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

Please Help! *** Warning Nasty Poop Pictures***


Britmum30

Recommended Posts

Britmum30 Newbie

Hello all..I'm new to this board and really need some help!!!

My youngest son is 4 years and 7 months old..he has mild autism and some serious poop issues. We can't seem to get a doctor to take us seriously so on a whim tonight I pulled out my camera and took some poop pictures to show the doctor...I'm also hoping that you guys may know what this is???

Some background...Nate's poop frequently looks like this...sometimes it's more solid than this but it's usually the consistency of peanut butter and usually light in color. I don't know if his tummy hurts, he most likely wouldn't tell us if it did. He was born in the 60th percentile for weight but is now less than the 5th percentile....he weighs 32lbs. He doesn't eat much...he's a very fussy eater...he doesn't drink a huge amount of juice mosly water. We cut all dairy and soy out of his diet almost a month ago but it hasn't helped. It smells nasty and sour and will often give him a diaper rash...he isn't potty trained.

summer2011174.webp

http://i1100.photobucket.com/albums/g402/Britmum29/summer2011177.webp

http://i1100.photobucket.com/albums/g402/Britmum29/summer2011176.webp

Please help!!!

Louise


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



Celiac.com Sponsor (A8-M):



mommida Enthusiast

He should be reffered to a ped. gastro. from the pictures alone.

The doctor should realize the force of the bm is so strong is blows up the child's back when it hits the diaper.

You can not stop giving him gluten until the testing is done!

mommyto2kids Collaborator

Our ds had ear infections alot. The med did that. He also had the roto virus a lot, a lot. Give him lots of yogurt and asidopholus, and break pill open and stur it into juice. Feed him firming food if you can. Try different formulas, don't mix formulas. We were there for a long time. Pampers and a size larger helped us. Hope is passes and they can figure out how to help him.

Britmum30 Newbie

Do you think this looks like celiacs poop??

Mommyto2kids...when you say formula do you mean infant formula? He's 4 years old. He never has really had any eat infections but when he was 2 he had severe bacterial pneumonia and they pumped him full of antibiotics...that was almost 3 years ago though.

I appreciate you all looking and apologies for the picture being so big!

Louise

alex11602 Collaborator

My youngest had poop like that 5-9 times a day until we cut out gluten and soy from her diet and if she has contact with either it will be like that for at least a week. I really hope that you are able to get to the bottom of what is causing this for your son and I would say that if the dr won't test him for Celiac that you try the diet for him, our dr diagnosed my youngest by symptoms and relief from them on the diet since she was so sick and my oldest after she had relief from non GI symptoms on the gluten free diet and while I think a dr diagnosis has its benefits, the health of our children is more important. Good luck to you.

suziq0805 Enthusiast

Did he have these poop issues before antibiotics? Just curious because my son was on so many antibiotics due to ear infections and ended up having something called c.diff. You can get that after being on antibiotics because the antibiotics can kill off the good bacteria in your body and the bad bacteria take over is my understanding of it. After a couple rounds of medicine my son's issues have cleared up.

domesticactivist Collaborator

Poor kid! I agree testing ASAP is a good idea.

I also highly recommend the book Gut and Psychology Syndrome by Dr. Natasha Campbell-McBride. She has a lot to say about diet and Autism. Our family has greatly benefited from the diet, though our problems are different. I have links if you search on GAPS Resources from the blog linked from my profile.


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



Celiac.com Sponsor (A8-M):



mommida Enthusiast

My daughter was diagnosed as probable Celiac when she was 17 months. She is 8 years old now. From my memory that looks like some of her "Celiac" poop. Some had undigested food, mucus blobs, really it was just nasty, nasty stuff. Seemed like her but just got raw from mere seconds of contact with it.

salexander421 Enthusiast

Neither of my girls are diagnosed celiac but they both had a positive genetic test and MAJOR improvements on a gluten free diet, we also are pretty sure our youngest has DH which would confirm a celiac diagnosis but she has not had any testing. This kind of poop looks very familiar. My girl's was often very light colored, grainy (like it had sand in it), extremely smelly, and really hard to wipe off their bottoms. Also there was often globs of mucous in it (looked like someone just blew their snot in it). This all cleared on the gluten free diet. I would definitely have him tested for celiac then, when all the testing is done, try him on a gluten free diet and see what happens. Even if he does not have celiac disease he could still possibly benefit from a gluten free diet so it would be worth a try either way. Hope you get the answers you're looking for!

AMom2010 Explorer

This is what my daughter's poop looks like much of the time, she is 15 mos old and has been having chronic diarrhea for the last 2 months. When it isn't this color, it is dark brown, but is the same consistency. We have had her on lactaid milk since Saturday and her poop was starting to look more normal, but as of this morning we are back to the nasty diarrhea I am sad to say. We go back to the GI Dr. on 9/12 and Dr. said she'd want to scope her if things haven't improved (DD had negative bloodwork for Celiac).

Edit: DD has never been on antibiotics...

Britmum30 Newbie

Thanks so much for all the comments. I really doubt the antibiotics caused this...that was almost 3 years ago now and he hasn't had any antibiotics since then. Amom210 good luck at the doctors, I would love to know if you get any answers.

Louise

tarnalberry Community Regular

I'm pretty sure that numerous doses of antibiotics for repeated respiratory infections over nine months is what triggered by celiac disease. So, if you feel it started at that time, there's no reason to discount your instinct. I can't tell you about the poop specifically, but if you feel like it's worth trying the diet, I totally support that. Testing first may well be a good idea, but I'd still try the diet after testing.

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. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      4

      Feel like I’m starting over

    2. - Scott Adams replied to Kirita's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Recovery from gluten challenge

    3. - Scatterbrain replied to Scatterbrain's topic in Sports and Fitness
      4

      Feel like I’m starting over

    4. - Kirita replied to Kirita's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Recovery from gluten challenge

    5. - Scott Adams replied to Kirita's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Recovery from gluten challenge


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,287
    • Most Online (within 30 mins)
      7,748

    Desert Ratt
    Newest Member
    Desert Ratt
    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

    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
    • Scott Adams
      Hopefully the food she eats away from home, especially at school, is 100% gluten-free. If you haven't checked in with the school directly about this, it might be worth a planned visit with their staff to make sure her food is safe.
    • Scatterbrain
      Thanks to those who have replied.  To Cristina, my symptoms are as follows: Dizziness, lightheaded, headaches (mostly sinus), jaw/neck pain, severe tinnitus, joint stiffness, fatigue, irregular heart rate, post exercise muscle fatigue and soreness, brain fog, insomnia.  Generally feeling unwell. To Trents, We didn’t do any of the construction but did visit the job site quite often.  While getting the old house ready we stirred up a lot of dust and I’m sure mold but haven’t been back there for over a month.
    • Kirita
      Thank you so much for your response! I have a follow-up appointment with her pediatrician next week, and also an appointment with her pediatric GI Dr. Your message gives me some ideas for questions to ask the doctors. My daughter went strictly gluten-free in January following her first endoscopy so I’m guessing her diet is pretty solid. She is compliant but also reliant on others to make her food (at school and home) but she didn’t have this problem prior to the gluten challenge when she went strictly gluten-free. It really makes sense to me that the gluten challenge inflammation hasn’t healed and I will be asking her doctors about nutritional issues. I ask for anecdotal stories because the research surrounding the gluten challenge seems to be inconsistent and inconclusive (at least what I’ve been able to find!). Thank you so much for your response!
    • Scott Adams
      While the positive endoscopy confirms the diagnosis, it's important to be skeptical of the idea that your daughter will simply "bounce back" to a pre-challenge state. The gluten challenge was essentially a controlled, prolonged exposure that likely caused significant inflammation and damage to her system; it's not surprising that recovery is slow and that a subsequent exposure hit her so hard. The persistent fatigue is a major red flag that her body is still struggling, potentially indicating that the initial damage hasn't fully healed or that her system is now in a heightened state of reactivity. Rather than seeking anecdotal timelines from others, her experience underscores the critical need for close follow-up with her gastroenterologist to rule out other nutrient deficiencies commonly caused by celiac flare-ups, like iron or B12, and to consult with a dietitian to scrutinize her diet for any hidden sources of cross-contamination that could be perpetuating her symptoms. The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs.      
×
×
  • 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.