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

"seizure Like" After Eating Contaminated Foods


Bexxa

Recommended Posts

Bexxa Rookie

Prior (1 week) to arriving at college I discovered I was gluten intolerant. I had been avoiding gluten and had improved greatly when suddenly my symptoms started to re-emerge. I found xanthan gum made me immediate feel like I was going to pass out so I started avoiding that. I believe I am also rice intolerant as I have been eating a diet heavy in gluten-free foods with rice flour. I eliminated - with great difficulty - rice products from my diet and have been going great (reduction in rash, acne, nosebleeds, etc) However, I have found that Corn Chex causes major issues. I did a quick search and found that Chex seems to be interacting with others as well. That brings me to today, since I was going along fine when I had this bowl of Chex you can imagine the shock that my body went through. I had a "clean slate" so I know that I was functioning along fine and then suddenly it's as if I ran into a brick wall. An overall strange feeling, incredible fatigue, just knew something wasn't right.

It's happened only a few times but I've had these "seizure like" episodes after eating foods that were contaminated with gluten. Basically I will find myself, like now, at 9:40PM and wonder where the rest of the day went (reference: I ate the chex somewhere after 10:40AM). I call them seizure like because my past actual seizures, from many years ago, were where I would just space out, the difference is that back then I wouldn't be able to talk, I would slump in my chair or to the ground. Now, obviously, I didn't do that. I continued on my day. It was as if I was in a haze but unable to remember clearly anything that happened. I haven't had seizures in years though. Oh, and I have no idea if it's related but, today I noticed flashes of bright little purple dots in my vision.

Any advice on this?

Thank you!


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



Celiac.com Sponsor (A8-M):



shadowicewolf Proficient

Generally speaking, it is adised to avoid all processed foods after diagnosis, then add them back in for this reason.You sure that your siezures haven't come back?

pricklypear1971 Community Regular

Do you have a corn issue? Xanthan gum is usually corn derived, Corn Chex.....

Frequently, when gluten is removed we expose other intolerances that have been lurking under the gluten umbrella.

There is a study that's been posted on this board about a percentage of Celiacs that are also sensitive to corn.

Pegleg84 Collaborator

First of all, Welcome to the forum. Hope you can find the answers and support you need.

How long have you been gluten free? A lot of us, after doing quite well for a while, will have other problems pop up out of nowhere, like PricklyPear said, either because the reaction to gluten was masking them, or our bodies just decide they don't like that food anymore.

If you have an intolerance to rice, then its quite likely you could have a problem with corn too. I'd cut it out for a while and see how you do (I don't think I can even get Corn Chex here in Canadaland...)

Also, I know what you mean about going totally out of it all day. I get really braindead and lethargic for a few hours, and while I usually don't start seeing spots, my vision often gets fuzzy. I hope you're seizures aren't coming back, but neurological symptoms are common.

Hope you can figure out what's bothering you.

Cheers

Peg

anti-soprano Apprentice

Prior (1 week) to arriving at college I discovered I was gluten intolerant. I had been avoiding gluten and had improved greatly when suddenly my symptoms started to re-emerge. I found xanthan gum made me immediate feel like I was going to pass out so I started avoiding that. I believe I am also rice intolerant as I have been eating a diet heavy in gluten-free foods with rice flour. I eliminated - with great difficulty - rice products from my diet and have been going great (reduction in rash, acne, nosebleeds, etc) However, I have found that Corn Chex causes major issues. I did a quick search and found that Chex seems to be interacting with others as well. That brings me to today, since I was going along fine when I had this bowl of Chex you can imagine the shock that my body went through. I had a "clean slate" so I know that I was functioning along fine and then suddenly it's as if I ran into a brick wall. An overall strange feeling, incredible fatigue, just knew something wasn't right.

It's happened only a few times but I've had these "seizure like" episodes after eating foods that were contaminated with gluten. Basically I will find myself, like now, at 9:40PM and wonder where the rest of the day went (reference: I ate the chex somewhere after 10:40AM). I call them seizure like because my past actual seizures, from many years ago, were where I would just space out, the difference is that back then I wouldn't be able to talk, I would slump in my chair or to the ground. Now, obviously, I didn't do that. I continued on my day. It was as if I was in a haze but unable to remember clearly anything that happened. I haven't had seizures in years though. Oh, and I have no idea if it's related but, today I noticed flashes of bright little purple dots in my vision.

Any advice on this?

Thank you!

I have a friend that had seizures as a child and recently had another. After many tests, the docs told her that it was due to a Vitamin B (I forgot which one) deficiency. After finding that she has another couple major Vitamin deficiencies, she is having an endoscopy this week to see if the malabsorption is being caused by celiac.

Memory loss- even if you're functioning through it- is nothing to mess around with. If you were my family member, I would make sure you saw a dr. as soon as possible to rule out things that could be unrelated to celiac.

nvsmom Community Regular

Yikes. I would talk to a doctor about that too. :(

I have low blood pressure and have had problems with fainting in the past. Whe my BP gets very low I see shapes and sharks when I'm near fainting; time does odd things then. If you have low BP, an intolerance could mess with you...

The visual distortions sound like a migraine aura. Is that a possibility?

Take care!

Gemini Experienced

Prior (1 week) to arriving at college I discovered I was gluten intolerant. I had been avoiding gluten and had improved greatly when suddenly my symptoms started to re-emerge. I found xanthan gum made me immediate feel like I was going to pass out so I started avoiding that. I believe I am also rice intolerant as I have been eating a diet heavy in gluten-free foods with rice flour. I eliminated - with great difficulty - rice products from my diet and have been going great (reduction in rash, acne, nosebleeds, etc) However, I have found that Corn Chex causes major issues. I did a quick search and found that Chex seems to be interacting with others as well. That brings me to today, since I was going along fine when I had this bowl of Chex you can imagine the shock that my body went through. I had a "clean slate" so I know that I was functioning along fine and then suddenly it's as if I ran into a brick wall. An overall strange feeling, incredible fatigue, just knew something wasn't right.

It's happened only a few times but I've had these "seizure like" episodes after eating foods that were contaminated with gluten. Basically I will find myself, like now, at 9:40PM and wonder where the rest of the day went (reference: I ate the chex somewhere after 10:40AM). I call them seizure like because my past actual seizures, from many years ago, were where I would just space out, the difference is that back then I wouldn't be able to talk, I would slump in my chair or to the ground. Now, obviously, I didn't do that. I continued on my day. It was as if I was in a haze but unable to remember clearly anything that happened. I haven't had seizures in years though. Oh, and I have no idea if it's related but, today I noticed flashes of bright little purple dots in my vision.

Any advice on this?

Thank you!

I'm gonna go out on a limb here.....I think if you have had seizures in the past and you are having such extreme "seizure-like" episodes, it might be prudent to go to a doctor and have yourself looked at. You may not be reacting to this food at all and have a really serious underlying condition.

I believe Chex cereals are manufactured in a dedicated facility so the odds of it being contaminated are pretty low. You may have an allergy to another ingredient but these are symptoms you should see a doctor for....pronto! Not everything is connected to gluten exposure.


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



Celiac.com Sponsor (A8-M):



Bexxa Rookie

Thanks for the replies everyone.

I'm still trying to navigate being gluten free (and whatever other intolerances may be lurking...). I think I will take your advice and cut out the corn, I've been dragging around lately in general (taking 3 alarms to get me out of bed, barely making it to class) but assumed it was a flu. I have also been consuming alot of corn pasta. However, I don't understand why these Chex would have caused such a strong reaction. Although, examining the overall eating structure, I ate the Chex in the morning versus normally eating the corn pasta at night - then obviously I might have slept the effects off. Interesting possibility.

I see a neurologist already because I have a history of traumatic brain injury and am being treated for migraines. I have never had a migraine aura that involved seeing dots, the only aura that I get is when I feel like I'm going to pass out. Soon after I'll have a migraine. And I've been on a medication that decreased the frequency of the migraines to such a degree that they are almost non-existant. I went from having them 5-6 days a week to having 10 within the past 3 months. I have a follow up appointment with my neurologist on the 28th which I was planning on mentioning this to him already. The seizures that I had in the past were, the doctors thought, a reaction to a medication. Now I'm on a literally a handful of meds to control mood and then the above mentioned migraine med - two are anticonvulsants so, this shouldn't even be happening (although I have been on one of the same anticonvulsants for years now so it might be the dreaded "pooping out"). Definitely will be addressing my concern with my neurologist.

I don't know if it's low BP. It's actually a possibility that I never thought of. When I was really ill and before I was diagnosed gluten intolerant, I went to the doctor and had low BP, I believe it was 94/68 or the diastolic around there. It definately was not the best BP to be walking around with. I don't feel dizzy but, if I'm reacting to the food my BP could be dropping. Although, according to the ER doc, I was dehydrated which was causing the low BP. So many possible avenues. This is confusing sometimes!

Anyways, thanks again for the replies everyone!

shadowicewolf Proficient

Is it possible your meds aren't gluten free?

Bexxa Rookie

Oh my gosh, that is so obvious I can't believe I didn't think of that.

The only problem is that I can't find any information about gluten-containing drugs. Invega has absolutly no information on it. And then I take generics for all the rest, the brand names are safe but there's no information on the generics. I'm going to change multivitamins as I found that it's not guaranteed gluten-free.

Wow. So obvious can't believe I didn't think of this!

frieze Community Regular

Seizures are not unknown in celiac disease. Maybe what is happening is that you are OVER medicated now, being gluten free.

pricklypear1971 Community Regular

Seizures are not unknown in celiac disease. Maybe what is happening is that you are OVER medicated now, being gluten free.

Excellent point!

Have you checked this list? Open Original Shared Link

gleegan Rookie

Hi,

I haven't experienced anything like a seizure when exposed to gluten. However, I do sometimes have this very weird thing where I feel like my brain is tingling. It's hard to describe in any other way. It's a disturbing feeling and it doesn't go on for too long. It took me a while to connect to gluten, but now it's one way that I know if I've been cross contaminated. Good luck with feeling better. It's a hard road sometimes and I know it can be frustrating.

Take care,

Kirstin

mushroom Proficient

My story is anecdotal only, about my brother. I come from a family of gluten intolerants; it wasn't clear at the time we were all living together, but in retrospect it all fits together. My brother had major symptoms after drinking beer with the boys. He also developed a seizure disorder in his 40's. It was really neither petit mal nor grand mal; He most often would either be sitting or at the table and suddenly this blank look would come into his eyes and he would cease interacting and just sit with no animation in his face. After a few seconds his face would reanimate and he would carry on like nothing had happened. No medication made any difference to this condition. It is sad. really, because a more violent seizure which was not witnessed caused him to hit his head in a doorway and led to complications from which he died. I remain convinced that it was a gluten response.

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
      131,953
    • Most Online (within 30 mins)
      7,748

    ramonaja
    Newest Member
    ramonaja
    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.