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?


krystal

Recommended Posts

krystal Rookie

I have been battling this gluten sensitivity thing for a while (actually, battling myself about it). I have gone through a really stressful time lately and have not paid ANY attention to what I am eating. Sometimes it takes a while for me to feel sick enough to force me to do something about my diet - I have evening symptoms mostly, and some of the daytime symptoms I have aren't bad enough that I really can't function with them. The migraines haven't returned this time around (yet).

But I have a question to ask of people who have seizures. I know how weird this is going to sound, but many times I have dreams that "explainn away" things going on in my real life. Often if I'm nauseous from eating something I shouldn't, I will have dreams about me vomiting. I had a dream once that my arm was trapped in a car when in fact it was just being laid on by my (very large) husband. I incorporate conversations by people around me into my dreams as well. The thing is, these "outside" sensations have a different quality to them in my dreams - I recognize them in my dream as being "not of the dream".

OK, now that you REALLY think I'm NUTS....

I am home by myself while DH is vacationing. My dream involved me being in a bed that was violently being shaken, to the point where my face, mouth, hands and feet were uncontrollable in my dream. It had that "not of the dream" feel, and in my dream I could HEAR the shaking as well. When I woke from the dream (at 4AM), I felt like I had been wrung out, I was full of sweat and was very nauseous and had trouble moving. )

I am wondering if this was possibly a seizure? It scared the crap out of me - I have never felt that way upon waking AT ALL. For the most part, I am an active healthy person, and to feel so debilitated upon waking is unprecedented. I had no other symptoms, though aside from what I mentioned. No sounds, smells, incontinence, etc. No damage inside my mouth or tongue. I would love nothing more than for someone who has firsthand knowledge of a seizure to say "No way, because you didn't have XXXX".

I have had weeklong episodes where my lips have gone numb, but that is about it for truly funky symptoms I believe are related to my diet. (I have nonconfirmed gluten issues as well as possible other food issues that I still have not gotten a handle on.

Thanks for your input.


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



Celiac.com Sponsor (A8-M):



mushroom Proficient

Since there were no witnesses, it is very hard to say whether or not it was some kind of seizure, though it sure sounds suspiscious. Do you have any other neurologic symptoms other than numb lips? My brother used to have mini seizures which I am now convinced were gluten related; developed them in his late 30's, had no residuals afterwards. Had other gluten suspiscious symptoms in retrospect.

I do understand about the dreaming thing. I always know when I should go to the loo at night because it gets incorporated into my dreams and I endlessly search for a loo. So, no, I don't think you're nuts, but I would think you were if you didn't get serious about keeping that nasty gluten away from your body

ravenwoodglass Mentor

I would mention this to your doctor. There is testing they can do, an EEG, during which they can try to bring on seizure activity. Even more important though is that you get strict with your diet.

TotalKnowledge Apprentice

Part of what has been happening to my sister is seizures. More over sticking with a gluten free diet has helped me with my restless leg syndrome, insomnia, and the general thrashing I used to do at night.

The benefits of maintaining a gluten free diet go way beyond any intestinal discomfort. If you know you have it I would stick to the diet.

gigantor98 Apprentice

I know all about strange dreams. But I can not say forsure that it was a siezure you had or not. I to suffer from siezures. I only started suffering from them that I was aware of Last June. These come around my ovulation cycle. Usually 2 within a 24 hour period and they last for 25 min. a piece leaving me feeling physically unplugged for 24 hours after the first attack. Than I am back to normal. These where not like anything any health provider around here had seen before. My hands and mouth draw up like a stroke than I can not feel anything from my knees down to my feet. A migrane usually triggers these with a intense knife stabbing pain behind the right eye. But I did have a siezure one time during a nap. I was not suffering from a headache than and my dream was of some one heavy setting on me. I woke up to find myself in that crazy postion and could not release my hands or mouth. I knew after several mins. that this was a siezure. Once my docs. found out that I had this attack during my sleep thats when they concluded it must be a siezure. I have taken several eeg tests to all come up neg. for this activity so in stead of doing a week long eeg test they assumed that was what was happening before being diagnosed with celiac disease. I am on siezure meds for 7 days out of the month and it lessons the side effects of these siezures. Does not stop the migranes. Since my celiac disease diagnoses in Nov of 08 last month was the best month I had had with these attacks. I am going to give myself a little more time before I update my docs on my progress with the meds and the diet before I ask them to try and release me off of the meds. I want at least 3 good months without these eposiodes before I give up the meds. I may never be able to but I am not sure. My docs just tell me I am an experiment.

It would be a good idea to keep a jounral of your daily activities as well as what you eat and if you are female your period cylce. I have just seen my endo and he is concerned with my parathyroid glands. He thinks celiac disease has destroyed at least one and hyperparathyroidism is known to cause seizures as well. I will let you know that I am fully aware of what is going on around me when these attacks happen I just can't control my body and it hurts. If I did not keep a journal of my activities they would have never tested me for celiac disease and I would still be on the anti depressent meds that left me in the corner of my living room drooling on myself while I was trying to take care of my 3 kid under the age of 7. My docs wanted to list me as paniac attacks. I am still upset at how easy our medical community can right you off as crazy and others around them believe them and their recommedations without listening to the patient. Having a siezure in my sleep was the only blessing that happened during this scary time in my life b/c it finally woke them up to listen to me.

May God Bless you and answer your prayers to your health problems. Jesus took this to the cross it is not yours to burden alone. Get off of gluten as soon as you can. If it is affecting your nuerologically than your small intestines is down to aobut a 1/4th of a gas tank full villi hair. At least that is how they described it to me. Once your nuero system is checking out than you are in some serious trouble but you can heal. YOU CAN HEAL. May God help you with your stress and burdens to allow you time to affectively stick to this diet.

DreamWalker Rookie

Definitely mention it to your doctor & get an EEG.

Right before I slid downhill, (losing 20+ lbs on an already bordering underweight frame + more GI issues) I *thought* I was having seizures. However, I never went to the doctor for them as there were no witnesses. A few times a week, I'd be lying on the couch, then suddenly find myself on the floor with my concept of time completely lost. And the next day, I'd have bruises up & and down the backs of my arms & legs. Anyhow, I had to move across the country so I continued putting it off, then the GI issues became more problematic & I was afraid of mentioning the episodes to any doctors lest they think I was crazy. (I was more afraid of the stomach pain continuing.) I'm not sure how many I had (or whether they were even seizures)... at least three... the rest are too fuzzy.

Although, for years before my gluten-free diet, I'd randomly fall asleep (in cars, during a movie, in the middle of a conversation). I vaguely recall that and probably wouldn't mention it had numerous friends never pointed it out. That, and I'd often just fall "out of it" my friends told me it was like I was in a trance. . .I just remember feeling sleepy(?) If I'm recalling anything at all.

All of it cleared up when I was diagnosed with Celiacs & went gluten-free though, which is why I never mentioned it....

I can't comment about the dreaming much. I remember half-sleepwalking to the bathroom numerous times at night. (D.) It felt like a dream and my housemate (who was always awake during the wee hours) said I'd pass by countless times when I'd only recall one or two.

Hope you find the answer.. :\

Mother of Jibril Enthusiast

Another idea for you to consider... anaphylaxis. That could definitely explain the "wrung out" feeling. Histamine levels naturally peak around 2am. I have idiopathic anaphylaxis (it's not food, medication, exercise, cold/heat, insects, etc... the classic allergy triggers) and my last two attacks started in the middle of the night. The main treatment is taking antihistamines on a daily basis... both H1 (zyrtec, claritin, allovert, benadryl, etc...) and H2 (pepcid, zantac, tagamet, etc...).

Incidentally, the brain has a lot of histamine receptors, so some people with IA also have problems with seizures. It's definitely something to ask a doctor about. My guess is that you'll need to be persistent to get answers :(

ps - I often get that "is this a dream?" feeling... and my sister has an unexplained seizure disorder


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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,963
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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.