Oh goodness where do I begin??
Genetics: we are waiting on the preauthorization to get the genome sequencing done. His microarray showed a duplication on 5p, but it is of unknown clinical significance. The sequencing is more detailed and will tell us more.
Endocrinologist: She ran some additional tests and based in those results she wants to treat him for hypothyroidism. We decided that we are going to go with her recommendation. I got really good vibes from her when we met with her.
G.I. doc: I was worried about this visit because it was local and not at the Childrens hospital we normally travel to. Also, I googled him and found horrible reviews. He wasn't bad at all. He was a little difficult to understand. He took his time with us and said based on what we told him that Grant's lack of eating is behavioral. He could have other problems, but he does not display these symptoms. We could do an upper g.I. if we wanted to, but it is likely to come back negative. We left with a few cans of elecare Jr. and decided to try an elimination diet for 10 days.
G tube: we are in the process of trying to schedule to surgery. Now if the elimination diet or thyroid medicine helps, then we will cancel, but the doctors don't think it will make a difference.
Allergist: we were given instructions to stay away from peanuts and anything made in a place with peanuts. We were told that with his number as high as it was that there a 50 50 chance that peanuts could cause him to go into anaphylactic shock. We also got an RX for episode pens in case of an emergency. We were also told to avoid penicillin and amoxicillin because of the rash he broke out in after getting it for an ear infection. We go back in a year to recheck things.
I am looking into getting Medicaid and Children with special healthcare insurance as secondary insurances for Grant. I'm also trying to find out all the resources that we qualify for.
There is more, but those are the big things
Re: Update
212 Facebook Admin.
You are a wonderful mother! It is so great that you are doing everything in your power to help him early!! My little sister has Medicaid and Children with special Healthcare insurance b/c she has Cerebral Palsy and a brain disorder. She sees LOTS of specialists, and my mom never has to pay anything. Good luck with everything, and keep us posted!
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BFP 3.8.16 EDD 11.20.16
Molly: Elecare is a non dairy based formula. We are eliminating dairy from his diet to see if it has any effect. It is doubtful, but it is relatively easy to check. Intolerances don't show up in allergy screens. They can only be checked by guessing and testing by changing your diet.
CSHC has been wonderful for us, we're in MI