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

Constipation


gflooser

Recommended Posts

gflooser Contributor

What can we use!!!???

I've been doing miralax, but thats starting not to work anymore. Is there any herbal remedies, cleanses?

What about mineral oils? It doesn't help that I'm on weight watchers. So I don't eat enough to MAKE me go! Sorry, tmi ;)

I had a massage and the therapist showed me how to do an intestinal massage and that helps a little.

Anyone???


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



Celiac.com Sponsor (A8-M):



dilettantesteph Collaborator

Prunes. Sunsweet don't seem to have any gluten in that I can eat them. 7 bite size a day.

skinnyasparagus Apprentice

I take all natural pure phyllisum husks as a fiber source. On days of constipation I take an extra one. They also make it in a powdered form but I prefer the gelatin capsules. For me, they work incredibly well and better than metamusil ever did. Prunes are great but don't always work and sometimes the extra sugar constipates you even more. They sell phyllisum husks at Whole Foods and GNC - but make sure its gluten-free because some companies produce them on machinery that manufactures wheat, soy, and nuts as well.

Hope this helps!

mftnchn Explorer

Prunes work better if they are boiled in water and softened. You might search the forum here as many people have posted their discoveries.

Magnesium is needed for the intestine to contract. You may try taking an oral magnesium supplement. You can gradually increase until it is enough to help. Vitamin C can help as well.

I have gotten a lot of help on the specific carbohydrate diet; in the literature I have found out that constipation is a sign of intestinal irritation, and if that is the case for you, extra fiber will make it worse instead of better. SCD helps by reducing irritants, eliminating carbohydrates that we can't digest (villa damage can hinder production of carb digestive enzymes) and that feed bad bacteria, helping to kill the bad bacteria and replace them with good bacteria.

babysteps Contributor

if your gut is irritated this would probably be a bad idea, but for me a meal heavy in garlic (say, one-third to half a head per person) speeds things right along. Prunes work great too.

mhb Apprentice

I am having good success using bitters from Italy. Years ago I tried the "Swedish Bitters" but they did not work for me. Recently I learned about "Dolce Digestivo". It has no sugar, alcohol or preservatives and is working well. The box says it has natural flavors and natural caramel color, but I called the distributor and they assured me, after researching its ingredients, it has no gluten. A friend of mine started using it and it's helping her a lot too. I paid $16.99 locally, but later found it online here for much less: Open Original Shared Link You could call the distributor to see if you can find it locally: Solaray, at 1-800-683-9640.

gflooser Contributor

You guys are GREAT!!! Thanks for all your help. Prunes used to work, but I think my body got used to them. Of course, I was only eating 3-5 per day. Maybe I should try to eat more per day!

What is the SCD diet???

Never heard of bitters....

I will have to research this stuff!!!!

B):):lol::P


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



Celiac.com Sponsor (A8-M):



mftnchn Explorer

Sorry, SCD stands for specific carbohydrate diet. It is designed to help heal the gut. For me, and possibly others who are celiac, damage to the villa means that we do not adequately produce carbohydrate digesting enzymes. Often mentioned is lactase, but there are at least two others that cannot be produced without villa.

When we don't break down sugars and starches to monosaccharides, they can't be absorbed. They should be absorbed high in the intestine. So if you are eliminating high amounts of sugar in stool (like I was) this is a sure sign of problems. It means further damage to the intestine and prevention of healing. The sugar in the lower intestine feeds lots of bad organisms.

The gut damage can produce either constipation or diarrhea. The answer of more fiber can actually worsen the condition.

The SCD eliminates the problematic carbs, then you follow a gradual introduction of foods beginning with those easiest to digest.

My main celiac symptom is constipation and gluten-free for 15 months, CF 10 months, and SF 12 months just didn't clear this up. One week after starting SCD I saw dramatic improvement.

So my question would be what is underlying the constipation? If symptomatic treatment isn't consistently helping...

Amber M Explorer
What can we use!!!???

I've been doing miralax, but thats starting not to work anymore. Is there any herbal remedies, cleanses?

What about mineral oils? It doesn't help that I'm on weight watchers. So I don't eat enough to MAKE me go! Sorry, tmi ;)

I had a massage and the therapist showed me how to do an intestinal massage and that helps a little.

Anyone???

Funny about the fiber. My nutritionist kept telling me to eat more fiber (before I was diagnosed) and the more I ate, the more constipated I got! I kept telling her it didn't work for me. After I went gluten free, my allergist told me to take magnesium for all of the neuro symptoms as well as the constipation. I had to get up to 1000 mgs. before it started to work. I tried everything else and nothing but the mag. worked for me. My allergist said, "your body will tell you when you have enough mag. because your stools will begin to be loose and if you get the "D", then start lowering the amount of mag." Have you had your vitamin levels checked? If you take magnesium, be sure its on a full stomach (or it will cause nasea) and build up gradually. I take half at lunch and half at supper.

gflooser Contributor

Thats very interesting Amber, thank you!

I'm going to the dr. for my regular yearly check up in a few weeks. I will be going with LOTS of questions!

mftnchn Explorer
Funny about the fiber. My nutritionist kept telling me to eat more fiber (before I was diagnosed) and the more I ate, the more constipated I got! I kept telling her it didn't work for me. After I went gluten free, my allergist told me to take magnesium for all of the neuro symptoms as well as the constipation. I had to get up to 1000 mgs. before it started to work. I tried everything else and nothing but the mag. worked for me. My allergist said, "your body will tell you when you have enough mag. because your stools will begin to be loose and if you get the "D", then start lowering the amount of mag." Have you had your vitamin levels checked?

Same for me. Actually this is what led me to my celiac diagnosis. I had tried the "tried and true" and it didn't work; I found the references to gluten problems when searching for answers.

I was up to 1600 mg of magnesium in the early months of gluten-free!!!! But was gradually able to cut it down to 300-400 daily and not every day. Now I am back up to about 1000 again after a hidden gluten exposure that took me several weeks to discover.

Also, YES on the vitamin d. My levels were horrendously low.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,021
    • Most Online (within 30 mins)
      7,748

    maltawildcat
    Newest Member
    maltawildcat
    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

    • NanCel
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
    • knitty kitty
      Please do more research before you settle on nicotine. Dr. Paul New house is a psychiatrist.  His latest study involves the effect of nicotine patches on Late Life Depression which has reached no long term conclusions about the benefits.   Effects of open-label transdermal nicotine antidepressant augmentation on affective symptoms and executive function in late-life depression https://pubmed.ncbi.nlm.nih.gov/39009312/   I'm approaching the subject from the Microbiologist's point of view which shows nicotine blocks Thiamine B1 uptake and usage:   Chronic Nicotine Exposure In Vivo and In Vitro Inhibits Vitamin B1 (Thiamin) Uptake by Pancreatic Acinar Cells https://pubmed.ncbi.nlm.nih.gov/26633299/   While supplementation with thiamine in the form Benfotiamine can protect from damage done by  nicotine: Benfotiamine attenuates nicotine and uric acid-induced vascular endothelial dysfunction in the rat https://pubmed.ncbi.nlm.nih.gov/18951979/   I suggest you study the beneficial effects of Thiamine (Benfotiamine and TTFD) on the body and mental health done by Dr. Derrick Lonsdale and Dr. Chandler Marrs.  Dr. Lonsdale had studied thiamine over fifty years.   Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/ I suggest you read their book Thiamine Deficiency Disease, Dysautonomia, and High Calorie Malnutrition.     Celiac Disease is a disease of malabsorption causing malnutrition.  Thiamine and benfotiamine: Focus on their therapeutic potential https://pmc.ncbi.nlm.nih.gov/articles/PMC10682628/
    • sleuth
      Thanks for your response.  Everything you mentioned he is and has been doing.  Tobacco is not the same as nicotine.  Nicotine, in the form of a patch, does not cause gastrointestinal irritation.  Smoking does. He is not smoking.  Please do your research before stating false information. Dr. Paul Newhouse has been doing research on nicotine the last 40 years at Vanderbilt University Medical Center.  
    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
×
×
  • 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.