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some of us who have been in Lymeworld for years have amassed contact lists and so if you post here or other sites we can get you info BUT a faster way may be for you to do the following: google "(your state) lyme disease support groups" then email the support groups and ask them for Dr referrals and even which Drs to avoid they will be a great local source of info for you and you may even make a few new friends!! good luck and if you need specific info or have a hard time finding help, we are here. Finette |