Just wanted to update everyone on what's going on with Caleb. Thank you so much to everyone who asks and tells us they are praying for him. We still don't have many answers but progress is being made.
The last big thing is we have an appointment with the Scottish Rite neurology department. It will be Tuesday August 30th. (soon!) I'm very hopeful that they will be able to give us some answers, or if not then be able to tell us for sure that there is no major problem just developmental delays. The Pediatric gastroenterologist did call back and say the upper GI came back normal. His next step would be to do things that the Neurologist will do so he wants to wait for those results. (thankful for that!) So I have no idea what the appointment on the 30th will look like and what tests they will be able to run but again, praying for answers and peace.
Jason and Caleb at Scottish Rite Caleb waiting for the Barium to reach his colon
On a fun note Caleb's vocabulary has exploded over these past few weeks. He talks A LOT! While many of the words are only understandable to me and Jason he is communicating so well! He is so expressive and loves connecting with people. He loves going to the store and flirting with anyone who will look his direction. He is so sweet!!
Love,
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Eating a sucker trying to help the barium move down, he loved it! (his first)
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