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

New W/ Questions - I'll Try To Keep It Short


wellsfamily

Recommended Posts

wellsfamily Newbie

Hi everyone. Here is my story:

I have a son w/ Type 1 D and a daughter w/ a milk allergy.

I have been having the normal GI issues that seem to be common around here - asked my Dr to run celiac panel.

It was positive for Antigliadin IGG, others were in normal range (but nothing had a 0 value)

Had an endoscopy last week, waiting for results. Gluten Free for 4 days. I also started thyroid meds same day as going gluten free, so not sure which thing is making me feel better.

Here are some of my questions:

If the biposy is negative, how do I know if I truly have a gluten allergy/sensitivity? Do I test myself after a while or go to an allergist?

Can you please tell me what you do when you eat at a party or are invited to dinner? I feel like I will always have to bring my own food.

What are some hidden gluten foods that I might be missing?

Thanks for any advise.

Heather


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



Celiac.com Sponsor (A8-M):



Offthegrid Explorer

Howdy - and welcome!

I'm not up on all the test results and what they mean, but I'm sure someone else will come along to explain.

I personally declined to have a biopsy after having a positive blood test. It is very obvious if I accidentally (or, in the beginning, purposefully) eat some gluten. You *could* do a gluten test if you go gluten-free for about a month, and then try some gluten. It is difficult in the beginning, however, to be completely gluten-free because it's hidden in so many things.

On the parties. If you can, I'd offer to bring a dish and then serve yourself some before anybody else touches it so it's not contaminated. Some gluten-free potato chips can be a good standby, as well as veggies, but these also can be contaminated.

As for dinners, if you feel comfortable, approach them about cooking at least one dish gluten-free. It can be difficult for people to comprehend, however. For now, maybe you could invite some friends over, cook everything gluten-free and talk about it?

Good luck. Don't be too hard on yourself, especially in the beginning. It takes time to figure this stuff out.

If you still find yourself getting sick and you're positive you've elimianted all the gluten, then you may have other intolerances. For me, that's dairy (casein) and soy. I'm working on eliminating soy with good results, but once in a while I find it slips in there even when I'm pretty careful, so still a learning process for me.

missy'smom Collaborator

Welcome. If you click on Celiac Disease Info above it will take you to a page that has a green box on the left. Towards the bottom of it is a link to a page of forbidden /unsafe ingredients.

debmidge Rising Star

My husband and I are the exception, not the norm as he has celiac disease & other food issues. This being said we do not eat food prepared at anyone else's home - we will bring a meal for him. He's only just recently been going to restaurants which have gluten free menus (Outback, Charlie Brown's, etc.).

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,634
    • Most Online (within 30 mins)
      7,748

    Linda whisenhunt
    Newest Member
    Linda whisenhunt
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • cristiana
      I think going back to your GI isn't a bad idea - my visits to the GI did not stop following my diagnosis as I had annoying issues on and off for some time.  Thankfully he is a fantastic GI, with  a great sense of humour, so it wasn't a chore to see him again although I'd rather not have had to, obviously!  But I needed my mind to be put at rest as my symptoms didn't seem to go away overnight as I'd hoped they would.  Initially I recall he recommended I went Dairy Free for three weeks, and he told me it would take that time to see an effect.  At that time, even lactose free milk went straight through me, so it is important, I would say, to even avoid that during a Dairy Free trial. My ongoing symptoms were bloating which did respond a bit to that trial.   However, within about 18 months there was a return to a very sore stomach, plus various aches and pains.   It turned out some gluten was sneaking in with my iron supplement (I was buying Floradix instead of Floravital), but I also think the dishwasher, the oven and eating out were contributors, too. Before my numbers normalised (from memory, about eight years!) I had several follow up appointments and a few more tests, but things gradually did get better.  Having read many accounts on this forum over the years, I don't think it is uncommon for symptoms to get a bit worse before getting better, that was certainly the case with me.  Your gut is damaged so you may well have issues digesting other food in the short term. But do try to be as scrupulously gluten free as you can possibly be as a first step, and I'd definitely try a three week Dairy Free trial.   Your villi because they are damaged are not able to create the lactase required to digest dairy at this time so you may well see some improvement if you come off dairy for a while.  Perhaps keeping a food diary of what you eat, where you eat it, whilst a bit onerous to do, will help identify foods that are causing issues.  For a while, apart from oats, I found peas, lentils and soya products hugely aggravating.  Things should calm down.
    • Rejoicephd
      Thankfully those are normal. B12 was on the low end of the normal range when I first got diagnosed. When I last got it checked, it had come up a lot (455 last time checked).
    • Scott Adams
      You can search this site for prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/  I didn't notice any gluten ingredients in Kirkland Almond non-dairy beverage, however it does contain Locust Bean Gum. Some gums may cause IBS-type issues in some people with celiac disease or gluten sensitivity:    
    • trents
      Have you had B12 levels checked?
    • Rejoicephd
      For the past few months, I've been taking several supplements (a multi-vitamin, an iron supplement, a vitamin C supplement, and a magnesium supplement), all of which state that they are gluten free on the label.  
×
×
  • Create New...