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

Color Of Stools With Children Of Celiac Disease


celia

Recommended Posts

celia Newbie

Hi Everyone

I am new to this board. As of last week, our Gastrointerologist is ordering my 2 1/2 year old a biopsy of the small intestine in another 5 days. He has been Failure to Thrive ever since about 9 months. He started out in the 50% percentile and now is in the 5th. He only weighs 24lbs at 2 1/2 years old. His stools have always been a dark green olive color - hardly ever brown. They are semi loose - not watery diarhea - but mushy with no form - outlined with running stools. He has never had an appettite since about 6 months old - basically when I stopped breast feeding and offered him more solid type foods. I have been told and told over by family members that oh he is just a picky eater. But deep down inside I know something is not right. If it is Celiac Disease - at least that is the answer to all these months of why he has not gained a pound and why he will not eat. I have to chase him around, distracting him just to get food down him. Has anyone experienced this constant dark green stool color with their Celiac positive children. And if so - after starting a Glutin free Diet - are the stools more normal per se (brown with form). I feel like a terrible mother not knowing that the color and texture of his bowel movements was an indication of something being wrong. We have been to numerous specialists trying to figure out why he is not growing - but I never stressed enough about the bowel movements he was having. Any replies would greatly be appreciated. Thank you.

Celia


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



Celiac.com Sponsor (A8-M):



kejohe Apprentice

First things first.... welcome to the board and you are NOT a terrible mother, in fact you are the opposite because you are doing what you can to get your baby better. My son was diagnosed at a year old and is now 3. He had very watery and very, very foul smelling stools, they were light in color and so loose they ran down his legs, or up his back. However, I don't know wht the significance is between dark and light stools, because I think everybody probably processes differently and it has a lot to do with what you are feeding them. For my son, he was eating mostly green veggies and pastas, chicken and so on, but always light colors, hardly any red meats, which can turn the stools very dark, also I think the amount of milk they driink makes a big difference, and my boy drank a ton.

Just out of curosity, if your gastro doc is already ordering a biopsy, does that mean that a blood test already came back positive? If so, I think it's a pretty good bet that he is a celiac.

Take heart, it's not as difficult to make the conversions as it looks, there as some times when you will feel frustrated and frightened, angry and sad. But I'll tell you what, that first time you go in for a check up and the doctor tells you he has gained a few pounds, you will feel like your floating on cloud nine! And it may take a little time, but when the appetite comes back, it will make you so happy to see him eat a full meal. I think that for me, the good times, the triumphs have far out weighed the dissapointments, and it gets a little easier everyday.

seeking-wholeness Explorer

Celia,

You are a fine mother! I understand your feelings, though, because I've had them myself. I keep reminding myself that it's not my job to clear away the obstacles from my children's path, but rather to make sure they have the resources to get over or around them on their own. It's hard to watch them struggle, though, and with young kids like ours (mine are 3.5 and 1.5 years old) more of the responsibility does end up on our shoulders. It's great that you are willing to accept that responsibility on your son's behalf!

My boys have had stools of all sorts of colors! Both have celiac disease (although we are admittedly self-diagnosed at this time--but I just got our new insurance cards in the mail, so we'll see what the doctor has to say soon!). Before we all went gluten-free, their stools were primarily orangey-brown, bulky, loose, and vile-smelling (like REALLY sharp cheddar cheese!), with occasional bouts of diarrhea that strongly resembled river mud and smelled sweet-and-sour! My older boy has also had some trouble with yellow, frothy stools (but not since we eliminated dairy products from our diet). My younger boy produced green stools one time, and I never did figure out why!

I just looked up "Stools, Green" in The Nursing Mother's Problem Solver, and it suggests that lactose intolerance may cause this problem. Does your son consume dairy products on a regular basis?

I wish you and your son the best of luck with the biopsy, and I hope the results are conclusive!

DLayman Apprentice

Ok.. I have a funny story about the color of poop..hehe

Have to tell it..

The hershey company put out promotional foods around the time the movie The Hulk came out last year.. Well being comic book fans we were drawn in by these items.. so I bought some 'Hulk" pudding and we made some yummy milkshakes with them. Well the next day my son had HULK GREEN poop.. yup.. Hulk poop.. heheh

But seriously.. Having had my son on a gluten-free diet then switched off before testing.. he had diahrea from last June to October. His stools were loose and like that story pretty much took on the color of what he ate.. and had undigested food in them often. We then switched his diet to a gluten-free diet. His stools became firm and formed. And for the most part medium to dark brown.

When we reintrroduced gluten in his diet to prepare for his endoscopy the first four days he had light yellow stools and there was no sleep in our house..

He had his endoscopy, no blood test, the biopsies came back negative, and now we have him on a regular diet.. but toddlers being invairably far superior in common sense than GI docs.. he is refusing most gluten containing foods.

Last year he went from at least 28 pounds down to 24. In the two months we had him on the gluten-free diet he went back to 27 pounds. From December to January21 he lost about 3/4 pounds. We were pushing fatty foods, giving him pediasure and he was getting 1/2 slice of bread a day.

My best advice.. don't be so hard on yourself.. I let my son go from June to August before we took him in to have him checked.. you think oh it will get better.. etc etc.. and there is nothing wrong with that..

And also if a blood test has not been done.. call your doc ahead of the endoscopy and INSIST they draw the blood then.. if possible while he is out for the scope.. kill two birds with one stone.. And relax and wait.. after the scope and blood work put him on a gluten-free diet and see what happens.

(lots of yummy [plain]chocolate breyers ice cream from the black box!!! gluten-free and good for mom too.) ;)

Also a good book.. Kids With Celiac Disease by Danna Korn.

ROYAL BLUE Apprentice

Celia, My son's stools were like that from the day he was born. I kept asking the dr about it. When he was nursing, the DR told me about the foremilk would cause this. then he started loosing weight, vary pale. The dr. ran a test for thyroid problems, it came back positive at 3 months for no apparent reason.

My son is now 6, been gluten-free for 2 months and for the first time ever his bowel movement are what you would call normal.

It took six years to find out what was wrong with him , but we finally did. As soon as I read a list of symptoms on this disease and saw a photo of another celiac child stomach, I instantly knew this is what he has had all along.

By the way, he grew 1/2 an inch in one month. hooray

Terri-Anne Apprentice

Could anyone tell me where I could view a picture of a celiac child's distended tummy? I'd like to compare my guy's big tummy to try to determine for myself whether he just has a typical little kid posture, or maybe a bloated celiac tummy.

thanks

ROYAL BLUE Apprentice

I can't say for sure where I saw the picture of a child with the distended abdomen, I think it was in Shelly Cases', or Danna Korns book.

The way I describe the tummy is like a child in Ethiopia. The Doctors always told me it was just the age he was at, he did not have the stomach muscles yet. I said no, with the way he always was coughing from his asthma, his stomach would get rock hard when coughing.


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



Celiac.com Sponsor (A8-M):



emsmom Apprentice

My 5 yr old DD has always had green stool I have mentioned this to dr's and they say it does not matter what color there stool is. I don't know if i agree it seems they are green after she has any kind of dairy, but she has had a lactose test and a milk allergy test both were negative. For some reason though she can not handle raw dairy products she gets bad stomach aches and usally vomits and gets green stool so i think it must mean something. we go for our biopsy wednesday good luck to your son.

emsmom Apprentice

error

celia Newbie

Hi Everyone

Just wanted to let you know my son did good with the biopsy on Wednesday. Now I have to wait until Monday for the test results. I just want an answer. Thank you to everyone that replied with the color of stools. You really are a great support group. If the biopsy comes back positive - I know who to turn to for support. Thanks again.

Celia :D

KimCrocker Newbie

Chelsea, my 9 year old, went from very dark and sticky to very pale (the color of a file folder comes to mind) and floaty. Celiac can make some really strange things come out of your body. We laugh about it now. Oh yeh, don't forget about the diarhea! Also, I think there are varying degrees of distention. Before we discovered Celiac, I just thought she had a chubby stomach and no back side. It's funny how we now talk about stools the way other people talk about the color of their shoes.

celia Newbie

Hi Everyone

Well we have the results and the biopsy came back negative for celiac disease. We are very happy over that. But still disappointed that we do not have an answer of why my little one is failure to thrive. We are now going through a 72 hour fecal test to see if there is malabsorption of fat. I just wanted to thank each of you for all your posts regarding this mattter. Im glad I found this forum with such wonderful people who take the time to respond to parents that are going through the initial testing of Celiac Disease. You are all terrrific. Thank you so much for your support.

Celia :rolleyes::D

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,960
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • 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
×
×
  • 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.