Dinny, Robin answered your question re LBD and PDD. As for doctors accepting info gleaned on websites, etc. it probably depends on the doctor. I have given my LO's neuro a copy of the LBD Bad Medication list which he found interesting not that he agreed with it all. And, I do mention things to the neuro and the GP that I have learned through my support groups etc. and they seem to handle it well. I am in Italy so maybe they are easier here and maybe not. When you go to the doctor, you are in need of answers so you should feel free to say and mention whatever you fee like within limits. IreneM
