Skip to main content

Rambling thoughts

My. brain. is. dead. So if I ramble, I apologize. I just took my Spanish final, and I am so glad that it's over with!! I did well on it, but that doesn't mean all my energy wasn't drained from taking the darn test. Three finals down, one to go! :)

Today was the CF walk in Austin. It was so weird not being there. I have been to a CF walk every year for as long as I can remember, and I have spoken at the event since I was in seventh grade as the ambassador for the Central Texas Cystic Fibrosis Foundation chapter. I know that I am still supporting the CF Foundation from afar, but I definitely wish I could have been there today physically, not just in spirit. I heard that the Walk was extremely successful, however. As of this morning, $110,000 was already raised!! Hopefully next year, my finals will be completed before the Walk, and I can participate as always.

My sister and I have finally decided on the May challenge (so sorry for the delay). We are compiling a book list to read over the entire month. These books will challenge us intellectually but also give us a way to enjoy the beginning of our summer break. We are both avid readers, so this challenge should be fun and exciting. There's nothing like opening a new book and diving into the character's lives, becoming a part of the storyline and feeling the emotions of the characters. I have never cried while reading a book or watching a movie (I know, what kind of a person am I??), but I thoroughly enjoy being held captive by an intriguing book. I could sit and read for hours (except that I like to stay active while reading, so I could probably walk and read or do calf-raises and read for hours..ha!) Once we decide on the final list, I will post it so you can know what we're reading.

I hope you all have a blessed, relaxing Saturday. Oh, and happy Cinco de Mayo. That's the last bit of Spanish I am speaking all day today!

Comments

  1. Can't wait to read your list! I'm a huge reader, as well. Books are my drug of choice. ;)

    ReplyDelete

Post a Comment

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...

CF Walk Letter 2018

Dear friends and family, I hope this letter finds you doing well! My life looks pretty different this year from last year. In May, I graduated with my master’s in communication sciences and disorders. I started working as a speech-language pathologist in June for a company called SpeechCare, and in July, Eric and I got married. That was a very busy couple months! I love my job; I work mainly with adults with intellectual and/or social disabilities to help improve their communication skills. My clients bring me so much joy! I love being able to help them communicate better with others. Eric and I are also loving being married. Living with Cystic Fibrosis has taught us to never take the time we’re given for granted, and we are making sure we soak up all the moments we’re given and go on plenty of fun adventures.  My health has been a bit of a struggle in the past few years. I had a round of IV antibiotics in May and then again in September and January. I will be starting IVs...