Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

What Does This Mean


eternity

Recommended Posts

eternity Explorer

My 17 month old was diagnosed with celiac about 2-3 weeks ago. My oldest three were tested and today they called and said that two of them were mildly positive. What the heck does that mean. One had a GLIABG level of 74 the other was 79. They are 6 and 9. The baby had results of 102. I don't know what these mean and why they are saying mildly positive. They said it is up to me whether I want them to be gluten-free based on whether or not they have symptoms. I thought if you were positive regardless of sypmtoms you were incurring intestinal damage. I am so stressed and confused, someone please help me out.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

Some docs think the diet is SOOO hard that, unless symptoms are interfering with your life, you shouldn't do the diet. I think that's poppycock (and I don't mean the popcorn based treat!), of course. I'd take the whole family gluten-free for the ease of it, but definitely those who test positive!

plantime Contributor

I agree with Tiffany. The diet is not as difficult as some people make it out to be. It would be even easier if your entire family is glutenfree. It is your decision to make.

celiac3270 Collaborator

Mildly positive....I think that means that they were borderline....probably positive, but not definite...mildly positive doesn't mean mild effects on the intestines. All three should be gluten-free.

Second, that is REALLY, REALLY stupid that they ask you based upon symptoms. They may not have symptoms now, but they're going to later. Arthritis, cancer, osteoporosis....if they don't follow the diet now, they'll die younger and will develop serious complications....all three should be gluten-free.

Sure, it would be easier for the entire family to be gluten-free, but it would also be expensive. If you have enough money to, I'd advise you to make the entire house gluten-free. However, gluten-free foods are really expensive, so if you're on a tighter budget, I would not advise you to put people on the diet if they don't need it -- I think this decision should be based on financial situation....over $4 for a loaf of bread is outrageous if you don't need it for medical purposes and it really adds up.

Finally, I, too, agree with Tiffany. The diet is not all that difficult to follow once you get the hang of it and symptoms should not affect your decision of gluten-free diet or not......if you catch it in them and make sure they follow the gluten-free diet, you're adding years to their life and saving them from miserable complications later in life. I find the symptoms the hard part...the diet isn't that bad or hard once you get the hang of it.

-celiac3270

tarnalberry Community Regular

I would add that a gluten-free diet doesn't have to be that much more expensive IF you stick with naturally gluten free foods. Instead of buying millet for a side dish, have beans. (And rice is always a good one.) Instead of buying fancy gluten-free noodles, get asian rice noodles (like pad thai noodles). Instead of buying bread, start making things that aren't sandwiches - or use corn tortillas. If you have to have baked goods, find a consensus on mixes that you can get and trust reasonably without having to throw away wasted efforts.

It doesn't have to be much more expensive to take the whole house gluten free if you're willing and able to get creative and cookin'! :-) (It can be cheaper if you're eating _really_ cheaply, but that's not particularly fun, as recall from my days in college trying to live on $20/wk for groceries. blah!)

gf4life Enthusiast

In my opinion, a positive is a positive. It doesn't matter if it is a higher or lower reading, some people just produce more antibodies than others and it has no bearings on how bad the symptoms are. There are people out there with outrageously high antibodies and NO symptoms, and other who have horrible symptoms and barely register any antibodies at all.

I found with my own kids that they all showed improvement on the gluten-free diet. Even the ones that tested borderline. My oldest child has a severe reaction to dairy, but his only symptoms from gluten seems to be behavior problems. Those were corrected with the diet and even his teacher noticed how much better he was behaving in class. My daughter mainly had diarrhea and occasionally vomiting. No more of that since being gluten-free. My younger boy has always been the sickest and he would have been the only one I had tested if the doctors had anything to say about it. He is so much better being gluten-free, and all of them have started growing at a faster rate.

Our pediatric GI doesn't think it is possible to keep a child 100% gluten free, but at home my kids are, and since I check ahead and send appropriate snacks whenever they go places, they are generally gluten-free away from home, too. The only time they have ever gotten gluten has been when we go out of town and have to eat out or at re4latives homes. The diet itself is not that hard, once you get used to it, but it is much easier if the whole house is gluten free. Before my kids were diagnosed I was getting contaminated all the time. Now the only things in the house that contain gluten are my husbands sauces and his jar of peanut butter (both kept out of reach of the kids) and an old toaster oven and one frozen loaf of regular bread, that kids and I don't touch. It had been easier than I thought, but it takes a lot of forethought when going out with the kids. The loss of convenience is the hardest thing to come to terms with.

And it doesn't have to be all that more expensive, you just have to be careful what you buy. I find we spend more on gluten-free foods, but since we eat out less, we end up spending about the same each month.

God bless,

Mariann

eternity Explorer

Just wanted to update and say that I found out that all three kids tested positive for the endomysial antibody. The lab said anything over 30 was moderate to high. My kids' levels were 74, 79, and 102. All three of them are gluten-free now and so am I since I am still nursing the youngest one. My dh I tested negative but I think he has a sensitivity. He is a truck driver and thus gone most of the time. That leaves my oldest son the only one not on a gluten-free diet in the house. He wants to be gluten-free as well to support his brothers. So long story short, we are all gluten-free. I don't buy many prepared gluten-free foods, I am pretty much making everything myself from scratch. It costs a bit to start with to accumulate the necessary ingredients, cooking supplies and such but I think it is cheaper in the long run than buying prepared gluten-free foods.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,946
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.