The Lie

This is one of the most sincere things I have ever written about myself. I am at a point in my life where I feel comfortable about sharing it, and for my closest friends this will be the first time you hear it. It’s a  story I was afraid to tell, but I hope it can serve a purpose now. This is the last post I will be writing.

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In life, there are times when the floor drops from beneath you.

Four years ago I asked if I could leave drawing class early to go to a doctor’s appointment. My instructor at the time asked me if everything was OK, to which I reassured, “Of course, I’m fine, it’s probably not a big deal.”

One hour later I was diagnosed with Takayasu’s Arteritis.

My mother and father were in the room, and I was shivering on the table, wearing a hideous hypoallergenic bag over my body. The specialist we had been sent to see, a cardiac surgeon, told us that there was no mistaking the diagnosis – it was a “textbook” case. And in such a tremendous moment in the lives of my parents and I, he was darkly fascinated.

“I’ve actually never seen a live case before, it’s so rare,” he said. Meanwhile, my father looked into his hands. My mother gripped the armrests of the chair as if she was about to shake it. I was furious. How could this young, hotshot surgeon do this to my parents? “Tell them it’s not a big deal,” I begged in my mind. “Please, just tell them that I can handle it. They don’t understand. Honestly…neither do I.”

I was nineteen years old and a freshman in college. Nothing felt wrong. I was just starting to find my footing, make new friends, and understand what living independently was like. It would all be wiped away.

I had to immediately start treatment and make time to take more tests. We were recommended a cardiologist, a rheumatologist, and secondary hematologist on the spot; rationed a handful of business cards and a dab of pity on top. I remember sitting in the car with my parents after the appointment, all three of us just stuck there in the parking lot, the snow falling steadily around us.

My mom got home and researched online feverishly. My father stood silently behind and watched her search. She looked into the disease, the online support groups, the best specialists. While she was reassured by the internet, I refused to look. To me it seemed a Pandora’s Box that I didn’t want to open. All I knew was that I was going to have to face whatever was about to come my way.

I can’t begin to describe the physical and psychological battle that ensued.  In order to slow the progression of this rare type of heart disease, I was prescribed a very high dose of steroids for about a year. The medication caused Cushing’s Syndrome, which had a toxic effect on my body. My face became completely rounded and I got acne. My back developed a painful hump. I gained 15 pounds. Into my legs, thighs and abdomen were carved huge, ugly stretch marks that would never heal. My hair thinned and fell out. I was tired and in pain. My body was falling apart day by day.

Because of how different I looked, I hid myself away at school. Every time someone stared at me on the bus, I was ashamed. Every time I ran into one of the new friends I made, I disappeared within myself. I ate quickly and alone in the corner of the cafeteria, afraid to look past my tray. I remember passing through entire days just looking at the cement of the sidewalk, avoiding questioning glances. One of the worst things was waking up every morning and facing the mirror with the hollow hope that it was all a bad dream.

Nightmares wove in and out of my conscious mind. I woke up from the anesthesia during a surgical test and watched the doctors finish their procedure on me. I passed by my reflection and could not recognize my own face in the mirror. Soon I forgot what I used to look like altogether. My identity slipped further away the more I looked into the face that wasn’t mine, the more I walked around in a body that I had never known. When I could be alone, I sobbed until my chest hurt and I couldn’t breathe. I cried enough for a lifetime.

What hurt me the most, though, was what this was doing to the people I loved most in life. I couldn’t prevent my mother from waking up in the middle of the night in terror, and I couldn’t stop my father from feeling guilty. When I asked my younger sister, “Does my face look that bad today?” I couldn’t stop her heart from sinking.

With all of this happening I made the choice to stay in school, and though it was one of the worst semesters I had completed grade-wise, it set the standard for how I was going to continue living. Just like that, the year I was 19 vanished, but I wasn’t going to let anything else be taken from me.

So I did the strongest thing I could do: I smiled.

I tore my gaze away from the sidewalk. I took deep breaths, looked straight ahead and walked without shame. With my swollen, ugly face I went to concerts. I made fun of myself in front of my friends. I devoted myself to studying. I showed my parents that I had enough strength for all of us. I eventually came off the harsh medication and for many months I focused on recovering. Slowly, my mom worried a little less, my father started telling jokes again, and in my sister’s expressive eyes I saw the reflection of happiness return.

Years later, I am here in Korea.

And I am here because of a lie.

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My pen hovered over that part of the application for a while.

“Known Illnesses/Diseases?”

“Medication?”

With pages and pages of paperwork spread out on the surface of the desk, my pen cast a thin shadow over those two little questions. Finally, the shadow twitched, and I wrote something that I am not proud of.

I made up my mind to teach in Korea shortly after my teacher and good friend recommended it during my junior year of college. I was immediately interested in the idea, researching the various programs, offers, and companies all offering a way for me to live and work abroad. It took a while for my parents to accept how determined I was to live abroad for a year, but with my health at a stable point and the doctor’s approval, they didn’t want to hold me back.

It was a long and arduous process getting all the paperwork together. Notarizations, those damned apostilles, my FBI Background Check getting rejected and returned; precious documents all stapled together with the anxiety that I would get found out and sent back before I even started. My fears stemmed from accounts of people getting rejected from the program for health issues as trivial as migraines. While researching I was also made aware of Korea’s social prejudice against those who are not in perfect health. With a complicated-sounding condition lumped into the category of heart disease, it would have been impossibly difficult to convince a recruiter that I was as healthy and functional as everyone else.

So I passed over the hurdles cautiously, one by one – the application, the paperwork, the TEFL courses, the interviews. On top of the normal anxiety of living abroad for a year, I was constantly afraid I would get pulled out of the program during orientation. Before leaving, I prepared with my doctor a note that described the nature of my condition and that it wouldn’t affect my job performance, just in case I needed a bargaining chip to stay. I was also aware that I would need to undergo a health check, but there was no certainty over what kinds of tests they would run or what they would look for.

Another problem I ran into was getting the medication I needed overseas. I was using a medication that needed to be refrigerated, and I had no idea how I was going to keep it cool. I managed to take a few months worth of it onto the plane with a prescription note and clearance, but when I got to the airport in Korea I was scared that someone would misunderstand, pull me aside and charge me for something. I bought some ice at a convenience store in the airport with my new Korean money and replaced it in the pack. I crammed onto the bus with other confused EPIK-ers, not knowing where I was headed or how long it would take before I could buy more ice.

All during orientation I bought cups of ice, frozen popsicles, and cans of energy drinks from the CU to keep the medication cool. Then, close to the end of orientation, the day of the health check arrived.

I was stricken when one of my friends came back and told me what the health check entailed: I had to take a chest x-ray. This was the same test that had been used to diagnose me back when it all started, so I was mentally preparing to pack up my bags and go back home then and there.

But, by some miracle, I passed the health exam.

After that, I got placed at a great school with amazing teachers, in a nicely-sized apartment just a few steps away. I made it.

One incredible (and healthy!) year later, this faulty little heart of mine is still pouring out gratitude.

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I haven’t written this to tell you it’s OK to lie on a job application.

I have written this to tell you that there is nothing holding you back in this world.

Go to a country you’ve only seen in pictures and breathe in its air. Squint against the sunrise of an unfamiliar horizon. Chase after something. Teach. Learn.

Live.

I will never find the identity I lost four years ago, but in its stead is a new one; one that I have made with my two hands, that others have strengthened with their kindness and support and love. It is the identity of a woman who is confident, bright, recklessly optimistic, and so, so happy.

In a way, through spending this year abroad I wanted to test myself; to prove that I could do it. In a way, I wanted to escape all semblance of the life that told me “You can’t.” Even if it was only for a year, I wanted to put far behind me the memories of struggle and self-defeat.

I wanted to be unstoppable…and I was.

To everyone who has read my blog this year, thank you. It’s been a dream that’s ended much too soon. Thank you for your comments and encouragement. Thank you for listening. As I start my new life in Chicago (law school, after all!), I will no longer write here, but this blog will always be here to those who want to relive this crazy amazing year with me, all over again.

My sketchbook didn’t exactly get filled this year, but my heart did.

I guess I’m addicted to fresh starts after all.

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