posted
I was just informed by another mom treating her child in NY that the state of New Hampshire has passed legislation that Lymes treatment is between the doctor and the patient and that insurance companies can no longer tell docs how to treat or when to stop.
Has anyone else heard anything to this effect?
Is it true? Your thoughts?
Posts: 20 | From eastcoast | Registered: Jun 2010
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Siciliano
Frequent Contributor (1K+ posts)
Member # 15920
posted
I sent you a pm.
-------------------- 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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