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Can Celiac Cause Your Body To Become Allergic To A Lot Of Other Things?
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I used to break out in hives all the time as a teenager and around the same time started to have anaphylactic reactions to carrots, bananas, avacado's, red delicious apples, watermelon, any melon including cucumbers, and tree nuts. I always went to the doctor but they never knew what was wrong. I also was in the hospital a lot for asthma. Then at 20 my joints became so painful I couldn't put weight on them. I went to a doctor who told me it was my adrenal. He gave me medicine and the pain andy symtom in my joints went away. I never had stomach pain, or excema but when I was pregnant with my second daughter I began to break out. After my fourth child I was diagnosed with Hashimoto's and autoimmune disease. My thyroid died within the month of diagnosis. I have gone gluten free and I feel so much better but I was never tested for celiac. I know I have often been anemic but can't tolerate iron without getting extremely sick and vomitting. Vitamin supplements in the past have made my neck stiff and I suffer severe body aches and flulike symtoms which subside after I quit with the supplement. Lately vitamins aren't bothering me, stomach bloating which I attributed to having six babies is gone and a depression I have always felt is gone. I think I have celiac. I don't want to eat gluten again. How important is the testing?

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I guess the real question is how important is the testing to you? And since you are asking the question you don't have a strong opinion one way or the other. :)

There are those who say you must be tested, you MUST know if you are celiac. But there are also those who say that a diagnosis is not worth making yourself sick for. You don't want to eat gluten again, and I don't blame you. Tlhe only reason, really, for you to want a diagnosis is because the disease is genetic and it is important that your children be tested for it. The recommendation is for all first degree relatives to be tested, every two to three years, or at first sign of symptoms. Are you the only one at home who eats gluten free or is the whole house gluten free?

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    • Cyclinglady is absolutely correct, after hours of internet research the only gluten-free food available at JNB is a fast food chain called 'Nandos'. I was hoping for a bit more variety, but I'll take what I get.   
    • I'm so confused about my daughter's diagnosis.  I hope somebody can help.   My 4 year old daughter has a swollen belly, stomachaches, and lots of gas.  She does not have diarrhea or delayed growth.  Because of her symptoms and because it runs in the family (2nd degree relatives) I had her tested for celiac.   She was weak positive for TTG (IGA)  and strong positive for DGP (IGG)   TTG (IGA)  8   (0-3 neg, 4-10 weak positive, greater than 10 positive) TTG (IGG)  2   EMA: Negative DGP (IGG)  47  (0-19 negative, 20-30 weak positive, greater than 30 positive) Last week, she had her endoscopy.  The doctor found inflammation and little holes or bumps on her duodenum.  He started her on prevacid and said based on his observations, he was suspicious of celiac, but he would not be able to confirm until the biopsy came back. The biopsy showed no signs of celiac disease.  He said that he could not diagnose her with celiac without the biopsy report saying there was celiac damage.  He said he would categorize her as a potential celiac, keep her on a gluten diet and redo the endoscopy in a year or two to check for damage again.  My questions are: 1.)  If it is not celiac, something is causing her duodenum to be inflamed and have little holes or bumps on it, right?  Could it be a wheat allergy or gluten sensitivity?  What else could it be and how do they test for it?  Given her elevated celiac antibodies, how likely is it to be anything besides celiac causing the damage?  2.)  How likely are false positives for TTG and DGP?  I've heard they are pretty sensitive and specific.  Does getting two positives make false positives less likely? 3.) What have you done in this situation?  I want her to have an official diagnosis to make things easier at school and to feel confident that we are eliminating gluten permanently for a worthy reason, etc.  But, I'm having a hard time imagining keeping her on gluten and waiting for her to get more sick and have more intestinal damage just for a diagnosis.     Thanks in advance for your help.  I'm so overwhelmed and confused.  I hope someone has some insight and experience that will help clear things up for me.            
    • Yeah I actually live in Japan which is pretty similar, because Coeliac disease is rare over here so is the understanding and accommodating it. When I mention Gluten to some restaurants they think I am talking in English and they are unfamiliar with the word in Japanese.    So it seems I can write off my chances of getting some authentic Chinese gluten-free food at the airport, but at least there is a Thai restaurant in T3 so I won't starve. Its called  'Phrik Thai' for future reference. http://en-shopping.bcia.com.cn/store/739.html  
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    • I always assumed plain coffee was, but I have seen some controversy online about this. I know someone who is gluten free and only buys whole beans and grinds them herself because she doesn't trust how the grounds are processed.
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