Skip to main content

Oh the Joys of a Colonoscopy!

Colonoscopy, Fun:




As you may remember from reading my October Posts ( Oct Post #1  & 2nd Oct Post) that I was admitted a second time that month for Gastrointestinal issues. I was having stomach cramps and what was believed to be Antibiotic Associated Diarrhea. However, CT scan revealed my colon and intestines were inflammed.  After having a rough 2 months of GI issues, and cuting out most food (diary, meat, grease, carbonated beverages, and sugar). I finally am getting a Colonoscopy to see what in the world is going on! I'm been taking Probiotics, was on meds for both C. diff and AAD. I even added driking Kefir to add to the probiotics and good bacteria.  Only now am I seeing any changes, less stomach aches, etc. I add a 1/2 cup pf the Kefir to my smoothie, its not bad -yum! I really reccommend it and Probiotics (so talk to your doctor about it), it could really help you out!

Read about Colonoscopies here!

So I'm glad to be getting the procedure done. Instead of being upset about the colonoscopy I'm excited. WHY? AM I CRAZY??? No, I'm excited to perhaps get some answers and will be able to fix it. I've always had GI issues. In fact: At birth I was born with a intestinal blockage and gangrene in my intestines. I've had surgeries for intestinal problems, etc over the years. I've had lots of weird medical complications and issues: Read about cystic fibrosis history here! For a Full history, including my family, school challenges, etc Read an essay I wrote about my history here! So I'm not new or nervous to this type of procedure.
I'm hoping it is a stupid lil problem, like bacteria imbalance. I know the doc said Crohns a couple times, but this test will be able to rule that out.

ANYWAY, that is scheduled for Friday. Apparently, my only choices for appointments were this Friday- FRIDAY the 13th or the day after Christmas...Well...considering the day before the surgery you spend a lot of it in the bathroom (after drinking the ever yummy- so I've heard- Go-Lightly stuff)... I don't think I want spend Christmas emptying my bowels, so I will have it done on Friday the 13th!!! LOL

Oh boy. I know what a pleasant topic for my blog... but hey CF and all that pretty... The two main things it does: Clogs up our organs with mucus and our intestines get clogged with bowel..... So it ain't pretty.  It is tough to write about stuff like this, it is a lil embarrassing, but it is imporant to know all the ways CF affects us, especially the ways it interferes with our lives. But it comes with having a blog and deciding to let the world know all the dirty details about CF.

It isn't all bad though, there are always some perks. Besides the fact my G-tube helped me gain all the weight when I was younger and maintain it through the years, it has some other helpful qualities.

For example, Not wanting to taste the colonoscopy prep liquid. Doc says I can put the Go-Lightly through my G-tube instead of drinking it! I've run water through before, when I was dehydrated and tired. I didn't want to drink anything. So Andrew and I put water through it. Sometimes stomach tubes have perks!
Labels:

Comments

  1. Inhaling HopeDecember 9, 2013 at 11:49 PM

    Good luck on the colonoscopy and I hope you get some much needed answers and it is an easy fix. My new obsession is plain kefir drizzled with honey. I don't even really like the taste of honey much, but something about the combo is delicious. Even my 18 month old is pretty obsessed with it.

    ReplyDelete
  2. CherizDecember 10, 2013 at 5:12 PM

    I have Plain Kefir too ( I use Plain in Smoothies) and I have honey. I will give it a try! Thanks!

    ReplyDelete
  3. AmandaDecember 18, 2013 at 9:48 PM

    How did everything turn out?

    ReplyDelete
    Replies
    1. CherizDecember 20, 2013 at 6:08 PM

      No Crohns- YAY! I had an infection, I have an issue with the levels of bacteria in there, So more Probiotics and watch what I eat, and for symptoms of other infections. But no biggie! Whew. Doc's Exact words: "Your intestines are clean and look good..." LOL :-) Thanks for Checking!

      Delete

Post a Comment

Popular posts from this blog

5K. I could cry. Beyond Annoyed.

My 5K I paid my registartion fee weeks ago, have been training and I'm ready for the 5K. However, I didn't get to run my 5K today. Why? Because Cystic Fibrosis decided to one up me. I got my spots back friday, and they just got worse and worse. They look like this: They take over my feet, and sometimes my calves. I posted about this a few weeks ago. I had them during the last few performances of Hairspray. I call it the "Mummy disease" because when it happens my joints freeze up and I can't move. So the morning of my 5K I wake up and they are on my thighs...     and on my arms. This is the worst they have been in years. I took pictures to show Dr. B at my clinic on the 11th.  I'm just really bummed and upset about my weekend! I was supposed to run my first 5K!!!!! I then had a bags tournament in Peoria for the Dream Factory, and was then going to head to Champaign for Sat night- Monday! My friend Alex, reserved me a ticket for Ren...
5 comments
Read more

Calling All Who Care!

     Please Read : Okay, so first off I want to say that this post is tough. It's tough to think about and write. However, it is extremely important and a huge topic in the CF Community, and is VERY NEAR AND DEAR to MY HEART!  First I want to ask you... What if I told you I needed a Transplant. That I needed to reach a certain weight, get my kindeys functioning better, get a higher pain tolerance, and get off a couple medications I take right now. What if I said I couldn't receive a 2nd chance at life unless I reached these goals and I raised a certain amount of money that seems impossible to raise. What if I had been in and out of the hospital off and on for the last year, with many surgeries, had multiple infections and my lung function dropped from 40s to the teens and now is slowly dropping still. What if I was starting to wonder if my decision to go through the grueling Transplant tests was worth it. What if I start to get down about my cf and wondering why ev...
8 comments
Read more

A Hospital at Home

Coming home from the hospital takes a balance..... Wait.... Did I just say home from the hospital??? That's right!  I get to leave Wednesday the 18th, after 8 days in the hospital. It was a logistical thing. I have a super important court date on for "Shoes (our AMAZING foster son) soon." So Doc knew before he admitted me that I would be leaving by that day... So what does this mean for me and my health??? Well, I need to make sure I continue the same treatment schedule I would in the hospital. So 4 sets of nebs a day. 8am, noon, 4pm, 8pm. Which means I finish my course of IVs at home. I will be on IV's at least until 27th (so 1.5 weeks left). I came into the hospital on Tuesday the 10th, but we didn't realize until Friday the 13th that my Psuedomonas is resistant to all of the antibiotic options for IVs except one med. So on the 13th we switched to Avycaz, which is a newer, hard hitting antibiotic that was brought to market less than 3 years ago. We were hoping I...
2 comments
Read more