Skip to main content

Updates and Cystic Fibrosis Clinic.

An Update:

I have my next CF Clinic this Thursday! Yipes, I'm a lil concerned. I didn't have my therapies for a week, so I'm gonna have to work really hard the next 4 days to get my lungs in better shape. Also, weight wise, not what I was hoping for. But otherwise, I'm doing good!

Its sooo weird how fast I can drop weight. Seriously, a couple days ago while weighing myself at mom's I weighed 98 lbs. I need to get back up to 107 again (dr. B wants 115).

However, today this is my weight:
Not sure how I dropped so much, especially since yesterday I had breakfast, lunch, steak n shake last night (with some friends) And I even hung out with a friend and had a couple beers last night. I didn't jog, or do any dance practices, just work, and went saw a show. Calorie wise, I shouldn't have lost any weight yesterday.

[side note: I don't drink much or often, but I did start drinking in 2012, when my dr. gave me the "green light" and said it is okay sometimes; But in no way do I think it is the best idea for every CFer, due to liver issues/ liver transplants. Be smart and Safe.]

 Guess, I'm just going to keep working at my weight, maybe start drinking nutiritional drinks before work. I think between waitressing and running around between classes and play practices the weight just melts off. 

Ps. Did you all notice my awesome socks :-)

Otherwise, I'm doing great. I'm back into the swing of doing my CF Challenge (read about it here!) Excited about the plays I'm in, keepin up with homework and work related stuff. Started to do a little jogging, not too much since my weight is low. My Stomach Tube is a lot better than it was and my surgery for the double hernias is March 12th @ 6:30 am. I have spring break from classes that week, then I will take off a couple days for work too. So that should work out perfect! Yay!

Everything is coming together very nicely :-)

And

Happy SuperBowl Sunday!



Labels:

Comments

  1. Inhaling HopeFebruary 3, 2013 at 7:26 PM

    Good luck at clinic. Sorry you didn't have your meds for so long :( It is hard to miss any treatments let alone a week. And hey, what is life without a few beers once in a while ;)

    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 ...
2 comments
Read more

Laura/Lara- two amazing gals

Laura and Lara Today, was a pretty normal day. Work, Meds, Jog, Blog. Instead of jogging, we walked 2.5 miles. (which I recorded in my spreadsheet and I will be doing data analysis later using all the variables I can come up with...) But here is the more EXCITING part of my day: I was asked a week ago to be a guestblogger for  Lara's Blog . She is climbing  Mt. Kilimanjaro to raise awareness & funds for CF in memory of her best friend Emma! I hope everyone goes to her blog and wishes her good luck! She posted my introduction and guestblog today!!! So check it out  Right HERE! Lara, Thank you for your hard work and dedication to helping find a cure for CF! AND then there is Laura ( a different Laura), she is my best friend. Laura has CF too (we met when we were really young)!!! I know she has been going through a tough time. But she is the one who got me invovled in CF awareness! My first CF fundriaser was in 2008 at a CF Walk that Laura to...
1 comment
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