Skip to main content

Trip to ER-back in the hospital

Trip to the ER, Back in the hospital:

Saturday was amazing! I loved going out and celebrating the fall weather. Sunday afternoon I started to not feel well and by sunday night I was pretty sure I needed to see a doc.

As you may have read in early posts: I had been having antibiotic associated diarrhea (I know, TMI)and not feeling the best. But it happens. So anyway. Saturday Night I noticed my gut was really distended and bloated. All day Sunday it  was the same, very big and bloated.

Saturday I was really upset by this. I wanted to wear jeans to the orchard, but I couldn't get any of them on. Plus I have gained over 10 lbs since I bought them... So add the bloated gut on top of that. No way! So I had to wear my black sweatpants to the orchard. And I had a hard time finding a dress to wear out to dinner too, most are slimer fits on me. So I chose a sweater dress. Luckily, it worked. But, I did not feel comfortable.

I was starving still from the steriods, so if you read the last post, you will see how much I ate. I pigged out! Probably not a good idea with stomach issues.

By sunday night, I was positive I had an intestinal blockage/ Bowel Obstruction. These can be common with some CF patients, and I'm one of those lucky ones. :-) lol

So, I waited until Andrew got off work and he brought me to the ER. Oh what joys ERs can be...

ER story time:

Well, it wasn't nearly as bad as (in march) last time... to read about my ER situation in March when I had a virus and Thrush read the blog post here! The only problem this time was the wait. We arrived at 11pm, but I wasn't admitted til 7am. In fact, my CT scan was at midnight and nobody followed up til 5am. The doc in ER told me I had a mild Urinary Tract Infection and my Colon was slightly inflammed. They put me on another IV antibiotic (on top of the 2 I'm on). And admitted me at 7am this morning.


Oh Doc:
 Doc. B came in this morning to see me. He said that I need to make sure to call his office, no matter what time, if I ever need to go to the ER. Wow, I've never had a doc tell me to call him after hours. Basically, his reasoning is this- well this is what he said:

"They say you have UTI, which you don't. So they put you on the Antibiotic for it, but you are allergic to it's relative Keflex. So I have to take you off that. Your colon is inflamed and your small intestine is constricted, so you are patially blocked. I think with you on a liquid diet and taking medication for the intestine/colon issues, you should be just fine. The ER's they try, but they have no idea about CF. They do pointless tests. " He proceeded to explain one silly test they had done over night...

For example: Apparently my insurance gets to pay for a test they did to prove I need my zenpep (digestive enzyme pills) and to say I was, infact, pancreatic insufficient. I have CF and have been taking enzymes since I was a couple months old. NO DUH!


But, Doc has a plan. Keep me at least through today and part of tomorrow. See if my stomach gets worse or better. If I keep my (oh, so awesome) clear liquid diet down and no fever then I won't be in long at all, unless the blockage gets worse.  I will take meds for the colon/intestines issues and in a couple weeks I may have an endoscopy done to re-check it all out.

So that's the plan. Bummed, missing classes again. But Blockages are nothing to mess around with. I've had some pretty scary encounters before. So, glad I got it checked out before it got worse.

And I guess our pumpkins will have to wait a lil longer to be carved... (perhaps it will be the next "At Home from hospital celebration")

Comments

Popular posts from this blog

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...

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...

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 ...