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

Question On Scoping


sjust

Recommended Posts

sjust Apprentice

So the G/I has decided that he wants to scope my 6 month old to find out what is going on. She is having green mucusy bowel movements. He says he is looking for damaged villi but not for celiac cause she is to little for that. My question is, has anyone had a baby this young scoped? It sounds pretty invasive and I really don't want to go that route. I am not even sure what it will accomplish. He has only decided to do this because we asked for a referral to Stanford.

Thanks

Sarah


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



Celiac.com Sponsor (A8-M):



Lisa Mentor
So the G/I has decided that he wants to scope my 6 month old to find out what is going on. She is having green mucusy bowel movements. He says he is looking for damaged villi but not for celiac cause she is to little for that. My question is, has anyone had a baby this young scoped? It sounds pretty invasive and I really don't want to go that route. I am not even sure what it will accomplish. He has only decided to do this because we asked for a referral to Stanford.

Thanks

Sarah

Don't do it and wait for the other moms to click on. They will.

hfsroyle Newbie

IMO, I would only let a GI specialist scope someone that small and even then, I'm not real sure about it. There is always the risk of perforation and then you've got a whole other set of problems. I'd go for other testing before I'd do that. Have you seen an allergist yet?

Nic Collaborator

I don't understand why he said that he wasn't looking for Celiac because she is too young for that. There are plenty of parents here that have babies with Celiac. But my question is, what else is he looking for? Are the suspecting another illness to be the cause and is that why he wants to scope?

Nicole

sjust Apprentice

My dr. is a G/I specialist but I have little faith in him. He flat out states that a child under the age of 8 months can't have celiac. We all know that is not true but try to get a dr. to change their mind. We have pretty much decided that we will get a second opinion and if they agree that scoping is the way to go then we will probably do that. I don't know what else to do at this point. It has been 4 months that we have been unable to figure out how to fix her issues.

Nic Collaborator
My dr. is a G/I specialist but I have little faith in him. He flat out states that a child under the age of 8 months can't have celiac. We all know that is not true but try to get a dr. to change their mind. We have pretty much decided that we will get a second opinion and if they agree that scoping is the way to go then we will probably do that. I don't know what else to do at this point. It has been 4 months that we have been unable to figure out how to fix her issues.

If it is any comfort to you, my son was scoped at 4 years old and handled it very well. It wasn't a terrible experience for him.

Nicole

CarlaB Enthusiast

Is your child eating gluten? If so, has she had a blood test? I'd do the blood test for celiac. The scope sounds too invasive for a six month old. But, if she's had no gluten, then celiac wouldn't be the problem, which is why I asked about her eating gluten.


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



Celiac.com Sponsor (A8-M):



sjust Apprentice

She is exclusively breastfeed and I have been gluten-free for about 4 months now. It seemed to correct the problem at first, then the bm issues returned. I realized I was eating gluten and cut it out but the bm has never returned to normal.

Ursa Major Collaborator

A six month old absolutely can have celiac disease. Are you breastfeeding your baby? If you are, and you are eating gluten, so does she. The same applies to dairy. A lot of babies are thought to be intolerant to breastmilk and are switched to formulas, when the problem is that the baby is intolerant to gluten and/or dairy or soy, and the mother is consuming these foods.

A breastfed baby eats what you eat. While breastfeeding my son I had to give up everything red, as it would cause him to have a raw bum, the skin would just peel off. That meant no strawberries, cherries, tomatoes (which I didn't know I was intolerant to at the time), peaches, red apples, rhubarb etc. for me that year. As long as I stayed away from naturally and artificially red foods, he was fine.

My oldest daughter's twins are intolerant to nightshades and dairy, and one of them to soy. They had terrible eczema and were not doing very well until she had them tested and stopped eating those foods while she was nursing them (a little over a year). Once she stopped eating those, their eczema cleared up, and they were much happier.

So, it might be gluten, or dairy or something else, or a combination. Rather than a scope on such a little baby (which will likely be negative anyway, as the baby is too small to have extensive damage to the villi yet) I would try an elimination diet for yourself if you are breastfeeding, or if she is eating solids, stop those altogether for a while and then reintroduce one at a time to look for reactions. If she is on formula, something in that might be the cause.

Ursa Major Collaborator
She is exclusively breastfeed and I have been gluten-free for about 4 months now. It seemed to correct the problem at first, then the bm issues returned. I realized I was eating gluten and cut it out but the bm has never returned to normal.

Oops, we were posting at the same time. Try eliminating dairy and soy to see if it helps, and if it doesn't, look for whatever else could be the cause.

sjust Apprentice
Oops, we were posting at the same time. Try eliminating dairy and soy to see if it helps, and if it doesn't, look for whatever else could be the cause.
sjust Apprentice

I am already off dairy, soy, corn, eggs, gluten, citrus, nuts, and beans. Total elimination of the corn is new as of Monday, prior to that I was only off big corn ie. popcorn, corn chips and tried to stay away from corn syrup. I am not sure where else to go on the elimination diet at this point.

Ursa Major Collaborator
I am already off dairy, soy, corn, eggs, gluten, citrus, nuts, and beans. Total elimination of the corn is new as of Monday, prior to that I was only off big corn ie. popcorn, corn chips and tried to stay away from corn syrup. I am not sure where else to go on the elimination diet at this point.

Oh goodness, you have already cut out the most common (and not so common) allergens! Try taking out nightshades (potatoes, tomatoes, peppers, eggplant) next to see if it makes a difference. It could also be rice, unfortunately. I can't tolerate rice, either, as it's a grain. And I am intolerant to all grains.

Once her issues resolve (if you figure it out), you should try those foods you eliminated one at a time to see if she has a reaction. If she doesn't, put the food back into your diet. There is no need for you to take more foods out of your diet than necessary!

It could be a combination, too. One of my granddaughters can't tolerate grain with eggs (their mom uses an egg substitute when baking) or grain with tomato (no spaghetti with tomato sauce, or hamburgers with ketchup). Those are almost impossible to figure out on your own. My daughter had the whole family tested with a Vega machine by a naturopathic doctor.

Another daughter can't tolerate tomatoes with meat, or potatoes with meat. She is also intolerant to sugar and wheat. One son-in-law is also intolerant to sugar, it gives him awful eczema. He suffered from eczema all his life until he was 25. Now they sweeten everything with honey, and his eczema is gone completely!

I found out about my nightshade intolerance at the same place. Too bad the Vega machine (which isn't infallible) didn't pick up on gluten, as it would have saved me four or five years of illness. It did pick up on my combination though, which is fruit and grain. I had never been able to figure out what caused me to have hives covering my whole body along with feeling really ill and breathing difficulties until then (a systemic reaction for sure).

Which makes me realize why suddenly I feel bad and am in pain, I ate a glutino breakfast bar, which has rice, corn and fruit! Yikes, so much for my good advice :ph34r: . I ignored my grain intolerance and forgot about my combination one as well (blushing in shame).

sjust Apprentice

Oh my :o that is a lot of possibilities. I am not sure how you cut out rice along with everything I have already cut out and still eat. If anybody can tell me, I would be willing to try it. We just found out we can go to Stanford though so that is exciting.

hfsroyle Newbie
Oh my :o that is a lot of possibilities. I am not sure how you cut out rice along with everything I have already cut out and still eat. If anybody can tell me, I would be willing to try it. We just found out we can go to Stanford though so that is exciting.

Congrats on the Stanford thing. I'm sure you feel better about that. I don't know what I would do if I couldn't eat rice either. That's pretty much what is sustaining me at this point. Katelyn is going through a growth spurt and nursing like crazy so I am STARVING!!!

Anyway....hope you get your appointment to Stanford soon!!

Heather

sjust Apprentice

I live on rice as well. I use rice flour for tortillas and waffles and eat lots of rice with meat.

Ursa Major Collaborator
I live on rice as well. I use rice flour for tortillas and waffles and eat lots of rice with meat.

I don't like saying this, but seeing how much rice you eat, it makes it even more likely as a culprit. I will just eat vegetables and meat (and I have just a few veggies I can eat that aren't high in salicylates), and the only fruit I can eat is peeled pears, and the occasional golden delicious apple. No spices, no herbs, no honey, no teas other than chamomile, and the only oil I can use is cold pressed sunflower oil.

And usually I stick to it, or I pay like I do now. I've been doing this for two years, and it is possible without starving! But it is difficult, no doubt.

The only starch I can tolerate in moderation is light buckwheat flour. I react to every other starch.

But if you eliminate rice and it makes a difference, it is possible that some of the other foods you eliminated aren't really a problem (even though dairy, gluten and soy may well be).

Darn210 Enthusiast

You've eliminated so much . . . it sounds like a lot of it is "guessing" what it might be and if so, chances are you'll be able to add most of that back in. Based on what you said, you saw a definite improvement when you went off of the gluten. Did you notice any kind of improvement when you went off any of the others? Did you do them all at the same time? (I don't really know how you do the elimination diet, so excuse me if I ask silly questions?) When you went off of the gluten, what did you turn to as your main staple? Did you start eating a lot of something (like the rice) that you didn't used to eat much of before? I would look hard at whatever that was. Those are the questions I would ask myself.

I was following (some) on your previous thread (about breastfeeding). One of the responses was about your baby could have an alergy to milk protein (which would then mean an alergy to breast milk). I know that you don't want to give up breastfeeding. I mention it again so that anybody that is new to this thread can respond if they know of a way to test for that without having to just stop. Also, you may want to ask a doc if there is a way to test for it.

sjust Apprentice

Dairy was definately a problem even the smallest amount caused scalding on her bottom, soy makes her spit up, she does not seem to tolerate corn although exactly how is still not clear, beans made her very gassy. The nuts we are off because my son has a cashew allergy so they said stay away from them and frankly it is the easiest. I have started adding back in egg in things like bread. She seems to be ok with that but it has been in very small portions. On Monday I took out all corn to see if we get anywhere with that, I was still using chicken broth with corn in it and drinking diet soda which I found out had corn syrup for coloring. They tested her for a milk allergy and it came back negetive. Not sure if that is the same thing you were asking about.

Sarah

CarlaB Enthusiast

I Googled "baby green mucousy bowel movement" and got this ... it's on www.justmommies.com

Some breastfed babies are very sensitive to certain foods in their mom
Ursa Major Collaborator

Sarah, an allergy and an intolerance are not the same thing. You can test negative for a dairy allergy and be very intolerant to dairy. The same goes for gluten. Allergy testing will only catch immediate reactions, but will miss delayed ones. Obviously, you know that already, as you have seen the reaction she has to dairy.

It is extremely unlikely for any baby to really be intolerant to their own mother's milk. Too many mothers give up on breastfeeding, when in reality the problem is something they are eating themselves. I believe you are on the right track with the elimination diet. Keep up the detective work!

janelyb Enthusiast

If a baby is allergic to their moms milk isn't that called PKU? If so she would have already been screened for that in the hospital after birth. Maybe it was the corn. Are you seeing any improvements yet? I'd give it another week and then maybe try the no rice option for 2 weeks to see if that makes a difference.

I'm so glad you are getting into the Standford Celiac Clinic, you will have to let me know how it goes.

Missed you today at Rori's party, hope all is well.

Janel

EmmaQ Rookie

When are you going to the Celiac clinic?

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. - knitty kitty replied to lizzie42's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Son's legs shaking

    2. - Scott Adams replied to Paulaannefthimiou's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Bob red mill gluten free oats

    3. - knitty kitty replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    4. - trents replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

    5. - SamAlvi replied to SamAlvi's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      High TTG-IgG and Normal TTG-IgA

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,868
    • Most Online (within 30 mins)
      7,748

    LMGarrison
    Newest Member
    LMGarrison
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • knitty kitty
      @lizzie42, You're being a good mom, seeking answers for your son.  Cheers! Subclinical thiamine deficiency commonly occurs with anemia.  An outright Thiamine deficiency can be precipitated by the consumption of a high carbohydrate meal.   Symptoms of Thiamine deficiency include feeling shakey or wobbly in the legs, muscle weakness or cramps, as well as aggression and irritability, confusion, mood swings and behavior changes.  Thiamine is essential to the production of neurotransmitters like serotonin and dopamine which keep us calm and rational.   @Jsingh, histamine intolerance is also a symptom of Thiamine deficiency.  Thiamine is needed to prevent mast cells from releasing histamine at the slightest provocation as is seen in histamine intolerance.  Thiamine and the other B vitamins and Vitamin C are needed to clear histamine from the body.  Without sufficient thiamine and other B vitamins to clear it, the histamine builds up.  High histamine levels can change behavior, too.  High histamine levels are found in the brains of patients with schizophrenia.  Thiamine deficiency can also cause extreme hunger or conversely anorexia.   High carbohydrate meals can precipitate thiamine deficiency because additional thiamine is required to process carbohydrates for the body to use as fuel.  The more carbohydrates one eats daily, the more one needs additional thiamine above the RDA.  Thiamine is water soluble, safe and nontoxic even in high doses. Keep in mind that gluten-free processed foods like cookies and such are not required to be fortified and enriched with vitamins and minerals like their gluten containing counterparts are.  Limit processed gluten-free foods.  They are often full of empty calories and unhealthy saturated fats and additives, and are high in histamine or histamine release triggers.  It's time you bought your own vitamins to supplement what is not being absorbed due to malabsorption of Celiac disease.  Benfotiamine is a form of Thiamine that has been shown to improve intestinal health as well as brain function. Do talk to your doctors and dieticians about supplementing with the essential vitamins and minerals while your children are growing up gluten free.  Serve nutritionally dense foods.  Meats and liver are great sources of B vitamins and minerals. Hope this helps!  Keep us posted on your progress!
    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
      @SamAlvi, It's common with anemia to have a lower tTg IgA antibodies than DGP IgG ones, but your high DGP IgG scores still point to Celiac disease.   Since a gluten challenge would pose further health damage, you may want to ask for a DNA test to see if you have any of the commonly known genes for Celiac disease.  Though having the genes for Celiac is not diagnostic in and of itself, taken with the antibody tests, the anemia and your reaction to gluten, it may be a confirmation you have Celiac disease.   Do discuss Gastrointestinal Beriberi with your doctors.  In Celiac disease, Gastrointestinal Beriberi is frequently overlooked by doctors.  The digestive system can be affected by localized Thiamine deficiency which causes symptoms consistent with yours.  Correction of nutritional deficiencies quickly is beneficial.  Benfotiamine, a form of thiamine, helps improve intestinal health.  All eight B vitamins, including Thiamine (Benfotiamine), should be supplemented because they all work together.   The B vitamins are needed in addition to iron to correct anemia.   Hope this helps!  Keep us posted on your progress!
    • trents
      Currently, there are no tests for NCGS. Celiac disease must first be ruled out and we do have testing for celiac disease. There are two primary test modalities for diagnosing celiac disease. One involves checking for antibodies in the blood. For the person with celiac disease, when gluten is ingested, it produces an autoimmune response in the lining of the small bowel which generates specific kinds of antibodies. Some people are IGA deficient and such that the IGA antibody tests done for celiac disease will have skewed results and cannot be trusted. In that case, there are IGG tests that can be ordered though, they aren't quite as specific for celiac disease as the IGA tests. But the possibility of IGA deficiency is why a "total IGA" test should always be ordered along with the TTG-IGA. The other modality is an endoscopy (scoping of the upper GI track) with a biopsy of the small bowel lining. The aforementioned autoimmune response produces inflammation in the small bowel lining which, over time, damages the structure of the lining. The biopsy is sent to a lab and microscopically analyzed for signs of this damage. If the damage is severe enough, it can often be spotted during the scoping itself. The endoscopy/biopsy is used as confirmation when the antibody results are positive, since there is a small chance that elevated antibody test scores can be caused by things other than celiac disease, particularly when the antibody test numbers are not particularly high. If the antibody test numbers are 10x normal or higher, physicians will sometimes declare an official diagnosis of celiac disease without an endoscopy/biopsy, particularly in the U.K. Some practitioners use stool tests to detect celiac disease but this modality is not widely recognized in the medical community as valid. Both celiac testing modalities outlined above require that you have been consuming generous amounts of gluten for weeks/months ahead of time. Many people make the mistake of experimenting with the gluten free diet or even reducing their gluten intake prior to testing. By doing so, they invalidate the testing because antibodies stop being produced, disappear from the blood and the lining of the small bowel begins to heal. So, then they are stuck in no man's land, wondering if they have celiac disease or NCGS. To resume gluten consumption, i.e., to undertake a "gluten challenge" is out of the question because their reaction to gluten is so strong that it would endanger their health. The lining of the small bowel is the place where all of the nutrition in the food we consume is absorbed. This lining is made up of billions of microscopically tiny fingerlike projections that create a tremendous nutrient absorption surface area. The inflammation caused by celiac disease wears down these fingers and greatly reduces the surface area needed for nutrient absorption. Thus, people with celiac disease often develop iron deficiency anemia and a host of other vitamin and mineral deficiencies. It is likely that many more people who have issues with gluten suffer from NCGS than from celiac disease. We actually know much more about the mechanism of celiac disease than we do about NCGS but some experts believe NCGS can transition into celiac disease.
    • SamAlvi
      Thank you for the clarification and for taking the time to explain the terminology so clearly. I really appreciate your insight, especially the distinction between celiac disease and NCGS and how anemia can point more toward celiac. This was very helpful for me.
×
×
  • 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.