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

New, Massive Pain When Glutened


Munzie

Recommended Posts

Munzie Rookie

Hi, I'm new and found you all by process of elimination. I was diagnosed with IBS several years ago, but the symptoms got worse and worse. So I started looking for answers. I am not under doctors care, have a ver limited income and no medical. My symptoms were to begin with constant diahrrea, then such severe cramps that I thought I seriously had to go to the ER (which I can't afford). So when I learned about Gluten allergy I went totally Gluten free -which I found to be a big chore- and was feeling really good for 2 weeks. Yesterday we went out to eat and a couple of hours later I felt the cramps coming on again. However at first I couldn't figure out why and was crying, cause I thought I had been wrong about being Gluten allergic. While I was laying in bed, massaging my gut and wracking my brains what it might be, I remembered eating Heinz 57 sauce on my steak and had my friend google the ingredients. So that's where the problem was. It scares me now to eat anything not basic enough for me to know it doesen't contain Gluten! You can't believe the pain -which by the way lasts for hours and leaves me totally drained and weak- and I just want to have it stop for good.  Oh, I also have Fibromyalgia, which I've read is also a symptom of the Gluten allergy. The FM symptoms were much better when I deleted Gluten from my diet.

Does anyone here have any tips for me, what I can do or has anyone experienced such massive pains?

 

Thanks, Dani


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I'm not familiar with the ingredients of Heinz 57 but couldn't find the ingredients on Heinz's website.  Eating at a restaurant has many ways you could get "glutened".  Was it a gluten-free menu?  Did you tell the waiter you needed gluten-free?  Even with all that, mistakes can be made.  Some places don't understand gluten-free and screw up the gluten-free menu - for example - saying French fries are gluten-free when they are fried in shared oil with something non-gluten-free like onion rings.  A waitress taking the bread off the plate before serving you. 

niese Explorer

I totally understand your pain I had abdominal pain for 2 1/2 months 24/7 dr tried different pain meds on me and nothing helped, I had to learn to deal with it.  Finally after several test and months later found our I had Celiac.  Since going gluten free that pain has left.  I do experience it when I am gluten from cross contamination, I am still new with gluten free and have had mistakes.  Plus I have Colitis so my intestines have a double whammy.  I am still healing so I do still get occasional abdominal pain but its usually around a level 2-3 which I can deal with.

 

Sounds to me since you ate out that you experienced cross contamination.  I agree with what kareng said.  I have only eaten out I think twice and both times was Wendy's only ordered a baked potato, but was scared to death the whole time.  

Hope you feel better soon.

niese Explorer

Hi, I'm new and found you all by process of elimination. I was diagnosed with IBS several years ago, but the symptoms got worse and worse. So I started looking for answers. I am not under doctors care, have a ver limited income and no medical. My symptoms were to begin with constant diahrrea, then such severe cramps that I thought I seriously had to go to the ER (which I can't afford). So when I learned about Gluten allergy I went totally Gluten free -which I found to be a big chore- and was feeling really good for 2 weeks. Yesterday we went out to eat and a couple of hours later I felt the cramps coming on again. However at first I couldn't figure out why and was crying, cause I thought I had been wrong about being Gluten allergic. While I was laying in bed, massaging my gut and wracking my brains what it might be, I remembered eating Heinz 57 sauce on my steak and had my friend google the ingredients. So that's where the problem was. It scares me now to eat anything not basic enough for me to know it doesen't contain Gluten! You can't believe the pain -which by the way lasts for hours and leaves me totally drained and weak- and I just want to have it stop for good.  Oh, I also have Fibromyalgia, which I've read is also a symptom of the Gluten allergy. The FM symptoms were much better when I deleted Gluten from my diet.

Does anyone here have any tips for me, what I can do or has anyone experienced such massive pains?

 

Thanks, Dani

 

Hi, I'm new and found you all by process of elimination. I was diagnosed with IBS several years ago, but the symptoms got worse and worse. So I started looking for answers. I am not under doctors care, have a ver limited income and no medical. My symptoms were to begin with constant diahrrea, then such severe cramps that I thought I seriously had to go to the ER (which I can't afford). So when I learned about Gluten allergy I went totally Gluten free -which I found to be a big chore- and was feeling really good for 2 weeks. Yesterday we went out to eat and a couple of hours later I felt the cramps coming on again. However at first I couldn't figure out why and was crying, cause I thought I had been wrong about being Gluten allergic. While I was laying in bed, massaging my gut and wracking my brains what it might be, I remembered eating Heinz 57 sauce on my steak and had my friend google the ingredients. So that's where the problem was. It scares me now to eat anything not basic enough for me to know it doesen't contain Gluten! You can't believe the pain -which by the way lasts for hours and leaves me totally drained and weak- and I just want to have it stop for good.  Oh, I also have Fibromyalgia, which I've read is also a symptom of the Gluten allergy. The FM symptoms were much better when I deleted Gluten from my diet.

Does anyone here have any tips for me, what I can do or has anyone experienced such massive pains?

 

Thanks, Dani

Dani,

 

Welcome  aboard! Please check out that newbie thread, you will learn alot there. This is an awesome place everyone understands and is very helpful.  If you have any questions just ask someone will be able to answer or direct you to the answer.  I was so blessed when I first found this site, learned so much and still learning.

 

https://www.celiac.com/pages/Newbie%3F.html

Munzie Rookie

Dani,

 

Welcome  aboard! Please check out that newbie thread, you will learn alot there. This is an awesome place everyone understands and is very helpful.  If you have any questions just ask someone will be able to answer or direct you to the answer.  I was so blessed when I first found this site, learned so much and still learning.

 

https://www.celiac.com/pages/Newbie%3F.html

Thanks to all of you :-). It's great to have finally found a place where I'm understood!   I share the anxiety when eating at a restaurant, always break out in a cold sweat when my companion suggests we go out to eat. He is very supportive, even read my new book I got today 'Living Gluten free for dummies', but he thinks I am talking myself into having something I don't :-(.   I understand this, cause I also run into people all the time who 'think' they have a desease if they have a little diahrrea *gruml*.   My symptoms have escalated over years and since I've learned about the Gluten and taken it out of my diet, I really feel much better (other than the episode yesterday). so I spent nearly $100 on gluten free bake goods today (money I really don't have) but I am a bread junkie and paying 7+ dollars for a mini loaf of bread at Walmart is just out of the question in the long run. I love to bake and have a breadmaker (no worries, it's squeekie gluten-clean lol). We'll see how it goes from here and I'm glad to have a new place to vent and get information. Thanks again....hugs, Dani

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. - RMJ replied to Samanthaeileen1's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

    2. - Samanthaeileen1 replied to Samanthaeileen1's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

    3. - JoJo0611 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Just diagnosed today

    4. - RMJ replied to Samanthaeileen1's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

    5. - Samanthaeileen1 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Thoughts? Non-endoscopic Celiac diagnosis in two year old

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

    • Total Members
      132,800
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • RMJ
      So her tissue transglutaminase antibody is almost 4x the upper end of the normal range - likely a real result. The other things you can do besides an endoscopy would be: 1.  Genetic testing.  Unfortunately a large proportion of the population has genes permissive for celiac disease, but only a small proportion of those with the genes have it. With family history it is likely she has the genes. 2.  Try a gluten free diet and see if the symptoms go away AND the antibody levels return to normal. (This is what I would do). Endoscopies aren’t always accurate in patients as young as your daughter. Unfortunately, without an endoscopy, some doctor later in her life may question whether she really has celiac disease or not, and you’ll need to be a fierce mama bear to defend the diagnosis! Be sure you have a good written record of her current pediatrician’s diagnosis. Doing a gluten challenge for an endoscopy later in life could cause a very uncomfortable level of symptoms.   Having yourself, your husband and your son tested would be a great idea.  
    • Samanthaeileen1
      here are the lab ranges.  Normal ranges for tissue transglutaminase are: <15.0 Antibody not detected > or = 15.0 Antibody detected normal for endomysial antibody is < 1.5. So she is barely positive but still positive. 
    • JoJo0611
      I have been diagnosed with coeliacs disease today after endoscopy, bloods and CT scan. I have also been diagnosed with Mesenteric Panniculitis today. Both of which I believe are autoimmune diseases. I have been told I will need a dexa scan and a repeat CT scan in 6 months. I had not even heard of Mesenteric Panniculitis till today. I don’t know much about it? Has anyone else got both of these. 
    • RMJ
      The normal ranges can vary for the tissue transglutaminase and gliadin antibody celiac tests because the units aren’t absolute.  Could you please tell us what the normal ranges are for the laboratory used? If her tissue transglutaminase results are 10-fold above the normal range some would diagnose her on that alone.  Endomysial antibody ranges are more standardized, and a titer of 1:5 would usually be normal.  Might that be the normal range and not her result?  Her total immunoglobulin A is normal for her age. (This is tested because if low, then the other IgA tests might not be valid).
    • Samanthaeileen1
      Hello there! New to celiac community, although I have lots of family in it.  My two year old was just diagnosed with celiac disease based on symptoms and bloodwork.  symptoms (swollen belly, stomach hurting, gagging all the time, regular small vomit, fatigue, irritability, bum hurting, etc) she got tests at 18 months and her bloodwork was normal. She just got tested again at 2 1/2  because her symptoms were getting worse and these were her results :   Tissue Transglutaminase Ab, IgA 58.8 Unit/mL (High) Endomysial Antibody IgA Titer 1:5 titer (Abnormal)   Gliadin Antibody IgA < 1.0 Unit/mL Gliadin Antibody IgG 8.5 Unit/mL Immunoglobulin A 66 mg/dL Her regular pediatrician diagnosed her with celiac and told us to put her on the strict gluten free diet and that we wouldn’t do an endoscopy since it was so positive and she is so little (26lbs and two years old). I’m honestly happy with this decision, but my family is saying I should push and get an endoscopy for her. It just seems unnecessary and an endoscopy has its own risks that make me nervous. I’m certain she has celiac especially with it running in mine and my husbands family. We are now thinking of testing ourselves and our 5 year old as well.  anyways what would y’all recommend though? Should we ask for an endoscopy and a GI referral? (We are moving soon in 5 months so I think that’s part of why she didn’t refer us to GI)    
×
×
  • 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.