Skip to main content

Surgery Still On, I Can Do This!

I can keep it up:

This past blog I discussed my fail at doing everything I needed to. I mentioned having a fever, well the Cipro is doing nothing. I'm not responding to it. I've probably built up a tolerance. So they are putting me on some steroids for the next four days and instead I'm supposed to focus on doing extra nebs A LOT and I'm supposed to do Cayston and Tobi, which usually I only do one a month, because they are nebulized antibiotics. But I will be doing both until after my surgery. And good news my temperature has been normal most of today and only went up to 99.5 for an hour ish.

So if I do tons of meds, walk on the treadmill and get my lungs working better. All should be well with my surgery on Tuesday. But I need to actually do it! So I apologize in advance if I don't hang out or do much this week. I need to get healthy by Tues. I have ONE WEEK to do this and  I need this surgery. Without it work won't happen. Without work I get farther behind in bills and it just can't go that way.

So here it is. Day 1 of kicking my booty in gear!

AND THANK YOU! I have reached my personal goal of $1,000 for the Cf Walk! I'm hoping my team can raise double what we did last year (roughly $2,500 this year)!!!! I'm sooo lucky to have my family and friends there to support me! I can't wait until Saturday to see everyone, you have no idea. I look forward to the CF Walk more than I do Christmas. It reminds me why we (Cfers) fight so hard. We fight for everyone we love. And I know I am very lucky to have so many people in my life who love me and are willing to donate, fundraise and walk every year! 

I am one lucky girl! http://www.cff.org/Great_Strides/dsp_DonationPage.cfm?walkid=8670&idUser=187918

Comments

Popular posts from this blog

How Fostering and CF impact my work

I haven't been on my blog much.... I think that is because most of my blogging is currently been done on Health Union's Cystic-Fibrosis.com (here is link to all my posts on their site: https://cystic-fibrosis.com/members/cherizkunkel/ ). I decided last fall to step away from real estate after 3 years in the business. It was tough to say good-bye, especially since I had tripled my volume and business in the last year. However, I didn't have time to add any new clients; I kept saying, maybe next week, next month I can fit more work into my schedule. The truth is fostering takes a lot of time. We have between 5-8 monthly visits at the agency, 1 court ate a month, 2 home visits from the caseworker a month, plus e have 2-3 doctors/specialist appointments for our current kiddo. We have lots of paperwork we fill out, gas mile logs, receipts to add, and more! Our kiddo also participates in gymnastics and dance two nights a week. We go to a fosterparent support group with our kid ...

Cystic Fibrosis Clinic Results. Not what I wanted, but...

My Results: I went down in lung function 2% points and lost  a couple more lbs. So I'm at 102. I was really disappointed with myself. I know that I have been doing  my meds and I have been doing my stomach feeding most nights too.  I have been making the right decisions and all my friends have been very supportive. I bring my nebulizers over to their houses to do them if we are hanging out, etc. It just wasn't enough this clinic. I really thought there would be a slight increase. However, I haven't been jogging since it is cold outside. And I know waitressing has been making it hard to gain weight. Plus, its winter. It is always harder for me to stay healthy in the winter. Dr. B was still pleased. He said "I should give myself a break, I have been doing everything he asked, I ran a 5K, and I'm still doing well." And that is true 2% increase isn't a huge decrease, only if I continue to decrease then there is a problem. Dr. B told me that I need to focus...

Black Plague ( known as Cepacia B)

Black Plague I had a long car drive home to think, so this is long, but heartfelt. Tonight I went to a meeting for a non-profit I help with and while discussing somebody's anger issues. I decided to share a part of my past with the board that was there. I still am in shock I did so, considering very, VERY, few people know this. But I'm not ashamed and feel like others have been in my place. Naturally, the next step, is to share it on a blog, where everyone has access to it. (heh.) When I was little around middle school age I had some anger issues. I used to get angry over nothing and scream and once in a while even push my mom ( luckily I was tiny and not very strong). She would just hug me and tell me she loved me, she never got angry back.  She knew I was angry because quite a few of my friends with Cystic Fibrosis were passing away, from Cepacia B and other infections that were spreading ( apparently at the parties, camps, and apts) around. About a yea...