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The TTG antibody IGA is .5 and the range is 0.0-6.9
Gliadin IGA is <10.0 It states that <20.0 is negative
Endomysial IGA gives no number. just says negative
Thanks again for all your input. I appreciate itView Thread
I live in Australia - my daughter Alex who is now 21 was a stop/start growing child, mostly in the 98th percentile for height, but with long gaps of no growth. As soon as she could toddle she would squat down with tummy pain several times a day. Once she could talk we knew she got dreadful stomach aches. She had huge brown shadows under her eyes. Doctors investigated but we drew the line at invasive procedures.
When Alex was 14 we went to the GP for the 500th time but saw a locum doctor. He arranged a huge number of blood tests. One of these was the sensitivity for gluten test, and her results were off the scale.
In one week she was in the local hospital having an endoscopy to confirm coeliac disease. As she came back from theatre the nurse confirmed that Alex had the worst case of Coeliac Disease the Gastoenterologist had ever seen - her villi were completly attrophied (excuse the spelling lolz). There is a lot more I could say about her symptoms, but my point to you, the reader, is more about the genetic connection.
My husband of 35 years (we had Alex late
) had been stick thin all his life. He is 6ft2in and when I met him weighed less than 9st. He had suffered from several illnesses but had recently had a heart attack and later nearly died from undiagnosed anemia 2 years after Alex had her endoscopy. Once they had given him iron transfusions we suggested they tested him for Coeliac Disease. The off the planet blood test results were comfirmed by the endoscopy. It was explained to us that nearly all his illnesses, including the heart attack and anemia had been caused by the undiagnosed Coeliac Disease.So when the medical people diagnose you or someone in your family with Coeliac Disease, remember the genetic link is not a myth. Get your family checked out too - you could save someone's life.
Poor Alex cried over never having wheat donuts again
(until they find a cure), but she agrees she would rather be alive than eat donuts.View Thread
I have NO other gastro symptoms (no pain, bloating, gas) although I've had hair loss and dry and aging skin since hyst. (Even though I'm on HRT these issues may be due more to hormonal issues than malabsorption.)
Due to the position of the pancreas and intestines and the anatomical effects of hysterectomy (settling of intestines), I thought this would more likely be an intestinal problem than a pancreas problem.
I've had the following tests:
- Celiac testing — Two blood tests (3 years apart) and endoscopy - negative
- Stool test for parasites (run by PCP) — negative
- Stool test for good and bad bacteria (run by integrative doctor) — normal results
- Ultrasound of pancreas, liver, bile ducts, kidneys, aorta. Images were very clear and all looked good.
GI doc now wants to schedule:
- EUS with another doctor to rule out pancreas problems — not sure I want to do this since U/S was clear and EUS doesn't always show pancreatitis early in disease.
- Small bowel follow through — what will this show? When I asked about adhesions or "blind loop" type abnormalities, he said I'd have much worse symptoms if I had these. So what would be the point of this test??
Are there any additional lab tests that would be useful before proceeding to all these imaging tests — non-invasive and invasive? And what imaging tests would be useful if all lab tests are normal or inconclusive?
I know I can do a gluten free diet to see if that helps. I did one in 2007 and don't think it made much difference but don't recall specifically. I've read that you have to go GF for 90 days and since I don't have many of the celiac symptoms, that's a lot of inconvenience (more so when eating out and traveling - not so much at home).
Thanks to anyone who can provide some input!!View Thread
The problem with the blood test for celiac disease is they are notoriously inaccurate. Many people can go years (!) before the disease will show up in the blood, unfortunately. There's a good stool test put out by enterolab.com that has proved invaluable to many who had trouble getting a true 'read' on whether or not they had problems with gluten/celiac. You can have the kit sent to you and find out for yourself without your doc's help if you want to.View Thread
It turns out I was diagnosed with Giardia,
and have two negative Celiac tests done since I last posted.
I hope this helps. It was from dirty water or seafood in Las vegas or Cancun, Mexico.
Put me out for 5 solid months, the recovery was worse than the Giardia itself.
Tingling, muscle spams, migraines, exhaustion.
Colonoscopy/endoscopy and only now am I starting to come better.
Also get checked for Lymes disease and thyroid problems and endogenous depression. I became quite depressed after 4 months of sickness.View Thread
last summer she discovered that cutting gluten, she is feeling much better. And me I have many digest problem since 12month, so i decied to cut gluten and I feel so much better, I don't take med any more and I fell good like the song
To me the cause of my gleten intolerance is Effexor.
happy ending for meView Thread
If you want to find out for yourself if you truly do have celiac, do the fecal antibody test put out by enterolab.com and see what results come up. It's the most reliable test I know and in some cases is better than the 'gold standard,' the biopsy. It's helped a lot of people find out they need to be GF when everything else has failed.
But if the smell of your fecal material or gas is really, really bad, make sure you ask your doc to run and stool test to rule out the presence of C. diff. It's a nasty bacterium that can cause miserable changes to the GI tract and the odor has a horrible, but characteristic smell of 'something died.' It causes a host of symptoms that can be mistaken for other conditions.
In the meantime you might want to give probiotics a try. There are several good brands on the market and for many they're very helpful in bringing some symptoms into line.View Thread
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On the off-chance the result of the celiac testing is incorrect - and it often is - you may want to consider giving gluten-free eating a try. Some people only find out for 'sure' by exclduing gluten and waiting to see what happens. Even the 'gold standard' - the duodenal biopsy - can turn out to be wrong.
I know going GF can be difficult, but it's worth a try.View Thread
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Yesterday I met a lady with her 13 yr old daughter at a Chick Fil A and she has Colitis and is on the Specific Carbohydrate Diet, so she said she heard or read that Celiacs should not eat any grain at all, even rice! I was taken aback at that. I eat a lot of rice and don't get sick. Well, at my age, 63, I think I am doing ok execept for this battle with stress and arthritis in my back. I survived breast cancer now for 13 years and many other situations that life has thrown at me. I have raised 5 children (2 stepkids) and I have 3 grandsons (& 3 stepgrandkids). Hope you are doing ok today and you have a wonderful tomorrow!!
God bless,View Thread
1. Bloating.2 Abdominal Pains.3.Diarrhea-severe eatery, voluminous.4.Nausea but not usually vomiting. Feeling Tired and easily winded.
Good Luck.View Thread
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