Thursday, July 2, 2015

Best Day EVER!

I've been in a funk - a very funky funk. But today, the first genetic therapy drug for my mutation of cystic fibrosis was approved, and I think I've broken free.

Never before have I experienced such nauseating, debilitating anxiety as I have these past two weeks. I cannot name the root of my nerves, and believe me, I wish I could. It feels impossible to fix yourself when you don't know why you're broken. But today, I felt as if I was slapped in the face by the mane of a unicorn made out of gummy bears. 

Guys . . . Orkambi is here.

We'll skip over the complicated scientific explanation of what Orkambi will do for roughly 8,500 Americans (those with the double delta F508 mutation who are over the age of 12) and get right to the good stuff. In clinical trials, patients taking Orkambi gained 3% lung function over time. This may not seem like a lot, but it is important to understand that cystic fibrosis is a progressive disease. This means that it only gets worse. Any improvement at all is, quite literally, a contradiction of the disease itself! And while some patients did not see any lung improvement, they saw a significantly slower decline. On top of that, patients in the trial had an easier time keeping weight on, which significantly aids to lung function as well.

Right now, people with CF are skydiving without parachutes - once the disease hits its breaking point (and this happens at a different age for everybody), our plummets are fast and unavoidable. Orkambi is our parachute. Orkambi can slow us down. Orkambi can save us.

Now, I won't pretend that Orkambi has worked/will work for everyone. Different people react . . . well, differently. But the results are there. The science is there. And where there is hope, there is life. Dum spiro spero. 

I just want to take this moment to thank everyone for their support. I want to thank you (yes, you!), the human who is reading this sentence. Together, we bought this drug. When the government refused to help us, we payed the scientists to do their jobs. We gritted our teeth and went door-to-door. We sold t-shirts, baked goods, and purple ribbons. We walked mile after mile, year after year, shouting to anyone who would listen that someday, CF would stand for "Cure Found." And no, this is not a cure. But it's the closest thing to a cure that any of us has ever seen, and that is something worth celebrating. 

Saturday, June 27, 2015

My Anxiety: Part One

I frequently worry, and I have for a long time. The physical manifestation of these worries can be observed by those who choose to be observant. Just a few weeks ago, a bus driver in Chicago locked onto my eyes as I hesitantly disembarked - Don't be nervous, honey, she said to me. But how couldn't I be?
  • I was travelling alone. I had a train to catch. I was running low on money.
  • My stop had either come and gone or had yet to come at all, but I wasn't sure which.
  • People were staring at my clothes. People were staring at my luggage. People were.
Of course I was nervous, and of course she could tell. When the world around me crumbles, idiosyncratic breadcrumbs fall behind my feet. Visually, it is quickened breath, teary eyes, bouncing knees, a clenched jaw, and hands that fly from fists to jazz hands and back again. Metaphorically, it is a plea for help.

Since puberty, panic has been Plan A. Though I strive to present myself as a rather self-sufficient young adult, the word "overwhelmed" is one I use often when on the phone with my mother. For years, my life has grown more and more into a puzzle that I cannot put together, and when I can't find a piece, I cry. I pull my hair, I hyperventilate, and I shout to whomever can hear me that I need them. 

I saw a counselor from the end of 9th grade to the beginning of 12th. My grandpa's battle with Alzheimer's had been growing more gory, as had mine with cystic fibrosis. Like any other heterosexual girl of my age, I was in love with a boy who didn't seem to notice me, and a very close friend of mine was diagnosed with severe anorexia. I was unhappy. That same close friend recommended her counselor to me, and I went, spending over $100 of my parents' paycheck every week to snottily sob on a beige loveseat.

Growing up with a life-threatening illness, I was (and am) a faithful believer in medicine. After more than two years, I was diagnosed with nothing, and since I wasn't any better and my meltdowns were only growing more frequent, I stopped going.

The triggers of my anxiety are patterned; I break when I feel lost, unloved, or judged. Unarguably, however, the most debilitating panic attacks stem from my feelings of failure. This is the anxiety that rips into my relationships. This is the anxiety that one social worker noticed. This is the anxiety that diagnosed me with Anxiety.

Tonight, I begin the healing process. Tonight, I swallow a little green pill before bed and lose myself in a packet entitled "Free/Low-Cost Counseling Services in Ann Arbor." But then again, I hate to be lost.

Saturday, June 20, 2015

Sixty-Five Roses

            I didn’t know that was going to be the last day. I swear I didn’t know. If I had known, I would’ve baked oatmeal raisin cookies instead of buying chocolate chip. I would’ve worn the earrings she liked—the ones that looked like little turtles. I would’ve brought a game she actually enjoyed playing. But I didn’t know, and I didn’t bake or wear or bring, and that was the day Rose died.
***
            “Took you long enough!” she yelled. I rubbed my hands with sanitizer upon entering room 223, trying not smirk at the way her voice cracked when she was irritated. Florescent overhead lighting mimicked noon in the worst possible way.
            “Oh, be quiet. It’s eight in the morning, you brat.”  A shiver seized the hair on the back of my neck as I adjusted the thermostat. There was no point in asking if she wanted a blanket—she didn’t. My eyes brushed her bones, knowing that drum-tight, moon-colored skin was the normality of her condition. Her blue lips fused into a firm line as she adjusted her oxygen cannula, then her floppy sunhat, which she insisted on wearing year-round.
“What’d you bring me?” she asked.
"I'll tell you what I should've brought you—nothing.” Rose laughed in reaction, mucus bubbling in the back of her throat. “Hey, can you even see with that thing on?”
            "Obviously. Not that there’s much to see here, anyway," she said. And she was right. With rounded furniture in varying shades of gray and a third story view of sidewalk cracks and bus station smokers, blindness seemed like a tumor worth trading for. Out came the cookies and the deck of cards.
            "Seriously? We played Uno yesterday," Rose said, not at all trying to conceal her disappointment. I constantly eyed the growing dullness of her corn stalk hair and wondered whether she was actually swallowing the pills I placed next to her milk. But when it came to what she was feeling, there was no guesswork involved. Methodically, I took off my coat, tossed it onto the empty recliner, and sat at the foot of the bed.
            "Well, Uno is a classic. And the classics are classics for a reason,” I replied, shuffling.
            “That’s what my dad says about his music.” I paused for a moment to watch her. Her freckles hid in response to January snow, clashing with the perennial power of her eyes. Her port dressing was coming loose, barely visible above the neckline of her t-shirt.
            “When was the last time you talked to your dad, Rose?” Now it was her turn to pause.
            “Last night.”
            “And what did he say?”
            “Nothing. Just the usual stuff.” She was growing more and more annoyed, her gaze refusing to set from my fingers and the cards.
            “Is he coming to see you, soon?”
            “Deb, does it matter?” Her eyebrows blew together and furrowed. “He’s too busy with work. Besides, you’re way more fun. And you’re a nurse. If I was dying, you would know how to save me.” She pushed her bangs behind her ears and I could see tiny dewdrops shimmering on her forehead.
            “Why would you say something like that?” I asked.
            “Because it’s true.” A cough rattled from within her ribs, proof that disease had rooted itself in a place neither of us could reach.
            “Here—we’ll start with more cards this time. It’s harder, but it’s also more fun.” Rose’s nostrils flared as I passed her seven Uno cards and straightened the deck between us. She froze, staring at her purpling fingernails.
            “You won’t stop coming, will you, Deb?”
            “Well, considering how often you tease me, I should.” I dug a finger into her side and a single, scratchy laugh was uprooted from behind her teeth. “But, no. I’ll always come. Life would be far too boring without you.”
            “Ugh. Stop mushing out on me and play.” She picked up a chocolate chip cookie, bit into it, and grimaced. “You know,” she said, chewing, “these taste like shit.”
***
            I often look back on that day and consider the things I could’ve done to give myself more time with her. I ask myself if the meticulous lip-liner was worth it—if my sedan really needed to be washed. They called it “Rose’s Celebration of Life,” but that’s not at all what it was. Or at least that’s not what it turned out to be. I withdrew into my skin, safe and unchanged, and peeked: thirty people in a dim room they could barely afford, listening to a man preach about a god they didn’t believe in, weeping over the loss of a girl they never paid attention to.