posted
Hello, I was diagnosed with chronic Lyme by a LLMD, but want to explore options of treatment and prices. I have been misdiagnosed for 20 years. Are there any LLMD's out there that are covered by insurance? I live in N. Arizona, but have family in MN and WI, so I can consider doctors there too. The support group in Arizona is hard to get a hold of. Thanks kindly!
Posts: 1 | From Prescott, AZ | Registered: Oct 2010
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janet thomas
Frequent Contributor (1K+ posts)
Member # 7122
posted
I'd check with the support groups in WI & MN-there are some Lyme docs around there.
-------------------- I am not a doctor and this is not medical advice but only my personal experience and opinion. Posts: 2001 | From NJ | Registered: Mar 2005
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littlebit27
Frequent Contributor (1K+ posts)
Member # 24477
pmerv
Frequent Contributor (1K+ posts)
Member # 1504
posted
Please consider joining your online state group to get help with local resources. The URL below is not your state group but will tell you how to find yours. http://health.groups.yahoo.com/group/statenamelyme
-------------------- Phyllis Mervine LymeDisease.org Posts: 1808 | From Ukiah, California, USA | Registered: Aug 2001
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