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

Stools - Horrible Topic


twe0708

Recommended Posts

twe0708 Community Regular

Are your stools normal since you have been gluten free? How long did it take? Seems like I get maybe three to four firm stools a month and the rest are soft. Not diarrhea, but soft like oatmeal. :rolleyes: Gluten free for a year and a half.


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



Celiac.com Sponsor (A8-M):



cassP Contributor

Are your stools normal since you have been gluten free? How long did it take? Seems like I get maybe three to four firm stools a month and the rest are soft. Not diarrhea, but soft like oatmeal. :rolleyes: Gluten free for a year and a half.

are you still eating dairy??

i cant remember how long mine took to normalize- probably 2 weeks to become normal. if i consume ANY or TOO MUCH milk one day- then the next morning there's a little "D". if i overdo the cheese- its not good at all... and if i overdo fructans/fructose in salad form or garlic/onion form then there's a little "D" too.

as long as i eat a healthy paleo type diet and get enough fruits & veggies- it's almost the "S" that Dr. Oz always talks about.

also- too many grains & gluten free substitutes especially corn will mess me up too.

i wonder what your diet is like? and i wonder how bad your intestinal damage was before you went gluten free?

sorry for all the poo descriptions :huh:

twe0708 Community Regular

are you still eating dairy??

i cant remember how long mine took to normalize- probably 2 weeks to become normal. if i consume ANY or TOO MUCH milk one day- then the next morning there's a little "D". if i overdo the cheese- its not good at all... and if i overdo fructans/fructose in salad form or garlic/onion form then there's a little "D" too.

as long as i eat a healthy paleo type diet and get enough fruits & veggies- it's almost the "S" that Dr. Oz always talks about.

also- too many grains & gluten free substitutes especially corn will mess me up too.

i wonder what your diet is like? and i wonder how bad your intestinal damage was before you went gluten free?

sorry for all the poo descriptions :huh:

This is what I usually eat daily.

Fruit smoothie in the morn. (blueberries, strawberries, banana)

Eggs

Snack - Apple with p-nut butter

lunch - white rice with slice of cheese and turkey slices or turkey meat with tomatos and cheese or sweet potato with cottage cheese

dinner is usually chicken and carrots, or chicken or steak fajita

Occasionally - a few pieces of dove chocolate or vanilla ice cream.

Nothing to alarming that would keep me this way. Doc never said anything about me being really bad off when I had an endoscopy done. :unsure:

cahill Collaborator

I wish i knew what a "'normal" stool was :unsure:

SaraKat Contributor

I was diagnosed in Sept, I never have/had abnormal stools- unless I was sick or something. So strange how this disease affects peopel differently.

ElseB Contributor

3 years in and I'm still waiting. Chronic constipation. And its not for lack of fibre or water in my diet.

cassP Contributor

3 years in and I'm still waiting. Chronic constipation. And its not for lack of fibre or water in my diet.

have you had your thyroid checked?? cause i always blamed my constipation on my gluten issues, or my battle with quitting smoking... but it wasnt untill i started on thyroid meds- that i noticed a change, i had NO IDEA that the slow motility i had for the last 7 years could be from a Hypothyroid.


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



Celiac.com Sponsor (A8-M):



cassP Contributor

This is what I usually eat daily.

Fruit smoothie in the morn. (blueberries, strawberries, banana)

Eggs

Snack - Apple with p-nut butter

lunch - white rice with slice of cheese and turkey slices or turkey meat with tomatos and cheese or sweet potato with cottage cheese

dinner is usually chicken and carrots, or chicken or steak fajita

Occasionally - a few pieces of dove chocolate or vanilla ice cream.

Nothing to alarming that would keep me this way. Doc never said anything about me being really bad off when I had an endoscopy done. :unsure:

wow, idk... it seems like you eat pretty healthy... do u have any stomach cramping? or bloating? or just too soft "bm"s?? that smoothie, apple, and sweet potato are so good for you and probably making your bms really smooth- but i dont think you should not eat them... cause it's so healthy. i think you could maybe be eating more greens- i think it's important to get your green colors too- different vitamins, etc.

??? not sure

this might sound weird- but have u ever tried metamucil? or bentonite clay? sometimes i actually have a harder bm after doing metamucil- and im guessing that maybe there was stuff stuck to the walls- and the psyllium grabbed it all- making the bm a little more substantial.

ok, idk, im thinking outloud..

ElseB Contributor

have you had your thyroid checked?? cause i always blamed my constipation on my gluten issues, or my battle with quitting smoking... but it wasnt untill i started on thyroid meds- that i noticed a change, i had NO IDEA that the slow motility i had for the last 7 years could be from a Hypothyroid.

Yup, thyroid checked and all was normal. I should note that in addition to adequate fibre and water, I'm also quite active (I run marathons) - all the things that doctors tell you to do to resolve constipation issues, I'm already doing!

cahill Collaborator

3 years in and I'm still waiting. Chronic constipation. And its not for lack of fibre or water in my diet.

Have you had any issues with other intolerances ?? I find my constipation is at its worst when i consume something that i have an intolerance too

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,056
    • Most Online (within 30 mins)
      7,748

    Dano2
    Newest Member
    Dano2
    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

    • Russ H
      This treatment looks promising. Its aim is to provoke immune tolerance of gluten, possibly curing the disease. It passed the phase 2 trial with flying colours, and I came across a post on Reddit by one of the study volunteers. Apparently, the results were good enough that the company is applying for fast track approval.  Anokion Announces Positive Symptom Data from its Phase 2 Trial Evaluating KAN-101 for the Treatment of Celiac Disease https://www.reddit.com/r/Celiac/comments/1krx2wh/kan_101_trial_put_on_hold/
    • Scott Adams
      BTW, we've done other articles on this topic that I wanted to share here (not to condone smoking!):    
    • Colleen H
      Hi everyone  This has been a crazy year so far... How many people actually get entire sensory overload from gluten or something similar ?  My jaw is going nuts ..and that nerve is affecting my upper back and so on ...  Bones even hurt.  Brain fog. Etc  I had eggs seemed fine.   Then my aid cooked a chicken stir fry in the microwave because my food order shorted a couple key items .   I was so hungry but I noticed light breading and some ingredients with SOY !!! Why are we suffering with soy ? This triggered a sensitivity to bananas and gluten-free yogurt it seems like it's a cycle that it goes on.  The tiniest amount of something gets me I'm guessing the tiny bit of breading that I took one tiny nibble of ...yikes ..im cringing from it .. Feels like my stomach is going to explode yet still very hungry 😔  How long does this last?! Thank you so much 
    • Scott Adams
      This is an older article, but may be helpful.  
    • gfmom06
      I have had orthodontic work done. The 3M invisalign material was no problem. BUT my retainers are another matter. They seemed okay for a few months. Now, however, they cause a burning sensation on my tongue, gums and insides of my lips. The burning sensation is now spreading to my throat. I notice it when I breathe. This is annoying and interferes with my enjoyment of eating. I am visiting with my provider tomorrow. We'll see where this goes from here.
×
×
  • 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.