I'm in a "something must be done" mood at the moment researching different approaches to helping Ds2 with his motor problems. (He has no diagnosis but motor and co-ordination problems along with communication, speech and language difficulties). He is at a special needs unit but even they seem surprised at how poor his motor skills are and this has activated me into thinking if there is anything else we can do for this. I remember Charlotte Moore writes that she had some success with one of her boys (George I think) using AIT but not the other, and I wondered if anyone else had tried this, how much it cost, where they went etc?