Hey everyone. As some of you know, my son was ill and unable to keep down any formula. The doctor switched him from normal Nestle Good Start to Enfamil Lipil to Nestle Good Start Soy to Nutraminigen to Alimentium... They even tried pedialyte but to no avail.. He kept throwing everything up. We went to the dotors two days ago and I told him no more formula changes. He suggested attempting a medicine that will possibly help... But we did not have a clue what was wrong so I didn't want to just try a medicine. Instead we got admitted to the local hospital and they ran tests on him. We got the results and were told only surgery would fix it and that we had to transfer to Arkansas childrens hospital. I forgot what the problem is called, but what it basically is is he has a valve at the bottom of his stomach that helps regulate the food that goes into your system that is too big. Even if he drinks like 20 ccs.. hes lucky to geta few drops that actually go into his system, the rest stays in his stomach til it gets overfilled and he throws it up. So, they discharged us yesterday, gave us all te paperwork we needed and copies of the x-rays and ultraound.. and off we drove four hour to this hospital. We got here at 4 pm and were stuck in the emergecy room til midnight.. then they finally admitted us and we went to our room...which we share with another family and baby that has the same thing... My son hasn't eaten in 12 hours.. they say he can't eat til after surgery.. he been practially starving to death for two weeks.. and they said he -might- have surgery today.. else wise tomorrow.. im really freaked out and angry... but i have to be here for my baby.. I mean he only is a month old and hes going through all of this.. i dont know what to do.. its not fair.