hello, i am a bit new to all this, my name is Dana and i am a stay at home mom to 4 kids, ages 7- 5 -3 -2, our youngest ---Silas is my reason for joining this group, his story is a long one so i will try to make it as short as possible...lol
Silas was a VERY quiet baby, he never cried or anything people would always say you never knew he was there, he did not make much noise either, he was late at everything...rolling over around 7 months, sitting at 10 months, standing at 14 months, walking at almost 19 months, he never really babbled as a baby either, so any way the ped was finally like you need to take him to a developmental doctor, so we did and this was his report
Gross motor delay, developmental delays, mixed expressive, receptive language disorder, low musscle tone
then came the visit to the neurologist and this was his report---Gross motor delay, developmental delays, mixed expressive, receptive language disorder, low musscle tone,some form of PDD-NOS, early signs of aspergers
then we also went to a endochronologist, who discovered his thyroid was elevated, and his tyrosine level was elevated and we still have no answer as to why
then came the visit to the gastrointerologist, for constant diarrhea, and they did the ph probe test and a upper gi and a endoscopy with biopsy, and a video swallow study and nothing signifigant was ever found
then came our visits to the ear nose and throat doc, they tested his hearing because he was not talking and both ears were flat.....so then we had cat scans and mri's and they foud he had a very large amount of fliud in his mastoids, how it got there is beyond me cause he never had a ear infection in his whole life...the neurologist said maybe it was there since birth, who knows not me...lol..well any way they put tubes in and drained both ears last summer, and then a few weeks ago we had another mri done and the neurologist said it looks like there is still fluid on both sides....:( so i dont know what they will do about that....
then we decided to take him to a holistic doc because we were getting nowhere, so we went to dr.buttram ....he found a moderate yeast overgrowth in his intestines, and his neurotransmitters were very elevated....he put him on child essence vitamins, and MB-12 injections and he told us to do a dairy free diet for 3 weeks so we did and then we gave him his bottle back and WAMOOOOO he pooed like 8 times in 20 minutes, so dairy is out..:(, and we are slowly finding more foods that go right throught him, corn and grapes and raisins come out like nothing ever happened to them...it is weird, and they come out like 20 minutes after he eats them....? well any way so far he gets speech twice a week and occupational therapy, and feeding therapy, he is very picky, he weigs 25 pounds and he is 2 and a half....he will chew stuff up and spit it out or gag on it, or stuff his mouth so full he cant chew,he seems to like food with a strong flavor, he will eat a whole can of black olives..lol.....the feeding team says it could be due to the low muscle tone, foods that have a strong flavor he can taste better, and when he stuffs he is able to feel the food in his mouth better, but then he cant chew, he also puts VERY disgusting things in his mouth and he still mouths on toys and stuff.... there is allot more but i think now i am just rambling..lol so i guess that is good for now..LOLOL..there is nobody around here to really talk to and it would be nice to make some friends you understand what we are going through!!!!!