Skip to main content

Home from Hospital, its great, but a lil tough.

Home from the Hospital

As you read in my last blog, some craziness happened, I got really sick and had to cancel my surgery. Which means I will be rescheduling that for May! I got a virus, which covered the inside of my mouth and throat in sores. Then I got Thrush, which covered my tongue... And then I got a sinus infection. I got transfered to a hospital in Chicago and have been camping out there over my spring break!

BUT... I'm home!!!!!! I have had no fever for a few days, my sores are gone, my tongue finally looks human again. Although, It was kinda cool looking, I could have been some strange alien on star trek :-)

I'm soooo glad to be home. But, now comes the "at home adjusting"; where I have to clean my house, cuz its a mess from me being sick. I have to de-bug my house so I don't get sick again, I gotta remember to take all the new meds they put me on, as well as my old. And make sure I have time to do my nebulizers and stomach feeding, etc. Also, I gotta pay all the bills I have received while in the hospital, but have no paycheck for the last week and a half... luckily, I know how to save money and cut corners :-)  I find it tough when I first come home, cuz I don't want to take it easy, I want to plunge right into my regular lifestyle. But I get wore down faster at first and have to remember I'm not 100%, which is hard for me to take. I really dislike not being able to keep up with my life. And sometimes that can be the most frustrating part of CF. I don't let it stop me, but when I get ill, it always slows me down for a while. As a CFer we are used to getting sick and being in the hospital for a week or 2 or a month at a time, but it never gets easier.

I got home late last night :-)

Today, I got the house picked up, fridge cleared out, dished done, 3 loads of laundry, and bathroom wiped down. I still have a lot of homework tonight, but I should be able to finish it while doing the rest of my nebulizers.

Other than being extremely tired still and kinda low energy, I feel pretty good :-) Very excited to get back to classes, my jobs, and play practices. I have missed everyone dearly and I can't wait to be 100% again!

Comments

  1. Glad you are on the mend! I have the same issue after getting sick- I want to jump right back into life and make up for lost time, but CF doesn't make that easy. Hope you feel 100% soon.

    ReplyDelete
  2. Hey Cheriz, gosh it's been a little while since I stopped over at your blog and have some catching up to do. Sorry to hear you have not been well, it all sounds awful! :( But so glad to hear you are doing better and love the positive attitude you have! Hope you back to 100% really soon!

    ReplyDelete

Post a Comment

Popular posts from this blog

Today's BIG Appointment

 I discussed last week about my recent struggles & goals. I have been dealing with a lot all at once! Family planning (update on that in 2 weeks), my Grandma's funeral, lower lung function. Through it all I have remained very compliant with my meds! My health is VERY important to me. So this last weekend I took my vest machine, wabi sterilizer system , and packs of ensure to my parent's for the weekend. I wanted to make sure I did everything. While it was a sad occasion, it was still pleasant seeing almost all of the family together again. Actually 27 out of 29 of the cousins made it to the funeral. Grandpa is in the middle of the picture (can you find me?) LOL   On top of my medications I have been doing some dancing & walking, but no jogging or anything. I'm still counting calories on my fitbit (hitting over 3000) a day (& 40 grams of protein, 50 grams of fat at least). I knew I was feeling a bit better than before, but wasn't sure what to expec...

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...

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 ...