Skip to main content

It's the most wonderful time of the year

Even though it's only November 26, the Christmas season has begun. A short walk through any sort of shopping area and you see busy buyers, rampaging the store's shelves in search of this or that gift that Johnny or Susie just have to get for Christmas. Public places are decorated with festive lights and Christmas trees. The weather hasn't caught the seasonal memo, but everything else is pretty much on board to celebrate the holiday season. Christmas is such a fun time. For starters, it is a celebration of the birth of the King of kings and Lord of lords. What a cause for jubilation! Secondly, Christmas is a time to enjoy family and friends and a time to show love to others. I love finding the perfect gift for the precious people in my life and watch them smile as they open their presents. It brings me joy to make them happy! Thirdly, although I always have to have a course of IV antibiotics over the holidays, I don't have to worry about school work, deadlines, or tests. It is freeing to have a complete break from my busy school life.

Speaking of school, I only have one more week of classes, followed by dead days and finals, and then I'm finished with my third semester at Baylor. It's crazy to think about!! I don't know how the semester is really about to end so quickly. The concept of time is just so strange. But, somehow, this semester's end is literally just around the corner. One more final push of energy and motivation, and I'll be in the clear to begin a new semester! I'm excited to see what the future has in store for me next semester.

I hope you all had a blessed Thanksgiving. Enjoy your week, and don't let opportunities to love other people pass you by!

Labels:

Comments

Post a Comment

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
2 comments
Read more

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
4 comments
Read more

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
1 comment
Read more