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

Symptoms Of Egg Intolerance


Christa1

Recommended Posts

Christa1 Newbie

I was just wondering what kind of symptoms anyone gets if they eat eggs or almond butter. I am having a hard time figuring out where my symptoms are coming from and if they even relate to eggs or almonds. I have trouble with peanut butter so I made cookies with almond butter, brown sugar, and egg whites. Those were the only ingredients and after I ate them my chest got really tight and my throat felt like it swelled up. I can't pin down the culprit because I don't even know if these symptoms correlate to the cookies. Anyone who could give me any input or advice would be greatly appreciated.


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



Celiac.com Sponsor (A8-M):



kimo Newbie
I was just wondering what kind of symptoms anyone gets if they eat eggs or almond butter. I am having a hard time figuring out where my symptoms are coming from and if they even relate to eggs or almonds. I have trouble with peanut butter so I made cookies with almond butter, brown sugar, and egg whites. Those were the only ingredients and after I ate them my chest got really tight and my throat felt like it swelled up. I can't pin down the culprit because I don't even know if these symptoms correlate to the cookies. Anyone who could give me any input or advice would be greatly appreciated.

It sounds like you might be allergic to the almond butter. My brother-in-law is allergic to all kinds of nuts and that is what happens to him. My daughter is allergic to eggs. At the time I didn't know and she had some and her eyes started to swell up and she got itchy all over her body.

Christa1 Newbie

Thank you for your input. Peanut butter has never settled well with me so I bet the other nut butters probably are affecting me as well. It is so hard to pin-point the culprit of the symptoms that pop-up. I will just have to stick to my eggless, dairy free, nut free muffins instead of trying to experiment with cookies. Thanks again!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,118
    • Most Online (within 30 mins)
      7,748

    Cwbtex
    Newest Member
    Cwbtex
    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

    • captaincrab55
      Hi Colleen H,   I suffered with the pins and needles/burning feeling in my legs and feet for at least  6 years until my Nephrologist figured out that I had to go on a low salt diet.  He said my kidneys weren't strong enough to remove the salt.  The simple fix was a diuretic, but that med leaves the uric acid behind, so that wasn't an option.  On the bright side the low salt diet lowered my BP over 20 points and and the pins and needles/burning feeling went away.  Good Luck and hope this helps.  
    • Colleen H
      Yes this is very frustrating for me ... not sure what to think.  Feels like I'm having reactions to a lot of things  Now applesauce?? I don't understand 😞 
    • Colleen H
      I did ... But aren't we going to be vitamin deficienct if we are not eating due to being sick ?? If the food we eat is gluten free and we have other sensitivities , how do we get out of the cycle??  Thank you 
    • Colleen H
      Anyone else get pins and needles. ??? Burning feeling ? Heat makes it so much worse 😔  Winter is here.  I had to lower my thermostat because I couldn't take that hot air feeling 😔  Hopefully it goes away soon     
    • trents
      I assume that you already know that genetic testing for celiac disease cannot be used to confirm a celiac diagnosis. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% actually develop celiac disease. It can be used to rule out celiac disease with a high degree of confidence, however, in the case where the genetic testing is negative for the genes. Until and unless you are actually diagnosed with celiac disease I would not raise this as an issue with family. However, if you are diagnosed with celiac disease through blood antibody testing and/or endoscopy with positive biopsy I would suggest you encourage first degree relatives to also purse testing because there is a significant chance (somewhere betwee 10% and almost 50%, depending on which studies you reference) that they will also have or will develop active celiac disease. Often, there are symptoms are absent or very minor until damage to the small bowel lining or other body systems becomes significant so be prepared that they may blow you off. We call this "silent 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.