Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Celiac Disease, Msg And Lactose Intolerance: How Severe?


David

Recommended Posts

David Explorer

Hi All:

I


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



Celiac.com Sponsor (A8-M):



Mike M Rookie
This week I had Tacos with Mission Corn shells, McCormick Mild Taco Seasoning, ground beef and fresh green onions. (Opted for no sour cream or cheese).

In reading ingredients he Taco Mix, I didn’t see any gluten sources, but I did see "whey solids (milk)."

I also snacked on Lays Stax Potato Chips a lot. I’m sure it wasn’t a source of gluten, since on their website it says they were gluten-free and are made on a dedicated line where cross-contamination isn’t an option.

Hello David, If you are sensitive to small amounts of gluten, seasoning mixes are a highly suspect area for gluten. I have learned this the hard way. Also, you may have a soy issue and the Lays Stax Potato Crisps , while gluten free, do have some soy ingredients in them. Hope this helps, Mike

David Explorer

Mike:

I hate to take up more of your time, but could you direct me to a resource for Soy allergens?

I

lbd Rookie

Your issues with dairy might be more with casein, a protein in milk products that has a similar structure to gluten, which some people (including me) have problems ingesting. Milk solids may contain casein and lactose, so maybe that is it.

wschmucks Contributor

Hey David,

It might take a while for your body to adjust. It took me about 3 months to start to notice a difference (not feel back to normal, but see any real improvement). If you are worried about other allergens I would try to get tested for them. This way you dont have to deprive yourself of the food (we are already so limited) and you will know for sure which will elleviate some worry on your part.

If you cannot afford/ dont have access I would elliminate the dairy and soy for a months or so and then add one of them back for 2 weeks and eat alot of it, the go off again for 2 weeks and see if you noticed a difference. That is just how I have tested out weather a food bothers me. Just make sure nothing else in your diet changes during that test period, that way you will really know.

As far as the food you listed: McCormicks is one of those wonderful companies that will disclose any source of gluten. So if you read the lable then you are good to go! Everything else looks good-- I beleive** (not sure) that whey was on the "OK" list for lactose intollerents? I thought there wasnt lactose due to the processing. Can someone help out here?

If you are Celiac...I'm afraid you just have to be patient. The healing process will have confusuing ups and downs. It wouldnt be a bad idea to remove other allergens you are wary of for the time being and then do a test (if you cant get an actual test). Good luck and hang in there.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,309
    • Most Online (within 30 mins)
      7,748

    jarheadmp3
    Newest Member
    jarheadmp3
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @Cathijean90! I went 13 years from the first laboratory evidence of celiac disease onset before I was diagnosed. But there were symptoms of celiac disease many years before that like a lot of gas. The first laboratory evidence was a rejected Red Cross blood donation because of elevated liver enzymes. They assume you have hepatitis if your liver enzymes are elevated. But I was checked for all varieties of hepatitis and that wasn't it. Liver enzymes continued to slowly creep up for another 13 years and my PCP tested me for a lot of stuff and it was all negative. He ran out of ideas. By that time, iron stores were dropping as was albumin and total protein. Finally, I took it upon myself to schedule an appointment with a GI doc and the first thing he did was test me for celiac disease. I was positive of course. After three months of gluten free eating the liver enzymes were back in normal range. That was back in about 1992. Your story and mine are more typical than not. I think the average time to diagnosis from the onset of symptoms and initial investigation into causes for symptom is about 10 years. Things are improving as there is more general awareness in the medical community about celiac disease than there used to be years ago. The risk of small bowel lymphoma in the celiac population is 4x that of the general population. That's the bad news is.  The good news is, it's still pretty rare as a whole. Yes, absolutely! You can expect substantial healing even after all these years if you begin to observe a strict gluten free diet. Take heart! But I have one question. What exactly did the paperwork from 15 years ago say about your having celiac disease? Was it a test result? Was it an official diagnosis? Can you share the specifics please? If you have any celiac blood antibody test results could you post them, along with the reference ranges for each test? Did you have an endoscopy/biopsy to confirm the blood test results?
    • Cathijean90
      I’ve just learned that I had been diagnosed with celiac and didn’t even know. I found it on paperwork from 15 years ago. No idea how this was missed by every doctor I’ve seen after the fact. I’m sitting here in tears because I have really awful symptoms that have been pushed off for years onto other medical conditions. My teeth are now ruined from vomiting, I have horrible rashes on my hands, I’ve lost a lot of weight, I’m always in pain, I haven’t had a period in about 8-9 months. I’m so scared. I have children and I saw it can cause cancer, infertility, heart and liver problems😭 I’ve been in my room crying for the last 20minutes praying. This going untreated for so long has me feeling like I’m ruined and it’s going to take me away from my babies. I found this site googling and I don’t know really what has me posting this besides wanting to hear from others that went a long time with symptoms but still didn’t know to quit gluten. I’m quitting today, I won’t touch gluten ever again and I’m making an appointment somewhere to get checked for everything that could be damaged. Is this an automatic sentence for cancer and heart/liver damage after all these symptoms and years? Is there still a good chance that quitting gluten and being proactive from here on out that I’ll be okay? That I could still heal myself and possibly have more children? Has anyone had it left untreated for this amount of time and not had cancer, heart, fertility issues or liver problems that couldn’t be fixed? I’m sure I sound insane but my anxiety is through the roof. I don’t wanna die 😭 I don’t want something taking me from my babies. I’d gladly take anyone’s advice or hear your story of how long you had it before being diagnosed and if you’re still okay? 
    • trents
      Genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out and also to establish the potential to develop celiac disease. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% actually develop it. To develop celiac disease when you have the genetic potential also requires some kind of trigger to turn the latent genes "on", as it were. The trigger can be a lot of things and is the big mystery component of the celiac disease puzzle at this point in time with regard to the state of our knowledge.  Your IGA serum score would seem to indicate you are not IGA deficient and your tTG-IGA score looks to be in the normal range but in the future please include the reference ranges for negative vs. positive because different labs used different reference ranges. There is no industry standard.
    • Scott Adams
      Since nearly 40% of the population have the genes for celiac disease, but only ~1% end up getting it, a genetic test will only tell you that it is possible that you could one day get celiac disease, it would not be able to tell whether you currently have it or not.
    • KDeL
      so much to it.  the genetic testing will help if i don’t have it right? If theres no gene found then I definitely don’t have celiac?  I guess genetic testing, plus ruling out h.pylori, plus gluten challenge will be a good way to confirm yes or no for celiac. 
×
×
  • Create New...