LymeNet Flash: LLMD's 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's in Maine

UBBFriend: Email this page to someone!

Author

Topic: LLMD's in Maine

CCP816
Junior Member
Member # 24905

posted

I live in maine and I am looking for a LLMD in the state. Anywhere in the state or north mass would be good. I can drive anywhere but live up towards the Bangor area.

Posts: 5 | From Maine | Registered: Mar 2010 | IP: Logged |

Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

posted

Hi,

CCP816 and WELCOME to our lyme site. We're glad you came to us for help.

I have sent you a private message (pm), click on the flashing envelope.

Also, check out our great "Medical Questions" forum where you can ask all the questions you might have and our wonderful, knowledgeable members will answer them. Just read some of the threads and you'll see just how informative they are!

[Smile]

--------------------
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 | IP: Logged |

MaineLyme
Junior Member
Member # 9611

posted

http://health.groups.yahoo.com/group/MaineLymeDisease/

For more information on Lyme disease in Maine.

quote:
Originally posted by CCP816:
I live in maine and I am looking for a LLMD in the state. Anywhere in the state or north mass would be good. I can drive anywhere but live up towards the Bangor area.

Posts: 7 | From Maine | Registered: Jul 2006 | IP: Logged |

CCP816
Junior Member
Member # 24905

posted

Thank you for the quick replies. I will look into all the infromation I hae recieved. Sorry if this is already a post someone has brought up.

Posts: 5 | From Maine | Registered: Mar 2010 | 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/