, going to the doctor and being told the lump is bad and is breast cancer, and the mother having surgery to remove the lump, then chemotherapy and radiation. At the end, the family is pictured on the beach and the mom is in the water, her hair having grown back, playing with one of the kids. Short and sweet.

I flipped through it and decided that it wasn’t half bad and would use it as a prop to guide my discussion. Now that I reread it, four months later and with some perspective, I actually think that it is pretty well done, considering the topic. Here’s why:

(1) It uses the word “cancer.” Using the c-word allows YOU, the parent, to contextualize the disease for your children, who may have terrifying associations with the word (or may develop them if you fail to contextualize it and they later hear or see something) if they have heard or seen something about it, say on TV or from a classmate.

(2) It explains that the cancer is not contagious, and that it is not the children’s fault (or anyone’s, indeed) that it occurred.

(3) It depicts the mom in a nice hospital room with flowers and chocolates (hey, these things are important!).

(4) It briefly outlines the treatments and explains that such treatments might make the mom feel poorly but that they will ultimately help (kill it!) and then she will feel better.

Now, there is no one perfect book for everyone. For instance, it appears to me that this particular book was written about someone having a lumpectomy rather than a double mastectomy with several reconstruction surgeries ahead. This doesn’t matter. You can pick and choose what you want from this or another book and fill in the rest.

When we told our kids about my cancer, it was very early in the process and we did not know what treatment I would be having. Nevertheless, we talked about chemo and radiation to help prepare the kids in the event I needed those treatments. We decided not to wait until we had a clearer picture of what was going to happen because the slinking around the house was getting old fast and Bill and I both knew that the kids would start to figure out something was wrong. Not telling them when we did, in our view, would have been insensitive and disrespectful.

Here is what I did not find in the book, and my own two cents, having thought about these issues and discussed them with a preschool educator whom I highly respect:

(1) Do not lie, but at the same time do not reveal to your young child any anxieties you have about dying. Your child wants to know that he or she will be cared for and that you will be around to do that. Sharing your own thoughts regarding this could produce a great deal of anxiety in a small child.

Let me qualify (1) above by saying that I am not giving any advice about later stage cancers or circumstances in which it is known that a parent is not likely to recover. I am focused here on early stage breast cancer, for which there is a good recovery rate. I am also not talking about discussing these matters with older children, which is a different ball game altogether and something that I haven’t had to think about.

(2) Explain to your children that it is all right to feel sad or upset about the cancer (and all it entails), and that it is okay to ask you questions about it. When we talked to our children, we told them that they should feel free to talk about the cancer and to ask me any questions they had about it, at any time. Of course, this has come back to bite me in all sorts of hilarious ways — but that is fodder for a separate blog on the funny things children say, which I promise to do in the near future.

I found that if I talked regularly (and joked, frequently) about my cancer with the children, it became less of a scary thing. I sprinkled it into conversations here and there, and it became the new (temporary — because I’m killing it) normal. Taboo isn’t good when it comes to something like this. Respect your child and allow them to hear about, process and talk about the issue. Then it might be a little less scary.

(3) Find someone at your child’s school (teachers, guidance counsellor, etc.) who is a safe person to talk to for your child and reach out to them to make sure they are keeping an eye on your child. Let your child know that they can go talk to this person about the cancer if they want to, but don’t force the issue. I know that my seven-year-old doesn’t talk about it at school. School is a safe haven for her where she doesn’t have to talk or think about my cancer. But she knows she can and whom she can go to if she ever wants to.

So how did it go? Well, I’d have to say really pretty well. The older child looked a bit stricken and went silent for a while. She had heard the word cancer before and definitely had some associations with it so I was happy to leap in and contextualize it for her as a disease that can be beaten. The younger child seemed to focus on the chemotherapy and the fact that I might lose my hair. She didn’t like that one bit and kept asking me (every day practically) if I would need “the medicine that would make my hair fall out.” Well if you have read my post “Cold Cap: From Rapunzel to Rambo,” you know that in the end she decided that bald wasn’t so bad. So for her it was all just a matter of easing into the idea.

What you don’t discuss can become very scary. Like the boogeyman. What you do discuss, however, you control to a certain extent. You can contextualize it. You can mock it. You can rock it. You can KILL IT.

You certainly can’t control everything, but feeling some control here is a very very good thing. Trust me.

 

Vag Toupee

WARNING: If you are a prude this is not the post for you. Take a deep breath and click on the following link, which will guide you to a topic equally fuzzy but more appropriate to your delicate sensibilities: http://www.dailypets.co.uk/.

Okay. Have we weeded out all the nice nellies? Good. Onward.

When I found out I was going to need chemotherapy earlier this year, a lot of jokes came to mind about losing hair in all sorts of places. Losing it on your head is obvious, of course, and people who haven’t been touched by chemotherapy (or alopecia caused by something else, such as an autoimmune disorder) might not stop to consider that there is a great deal more hair on the average (particularly adult) human body than on the head.

Most chemo patients I have spoken to or read about have lost at least some of their eyebrows and eyelashes in addition to the hair on their heads during treatment. And many have joked about no longer needing to shave or wax their legs or underarms in order to optimise appearances in the latest jort or halter top (both of which most people shouldn’t be wearing anyway — ah-hem — whether or not they are currently featured in InStyle Magazine).

I started to consider the possibilities. This could be a good thing, I thought. After years of unsatisfactorily bleaching the brunette peach fuzz on my upper lip, which frankly resulted only in a blonde moustache that caught the sunlight just so, I might be able to cut down my personal grooming efforts by a sizeable chunk every week.

Yessir. Goodbye as well to plucking those pesky industrial-strength eyebrows that once threatened (they’ve given up a little after years of maintenance, sigh) to weave my two prominent arches into something resembling Bert on Sesame Street or the actor, Peter Gallagher.

But what else? Ah yes. The bikini area.

Although initial thoughts of losing my hair “down there” made me cringe, because I don’t fancy resembling a prepubescent girl, it didn’t take me long to find humour in the situation.

“Well,” I joked with my very best friends who were already intimately acquainted with my raunchy self, “if the pubes go I can always just get a ‘vag toupee.'” I laughed at my own joke and started to come up with alternative names for such a prosthesis (although vag toupee is kind of my fave). “I could call it a ‘vig,’ after ‘vag wig,'” I quipped. Peals of laughter. “And if you would rather not have hair but you want something down there you could bedazzle your area and have ‘vling!'” (Umm, that’s “vag bling” for our octogenarian readers).

Little did I know, I was not original. Not even a little bit. That’s right; it turns out the vag toupee has been around for a very very very long time. I mean longer than chemotherapy. Longer than America has been independent. Seriously!

And this brings me to a brief history of the vag toupee, a/k/a the merkin.

The Oxford Companion to the Body dates the use of a merkin, or pubic wig, back to the mid 1400s! Back in the day, women used to shave their pubic hair to ward off crabs. Prostitutes would take it all off to hide evidence of sexually transmitted diseases. In both such cases, a pubic wig was employed in order to hide the evidence and make their goods look, well, good.

But wait, that’s not all!

Today, merkins are used by fetishists and drag queens (everything else on a drag queen is false so why not the muff). In addition, Hollywood employs merkins all the time to cover up inappropriate pubic hair styles (for example, if the movie takes place in the 1950s and the actress has a Brazilian, which is not true to the period), to make an actress’s cuffs match her collar (e.g. The Girl with the Dragon Tattoo) and perhaps most often, to conceal the labia so that a film doesn’t get the dreaded NC-17 rating, which is somewhat lethal to wide cinematic distribution.

Sort of ridiculous, by the way, that a man can have his hog out in a film and it doesn’t warrant an NC-17 rating, but God forbid a labium creeps onto the corner of the screen and everyone runs for cover. Puh-lease, people. But that’s a blog for another writer. I am not here to protest inequalities between the sexes. After all, men can get boob cancer too!

Total aside — if you have ever seen Last Tango in Paris, that was not a merkin. That was a real bush. It is no wonder the poor actress who played that role was so screwed up after that movie. If zillions of people had seen my vag fro looking like that I would have been screwed up too. Actually I don’t think I could even attempt that look without a dozen merkins, or at least some pube extensions. Just sayin’…

The long and short of it (tee hee) is, I got an unexpected education on the subject of the vag toupee when I started to poke around there (tee hee hee — sorry I couldn’t help it). And when you think about it, the merkin really is a clever little device.

But I am sorry. The word merkin is completely unacceptable. I don’t care what the origin is, and from what I have read it may be a variant of the word malkin, meaning “mop.” See http://www.etymonline.com/index.php?term=merkin.

Vag toupee is much better.  🙂