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

Anyone Else Reacting To Gluten Fed Poultry (and Eggs) And Fish


mm54

Recommended Posts

mm54 Newbie

I have DH and was diagnosed three years ago. About a year ago, I started to have the typical DH rash almost every time I ate rice, even with brands clearly labeled "gluten free". At the end I was ordering special exotic rices from Bangladesh and other places and I was not reacting to these, but I eventually decided to eliminate even those - too much hassle and it seemed like a crapshoot every time I ate rice.

About six months later, I started to have the DH reaction most of the time when I ate chicken, which I had carefully prepared........not a spec of gluten in my home. So I went to the butcher and inquired about breading or stuffing in the back room where they package the stuff. Yes, they do breading. So he was super nice and used special latex or rubber gloves when he handled my order, and my chicken never touched the countertop. However, I still broke out. I called the chicken production/slaughter plant and the customer service lady told me there was not any gluten in their plant whatsoever! So then I spoke with the butcher again. He suggested perhaps I was reacting to the gluten/grain pellets the chickens are fed. He told me poultry do not have stomaches, but rather gizzards............that grind up their food. Being still skeptical, I tried all kinds of chicken from other grocers, and I broke out every time. I tried turkey and even ostrich! (Like eating a cardboard box.) Anyway, he was right. I reacted every time. At the same time I was reacting to some fish. After carefully scrutinizing the problem there, my local fish store told me the fish I was having problems with were all pond fed.........pellets again!

I started to wonder why I was still able to tolerate eggs...............until about a month ago and started breaking out every time I ate eggs, so I've eliminated eggs. The diet I'm on now is super restrictive, but I think it is probably quite healthy. Pretty simple fare - beef, pork, lamb, elk, buffalo, and wild fish, some legumes, lots of veggies, salads, fruit, and nuts. Even with nuts, I have to be exquisitely careful with the brands I buy. Many are contaminated.

Seems as though my sensitivities to gluten are way off the charts. Anyone else experience this problem?


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



Celiac.com Sponsor (A8-M):



Franceen Explorer

I had been told (and found it to be true) that while you are suffering a DH breakout, you are hypersensitive to IODINE - mostly from table salt and salt injected and included in foods, including fresh foods. I bought table salt without iodine, and was very careful about the foods known to be high in iodine (fish, especially). I believe that poultry can have added salt and definitely ham and pork do.

You might be adding salt to eggs and the other things you are unexpectedly reacting to.

Once my DH had completely gone away, I became less and less sensitive to iodine and eventually became back to normal. When I get accidentally glutened and breakout (now much less frequently), I have to go back to avoiding table salt, restaurant food, and frozen food, hams, poultry etc until the rash goes away.

One of the old fashioned tests for DH was to put an iodine patch on your skin and if you broke out it was considered DH!!

You may want to try that before you go completely crazy with eliminating so many foods. Eventually that can become unhealthy and may not cure the problem!

Good luck.

tarnalberry Community Regular

nope, never had an issue with grain fed animals. the protein is broken down and isn't something that can be really put into the flesh of an animal without changing it to an animal protein. such is metabolism. :)

but franceen is right - the DH reaction in the skin is mediated by iodine, so - even without eating gluten - until you are well and completely past healed, taking in much in the way of iodine will exacerbate DH symptoms. that means not just iodine enriched table salt, but also sea vegetables (like nori in sushi), fish, shrimp, potato, turkey, beans, milk, and egg.

mm54 Newbie
I had been told (and found it to be true) that while you are suffering a DH breakout, you are hypersensitive to IODINE - mostly from table salt and salt injected and included in foods, including fresh foods. I bought table salt without iodine, and was very careful about the foods known to be high in iodine (fish, especially). I believe that poultry can have added salt and definitely ham and pork do.

You might be adding salt to eggs and the other things you are unexpectedly reacting to.

Once my DH had completely gone away, I became less and less sensitive to iodine and eventually became back to normal. When I get accidentally glutened and breakout (now much less frequently), I have to go back to avoiding table salt, restaurant food, and frozen food, hams, poultry etc until the rash goes away.

One of the old fashioned tests for DH was to put an iodine patch on your skin and if you broke out it was considered DH!!

You may want to try that before you go completely crazy with eliminating so many foods. Eventually that can become unhealthy and may not cure the problem!

Good luck.

I had not heard about the issue with iodine in relationship to DH. If it is iodine that is exacerbating the problem, why is it I have never had a breakout with wild fish? I have a freezer full of wild salmon, orange roughy, tuna, and halibut. I eat these several times a week and I do not have any DH reactions with any of these. Certainly they have just as much, if not more iodine, than farm-raised fish.

ravenwoodglass Mentor

"I had not heard about the issue with iodine in relationship to DH. If it is iodine that is exacerbating the problem, why is it I have never had a breakout with wild fish? I have a freezer full of wild salmon, orange roughy, tuna, and halibut. I eat these several times a week and I do not have any DH reactions with any of these. Certainly they have just as much, if not more iodine, than farm-raised fish."

The issue may not be the fish itself but the way it is processed. If they use salted water in the processing of the farm raised fish that may explain it.

To completely clear my DH I had to eliminate iodine from everything for a while, even my vitamin. I also had to be really really strict about CC as even the tiniest amount would cause an outbreak for the first couple of years gluten-free. It takes up to 2 years for the antibodies to leave the skin. After that I found I was able to tolerate a bit more iodine and added the vitamin back in but I still use uniodized salt.

Franceen Explorer

Several things come to mind here:

DH takes a VERY long time to completely clear up - even 100% Gluten Free and with much reduced Iodine in diet.

Also, the typical reaction to Gluten with DH is very delayed, especially in the beginning. That made it very hard, and sometimes impossible to determine what it was that caused the outbreak. Over the first two years of gluten-free and the first year of reduced iodine, the reaction time very gradually reduced to about 3 days.

Now a couple of years into gluten-free (very strict) and still using uniodized table salt, my DH still takes 1 - 3 days to show up - but now I am also getting a much quicker intestinal reaction! (Gas, grumbling, bloat within hours of eating the gluten and if a bad glutening - diarhea for about 1 day).

I still can only guess at what the source was though.

I no longer avoid high-iodine foods - I eat "lox" (Salmon) for breakfast nearly every day and lots of other fish, but I use un-iodized salt and still watch the vitamin iodine content (there is SOME, but I buy the vitamin with less).

The iodine connection to DH is well documented and understood by the medical community - and really does exist. I just think that people's levels of iodine intake vary very greatly (many people eat NO fish at all and that is a significant source).

Trying to reduce iodine (never never eliminate it 100% - thryroid problems will ensue!), might be a good way to tell if it is a potential source for you.

mm54 Newbie
Several things come to mind here:

DH takes a VERY long time to completely clear up - even 100% Gluten Free and with much reduced Iodine in diet.

Also, the typical reaction to Gluten with DH is very delayed, especially in the beginning. That made it very hard, and sometimes impossible to determine what it was that caused the outbreak. Over the first two years of gluten-free and the first year of reduced iodine, the reaction time very gradually reduced to about 3 days.

Now a couple of years into gluten-free (very strict) and still using uniodized table salt, my DH still takes 1 - 3 days to show up - but now I am also getting a much quicker intestinal reaction! (Gas, grumbling, bloat within hours of eating the gluten and if a bad glutening - diarhea for about 1 day).

I still can only guess at what the source was though.

I no longer avoid high-iodine foods - I eat "lox" (Salmon) for breakfast nearly every day and lots of other fish, but I use un-iodized salt and still watch the vitamin iodine content (there is SOME, but I buy the vitamin with less).

The iodine connection to DH is well documented and understood by the medical community - and really does exist. I just think that people's levels of iodine intake vary very greatly (many people eat NO fish at all and that is a significant source).

Trying to reduce iodine (never never eliminate it 100% - thryroid problems will ensue!), might be a good way to tell if it is a potential source for you.

Before being diagnosed with DH, I did not use salt in cooking for nearly 20 years, because I thought it was the healthy thing to do! And into the first year after being diagnosed with DH, still no salt. So I have a hard time believing iodine was a contributing or exacerbating issue to developing DH for me personally. I use a little salt now, but not much. I appreciate your input, but it really doesn't jive with my experiences. When I first caught on, breakouts would appear about 1/2 - 1 hour after eating a questionable meal (dining away from home usually or trying some new product at home) not days and days, not even remotely. I rarely have problems now, I go for months without a problem. The first year of going gluten free, I was having breakouts all the time because I really didn't understand all the sources of gluten that were causing me problems. Once I developed a better understanding and became more assertive in my inquiries, I had far fewer problems. When I do break out now, it generally takes about an hour to several hours and I know what it is because I was not completely sure I was safe - dining out, etc. You are right about the thyroid issue, am dealing with this problem presently. I think going without salt for so long didn't help a bit.

I have already asked about the chicken being plumped up (injected) because my butcher told me with turkey they are generally injected with a filler, that often includes water, some gluten, and salt. I haven't been able to eat turkey for a couple of years because of this. He told me the brand of chicken I was purchasing was not injected or treated - it's all organic, etc. I even spoke with the butchering and processing plant and they assured me there's nothing added.

My doctor has told me on many occasions that every body is unique. What is true for you is not necessarily true for me, and the other way around as well. I have been researching the thyroid condition I have, and I think it may have made me super super sensitive in the past two years. My chemical sensitivites and allergies have also gone through the roof, in addition to becoming super super sensitive to gluten. Alot of products that say "gluten-free" have proven not to be, atleast not in the low enough range for my body to tolerate. Anyway, thanks for the comments. I wish it was as easy as cutting down on salt.


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



Celiac.com Sponsor (A8-M):



Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to emzie's topic in Related Issues & Disorders
      1

      Stomach hurts with movement

    2. - emzie posted a topic in Related Issues & Disorders
      1

      Stomach hurts with movement

    3. - Flash1970 replied to Ginger38's topic in Related Issues & Disorders
      3

      Shingles - Could It Be Related to Gluten/ Celiac

    4. 0

      NCA Tennessee/Vanderbilt – Parents & Caregivers of Children with Celiac Virtual Meeting

    5. 0

      NCA Tennessee/Vanderbilt – Parents & Caregivers of Children with Celiac Virtual Meeting


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,451
    • Most Online (within 30 mins)
      7,748

    emzie
    Newest Member
    emzie
    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

    • cristiana
      Hi @emzie and welcome to the forum. Perhaps could be residual inflammation and bloating that is causing sensitivity in that area.  I was diagnosed with coeliac disease in 2013 and I remember some years ago my sister telling me around that time that she had a lady in her church, also a coeliac, who  had real pain when she turned her torso in a certain direction whilst doing exercises, but otherwise was responding well to the gluten-free diet. As far as I know is still the picture of health. I often end up with pain in various parts of my gut if I eat too much rich food or certain types of fibre (for some reasons walnuts make my gut hurt, and rice cakes!) and and as a rule, the pain usually hangs around for a number of days, maybe up to a week.   When I bend over or turn, I can feel it.  I think this is actually due to my other diagnosis of IBS, for years I thought I had a rumbling appendix but I think it must have just been IBS.  Reading the experiences of other sufferers, it seems quite typical.  Sensitized gut, build up of gas - it stands to reason that the extra pressure of turning can increase the pain. When I am glutened I get a burning, gnawing pain in my stomach on and off for some days - it isn't constant, but it can take up a few hours of the day.  I believe this to be gastritis, but it seems to hurt irrespective of movement.   Anyway, you are doing the right thing to seek a professional opinion, though, so do let us know how you get on.   Meanwhile, might I suggest you drink peppermint tea, or try slices of fresh ginger in hot water? A lot of IBS sufferers say the former is very helpful in relieving cramps, etc, and the latter is very soothing on the stomach. Cristiana
    • emzie
      Hi! One of the usual symptoms I have with a gluten flare up has deviated a bit and I thought I'd search for advice/opinions here. Also to see if anyone goes through similar stuff. Monday all of a sudden I got really bad pain in my stomach (centre, right under the chest, where the duodenum would be located). I ended up having to throw up for 2 hours, my body was trying to get rid of something from all sides and it was just horrible. Since then I havent been nauseous anymore at all, but the pain has stayed and it always worsens the moment i start moving. The more I move the more it hurts, and when i rest longer it seems to dissapear (no movement). I've had this before, but years ago I think around when I first got diagnosed with coeliac, where each time I moved, my stomach would hurt, to the point where I went to the ER because doctors got freaked out. That only lasted 1 night though, and Now it's already wednesday, so 3 days since then, but the pain persists and remains leveled. it doesn't get crazy intense, but it's still uncomfortable to the point I cant really go out because Im afraid itll turn into a giant flare up again. I couldn't think of where I could possibly have been glutened at this bad of a level and why it hasn't passed yet. I went to the GP, and as long as I have no fever and the pain isnt insane then its fine which I havent had yet. Tomorrow im also seeing a gastroenterologist specialized in IBS and coeliac for the first time finally in years, but I thought I'd ask on here anyway because it still hasnt dissapeared. It also hurts when someone presses on it. Maybe it's just really inflamed/irritated. I'm just frustrated because I'm missing out on my uni lectures and I do a sports bachelor, so I can't get behind on stuff & next to that i'm also going to go to the beach with my boyfriend's family this weekend: ( 
    • Flash1970
      Hi. So sorry to hear about your shingles. There is a lidocaine cream that you can get at Walmart that will help numb the pain.  That's what I used for mine. It can't be put near your eyes or in your ears. I hope your doctor gave you valacyclovir which is an antiviral.  It does lessen the symptoms. If it is in your eyes,  see an ophthalmologist.  They have an antiviral eye drop that can be prescribed.  Shingles in the eye could cause blindness.  I was unsure whether you have celiac or not.  If you do,  follow the diet.  I believe that extra stress on your body does affect everything. Shingles can recur. If you start getting the warning signs of nerves tingling,  see the dr and start taking the valacyclovir to prevent a breakout. If I sound technical,  I am a retired pharmacist. 
    • Scott Adams
      You are right to be proactive, as research does indicate that individuals with celiac disease can have a higher predisposition to enamel defects, cavities, and periodontal issues, even with excellent oral hygiene. While many people with celiac successfully undergo orthodontic treatment without complication, your caution is valid. It may be beneficial to seek a consultation with an orthodontist who is familiar with managing patients with autoimmune conditions or who is willing to collaborate with your daughter's gastroenterologist or a periodontist. They can perform a thorough assessment of her current oral health, discuss your specific concerns about recession and decay, and create a tailored hygiene plan. This second opinion could provide a clearer risk-benefit analysis, helping you decide if addressing the cosmetic concern of the lower teeth is worth the potential risks for your daughter, especially if they are not currently affecting function or her confidence. 
    • Scott Adams
      This is an older article, but still helpful:  
×
×
  • 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.