selective IgA deficiency test

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birdlover3
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selective IgA deficiency test

Post by birdlover3 »

SHould a person who has the MC have the selective IgA deficiency test BEFORE doing the Enterlab tests?? Would that be the protocal?
Diagnosed with Collagenous Colitis November 2012.
jgivens
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Post by jgivens »

Birdlover,
Having that test BEFORE the Enterolab testing is what Tex recommends in his book. Many people have to pay out of pocket for the lab test and why go to the expense if you are IgA deficient? Leah I think, speaks from the experience of having had the tests only to find out she is IgA deficient.

I am going to ask my Dr. for the IgA and IgG (?) before I do the Enterolab testing.
Jane
Diagnosed with Lymphocytic Colitis 12/19/12
"When it gets dark enough,you can see the stars."
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Doug
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Post by Doug »

From everything I have read here and in Tex's book says yes. I called my doctor and I had a test done back in June 2012, I didnt even know I was tested. You may already have the results in some blood work that was done for you.

My results are

Immunoglobulin A Within range



Tissue Transsglutaninase Antibody Iga TTG antibody, IGA

Results <3

Reference Range <5


Immunoglobin A
197 .......... Reference Range 81-463 mg/dl

I appear to be in the normal range, but I am not sure, Can any one read this for me. I really want to get tested by Enterlab
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birdlover3
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Post by birdlover3 »

Thanks for your comments on this. I will ask my doctor about this.
Diagnosed with Collagenous Colitis November 2012.
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birdlover3
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Post by birdlover3 »

I will take both of your comments to my doctor on my appt. and show him this. I did have blood work but don't understand it.
Diagnosed with Collagenous Colitis November 2012.
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tex
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Post by tex »

Doug,

Yes, your celiac screening test results were both negative, and your immunoglobulin A production appears to be close to mid-range, so your EnteroLab test results should be accurate and reliable.

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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Post by tex »

Barb,

Just ask your doctor if you have already been tested for selective IgA deficiency. As Doug said, you may have already been tested. If you've already been tested, your doctor should be able to tell you if you should happen to have the problem.

And if you haven't been tested, just ask your doctor for a blood test to rule out selective IgA deficiency.

Tex
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It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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Post by Leni »

My doctor told me I was IgA deficient. I know she didn't include the term "selective". Is there a difference?
Leni

Diagnosed with lymphocytic colitis and IgA deficiency on 1/21/13.

Anything is possible one day at a time!
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tex
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Post by tex »

Hi Leni,

She probably just left out the "selective" part of it to make it sound less confusing. I'm sure she was talking about the same condition that we've been discussing here. The "selective" part of the name is just part of the doctorspeak tradition. Sort of like the term "essential tremor".

Why doctors picked the term "essential" is beyond me. Surely there are better options. I'm pretty sure they used that term to imply that the tremors are not associated with an underlying disease. But most of us consider the term "essential" to mean absolutely necessary, or indispensable, and tremors are hardly indispensable. :roll: Why couldn't they just associate the tremors with their old standby favorite, "idiopathic", to make it "idiopathic tremors", meaning tremors with no known cause? Whoever first describes diseases, syndromes, or health issues probably gets extra points if they're able to add a bit of obfuscation to the name. :lol:

Sorry, I tend to get sidetracked sometimes. :lol:

Tex
:cowboy:

It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
Leni
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Post by Leni »

Ted, thank you and you're funny. I happen to agree with you. My son was diagnosed 25 years ago with benign essential tremor and I've always thought it was an odd term. :smile:
Leni

Diagnosed with lymphocytic colitis and IgA deficiency on 1/21/13.

Anything is possible one day at a time!
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