Skip to main content

Food, Food, Food ( A day of Food)

Food, Food, Food, ever get sick of eating food?

Okay, so that's the main reason I still have my G-Tube is that don't like eating constantly, feeling full all the time, and I'm not a fan of high cal. food.

Born with CF, but don't care for fast food, sweets, or anything that potentially could help me gain weight. So I compromise: eat what I want, when I want, and do 1,400 cals over night while sleeping.

However, as you know I'm trying to really, REALLY, get my lung function up. 1. Dr. Boas is challenging me and I don't step down to challenges 2. and of course, I want to be healthy!

So weight affects lung function, so the easiest way to bring up my lung function is bring up my weight. So I figured I would let everyone see what I eat on day to day basis.

(Note: Todays breakfast was bigger than usual, I usually will drink an ensure, eat a powerbar, cereal and reach 700 cals. Then eat more cals at lunch/dinner!) I Always try to eat 2,500 cals a day + 1,400 night= 3,900

BreakFast

Banana, Cream Cheese French Toast Sandwich, eggs (w/condensed milk), and iced coffe total.....................................................1,500


(This nows means I can have something more simple and smaller calories for dinner, I really prefer a salad or soup, etc)

I ended up running errands in the town next to my hometown, so ended up eating at a HyVee......................................................700ish calories.

For Dinnner I had pecan encrusted cod and parmesan noodles.....500

Had a snack of pretzels, mango applesauce, ..................................200
                                                                 Total for day ................2,900 cal.
                                                                  After Fedding..............4,300 total

check out this site for high cal meals to prepare! ( i got the french toast sandwich there, but I used the whole banana and left over milk/egg mixture for scrambled eggs (but added two more eggs))
http://www.chef4cf.com/

I checked my weight today 102 lbs. Yay! I lost some when the pharmacy held my supplies for my feeding, due to insurance carrier switch( no worries same coverage though)

Comments

  1. You're the only person I know who has to work at finding high calorie foods. Congrats at having a three digit weight!

    ReplyDelete
  2. Thanks Kym, I shooting for 106 at my appt.. Remebering growing up and how I would constantly take time outs to run inside and grab snacks...lol

    ReplyDelete

Post a Comment

Popular posts from this blog

Planning ahead (yay, for being organized).

Organization: it is a great thing! I'm doing another CF Walk in October! It's on the 6th at 9am. Why am I posting this now? In the past I wasn't organized. I would end up asking a couple friends to walk it with me. I didn't fundraise much, but I want that to change! I've had people tell me they would have walked if they knew about it. I'm blogging now, being more active on CF communities online, and there is no reason why I shouldn't invite others to do the walk. Everyone knows I have CF, why did I never invite more people?? No clue. So here I am inviting everyone to come and walk with my team! Here is the link the Facebook Event: Cheriz's CF walk FB event Also a link directly to my GreatStrides Walk page is on the upper lefthand side of the blog! I want to start to be more active in fundraising walks (along with 5ks). I'm planning on doing 2-3 CF walks a yr, and the ALS/PLS Walk every year! If you want to cheer me on at my first 5k i...

Why I Hope this Hospital Stay is Different

Typically, I've been very stable as an adult. I'm very lucky for that stability. However, 2018 started out nowhere near where I wanted. I was admitted mid March for a virus. We aren't sure what virus I had (every test came back negative). However, I had a consistent fever over 102 the entire 5 days I was in the hospital. Once I was fever free for 24 hours and I started eating better, they let me return home. I was excited to leave and get back to my everyday life. But, considering now a month later (and re-admitted), I think I should of just done a two week tune-up last month while I was in already. Live and learn. As you know (I'm sure) I have been trying to get my lung function back up to around 55-60%. 60% is my goal and it really is the highest my lung function can get, due to all the permanent scarring. I started Orkambi in October 2016. At that time it was the newest gene-modifier drug on market for CF patients (with my mutations).  After going on Orkambi I droppe...

End of Summer -Updates!

Wow, I can't believe it's been a year since we moved our blog to www.MoreThanDNA.org! A lot has happened in that year. My husband and I became Foster Parents to some amazing kiddos and still have one of those kiddos living with us. We have loved having "Shoes" with us and can't believe how much he has grown and learned in the year!I'm so proud of him! We have court next week, so prayers that it goes okay (and doesn't get continued again- that just drags it out longer for the kids). He is now 39 months old and starting Pre-K this month! Other big changes include: Some renovation to our home (complete Bath rehab & updated plumbing throughout), I started a new gene-targeting medication (symdeko) that is helping to keep me stable these last 3 months, and I got an AffloVest! I'm loving my new portable vest! Also, career wise...we both switched jobs! Andrew also started Seminary this summer to get a Masters Degree in Divinity. He has always wanted to be ...