Hi, my daughter has Noonan's syndrome and was diagnosed age 3. She is now 11. She has no problems in terms of any learning disability except that she does need lots of repetition before something clicks with her. She is average in the class. She has small stature and is about the size of a 7- 8 year old at age 11. So this is where the OT and paediatrician have been involved . She has been provided with wobble cushion and step under her feet and a slope to enable her to write comfortably. She has never had a statement as all this has been put in place without that. She is going to high school in September and the school nurse , OT and high school have all been talking about EHCP and IHCP . I don't understand the difference . I have been advised to get the primary school to start the application for EHCP now before the end of term as they know her history. Is this all the right thing to do? The school do seem to be putting everything in place anyway for her for next term or is it important to have it down in one of these documents. She is going to be allowed to use the lift, she would have trouble with stairs carrying books, she will have a toilet pass and they are going to speak to the PE staff about the problems she has, she will get a lunch queue pass so she doesn't get trampled on and it is obvious when new staff meet her that she faces difficulties. Sorry for long long message but am very confused