Showing posts with label dream. Show all posts
Showing posts with label dream. Show all posts

Friday, July 24, 2015

Since Coming to College . . .

. . . I've learned not to place my happiness on the shoulders of those around me.
It took hours of sleeplessness, tears, and phone calls to my mother, but I have finally realized that putting the entirety of my emotional health into someone else's hands ends up being detrimental to both parties. This habit is one which I developed halfway through high school.  The silver lining? The fact that I developed it at all was because there was a very special person in my life at the time who was willing to carry me through the peaks and troughs of 16, 17, 18, and 19. But, as Chinua Achebe wrote, "things fall apart." During that age of heavy maturing, I realized that my happiness was at the mercy of someone who wasn't me, and why would that ever be something to desire? Now, as long as I have myself, I'm okay - and I'm very thankful to the person who taught me that, however painful it was for both of us.

. . . "cystic fibrosis" is no longer abstract.
Since the fifth grade, I've been admitted to the hospital two times a year. That was my routine, and as much as recurring lung infection can "work" for a person, it worked for me. Now, after watching my health decline more significantly and more quickly during these past 11 months than it ever has before, I've come to understand why the median life expectancy of someone as mutated as me is 37-years-old. Never in my life have I been able to imagine myself as an old lady, but I've never been able to imagine myself dying young, either. When I pondered the demise of my existence, it was always fuzzy. At the hand of my freshman year of college, with its loneliness and excitement and independence and busyness, there is a port permanently in my chest. Health insurance companies are knocking on my parents' door every day to collect bills I never used to acquire. I can no longer run up a flight of stairs (though I'm working on it). My health is now at a very tricky stage, and I'm forced to face that if I let myself go, today, I'd plummet. If I ignored my pills and physical therapy, I'd plummet. If I stopped exercising, I'd plummet. If I chose to stop fighting for my life, right now, there is a very big chance that I could begin to die. This is something I'm thinking about for the first time, but now that I am, I'm choosing to win. Now I CAN imagine myself dying young, but that's the only place where that scene will play: in my imagination.

. . . sandwiches have replaced cereal as my official "lazy meal."
Milk expires quickly. I don't have time to keep buying milk.

. . . I've stopped waiting.
There's something magical about saying "When I grow up . . . " with stars in our eyes. It elicits the idea that the future is a place of more possibility, luck, and motivation. Operating with the future in mind, we - naturally, as humans - become complacent. There's always tomorrow. There's always tomorrow, tomorrow, tomorrow. But what if I don't want to grow up? What if my best friend revealed that my most sunshine-y quality is the fact that I am childlike? If I never grow up, where is my magical future where dreams are possible and motivation floods my blood? Well, I know I'm still (barely) a teenager, but I think it's here. I want to read and write and make videos and help people and spread awareness for cystic fibrosis, and I want to do those things seriously. Professionally. I'm never growing up, so I'm never going to receive a message from the universe that reads "Do it now." Why would I wait until graduation day to begin chasing my passions? To begin helping people? I wouldn't, so I'm not. And let me tell you, there are big, big things on the horizon.

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. 

Sunday, November 3, 2013

What is College?

I haven't blogged in a while...

I'm gonna work on that.

Promise. :)

So, where to start. Since my last post, all of my attention has basically been on college applications. I won't post my number one (mainly because I don't want to jinx anything) but it's elite and super hard to get into and expensive and blahhh. But, I'm in love with it: I've visited twice, and I know with everything I have that it's the place where I would be happy. It's just stressful, because even though I take all honors and AP classes at school, my GPA really isn't that high. Missing a lot of school really takes its toll on your grades. I'm hoping that admissions counselors will be able to look past my marks and realize that I'm at least a little bright--I have an okay ACT score and I'm really proud of my essays, so we'll see what happens. I only have one more school to apply to (by Friday) and then I will have applied to four schools. Those results will be ready before Christmas, and if I don't get into any of my top four, I'll send out another batch of applications to slightly easier schools by January 1st.

Other than applications, I've been doing a lot of writing, a lot of homework, and a lot of coughing. Band is STILL GOING ON because our football team has been kicking butt, which I like as a senior but dislike as someone who's basically allergic to fall. Spending so much time in the cold and the rain has got me pretty sick, at the moment. I'm not sure if I'll schedule an appointment at the clinic tomorrow or not--the marking period just ended at school and I missed all of last week, so I really really need to get back in the classroom. Too many decisions. I wish someone would just make them for me.

All of this craziness with college and CF has just made me get really stressed, and I'm just not feeling happy. And after weighing my priorities, I've decided that after my health, my happiness should come first. Writing makes me happy. Or, at least, a little calmer. That's why I'm rededicating myself to this blog, my poems and stories, and I'm going to try to start journaling. (We'll see how that goes!) Other than that, I'm just going to pray pray PRAY that the admissions counselors at my dream school are impressed by my application. I wish they could meet me . . . it's hard to imagine that my entire being could be correctly and seamlessly transposed on a piece of paper.