LymeNet Flash: Hemex and bartonella

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 » Medical Questions » Hemex and bartonella

UBBFriend: Email this page to someone!

Author

Topic: Hemex and bartonella

susanschn
Member
Member # 19352

posted

My mother just received the following message from her LLMD. What do you all know about these conditions?
BARTONELLA POSITIVE, HEMEX POSITIVE, EVEN WITH NORMAL CD57, EVERYTHING POINTS TO LYME

Posts: 34 | From Florida | Registered: Mar 2009 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

HI Susan... so is she waiting on results of an Igenex Lyme test as well??

Here is a link with info on bartonella symptoms:

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/81386

(scroll down until you see it)

The hemex test may be for hypercoagulation. I had that too and was treated with heparin. It really helped.

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

Posts: 96222 | From Texas | Registered: Feb 2001 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

up for help... can anyone give more info on bartonella or hemex??

There should be info here on bart:

www.wildcondor.com/lymelinks

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

Posts: 96222 | From Texas | Registered: Feb 2001 | IP: Logged |

treepatrol
Honored Contributor (10K+ posts)
Member # 4117

posted

My answers here
http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/88544

--------------------
Do unto others as you would have them do unto you.
Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.

Newbie Links

Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

More info for susan:

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/88544

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

Posts: 96222 | 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/