Skip to main content

Limits

This has been the semester of realizing I have limits. Here's how it has gone down, in dialogue form:

Me: This semester is going to be so great! I'm feeling on top of the world right now. Nothing's going to stop me!
CF: Oh, you think you can go to Passion 2013, get very little sleep, skip treatments, and then NOT need IVs? False.
Me: Whatever, I can handle doing IV antibiotics while starting a new semester. No big deal. Passion was the absolute best thing for me to do this Christmas break.
CF: Handle this nausea with the IVs, why don't you?
Me: No problem.
CF: Oh, you think you can balance Sing practice, school, work, church, friends, phi lamb, and CF? Let's see how you handle the flu.
Me: Okay, that one was rough. But it's okay, God helped me through.
CF: You're STILL trying to do everything like a normal person? What's wrong with you? Maybe severe anemia will make you realize your limits.
Me: I'll drop Sing and start taking iron supplements.
CF: Ha, you think you're going to make it through the semester without another problem, but you're not. Let's throw a lung infection into the mix!
Me: Maybe I can wait until the end of the semester to start IVs...
CF: Yeah, right!
Me: Fine, I'll start IVs.
CF: And the lung exacerbation wouldn't be complete without nausea, a lung bleed, and a few port problems.
Me: (silence)
CF: Ha! Who's winning in the fight now?
Me: Me. Because no matter what happens, my God has never left my side. But maybe I can't handle everything I thought I could.
CF:...

I can't do it all, and I'm slowly realizing this as I get older. My body simply isn't capable of running 120 mph, even though I'd like it to. I'm not a normal college student. I have very real physical limits that I must acknowledge or else I'm going to run myself into the ground.

The good news? I am not trying to balance all aspects of life on my own. My God will never leave me. I love the verse in Psalms that says, "My flesh and my heart may fail, but God is the strength of my heart and my portion forever." Amen and amen. Even as I am realizing I can't do everything I'd like to, God is pointing me in the direction I should go and the opportunities in which I should invest my time. I am not having to figure out these aspects of my life on my own. Thank goodness, because my life would definitely be in shambles if I had to navigate my limits on my own!
However, I do need to learn to recognize what I can and cannot manage in my life. I like to stay busy, but busyness is good only to an extent. I can't sacrifice my health, my spiritual walk, or my fellowship time with friends. Acknowledging my limitations is definitely a work in progress.

Comments

Popular posts from this blog

CF Letter 2020

Dear friends and family, It's May 2020, which means it is another CF Awareness month and another time to talk about all the amazing things happening in the CF world! This has been a very good year in the CF community. In October of 2019, Trikafta was approved by the FDA for all people with CF with at least one copy of the dF508 mutation. 90% of people with CF have at least one copy of this specific mutation. This is a HUGE deal in the CF community because it is one of a handful of drugs that addresses the underlying cause of CF and the only drug that such a huge percentage of people with CF can take. Trikafta is a total game-changer for so many, including me. I have gained stability, I require fewer IV antibiotics, I gained lung function I thought was long gone, and I feel like I can plan things in my life again. The hard work of the CF Foundation, willing researchers who continue to search for a cure and medicines that will increase quality of life, and the generous donations fr

CF Letter 2019

Dear friends and family, I hope you all are having a happy and healthy 2019! The Great Strides CF Walk is just around the corner, and we are gearing up for a great walk day! Since my last CF Walk letter, my health has had its ups and downs. Just before the CF walk last year, I got the sickest I have been in awhile and had to fight off pneumonia with the help of 4 weeks of IVs. I also had to do IV antibiotics in August and November. However, I have stayed relatively healthy in 2019, and for that, I am extremely grateful! Although I’ve had to fight off 2 colds, my body has been able to get through it without needing IV antibiotics. While I know I will need another round of IVs eventually, I am thoroughly enjoying being IV free. I credit this to the amazing CF therapies available to me, my compliance to my treatments, and all of your prayers for my health. I continue to take 30+ pills a day including enzymes to digest my food, vitamins and supplements that my body cannot absorb

The spirit of giving

It’s the end of 2017. That means it’s time to send in those end of year donations. Want to give to some amazing charities actually doing good in the world? I’ve compiled a list for you!  The Cystic Fibrosis Foundation- Obviously, I’m biased toward CFF. They fund amazing research that is saving people’s lives! Don’t you want to be part of that? Not only that, but 90 cents of every dollar goes directly to advocacy and CF research. If you donate to the Cystic Fibrosis Foundation, you know your money is going to be spent wisely and is going to make a difference. Since cystic fibrosis is an orphan disease (that means it’s really, really rare), people with CF rely on your donations to fund research. As well, Congress just cut the orphan drug tax credit, meaning companies are not going to get as much incentive for studying orphan diseases and creating drugs to treat them. The CF Foundation needs people like you to donate to CF research so we can find a cure for CF SOON. —www.cff.org