Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

York Food Allergy Tests


lindasheppard

Recommended Posts

lindasheppard Newbie
:ph34r: I received the test back and am allergic to almost everything (in addition to being Celiac with severe intestinal damage) - Rice, corn, eggs, nuts, milk, soy, etc. I also have gastroparesis (trouble with food moving from stomach to intestine - especially fiber & fats). I am at a loss about what I should eat anymore. Are these tests really accurate? If so what am I supposed to do - live on a feeding tube? This is getting ridiculous.

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



Celiac.com Sponsor (A8-M):



KaitiUSA Enthusiast

Did it say how sensitive you are to these things? I know I am sensitive to dairy if I have alot of it but I can have some in moderation. Also I would value what these tests have to say...I for one did not have one done yet but plan to sometime in the near future.

Fruits and veggies are good though :D

tarnalberry Community Regular

As vote said, how allergic? You may be able to include them in your diet rotationally (have them one day, but not the next few) which could help your options. You'll also want to investigate the widest possible variety of food. (Other grains, other fruits/vegetables, etc.) What's the full list?

mela14 Enthusiast

I had that test done about a month ago and also have LOTS of food allergies. I didn't need the York test tell me that I was reacting to food but it did help to pinpoint or at least validate my intolerances. It IS very hard but you will figure out what you can and cannot eat. I was working with a dietician when I was first told about the gluten intolerance and she had me eating sooooooooo many new and different foods that I was reacting almost daily. Then it made sense to me why I was not eating the foods that she put in my diet......I probably reacted to them before and avoided eating them subconsciously. Most fruits, fresh meats, fish and salads are ok. Nothing canned or processed. Think natural.....but eliminate the things that make you ill. If you tested positive and are not sure if you get sick from it try small doses to see how you react.

It's been 3 months since going gluten free and I am still having a hard time with other intolerances. This morning I reacted to hot brown rice cereal and remembered that I felt the same way when I had buckwheat, which I tested positive for, coincidentally made by the same manufacturer. So....it could be cross contamination. This is a learning experience. I'll never eat that hot cereal again....or any other made by that manufacturer! Of course it ruined my day and I am still feeling awful but what is the other option....Not eating???? You have to figure out what doesn't hurt you so that you can eat and maintain nutrition.

I don't do eggs or soy or peanuts anymore....just to name a few.

One of the good things that came out of my appointments with my dietician is that she had me keep a food diary. Everything I put in my mouth was documented along with the time and how I felt afterwards. When you don't feel well it's hard to figure out what did it but if you see it in black and white over and over then you know you can't have it. Consider keeping a food diary.

Email me anytime if you need to talk.

good luck!

cdford Contributor

Here is what the CDers in my family had to do.

Start with some simple meat such as chicken that you do not react to. Grill it without extra spices or sauces. Use only a little salt for flavoring and some garlic if you do not react. Be sure you are starting with a clean grill if you used to use it for non-gluten-free items or the cross-contamination can get you.

Next, buy some white rice (or brown if you are like me and a nutrition nut or get constipation badly). Use that as your starch to start with since it is rare to have a reaction to rice.

Pick out a couple veggies and fruits that you like and are not reactive to. Keep it minimal and simple.

Use this simple meal for several days rotating among the couple of fruits for breakfast and snacks and among the couple of veggies for your other meals.

After a week or so and you are not reacting, add in foods like you do a baby learning to eat...one at a time. Keep a food diary. Only add one fruit or one veggie and eat it once daily for several days. If you react, go back to what you were eating before and let it get out of your system. If you don't react, put this food into your rotation.

When you have a little variety in your fruits and veggies, add some potatoes instead of rice. We did mashed potatoes made with gluten-free chicken broth instead of dairy. Now you have two starches you can alternate along with your veggies and fruits so you shouldn't be having to eat the same thing more than two or three times a week.

Next add a different meat. Again, keep it simple and grilled. No added fats, fancy spices, or sauces.

You get the picture. After several weeks, you will find that you have quite a bit of variety and are letting your body relax and heal. After a couple of months more, you will have significant variety and a clear list of what you react to.

After you have been six months or more without a reaction, try adding back an item you were only a little reactive to and see if your immune system will handle it now. We found that we were able to add back almost everything within a yr or two. We each still have a couple of things we don't dare try again, but we are a whole lot better off than before.

mela14 Enthusiast

Donna,

I'm reading the advice that you gave linda...I'm going to have to take it myself.

I am having such a hard time with food. I eat things that I think are ok but then react terribly. The advise you gave to keep it simple is what I have to do. The thing is that I thought I WAS keeping it simple! Chicken seems to be ok......white rice is now bothering me too! My gut is always inflamed and bloated. Even certain veggies are doing me in. I have been trying to be gluten free for about 3 months now but have realized there are so many other intolerances and then the IBS acts up too! OKay, so i have to get back to basics and simple food. It seems that the less variety of food the better off I . One thing sets me off and then my gut is irritated for days!

soooooooooooo here I go again..think simple.........and gotta watch those veggies!

Will think of your words whenever I dare to venture onto something that is questionable! "Simple"!!!

kactuskandee Apprentice

Good advise Donna, I agree with Mel... Keep it simple. Like you Mel, I react to so many things...My IBS, after being great for many months started up again, so I too have had to go back to the tried and true....a few days of mostly rice or rice products, then I know I can safely add puffed millet, puffed corn...and when the pains/bloating/gas goes away I add simple things back in, plain potatoes, peas, carrots, a LF white fish...but only salt as my seasoning.

I still don't know who to go to for the food allergy test...I want to be tested for as many as possible although like some of you I can already tell what I'm sensitive to. Dairy for sure and soy for sure and to many raw fruits or veggies, and then there is chocolate...oh don't even start me on that..I'm a chocoholic but it sure can do me in. I know in part because of the fats. I can do a cocoa based smoothie with no problems.

Anyway you look at it, it's tough. But something challenging always is, and after all, aren't we worth it?

Kandee


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



Celiac.com Sponsor (A8-M):



aaascr Apprentice

lindasheppard -

You are not alone! And I felt pretty much the way you do now, when I found out that I had celiac disease.

I am allergic to most proteins and lots of fruits and veggies too.

I had to eliminate them from my diet. The only thing I can tolerate is a (very) small amount of corn, which is fortunate because similar to gluten, corn is in everything, including tylenol and ibuprofen. Once your system has calmed down it should be able to tolerate more fresh fruit and vegetables though stay away from things in the cabbage family if you're having fiber issues. While I can eat rice, I have found that I like quinoa better and it has more protein, haven't had a reaction to it either. It can be purchased as natual, flakes and flour. Due to my allergies I eat organic, and I pretty much stay away from mainstream and processed foods. It has taken me a long time to figure out what I can/cannot eat, so don't get too frustrated. I'd be happy to help you with any food suggestions - just let me know..

mela14 Enthusiast

aaascr,

i read your post and found it interesting that I used to eat quinoa too and I don't think it gave me a reaction. Then I started seeing a nutrionist who wanted me to have a little protein at every meal. I would have 2 hard boiled egss with the quinoa for lunch. That's when the trouble really started. I would get soooo sick. Not knowing I had food allergies other than gluten I figured there was something up with the quinoa so I stopeed eating it. Then I had the YORK allergy test done and eggs were at the top of the list for allergies...both the white and the yolk. I have never attempted to try the quinoa again as I am afraid. Could there be any cross contamination with quinoa? Not sure. My gut has been in a bad sate for weeks and I can't seem to get it to calm down. I guess I have to scrutinize more and definately stop the espresso that I love so much! it is starting to irritate me regardless of how little of it I drink right now. maybe..........when my gut is better I can sneak in a few sips from hubby's cup! Between the IBS and the allergies this is really tough. I am happy that you finally figured out what you can and cannot eat. I am still trying to get it right. Please pass along any tips that you might have. Even after I have a BM the pain and twisting are there....sometimes I even get bloated! oh well...............................

debmidge Rising Star

I have a different take on the York testing.

My husband is celiac & we did the full test and it came back that he was highly sensitive to soy, yeast, almond, milk, egg yolk, certain nuts like hazelnut, cashew, lentils, chili pepper and mildly sensitive to other items such as garlic & brazil nuts.

We showed the report to his gastro, who is the ONLY gastro who diagnosed him with celiac disease properly in 30 years, he was not familiar with this type of testing, but he said not to put too much faith in it as we could run another test in several months and get differing results, as the body does change.

Why I am skeptical about this test: For example, my husband has not eaten lentils or chili pepper in 30 years! nor hazelnuts or cashews in 30 years; not even in a baked item or processed item as nuts upset his IBS (that he thought he had). Anyway, my question to York was how can someone have an antibody in their blood for a foodstuff that they have not eaten in 30 years? Their reply is that it has to be in something he has eaten recently, maybe as a hidden ingredient. Well, sorry, but that's not possible. From 11/03 to the test date of 8/04 everything he ate was made by me or him from scratch with plain/bland gluten-free ingredients. I am not questionning sensitivity to the soy, yeast, milk or egg yolk, admittedly, he does eat this stuff, but I am questionning the items he hasn't eaten for many, many years. How does the body have a measurable sensitivity to something that the person is not eating?

Anyway, I'd say "proceed at your own risk" and buyer beware. If you get a test, go over it with your GP, gastro or nutritionist (as a matter of fact, the York report tells you to do just that).

KaitiUSA Enthusiast

I think they are good to have done however they are not widely accepted by the medical community yet.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,187
    • Most Online (within 30 mins)
      7,748

    Kris46
    Newest Member
    Kris46
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...