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

Painful Bowl Movements


med5224

Recommended Posts

med5224 Newbie

I found out that I had celiacs a little more then a year ago. Before I found out about it I was lucky if I was able to have a bowl movement once a week and when I did it was painful or it wasn't that much. When I started my diet it was no longer painful to go and I was relieved and over whelmed with happiness, as weird as it sounds, to just be able to be in the bathroom and not be in pain, the first time in I can't remember how many years.

But lately I am started to hate having to go to the bathroom again. Almost the whole time since i have been gluten free and before i have had blood on my toilet paper. It was something I could deal with and my gastroenterologist didn't seem worried because when I last talked to her they had just run all the tests and checked my insides and everything was fine. Since she thought it was fine i thought it was fine, I trust her a great deal since she is the only doctor that has ever actually investigated into my complaints and pain instead of dismissing it as "growing up". The problem is in the last few months it has gotten more painful.

When I go and it is hurting usually rubbing the side of my tube helps just because its smooth and some how it comforts me. This has stopped working. The stools have gotten bigger in some cases or shaped in such a way that I cry out when I am on the toilet. It is really embarrassing but luckily no one has noticed yet. After I leave the bathroom it even hurts to walk just because of the pain that I feel from it. The other night it took me 30 minutes to fall asleep just because of the pain. I haven't been exposed to any gluten lately because i haven't had a reaction but I did have a reaction to nitrates about a week ago but thats it. It just doesn't make sense and i guess i want to know if anyone else has felt this way before I start freaking out about it.

I appreciate any help or advise anyone can give me,

M


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



Celiac.com Sponsor (A8-M):



burdee Enthusiast

You may have developed hemorrhoids during all your years of constipation. Those will make bowel movements very painful and cause you to bleed when you 'go'. There are many OTC hemorrhoid ointments. However none of them are as effective as using a 'sitz bath' to shrink hemorrhoids. That doesn't mean sitting in the bathtub. A sizt bath is a device that you put on your toilet. You fill the sitzbath with very warm water and sit in the 'bath' for at least 10 minutes. That will shrink the hemorrhoids, decrease the pain and stop the bleeding. You can usually buy sitzbath at medical supply stores. Maybe your local pharmacy carries those. (I actually got my 'sitzbath' AFTER hemorrhoid surgery, which is another PAINFUL, albeit last resort option.)

Nevertheless, you may also want to consider why you still have hard, painful bowel movements after abstaining from gluten. I'm surprised your gastro didn't seem concerned about your symptoms. Maybe she doesn't think hemorrhoids are serious. Maybe she never had them or experienced hemorrhoid surgery. As someone who experienced years of hemorrhoidal pain and then 3 months of painful recovery after surgery, I'd recommend you address your symptoms ASAP.

SUE

I found out that I had celiacs a little more then a year ago. Before I found out about it I was lucky if I was able to have a bowl movement once a week and when I did it was painful or it wasn't that much. When I started my diet it was no longer painful to go and I was relieved and over whelmed with happiness, as weird as it sounds, to just be able to be in the bathroom and not be in pain, the first time in I can't remember how many years.

But lately I am started to hate having to go to the bathroom again. Almost the whole time since i have been gluten free and before i have had blood on my toilet paper. It was something I could deal with and my gastroenterologist didn't seem worried because when I last talked to her they had just run all the tests and checked my insides and everything was fine. Since she thought it was fine i thought it was fine, I trust her a great deal since she is the only doctor that has ever actually investigated into my complaints and pain instead of dismissing it as "growing up". The problem is in the last few months it has gotten more painful.

When I go and it is hurting usually rubbing the side of my tube helps just because its smooth and some how it comforts me. This has stopped working. The stools have gotten bigger in some cases or shaped in such a way that I cry out when I am on the toilet. It is really embarrassing but luckily no one has noticed yet. After I leave the bathroom it even hurts to walk just because of the pain that I feel from it. The other night it took me 30 minutes to fall asleep just because of the pain. I haven't been exposed to any gluten lately because i haven't had a reaction but I did have a reaction to nitrates about a week ago but thats it. It just doesn't make sense and i guess i want to know if anyone else has felt this way before I start freaking out about it.

I appreciate any help or advise anyone can give me,

M

jennifert Newbie

I had the same issue- at first I was going better and then I was more constipated. ..figured out that i was not getting enough fiber and bought a multigrain gluten-free bread instead and started drinking prune juice and adding lots more fluids and salads. Things are much better now in that regard. Also, I think I have noticed that i have an intolerance to milk, which was causing more consitpation...tried lactaid pill for a couple days and started going easier...

good luck!

burdee Enthusiast

I had the same issue- at first I was going better and then I was more constipated. ..figured out that i was not getting enough fiber and bought a multigrain gluten-free bread instead and started drinking prune juice and adding lots more fluids and salads. Things are much better now in that regard. Also, I think I have noticed that i have an intolerance to milk, which was causing more consitpation...tried lactaid pill for a couple days and started going easier...

good luck!

I also noticed that dairy products influenced constipation. After I was diagnosed with IgA mediated dairy allergy and abstained from all dairy products, I rarely had hard stools. The lactaid tablets did nothing for my constipation, because I reacted to the casein protein.

Consuming more fiber, fluids, magnesium and vitamin C all helped reduce constipation. However, treating for gut bugs (bacteria, parasites and especially candida) completely eliminated constipation. Taking daily probiotics keeps me more 'regular' than anything else I've tried.

SUE

  • 8 years later...
espinmari Newbie

I having difficulty staying in bed with such pain, last few days when I walk I felt lower abs pain that went away .. but every time I have the urge I feel like I must call for help.    This is all after I cut Glutten for almost 3 months now... I was thinking maybe is part of the healing process since abs have been in bad shape, but do wanna find out if there is something else going on.. 

Ennis-TX Grand Master
1 hour ago, espinmari said:

I having difficulty staying in bed with such pain, last few days when I walk I felt lower abs pain that went away .. but every time I have the urge I feel like I must call for help.    This is all after I cut Glutten for almost 3 months now... I was thinking maybe is part of the healing process since abs have been in bad shape, but do wanna find out if there is something else going on.. 

This is a old post with the last poster being from 2010. If your having issues you might want to start a new thread to better address your symptoms. NOTE constipation with celiacs can be caused by multiple factors the No1 being magnesium deficiency, which will require you to take stuff like Natural Vitality Calm which is a magnesium Citrate which will also help stimulate your bowels and keep more moisture in your stools. Start with 1/4 tsp (1-2grams) and over a week slowly up it by another 1/4tsp or 1gram til you reach the full dose OR til you get loose stools and back it back down to find your tolerance (dosing to tolerance) other causes can be low fiber if you eating processed gluten free and not a WHOLE foods diet which we highly suggest with this when starting. Other factors can be vitamin C, not enough fluids or bad gut bacteria and in some cases a SIBO or candida overgrowth can be a factor but these have other signs like bad gas, bloating etc.
If your new to the diet please look over the newbie 101 thread as there is a steep learning curve...and you sorta have to decon your kitchen to be gluten free. And whole foods only really makes the transition easier and the healing progress faster.
PS remove dairy and oats for the first few months, dairy intolerance is very common as the vili that help with the enzymes to break it down are damaged. Oats are commonly contaminated and some celaics also react to oats.

ravenwoodglass Mentor
11 hours ago, espinmari said:

I having difficulty staying in bed with such pain, last few days when I walk I felt lower abs pain that went away .. but every time I have the urge I feel like I must call for help.    This is all after I cut Glutten for almost 3 months now... I was thinking maybe is part of the healing process since abs have been in bad shape, but do wanna find out if there is something else going on.. 

Welcome to the board. Were you diagnosed by your doctor?  If so you may want to contact the doctor to make sure nothing else is going on.  Many doctors don't tell us all we need to be aware of when we are diagnosed. Keeping safe involves more than just the food we are eating. If you haven't already please read the 'Newbie 101' thread at the top of the Coping section to make sure you are doing all you need to do to keep from being glutened.

If by chance you are not diagnosed and went gluten free on your own do be sure to get in touch with a doctor. Go back to eating a slice or so of bread a day so you can be tested.  It is important to get a formal diagnosis if possible so we can be looked after properly for follow up testing and have our dietary concerns followed if we should be hospitalized. It is also important for your other family members as if you are positive all your first degree relatives should be tested whether they have symptoms or not.


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,542
    • Most Online (within 30 mins)
      7,748

    Carol Zimmer
    Newest Member
    Carol Zimmer
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.