posted
Somewhere that accepts insurance would be preferable but I get that probably wont happen. I had heard of a center in DC that has a pretty informative website, but I dont know anything else about them or the actual doctor's name. Anyone have ideas?
Posts: 7 | From Maryland | Registered: Jun 2010
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Siciliano
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-------------------- I'm sorry but I am no longer accepting any private messages due to my own battle with lyme. Posts: 3897 | From New Hampshire | Registered: Jun 2008
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Check out the support groups listed under "Chapters" at www.natcaplyme.org. Attending a meeting may give you a chance to meet other patients and discuss physicians.
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