LymeNet Flash: Seeking 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 » Seeking LLMD in Minnesota

UBBFriend: Email this page to someone!

Author

Topic: Seeking LLMD in Minnesota

BGearhead
Member
Member # 30840

posted

Hi
I started the many trips to different docs to only get worse..tremors starting. I hope there is a LLMD near me in Minnestota...can I get some info....thank you.

Posts: 27 | From MN | Registered: Mar 2011 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Information sent!!

Please read in Medical Questions for great information and help:

http://flash.lymenet.org/ubb/ultimatebb.php/forum/1

Each forum also has special links at the top of each page containing information you may find helpful.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001 | 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/