Skip to main content

Exciting News, even in a Hospital!

Exciting News: Even in the Hospital:

3 Exciting things!!


Yes, I know. exciting news in the hospital...Nope, I don't get to go home. Not yet. BUT, I'm excited to share some othe GREAT NEWS! First, of all since I was admitted last Thurirsday morning, I have gained weight. 1. because I don't have time to make food and eat at home as much as I need and 2. Who wouldn't devore a meal of roast beef, potatoes, veggies, fruit, and pudding at 6pm then order anothertray with shrimp and rice, and more dessert at 7pm?

1. So as of today I am 107.4 lbs!


This is the highest I have been in a very long time. To check out my weight and lung functions changes over the years click here- Clinic-My Health Page!

Only, down side...I need to buy new pants and running shorts, none of them fit me...I'm cheap and picky with clothes..so it may take a while. However, I'm sure a trip to Delia's will change my mind. Ps. for some reason Delia's usually fit, when others are too big. So maybe...


2. We were discussing the CF fundraisers And Andrew is going to be doing the CF Climb in November this year!

The CF CLIMB on November 10th is way to committ to the challenge of climbing the 58 floors in honor of everyone affected by CF. This events raises, just like GreatStrides, to provide research for CF and in hopes to find a cure!

I'm going to help them fundraise for the event, so if you'd like to donate, feel free to give the money to one of them, to me, or my mother by November 8th! :-) Sorry, no online link for the Climb. (checks can be made to CF Foundation)


AND 3. I got a Pulmonary Function Test Today (PFT) and I get to find out the results and discuss it with Dr. B tomorrow!

So here is to hoping my lung function goes back up. (currently 45%). So many good things. Weight, friends supporting me, fundraising for CF, keeping up in classes, getting healthy and hoping to get lung function back in the hospital!

YAY! Now, to eat my berry smoothie and wait for Andrew to get here. Well, after my 4 nebulizers and vest treatment of course....
Labels:

Comments

  1. AshleyOctober 16, 2013 at 1:16 PM

    I need to go to your hospital. My hospital's food was awful. I had my mom bring me every meal when she could and leave behind a cooler with snacks for when she wasn't there.

    Congratulations!!

    ReplyDelete
    Replies
    1. CherizOctober 16, 2013 at 8:38 PM

      I used to go to a different doc and hospital, and the food was bland and limited. Now, I'm in Chicago. Bigger Hospitals, means bigger bucks and better food :-) But yeah, I feel ya. At the old hospital, I had a doc who brought CFers pizza and take out. lol

      Delete

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...
2 comments
Read more

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...
3 comments
Read more

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 ...
2 comments
Read more