Food, tasty with a side of shame and guilt

Trigger warning: Discussion of food and disordered eating.

When was the last time that you ate something without thinking about it? And by that I mean, when was the last time you ate something without weighing the positive and negative consequences that that food stuff may have on your body? When was the last time you ate a chocolate chip cookie without playing mathematical gymnastics as you count the calories you’ve consumed for the day minus the calories you’ve expended?

For me, I can’t even remember.

JK Rowling

I don’t know when it was that food became laden with guilt, shame, and turned into a complete mathematical nightmare. But I imagine it was probably around the same time that I hit puberty and realized that I was much bigger than most of my classmates. I don’t mean bigger in that I was chubbier or obese, but I was quite literally the tallest kid (male or female) in any class. My friends could still fit into children’s wear and I was shopping at women’s stores.

It was probably also around the time that I was swimming. I started competitive swimming around the same age and spent 8 to 10 hours a week in a pool. I also spent 8 to 10 hours a week with girls whose bodies had barely any body fat. The other girls walked around the pool deck on their toothpick legs, thighs never rubbing together in the humidity (they had what we now call the thigh gap), without a towel covering their non-existent cellulite.

Watching these lithe swimmers was the beginning of when I stopped thinking of food as nourishment. Food was not something to make my body stronger or make me swim better. And it definitely wasn’t something that I could enjoy without consequence.

SupermodelsMy obsession with food became worse when I decided that I wanted to be a model. I had been watching Fashion Television with Jeanne Bekker since I was 6. I watched Naomi, Cindy, Christy, and Claudia prance down runways wearing clothes that I didn’t understand but loved. I made my Barbies imitate these glamazons and made my sister play Supermodel with me. My love for fashion and supermodels, coupled with the fact that when I hit puberty people kept telling me I should be a model (I guess because I am tall?) wanting to be a model seemed like a natural decision.

What I learned very quickly was that being tall wasn’t enough to be a model. Agencies were looking for a tall girl with a unique face who had very precise measurements; measurements I didn’t have. However, the agency woman who had sized me up (literally, she had taken a tape measure to me) assured me that if I stuck to a healthy regimen and worked out (they didn’t want unhealthy girls here, oh no!) that I could probably be a model.

That summer I spent carb-less, counting and weighing all of my food, and working out like a maniac. I ate my 1/2 cup of All Bran Buds with my low-fat yogurt cup and kept my hunger pangs at bay throughout the day with countless cups of coffee (it wasn’t like it was going to stunt my growth), diet coke, and if I was too dizzy juice. At dinner I ate very small portions of whatever my mom cooked, minus whatever carbohydrate she would put on the table. I returned to the agency in the fall with the exact measurements I was missing 2 months earlier.

At 5’10” I weighed 115 lbs. I was cold all of the time. I was ravenously hungry. But the agency said I could be a model, so it was totally worth it.

As you can imagine, this eating regimen couldn’t last forever. Despite fasting during the day, when I got home from school, I couldn’t stop myself from raiding the pantry. I would shove spoonfuls of peanut butter into my mouth while crunching down on chocolate chip cookies. I would eat ice cream directly from the tub while crumbs of chips were on the front of my shirt. I would eat until I felt sick. And it wasn’t just at my own house that this would happen. I used to babysit for a family across the street and as soon as the kids were in bed, I would snack on whatever they had in the house. To this day I think they had a nanny cam and stopped letting me babysit once they saw me shoving my face with all of their food.

I was binge eating, without the purging. As you can imagine, this eating pattern made me slowly start putting weight back on. I would measure myself and was seeing myself grow in the process. I hadn’t booked any real modelling work and told my mom, “I don’t want to be a model anymore. I’m too hungry.” And that was the end of my career.

Unfortunately, it was just the start of a pattern of disordered eating that follows me to this day. I am currently the heaviest I have ever been, mainly because of the anti-psychotic Seroquel. It causes cravings for carbohydrates. It overrides the brain’s “I’m full” sensor and wreaks havoc on my metabolism. It also makes it incredibly difficult to lose weight. Some days I am embarrassed by my current body while other times I just don’t give a fuck. Except no matter how I feel about my body, I still feel the same way about food; it’s the enemy.

salad

Seriously this was the best salad ever.

As I get older, I’m slowly trying to approach food in a different way but my disordered eating is deeply embedded in who I am. I am trying to value food as either good or bad based only on its relation to my health. Eating a beautiful salad is preferable to a bacon cheeseburger with fries because the nutrients in the salad actually fulfill dietary needs. The cheeseburger fills a craving or laziness because I didn’t prepare my lunch. However, even as I eat a salad filled with healthy items like avocados, berries, quinoa, arugula, and feta cheese — I wonder, wouldn’t it be better if I just didn’t eat? I still value skipping a meal over nourishing my body. And that makes me incredibly sad.

It makes me even sadder because I know there are countless other women and men who think just like me. There are many other people who are so embarrassed by their bodies that they almost kill themselves trying to attain an unobtainable goal — like that pesky thigh gap. I am lucky that I do not have a full blown eating disorder because they take lives.

But, I would like to be able to eat a damn chocolate chip cookie without wondering how many calories are in it.

My breakup letter to alcohol

Dear Alcohol,

You and I have had some fun times. Wino Wednesday with my best friends, which almost never really fell on a Wednesday but seemed to funnier to name it. Numerous pints on patios with colleagues after work to blow off steam. I’ve enjoyed you at whiskey tastings and wine pairings; there was this particularly amazing one in San Francisco where someone had the amazing idea to pair you with chocolate. I have shared incredible bottles of amarone with my partner over fancy home cooked meals that were better than anything we could get in a restaurant.

Despite all of these great times, there have been countless others where you have caused me, and those I love, shame and embarrassment.

Me & my friend E. during Halloween at Bishop's University -- beers in hand.

Me & my friend E. during Halloween at Bishop’s University — beers in hand. I was 17 in this photo.

Let’s rewind to first-year university where I ended up in the university “drunk tank” too many times that I started giving fake names to avoid mandatory alcohol abuse meetings. There was that sleepover in grade 11 when I passed out after consuming countless jello shots and Peach Schnapps (the drink of choice for any well respected high school girl) after a particularly cruel boyfriend broke up with my via e-mail. I collapsed mid speech about how all men were bastards and “we were all fucking fabulous!”

Or what about that time the same wino Wednesday ladies and I got so bombed during a birthday dinner that a taxi wouldn’t take us home. We had to wander until we (me) sobered up. Oh and what about that work party that colleagues had to call my parents to come and get me because I was puking in the bathroom? Or, even more embarrassing, almost five years ago when my grandfather suddenly passed away and I got blackout drunk after his funeral in front of family and friends. My husband and parents had to put me to bed.

Now a lot of this behaviour most people would chalk up to youth and sheer stupidity, and I would agree. A lot of these stories happened when I was between 16 and 21. This was before I learned about tolerance and when to trade you for water. But there are still these moments (more than I wish to admit), even at 29, where I get so drunk I’m puking in a bathroom or waking up with a wicked hangover trying to piece together what happened the night before.

I have been so open and honest in this blog — more honest than in “real” life — that I sometimes find it frightening how much the public knows about me and my struggles. But this is one thing that I haven’t addressed. It’s a secret that I’m even afraid to admit myself. It is the last card that I hold to my chest.

I self medicate with you, alcohol. And I particularly abuse you when my mental illness is triggered. This means that I am either floundering in depression or enjoying the high tide of hypomania.

10400495_539304528140_3669_n

A family photo from my convocation. That’s me in the middle row on the far right and my grandfather is on the left of my sister who is in the middle.

Let’s use my grandfather’s death as an example. I loved that man more than anything. He was taken from me in a flash, a month before I got married. I have so many incredible memories of me and him from when I was a child and just seeing a picture of him now still brings me to tears. Hearing a Johnny Cash song brings a swell of emotions so strong that I often have to stop and remind myself to breathe. I found a book of poetry by Robert Service and had to buy it just because it reminded me of him. I have become Scrooge at Christmas because, to me, he was the embodiment of all the Christmas-spirit. He used to have Christmas Tree parties where everyone bundled up and cut down fresh trees and then the house would be filled with 20 to 30 people as they celebrated the holiday season. He would always be there on my own birthday (December 18). His birthday was December 31st and he always said he was born to party.

This New Year’s Eve I drank gin martinis just trying to get through it, and ended up where I usually do with you when I’m that upset, puking in some bushes.

Many of these moments where I’m drunk, stumbling, and puking correlate to a moment where I was feeling like utter shit. Despite the infinite number of therapists I have seen over the years, I struggle to vocalize and identify negative feelings and dealing with them. It’s just easier to drink until I’m numb.

Do I think I’m an alcoholic? Absolutely not. I don’t drink to function. I don’t drink every day or even every week. I can easily go months without touching a glass. However, what bothers me is that when I do choose to drink it’s always over the top. It can never be a glass of wine, it has to be several. It’s never one pint, it’s five. I have no sense of moderation. This is part of my personality and my bipolar disorder. I have an extreme personality and I either go in 110% or I don’t do it at all.

With my recent bipolar instability I have realized that consuming you, alcohol, just isn’t an option. Every time I touch a glass of something, I risk becoming drunk. Besides, I know you fuck up my mood. Plus, with the amount of medication that I take, I know you’re not great for my liver. And, any bipolar expert will tell you that you’re a big no-no. I mean, it says it right on the bottles of pills I take, but for the past 10 years I have ignored the warnings in an attempt to fit in, in an attempt to numb the way I feel.

So alcohol, you and I are taking a break. I don’t want to say it’s a break up because I don’t want to put that pressure on myself. But those pints on patios will be few and far between, I’m glad I live far away from my two best friends because Wino Wednesdays are no longer a thing, and those beautiful bottles of wine will almost never happen.

I might see you again in the future, but right now you need to go.

Rage & love: A glimpse into a bipolar relationship

“Are you mad at me?” He asks from the sofa. I’m standing in the kitchen about to start dinner, and our dishes from lunch are still sitting in the sink.

“No, I’m not mad. Why would I be mad?” I’m doing that stereotypical female thing that, as a feminist, I hate so much. I hate being that trope of a wife. But the fuse in me is lit and it’s short.

“You sound mad…”

Boom!

Explosion

“Well I guess it’s up to me to do all these fucking dishes and make dinner!” I scream, throwing the dishes into the sink. Rage possesses me like a demon. It’s like there’s a little voice inside of me shouting at me to shut up, telling me that my anger at him is irrational, and brought on by the hypomania but it’s fighting a losing battle. I am the demon’s bitch. I don’t have control over my words or limbs.

“Well that’s unfair,” he says, joining me in the kitchen. “I was just going to check something quick on the computer and then I thought we’d cook together. I wasn’t leaving you to do all of this on your own. You know I wouldn’t do that.”

Of course I know that. For a moment the little voice inside of me has beaten the demon down. “I’m sorry, I’m sorry,” I say clutching my head, as if holding my head between my hands will somehow keep the demon at bay. “That was totally irrational.”

“It’s okay, you’re not feeling well.” He tries to rub my back, but I feel myself shirk back. I try and mask my aversion to his touch by grabbing a head of broccoli out of the fridge, I reach for a cutting board, and a knife.

Bear

He’s right. I’ve been hypomanic for about 2 weeks and the rage is an indication that it’s about to break. I had felt a murderous pressure in my chest all day.I could have ripped the face off a bear. I scowled at anyone who looked at me the wrong (or right) way. It didn’t matter what was said or how someone smiled or even how they complimented my outfit. Everyone was out to get me. Everyone was an idiot. Everyone was in my way. Everyone was just so fucking slow.

The demon is back with a vengeance as I recall my day. Why can’t everyone just do what I want them to do at the speed and capacity that I want them to do it? I wonder, savagely attacking the head of broccoli like it has murdered my puppy. Like, why doesn’t my husband know that he should be fucking washing these dishes right now while I prep dinner? It’s all part of the plan so that we eat by 7 p.m. Why can’t he just see the fucking plan? Why can no one ever see the fucking plan?

“You know,” I say turning and pointing the knife at him. “You should just fucking leave me.” The words come out of my mouth like a flood. They come out before I even think of them because I don’t control them. “You’d be better off without me. Actually, everyone would be better off with out me.”

He takes the knife from my hand and places it on the counter away from my reach. He’s not afraid for his life, but he’s afraid of what I might do to myself.  But I’m not threatening suicide. I truly believe that he would be better off with a partner who wasn’t bipolar. I believe my parents would be better without a bipolar daughter. I know my employer would be better off without a bipolar employee. My existence is just a fucking disaster for everyone.

I have this sickness that turns our lives upside down. I have this sickness that makes me dependent on him in so many ways. He is my support system. He comes to doctors appointments with me. He worries about whether or not this will be the episode when I kill myself. He has been working on his thesis while picking up the slack at home. He does groceries when I cannot handle the people. He cooks. He cleans. He does all of those things that we would normally split because I have been mired in this sickness.

“I have some fucking audacity to be angry with you for not helping out. These past 6 months have been all you taking care of me and the house. Aren’t you tired of babysitting your wife? Fuck I’m such a mess and here I am, angry at you over some fucking dishes. You should just leave me before you just end up resenting me.”

He is crying now. But I’m not sure why. I’m giving him this out that so many men in relationships much worse than ours would beg for. I’m giving him permission to leave me; to be free of me and this illness. I often wonder whether he’s a masochist because the reality that he could actually love me this much is currently beyond my understanding.

The rage has now left me, as if I have gone through an exorcism. Now we can talk through the issues. I explain how guilty I feel. How sorry I am for yelling, for the sickness, and for everything I have ever put him through. And he tells me that he never feels like a babysitter because he loves me. He loves me and all my flaws. He has stayed with me this long and is not going to leave me, ever. I am stuck with him, not vice versa.

And then we fall back into our regular routine. He washes the dishes as I finish preparing dinner. But we both know that this isn’t the end. This won’t be the last time. But we take the calm as it comes.

That thing you can understand

Here’s what I’ve decided: People generally get depression. By that I mean, they understand what it’s like to feel sad and self-loathing. They get the feeling of being helpless. They may not understand the complexities and nuances or how hard it is to do simple tasks like brush your teeth. But they get the general sentiment about what it feels like to be depressed.

People also generally get anxiety. We all experience anxiety to a certain extent. It’s like that moment before a test or the big game. Perhaps you’re waiting for news and you can’t sit still. Although anxiety is 100 times more complex than that the literal how it feels people are able to get.

What people don’t get are the other aspects of mental illnesses. They don’t know what it’s like to have hallucinations — auditory or visual — they don’t know what it’s like to be manic. These are experiences beyond the human spectrum of understanding; unless you live with someone who is Schizophrenic or Bipolar or you have Schizophrenia or Bipolar.

I could explain all day what it feels like to be hypomanic — it feels like I’m constantly late for something. It feels like I’ve forgotten something important. My skin is crawling and I want to rip it off. It feels like there are ants in my brain. I’m twitchy like a tweaker in need of a hit. I’m paranoid as fuck. I ramble about things that I think sound profound, but really sound illogical and dumb. My voice is too loud, words tumbling out too fast. But at the same time, I am hyper focused and aware. You need that project done — it’s getting done, like TODAY!

But this, all this energy. It could be gone tomorrow. And I’ll be a pile of depression — that thing you can all understand.

Is it so much to just want to feel normal?

Orphan Black

The clones from Orphan Black, which admittedly i have been watching and probably why I asked this question.

“If there was a clone version of me, would you be able to differentiate between me and the clone? Like could you tell that it wasn’t the original? This troubles me. I think if there was a clone version of you, I’d totally know that it wasn’t you. It would say something and I’d be like, bam, you’re not Shane you’re a replicate. What’d you do to my husband?”

We were sitting in a small examination room with walls that reminded me of The Yellow Wallpaper. In a few steps, I could walk the length of the room and if I stretched I could touch it wall to wall.

Alice in WonderlandMy husband, who is 6’4, looked gigantic in this tiny room and sitting in an even smaller chair. It was straight out of Alice’s Adventures in Wonderland and he ate the mushroom that made him grow ten feet tall.

Meanwhile, I feel like a caged animal as I pace back and forth and ramble about clones.

“I would know it’s not you because the clone wouldn’t ask me questions like this.” He looks at me and laughs and I laugh too. Was it inappropriate? Was it too loud? I have no control over the volume of my voice.

In these situations where I’m in the grips of my mental illness — in this instance deep in hypomania — my husband has the ability to bring levity to the situation while also keeping me calm.

“Why haven’t we seen the doctor yet?” I asked. We had been waiting in the walk-in clinic for 3 hours. My doctor was working at the walk-in clinic today so I had to spend the long wait in the waiting room with people who are physically ill. I will probably contract some virus from them in the coming days. So that when I finally come down from my hypomania, I will be depressed and sick. I considered putting on one of those masks they give you if you have a cough, but I didn’t want to look crazy. “What if she’s taking so long because she’s calling the hospital thinking that I need to be admitted?”

“That’s a paranoid thought Marisa,” Shane reminds me gently. Logically, I know he’s right. That’s not how the system works. Hypomania overrides all logic and, for me at least, brings in paranoia.

“It’s the waiting, it’s getting to me.” I keep scratching my arms like I’m tweaking. We’ve been here for what seems like forever and I’m about ready to tear my skin off. I can’t sit still. I’m sure the pacing is driving him nuts.

I poke my head out of the room and I can see my doctor on the phone. She’s speaking french. I have to listen hard to understand her because her voice is lowered, and for some reason when I’m hypomanic, understanding french is more difficult. She’s definitely not talking about me.

After 40 minutes of waiting in the Yellow Wallpaper room, my doctor finally comes in to see me. This is the second time I’ve seen her this week. The first was when the hypomania started.

“Ça va mieux Marisa? Are you doing better?” Although she knows I’m an anglophone she speaks in both languages. It’s sort of endearing. We speak in a mixture of French and English. Something that only really happens in Montreal.

“No, I’m not doing any better. It’s getting worse actually.” I try and speak in short succinct sentences because I know that if I talk too much, the words will come out in a loud flood. Hypomanic speech embarrassing. As someone who already speaks fast when I’m healthy, my hypomanic speech is a flood of words that don’t always make sense.

“Oh ma pauvre.” She looks at my husband. “I feel really sorry for your wife. Ce n’est pas facile ça. It’s not easy.”

“So what do we do now?” I ask.

She writes me a script for 1 mg of lorazepam that i’m to take twice daily, plus an extra 50 mg of Seroquel that I’m to take at lunchtime and then at night I take 200 mg of Seroquel. My insurance company is also demanding another note from her with a consultation report.

“I do not think you should start working full-time yet. I want you to go back to 3 days per week.”

“No!” I shout at her. My tone and volume startles her. “No, no, no. I’m not taking steps backwards from going back to work because of this. No. It’s not happening.” I’m shaking my head and pulling my hair back in anxiety.

“But they’re going to ask why if I saw you and you are hypomanic, why are we going to stay the course? Tu comprends?”

“Okay, well I already started at 4 days a week this week. I don’t want to go back to 3 days a week.”

“Okay, so I write that you remain on 4 days a week because of the hypomania. Does that work?”

“I guess…” I’m sitting on the examination table and I kick my legs back and forth like a child. I feel like a loser because of this. Why are my moods cycling so much? Why can’t I just return to work like I wanted to? Nothing ever works out the way I want it to.

“Doctor,” my husband speaks up. He’s been mostly silent during this appointment letting me speak for myself, except when I ask for his observations. He’s a good man. “I’m concerned by the frequency that her moods have been cycling. We’ve had a mixed episode a few weeks ago, depression a few weeks before that, and now this. Should her medications be reevaluated?”

“Je comprend, mais je suis pas psychiatre. I’m not a psychiatrist. Maybe I refer your wife to one.”

I wonder if I look as dejected as I feel.as I stare at my husband. He knows how much I hate psychiatrists. I’ve had so many bad experiences. But ultimately, my doctor is a GP and doesn’t have the expertise to deal with Bipolar Disorder. Perhaps it’s time to bite the bullet and go and see one.

We left the office with a medical consultation report for my insurance company, a referral to the agency that can refer me to a psychiatrist, and more anxiety than I know what to do with.

I call my therapist, who was once a psychiatrist back in Europe but is non-practicing in Quebec, and explain everything that has happened, Once I’ve stopped talking she finally says, “Well you could present yourself to the ER at the Douglas to ensure you see a psychiatrist there. They have a good team that I trust.”

My stomach drops. That’s the last thing I want. I don’t want to be hospitalized. “Isn’t there another way?”

It turns out, at the Douglas Institute that specializes in psychiatry and is more advanced in the way that they treat people, the only way to see one of their psychiatrists is to admit yourself into the ER. The admission into the ER could result in a hospitalization, which would completely ruin my back to work plan. My husband and I discuss this and decide that my fear of hospitalization is greater than my fear of dealing with hypomania.

Right now, I can at least channel my hypomania. I work with it. It’s not pleasant, but I can mold it into useful energy to get shit done. I work out. I socialize. I clean the house.

Hypomania is wrapped up in productivity, which makes me appear normal and ultimately that’s all I really want — to appear normal.