Skip to main content

Not Again!

Weekend Luck:

Doctor's offices are open Monday through Friday. Yet I always start feeling sick on Fridays. Luckily, I don't get "sick" too often. Which is pretty lucky considering my pathetic immune system. My immune system can't fight anything and even a simple cold could become more serious and life threatening.

For example:  I had to break down and call Doc's after office hours (this morning) to figure out what to do, thanks to a simple cold sore, AGAIN!

Yep, you heard me right. Again, thanks to a cold sore. Not sure if you remember in 2013. In 2013:  I had a cold sore that turned my  mouth and lips full of cankers, sore, and lesions. My jaw/mouth was so swollen that I couldn;t talk (which is really funny if you know me, since I gab all the time) or barely swallow liquid. My throat and tongue covered in bacteria and fungi (my tongue was covered in pure white - it was thrush). My fever reached 104 and my pulsox dropped into 80s, Andrew took me to ER, I was transported to Chicago & in the hospital for over a week, fighting this silly virus that turned ugly. 

 (picture: That's not lipgloss or the lighting, that's the fungi)

The doctor said it was the cold sore virus (also know as Herpes simplex 1), which I thought was amusing, but it's the simple virus a body has when someone gets a cold sore. It stays dormant in your body, until you get another cold sore. Which is why some people are more prone to them. I had never had them until 2013. Which is why docs think it happened so fast and got so serious. Honestly, being rushed from my hometown to Chicago via ambulance, didn't bother me. But, they had to make sure my throat didn't close and kept checking it. The thought of having to quickly trach my throat terrified me. But whew, I started to slowly get better and once my sinus infection and virus were gone, I could eat solids. One I had no fever, I got to go home!!!

Most people, put medicine on the cold sore and it eventually goes away. For example: Abbreva. Their bodies can fight simple viruses and colds. Apparently, mine cannot. I took me a total of 2 days last time to progress to that point, which is why I'm being super carfeful to keep an eye on it this time! 

This weekend it isn't nearly as bad. I knew what it was and did everything I could. I had a cold sore off and on for the week, then thursday night my lips got swollen and I noticed I had 3 cold sores on one lip. (I look super gross right now). Then Friday, I woke up with a stuffy nose (plus the 3 sores), but felt fine. I did some shopping/errands. An hour after getting home. BAM! 100 fever, and noticed canker sores on my cheek and tongue. I couldn't sleep Friday night. My fitibit says I slept an hour. Satruday, I woke up feeling like I had a head full of crap (yay, sinus infection too!) - I got a sinus infection last time, so I figured it was coming.

However, I have kept my fever below 100 and it goes away with motrin/tylenol. I'm drinking and resting. I got the pleasure of watching 10 hours of Law and Order (on that beautiful 60 degree weather day). But Andrew was a work and I was told to rest and text him updates.. So I did. 

Today, my cold sores are bigger, and my breathing is a little harder, but it isn't really affecting my lungs or pulsox too much. My throat and tongue don't have any bacteria or fungi, they are clear, and I can still eat! So, Doc and I are still hoping I can beat this without hospitalization. I called this morning and they are writing me a prescription for acyclovir, which I went home on last time. I'm to watch the sinus infection, if it get's worse, i  may need antibiotics, but I'm allergic to all the ones you can get orally (and we don't want to need to do IVs). So keep your fingers crossed that the Acyclovir get this virus under control!!!!

Isn't it crazy to think, one silly lil cold sore could do so much harm in my body! Doc said this could happen every single time I get a cold sore. Which is just annoying. But at least it's not as serious this time around. Hoping to feel well enough to keep my appointment Tuesday. I'm supposed to meet with my eye surgeon and talk about my eye surgery. (I will save that for another post)...

I will keep you all updated on my CF Facebook page! Sometimes I feel like an operation board game! 

Comments

Post a Comment

Popular posts from this blog

CF isn't all tears and saddness. Get a Full Picture.

  CF and Laughing Cystic Fibrosis can bring sad times and times of tears (like losing a close friend with CF, etc) BUT, it can bring so much joy and love. I've noticed most people love to talk about the people they meet while traveling. This is usually, because they have learned something from the person. Or the person is considered unique to them. I can do the same thanks to my Cystic Fibrosis. I may not have traveled much in my life thus far, but I have learned mountains of lessons from my CF. [Picture right:  Me ready for surgery in 2nd grade!] Forgive my shoutouts (but I must recognize a few amazing people) I have met some of the most amazing doctors: Chatrath, Dr. B Nurses: Sara & Marie (from Clinic), Lizzard, Melody (best IV stick ever), Deb, and Kris (you know a nurse is amazing if you love her after putting tubes down your nose!) Respitory Therapists: Jeannette, Lanell, and Don (you da Man) And Cookie Marrow (Musical Therapist- She would sing to me a...

Video Blog: Life in the hospital (as a child)

The daily life in the hospital! Most people cringe at the idea of a hospital. However, when I was little I never minded going into the hospital. I usually would have at least one other friend with Cystic Fibrosis to hang out with there (before we knew about the "CF Bugs"). I didn't love being sick, but I loved my CF friends that I would hang out with. Also the hospital, nurses, and my parent's tried to make it a "normal" environment. I got up and put on cute clothes, "walked to school", flirted with a couple CF boys, did homework, came "home" (back to my room), my friends would ask my parent if I could go play with them. We'd hang out in the play room or go on a walk with one of my parents! My dad loved taking me on walks and I LOVED going on our walks! Here is a video blog of the route we took and bit of information on what is was like growing up (for a chunks at a time) in the hospital! (it is posted via youtube, let is dow...

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 ...