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

Glutened - But The Result- Constipation

kim307

By kim307
in Coping with Celiac Disease

Recommended Posts

kim307 Newbie
kim307
Posted

Hi everyone,

I am only 2.5 months into being diagnosed...and so far, things have gone well. I made a beginner mistake this weekend and took a few bites of chicken picatta...which def had flour (although the waitress said no). Being Italian I should have known this...but I was caught up in the moment.

Here's the weird thing...instead of getting the "d"...I became VERY constipated and in so much pain, and just fatigued. Could this even be possible??? I thought the opposite would happen. I wish it did. Any thoughts? Now my stomach is still in a knot. Ugh!

Kim

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

Celiac.com Sponsor (A8-M):


GFreeMO Proficient
GFreeMO
Posted

Hi everyone,

I am only 2.5 months into being diagnosed...and so far, things have gone well. I made a beginner mistake this weekend and took a few bites of chicken picatta...which def had flour (although the waitress said no). Being Italian I should have known this...but I was caught up in the moment.

Here's the weird thing...instead of getting the "d"...I became VERY constipated and in so much pain, and just fatigued. Could this even be possible??? I thought the opposite would happen. I wish it did. Any thoughts? Now my stomach is still in a knot. Ugh!

Kim

That has happened to me several times. I usually get the d 3 or 4 days after if that happens. You could try drinking some warm apple juice or eating some canned fruit or raisins to get things moving along. Hope you feel better soon.

kim307 Newbie
kim307
Posted
  • Author

Thanks! I will try that:( I didn't know what to expect...but my stomach is in a knot and I can't "snap out of it". Honestly, I didn't really believe I would be able to tell I was "glutened". And I was considering cheating this summer on my favorite pizza, guess not. I expected to be running to the bathroom if I was glutened, but not this.

cassP Contributor
cassP
Posted

Hi everyone,

I am only 2.5 months into being diagnosed...and so far, things have gone well. I made a beginner mistake this weekend and took a few bites of chicken picatta...which def had flour (although the waitress said no). Being Italian I should have known this...but I was caught up in the moment.

Here's the weird thing...instead of getting the "d"...I became VERY constipated and in so much pain, and just fatigued. Could this even be possible??? I thought the opposite would happen. I wish it did. Any thoughts? Now my stomach is still in a knot. Ugh!

Kim

yes it's definitely possible... for me (and so many members on here)-> "C" is usually what i get from gluten. way more than "D".

Jenbeans77 Newbie
Jenbeans77
Posted

This is also the case for me. I very rarely get "d".....but every time I get "glutened"....i always get extremely bloated and have a case of the "c"... I got glutened last weekend...and am just now starting to get things rolling so to speak. i take probiotics, and drink aloe juice to help. but no matter what i do, it usually takes at least a couple of weeks to get back to feeling somewhat better...

rustycat Rookie
rustycat
Posted

Same here. I'd say about 90% of the time, I get the "C". It's like my colon just seizes up and it's very uncomfortable.

Probiotics usually work well and sometimes I take a small amount of psyllium to get things moving along. It can take several days to get things back to normal, though.

Hope you're feeling better by now.

jazzbaby Rookie
jazzbaby
Posted

yes it's definitely possible... for me (and so many members on here)-> "C" is usually what i get from gluten. way more than "D".

same here, have never had "d" through all of this but "c" is always the problem

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

Celiac.com Sponsor (A8-M):


plantime Contributor
plantime
Posted

I get constipated if I consume wheat, diarrhea if I consume barley, and I don't want to know if I eat rye. Celiac reactions can go either way, and they both hurt.

ElseB Contributor
ElseB
Posted

I have NEVER gotten D, not once. Its ALWAYS constipation. And one tiny crumb of gluten results in 4-6 weeks of constipation. Try magnesium pills. Magnesium draws water into the intestines which will help reduce constipation.

shopgirl Contributor
shopgirl
Posted

Sorbitol helps too. Apples, pears, prunes. Drinking juice warm, like someone suggested, helps. Hot anything helps: straight water, tea, even coffee because it stimulates the muscles. Olive oil is good too: either over a green salad or straight from the bottle with a spoon.

If worst comes to worst, Miralax is a very gentle, easily tolerated medication that is definitely not a stimulant and always safe to take.

cassP Contributor
cassP
Posted

OMG i wish i could eat pears (but cant cause of fructose issues :( ) cause PEARS always gave me the best results the following morning!!! i hope i can eat those again in the future

  • 2 weeks later...
beefree11 Newbie
beefree11
Posted

Hello everyone, I am new to this site and it is my 24 yo daughter that is gluten intolerant (same blood work in 2009 also showed wheat allergy, egg white, soybean, egg yolk, casein/cow milk, maize/corn, gluten). She is also Hashimoto's, hypothyroid, PCOS and symptoms of a parasitic infection to name just a few ;-0).

This am (4:30) she woke me up due to extreme abdominal pain. She claimed to have a huge knot in her stomach and was up all night tossing and turning. She claimed she was having significant worrisome and negative thoughts, that truly were frightening. All she could think of was all the things/decisions she had done wrong recently. ???

Have any of you experienced this? She has been "c" for a week. We have tried them all - am thinking of some type of message to help intestines MOVE? I can only think that she was glutened at work and it was extreme!!! She was laying on the floor of the bathroom, praying to God for a miracle and asking if I would take her to the hospital. It was bad. Of course on New Years Day! arrghhhhh. I offered to take her,or call ambulance but she said she could NOT stand. She was also complaining of feeling stuffed in head and had difficulty breathing!

We stayed like that for an hour until I began reminding her of all the good she has done and kindness she brings to people and animals. How compassionate she is. That she is a wonderful human. The severity of the spasms ceased and she returned to bed. I had her drinking lots of water, I feared dehydration which is BAD, too. I put a damp cloth on her forehead for she claimed that she felt secure with it on...and she relaxed enough to fall asleep. She is feeling somewhat better, but is still bed bound. I am a mess.

Should the C be the main concern? Could it be poisons leaking thru her gut and getting into her bloodstream? (Her blood pressure was 107/60) No fever.

With her not having health insurance, I really don't know what to do. Of course if things become worse for her, my credit card has a huge limit and I would not let her go without care...but the doctors around here don't actually recognize gluten intolerance without a biopsy. I am sure that is where it would be headed but she has been gluten free since 09/2009.

Is this the beginning of many more to come? I would love to stop it or alleviate these occurrences as soon as possible and my next question: Are there more frequent attacks of this "type" when constipated? Is remaining as "regular" as possible the goal to relieving some of the more confusing symptoms? Of course not eating any gluten is the main priority - but would you agree that keeping sluggish to non-working bowels would be the next most important factor in alleviating symptoms and/or attacks??? Thank you sooo much.

  • 2 months later...
hockeymomofceliacchild Rookie
hockeymomofceliacchild
Posted

My kids are always constipated my 2 year old actually asked for a supository she was in so much pain. I give my kids lactulose to help them out. If it wasn't for my son being consitpated his DH would not have flared the doctor prescribed more fibre and we were putting bran buds in meatloaf and spagetti wow did his rash flare and thus concluded he had celiac.

All my kids get constipated so it will be interesting if they all have celiac or not.

A nice warm cloth on there bum and massage their bellies helps alot. I also give them ribena juice which is a natural laxative. However I havent checked the label to see if I can give it to my son with celiac I can't see why not but of course you have to check everything :)

missj Rookie
missj
Posted

The knotting is exactly how I feel. I used to be able to feel the digestion process after I ate. Now I eat, there is no movement and when it's time to go, it's TIME! Find a bathroom NOW!

Even though I have no dx yet, this is my exact problem and I'm glad I was directed to this thread. I am on magnesium oxide pills (by the doc) and a high fiber diet that is NOT helping. I'd like to know about this Aloe Juice...I have been drinking hot teas everynight, although I don't know if I can see a difference.

shopgirl Contributor
shopgirl
Posted

I have been drinking hot teas everynight, although I don't know if I can see a difference.

What kind of teas? Black tea can be constipating in some.

missj Rookie
missj
Posted

Sleepytime Tea is my favorite. Chammomile blend I think is what that one is. I also drink Yogi brand Kambucha and Detox. Plus just your typical Lipton stuff but that is usually of the iced variety! Mmmm.

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748
    Tara M
    Newest Member
    Tara M
    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
      Celiac and dermatitis herpetiformis has taken Me from Me

      By trents · Posted

      Is this man the father of your children?
    • Jillian83
      Celiac and dermatitis herpetiformis has taken Me from Me

      By Jillian83 · Posted

      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      Ibuprofen

      By cristiana · Posted

      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      Knowing what to do when feeling unwell.

      By Me,Sue · Posted

      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      The Happy Tart review

      By Francis M · Posted

      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.