LymeNet Flash: LLMD in Minneapolis

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 Minneapolis

UBBFriend: Email this page to someone!

Author

Topic: LLMD in Minneapolis

JohnSmith
Junior Member
Member # 30729

posted

Hi, I was diagnosed with Lyme Disease last year, put on oral antibiotics and thought I was in the clear. However, some of the symptoms seem to be coming back along with some new symptoms (e.g. severe anxiety).

Now, I'm not positive it's a result of the Lyme disease, but I would really like to find an LLMD in Minneapolis to help me get through this. Some of my friends and family have let me know that I'm just not acting like myself and it's starting to impact my performance at work.

Could someone please recommend a LLMD in the Minneapolis area? Thank you!

Posts: 1 | From Midwest | Registered: Feb 2011 | IP: Logged |

ktkdommer
Frequent Contributor (1K+ posts)
Member # 29020

posted

Sending PM

--------------------
Things are never dull. After 3 fighting Lyme, 2 are in remission. Youngest is still sick, age 22. He has new diagnosed Chiari Malformation and Ehlers Danlos Syndrome.

Posts: 1366 | From Perrysburg, Ohio | Registered: Nov 2010 | 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: 96223 | From Texas | Registered: Feb 2001 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

More info:

http://flash.lymenet.org/ubb/ultimatebb.php/topic/2/13239

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

Posts: 96223 | From Texas | Registered: Feb 2001 | IP: Logged |

littlebit27
Frequent Contributor (1K+ posts)
Member # 24477

posted

I answered your PM

--------------------
*Brittany Lyme Aware on FB*
http://littlebithaslyme.wordpress.com/

Posts: 2310 | From Southeast | Registered: Feb 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/