Skip to main content

In the Hospital: I'm not a car, but I need a tune-up



In the Hospital: Tune Up Time

IEvery so often as a child I would go in the hospital for a "tune-up." However, I switched to a different doc in May of 2011 and this doc doesn't really believe in "tune-ups" in the same sense my old doc did. My old Doc put me in at least twice a year on meds, even without a big decrease in lung function. My new Doc explained that he doesn't put CFers on antibiotics or IVs unless it is necessary, due to superbugs and growing immunity to them. Plus, I'm allergic to Bactrum, Levaquin, and Keflex and their cousins (3 main antibiotics they use for us). So gotta be careful.
 But as you all know, from reading previous blogs, that my lung function has decreased from 61 to 49% since summer of 2012. But last month, it went from 54 - 49%which is quite the drop for two months,especially for me. I'm pretty healthy and stable most the time.
Well, in the last couple weeks I noticed walking into to school and even work would take a lot of energy out me and I would get out of breath easy. I was reluctant to admitt it,but eventually I started coughing and wheezing more. Andrew basically put me in my place and told me I had to call doc. He always explains to me how much he loves me and wants me to be healthy, because he can't stand to see me sick or struggle. So I give in and call doc (and he's always right).
Sure enough, here I am in the hospital, he thinks my lungs have just accumlated a lot of junk in them and it may take some time to get them cleared out. They have me on antibiotic and steriod ivs, so they have to watch my blood sugar. Also, they are taking my blood to watch my cell counts, vitamin levels, etc. I'm doing 4 rounds of treatments a day. I'm hoping to be out next week and back home, where I can start making sure to keep up with meds and walking/jogging on the treadmill. Exercise really helps with keeping my lung function up. So I need to get back into jogging and training again.
I'm so lucky to have a guy who supports me. He convinces me to call doc when I need to! And this week when I wasn't feeling well and sleeping most of the time, he would go to classes, make me lunch, get my meds ready, go to work, and come home that night and he cooks more food and gets my feeding ready. I feel bad when I'm sick, cuz he does all of the work, but he never grumbles, he enjoys doing it. I once asked him if he would ever resent it or get tired of it. and he always responds  "I love you, I enjoy doing this, because I can help you, you have so much you have to deal with and all I want to do is make it a little easier, so you can focus on be healthy and happy, because that is  what makes me happy"
(above: my iv is accessed in my port in my chest and I'm wearing the mask from admission)
I'm so lucky to have such an amazing guy, it makes me want to work harder, be healthier, and I'm definetly happier :-) I love you, Andrew! You are amazing!
We are hoping my lung function will increase from this hospital stay and give me back some energy. Then when I get out, we are going to figure out a schedule, so I can do all my meds, stomach feeding, lift weights, jog, and do school and work. I want to get healthier, I can get healthier. Every time I go into the hospital, I take it as an opportunity to look at my life and fix it to get healthier. Its a chance to reboot and start over. A clean slate and I'll take it....


Comments

  1. were a like in many ways I love you laura

    ReplyDelete

Post a Comment

Popular posts from this blog

Close to a Cure?!?!?! and Thank You!!!!!!!!

Help Us Find A Cure & Thank you! Lots of new meds and treatments are being researched thanks to the CF Foundation and the people who support it! Thank you soooo much everyone for supporting me and the CF GreatStrides Walks! I hope you enjoy hearing about the cool new ways steps are being taken towards finding a cure for CF and how everyone has helped me and us (the cf community)! New Treatments And Break Throughs: As you may know, from reading my last couple blogs. Some exciting news was released!  VX-809 + Kayldeco Phase 3 (6 month clinical trials) has started! Which means if all goes well, this could be on the market in the next year or two. This drug helps target the actual faulty gene. It will help improve our lung function (hopefully gain some back, the part that isn't damaged) and will help us to slow the decline of our lungs health tremendously! This is the treatment for my mutations!To read more about this new treatment click Here! Also, there are other medic...

First blog: Hello

My first Blog: A little About Me I'm not sure why I have decided to start a blog, however, here I am.  I have honestly thought about writing about my life for years, but have always chickened out. I have finally decided to share the experiences life has thrown at me. The biggest reason I have been asked to blog by people is because of everything I have dealt with medically. I have Cystic Fibrosis and a few other medical problems...This is probably the best reason why I should blog. I can relate to others who are dealing with medical problems, however,my CF is also why I did not want to write this blog. CF can be embarssing and annoying sometimes... but it  has helped define who I have become to be as a person. Therefore, (yes, even though I want it cured) I don't hate having CF. Let me start off with some basic info and statements. I'm 26 yrs old and have dealt with CF all my life. In this blog you will hear recent stories (good, bad, embarassing); a...

Holding Down the Fort

My husband, Andrew, is currently at Wartburg Theological Seminary and is starting his first week of his second year there. Every year he lives on campus for one week. He enjoys starting each semester on campus where he can build friendships with other students and professors. It's the only time he is on campus. Usually he does long-distance learning, online, from home. It was the only way we could manage him doing a four year Master degree program while working. This week is the hardest for us. However, we have something on Thursday and Friday this week, so Andrew will only be gone 3 days instead of the typical full five. So that will make this week a bit easier than the other semesters. It's hard for Andrew to be away, although I know he is having a blast. We send random pictures back and forth like a book he may be reading or a game I may be playing with our kiddo. It is hard for the kid(s) to not see Andrew every day. We are foster parents and stability is a BIG issue for ...