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

This Is Ridiculous, Everything Has Gluten In It.


groogle

Recommended Posts

BabySnooks Rookie
My understanding is that 1 in 133 have Celiac (whether it has been diagnosed or not).  I understand your frustration.  It does seem like an impossible diet at first.  You are actually lucky to live in Europe.  Restaurants seem to be more accomodating than in the U.S.  As for bread products, I order from www.kinnikinnick.com.  I really love their muffins and donuts for a treat.  All vegetables and fruits are gluten free in their natural form.  Plain meat (steak, chops, etc) will be gluten free. Potatoes are safe (boiled, baked, fried-- just not breaded or in a sauce thickened with flour)  I have been gluten free for over a year.  I have been able to travel all oveer Europe and the U.S. without difficulty.  By the way, your parents may very well be celiacs, so you may as well tell them as soon as possible.    Good Luck!

<{POST_SNAPBACK}>

Thank you Pegster, another thing I am curious about is in that same area, it mentions that if there is hydrolyzed vegetable protein in the product, the label will say so. Somewhere I have read that if it says hydrolyzed corn protein instead of vegetable protein, that is ok. Do you feel this is true?


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



Celiac.com Sponsor (A8-M):



judy05 Apprentice
I've been feeing really bad for about a year, now I have finally been dianosed with celiac disease.

I dont understand this I was eating gluten foods for all the prior 18 years of my life, how can I suddenly be allergic to gluten.

I'm a young man, I can't eat gluten free stuff only, I don't even know what has gluten in it or not and it seems pretty much everything. I hate food shopping too. If it was just bread I couldn't eat  I guess I could handle that but glutens in everything.....

Is there any other way to get back to the way I was before. I really dont wanna learn about this disease and be sick.

This diet is completely unworkably for me, does that mean I'm completely screwed?

Thanks for any help,

Greg

Dear Greg, I want you to know that your reaction is familiar to all of us. I tried to deny it and I didn't want to learn about the diet but it is the only way to feel better and you will feel better. I eat very little gluten-free foods, except for the pizza and a few frozen foods. Most foods have at least one brand of gluten-free food, such as Bush Baked Beans, Oscar Meyer hot dogs, etc. Just think of it as substituting not giving up your favorites.

As for telling other people, friends and family, I think of it as spreading the word. My husband,who loves to talk to people, tells everyone he comes in contact with all about the disease and the diet. He is even in the process of being tested for it because he has severe pain, numbness, and tingling in his legs and the Drs are clueless. You may be helping others who are having problems.

In the beginning, keep it simple so your gut can heal. I spent a whole summer living on chicken, pork, rice, potatoes,veggies and fruit. Most of these meals are very simple and easy to prepare and shouldn't make you any sicker. I found that

peppermint tea was very helpful. I also had to give up dairy because I had severe neurological symptoms.

I hope you feel less depressed about this. Keep on reading on this board, it has been a lifeline for me!

<{POST_SNAPBACK}>

moe1981 Newbie

Hello everyone

I have a 16 month old daughter that had the bloodwork come back elevated for the antibodies. Now the next step is to do endoscopy. Ever since she was a year old we noticed she was losing weight. I was really concerned because she started looking like she was malnourished, but she would eat more than I would. Finally her pediatrician scheduled her an appointment at Pittsburgh Childrens Hospital on the 14th. We went and had her bloodwork done that day. So now we have to wait for the endoscopy appointment. I'm glad to see there is support for this disease. She is a picky eater so any suggestions on foods she will like or where I can get them? Any help would be great

Thanks

Melissa

Jnkmnky Collaborator

Melissa,

go to the parents of kids with celiac disease section and browse through old posts. There are plenty of great answers to your questions there! :)

2old4 Rookie

Hi Groggle,

I have only been on the gluten-free diet for 2 months and I must say, it is getting easier all the time. Keep reading here, these guys are fantastic, supportive, and full of knowledge on this disease. I felt very overwhelmed about it and for a week all I ate was chicken breast meat and green salad with cidar vinegar. Now I am eating nachos (pretty much all white corn tortillas are fine), cheeseburgers (Kinnikinnick buns), pasta salads (Tinkyada pasta) Mac & Cheese, Mrs. Leepers makes some great Hamburger Helper "type" of mixes, real easy & quick (Chicken Alfredo, Beef Stroganoff, Beef Lasagna) I drink Coke, and eat 3 Muskateers bars. Oh by the way, I do eat Fruits and Vegetables too, not all junk food. :lol:

The biggest thing though is how good I feel. Everyone has a different time frame on how they heal and what they can tolerate. I was one of the lucky ones. Once I completely eliminated gluten, I noticed increased energy in less than a week. I slept less, I had wayyyyyyyy less bowel movements, I didn't have the "sick/nausea" feeling after I ate something, and the bone pain in my legs was less. It was quite a change from how I felt before. Try it please, it gets easier, I promise, and it is so worth it. Good luck!

Patty

Merika Contributor

Hi,

It takes a while to get used to, and it takes a while to find the best stores, restaurants, and support groups/people near you. I would think there must be stuff in Ireland because recent research has shown that Ireland has THE HIGHEST rate of celiac anywhere in the world - 1 in 50 people. For the USA it's 1 in 133. So you should be in good company :)

Merika

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,549
    • Most Online (within 30 mins)
      7,748

    Trina Morrow
    Newest Member
    Trina Morrow
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Thanks for the update @TerryinCO! Would you elaborate what you mean when you say your genetic tests show that you are "10x higher" for developing celiac disease? 10x higher than what? There are two main genes, HLA-DQ2 and HLA-DQ8, that have been identified as providing the potential for developing celiac disease. Since 40% of the population carries one or both of these genes but only 1% of the population actually develops celiac disease, the genetic test cannot be used to diagnose celiac disease, simply to establish the potential for developing it. Gene testing is usually done to rule out celiac disease vs. NCGS (Non Celiac Gluten Sensitivity). In other words, if gluten consumption is definitely causing someone problems but they don't have the genetic potential for developing celiac disease then the diagnosis would be NCGS. We also know that having both DQ2 and DQ8 puts one at higher risk for developing celiac disease than having just one or the other. But I'm not sure I've ever seen it quantified as in "10x higher". Not sure what you mean by this.
    • Jordan23
      I would stop Xanax. It will eat away at your DAO enzymes needed to break down histamine . No energy drinks will do the same. I use to have all reactions in stomach now it's changed and started in my chest , which completely sucks and bummed. Maybe your reacting to high histamine foods. But it's hard to avoid cross contamination.  I would get pea milk made by ripples .it's a blue bottle . Ru getting cross reactions? Corn gets me. If it says gluten free it's probably not. Nibble at new foods and wait for reactions. Could be sudden or take 2 hours but some people think it hits 2 days later no way. Avoid coffee. Stick to free range chicken and steak or fish . Do lentils package by kroger works for me it doesn't even say gluten free but works for me just rinse well. Make big soups with sweet potatoes, cauliflower,  brocoli,  cucumbers, and add lentils or cook lentils separate taste better. If you can do potatoes add those inn huge plus. If you can do dairy yogurt try Noosa or a certified gluten free one. Don't smoke I had to quit creates heat and acid in your stomach which lowers your vitamins to break food down. Your reactions are in your chest . Do smoothies everymorning with apple.  🥒 cucumbers, arugula , oranges or add what you can tolerate with water. Try a peppermint tea certified gluten free that works for you. Watch out for spices like turmeric they add flour fillers to prevent caring. I got hit hard by that.  If you have a huge attack get the pin or eat oranges quick. If quinoa works for you get certified huge plus. I could go on and on . Just nibble first wait and see then continue eating it.  It's hard to find nuts that work for you. Maybe try nuts.com..... enter with caution
    • TerryinCO
      I haven't been on the site for a while and I have some update info.   Genetic tests show I have the Celiac markers and high risk for Celiacs's  (10X it shows).  Immoglobulin A and G are low - just below the 'green' range; immoglobulin M is in the 'green'.  Zinc, Iron, magnesium, ferritin, and b12 are all in the 'green' range. I've been off the PPI for two weeks now and no real problems...minor heart burn and OTC antacids fix that.  So that's good to be off of that for good. I switched to a b complex sub lingual vitamin. I was surprised about the genetic results on Celiac markers. To my knowledge no one in my family had it or were diagnosed with it.  But they could have had and never been diagnosed.  And at 76 this has come up for me. Gluten free diet is going well and I do feel better on it - nothing major in changes - just better. I appreciate all the advice I've gotten on this site - lots of experience knowledge to draw on here. So thank you, all.
    • ALBANICKAP
      Thank you Scott, I will try what u suggested. 
    • pplewis3d
      Does anyone know if Citracal Petites supplements for Calcium and Vitamin D3 are gluten free?
×
×
  • Create New...