The best part of Dylan’s visit was his mood he was happy. His VNS was finally checked and in working order. The new neurologists attitude is that she knows what is best for our child. One of her questions for us was why is he on such a low dose of Keppra and we said with a higher dose of the medication he was unable to function properly. When he was on the higher dose of Keppra he just sat there and wouldn’t move or do anything. Maybe the next visit will be better. The office he goes to has a beautiful garden outside for families to enjoy.