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05/19/2008 21:34
fin24

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

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