Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

We Had A Scope And Biopsy....now What?


crstnol

Recommended Posts

crstnol Rookie

My almost 18 month old daughter had a scope and biopsy done last Thursday. She has multiple food intolerances and has been dx failure to thrive, has borderline anemia and had a celiac blood panel done and the only thing that came back abnormal was the glaiden antibody IgG (it was 94). Anyways, GI said the scope showed no signs of celiac what-so-ever. What it did show was a dozen or more clusters of ulcers. Yesterday he called me and said the biopsy results were completely normal, so he is going to talk to another pathologist and show them the pictures of her stomach with all the ulcers in it to see if they can figure out what is going on. Meanwhile, her and I went wheat free last Thursday (I breast feed her) and so far, I don't see much of a difference in her. We added in spelt and have been shopping for glutten free items (although I'm not sure we've gotten all the derivatives out yet) and Tuesday she had mucousy stools with noticable amounts of blood. She's still happy and sleeping at night so the GI said not to worry about it right now. I'm so confused! Could she have celiac and have a negative biopsy? And can celiac cause ulcers? The other thing I just realized is that rice milk has wheat glutten in it?? I've tried giving her rice milk to drink and she breaks out in a terrible diaper rash every time. Her ped said that the glaiden antibody being high indicated "a severe wheat allergy" although her RAST testing came out negative for all the big 8 allergens--so I'm wondering if maybe it's the wheat in the rice milk that she's reacting to. Is rice well tolerated for most celiacs? The other one she reacts to every time is oats--we've never really tried barley or rye.

Anyone have any insights? I would greatly appricate any help!

Christy

Lainey 10/5/04


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



Celiac.com Sponsor (A8-M):



Nancym Enthusiast

Just a suggestion but until you identify exactly what she is sensitive to, can you keep her on a very simple diet of fruits, veggies and meats? I'd avoid all grains and beans and nuts and dairy, including soy, rice and corn. I think a lot of us are sensitive to mulitple things and it takes a really minimalistic diet to eliminate them all, at first.

ravenwoodglass Mentor
My almost 18 month old daughter had a scope and biopsy done last Thursday. She has multiple food intolerances and has been dx failure to thrive, has borderline anemia and had a celiac blood panel done and the only thing that came back abnormal was the glaiden antibody IgG (it was 94). Anyways, GI said the scope showed no signs of celiac what-so-ever. What it did show was a dozen or more clusters of ulcers. Yesterday he called me and said the biopsy results were completely normal, so he is going to talk to another pathologist and show them the pictures of her stomach with all the ulcers in it to see if they can figure out what is going on. Meanwhile, her and I went wheat free last Thursday (I breast feed her) and so far, I don't see much of a difference in her. We added in spelt and have been shopping for glutten free items (although I'm not sure we've gotten all the derivatives out yet) and Tuesday she had mucousy stools with noticable amounts of blood. She's still happy and sleeping at night so the GI said not to worry about it right now. I'm so confused! Could she have celiac and have a negative biopsy? And can celiac cause ulcers? The other thing I just realized is that rice milk has wheat glutten in it?? I've tried giving her rice milk to drink and she breaks out in a terrible diaper rash every time. Her ped said that the glaiden antibody being high indicated "a severe wheat allergy" although her RAST testing came out negative for all the big 8 allergens--so I'm wondering if maybe it's the wheat in the rice milk that she's reacting to. Is rice well tolerated for most celiacs? The other one she reacts to every time is oats--we've never really tried barley or rye.

Anyone have any insights? I would greatly appricate any help!

Christy

Lainey 10/5/04

Celiac can cause ulcers, it did in both my kids. You can have a false negative on the biopsy and you can also have changes that are really preceliac changes that doctors don't always recognise. Also please be sure to check all the different names for wheat. Spelt is an ancient form of wheat and is not gluten free. Rice is well tolerated but barley and oats are a no no. Please also be sure to look for malt in the ingredients that is not safe either. Some thing called buckwheat makes a great warm cereal and is actually not related to wheat at all, if she likes cream of wheat that might be a good one to try. I would get the phone numbers off of any product I used for her for awhile and call the company to make sure it is gluten-free.

mouse Enthusiast

Most rice milk is gluten free, but NOT all. I use Pacific. Avoid Oats because there is a big problem with cross-contamination. No barley, rye or spelt. It is so hard to watch your child be sick.

crstnol Rookie
Just a suggestion but until you identify exactly what she is sensitive to, can you keep her on a very simple diet of fruits, veggies and meats? I'd avoid all grains and beans and nuts and dairy, including soy, rice and corn. I think a lot of us are sensitive to mulitple things and it takes a really minimalistic diet to eliminate them all, at first.

Thank you for responding. I should tell you what we are eating. Chicken, Beef, Carrots, Black beans, Grean Beans, Potatoes, Oranges, Peaches, Pears, Bananas, Rice and Spelt. That's it for both of us. Now, about once a week I drink about 1/2 of a can of pop just to stay sane, but that's it. We have tried several other foods, but they always end in a reaction of some sort. The last time we tried Allementum (a milk based hypo-allergenic formula) she had about 2 or 3 ounces in 3 bottles one day and the next day had blood in her stools--almost as if she was having a period. So we still havn't found any fluids that she can handle.

I'm just frustrated with the drs. and hoping to try to find some insight as what may be going on with her.

Thanks,

Christy

So, spelt is not OK? I could have sworn it was in the store as "glutten free" I'll have to look at it again when I get home. So is there any "bread" products that are safe?

Guest nini

if her antibodies were elevated, she has Celiac, even if the biopsy was negative. The biopsy can never ever completely rule it out, it can only confirm it. Dr.s that cling to the outdated dangerous methodology of relying on the biopsy to diagnose celiac are missing many many people in the early stages of the disease. Tests are especially unreliable in children, (if they are negative) so the fact that she did show elevated antibodies is a huge indicator of Celiac.

Spelt is absolutely NOT SAFE. There are companies (like Kinnikinick) that make wonderful gluten-free bread and other baked goods.

My daughter was dx with all the things you described yet was not tested for Celiac until I was dx'ed with it when she was 3. The tests they did on her were not the correct tests and hers were "negative" and the Dr. refused to explore celiac any further and said that she JUST had IBS and that I needed to feed her more whole wheat. Never mind the fact that when she ate anything with wheat she broke out in hives all over her body (what was it doing to her insides?)

I have a huge file of lists of safe foods and menus and so on for newbies if you would like it, just e-mail me at nisla@comcast.net and in the subject put "request newbie survival kit"

Rachel--24 Collaborator

Just wanted to reitterate whats already been said. Spelt is NOT gluten-free and should not be eaten on a gluten free diet. Her blood test was positive so she's either Celiac or gluten intolerant....either way the treatment is the same. Gluten Intolerance is not an allergy so it will not show up in allergy tests...which is why hers was negative for wheat. Celiac or intolerance does not produce the same immune response that an allergy causes.


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



Celiac.com Sponsor (A8-M):



Jen H Contributor

Rice bread is safe. Whole Foods makes some good ones and I hear Kinnickinick does too (haven't tried them yet). I agree with sticking to a very simple diet until you know more-fruits, veggies, plain meats. Let us know if you have more questions.

crstnol Rookie

Thank you all so much! My understanding (from someone on this board) was that the glaiden antibody IgG was not a definate indicator of celiac and that if her glaiden IgA had been positive, then that would have been a positive celiac result. I am new to all of this, so I don't know. I went home yesterday and read the spelt bread package and it said "a wheat alternative" I will stop giving it to her and eating it myself. I did find the Kinn........??? glutten free bread, so I bought a loaf of that and we'll give it a try. What do you think of doing the entrolab tests? I am considering ordering that test to see if it would show anything.

Thanks again!

Christy

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,685
    • Most Online (within 30 mins)
      7,748

    Janahawk
    Newest Member
    Janahawk
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.3k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Thanks for the additional information. I was thinking of asking you if your daughter was taking methylated vitamins since she has the MTHFR gene but you beat me to it. To answer the question you posed in your original post, as I explained, celiac disease does not damage the colon but the lining of the small bowel. If the damage is pronounced enough and the doc doing it is experienced, yes, the damage done to the lining of the small bowel can be spotted with the naked eye.
    • cameo674
      I could not locate the correct Gary Brecka video where he explains the methylation process and specifically states things about how people with the MTRR homozygous gene mutation are known to suffer from heartburn due to a weakened valve/sphincter where the esophagus and the stomach connect.  My brother had the youtube video sent to him from 10x health which is probably why I cannot locate it.     I will have read up on mast cell activation.  I do not know anything about it.  Tums is my preferred gerd treatment.  I always figured a little extra calcium could not hurt me.  
    • cameo674
      Trents: Due to a genetic mutation, my daughter has inherited from both parents she cannot process the Folic Acid provided in the fortified American grains.   An MD told her to avoid eating fortified grains.   My daughter makes the assumption that unless she makes the food item, that the baker used a fortified grain so she has been limiting her gluten intake since 2020.   Her Psychiatrist was who tested her for MTHFR gene issue because she suffers from depression and severe anxiety. The Psychatrist also instructed my daughter to supplement with a methylated version of folate once she knew my daughter was homozygous, because the methylated version bypasses the mutated gene step so her body can absorb it.  Low folate absorption impacts serotonin and dopamine production.  My husband and I also both have two other homozygous gene mutations that interfere with vitamin absorption: MTRR and VDR taq.  The first interferes with B-12 absorption which requires us to take a methylated B-12 vitamin and the second with Vitamin D absorption so we have to take higher doses to stay within normal levels.   My brother, who has the exact same gene mutations, went through 10x health genetic testing for vitamin supplements (paid by his employer) and received a huge report saying the same things about which types of supplements had to be taken.  Gary Brecka does videos on how these gene mutations impact the vitamin absorption pathways.       If my brother had not gotten his testing through work, he would never would have started his supplement journey.  His testing is what triggered my getting functional health testing that tested similar biomarkers to his.  Again the celiac testing was an add-on test that I did off the cuff.  
    • trents
      Welcome to the forum, @growlinhard1! If eliminating gluten from your diet makes significant improvement in your symptoms then there are two possibilities. Either you have celiac disease (aka, gluten intolerance) or NCGS (Non Celiac Gluten Sensitivity, aka, gluten sensitivity). The difference is that celiac disease is an autoimmune disorder that creates inflammation and, over time, damages the lining of the small bowel which inhibits nutrient absorption whereas NCGS does not damage the lining of the small bowel. They share many of the same symptoms. At the end of the day, the antidote for both is to abstain from foods that contain wheat, barley or rye, the three gluten-containing grains. Some countries supply stipends and healthcare benefits for those with an official celiac diagnosis. If you live in the USA that does not apply. The main reasons for seeking an official celiac diagnosis are psychological and social. Many people have a hard time not falling off the gluten free bandwagon without an official diagnosis. They find it easy to rationalize it all away as being temporary or due to something else. When you have an official diagnosis, you tend to take gluten-free eating more seriously. Socially, family and friends are more likely to respect and attempt to comply with your need to eat gluten free if you have an official diagnosis of celiac disease. Your physician is more likely to take you seriously as well if you have an official diagnosis because there are typically other health problems that are spinoffs which develop from celiac disease in time. One autoimmune disease invites others. There are no tests for NCGS. Celiac disease must first be ruled out. We do have specific tests for celiac disease. By the way, some experts believe that NCGS can transition into celiac disease. If your endoscopy/biopsy is only a month away, I would encourage you to stick it out and go back on gluten to get an official diagnosis. You still have time to get a valid test result if you start back on gluten now, 10g of gluten daily which is about the amount found in 4-6 slices of wheat bread.
    • BoiseNic
      I have the same problem. No matter what I eat, I seem to get a break out every 1 to 2 months. I do not do oats, citrus fruits, apples, onions and other foods also, as those cause reactions. The only time I have zero problems is when I fast. The only staple grain I have is quinoa, as that doesn't seem to cause me issues. I have linked mine to a microbiome imbalance. I am currently on month 3 of Skinesa. It's supposed to take 3 months before seeing results. I guess we'll see.
×
×
  • Create New...