Guest guest Posted September 12, 2010 Report Share Posted September 12, 2010 I have been reading on this board for about a month and have started 2 EFA's a day for my almost 3 year old son with apraxia. We saw some improvement but not much. Then I have been trying to get him to take NV. I've tried chocoloate milk, the no bake cookies, syringing it, etc. Basically, he has maybe gotten half a scoop a day (on the optimistic side of things) for a week. It is a struggle and it takes some bribing to get it down. He has had diarrhea for two days now and I am not sure if it is related. Has anyone else had this problem? We have seen improvements in his imaginative play, more progress with potty training, and more approximations than before. His SLP was thrilled with how focused he was during therapy last week. So, I really want to give NV a complete try but am unsure of what to do at this point. Open for input... Quote Link to comment Share on other sites More sharing options...
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