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

Intestinal Bleeding


alex11602

Recommended Posts

alex11602 Collaborator

Our doctor diagnosed my 15 month daughter over the phone with celiac disease about 2 1/2 weeks ago and also sand that since she had a few gritty diapers that there was probably intestinal damage. They wanted to do a colonoscopy, but it had to wait since we don't have health insurance. Well yesterday I went to change her diaper and there were what looked like coffee grounds in it and since my grandmother always told me that black means blood I called the doctor. They ended up having me take her right to the ER and her diaper tested positive for blood. Since it was not a large amount they sent her home with directions to follow up on Monday and come back if it gets worse. They say that it is probably intestinal bleeding, but they do not know what it is from. Could the intestinal bleeding be from the damage from celiac disease? And does anyone know what they would do, I know it has to be taken care of right away, but I need to have an idea on how much we may be talking price wise...I just want to be prepared. Thank you in advance.


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



Celiac.com Sponsor (A8-M):



Kimmik95 Rookie

Is your daughter on a gluten free diet? I'm not sure I understand how she would be diagnosed over the phone. My son had bloodwork done and then, based on that and symptoms, he had an endo which confirmed villa damage, which is kind of the golden rule for diagnosing celiac disease these days. celiac disease damages the small intestine, among other things, so I would imagine intestinal bleeding could be a result of celiac disease. I'm no doctor, but here's what I would do. If you feel comfortable that she has celiac disease, I would just put her on a gluten-free diet and stick with it. If she continues to have these bad reactions, then it's probably not celiac disease.

Our doctor diagnosed my 15 month daughter over the phone with celiac disease about 2 1/2 weeks ago and also sand that since she had a few gritty diapers that there was probably intestinal damage. They wanted to do a colonoscopy, but it had to wait since we don't have health insurance. Well yesterday I went to change her diaper and there were what looked like coffee grounds in it and since my grandmother always told me that black means blood I called the doctor. They ended up having me take her right to the ER and her diaper tested positive for blood. Since it was not a large amount they sent her home with directions to follow up on Monday and come back if it gets worse. They say that it is probably intestinal bleeding, but they do not know what it is from. Could the intestinal bleeding be from the damage from celiac disease? And does anyone know what they would do, I know it has to be taken care of right away, but I need to have an idea on how much we may be talking price wise...I just want to be prepared. Thank you in advance.

alex11602 Collaborator

Is your daughter on a gluten free diet? I'm not sure I understand how she would be diagnosed over the phone. My son had bloodwork done and then, based on that and symptoms, he had an endo which confirmed villa damage, which is kind of the golden rule for diagnosing celiac disease these days. celiac disease damages the small intestine, among other things, so I would imagine intestinal bleeding could be a result of celiac disease. I'm no doctor, but here's what I would do. If you feel comfortable that she has celiac disease, I would just put her on a gluten-free diet and stick with it. If she continues to have these bad reactions, then it's probably not celiac disease.

She has been on a gluten free diet for about 2 1/2 weeks now. The ER doc was saying that it was damage that was already done. She was diagnosed over the phone based on symptoms. Our doctor refuses to do tests on either of us because of the rates of false negatives and because of the cost.

GFinDC Veteran

I used to have black stool and bleeding before going on the gluten-free diet. Celiac does destroy the lining of the small intestine, so its no surprise if it causes bleeding. A positive response to the diet is a better test than any test a doctor can give you, no matter how much it costs. If it makes you sick don't eat it. Your body doesn't care about test results, it reacts to real life.

A dairy intolerance is also fairly common with celiac disease due to damage to the villi of the small intestine. The villi produce an enzyme called lactase that digests the sugar (lactose) in dairy. So, damaged villi equals no or low lactase production. That's why many celiacs have problems with dairy. After being on the gluten-free diet for a while some people regain the ability to eat dairy but not all do.

It is helpful to start the gluten-free diet by eating whole foods and avoiding processed foods. It also helps to cut out dairy and soy at first. Many of us have problems with soy also, although not all do.

There is lots of great information on this board, so stick around and read and ask questions. Since the tendency to develop celiac is genetic, it is good to have your immediate relatives tested for antibodies to gluten. Gene testing is ok, but there are lots more people with the genes than there are people with celiac. Not everyone with the genes develops it.

The typical tests the docs do are blood antibodies first, and then a biopsy of the small intestine via endoscopy. But if your body is already doing better being off gluten, the tests are not nessecarily going to tell you anything you don't already know.

I think it is better to start the diet myself, and do a good strict job of it too. No cheating, watch out for cross-contamination, no sharing of peanut butter jars etc with gluten eaters, no processed foods, no dairy, and no soy, no oats. If it doesn't help after a month or two, then it would be good to think about further tests. But the only treatment for celiac disease is the gluten-free diet. Some people do get vitamin shots, but most can get by without them. Sub-lingual B-12 is often used at first.

Make sure to check all your vitamins and meds and drinks for gluten also.

alex11602 Collaborator

I used to have black stool and bleeding before going on the gluten-free diet. Celiac does destroy the lining of the small intestine, so its no surprise if it causes bleeding. A positive response to the diet is a better test than any test a doctor can give you, no matter how much it costs. If it makes you sick don't eat it. Your body doesn't care about test results, it reacts to real life.

A dairy intolerance is also fairly common with celiac disease due to damage to the villi of the small intestine. The villi produce an enzyme called lactase that digests the sugar (lactose) in dairy. So, damaged villi equals no or low lactase production. That's why many celiacs have problems with dairy. After being on the gluten-free diet for a while some people regain the ability to eat dairy but not all do.

It is helpful to start the gluten-free diet by eating whole foods and avoiding processed foods. It also helps to cut out dairy and soy at first. Many of us have problems with soy also, although not all do.

There is lots of great information on this board, so stick around and read and ask questions. Since the tendency to develop celiac is genetic, it is good to have your immediate relatives tested for antibodies to gluten. Gene testing is ok, but there are lots more people with the genes than there are people with celiac. Not everyone with the genes develops it.

The typical tests the docs do are blood antibodies first, and then a biopsy of the small intestine via endoscopy. But if your body is already doing better being off gluten, the tests are not nessecarily going to tell you anything you don't already know.

I think it is better to start the diet myself, and do a good strict job of it too. No cheating, watch out for cross-contamination, no sharing of peanut butter jars etc with gluten eaters, no processed foods, no dairy, and no soy, no oats. If it doesn't help after a month or two, then it would be good to think about further tests. But the only treatment for celiac disease is the gluten-free diet. Some people do get vitamin shots, but most can get by without them. Sub-lingual B-12 is often used at first.

Make sure to check all your vitamins and meds and drinks for gluten also.

Thank you so much for the information. I will definitely check all her vitamins and drinks too. And I will cut out dairy and soy to see if that helps. Again thank you.

potatopeelingmom Newbie

Hi Alex,

I hope your little girl is feeling better, but if not I think you need to ensure she sees a Pediatric Gastroenterologist. Bleeding could be indicative of something other than Celiac. She could have Ulcerative Colitis or something else (the root cause could be Celiac however). If it is Ulcerative Colitis it needs to be brought under control. I agree with others that have written to ensure she is gluten, dairy and possibily soy free for awhile.

Good luck,

Monica

alex11602 Collaborator

Hi Alex,

I hope your little girl is feeling better, but if not I think you need to ensure she sees a Pediatric Gastroenterologist. Bleeding could be indicative of something other than Celiac. She could have Ulcerative Colitis or something else (the root cause could be Celiac however). If it is Ulcerative Colitis it needs to be brought under control. I agree with others that have written to ensure she is gluten, dairy and possibily soy free for awhile.

Good luck,

Monica

Thank you. She has a doctors appointment today and the ER doctor was mentioning possibly sending her to a pediatric GI. I will definitely push for it though. Thank you again.


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



Celiac.com Sponsor (A8-M):



alex11602 Collaborator

We took her to the doctor earlier in the week and they told us to call a pediatric GI. I called the name they gave me and they told me to take her to a children's hospital since she would be able to get all her care in one place and they could work with us financially. Another thing the doctor said was to cut common allergens out of her diet and the list included....the gluten (of course), dairy, eggs, soy, peanuts, tree nuts, citrus fruits, fish, shellfish, nitrates, artificial coloring and dyes and preservatives. So she is on a fairly strict diet while we wait for the hospital visit. She is still having old blood in all her runny stools and she goes 5-8 times a day. If it gets worse I am just going to take her back to the ER. Thank you for all your tips.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,583
    • Most Online (within 30 mins)
      7,748

    Lindy Lulu
    Newest Member
    Lindy Lulu
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Ben98! If you have been consciously or unconsciously avoiding gluten because of the discomfort it produces then it is likely that your blood antibody testing for celiac disease has been rendered invalid. Valid testing requires regular consumption of generous amounts of gluten. The other strong possibility is that you have NCGS (Non Celiac Gluten Sensitivity) which shares many of the same symptoms with celiac disease but does not have the autoimmune component and thus does not damage the small bowel lining. It is 10x mor common than celiac disease. There is currently no test for NCGS. Celiac disease must first be ruled out. Some experts in the field believe it can be a precursor to the development of celiac disease. Having one or both of the primary genes for developing celiac disease does not imply that you will develop active celiac disease. It simply establishes the potential for it. About 40% of the population has the genetic potential but only about 1% develop active celiac disease. 
    • Ben98
      TTG blood test and total IGA tested on many occasions which have always remained normal, upper GI pain under my ribs since 2022. I had an endoscopy in 2023 which showed moderate gastritis. no biopsy’s were taken unfortunately. genetic test was positive for HLADQ2. extreme bloating after eating gluten, it’ll feel like I’ve got bricks in my stomach so uncomfortably full. the pain is like a dull ache under the upper left almost like a stitch feeling after a long walk. I am just wanting some advice has anyone here experienced gastritis with a gluten issue before? thank you  
    • Wheatwacked
      "Conclusions: The urinary iodine level was significantly lower in women with postmenopausal osteoporosis, and iodine replacement may be important in preventing osteoporosis"  Body iodine status in women with postmenopausal osteoporosis Low iodine can cause thyroid problems, but Iodine deficiency will not show up in thyroid tests.  Iodine is important for healing, its job is to kill off defective and aging cells (Apoptosis). Skin, brain fog, nails, muscle tone all inproved when I started taking 600 mcg (RDA 150 - 1000 mcg) of Liquid Iodine drops. Some with dermatitis herpetiformis, Iodine exacerbates the rash.  I started at 1 drop (50 mcg) and worked up to 12 drops, but I don't have dermatitis herpetiformis.
    • cristiana
      That's great news, you can do this.  Let us know how things go and don't hesitate to ask if you have any more questions. Cristiana 😊
    • petitojou
      Thank you so much for sharing your experience and I found myself giggling with happiness as I read how your body reached such spring! And I hope that your current journey is also successful!! Definitely starting the food diary! So many amazing advices. And it’s very scary. It really hits all our soft spots as well as our confidence system. Most doctors I went thought I was underage despite being in my late 20s. Right now I look like am I twelve, but is also this body that’s taking so much, so I might as well love it too! Going to make the necessary changes and stay in this path. Thank you again! 🫶
×
×
  • 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.