Hi All! I am a first time poster, although I've been lurking for a while. My six year old began ticcing this summer as soon as school got out. We have an appt with a ped neurologist Aug 19 but after reading what others have experienced I am not expecting much. I got the Sheila Rogers book and was immediately encouraged. However, after doing some food eliminations, introducing supplements, etc the ticcing is basically the same. Has anyone else experienced this. I guess after reading the book I was expecting big changes but none yet. How long does it typically take to notice changes after introducing supplements and dietary mods. I am also a little worried about the supplements I have chosen and the dosages I'm giving. Right now we are doing a kid's multivitamin, a kids Omega 3/6/9 blend, Vitamin c (500 mg), vitamin b6 (100 mg), and magnesium (250 mg). These are adult sized dosages I know so I am a little worried that I am overdoing it. Does anyone have any inight into other suppements that might be beneficial? I am interested in the amino acid component but don't know where to start there. Any advice from more experienced TS parents would be greatly appreciated! My husband thinks that I am now obsessive about finding treatment but if there are things we can do to make it better than I am willing to do whatever it takes.