Hi Kori Anders.

I know what you mean about the voices. It is very difficult to deal with. My pdoc just recently lowered my dose of Invega for my schizophrenia. I have Tardive Dyskinesia too. I take meds for that but they don't work. My doc thinks the Invega is interfering with the TD meds. I have been on a lower dose of Invega now for 5 days. There is no change. I'm hearing voices more often now. I'm seeing things that just don't make any sense. The voices are louder, and more pronounced. I can actually make out what they are saying. Usually it's just bad stuff about me. Like, I am worthless, or I am lazy. I wish my doc would increase my Invega again. I hate the voices.

Sincerely,

Piraeus