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Hope for Misophonia through NFB

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I just got off the phone with a Dr. Gurnee. He runs the sdale Neurofeedback center here in sdale, AZ. His website: http://www.scottsdaleneurofeedback.com/He is the one I am planning to do my Neurofeedback with. He said that he has treated many people with sound sensitivities and considers it a form of OCD. I told him about other sensitivities like visual and tactile and he said that he sees that all the time and that they come from the samearea of the brain. Funny, but he mentioned many of his patients hated eating and chewing sounds. They are no longer bothered by the sounds and can

choose whether to obsess about them or not, but now chose not to and have the power to do that. He also said that he knows exactly what part of the brain causes this problem and focuses on that area but still requires that I get the QEEG mapping done. I told him about Clyle and how he needed over 100 sessions and said that it would take much less than that ( I guess since he already knows the area of the brain to focus on) but the number would depend on the severity of the condition. I feel very hopeful right now, and that is a nice feeling. I start in 2 weeks, since I am visiting family first in N.Y. Can't wait to report on this to the group. I sure hope it works!Funny how this is happening right now with all that has been going on here on this

site. Mike

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