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

What Was In My Dinner?!


scole2

Recommended Posts

scole2 Newbie

Hi,

I am a newly diagnosed celiac and have been doing my best for the past few months to be as gluten free as possible.

Symptoms are....better but not gone. My dietician recommended going dairy free for a few weeks to see if that helps. Keeping the dairy free/gluten free thing in mind I thought dinner tonight was safe until I was running for the bathroom about 10 min after dinner.

Dinner consisted of:

Grilled chicken rubbed in cumin and olive oil

pre-made polenta

grilled nectarines/blackberries and cilantro w/ lime juice

Very basic ingredients and yet my stomach is quite unhappy. Anyone have any ideas?

It is so frustrating to be diagnosed and yet still not understand what is making me sick. Any ideas will be much appreciated!

Sara


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

Is this stuff you usually eat? I don't eat corn products a lot, so, sometimes I get tummy aches from them.

Gfresh404 Enthusiast

My guess would either be (as previously mentioned) the corn and or the berries. I myself have to be very careful about when and what I eat fruit with. I make sure to always eat it first and to wait at least 20 minutes before eating anything else.

I remember a couple of times before I used to eat a banana and a brown rice bar at the same time. This would send me running to the bathroom. I believe it has something to do with the fact that the fruit digests so much faster than everything else.

Or it could just be the combination of the corn and the fats (the olive oil). I try to avoid all insoluble fibers at all cost. For some reason they seem to completely throw my digestion of fats out of whack. This includes all whole grains (white rice is ok), cruciferous vegetables (brussel sprouts, lettuce, etc.), and skins of fruits and vegetables. It has been difficult to eat healthy while avoiding insoluble fiber since a lot of the healthiest foods contain this type of fiber. I try to stick to a lot of potatoes without the skin, carrots, peas, bananas, apples w/o skin, oranges, strawberries, grapes/raisins, and lean meats. I also eat a fair amount of white rice but have been trying to cut back.

Have you noticed any other disturbances when you knew you were being gluten free?

How long have you been gluten-free?

And do you tolerate other grains well?

ravenwoodglass Mentor

It could have been the premade polenta may not have been gluten free, not all are.

Also were you using a grill that had been used or was also being used for nongluten free food? That could be another source of CC.

Or because some of us have delayed reactions it could have been something from the day before.

OptimisticMom42 Apprentice

I would think CC on the grill or in the polenta. Also check your spices. Some of the off brand ones have fillers. I found a "chili pepper" spice that my son purchased that had three ingredients. Although they all seemed OK I haven't been the same since using it to make taco seasoning. I'm in the C club rather than D so I'm not up on the fruit and fiber part but it sounds like you have recieved some great advise in that area.

Take Care,

OptimisticMom42

scole2 Newbie

Thanks for the help!

I double checked the polenta, nothing suspicious in the ingredients. I eat other corn products and grains fairly often with no effects.

Double checked the cumin, companies website says all the spices are single ingredient and gluten free.

The grill has not been used for anything w/ gluten recently, but could probably use a good cleaning.

The only thing in the dinner I have not eaten since diagnosis is the nectarine. Judging by Gfresh404's comments maybe it was the skin.

I was diagnosed in March of 2009 so this is all still pretty new. In the past few weeks I am learning that it is more than just about being gluten free since I seem to be reacting to things that I know are gluten free. I have tried to reduce CC as much as humanly possible. Hopefully these intolerances that are popping up are a result of healing villi and will get better with time. Or I could be just deluding myelf! :)

Thanks for the suggestions. I never feel more frustrated than when I get sick after a meal and I did everything I could to not use gluten containing ingredients and avoid CC!

Sara

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - tiffanygosci posted a topic in Coping with Celiac Disease
      0

      New Celiac Mama in My 30s

    2. - knitty kitty replied to klmgarland's topic in Dermatitis Herpetiformis
      8

      Help I’m cross contaminating myself,

    3. - Yaya replied to Jhona's topic in Introduce Yourself / Share Stuff
      29

      Does anyone here also have Afib

    4. - larc replied to Jhona's topic in Introduce Yourself / Share Stuff
      29

      Does anyone here also have Afib

    5. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      8

      Help I’m cross contaminating myself,


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,921
    • Most Online (within 30 mins)
      7,748

    Serena Rodriguez
    Newest Member
    Serena Rodriguez
    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

    • tiffanygosci
      Hello all! My life in the last five years has been crazy. I got married in 2020 at the age of 27, pregnant with our first child almost two months later, gave birth in 2021. We had another baby in April of 2023 and our last baby this March of 2025. I had some issues after my second but nothing ever made me think, "I should see a doctor about this." After having my last baby this year, my body has finally started to find its new rhythm and balance...but things started to feel out of sorts. A lot of symptoms were convoluted with postpartum symptoms, and, to top it all off, my cycle came back about 4m postpartum. I was having reoccurring migraines, nausea, joint pain, numbness in my right arm, hand and fingers, tummy problems, hives. I finally went to my PCP in August just for a wellness check and I brought up my ailments. I'm so thankful for a doctor that listens and is thorough. He ended up running a food allergy panel, an environmental respiratory panel, and a celiac panel. I found out I was allergic to wheat, allergic to about every plant and dust mites, and I did have celiac. I had an endoscopy done on October 3 and my results confirmed celiac in the early stages! I am truly blessed to have an answer to my issues. When I eat gluten, my brain feels like it's on fire and like someone is squeezing it. I can't think straight and I zone out easily. My eyes can't focus. I get a super bad migraine and nausea. I get so tired and irritable and anxious. My body hurts sometimes and my gut gets bloated, gassy, constipated, and ends with bowel movements. All this time I thought I was just having mom brain or feeling the effects of postpartum, sleep deprivation, and the like (which I probably was having and the celiac disease just ramped it up!) I have yet to see a dietician but I've already been eating and shopping gluten-free. My husband and I have been working on turning our kitchen 100% gluten-free (we didn't think this would be so expensive but he assured me that my health is worth all the money in the world). There are still a few things to replace and clean. I'm already getting tired of reading labels. I even replaced some of my personal hygiene care for myself and the kids because they were either made with oats or not labeled gluten-free. I have already started feeling better but have made some mistakes along the way or have gotten contamination thrown into the mix. It's been hard! Today I joked that I got diagnosed at the worst time of the year with all the holidays coming up. I will just need to bring my own food to have and to share. It will be okay but different after years of eating "normally". Today I ordered in person at Chipotle and was trying not to feel self-conscious as the line got long because they were following food-allergy protocols. It's all worth it to be the healthiest version of myself for me and my family. I would be lying if I said I wasn't a little overwhelmed and a little overloaded!  I am thankful for this community and I look forward to learning more from you all. I need the help, that's for sure!
    • knitty kitty
      On the AIP diet, all processed foods are eliminated.  This includes gluten-free bread.  You'll be eating meats and vegetables, mostly.  Meats that are processed, like sausages, sandwich meats, bacons, chicken nuggets, etc., are eliminated as well.  Veggies should be fresh, or frozen without other ingredients like sauces or seasonings.  Nightshade vegetables (eggplant, potatoes, tomatoes, peppers) are excluded.  They contain alkaloids that promote a leaky gut and inflammation.  Dairy and eggs are also eliminated.   I know it sounds really stark, but eating this way really improved my health.  The AIP diet can be low in nutrients, and, with malabsorption, it's important to supplement vitamins and minerals.  
    • Yaya
      Thank you for responding and for prayers.  So sorry for your struggles, I will keep you in mine.  You are so young to have so many struggles, mine are mild by comparison.  I didn't have Celiac Disease (celiac disease) until I had my gallbladder removed 13 years ago; at least nothing I was aware of.  Following surgery: multiple symptoms/oddities appeared including ridges on fingernails, eczema, hair falling out in patches, dry eyes, upset stomach constantly and other weird symptoms that I don't really remember.  Gastro did tests and endoscopy and verified celiac disease. Re heart: I was born with Mitral Valve Prolapse (MVP) and an irregular heartbeat, yet heart was extremely strong.  It was difficult to pick up the irregular heartbeat on the EKG per cardiologist.  I had Covid at 77, recovered in 10 days and 2 weeks later developed long Covid. What the doctors and nurses called the "kickoff to long Covid, was A-fib.  I didn't know what was going on with my heart and had ignored early symptoms as some kind of passing aftereffect stemming from Covid.  I was right about where it came from, but wrong on it being "passing".  I have A-fib as my permanent reminder of Covid and take Flecainide every morning and night and will for the rest of my life to stabilize my heartbeat.   
    • larc
      When I accidentally consume gluten it compromises the well-being of my heart and arteries. Last time I had a significant exposure, about six months ago, I had AFib for about ten days. It came on every day around dinner time. After the ten days or so it went away and hasn't come back.  My cardiologist offered me a collection of pharmaceuticals at the time.  But I passed on them. 
    • klmgarland
      So I should not eat my gluten free bread?  I will try the vitamins.  Thank you all so very much for your ideas and understanding.  I'm feeling better today and have gathered back my composure! Thank you kitty kitty   I am going to look this diet up right away.  And read the paleo diet and really see if I can make this a better situation then it currently is.  
×
×
  • 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.