LymeNet Flash: LLMD in Bangor Me

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 Bangor Me

UBBFriend: Email this page to someone!

Author

Topic: LLMD in Bangor Me

MaineHelpInMaine
Junior Member
Member # 23612

posted

Hi...I'm new here and would like someone to please recommend a Lyme Literate MD in the Bangor Maine area. I am currently having Ear and Face Pain with burning sensation and know that there is lyme on my property. Please Help

Thanks!
Ron

Posts: 1 | From Bangor Me | Registered: Dec 2009 | IP: Logged |

Meg
Honored Contributor (10K+ posts)
Member # 22

posted

PM Sent

--------------------
Success Stories---Treatment Guidelines

Posts: 10010 | From somewhERE OVER THE Rainbow | Registered: Oct 2000 | IP: Logged |

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

posted

Hi,

Maine and welcome to our site.

I sent you a private message, click on the flashing envelope.

--------------------
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 |

z15
Junior Member
Member # 22217

posted

Hi,

I'd very much appreciate the name of LLMD's around Bangor as well. My son is still having joint issues after approx 7 months of doxy and he is now located in Northern Maine with difficulty getting back to Boston.

I'd like to work with his Mass General doc to help engage a Bangor area LLMD.

Thank you,

Z

Posts: 5 | From Groton, MA | Registered: Sep 2009 | IP: Logged |

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

posted

Hi, Z and Welcome to Lymenet! [hi]

We are happy to have you. I sent you a private message (pm), click on the flashing envelope. [Smile]

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!

We also have the General Support forum that you should check out too! [Big Grin]

--------------------
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 |

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/