Skip to main content

Hidden Treasure

I apologize for not blogging for several days now. I've been very busy! That's college life for you, I suppose.

This past weekend was parents' weekend at Baylor. My whole family came to Waco, which was loads of fun. I enjoyed having my family in my home away from home because I got to show them why I l love living here. I believe that God has placed me in Waco at this time in my life for a specific purpose, and while I'm here, I will make the most of every opportunity I'm given, including the opportunity to explore and discover a new city.

People don't always appreciate Waco for the city that it is. From the outside, it does look a little sketchy. And I don't recommend walking the streets at night. However, Waco has many hidden gems nestled in its antique exterior. It is home to one of the best universities in Texas (of course, I may be a bit biased.) The city of Waco cares deeply for the homeless and has many opportunities for people to get involved serving through organizations like Mission Waco, the Salvation Army, and other ministry groups. It is also one of the most churches areas. You could go to a different church every Sunday for several years and still not attend all of them (there are roughly 230 churches). Cameron Park is a beautiful, complex park in the center of Waco, the suspension bridge at sunset is stunning, and the farmers' market on Saturday morning is full of fresh produce and unique food trailers.

Waco is definitely a hidden treasure in the heart of central Texas. I wouldn't trade living here and attending Baylor for anything in the world!

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