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

Suspecting Nc Gs- Starting Probiotics


Lys-88

Recommended Posts

Lys-88 Newbie

First a very brief history - I'm a 23 year old girl diagnosed with crohns 8 or 9 years ago, and have been making minor diet changes ever since. In Spring 2009 I was at my worst, celiac panel came back negative, but frustrated with symptoms I went raw anyway, felt almost great. Had a tough time staying strict and during the colder months started eating some cooked, vegan, grain-free foods (organic soups, hummus, etc). Come the following spring, I was taking a bite of this, bite of that.. no matter it was vegan or not. A bite of cracker or pretzel, or 3 croutons on my salad weren't a big deal to me, because it was such a small amount I didn't feel it'd cause too much damage.. But maybe I was wrong. I mean, three croutons?

I'm not sure if this is the cause, but once again regardless of my high-raw diet (with only the few 1-3 bite a day cheats usually a cracker, pretzel, crouton, noodle of pasta, teriyaki vegetables, etc)my symptoms are unbearable to the point I do not want to leave my house. I come home from work and lie in bed. Maybe 1-2 bites a day of gluten really DOES make a HUGE difference??? I don't know. I'm sick of pretending it might not though, so 4 days ago I cut gluten 100% out of my diet (as well as any dairy or soy 1-2 bite cheats). My only cheat has been a gluten-free english muffin (and yes, rice does make my "arthritis" flare).

Symptoms-

intestinal discomfort, bloating, gas (worst it's ever been and suffer 24/7 literally), abdominal pain, cramping, diarrhea, all GI symptoms worsen dramatically when I eat ANY amount of fat!.. Arthritis, puffiness of face, edema in lower legs/feet, water retention, extremely dry skin, severe fatigue and loss of energy, forgetfulness, depression.

My main concern is the GI symptoms. Everything I eat has my stomach churning, causes bloating/gas. But also ANY amount of salt (I usually use organic Himalayan sea salt) has my body puffy and my ankles tightly swollen and "woody" feeling.

So enough is enough, I'm ready to begin healing. Four days in and no major improvement, the gas and tightness has lessened slightly but discomfort continues. I don't expect magic. But maybe it's not improving due to part 2 of my healing regimen: I decided after cutting out gluten that I need to get in some good probiotics, hopefully to help the GI heal up and become symptom-free a little quicker. I had floragen3 and one other kind of probiotic, I started taking those daily. I bought kimchi and would take a few bites here and there, usually with dinner (beyond simple low-fat raw salad). I also bought kombucha tea to sip on which I've had 2 bottles of so far. My new Garden of Life Raw probiotics arrived today so I took one with dinner and a few bites of kimchi. My intestine is churning, noisily.. Tight and uncomfortable, and immediately I get gassy. I don't really overdo it with the kimchi because it's only a few bites, but for some reason any amount does this, and also I notice I get churny-gassy when sipping Kombucha. Not sure if pills are making difference with those symptoms or not but it's easier to tell when I eat/drink the probiotic foods.

So mainly I'm just wondering if this is going to go away? Should I stop the probiotics if going 24 hours without them seems to calm the stomach (in a way, still eating a spinach-cucumber-tomato-lemonjuice salad has me slightly upset) or should I keep up with them because this is normal for your gut to react this way starting them? I've never kept up with the things because this happens every time I try to take probiotics fo 5-7 days, it's constant discomfort and more gas. But maybe that's just them starting to work and push out the bad bacteria.

Also, is it really possible that TINY amount of gluten I'd eat, and not everyday, would cause the symptoms to be THAT severe? The GI upset to be that intolerable and the gas to be that bad?? It just seems like SOOO much GI discomfort for such a tiny amount..

Thanks for anyone who takes the time to read and even more to those who take the time to respond..


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



Celiac.com Sponsor (A8-M):



Bubba's Mom Enthusiast

It's possible you have some other issue going on, but as an answer to your question about the amount of gluten you were ingesting and it causing symptoms..yes. That amount can cause your symptoms, and they can last for days.

I ate a sample of cheese from the grocery store on Saturday. They wre serving it with crackers.

My hubby tried the sample and raved about how good it was, and said I should try it. I asked for a small piece of just the cheese because the cracker had gluten. As I chewed the cheese there was a crunch..and I realized there was a crumb of cracker.

That crumb caused a severe reaction. It's now 3 days later and I'm still feeling it.

Ingesting even a tiny crumb like that if you have Celiac disease can cause symptoms for up 2 weeks..and longer in some people.

Try going completely gluten-free, avoiding even trace amounts..and see if your symptoms settle down?

Lys-88 Newbie

Thanks for the reply. I have been doing my best at avoiding all trace amounts and possible cross-contamination. I've also been avoiding soy (except a little tamari), all beans/legumes, all dairy as before, and peppers, broccoli, hard-to-digest vegetables as well. Trying to stay low-fat but finding it a little hard, and still am having a hard time digesting fats. Probiotics are still causing discomfort too, and it's been over a week of being on them now. I wish this adjustment period- if that's what it is- would pass. I'm feeling very bloated, some symptoms have improved though and my energy is slowly coming back for the most part, so I know I'm making a little progress. Just trying to stay motivated and stick to it. I wonder if I decrease the amount of fruit I eat if that may help reduce symptoms until I can adjust? I just want to feel normal again.. it's been so long, and I don't even remember what it feels like anymore. My dad has almost every last symptoms of celiac so I'm convinced that gluten is the culprit here (as well as trace amounts of soy, beans, rice, etc in my diet).

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. - Teaganwhowantsanexpltion posted a topic in Introduce Yourself / Share Stuff
      0

      A little about me and my celiac disease

    2. - trents commented on Scott Adams's article in Winter 2026 Issue
      2

      Celiac Disease and Longevity: Can Treatment and Healing Improve Long-Term Survival?

    3. - Paulyw commented on Scott Adams's article in Winter 2026 Issue
      2

      Celiac Disease and Longevity: Can Treatment and Healing Improve Long-Term Survival?

    4. - xxnonamexx posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Healthy Gluten Free Foods low sugar that you found?

    5. - Jmartes71 replied to Jmartes71's topic in Gluten-Free Foods, Products, Shopping & Medications
      2

      Medications

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

    • Total Members
      133,232
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Teaganwhowantsanexpltion
      I was diagnosed at 6 after having severe stomach pain after eating white bread or any kind of gluten my sister had one done aswell I was scared for the biopsy but thats bc the gas mask thing but now that I am a 14yr old female struggling with severe chronic pain making my body ache for no reason making it hard to sleep and do the things I love like playing spot which I love to do but I can sometimes not even be able to walk bc my knees hurt so bad I can or my hips or back the only think I wish for is to be a normal kid which I can't even be and I get accused of faking pain bc there is no physical things to notice especially at school when one day it will be so sore im limping the next im walking perfectly fine idk if its all from celiac disease but im the only one in my family that has this problem 
    • xxnonamexx
      I noticed eating gluten-free or CGF foods have higher sugar and sodium some. No added sugar protein bars I found better with plant fiber. I wanted to know what are you go to besides whole fruits/veggies that you find are healthy for you where you can feel eating normal without hurting yourself or health. I was looking into subscription based like Thrift to see if there is something that is healthier CGF that can make me feel normal. Thanks
    • Jmartes71
      Thankyou because I met up with K B with well known bay area hospital once and she said she knows I don't like to take meds, I said thats incorrect, I have issues.Thats the one that said I was deemed " unruly " when she admitted I was celiac when I asked why am I going through this.
    • cristiana
    • trents
      Cristiana, that sounds like a great approach and I will be looking forward to the results. I am in the same boat as you. I don't experience overt symptoms with minor, cross contamination level exposures so I sometimes will indulge in those "processed on equipment that also processes wheat . . ." or items that don't specifically claim to be gluten free but do not list gluten containing grains in their ingredient list. But I always wonder if I am still experiencing sub acute inflammatory reactions. I haven't had any celiac antibody blood work done since my diagnosis almost 25 years ago so I don't really have any data to go by.   
×
×
  • 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.