Skip to main content

Thankful Thursday

WOW. This week has been a complete whirlwind. I can hardly believe it's Thursday. I moved back to Baylor last Friday and have been slowly adjusting back to college life. It is crazy how much life can change in just one week.

1. I am thankful for my family for helping me move in. It is a little bit overwhelming, unpacking all your precious belongings into a new space. You want to make everything look perfect, but you don't know what "perfect" will look like. At least, that's how I felt! My family was patient with me, helped me build furniture, and became my "interior decorators". I'm very thankful that they live close enough to help me in this transition.

2. I love almost all my classes. They just seem so interesting! I'm not going to lie, this semester is going to be difficult. But I am so excited to get started. My professors all seem wonderful, and I know that I will learn a lot!

3. My roommate is just so awesome. We are in the same small group at church, so we have similar thought and beliefs. She is one of the sweetest girls I know, and she is always striving to live as God has called her to live. I know we are going to have a wonderful year :).
Labels:

Comments

  1. AnonymousAugust 25, 2012 at 2:10 AM

    Your positive outlook on life even with everything the world has thrown at you is very encouraging. You are a blessing to everyone around you. Know you are being prayed for.

    ReplyDelete
  2. Emily IngramAugust 28, 2012 at 8:00 AM

    Thank you so much! To God be the glory. I appreciate your prayers and words of encouragement!

    ReplyDelete

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