My beautiful 19 month old DD saw two SALTs last week for a swallow assessment. She got the all clear on that, but the therapists picked up a few behaviours they said show she requires further assessment.
Having had a chance to observe her at home now following their comments, I am very concerned that she is at risk for developing/is developing ASD. She is poor at eye contact when focussed on something (usually a toy or a book), and often doesn't respond to her name when called, if she is engrossed in something. When asked to look in my eyes she sometimes gets annoyed. She is not very interested in other children, and doesn't seem to mind if we go out of sight for a time. She can say quite a few words, but doesn't tend to use them functionally. On the other hand, when we are joking with her or singing she maintains great eye contact, will laugh and hold our eye-gaze while we are connecting. She looks pleased to see us and other people she knows, will grin broadly etc, sometimes bring us stuff to show us, does a little pretend play etc. Waving good-bye is hit and miss, sometimes it happens unprompted, but mostly it is prompted (which she occasionally ignores). It is like a fog descends upon her at times, while at others she seems fully alive.
We have been referred for a SALT speech and communication assessment, but we waiting on a date. I am extremely stressed and upset (apologies if that sounds insensitive to those on this board), and desperate to know what I can do to help her. Everything I read suggests early intervention results in the best outcomes. What can I do now to help her? Does anybody have any recommendations for books or websites to read?
Also, can anyone let me know what the process is for diagnosis and getting support? Assuming the SALT says there is cause for concern, as I am expecting, what happens next? Does she get referred to a paediatrician? How long does it take? We are willing to go private to speed things up, but don't know who we should see, in what order.
Also, I am aware there are various therapies available, like ABA, Floortime etc. Is there funding for these? Has anybody any experience with these for such a young child, and/or before diagnosis?
Sorry for the mammoth set of questions. I am just very worried and trying to get things moving for my DD.