Skip to main content

New semester

The beginning of a new semester is at hand. People are still excited about their classes, professors are getting used to new dynamics, and you see smiling faces everywhere. Of course, all of this changes as the semester goes on and students get frazzled, worried, and sleep-deprived. But the inevitable semester slump hasn't hit yet--we're just getting started! 

Like most people, I enjoy starting off a new semester. I am excited about my classes (This semester, they are all either related to speech pathology or linguistics, which is fantastic since I am very interested in those things). I take (too much) joy in writing assignments and activities down in my planner. I even like getting all of my books and skimming through them to get an idea about the class. 

However, I also like finishing a class. I love the feeling of accomplishment I get when I see the reward of hard work and studying. I am thrilled when I feel I understand the content I was supposed to learn. I love adding knowledge to my brain's toolbox of information! 

I am looking forward to this semester, including the beginning, middle, and end of it. I cannot wait to learn new information, experience new things, and grow in my friendships. I know that God is leading me day by day, and He is fully trustworthy. I will not be one of those people dragging through when they reach the end of the semester--I will go every step with my head held high and my eyes on my Savior. 

"Rejoice always, pray without ceasing, give thanks in all circumstances; for this is the will of God in Christ Jesus for you."--1 Thessalonians 5:16-18. 

Comments

Popular posts from this blog

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 ...

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...

Traveling abroad

In May, I will be going on a mission trip with my church to the UK. I'm so excited to be a part of this mission team!! I know that God is going to work in and through us for His glory. However, I can't say I'm not nervous about taking care of all my health stuff while I'm over there. This will be my first international trip without my parents and first time to fly with all my medical equipment by myself. Even when my band flew to Seattle in high school, my mom was a chaperone and helped me check baggage, go through security and lug all my equipment around. This time, I'll have to manage all of that on my own (of course, the other team members will be with me, but I'll be the only one intricately connected to my CF and who actually knows what all I have to bring with me on the trip). On top of that, when we went to Europe for my make a wish trip, my Vest and compressor "burned up" due tonthe voltage difference, even though we used the power converter li...