Hello! My son was born with cord wrapped around his neck at birth in 1965 according to his doctor 6 months later. His development was slow and was categorized as "brain damaged". Later diagnosis changed to cerebral palsy. He has had Jacksonian seizures sporadically. He takes no medications. He knows some sign language. He is basically non-verbal, but understands much of our communication. However, he cannot tell or describe verbally how he feels. My question: What sensations and feelings does one have when experiencing the Jacksonian seizure? Thank you.