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Official Diagnosis


Forty320

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Forty320 Newbie

(I like these cute faces)

I posted this message on another thread, but decided perhaps it deserves its own.

I had been gluten-free for about 3 months with miraculous results. I had absolutely no problems with my health at all as long as I was gluten-free. However, my family were pushing me to get an official diagnosis. So I finally made an appointment and went in. My doctor has placed me on a non-gluten-free diet until further notice. I have been in physical distress all this time since. This was only about 5 days ago, but I began to feel the results imediately. I've spent more time in the bathroom these last five days than in all the three months before. It seems like everything I eat makes me sick. I also can't help but imagine how much damage I must be causing my body. I should also point out on a different note that since I'm eating food with gluten in it, food containing gluten seems to have no taste since I've been gluten-free. I even ordered a dominos, which used to be my favourite pizza, and it tasted like glue with a touch of grass. I think I know what I want to hear, but I don't have the emotional strength on my own to defy my family's wishes, and I feel they will respect my condition better with an official diagnosis. I was sent to an allergy specialest also, who discovered I'm allergic to natural vegetation growing everywhere within 800km of my home, and that wasn't what I wanted to hear. It did explain why I have a cold most my life. But I was there to rule out wheat allergy. Am I going about this all wrong?

- Dan


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tarnalberry Community Regular

If you know the answer to the question ("Am I gluten-intolerant or not?"), and are having trouble with your family causing you to doubt what you know to be true, then I would suggest working having the confidence to believe in yourself. I know that this probably isn't the answer you wanted to hear, but having people question you on this will happen ... unfortunately, probably the rest of your life. If you think you can stay on gluten for another 85 days (the rest of three months) for the blood tests and biopsies, and you feel that method of diagnosis is best for you, then stick with it - it certainly isn't a "wrong" way to go. But I worry about the tone of your post - it seems that you are saying you can't do what you know to be best for you if your family questions it. They may still question you after the formal testing - and you've already done one formal test, and that's a gluten challenge. Are you prepared to do what is best for you against their advice even after the tests? If the test are inconclusive, or even a negative (though potentially a false negative), will you go back on gluten, even if eating gluten-free makes you feel better?

Forty320 Newbie

I will guarantee you I will go on a gluten-free diet again no matter what the doctor says. I will not live the rest of my life this way. I may have to do it without the support of my family, but I hope not. What I really wish I could do is teach them about this condition. They don't understand why it is so important that I am exposed to no gluten. I have a hard time understanding my own mind. It's hard for me to make decissions when I'm like this. I suppose I should set a limit to how far I'm willing to go before I give up and return to a gluten-free diet. I don't want to put myself in danger by eating something that could be poison to me.

Oh, does it really take three months of eating gluten to get to where I can be tested properly? :o Yikes! I hope there is a faster way! If I can call what you call a "gluten challenge" a formal test, I think I'll just accept that as such and tell my family I've been formally tested! Then, whether they want to believe me or not is up to them. If they choose to alienate themselves from me, that's their decission, and it's their problem. I won't accept the consequences.

I'm curious, however, if you happen to know, considering the new law that is supposed to go into affect here in the US in january of 06, making it easier to see if wheat is in stuff, if I were not gluten intolerant, and were simply reacting to a wheat allergy, would my symptums be the same? I know they're two different things, but merely avoiding wheat would be easier than avoiding everything with gluten in it. If I had a wheat allergy, would I react the same to wheat as I would react to gluten if I were gluten intolerant? Does that make any sense?

- Dan :unsure:

tarnalberry Community Regular

I'm glad I just misread your post, and that you'll do what you need to do to keep yourself healthy! I know it can be tough when people don't believe you, but you're right that we're not supposed to feel crappy! :-)

Most allergists will tell you that if you have a wheat allergy (which is an immune response mediated by the IgE molecule), you'd have itchy eyes/nose/face, hives, or other classic "allergy" symptoms caused by histamine release. This is as opposed to an intolerance (which is an immune response mediated by the IgG and IgA molecules), you'd have intestinal discomfort, bloating, and so forth.

But really, the symptoms can overlap more than that. You can get a blood test for an allergy to wheat (IgE) as well as the celiac panel for an intolerance (IgG/IgA), but you can also be both. If you really aren't sure, I'd suggested doing a separate dietary challenge, and after being totally gluten-free for a week or so, eat a big bowl of oats, or a big bowl of pearl barley.

I should be clearer on the "dietary challenge as a formal diagnosis". It's _part_ of a formal diagnosis. Many doctors will not take it as proof - ON ITS OWN. Mine took it for a diagnosis in combination with inconclusive (not negative) blood test results. But, unfortunately, you DO have to be gluten-free for quite a while to have positive test results. You can't diagnos celiac via biopsy without intestinal damage, and there's evidence that you won't get accurate positives on blood work without intestinal damage that allows the antibodies to escape into the blood stream. That's why many good celiac doctors recommend at least three months back on gluten for testing.

Some people around here have used Open Original Shared Link, which is a stool test that has not been peer reviewed yet but was developed by a doctor who deals with celiac. Many of them have found it to be the best way to go for them, and you can be gluten-free for (approximately) up to a year before testing and still get reliable results. Many regular doctors will not accept their findings for a formal diagnosis, however. (Then again, there's arguments about getting insurance and whatnot with that as a formal diagnosis... so there are pluses and minuses...)

Racheleona Apprentice

I have been having the same problem, my IgG number was the only positive and was one point difference from being negative. I have not been getting straight answers, and wonder if only wheat is causing all of my problems ( if that is possible for wheat to cause loss of menstruation, hair loss, graying etc.) A blood allergy test I did, showed no allergy to gluten but allergies to buckwheat, wheat, barley, and I think oats. I'm so confused as to what I should do! So I know how you feel.

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    • Mmoc
      Thank you kindly for your response. I have since gotten the other type of bloods done and am awaiting results. 
    • Aretaeus Cappadocia
      I wanted to respond to your post as much for other people who read this later on (I'm not trying to contradict your experience or decisions) > Kirkland Signature Super Extra-Large Peanuts, 2.5 lbs, are labeled "gluten free" in the Calif Costcos I've been in. If they are selling non-gluten-free in your store, I suggest talking to customer service to see if they can get you the gluten-free version (they are tasty) > This past week I bought "Sliced Raw Almonds, Baking Nuts, 5 lbs Item 1495072 Best if used by Jun-10-26 W-261-6-L1A 12:47" at Costco. The package has the standard warning that it was made on machinery that <may> have processed wheat. Based on that alone, I would not eat these. However, I contacted customer service and asked them "are Costco's Sliced Almonds gluten free?" Within a day I got this response:  "This is [xyz] with the Costco Member Service Resolutions Team. I am happy to let you know we got a reply back from our Kirkland Signature team. Here is their response:  This item does not have a risk of cross contamination with gluten, barley or rye." Based on this, I will eat them. Based on experience, I believe they will be fine. Sometimes, for other products, the answer has been "they really do have cross-contamination risk" (eg, Kirkland Signature Dry Roasted Macadamia Nuts, Salted, 1.5 lbs Item 1195303). When they give me that answer I return them for cash. You might reasonably ask, "Why would Costco use that label if they actually are safe?" I can't speak for Costco but I've worked in Corporate America and I've seen this kind of thing first hand and up close. (1) This kind of regulatory label represents risk/cost to the company. What if they are mistaken? In one direction, the cost is loss of maybe 1% of sales (if celiacs don't buy when they would have). In the other direction, the risk is reputational damage and open-ended litigation (bad reviews and celiacs suing them). Expect them to play it safe. (2) There is a team tasked with getting each product out to market quickly and cheaply, and there is also a committee tasked with reviewing the packaging before it is released. If the team chooses the simplest, safest, pre-approved label, this becomes a quick check box. On the other hand, if they choose something else, it has to be carefully scrutinized through a long process. It's more efficient for the team to say there <could> be risk. (3) There is probably some plug and play in production. Some lots of the very same product could be made in a safe facility while others are made in an unsafe facility. Uniform packaging (saying there is risk) for all packages regardless of gluten risk is easier, cheaper, and safer (for Costco). Everything I wrote here is about my Costco experience, but the principles will be true at other vendors, particularly if they have extensive quality control infrastructure. The first hurdle of gluten-free diet is to remove/replace all the labeled gluten ingredients. The second, more difficult hurdle is to remove/replace all the hidden gluten. Each of us have to assess gray zones and make judgement calls knowing there is a penalty for being wrong. One penalty would be getting glutened but the other penalty could be eating an unnecessarily boring or malnourishing diet.
    • trents
      Thanks for the thoughtful reply and links, Wheatwacked. Definitely some food for thought. However, I would point out that your linked articles refer to gliadin in human breast milk, not cow's milk. And although it might seem reasonable to conclude it would work the same way in cows, that is not necessarily the case. Studies seem to indicate otherwise. Studies also indicate the amount of gliadin in human breast milk is miniscule and unlikely to cause reactions:  https://www.glutenfreewatchdog.org/news/gluten-peptides-in-human-breast-milk-implications-for-cows-milk/ I would also point out that Dr. Peter Osborne's doctorate is in chiropractic medicine, though he also has studied and, I believe, holds some sort of certifications in nutritional science. To put it plainly, he is considered by many qualified medical and nutritional professionals to be on the fringe of quackery. But he has a dedicated and rabid following, nonetheless.
    • Scott Adams
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