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

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.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Mari replied to Jmartes71's topic in Related Issues & Disorders
      15

      My only proof

    2. - Rejoicephd commented on Jefferson Adams's article in Gluten-Free Cooking
      1

      Your Complete Gluten-Free Thanksgiving Plan: Recipes, Tips & Holiday Favorites

    3. - marion wheaton replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    4. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,420
    • Most Online (within 30 mins)
      7,748

    maggie23
    Newest Member
    maggie23
    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

    • Mari
      Years  ago a friend and I drove north into Canada hoping to find a ski resort open in late spring,We were in my VW and found a small ski area near a small town and started up this gravelled road up a mountain. We  got about halfway up and got stuck in the mud. We tried everything we could think of but an hour later we were still stuck. Finally a pickup came down the road, laughed at our situation, then pulled the VW free of the mud. We followed him back to the ski area where where he started up the rope ski lift and we had an enjoyable hour of skiing and gave us a shot of aquavit  before we left.It was a great rescue.  In some ways this reminds me of your situation. You are waiting for a rescue and you have chosen medical practitioners to do it now or as soon as possible. As you have found out the med. experts have not learned how to help you. You face years of continuing to feel horrible, frustrated searching for your rescuer to save you. You can break away from from this pattern of thinking and you have begun breaking  away by using some herbs and supplements from doTerra. Now you can start trying some of the suggestions thatother Celiacs have written to your original posts.  You live with other people who eat gluten foods. Cross contamination is very possible. Are you sure that their food is completely separate from their food. It  is not only the gluten grains you need to avoid (wheat, barley, rye) but possibly oats, cows milk also. Whenever you fall back into that angry and frustrated way of thinking get up and walk around for a whild. You will learn ways to break that way of thinking about your problems.  Best wishes for your future. May you enjpy a better life.  
    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
×
×
  • 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.