At 3 weeks old, we discovered our daughter, Olivia, has cystic fibrosis. Originally, I created this blog to document her CF journey. At this time, I will be using it to document our toddler/preschool homeschool journey that we will be doing during some of her treatment times.
Saturday, June 8, 2013
Eating frustration ... Ugh
For two or three days, Olivia has been drinking 3-4 oz of her Pediasure consistently at a time. At those rates, I have a chance of actually getting her all the way off the NG tube. However today, she has decided to drop back down to 1.5-2 oz consistently. Argggghhhh!!! Hopefully the latter is the fluke and not the former. /sigh
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