Skip to main content

Quote day

It's quote day on my blog today! Enjoy the quotes below along with my comments about how the quote touches my life. 
Outward beauty will fade. I don't care if you're Miss America or the highest paid model on the runway. Our physical bodies are wasting away. No exceptions. Sorry to burst your bubble.  Five, ten, even  twenty years from now, will people see beauty pouring from you by the way you live your life and through the confidence you have in your identity in Christ? Or will they simply remember a pretty face? 

The world we live in is constantly changing. When we think we've found some solid footing, an earthquake shakes through our lives, and we fall flat on our faces. I personally NEED the assurance from God that He is my rock and my foundation. With Him, my solid ground will not be shaken; I will not sink. "On Christ the solid rock I stand, all other ground is sinking sand."

Loving God and loving people are what we are called to do. All of our actions should be driven by these two commands. This year, I am working on loving ALL people the way Christ does. I want people to see my Father through the way I love. 

My house will always serve the Lord!!

I love the power of language. It is the way we communicate, the way we persuade, the way we discuss ideas, the way we explain, the way we understand others. Language is no ordinary ability--it truly is remarkable. Don't take advantage of your linguistic abilities. They are more useful than you probably realize.

Life for me is about more than just getting through the day. I want to be challlenged by my friends and family members to live a life of influence. I want to grow in spiritual ad emotional maturity on a consistent basis. I want to dream big dreams for the future, all the while putting my faith in God's timing and will for my life. Yeah, I have cystic fibrosis. And yeah, my life looks different than the average young adult's life. I have to think about making my energy last throughout the day, staying away from germs, taking care of my health needs, doing breathing treatments, and sometimes making difficult decisions I'd rather not be faced with. "But, I have bigger dreams than just breathing." 







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