UPDATES

I met with the new GI this week. She seemed pretty nice, however I don't really judge first impressions anymore. She said that we were basically doing all we can do for Hannah's reflux. She did change her from Previcid to Nexium b/c of insurance stuff, but so far the insurance hasn't approved the Nexium either. I expressed my frustration about the arching and how neurology says its GI and GI in the past as said its neurology. This GI said an easy way to test it is when Hannah is arching give her some Maaloxx. If its GI related, she will feel better and stop arching and if it is neurological it won't make a difference. Of course Hannah hasn't really arched since then to test it out. She wants to see Hannah back in two months, so at least she still plans to treat Hannah and not just chalk it up to neurology.
Hannah had her sleep study last night. She slept like a champ for almost 7 hours straight which she doesn't do at home. However she hardly jumped at all. They kicked me out of the hospital at 5 this morning and said I didn't need to wait to speak to a DR which to me indicates everything was "normal". Of course when we got home and went back to sleep Hannah just about jumped out of her skin. So this was another wasted test. I am getting really frustrated and feel like we are never going to find answers or solutions to these issues. Please pray that I will not loose hope and will not be so frustrated.