Skip to main content

San Antonio Fun!

This weekend, I had the joy of going to San Antonio with one of my friends and her family. We left at 7:00 am on Saturday (yes, college kids can get up that early on a Saturday) and followed the signs down I35 to San Antonio. It was a fantastic weekend, SO nice to get away from Waco for awhile. We went to Sea World, which has changed a lot since the last time I was there. All the exhibits and shows are bigger and more lively, trying to draw people into the many different attractions. They are even opening up a water park right next to Sea World in May. (Very smart, Sea World, very smart). We saw the dolphins and, of course Shamu. We also got to feed dolphins and see the sharks/coral reefs. Although the weather was a little overcast, it never really rained on us, which was definitely a blessing! That night, we went to a Mexican restaurant for dinner. San Antonio is pretty much famous for their Mexican food, and this restaurant did not disappoint. There was even a prom group eating in the restaurant, so it must've been pretty delicious all-around! We tried to go to the Alamo, but it was closed. (Sad day!) However, we saw it from the outside, and it looked smaller than I remembered. Of course, the last time I was there, I was in elementary school. Everything seems bigger when you're younger! We also walked around the downtown area of San Antonio to get to and from our hotel to various locations. San Antonio is overall a lively city, full of mariachi music, antique buildings, and awesome venues.

For all you people wondering how I got my breathing treatments in and if I took care of myself, the answer is yes, I was a good, compliant CF patient and did every single treatment. I know taking care of my health is of utmost importance, even on road-trips and mini-vacations. I didn't take the whole shebang of equipment, but I did take my nebs, cayston machine, and albuterol. For Saturday-Sunday, I felt like this was a good compromise because lugging my Vest around would not have been pleasant or realistic, but I still got good treatments in over the course of the 32 or so hours I was gone.

I am so glad I got to travel down to San Antonio with my friend and her family. Road-trips are always quite the adventure, and this one was no exception. I hope you had a fun-filled weekend, as well, and are rejuvenated for another busy, busy week!

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...