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

I'm New To This....could Eggs Be The Culprit?


Guest JEN

Recommended Posts

Guest JEN

Hello everyone,

First off - thanks for all the wonderful dialogue on this board. Where would we be without the internet for information sharing??? WOW

Anyway - a little about me. I was accidentally diagnosed with celiac disease in June, 03 by way of a biopsy during an enderoscopy (throat scope-whatever that's called). Anyway - after some initial research and preparation, I went gluten-free on September 9th (I have not had a beer in over 4 months - not even a sip - and it's near killed me...ha). Ok, on with the serious stuff.....

I have been gluten-free for 4 months and a week (with only one "known" accident). I can't tell you that I feel better because I was asymptomatic in the first place (as I said, I was diagnosed accidentally while ruling out a GI problem for some female problems I was having at the time). I have two questions for all of you:

1) When I had my follow-up appt. last week with the GI doc - we couldn't measure my improvement by talking about my symptoms because I never had any to begin with. So, he did a celiec-panel bloodwork to compare it with my baseline that I had back at time of diagnosis. He said I was improved in every antibody test (I think he said there were 4 or 5 categories?) that they ran. I went from a total antibody count of 308.6 down to a 26.8. I was elated (because that is over 90% improvement). But he basically said that, "if I thought I was gluten-free to think again...beacuse if that were the case my antibody levels would be at zero". After that comment, I wanted to kick him in the you-know-what. But I didn't. I was feeling so down after my appointment that I went and ate a half of a pizza (but no beers). Again, absolutely NO SYMPTOMS after having a half of a pizza and some fried cheese sticks. OK - so I haven't fallen off the gluten-free wagon - just had an angry episode. I just need to try harder to get that to a zero, I guess. I need to be more careful about cross-contamination and make less assumptions that things are ok. But it's very difficult when I have no outward symptoms to gluten.

This leads me to my next question.

2) It seems that since going gluten-free, I am reacting to EGGS. I seem to get terrible rumbling stomach pains and have endless watery diarrhea (like turning on a hose-sorry) shortly after I eat eggs. Could that be a culprit? And if so, how do I really find out if I am allergic to eggs? Is there a blood test I can ask the doc to order to determine if I am allergic to eggs?

Any advice or words of encouragement would greatly be appreciated at this time.

Thanks, in advance, for your support. God Bless.

Jen


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



Celiac.com Sponsor (A8-M):



gf4life Enthusiast

Hi JEN,

It could be the eggs causing problems, but it wouldn't change your antibody levels to gluten. Although after 4 months the tests would not necessarily be at "zero" some people take 6 months or more to be able to reduce their levels to zero, and yours were exceptionally high. I have a few questions for you.

Do you routinely have anything else with the eggs that might also cause a problem?

Was there a significant amount of damage in your intestines, and if there was did you stop having dairy products, at least temporarily to allow yourself to heal?

As for testing, you could ask your doctor to order the RAST food allergy testing. They take a blood test and check for IgE reaction to certain foods, eggs being one of the top eight. The others being wheat, soy, milk, shellfish, fish, peanuts, and tree nuts (like walnuts or pecans). There is also a more detailed test of more than 100 foods, and I don't know much about that one. I know that with most true food allergies the reaction is typically outward, rash, hives, throat swelling, and such. Food intolerances are typically GI reactions. They are also harder to test for. You could check your self by doing an elimination diet of the suspect foods,

I imagine it would be hard to stick to the gluten-free lifestyle when you didn't have symptoms to begin with. Try not to have too many of those "angry eposides" though. :rolleyes: You don't want to continue to damage yourself inside.

By the way, did they ever figure out the "female" problems you mentioned. I was just wondering if they were caused by the Celiac Disease?

God bless,

Mariann

Lily Rookie

Hi Jen,

I'm getting ready myself to go on an allergy elimination diet and cannot have eggs while I do that. When I add them back in I'll be able to tell if I can take it or not. I have grown not to trust lab tests so I'm in the mindset to listen to my body. Good luck !

Mariann.......you have such wonderful information, we're lucky to have you here :).

Lily

gf4life Enthusiast

Thanks Lily, I'm happy to share. I've always had a weird obsession with medical books and since I got on the internet it's been insane! :P I just seem to absorb what I read, at least when the topic interests me. My sister and a few of my friends lovingly refer to me as Dr.Mariann and call me to ask me what I think about their symptoms before they call the doctor... I study my medical encyclopedias and love to do research. I think it is because I have been suffering from the effects of gluten intolerance since I can remember (my earliest symptom I can remember was at 4 years old) and since the doctors couldn't figure it out, I have been on a lifelong quest for health...

God bless,

Mariann :)

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.