Skip to main content

Hospitalization and Worries

Hi everyone!


Sorry, we haven't had a chance to blog much since we got some foster kiddos! If you are new, make sure you check out the last few posts.  Trying to make sure the kiddos make it to all their appointments and are learning as much as they can is very important. So yes, I put 100% of myself into working hard for my kids.


What did that mean? Well... I did all my nebs and oral pills, but honestly struggled to do my vest, exercise, eat, or sleep much over the last 2 months.


No vest, no sleep, no exercise, and honestly only eating 1 meal a day... I knew I'd take a toll on my body. But, I knew for the first 2 months I had to do what was needed. Both or safety reasons for my kiddos and me! I had clinic at the beginning of September... Weight was down from 116 to 112 and lung function down from 60 to 40. However, I pleasantly supported by my whole care team in my decision to stand by the kids. However, we needed a game plan to make sure I didn't jeopardize my health. I have a history of allergies to Keflex, Bactrim, Levaquin. However, I wasn't ready to be admitted without seeking out all my options. Doc said since my allergy to levaquin was minor and when I was really young, we could try oral Cipro. I took my first dose and waited in clinic a bit ( I also took Benadryl with them). I had a follow-up two weeks later...yes down to 110 lbs and 36% can't wait any longer. I set admission date for one week from them (because Andrew was gone for a few days for work conference and I had to watch the kids).


By the time Thursday the 5th came... I was beyond ready for the hospital.  Fast forward to today, Monday the 9th... Still struggling with breathing and daily activities. I get out of breath showering. I'm constantly waking up at night coughing. There was talk for the last few days that my port my have an infection.. Although, I never thought it did. However, I had fevers around 103.5 - 102.9 for over 2+ days straight and doctors thought that might be the culprit. Luckily, I'm more running 99.3-100.0 now, so we are heading the right way as far as fevers.. We did talk about possible port replacement down the road, mine is overdue (over 20 years old). However, I am hoping to schedule that post hospital when I have my full health at the time. Right now.. my latest lung function tests were between 28-36%... I still don't have my appetite back and I'm super tired every day.. However, in the 6 hours of sleep I got last night I was woken up 7 times for vitals, blood draws, meds, etc...

Before I was admitted I had 5 days to get all laundry done, snack and med charts made for the afterschool babysitters. I made sure to have all the Foster Care paperwork caught up, etc. Hopefully, my organization has helped Andrew and the kids (and sitters). For now there isn't much of an update. I just want to get back to 60% and 115 lbs! I want to come home to Andrew and the kiddos. It broke my heart seeing them cry when they left me here or hearing them tell me "Love you" <3

I just hope I can fully bounce back and that I can do it fairly fast!!!

Comments

  1. I am rooting for you !! You got this. Love ❤️ you

    ReplyDelete
  2. Hope you get better soon. How are Andrew and the children doing. Is he able to bring them to visit. Don't overdue things when you get out. Try to take it easy for a few days if possible and gradually increase what you can do. Don't want to be turning around and have to go back to the hospital again. Well hope everything gets back to normal soon. Or at least what passes as normal.
    Take care

    ReplyDelete
  3. Thanks Aunt Tammy! love you too!

    ReplyDelete
  4. Thanks Doug! Our two older kids don't seem to want to come up to visit, so we don't push it. It's been hard not seeing Andrew, but overall it has been going okay. I have to remind myself to slow down all the time, it's a good reminder. and Thank you!!

    ReplyDelete

Post a Comment

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 ...

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 g...

What Else Should I Do?

Need Some Feedback.       May has almost come to an end. I love May, nice weather, summer starts, AND its Cystic Fibrosis Awareness Month! A lot of the CF walks are in may and its a great time to raise funds and awareness for CF! However, I'm also excited that it will be June soon! June 28th is the Princeton Cystic Fibrosis Walk. I've helped organize other events in the past. Whether for school or other non-profits I've volunteered at, but this CF Walk is a little different. It is the first time, I've put together a City event. Or put together an event that is so near and dear to my heart. I'm so thankful that I had so many people sign up so quickly. Pretty much everyone family member I have on my mom's side signed up the first day. And I've have had some family and friends help me (giving me ideas, helping me recruit, etc). But, Its the first time I didn't have a committee or team behind me to help execute the ideas and actually plan the event. I lo...