Does anyone know how to contact Andrews Reiter Clinic or have their web address? For some reason I'm having trouble finding it. Incidentally, has anyone had success with them? They are probably my last resort. I don't know what else to do from them. Some people have been urging me to have surgery on my son, but that frightening option is just not an option for me.
Thanks!
Lori
P.S. I'm just conspiratorial enough to think that there already is a cure for it out there, but who benefits from there not being a cure? You guessed it -- Big Pharma, neurologists won't get office visits, etc. When my son was on medication it cost an average of $450/month. That's just one person. I'm very angry and cynical over the whole thing. It just makes me sick. Does anyone else feel this way or is it just me?