Skip to main content

I'm a Hungry Monster

Gaining weight? Losing Weight? Who doesn't struggle with weight some way or another? Well a big part of Cystic Fibrosis is a struggle with nutrition and weight. I have always struggled to gain weight, I was 45 lbs in 7th grade, and only in the last 5 months has my doctor/care team started feeling satisfied with my weight. whew, only took me 32 years!

Slowly over the last year I have been gaining 1-2 lbs between clinic appointments. At my last appointment (just in July) my weight was 110 lbs. Which is pretty much the highest it has ever been. In 2012, I hit 109 briefly. (see side-by side picture)  However, the goal is now around 115-120 (to have a few pounds extra for when I get sick). Doc K suggested I started taking a med to increase my appetite (non-steriod). I agreed, I usually always agree to what my doctors suggest. Doc said he hoped I reach my goal by my next appointment in September. However, after only 1 week on the med I had gained 6.5 pounds (116.5).  He cut my dose down (to half dose). I'm currently not taking it for a week (do to it conflicting with an allergy test I have coming up next week). Even half dose I was still hungry all the time. But full dose was horrible.

Normally, I'm cranky only when I get really hungry. Anyone seen those funny memes? The "I'm hungry vs. after I eat" memes? Yes, that is me. Anyone who knows me will agree. Well, since starting this new med in July I have been super cranky. I'm always hungry, always miserable. I am always starving, feels like I'm starving to death. The weight gain was fast. Adding well 5% of your total body weight in a week. It made me lethargic and lazy that whole week.

So now it's beginning of August and I am trying to work on being more active & gaining muscle.  Now that I have reached the goal weight range, I need to focus on getting more endurance walking and muscle mass. I am starting small, walking more during the week. I'm adding little workouts in the mornings a few days a week.

I try to remind myself how far I have come. Managing to get rid of my stomach tube after needing if for 17+ years. I had my stomach tube put in during  7th  grade, when I only weighed 45 lbs. and within 2 years I doubled my weight. The picture to the right is me freshmen year in high school (weighing about 95-100). After college,  my stomach tube was having a lot of infections/leaking issues. It hurt and was raw and bleeding a lot. Up til the last 2-3 years was fine though (so I really do advocate people consider getting them if they are needed). But it was rough towards the end. I had to prove to myself and doctors I didn't need it. I started calories counting in 2012 and with Andrew's support & help I had it removed in 2014. Removing it had some complications. I had developed a fistula, where my stomach had adhered to my skin.  So needless to say, I'm so glad that part it over! I'm proud of what I have accomplished. I hope to be able to keep this weight up & gain muscle/become a stronger.

It's hard to find all the time I need in the day to work out. Wake up, 2-3 hours of med treatments, pills, high fat/calorie breakfast, work, 2 more hours of meds, dinner, etc..I tend to sleep 8-10 hours per night and need every bit. But I will keep at it. I know I need to make it priority, just like my meds. I have stumbled a bit this week, because I'm coughing more and it feels like starting to get sick again. So we will see what happens. But, I want to remain focused on my weight and workout plans. Hopefully, in September my weight will still be up & I am even healthier. I have tried working out in the past, but it never lasts more than a few weeks. Any suggestions, tips, better workouts?

What workout videos/ YouTube channels, or protein drinks do you like? Feel free to pass on advice & words of encouragement :-) -this is my biggest challenge (weight/Muscle gain/exercise). Thanks!!!

We will keep everyone updated on my Allergy tests & dexascan too! Follow our FB page to read more updates!

Comments

  1. By any chance was your appetite stimulant also a antihistamine? Just got out of the hospital a few days ago from my tune up and a collapsed lung. My appetite hasn't been that great the past year and was curious what other cfers use?

    ReplyDelete
  2. Hi Breeann,
    Yes it was! Which is why I have to go off it for my allergist appointment. It has been working and I'm hoping to put off a tune up for a while. Hope you are feeling better since you got out of the hospital! Talk to your doctor, he may have a suggestion like mine did! :-) Take Care.

    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...

Um..Need to clear my head.

I was having a good day, it was one of my babysitting girl's bdays! We went for ice cream, I hung out with a friend and watched "Game of Thrones". I really liked it and I'm hoping to watch more this wknd. Then I logged onto Facebook to see that my best friend Laura (with CF) is down in lung function, on oxygen at night and her doctor is putting her on the Transplant list. I have lots of thoughts going through my head the MAIN one is "Please let her get a Tx soon, heal well and fast, and live her full life, they way she deserves to! PLEASE, PLEASE, PLEASE!" I can't imagine how she must feel, I know I'm sad knowing she is at point she needs one, but HAPPY she will get on the list! Happy, Sad, Scared, Excited. How do I feel..? The worst part is knowing that she is pain. I just want to take all that away, give her some good n plentys (one of our fave candy), kiss her on the forehead, tell her I love her, and that before she knows it she will have...