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» LymeNet Flash » Questions and Discussion » Medical Questions » IGeneX Results

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Author Topic: IGeneX Results
jedibelle
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Member # 3794

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I got my results from IGenex and they are as follows:

IgM:
18 +
30 +
31 ++++
34 +
39 -
41 ++
45 -
58 +
66 +
73 -

and IgG:
18 ++
30 -
31 IND
34 IND
39 +
41 +++
45 -
58 -
66 -
73 -

My understanding is that I am CDC neg but IGeneX Pos. Does this mean I have an active infection or could it just be the result of having late stage LD for so long? All of my testing going back to 2002 has very similar results. Oh, my ELISA came back reactive as well.

Posts: 41 | From Toronto, formerly of CT | Registered: Apr 2003  |  IP: Logged | Report this post to a Moderator
Michelle M
Frequent Contributor (1K+ posts)
Member # 7200

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Crikey! Looka that 31 band!

That is positive enough for even an idiot doctor to recognize.

LOTS of specific bands, and then some!

Don't think this is a result of having lyme in the past; if you were really "cured" you wouldn't have so many reactive IgM bands.

Of course, I'm assuming you are symptomatic for lyme.

Hope you'll be getting treatment!

Best,

Michelle

Posts: 3193 | From Northern California | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
treepatrol
Honored Contributor (10K+ posts)
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Its a active infection sorry
you need llmd
keep treating

--------------------
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 | Report this post to a Moderator
jedibelle
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This is where I start to doubt things, I am symptomatic... I think... but I have never had physical sx, only neuro, so I wonder if its just all in my head and nothing is really actually wrong. What a fun disease... grrr
Posts: 41 | From Toronto, formerly of CT | Registered: Apr 2003  |  IP: Logged | Report this post to a Moderator
Michelle M
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Hi Jedibelle.

Don't feel weird about having only neurological symptoms.

That is plenty common!

We've had threads on here where many people with lyme have only neuro symptoms. I'm one of em! I wish I knew how to search for those threads and I'd link them.

Neuro lyme means spirochetes are in your brain. It's a hard space to defend for your body. You need good abx that will pass the blood-brain barrier. Such as doxycycline. There are others. Sometimes your body can fight off the spirochetes, thus you have no physical maladies, but your brain has little protection.

Keep treating; hope you have a good doctor. I know they're kind of scarce up there!

Michelle

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Michelle M
Frequent Contributor (1K+ posts)
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Threads about neuro symptoms...

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=043879#000000

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=043996#000000

You're not alone!

Michelle

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5dana8
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Member # 7935

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Hi Jedibelle

Very possitive specially with ***** at band 31. Sorry to say this. Many people here just have neuro-lyme.

I have a friend in CT that just has it in his heart. It can pick one area & hang out there. But can also spread to other area's of the body,

So it is very important to get treatment now.

I had *** on my band 31 . A very wise LLMD told me once that you have a zero chance of not having lyme with that band lighting up so much. It is highly reactive to lyme. Here is a link that explains the WB better than I can:

http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=042077

Here is a link that explains why you can still have lyme and test CDC negative:

http://www.anapsid.org/lyme/lymeseroneg.html

I just wanted to leave you with one more link-my fav:

http://flash.lymenet.org/ubb/Forum1/HTML/008359.html

Good luck & hope you have a good Lyme Literate MD to help you get better

Stay in touch & keep reading

Hugs & healing
Dana

--------------------
5dana8

Posts: 4432 | From some where over the rainbow | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
jedibelle
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Thanks guys. Fortunately I have a great LLMD who pretty much said the same things as you (I just wanted to hear it from another source) but he is in the states and I no longer have insurance. I am so lucky to have him though, hopefully I'll figure out the financials soon. Thanks for being so helpful and supportive [Smile]
Posts: 41 | From Toronto, formerly of CT | Registered: Apr 2003  |  IP: Logged | Report this post to a Moderator
   

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