Ok, so not too much has happened in the last couple of days. We are up to 4ml and hour continuous feeds. We upped the amount of Pectin to 2% (we were at 1%), to help with Caleigh's loose stools. Eric and I met with another GI doctor, and he ordered a special kind of feeding bag for Caleigh. It's called a Farrell Valve Bag (click on the 1st choice on Google) and it lets us feed Caleigh and vent her tummy of air & gas constantly. They seems to think a lot of her discomfort is from gas and air trapped in her belly. We'll see how it goes and maybe it will help get her volume up because she is feeling better.
Eric and I are running off to the hospital now, but I will update more later. XOXO