Yesterday I took Camden to his GI appointment at Children's. First let me say that I didn't call until Monday at 3 p.m., after much urging from my two sisters, to get an appointment. I was able to get in the next morning at 9 a.m. due to a cancellation. The nurse on the phone stressed that that NEVER happens. I really felt that we were supposed to be at that appointment then. I had to race there after I dropped I and E off at school. Grandma H. came to stay with Logan--thank goodness!
We first met with a nurse practionier. She has been in the field of gastroenterology and nutrition for 28 years so I felt like she probably knew quite a bit. I was very disappointed within 20 minutes of talking with her though. She criticized me for not vaccinating until my babies are a year old and then told me that Logan was not allergic to dairy because boys do not get yeast infections! I said, well, that's what he had, the doctor diagnosed it. And he had ear infections. She said that's not an allergy symptoms. WHAT?!?!?!?! I felt almost like bursting into tears thinking we had made a senseless trip in. Things did get better though.
Basically, Camden does have gastroesphogal reflux disease. It peaks at four months of age, which may explain why Camden is struggling now (he'll be four months on the 20th of this month). He has many symptoms and all the choking, difficulty breathing is just that, a symptom of the disease. The fact that his "spit up" goes back down and he chokes on it and it could aspirate into his lungs and cause pheumonia is just a symptom and something you deal with. This was very frustrating for me to hear!!!! I wanted to cry for my lil' guy. I guess part of me was hoping for some miracle, which is crazy, I know. Reflux also gets worse whenever he's sick so he'll struggle more when he's got a virus .
Most babies are taken off of their reflux meds after two months. They highly suggested I not take Camden off of his Prevacid any time soon. It will be two months that he's been on it on the 25th. She actually increased his dosage to see if it helps with the amount of choking episodes he has.
We are also supposed to keep a log of all his choking/spit up episodes for a week and then report in to her every week for the next three weeks. If he is still having a considerable amount of "episodes" after the three weeks, then they may do a swallow study with a speech pathologist and radiologist to be sure nothing is physically wrong inside.
She suggested giving him a tablespoon of cereal at night to help calm his stomach and keep things down so he'll sleep better. We're also supposed to give him a bottle once a week. He shouldn't choke with a bottle, but the few times he's gotten one, he has. If that continues, I'll have to report that too.
They were more than willing to do a upper GI on him but didn't recommend it. It will show that he's refluxing and how often for an hour, but it wouldn't help us in our treatment of him. I opted not to do that. I didn't see the point of putting him through something miserable when it wouldn't help us out in the end.
So all in all, I was frustrated but I did learn some things. It seems there's conflicting information among some physicians regarding reflux and I think it's because much is unknown, like why it's caused.
I continue to pray for Camden and continue to do all I can naturally for him. I hate having him on meds but he really needs it. I know God is the ultimate physician and He can heal him. Until then, I keep Camden close and I am learning to enjoy it. Some day I will look back on all this and maybe actually miss it as Camden is running around me like crazy! :)