LymeNet Flash: Need an LLMD in Minnesota

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 » Need an LLMD in Minnesota

UBBFriend: Email this page to someone!

Author

Topic: Need an LLMD in Minnesota

SouthernGirl
Junior Member
Member # 32702

posted

Hey all

I just recently moved up north. I have an amazing doctor "back home" but would like to find someone a little closer to where I am now. I have a few names of dr's in Minnesota and Wisconsin but I have no idea who to try and who is the best.

Would any of you be willing to tell me about your personal experiences with a dr. up here?

Thank you so much!

--------------------
http://confessionsofalymie.wordpress.com/

http://letterstoasoldier.wordpress.com/

Posts: 8 | From Down South | Registered: Jul 2011 | IP: Logged |

SouthernGirl
Junior Member
Member # 32702

posted

(I forgot to say that I have medication sensitivities that has made it really difficult to find an LLMD who can work with me!)

--------------------
http://confessionsofalymie.wordpress.com/

http://letterstoasoldier.wordpress.com/

Posts: 8 | From Down South | Registered: Jul 2011 | 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/