Skip to main content

Sick Update

Just a Lil Update:


If you haven't read my last blog, you may want to do that so you know what I'm talking about (read it here!).  As you know I had a lot going on last week with the clinical trial, picnic, and then getting sick. Monday I called Doc and got some oral antibiotics prescribed. I'm now on (month's worth of) Cipro and doing a two week round of inhaled (neb) Tobi. As you know I've always done Tobi my whole life on and off every other month switching it out for Cayston. Since doing this clinical trial a month and half ago I've been off antiobitic nebs to test the effectiveness of the new drug. Now, it just so happens I had been doing great since off the nebs. Even on Thursday of last week I had a high lung function that hasn't dropped at all soince been taking off the nebs. But unfortunately, I caught something over the weekend and got sick.

Of course the first thing that comes to my mind is "Oh no, I hope this doesn't hurt the trial if I'm getting the real drug". But I gotta remember that we get sick and 6 months is a long trial and things happen. They take all that into account. So phew. I love this trial. In fact, even though I'm sick, I'm already starting to feel better. I only have been doing Tobi nebulizers and oral cipro antibiotic pills for 3 days now. I've been sick for 5 and usually it lasts a lot longer and I end up needing IV infusions to battle. So hoping this is a quick turn around!

My immune system may suck and I catch everything, but at least right now my body is fighting this without IVs. Cipro is pretty heavy duty stuff though and inhaling Tobi for the first time in almost 2 months is really making a difference.

ONLY downside is the Cipro. I'm very allergic to 3 of the main antibiotics that they use to fight psudeo (psudeomonas aeruginosa) infections in CFers. Keflex, Levaquin, Bactrum. Yep so pretty much every big antibiotic they use to fight I can't take. So I take Cipro which is related to Levaquin, but I can tolerate it. I've had some minor problems in the past. 1 time I had a small rash for a few days. This time I'm getting headaches. And the headaches suck!!!!

But I can stick it out for a while until my lungs are better. I can tell the Cipro is working, I just gotta deal with the headaches until I'm better. 23 more days (hopefully once I'm better we can discuss stopping the med early). I'm not ready to call Cipro quits and have to find a new way to treat the infections, because honestly I'm limited with what the docs have left that they can do without those antibiotics. And who wants to exhaust all their options (I'm only 29).

So I apologize ahead of time to everyone I'm not very responsive to, my lack of communication, and everything else. I'm trying to get better, keep up with my meds, my homework/classes, and deal with some headaches. But I'm doing it without the hospital and that's the main thing.

Pic: Is from last time I was in the hospital in 2013 (November). Andrew's always right there for me, love him!

So a big thank you to Andrew! Who not only works full time, goes to school full time, but has been doing all the errands for me and taking care of me. In the last 2 years we have been together, he has dealt with so much. Actually (click here to see what he's gone through), I posted a year in reveiw with pictures and it shows the best and worst that we went through last year! He nevers gets upset, he just always wants to help me. He is simply amazing and I'm so lucky!

So I'll keep y'all posted on how I'm doing and keep those fingers crossed my allergic reactions don't get worse and I continue to improve!




Comments

Popular posts from this blog

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...

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...

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 ...