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

Diagnosed W/ Too Many Food Allergies?


jsb727

Recommended Posts

jsb727 Newbie

I got tested for food allergies (prior to looking into celiac disease), and the test came back with TONS of food allergies. None of which I had ever noticed a reaction to before. Has anyone else experienced what I would call an "over-diagnosis" where they say you have tons of allergies you don't really have? I had the IgG Antibody Assessment through Genova Diagnostics.

The test showed I was allergic to dairy, alfalfa, broccoli, celery, cucumber, lemon, white potatoes, asparagus, cabbage, gluten, lettuce, spinich, avocado, cane sugar, corn, grapes, pecans, tomatoes, bananas, carrots, green peppers, and pineapple. Not to mention several others that were "low level."

My naturopath even said she'd never seen anyone's test come back with so many allergies. She had me go off all these items for 3 months to see if there was any change. I called her after two months (survived this diet from 12/1/07 to 2/1/08) and told her I couldn't take it any more. :blink: I still can't believe I made it through Christmas.

The only thing that concerns me is that even though I know I have celiac now, I have no symptoms if I eat something w/ gluten in it. I've been gluten-free for almost 4 months now (was diagnosed by biopsy in May). I'm sure I have to have had something with gluten in it within that time, either by cross contamination or accidentally. What if I just have no symptoms when I eat food I shouldn't eat?


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



Celiac.com Sponsor (A8-M):



Rachel--24 Collaborator
I got tested for food allergies (prior to looking into celiac disease), and the test came back with TONS of food allergies.

I've been gluten-free for almost 4 months now (was diagnosed by biopsy in May). I'm sure I have to have had something with gluten in it within that time, either by cross contamination or accidentally. What if I just have no symptoms when I eat food I shouldn't eat?

I'm assuming that you must have had symptoms which led you to have the food intolerance testing....and then to be tested for Celiac Disease?

If you are now symptom free...(after having been diagnosed and after 4 months on the diet) I would probably consider that to be a sign that you are doing well on the diet and that you are healing.

If you are concerned that you may still be consuming gluten (without having any noticeable reaction) you can have your bloodwork repeated to be sure that the antibody levels are going down and that they stay down.

The IgG testing is for food intolerances......which are different from food allergies. Allergies are IgE mediated and it would be unusual to have that many "true" allergies.

IgG mediated food intolerances can be temporary and may have been a result of intestinal damage (leaky gut) caused by undiagnosed Celiac Disease.

Food intolerance reactions are typically delayed reactions.....it can be difficult to link a particular food to the symptoms and the symptoms may seem unrelated to diet.

If you are still experiencing symptoms that you think might be caused by accidental glutening or by additional food intolerance....I would recommend keeping a food journal to help figure out what might be causing it.

jsb727 Newbie

The original symptom I had that made me seek help is bone hypersensitivity (sometime around '93). Over the years I got sent to a couple rheumatologists, physical therapy, and a spine/sports specialist, none of which had the answer. I would go through phases where I would tell myself "this is not normal, someone should be able to diagnose this" and then I'd go to a couple doctors and not get any answers. So I'd wait a couple years and then go through the same series again. At one point I was diagnosed with fibromylgia (a diagnosis that didn't seem right to me... but I'm not a doctor). Finally I went to a naturopath, who tested me for food sensitivities, and eventually did the blood test for celiac at which point she referred me to a gastroenterologist for the upper endoscopy.

I have, however, noticed that I no longer get canker sores (which previously I had several of them at a time, and I would have them more often than not). I also don't have the sinus problems I've had for years. Those two symptoms I hadn't previously associated with gluten.

So, I don't get any symptoms from eating gluten or different foods. Although, I've gotten maybe 2 or 3 canker sores over the last several months... I haven't correlated it to eating gluten, but I'll keep an eye on it.

SGWhiskers Collaborator

My testing for food allergies was only for the big 8. I came back positive for Milk and Egg. I had never had what I would consider allergic symptoms before and was surprised by the food allergies. I eliminated every trace of milk and egg in my diet for 1.5 years. The only changes I noticed were elimination of canker sores, and (gross alert) healing of a very small fissure or maybe tiny bleeding hemorroid. This tiny bit of blood came back if I slipped up and ate any milk. Since my other (undiagnosed Celiac) symptoms were not better, I added milk and eggs back with no other problems. 7 weeks ago, I started the Celiac diet and reduced my milk and egg comsumption to just what was in a little milk chocolate. The little blood remained until I again cut out all milk 3 weeks ago. Logic tells me that that tiny speck of blood is indicative of continued damage in my lower digestive system. Not a coincedental hemorroid like my earlier MD thought.

Anyway, my point is that even if you can't see the intestinal damage from food allergies, it may very well be going on inside. My new/good doc has recommended that for the first 6 months of healing, I don't have any allergens. Then I give them a test one by one. I don't think I'm going to challenge for 2 years.

Of course, I don't have as many allergies as you. Or maybe I do and have not been tested. Good luck. I'm sorry about the restricted diet.

SGWhiskers

Juliebove Rising Star

My daughter was initially diagnosed with IgG allergies to wheat, gluten, peanuts, dairy, eggs, soy and banana. About 4 years later she was tested again. Now it is wheat, spelt, peas, lentils, peanuts and almonds.

The Dr. explained that those foods we eat a lot of tend to show as IgG allergies. She said my daughter could resume eating those foods she used to be allergic to, but only twice a week and not on consecutive days.

I was tested once and found to be allergic to dairy, eggs and almonds. I used to get canker sores when I'd get a virus, but have had them only a couple of times since and the last time they went away in a day. The dairy was also causing sinus and ear infections.

Amyleigh0007 Enthusiast

My son was dx with allergies to corn, wheat, egg whites, clam, soy, walnuts, and peanuts. His dr also told us that he could eat these foods but with limits. We have to watch how much he consumes and if he has any reactions (because he has never had any visible reactions). For example, he can have waffles that contain egg but I would never give him a scrambled egg. So far he has not had any reactions except the hives on his esophagus that was discovered when he had his biopsy. The dr didn't think that was a reason to totally avoid those foods. He said the gluten free diet was hard enough to follow, adding all the above foods to that list would make finding foods that a picky 8 year old would eat nearly impossible.

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. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    4. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

    5. - nanny marley replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      nothing has changed

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

    • Total Members
      133,343
    • Most Online (within 30 mins)
      7,748

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

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
×
×
  • 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.