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

What Am I Missing?


almostnrn

Recommended Posts

almostnrn Explorer

I am so aggrivated right now with this disease. A couple of weeks ago my DH flared pretty bad (the cause is still kind of a mystery to me) which only seems to happen to me with large and consistant quantities of gluten, prior to that I had been good as gold for quite some time. Thought I had it all under control until this week. I went to my first celiac support group meeting which just happened to be hosting their annual gluten-free potluck. There were 2 vendors there; one with desserts, and I've had those before with no reaction and one with gluten-free bread. This is by far the best bread I've had and the only I've found pallatable. As a matter of fact prior to this I had given up on the idea of bread peroid. Here I was all giddy with delight....until I got home. By then the gas and bloating had started which was followed by two days of nausea, fatigue, etc. So I finally felt like I could eat something yesterday. I pulled out the new bread (which is certified gluten-free) and make the most wonderful grilled cheese. Glad I enjoyed it then because this morning has been a different story. New spots, GI distress, gas...you all know the routine. So clearly it must be the bread right? I know that lots of you have several other food intollerances as well and I"m wondering if I"m developing others too. But are the symptoms of other food problems the same as those of a glutening? The only thing my husband and I can come up with in the ingredient list would be yeast. I"ve had all of the other flours used in the bread without consequence. I am quite litterally at the end of my rope here and I'm getting to the point where I"m terrified to try anything different or new. I'm not sure if the DH is popping up new spots from the last bad flare a few weeks ago or if its related to this. I asked my dermatologist if he had any idea on how delayed a flare could be or not be and get this he encouraged me to "cheat" on my diet and then keep a journal. Why oh why can the medical community not get it....and why aren't they doing a better job of educating themselves? With current statistics suggusting 1 in 135 people having celiac its not like there is just a handful of us out there!! Sorry for the rant all, but I'm just feeling incredibly frustrated right now and I'm really tired of something so simple as eating being such a chore. Mostly....today I'm just tired of not being "normal" and healthy.


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



Celiac.com Sponsor (A8-M):



ArtGirl Enthusiast

I'm so sorry you've had to got through all this. Hope you get to feeling better soon.

Almost all my food-allergy related symptoms are GI in nature (gas, cramps and D). Gluten causes the most severe symptoms, then corn, then everything else. I've yet to get a real handle on what causes what exactly, as I do have some other minor symptoms such as runny nose, mild headache and itchy skin.

Is this bread a loaf you bought at the meeting? If it is, I'd throw it away. You'd probably be safe making your own bread from the same ingredients you purchase separately. However, iff it IS yeast that's causing the problem, you could do a challenge with just yeast to either rule it out or confirm your suspicions.

Hang in there. Remember, this journey has its hills and valleys - you just have to keep on walking to get out of the valley and back up on the hill. And, yes, it's a bummer to have to be thinking about one's body and food and all that. When I get down about this (which I have been these last few days) I tell myself that although these food intolerances and allergies are a great inconvience, there are certainly other diseases that would be far worse. (It helps sometimes to put this into perspective - but not always <_< .)

Guhlia Rising Star

I really don't have anything useful to add. I just wanted to say that I hope you're feeling better soon. I agree with Artgirl, I'd get rid of the bread. I wouldn't necessarily dismiss the manufacturer though. Perhaps you could call them to find out if their bread is made in a dedicated facility.

L.A. Contributor

I understand your frustration. I have had reactions to products that are gluten free and left wondering was it the new gluten free product I just tried or did I get glutened in an other way I was unaware of. I find I eat the same "safe" things over and over and am very hesitant to try anything new for fear of getting sick--makes one rather paranoid doesn't it. Big Hug. :)

Green12 Enthusiast
But are the symptoms of other food problems the same as those of a glutening?

Many people on this board, including me, report having the same symptoms of a glutening when eating other foods they are intolerant to- so that could be a possibility.

I don't know anything about DH, so I'm not sure if it can appear with other food intolerances, outside of gluten?

Since you reacted twice to the bread, I would stay clear of it.

Hope you feel better :)

Guest cassidy

I know you said the bread is gluten-free, but is it produced in a facility that contains gluten? In the beginning I thought people were crazy for worrying about this until I got glutened by gluten-free products that had cc issues from being produced on the same lines. We have a local bread company but I checked and they just wash everything down between gluten foods and gluten-free foods. I won't try anything because I'm afraid I'm going to get sick.

I realize that other intolerances may cause problems, and I don't have dh, but I have never heard of dh symptoms from anything other than gluten. I had never heard of them until I found out about celiac and I would like that if people got dh from peanuts or soy or something, that they would be more common and in the news. I don't have any knowledge on this, it is just my opinion.

Hope you feel better and figure it out. What type of bread was it? Maybe someone has had an experience with them.

mamaw Community Regular

I hope you are feeling better & I agree the mediacl doctors need to get up tp speed with this issue.It's bad enough when family & friends feel you may have went over the edge but it just kills me when a doctor has no clue.

Also it could have been a combo of flours & such. I sometimes can eat a certain food with no problems then next time I eat the same thing with more things added with it --- all of a sudden I'm down & out.Remember to some have issues with rice...my sister who is not gluten-free eats rice or chicken she instantly starts sneezing her head off. We alway know when she eats it!!!

hope things get better

mamaw


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



Celiac.com Sponsor (A8-M):



almostnrn Explorer

Thanks to all of you for commenting. The bread is now in the trash :) . I spoke with the gentleman who started the company and it is indeed a dedicated facility and guaranteed gluten-free. He was a retired baker and his grandson was diagnosed with celiac. The family was concerned because he wouldn't eat any of the current breads out there so they started making their own. What a shame this is happening to me because man is it good!

I think on the topic of other food allergies/sensitivities I have been in denial. I guess I can't imagine eliminating even more food, but unfortunately that is most likely what is going on. The 2 big differences I've noticed with this last reaction are...no brain fog and no headache. I've also started to develop a rash that is definately not DH. I will be calling to schedule an appt. with my MD to look at the possibility of testing for other food allergies. Since we are a military family that could take a little bit so I will try to keep track on my own as well. There were some other symptoms mentioned as well like a stuffy nose, etc. which I can relate. So the search will continue... Geez, with all of my limitations I'd expect to be in a much smaller size by now. Guess as long as I can still eat snickers bars and Graters ice cream that won't be an issue! :D

almostnrn Explorer
When I get down about this (which I have been these last few days) I tell myself that although these food intolerances and allergies are a great inconvience, there are certainly other diseases that would be far worse. (It helps sometimes to put this into perspective - but not always <_< .)

You are soooo right about that. I lost my mom this year to cancer. She was way too young and too wonderful to go through what she did. When she was still alive it was unbelieveably easy to keep my "illness" in perspective. Although, we used to laugh all the time that she could eat any and everything she wanted and wouldn't and I wanted to do that but couldn't. Isn't it funny how that works out sometimes. Anyways, thank you for that gentle reminder.

daffadilly Apprentice

Dear Almost,

One word: cross contamination, (okay it was two) if it was not at the bakery it was in one or more of the gluten-free grains that they used. If it is the same grain that you use without a problem it could be the supplier of the grain, maybe ground on different equipment etc. I do not have DH, but I get glutened by most of the gluten-free stuff, so I just do not eat it. I also get glutened by Almond Flour from a certain common brand. I need to grind my own, because I can eat almonds all day with no problems.

I keep a dish of almonds and walnuts sitting out in the kitchen at the office, yesterday I forgot & reached for ONE walnut half, ate it, then got a severe stomach cramp, & yep a little bit later it was a trip to the bathroom. I had forgotten that I cannot eat out of that dish of nuts, because the guys in the office eat toast etc, & then scoop out the walnuts or almonds with their wheaty hands. With me gluten is like the peanut allergy - there is no amount that I do not react to.

Also, did he start that bakery with spanking brand new pans and equipment, or get used stuff? I would guess used stuff since he was already a baker and probably had the equipment or knew someone that did.

kbtoyssni Contributor

If it is the yeast that's a problem, it might not be unusual that you're reacting to it now when you didn't before. Before your body was so overloaded from all the gluten it probably didn't have much left to fight the yeast but now that it's healed the yeast is starting to become the "dominant" food intolerance.

I sometimes get random symptoms, too. I have a lot of trouble tracing them and most of the time I am 99.999% sure it has nothing to do with gluten. I try to find a pattern, but I just can't. Sometimes I wonder if it's quantities of food that I eat. Maybe I only react if I eat a certain amount. Or I only react when my immune system is already stressed out from illness.

almostnrn Explorer

Wonderful information indeed!! I guess the farther I get into my gluten free journey the more I realize I have so much to learn. This message board has been an invaluable resource for me, not just for learning new things like recipes, good products to use and such but the sheer knowledge everyone on here has about celiac and the gluten-free lifestyle. CC is an issue that I am just really starting to get a grasp on. Thanks again to all, your imput has not only been very informative but uplifting in a moment I was feeling so down.

susan in colorado Newbie

OK...I have been gluten-free since April this year and have felt great...then today I went hog wild...so far I have had a big muffin from the convenience store...a halloween cupcake and a kit-kat bar...what happened to me...I woke up depressed today and the only thing I could think of is I WANT FOOD, esp food I can't have.

almostnrn Explorer
OK...I have been gluten-free since April this year and have felt great...then today I went hog wild...so far I have had a big muffin from the convenience store...a halloween cupcake and a kit-kat bar...what happened to me...I woke up depressed today and the only thing I could think of is I WANT FOOD, esp food I can't have.

How are you feeling? I'm hoping you will continue to be ok and not have too serious of a reaction. I did this once or twice shortly after I started the gluten-free diet but have not done so intentionally since my EGD this past summer when they made me eat the stuff. I think quitting a gluten filled diet can be as difficult for some as quitting smoking. Not to mention the fact that a gluten-free diet can certainly be more time consuming to prepare, that alone has been the source of many meltdowns for me. I hope you don't mind if I give you a tip....I try to keep at least 1 mix in the house. Sometimes its for gluten-free cookies, brownies, muffins, etc. That way when I wake up in a mood there is an easy solution in sight. I know its a lot easier said than done sometimes. Oh one more thing...I have tried to mentally change my idea of things I can't have to gluten-free foods that I could eat but shouldn't like a Snickers or Ben and Jerry ice cream. That way I can still feel as if I have "indulged" without falling off the wagon. I hope this helps, and like I said before I hope you feel ok!!!

Aerin328 Apprentice

You said you had grilled cheese before you got sick... perhaps it is actually casein intolerance? From what I understand a lot of celiacs who are have immune reactions to gluten also have reactions to casein (the protein in dairy products). In fact Enterolab tests casein automatically when you order the celiac panel. Just a thought!

Christian

CMCM Rising Star

Christian is right about the casein intolerance.....I always thought I was lactose intolerant (that's a sensitivity to milk SUGAR), and I probably am, but I found out thru Enterolab testing that I am also casein intolerant...casein is the milk protein. I actually think casein and/or lactose in dairy gives me more problems than does the gluten. Or the two go hand in hand and pack a double whammy. Also, allergies/sensitivities/intolerances don't usually occur in isolation. If you have a system that is intolerant to one thing, the likelihood is great that there are a whole list of things you don't do well with.

An allergist once told me that for virtually ANY food it's best to rotate eating it....i.e. if you have a particular food one day, wait about 4 days before you eat it again. I have seen with myself that continually eating something can have a cumulative effect. The 4-day window between eating something again seems to help a lot in preventing reactions.

There are just so many reactive foods out there....probably less variety is better for you, too. Find out what never bothers you and make those things central to your diet. For other things, try them on an occasional basis but never day after day.

daffadilly Apprentice

Almost, that is what I do about eating something that I really should not, I of course would never put a crumb of gluten near my face but now a candy bar or better yet, I made myself a huge pan of gluten free dairy free fudge, now that stuff was baddddddd in such a good chocolatey way.

I also would never be without a bag of Gluten free Pantry brownies, not that I ever eat them, but they are in the pantry if I want to or if I need to bake a gluten-free treat for some of my friends.

another badish treat for me is a fried sweet potato with an onion - they fry up just like regular potatoes (which I am allergic to). At least I use extra light olive oil to fry in.

So I would second what Almost does if you feel like being bad and cheating better to cheat on something that is allowed like a banana split, ice cream & chocolate syrup, candy bars, or whatever is your comfort food treat.

almostnrn Explorer

Christian and CMCM, thanks for the heads up on Casien. I'm wondering if that is something I should look into even though I have never had any problems (as far as noticeable affects) with cheese and use it fairly frequently. I will read up on it for sure though!

jukie Rookie

I also thought I was tolerating cheese but eliminated all dairy after testing positive for casein. Then one day I forgot to wash my hands after making a gluten-free pizza for DS and found out the hard way just how much of a problem cheese really was for me...from an accidental cross contamination :blink: It's definitely worth considering the possibility. Hope you're feeling better soon!

almostnrn Explorer

HOw do I go about getting tested for that? Just my family doc?

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,955
    • Most Online (within 30 mins)
      7,748

    Mabelie
    Newest Member
    Mabelie
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.