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!
Posted by janet thomas (Member # 7122) on :
I'd check with the support groups in WI & MN-there are some Lyme docs around there.
Sending you a PM.
Posted by pmerv (Member # 1504) on :
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