LymeNet Flash: LLMD in Maine?

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD in Maine?

UBBFriend: Email this page to someone!

Author

Topic: LLMD in Maine?

mindy
Member
Member # 8837

posted

Hi,
New here, looking for a Lyme doctor in Maine. I have not been diagnosed with Lyme, in fact test was negative, but with fibro. I really don't fit into that..no tender points, etc and the more I read the more it sounds like Lyme. I will see my doctor in March and will talk the to her and see what she thinks, But need to know if anybody knows where in Maine I can be treated...thanks.
Mindy

Posts: 12 | From Maine | Registered: Feb 2006 | IP: Logged |

lpkayak
Honored Contributor (10K+ posts)
Member # 5230

posted

if you still need #'s for maine, nh, mass email me tomorrow-i will be home and able to give them to you... [email protected]

anyone feel free to email me for new england states

--------------------
Lyme? Its complicated. Educate yourself.

Posts: 13712 | From new england | Registered: Feb 2004 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/