Hi Kirsty

At least we now know we are not alone. Jett had an NG for 8 weeks while he was in NICU, then 4 weeks at the Childrens Hospital, I had been given LIGHT reading on NG tubes as the hospital was more than certain Jett would come home with NG feeding tube, but fortunately the day before discharge he took 100mls from a bottle, HOORAY. It was a slow uphill battle from there at first, but slowly now we are seeing more and more progress. He now will eat off a spoon, but gags and throws up when he has, say for instance, a sandwich, it is like there is too much for him to concerntrate on...(the whole holding, putting to mouth, chewing, swallowing etc) I share your frustration. He has a visit with the speechy and OT this week, so hopefully they can open a few more doors for us, will let you know how all goes, maybe we can help each other

Take Care