Zak is up to 28 pounds again. He likes to eat now that he is fully recovered from his tonsil surgery. Keep it up big boy! What a difference that has made is his sleeping too. Callie is still around 7lb11oz. The poor girl is getting plenty of calories but just burns so much trying to eat. She is also getting more playful since she has been feeling good.
We now have a big decision to make about Callie’s weight. We have been putting off a feeding tube, playing the waiting game. We are finally to that point. Several doctors have asked If we have considered it. Of course we have, we just are not ready. We have had some very long talks with our GI doctor. He has even called us at home on several occasions. He is one of the most amazing people I have ever met. He truly takes everything into consideration. Last week Chris and I finally agreed to move forward with a feeding tube. Callie had a rough week with an ear infection, antibiotics which lead to lots of stools and reflux. Now we need to determine if the reflux was more because the antibiotics or just because she is finally eating more.. or just because that is her and that is the way it is. Unfortunately no one knows the answer. Where is the magic ball when we really need one. So now we have begun the discussion if she needs the Nissin.. after even more discussions (yes all in one week) we said fine, go ahead. Our GI doctor said we should meet with the surgeon and himself again before we move forward. I just wish this was a simple decision like it was for Zak. This time it is not a cut and dry decision. I think this is one of the hardest choices we have had to make regarding our kids medical care. Thankfully our doctor is amazing and we trust his judgment. It is in God’s hands to guide us and I know it will work out in the end.
On a good note.. Chris and his Dad went out on Duck opener this weekend. They eac
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