






So we have been MIA for about a week now... We traveled down to Little Rock on Monday, the 8th for an appointment with a pediatric GI specialist and during our visit the doctor decided she wanted to admit Cohen to Arkansas Children's Hospital for what turned out to be an 18 hour fast to figure out what has been causing all of Cohen's diaherra! There is no nice way to describe his poop but that. Basically, Cohen has never had a real poop, just water stools. Yuck... The GI doctor decided to do the fasting because Cohen is weighing in under 15 pounds and is 7 months old so they consider this a failure to thrive and this is of concern and the cause of his failure to put on weight is his cronic pooping. After two days in the hospital and lots of test they determined that Cohen has a very unique protein difficieny called Sucrase Isomaltase Dificiency. Basically he was born without the enzyme to be able to digest table sugar and sucrose which we all know is in everything.
It will be challenging but he will probably be heathier than most kids because of this. For me it is sad to think that he cannot have the guilty pleasures in life like birthday cake, Halloween candy, Christmas cookies or ice cream on a hot summer day. I am sure as I do research and meet with nutrionists we will all learn how to get around some things but Jeremy and I have both decided that we will alter our life style too to make sure he is not the only one going without the guilty pleasures and some of just the regular day-to-day foods that we all consume.
The important thing is that he is putting on weight, and he is happy and healthy. We are happy to be home!

















