I'm Jenny, mum of 4, girl 14, boy 10, girl 7 and boy 21months. Our second child has AS, which was finally diagnosed at 8. Far too late for early intervention, and in fact too late for any government assistance in our small town. So we regularly traipse to Perth to see our speechie or to see the psych, or any other treatment. The only treatment we can access here is physio, which is actually quite useful as he has some strange postural things going at the moment.
Thanks for creating this forum, hopefully it will be useful and fun for all.