Skip to main content

Trying to Gain Weight

Unlike most of America, my youngest needs to gain weight. Being a micro-preemie and having kidney failure are both high-risk conditions for developing eating problems.  Basically, we've been working on this since she was born. A few months ago, things weren't going well so I decided to get more serious and I made a schedule.

Here's the schedule:


The scheduled daily goal is 1750 calories and 76 ounces of fluid.

Every morning I give her Carnation Instant breakfast made with whole milk or Pediasure:  280 calories.  She also gets one box of Boost Kids 1.5:  360 calories.


For dinner she has the high calorie chocolate milk from Costco:  210 calories.  Those three added together are 850 calories--about half her calories.  We try to get the rest of her calories in the food she eats at meals and snacks.



Obviously she's not eating a lot of food.  I think her many medical issues have messed up her hunger cues.  Plus eating basically nothing for the first 3.5 years of her life until she got her transplant meant she didn't get used to eating different foods. Eating is actually a skill you have to learn. So we're working on expanding her palate. At breakfast and dinner she has to try a little bite of everything I'm serving.

Before this schedule, Camille wasn't eating any lunch at school.  She would drink a juice box and that was it. But looking at the schedule, I realized that skipping lunch was not an option.  Discussing this with her teacher, we decided that Camille had to stay in the lunchroom until she finished even if her class had to leave without her because learning how to eat lunch is an important life skill. I send a very small lunch with her of about 150 calories. So far, it seems to be working.

What I realized in making this schedule is that every little thing we do matters. If I give her water instead of whole milk in the afternoon, that's 150 less calories.  If we don't have dessert, that's another 150 lost calories.  No snack? 150 lost calories. The schedule helps me stay motivated.

I wish I could say that my schedule is working but so far she doesn't seem to be gaining weight.  I'm hoping it's because she has been sick this winter.

With her cousin's toy pet dog Cream Puff that she loves.

My long-term goal is for her to get rid of her feeding tube and have her enjoy eating a wide range of foods.  Hopefully we'll get there.



Comments

Popular posts from this blog

2024 Hansen Family Reunion, Wednesday

Recently we had another Hansen Family Reunion at Bear Lake. We've been having these destination reunions since 2008. There were about 70 of us in attendance. Bruce and Michelle organized the activities and did a good job. I enjoyed myself! Hopefully lots of other people did too. We showed up on Wednesday afternoon and enjoyed a taco salad dinner, served by Neil and Kristie's family. We also worked on two mixer games:  a word search with the names of all 100 Hansen family members as well as a Bingo card that involved finding people with different attributes like recent high school graduation, birthdays in certain months, etc. The word search was definitely the most popular. Also popular was playing Nine-Square and Sandy Pickle (a cross between pickle ball and badminton). Thys and Katrina might have won! After dinner, we had an FHE activity/lesson. Liz had made a book with stories of the first ancestors to join the church. She had selected different stories for us to act out in g...

Hansen Family Reunion 2024, Thursday afternoon

For lunch on Thursday, Lauren and Kurt made Cafe Rio which was delicious.  On Thursday afternoon, we had free time at the lake. Heidi and Aaron rented a pontoon boat and took people out for rides. This was very popular. Some of us went on the kayaks and/or swimming or just hung out on the beach.

Book Review: Out of My Mind by Sharon Draper

This is a juvenile fiction book about a young girl named Melody with severe cerebral palsy.  Her body doesn't allow her to feed herself, speak, or do much at all.  She's very intelligent with a photographic memory but she can't really communicate.  Finally, in 5th grade, she gets a "Medi-Talker" which is a computer that speaks what she types in.  Finally she has a voice. This book explores what it is like to be severely physically disabled but not mentally disabled. It seems like one of the most frustrating of all scenarios.  She is completely aware of all the cruelty (subtle and otherwise) that her classmates inflict on her because they don't really want to include her in their activities.  One of the saddest moments in the book comes when she realizes that every one of her special ed classmates is kind, where the "normal" ones are not.  Who really has the worse disability? The book was a quick read and fairly enjoyable.  Wha...