LymeNet Flash: Looking for LLMD in Atlanta area

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 » Looking for LLMD in Atlanta area

UBBFriend: Email this page to someone!

Author

Topic: Looking for LLMD in Atlanta area

AC
Junior Member
Member # 8438

posted

Haven't heard of any Lyme in the Atlanta area but my son has been sick for over a year and dozens of doctors do not have a clue as to what is wrong. He has displayed a great number of the listed symptoms for Lyme disease but the doctors here are not to keen on making a diagnosis of Lyme. Until recently we have not made a connection with Lyme disease but recently we did come to the realization that my son started getting sick about one month after a vacation to California. While in California we visited Muir Woods and stayed in Tahoe for several days. This trip occurred in late July 2004. I am trying to find out if anyone has any pertinent information regarding ticks and (or)Lyme in these areas of California and during that time of year.

AC

Posts: 6 | From Atlanta, GA | Registered: Dec 2005 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Lyme is found in 49 states.

California has plenty of Lyme all times of the year.

Lyme Disease State Info
http://www.lymeinfo.net/support.html

Treepatrol's links
http://flash.lymenet.org/ubb/Forum5/HTML/000569.html

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

Posts: 96239 | From Texas | Registered: Feb 2001 | IP: Logged |

Dalphia
Member
Member # 8305

posted

I was diagonsed with Lyme, Babesisa (both tick bite infections) at the FFC in Atlanta. They specialize in CFS/Fibromyalgia and of course Lyme and Lyme coinfections. If anyone can get to the root of your son's problem it will be there.

You can get more information on the website.
Good luck,
Dalphia

Posts: 97 | From Tennessee | Registered: Nov 2005 | 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/