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. - catnapt posted a topic in Related Issues & Disorders
      0

      anyone here diagnosed with a PARAthyroid disorder? (NOT the thyroid) the calcium controlling glands

    2. - catnapt replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      how much gluten do I need to eat before blood tests?

    3. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Curious question

    4. - Amy Barnett posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Question

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

    • Total Members
      133,322
    • Most Online (within 30 mins)
      7,748

    avery144
    Newest Member
    avery144
    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

    • catnapt
      learned I had a high PTH level in 2022 suspected to be due to low vit D  got my vit D level up a bit but still have high PTH   I am 70 yrs old (today in fact) I am looking for someone who also has hyperparathyroidism that might be caused by malabsorption    
    • catnapt
      I am on day 13 of eating gluten  and have decided to have the celiac panel done tomorrow instead of Wed. (and instead of extending it a few more weeks) because I am SO incredibly sick. I have almost no appetite and am not able to consume the required daily intake of calcium to try to keep up with the loss of calcium from the high parathyroid hormone and/or the renal calcium leak.    I have spent the past 15 years working hard to improve my health. I lost 50lbs, got off handfuls of medications, lowered my cholesterol to enviable levels, and in spite of having end stage osteoarthritis in both knees, with a good diet and keeping active I have NO pain in those joints- til now.  Almost all of my joints hurt now I feel like someone has repeatedly punched me all over my torso- even my ribs hurt- I have nausea, gas, bloating, headache, mood swings, irritability, horrid flatulence (afraid to leave the house or be in any enclosed spaces with other people- the smell would knock them off their feet) I was so sure that I wanted a firm diagnosis but now- I'm asking myself is THIS worth it? esp over the past 2 yrs I have been feeling better and better the more I adjusted my diet to exclude highly refined grains and processed foods. I didn't purposely avoid gluten, but it just happened that not eating gluten has made me feel better.   I don't know what I would have to gain by getting a definitive diagnosis. I think possibly the only advantage to a DX would be that I could insist on gluten-free foods in settings where I am unable to have access to foods of my choice (hospital, rehab, nursing home)  and maybe having a medical reason to see a dietician?   please let me know if it's reasonable to just go back to the way I was eating.  Actually I do plan to buy certified gluten-free oats as that is the only grain I consume (and really like) so there will be some minor tweaks I hope and pray that I heal quickly from any possible damage that may have been done from 13 days of eating gluten.    
    • Jmartes71
      So I've been dealing with chasing the name celiac because of my body actively dealing with health issues related to celiac though not eating. Diagnosed in 1994 before foods eliminated from diet. After 25 years with former pcp I googled celiac specialist and she wasn't because of what ive been through. I wanted my results to be sent to my pcp but nothing was sent.I have email copies.I did one zoom call with np with team member from celiac specialist in Nov 2025 and she asked me why I wanted to know why I wanted the celiac diagnosis so bad, I sad I don't, its my life and I need revalidaion because its affecting me.KB stated well it shows you are.I asked then why am I going through all this.I was labeled unruly. Its been a celiac circus and medical has caused anxiety and depression no fault to my own other than being born with bad genetics. How is it legal for medical professionals to gaslight patients that are with an ailment coming for help to be downplayed? KB put in my records that she personally spent 120min with me and I think the zoom call was discussing celiac 80 min ONE ZOOM call.SHE is responsible for not explaining to my pcp about celiac disease am I right?
    • Amy Barnett
      What is the best liquid multivitamin for celiac disease?
    • Jmartes71
      I've noticed with my age and menopause my smell for bread gives me severe migraines and I know this.Its alarming that there are all these fabulous bakeries, sandwich places pizza places popping up in confined areas.Just the other day I suffered a migraine after I got done with my mri when a guy with a brown paper bag walk in front of me and I smelled that fresh dough bread with tuna, I got a migraine when we got home.I hate im that sensitive. Its alarming these places are popping up in airports as well.I just saw on the news that the airport ( can't remember which  one)was going to have a fabulous smelling bakery. Not for sensitive celiacs, this can alter their health during their travel which isn't safe. More awareness really NEEDS to be promoted, so much more than just a food consumption!FYI I did write to Stanislaus to let them know my thoughts on the medical field not knowing much about celiac and how it affects one.I also did message my gi the 3 specialist names that was given on previous post on questions on celiac. I pray its not on deaf door.
×
×
  • 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.