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

Maybe A Stupid Question


Danijela

Recommended Posts

Danijela Contributor

Hey there!

Ive heard people say if you don't have a BM for a prolonged period of time your body can become toxic.....

what are the signs that this has happened......

I have 1 mb per week so i'm sure i have this and feel lousy i'm just wonder what symptoms can i blame on this???

thanks


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



Celiac.com Sponsor (A8-M):



Kasey'sMom Enthusiast

When I don't go often enough, I just feel sick all over. My tummy gets swollen if I haven't gone in awhile and is sore to touch. I seem to be a little more in touch with things than I used to be and I can really tell if I've gotten toxin overload. I start to notice that I don't have as much energy. Sometimes I have lower back pain with it as well. I've also had joint & muscle pain with toxic overload. I think some people even have headaches when they're overloaded.

My dd gets constipated and her Dr. has put her on Murilax. This has helped her go more often without all the pain. He also has her drinking 100% juice such as blueberry. He also recommended eating blueberries and watermelon together. :) She complains with a tummy ache and gets cranky when she's not regular as well. Her Dr. wants us to try to get her to go twice a day.

Hope you get to feeling better soon.

skbird Contributor

What happens is that if you are constipated, your waste doesn't leave your body and it further ferments or decays (or becomes rancid, supposedly) in your gut, which is a permeable membrane, so this stuff is reabsorbed in your system and can make you feel terrible. Having migraines, illness, feeling like you have the flu, difficulty concentrating, etc, are all signs.

If I am constipated, I still seem to go every day, but it's just harder, so I try taking psylliam and drinking more water, or taking extra magnesium capsules until things get moving. I definitely feel better. Sometimes if I have to go and haven't had an opportunity, I start to feel bad, and have noticed that right after finally going, I feel much better right away. I'm pretty sensitive though...

Stephanie

Guest BellyTimber

Also, bad breath can be a symptom (as of much else).

In addition I would recommend, when you do eat, lots of green leaf veg like spring cabbages and also the older and whiter kind of cabbage. If you've not got a steamer don't worry, drain off the liquid into a couple of mugs and when it's cooler it's a delicious drink.

If you use live yoghurt, stir into it a little psyllium husk, rice bran or cinnamon-flavoured finger millet powder (ragishira) all of which I have found help me. (Live yoghurt, if it contains serious numbers of organisms, has had its lactose changed into something else so permissible unless on an ultra strict lactose regime, is delicious, and the organisms promote internal health.)

A supplement of magnesium has helped me in this situation in the past.

Epsom salts in the bath can help (a good handful maximum per bath).

'Normal' for BMs is reputedly anywhere from 3 times a week to 3 times a day so, while you've some way to go, it's not too far. Also, as you explore with support your gluten and any other dietary issues the system will get more and more balanced so there's plenty of hope!

:lol:

jenvan Collaborator

danijela-

oh no! you definitely need to be going more often!! i totally disagree when doctors say 'everyone is different and some people only go every few days.' not true! our bodies weren't designed that way. i would definitely evaluate your diet, make sure you aren't continuing to get gluten. (are you gluten-free?) my constipation vastly improved after going gluten-free. make sure you are getting fiber--eat fruits, beans, drink lots of water. try some psyllium or magnesium too--those definitely help. hope things improve soon!

Danijela Contributor
danijela-

oh no!  you definitely need to be going more often!!  i totally disagree when doctors say 'everyone is different and some people only go every few days.'  not true!  our bodies weren't designed that way.  i would definitely evaluate your diet, make sure you aren't continuing to get gluten.  (are you gluten-free?)  my constipation vastly improved after going gluten-free.  make sure you are getting fiber--eat fruits, beans, drink lots of water.  try some psyllium or magnesium too--those definitely help.  hope things improve soon!

<{POST_SNAPBACK}>

Hi Jen

I'm not gluten-free yet, i just started seeing a GI specialist and I found out from my GP secretary what celiac antibodies were run and it wasn't the full panel so when i see him in a few weeks i'm going to ask him to re-order the test, ive been trying to eat the 2-3 pieces of bread in order for it to be acurate....

Thanks for the advice !

Rachel--24 Collaborator

I was very constipated before I went gluten-free. I did feel very toxic all the time as well. Since eliminating all gluten I immediately became "regular". I even have more than 1 bm a day now.

Not being gluten-free probably explains your constipation. Keep doing what you're doing for the tests...hopefully you are having them soon? If the tests are negative try going gluten-free anyways. My bloodtests were negative but I wasnt eating gluten all the way up to testing cuz I didnt know any better.


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



Celiac.com Sponsor (A8-M):



judy05 Apprentice
danijela-

oh no!  you definitely need to be going more often!!  i totally disagree when doctors say 'everyone is different and some people only go every few days.'  not true!  our bodies weren't designed that way.  i would definitely evaluate your diet, make sure you aren't continuing to get gluten.  (are you gluten-free?)  my constipation vastly improved after going gluten-free.  make sure you are getting fiber--eat fruits, beans, drink lots of water.  try some psyllium or magnesium too--those definitely help.  hope things improve soon!

<{POST_SNAPBACK}>

I have to agree with Jen. If I don't go everyday I feel terrible. I drink a lot of water, eat lots of fruit and fiber, and take 2-4 Citracel /day. It's good for both diarrhea and constipation and it forms a gel action in your intestine and I usually have a "masterpeice" B) every day. You will feel so much better if you go every day. Also Citracel is gluten-free!!!

Guest BellyTimber

I was only trying to be encouraging! :lol:

I found magnesium good, also green leaf veg, and live yoghurt. For fibre I'm now recommended, hemp protein powder which has a lot of fibre, or sprouted flaxseed, which is also fibre rich. Rice bran from Ener-G is cheaper though, as is psyllium.

I vary in my regularity but on average at least once a day, an improvement on previous, so there's light at the end of the tunnel when you complete 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. - asaT replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      nothing has changed

    2. - nanny marley replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

    3. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      45

      Supplements for those Diagnosed with Celiac Disease

    4. - par18 replied to Woodster991's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      9

      Is it gluten?

    5. - SilkieFairy replied to SilkieFairy's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      IBS-D vs Celiac

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,342
    • Most Online (within 30 mins)
      7,748

    Muhammad
    Newest Member
    Muhammad
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      Scott, I am mostly asymptomatic. I was diagnosed based on high antibodies, low ferritin (3) and low vitamin D (10). I wasn't able to get in for the biopsy until 3 months after the blood test came back. I was supposed to keep eating gluten during this time. Well why would I continue doing something that I know to be harmful for 3 more months to just get this test? So I did quit gluten and had the biopsy. It was negative for celiacs. I continued gluten free with iron supps and my ferritin came back up to a reasonable, but not great level of around 30-35.  Could there be something else going on? Is there any reason why my antibodies would be high (>80) with a negative biopsy? could me intestines have healed that quickly (3 months)?  I'm having a hard time staying gluten free because I am asymptomatic and i'm wondering about that biopsy. I do have the celiacs gene, and all of the antibody tests have always come back high. I recently had them tested again. Still very high. I am gluten free mostly, but not totally. I will occasionally eat something with gluten, but try to keep to a minimum. It's really hard when the immediate consequences are nil.  with high antibodies, the gene, but a negative biopsy (after 3 months strict gluten-free), do i really have celiacs? please say no. lol. i think i know the answer.  Asa
    • nanny marley
      I have had a long year of testing unfortunately still not diagnosed , although one thing they definitely agree I'm gluten intolerant, the thing for me I have severe back troubles they wouldnt perform the tests and I couldn't have a full MRI because I'm allergic to the solution , we tryed believe me  I tryed lol , another was to have another blood test after consuming gluten but it makes me so bad I tryed it for only a week, and because I have a trapped sciatic nerve when I get bad bowels it sets that off terribly so I just take it on myself now , I eat a gluten free diet , I'm the best I've ever been , and if I slip I know it so for me i have my own diagnosis  and I act accordingly, sometimes it's not so straight forward for some of us , for the first time in years I can plan to go out , and I have been absorbing my food better , running to the toilet has become occasionally now instead of all the time , i hope you find a solution 🤗
    • asaT
      I was undiagnosed for decades. My ferritin when checked in 2003 was 3. It never went above 10 in the next 20 years. I was just told to "take iron". I finally requested the TTgIgA test in 2023 when I was well and truly done with the chronic fatigue and feeling awful. My numbers were off the charts on the whole panel.  they offered me an endoscopic biopsy 3 months later, but that i would need to continue eating gluten for it to be accurate. so i quit eating gluten and my intestine had healed by the time i had the biopsy (i'm guessing??). Why else would my TTgIgA be so high if not celiacs? Anyway, your ferritin will rise as your intestine heals and take HEME iron (brand 4 arrows). I took 20mg of this with vitamin c and lactoferrin and my ferritin went up, now sits around 35.  you will feel dramatically better getting your ferritin up, and you can do it orally with the right supplements. I wouldn't get an infusion, you will get as good or better results taking heme iron/vc/lf.  
    • par18
      Scott, I agree with everything you said except the term "false negative". It should be a "true negative" just plain negative. I actually looked up true/false negative/positive as it pertains to testing. The term "false negative" would be correct if you are positive (have anti-bodies) and the test did not pick them up. That would be a problem with the "test" itself. If you were gluten-free and got tested, you more than likely would test "true" negative or just negative. This means that the gluten-free diet is working and no anti-bodies should be present. I know it sounds confusing and if you don't agree feel free to respond. 
    • SilkieFairy
      I realized it is actually important to get an official diagnosis because then insurance can cover bone density testing and other lab work to see if any further damage has been done because of it. Also, if hospitalized for whatever reason, I have the right to gluten-free food if I am officially celiac. I guess it gives me some legal protections. Plus, I have 4 kids, and I really want to know. If I really do have it then they may have increased risk. 
×
×
  • 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.