Hope may not recognize her numbers or alphabet, but I am sure her difficulties do not include FASD. I have been having difficulties with my hip, and the Dad took over Hope and her physical aggression for the last three days. He used the time out chair and our big red 5 minute timed (thanks, Sherri ). As Hope is tantruming, she pulls on him the same stuff she pulls on me – trying to bite, kicking , throwing things (including the chair), name calling, spitting, etc. He deals with them differently. He does keep her from hurting him, which is easier for him then me, but her time out is based on the number of times he turns over the timer. I don’t know if it is an art or a formula I just don’t grasp, but during Hope’s tantrum, the Dad adds on *Timers* as in “Hope you are up to three timers”. After the tantrum ends, Hope needs to sit in the time out chair for as many 5 minute timers as he has said. She has earned up to 30 minutes and has completed them. She knows that 6 timers is a lot longer then 2 timers! This is still a mystery to GB- she still hasn’t grasped that a single Hanna Montana show, with commercials, is a half hour, last year, now, next week. GB only has *now*, which makes it very hard to prepare her for anything. Hope knows that today always turns into tomorrow and you can communicate a rough sense of how long she will have to wait by counting *sleeps*. She can understand around two weeks, 14 sleeps.
Hope still takes constant supervision and hasn’t gone a day without a major blow up, but I think her future will be easier than GB’s. RAD kids are never easy, but with a RAD kid without other medical conditions, at least you know where the problem is coming from. Since my first RADish came (1986), there is so much more identification of children with RAD and so many more treatments available. I think Hope has a bright future ahead of her.