His reflux is still an issue. We are stopping one of his meds (reglan) today to see if he still needs it and if being on it has really made a difference. I would rather not play around with his meds, but the pediatrician prefers this. He is not spitting a lot, he is just truly uncomfortable for periods of time throughout the day. This sometimes interferes with his feedings as it hurts him to eat when he is refluxing. And it makes him choke, which is never fun while simultaneously trying to eat. It can be quite frustrating for us and obviously for him. He is hungry, but just can't eat.
Carter's mom Kellie had a great post on her blog explaining reflux a couple of weeks ago. I asked her if I could "borrow" it because she did such a good job with it. Reflux is something that many people deal with, but due to the defect CDH babies have a somewhat different struggle with it. Hopefully this information will help you understand more about the whys and hows of our reflux situation!