LymeNet Flash: Test results?

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 » Test results?

UBBFriend: Email this page to someone!

Author

Topic: Test results?

MrsSAM
Member
Member # 7079

posted

Hi Everyone: Just wondering if anyone knows what it means to have the lyme test come out 1.32. It states that 1.10 is negative and 1.64 is positive, does anyone know what 1.32 means?

------------------
Thank you MrsSAM

Posts: 31 | From Canada | Registered: Mar 2005 | IP: Logged |

MammaLyme
Frequent Contributor (1K+ posts)
Member # 1257

posted

What test is this?

Posts: 2173 | From Maryland | Registered: Jun 2001 | IP: Logged |

MrsSAM
Member
Member # 7079

posted

HI: Its for Lyme I am not sure exactally, I guess I should have know before I asked this. I just know it was for lyme?

Posts: 31 | From Canada | Registered: Mar 2005 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Probably the ELISA...but do try to get a copy of the test. Keep it for your own records. The ELISA is notorious for false negatives so anything slightly in the realm of positive, should be considered very suspicious.

Can you get your dr to follow up with a Western Blot test by Igenex Labs?...not just any lab will do, trust me!

Here are some links........Be sure to read the one on the Western Blot test.

Tincup's Links for new members
http://flash.lymenet.org/ubb/Forum1/HTML/009342.html

Dr. Joseph J. Burrascano's Guidelines http://www.ilads.org/burrascano_1102.htm

Rose's 15 Facts for Newcomers http://flash.lymenet.org/ubb/Forum1/HTML/011977.html

Camp A and Camp B http://flash.lymenet.org/ubb/Forum1/HTML/021395.html

Abbreviations for Lyme-speak
http://flash.lymenet.org/ubb/Forum1/HTML/020494.html

Making the most of your LLMD visit
http://flash.lymenet.org/ubb/Forum1/HTML/020605.html

Success Stories http://flash.lymenet.org/ubb/Forum1/HTML/022173.html

Western Blot explanation: http://flash.lymenet.org/ubb/Forum1/HTML/022767.html

The cause and spread of Lyme http://flash.lymenet.org/ubb/Forum1/HTML/032259.html

More info: http://www.ilads.org/

Lyme Wars http://www.wildernetwork.org/Lyme_Wars.html

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

http://www.anapsid.org/lyme/matthewgoss/index.html

------------------
oops!
Lymetutu

[This message has been edited by Lymetoo (edited 29 May 2005).]

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

MammaLyme
Frequent Contributor (1K+ posts)
Member # 1257

posted

Get yourself tested by Bowen Research lab. Call them in FL at 727-937-9077. You donate $250 and they test for babesia, lyme, HME and HGE. This test saved my life. I had it all but I only had bits and pieces from other labs.

You get pictures of what is in your blood. You also do not have to take antibiotics for it to show up either.

As soon as your blood arrives in FL, you get the test results faxed to your doctor within 24 hours. Then about a week later, you will get the pictures sent to your doctor. We take the results and color copy them on our printer.

Always keep copies of all of your reports.

Go to www.bowen.org and click on lyme research and go to www.lymediseaseinformation.com and look at the Pfizer pamphlet for the coinfections that Bowen shows.
Good luck.

Posts: 2173 | From Maryland | Registered: Jun 2001 | IP: Logged |

MammaLyme
Frequent Contributor (1K+ posts)
Member # 1257

posted

Go to www.bowen.org and click on lyme research and go to www.lymediseaseinformation.com and look at the Pfizer pamphlet for the coinfections that Bowen shows.
Good luck.

[This message has been edited by MammaLyme (edited 29 May 2005).]

Posts: 2173 | From Maryland | Registered: Jun 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/