Anything is possible. You can be told that you have a 90-percent chance or a 50-percent chance or a 1-percent chance, but you have to believe, and you have to FIGHT



Lance Armstrong

Saturday, April 25, 2009

19 oz in first 24 hours!

So the first 24 hours on reflux medicine she ate her full 19oz!! YAY!! Either she does have reflux or we are just lucky! Time will tell.. Stayed tuned for the next 24 hours of feeding..

5 comments:

Katie said...

Your daughter is so cute! Found your blog through baby Grant's. I just wanted to say hello. Our baby girl also has Ebstein's. I've only met one other family whose daughter has this defect, it's so rare. Maddie, our daughter, has had 2 surgeries and 3 caths. Unfortunately, her right ventricle isn't sufficient and we're down the Fontan pathway with her, BUT she's doing really awesome and we have much hope for her future with this. Just wanted to wish you the best and say hello! Congratulations on such a cutie pie too!
Love,
Katie Allred (Maddie's mom, HRHS)
http://allredbabygirl.blogspot.com

kdance10 said...

Yeah! Way to go libb:)That medicine helped both my girls too.

Unknown said...

Good job baby girl!! Keep up the good work!!

Amy said...

Yeah!! If you need any tips on 'how to be a good eater' I am your woman.

She is darling.

Dennison Family said...

Way to go LIBBI!! Rah rah libbi!! You can do it!!
I hope she does great today too!!!

This is Paul Cardell's CHD video. (I put it at the bottom of the blog, it fits best there..) It is shocking how many people, young and old are dealing with the same type of things we are. Take 9 minutes and watch, these are some of the cutest babies i've seen!! Libbi is about 6 and a half minutes into the video. (make sure you scroll down and pause my music playlist so you can hear his music, he is a pianist, it is very pretty!)

Paul Cardell CHD Video