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

Help with gluten coming out. Painful.


Meak

Recommended Posts

Meak Newbie

Hey, all. I'm on the celiac Facebook group but I feel better talking here because I can write way more and it's more discreet. I haven't been diagnosed with celiac, because my doctor had me eat gluten for only two weeks and I was already gluten-free for a while before that test, so it came back negative. In 2010, my endoscopy was normal, just inflamed. Doctor said Gastritis. In 2015, I had a colonoscopy and the gi doctor said my colon is pink and healthy and said 'ibs' 

 

I have ehlers danlos syndrome, and brain damage, math disability, severe. Learning disability, somatic symptom disorder, Ptsd, panic disorder, agoraphobia. I don't know if these are important for this post, but I like being very honest and detailed. 

 

When I eat gluten, I can eat it for about three days, and I seem to feel good, really good, almost like a normalcy, like a high on life. Well, I ate gluten meals for a week, I reintroduced it after not eating it for a while. I'm Vegan and I was eating very clean. No sugar, veggies, fruits. After a week of gluten, my stool smelled horrendous like it always does when I consume it. Smells like motor oil, so foul, makes me gag. Stool gets lighter, HUGE and painful, no matter how much water I consume. I get itchy with a fee tiny blisters on my skin, and I've always been very constipated since I was little along with bleeding sores on my scalp. I also get scaly or flaky itchy 'cuts' on the top of my ears, in the inside of my ears. If I scratch at them, I bleed and pus comes out and it's super stingy. 

Joint pains get worse, panic attacks, suicidal thoughts, carpal tunnel, severe bloat. When I wait long enough and quit eating it, I poop a lot and my stomach goes instantly flat. Eating it, I can go from 142 lbs to 150 within a day, not exaggerating. I get so bloated, that wearing even leggings or pajama pants or underwear makes me feel short of breath, it pushes down on my stomach. My hearing is extremely sensitive, with constant ear ringing. I will jump at even the slightest noise. This only happens after I consume gluten. If I over eat on vegetables, I feel pain but ok, but gluten, I end up having panic attacks and feel 'delusional' if I watch a horrid film, I feel like it's going to actually happen. It's crazy, but not eating it long enough, and I feel normal again. 

 

My stool has started to slowly become darker now, not as light. Mostly after I poop, I have severe pain that can spread from my rectum to my lower right abdomen and even to my hip, and lower back. A nurse assumed I had pelvic inflammatory disease, turns out I didn't, it was my bowels. When I come off of Gluten, I start having chills all over, freezing, then I poop and I'm even colder. I have reactions to potatoes, rice, corn, yams, quinoa, so much pain and bloating. Cannot eat sugar, certain fruits. More than half an avocado and I feel awful. Oats are horrible. Can't eat cream of rice. Any kind of rice. Tempeh hurts me as well. 

 

I have four teeth that have rotted out and broken off. Thankfully the front one, a dentist filled for very cheap since I was 18. I'm 33 now and it's still filled. I've always experienced tooth aches, infections. When I eat gluten, I can't pass gas, I feel it trying to come out but it won't. I used to be able to and it made me feel way better. I have to also manually remove poop sometimes. I was going normally before and eating it, the rabbit pellets and huge stool started coming back. 

 

In Feb this year, I admitted myself to the ER for severe pains and anxiety and xrays showed I had stool backed up. I went to the ER five times in Feb and March, and every time, I had large thick stool stuck in my intestines. 

 

I've had missed periods, and severely heavy painful periods, fatigue, especially after pooping. My finger tips goes numb, my toes go numb and migraines.

 

After I eat gluten, I'll have sneezing fits about an hour later, and the sneezing lasts for a week and it happens every single week. I know I should avoid gluten, and I am, but I wanted to see if this sounds like celiac or just I tolerance. I'm not seeking medical advice. I've had very useless doctors who can't do the celiac test properly and dismiss my concerns and they all say it's ibs, change my diet. I also think I'm experiencing cross reactive symptoms from foods like corn and rice and potatoes. Also, I cannot ever eat beans. They hurt me severely. Pain, gas, massive pregnant looking belly. 

 

I just want to know, mostly, when you quit eating gluten, when do you feel better again? I miss myself. :( I've always been kind of sick but I miss even having the symptoms I can manage, not this overwhelming horrible nightmare. Thank you to anyone who even reads this. I don't want to feel alone in this.

 

I wanted to add that it's been four days since I ate lasgana, not gluten free, and the food ingredients from that dish are still coming out in my stool. 


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



Celiac.com Sponsor (A8-M):



Ennis-TX Grand Master

Since you tested on a gluten free diet...they do not count, testing requires you to be eating gluten for 12 weeks to get the antibodies up. Obviously not a option, if it is giving you so much pain, but a gluten challenge might be worth it, your call.

Open Original Shared Link

If you are celiac, reactions vary but worst of them can ease off after a few days, but will have other symptoms for months til the antibodies go back down..I heard some take 6 months.

You have some issue with gluten, if you do not want to get tested then going gluten free with the assumption you have celiac is a good idea. Constipation used to be my number one issue growing with undiagnosed celiac...BM every 2-3 days up to 11 days was normal back then. Celiac constipation is normally directly related to magnesium deficiency. The one you must take to fix this is Natural vitality calm, start off 1/4tsp (1-2g) a day and slowly up it 1/4tsp (1-2)g a day til full dose or go beyond til you get loose stools then back back down 1/4tsp (1-2g) this is referred to as dosing to tolerance.

Your neurological symptoms can be from 2 things.
1. Gluten ataxia, where your body might have been attacking the brain in a confused auto immune response to gluten. I have this myself...math can not be done with more anymore, I can no longer do computer programing, and my thoughts would loop like crazy and not move forward when I was on gluten. It also caused nerve damage with loss of feeling, heat sensitivity, and some spinal damage for me it seems.
2. B-vitamin and other nutrient deficiency like magnesium etc. can lead to nerve damage. Celiac means you will not be absorbing it effectively with a damaged intestine. I would suggest a Liquid version like what I take Liquid Health Neurological Support and their Stress & Energy formula 1tbsp each 3 times a day. Also consider their vitamin D and perhaps a multivitamin.

You mentioned recent issues with grains/sugars.....sounds like Ulcerative Colitis that I got. Probably not but I had to remove all grains from my diet, all fruit, sugar. My Ulcerative Colitis would flare up from not just the standard triggers of gluten, dairy, soy, but also the rare triggers of fructose and glucose. For now try a paleo/keto diet removing all grains, beans, soy, fruit. Try adding in more healthy fats like nut butters and seed butters that are smooth and easy on the gut for keeping your calorie up.
Other thoughts to the cause could be a SIBO or Candida issue which would require the same low carb diet to starve off the offenders.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,029
    • Most Online (within 30 mins)
      7,748

    Jen72
    Newest Member
    Jen72
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • 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.
×
×
  • 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.