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Sleep Problem

Lister

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Lister Rising Star
Lister
Posted

everytime i go to try to sleep once i get almost to the point of sleep i end up flinging up out of bed gasping for air, is this related to celiac or is it just me beeing stupid. People have told me that its because i am worrying and making my body panic. But im completly relaxed lay my head down then next thing i know i cant breath its really frightning

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Guhlia Rising Star
Guhlia
Posted

That sounds like sleep apnea which can cause a whole host of other health problems. You should definitely mention this to your doctor and push him to pursue sleep studies.

GravStars Contributor
GravStars
Posted
everytime i go to try to sleep once i get almost to the point of sleep i end up flinging up out of bed gasping for air, is this related to celiac or is it just me beeing stupid. People have told me that its because i am worrying and making my body panic. But im completly relaxed lay my head down then next thing i know i cant breath its really frightning

it COULD be anxiety/worry/panic. i have a thing sometimes, not so much gasping for air, as a quick inhalation that jerks me awake, right as i'm about to drift off. but if it's sleep apnea, that would be different i think (not sure what apnea is caused by). consciously relaxing and breathing with your abdomen (deep belly breaths) before falling asleep might help.

Nancym Enthusiast
Nancym
Posted

Sounds like sleep apnea to me. That can be deadly at worst and it can seriously compromise your health at best. See a doctor!

flagbabyds Collaborator
flagbabyds
Posted

That does sound like sleep apnea, i would do that before i had my jaw surgery, it can be deadly, so you should go to a sleep doctor.

plantime Contributor
plantime
Posted

Does it happen when you sleep only on your back, only on your sides, or all the time? I have apnea if I sleep on my back, but not if I am on my sides. Try changing your position. However, I really recommend seeing your doctor about it.

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    • rei.b
      High DGP-A with normal IGA

      By rei.b · Posted

      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • knitty kitty
      High DGP-A with normal IGA

      By knitty kitty · Posted

      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      High DGP-A with normal IGA

      By rei.b · Posted

      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
    • knitty kitty
      High DGP-A with normal IGA

      By knitty kitty · Posted

      Food and environmental allergies involve IgE antibodies.  IgE antibodies provoke histamine release from mast cells.   Celiac disease is not always visible to the naked eye during endoscopy.  Much of the damage is microscopic and patchy or out of reach of the scope.  Did they take any biopsies of your small intestine for a pathologist to examine?  Were you given a Marsh score? Why do you say you "don't have intestinal damage to correlate with lifelong undiagnosed celiac disease"?   Just curious.  
    • rei.b
      High DGP-A with normal IGA

      By rei.b · Posted

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