Ezra is 5 months old and was diagnosed with Tetralogy of Fallot with Pulmonary Atresia at birth. He's gotten the majority of his food via an ng tube since he was only a few days old. He was born weighing a healthy 9lbs 2oz, so his weight has never been a problem. However, he has never been able to be off of the ng tube.
Here he is at about a month old & now:
We always thought that after his open heart surgery he'd have more energy and feel better, allowing him to eat completely on his own. Unfortunately, the surgery came (April 8, 2015) and went with very little change in his feeding habits.
More recently, his feeding has gotten even worse, which can attributed to the fact that he is becoming more and more aware of his ng tube. He hates it, and it's worsening his oral aversion.
He now goes to weekly feeding therapy, which isn't super helpful because the therapists think he's too old to relearn how to take full feeds. I don't believe that, and I refuse to give up trying. He will also be getting a g-tube in the near future. I'm sad about that because it just seems more permanent and serious.. But I know that it's what he needs & it will be good for him.
I'll try to update this blog weekly, maybe more often if he has any appointments of notable things going on. Thanks for reading! :)