Has anyone had the Wada Test done? What was you all's experience like with it? What happens after the test is done? Do you have to meet with the neurologist again and the neurosurgeon to see what will happen? I have an appointment to get the Wada Test done on October 23rd and I am scared to death. The visual of getting a catheter stuck up your leg is traumatizing but at least it is for a good reason. I hope that it goes well and that they find which side of my brain has the best memory and see if my language and/ or memory will be affected by the surgery. I need all the support and information that I can get so my anxiety can go away.