Guest guest Posted May 15, 2012 Report Share Posted May 15, 2012 My NFB speaks with 's as well as Cyle's and one in Seattle who contacted me after hearing that I was trying it and twoMisophonia patients came to him. Once you find someone see if you can give me his/her name so he/se can be part of the discussion among allof them on figuring out the best protocols. This goes for everyone trying it. I'dLove to get them all together to talk. I'm also trying to encourage them all to post there contact info on www.misophonia.net so those with miso can find them. None of these providers ever heard of Misophonia before we all contacted them. So chances are you'll have to find one, then educate him/her. If you can find someone in your network then chances are good your insurance will pay for it. I go out of network so I'm paying out of pocket. Sigh One way to find someone is on www.bcia.orgGood luck,HeidiSent from my iPhone Thanks to everyone who responded to my previous thread. I'm willing to try CBT and NFB for my 14 year old son. Does anyone know or recommend any CBT and/or NFB provider in the San Francisco Bay Area who is familiar with Misophonia? Quote Link to comment Share on other sites More sharing options...
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