posted
I am re-posting this, after reading the feedback and reading my post. I now understand the problems with my text. My rheumotolgist did some blood work. My results came back with Lyme co-infection tests for Ehrlichia and Anaplasma originally I posted this question without the markers. Wondering if this makes a difference, since the nurse said I was negative. It reads:
Ehrlichia Ab panel my result <1:64 there expected value titer <1:64
Anapalasma phagocytophilum my result <1:64 there expected value titer <1:64
-------------------- +++++++ do i have lyme, please comment, derealisation,anxiety,floaters,hypertension,tinnitus,dizziness,minor aches,igenix results,igm,**83-93ind,igg**41++ what do u think,please comment Posts: 195 | From california | Registered: May 2011
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posted
First-- alot of people here have trouble reading computer screens because of how lyme can effect the eyes. So it will be helpful if you use lower case and if you break up your paragraphs, so its easier to read.
Also, can you let us know what test you are refering to?
Giving more information on what you're testing for and what types of symptoms other symptoms you have.
Have you been diagnosed with Lyme, or had a Western Blot test, with Bands? That test will help be more specific on if you do or do not have lyme. People here have tons of knowledge-- i'msure we'll be able to help :-)
Posts: 844 | From CA | Registered: Apr 2010
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poppy
Frequent Contributor (1K+ posts)
Member # 5355
posted
A titer test is going to be an ELISA, not a good test for lyme. But did you have a lyme test? You only posted anaplasma and ehrlichia. And I am confused because your previous post said you were positive....this says negative for these two coinfections. Babesia should also be looked for.
That said, lyme is a clinical diagnosis (symptoms, history).
[ 10-15-2012, 05:04 PM: Message edited by: poppy ]
Posts: 2888 | From USA | Registered: Mar 2004
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Sorry, I can't form a full reply because, sadly, I cannot read one word of your post but the headline pretty much explains it.
All UPPER CASE is like a hammer to the eyes.
All solid text, too, with no white space breaks just sends many eyes into spasm. It all becomes on sea of swirls.
Many here have trouble with vision so mostly lower case is kindest to the eyes - UNLESS there is just one word here or there to make a point.
Paragraphs of no more than 3-4 lines seem to work best. And, to help our brains sort it all out, new thoughts that get a new paragraph also work best so we don't miss anything for you.
This way, you'll have more be able to read and reply.
Please hear this in a neutral tone of voice: you must become educated about this. Yes, there is much to learn as to even what kind of doctor will have the knowledge to help.
Reposting from your "Need Help with Test Results" thread: this is very important for you to read - or get someone to read it to you.
------------------------------------
Although your regular doctor tested you and started you on treatment, he or she may or may not be able to actually treat you. Sadly, there is a lot to learn in order to be a wise patient.
FIRST: you need to also be on PROBIOTICS now. Take a couple hours both directions of the clock from when you take your abx (antibiotic).
SECOND: Liver support is vital with any antibiotics and espeically with toxic tick-borne infections. MILK THISTLE is the most basic. Link below is more detailed.
LEARN THE TERRAIN
Connect with local, regional and state lyme support groups:
kelkat posted on Oct. 12: Need help with test results -
Posts: 48021 | From Tree House | Registered: Jul 2007
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- I recall from a previous post that you got a steroid shot in a joint recently.
Any LLMD whom you call for an appointment will need to be made aware of that at the time of the call. Tell them the symptoms you now have.
They will need to address this a bit differently after the steroid shot. Many have gotten worse with steroids.
I don't want to tell you now that no one with lyme should every get a steroid shot or take steroids, as I don't want to make you sad. Still, you need to know this. And life can go on but you know it's vital to find a well educated doctor.
I'm so sorry to hear about all you are going through.
First, connect with your state lyme support group. I hope you find the kind of guidance you need.
Take care. -
Posts: 48021 | From Tree House | Registered: Jul 2007
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posted
Thank you all so much. I am learning as I go. I was negative for Lupus and she said I was vitamin D defiecient, and I should get tested for allergies.
Posts: 23 | From mn | Registered: Oct 2012
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posted
I can see why, sorry about that.
Posts: 23 | From mn | Registered: Oct 2012
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- About that steroid shot you had recently. Be sure to ask your doctor about whether it might be traced to any of the recently contaminated lots.
Even if these Rx were mostly used for spine treatments, it's important to be sure of the lot number, name of Rx, manufacturer and vendors:
posted
I have been worried about that, then I noticed my clinic was not on the list. But now I see they just added 129 clinics to the list and sold drugs to my healthcare provider. Their is no new name list, so I think I should call my clinic tomorrow. I have been 2 the doc 3 times last week. Noonne did any blood work, I did recieve a head/neck scan and was told the results were inconsitent, and to follow up with a neuro in 2-3 weeks.
Posts: 23 | From mn | Registered: Oct 2012
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