I am surprised and saddened by the two messages that followed my post but I do encourage you to keep on your own journey with respect to your son's health. Ultimately, you must choose for yourself and him what is the best path. Dr. Clark is a researcher who has totally devoted herself to her work--and to helping whomever she can with her research. I am saddened by the two previous posts because I suspect they really could benefit from Dr. Clark's work if they had had ongoing contact with her and those of us who have used her methods to our benefit. Please don't give up on Dr. Clark or on others who are working with alternative methods of treating cerebral palsy. And your personal hunch about your son's seizures is important--no matter what any of us has to say! Even if it turns out to be your own attitude that gets help in your search, it will be a positive step that benefits you and your son in the end. God bless you and keep on looking into whatever information that becomes available and don't let the two previous posts get you down.