I have posted before regarding DS (16m) babbling but having no words, and SALT assessment indicating an expressive language delay. Now about six weekslater, we have visited with her again and been told that we should "read up on" apraxia (think it is called dyspraxia in UK?). Apparently this would not be diagnosed officially until he is 2, but we are taken aback by the direction to read up on this as that must mean she thinks that's the situation.
DH and I still feel he is so young, but she is the pro and must have a reason for telling us that other than now being even more obsessed with worry.
We know we are a little sensitive about what seems like so much negativity around his not talking. On the way home from the meeting a little old lady in a parking lot was talking to DS as we were packing up and wanted him to reply...when I told her casually that he wasn't talking just yet, she gave me the most rude tirade about something obviously being really wrong as he should be saying SOMETHING. My jaw actually dropped that a stranger would be so mean!
So knowing that we are now a bit sensitized to this "no words" situation, really want to know what I am supposed to be taking out of the "read up on" apraxia direction. I can't imagine she'd say this unless she thought it was going to be the case - but really, isn't he soooo young to be thinking that already?
(His receptive language is within normal range, started pointing at 14m, hearing fine, responds to his name when he feels like it, very social, etc. - he just has no words).
Would appreciate other's perspectives?