Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Yawn To Breathe


Happyw5

Recommended Posts

Happyw5 Explorer

For the last few days I can't seem to get a deep breath unless I yawn...It is so exhausting! Has anyone else had problems like this? Mine seems to come and go every month. I don't know if maybe its hormonal-anxiety-or food. I have been gluten free for about 2 months...I am out of breath just coming up steps and even sitting. I sleep ok so maybe it is in my head!


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



Celiac.com Sponsor (A8-M):



gemmaarm Newbie

Hi, I'm the exact same, have been like this for a week. I think it must be a vitamin deficiency such as b12 that's causing mine. I would get your blood checked.

Looking for answers Contributor

Yes, I used to go through spells like this that would drive me mad. I haven't had them since I got on a good supplement program, so my guess it's what the previous poster suggestion (B 12) or iron. I was low in both.

glutenfr3309 Rookie

that's interesting. i think this has happened to me, except when i would breathe in deeply it would hurt in my ribs. i'm wondering if when this happens to me if it's a glutening symptom. i'm 10 months gluten-free but am still trying to figure out my sensitivity and what my symptoms are if i've accidentally been glutened.

  • 3 years later...
WilliamCDaniels Newbie

For the last few days I can't seem to get a deep breath unless I yawn...It is so exhausting! Has anyone else had problems like this? Mine seems to come and go every month. I don't know if maybe its hormonal-anxiety-or food. I have been gluten free for about 2 months...I am out of breath just coming up steps and even sitting. I sleep ok so maybe it is in my head!

I have had this same problem for years and I finally found out what was going on. I (and I imagine everyone in this discussion) have something called "Hyperventilation Syndrome." Basically, over the years, we have learned to stop breathing deep in our bellies, as all newborns do, and learned to breathe in our chest's. Most of the time this is completely unconscious. Anxiety CAN exacerbate this, but most likely would go completely unnoticed. 
 
Before you say "Its not anxiety! I've tried every antidepressant and gotten all of the tests and nothing came back!" I would tell you that I did the same thing, and it all came back clear. Not being able to breathe and not knowing why is probably one of the most terrifying feelings there is and there have been many times where I have just wanted to take a swan dive over a high bridge. But believe me, there is a solution. First of all, realize that you absoloutely are getting enough air. That is not the problem. You will not die from this. The reason you feel like you are constantly out of breathe is because you are expelling too much carbon dioxide. Carbon dioxide is essential for maintaining oxygen levels; so when you don't have enought CO2, your brain realizes this, and attempts to take in more air, giving you that "air hunger" feeling. All you have to do to cure yourself of this is to relearn how to do belly-breathing. Google "Buteyko Method". It is excellent. Also check out the book Hyperventilation Syndrome by Dinah Bradley. Believe me when I tell you that it works and once you learn how to do this you will be fine. Sorry to everyone who is going through this horrible feeling. When it was at its worst, I literally felt like I was suffocating. If you find yourself panicking, just remember - you're expelling too much CO2. The best way to fix this is to breathe "low and slow". Lie on your back and breathe deep into your belly, as slowly as you can. Your chest shouldn't move at all. At first, it will feel very incomfortable; this is because your brain still feels like it needs more air. But what you are doing is slowly restoring the CO2, which will in turn modulate your oxygen. As I am writing this it sounds like a bunch of mumbo jumbo, but believe me it works. If you can't trust some random dude posting on this forum, and who would blame you if you couldn't, then just google "Hyperventilation syndrome" and try the deep belly breathing. You should also go for brisk walks and ONLY breathe through your nose. Never your mouth. Every time you breathe through your mouth you are expelling more CO2 and thus receiving less oxygen. I hope this works. It did for me. 
GF Lover Rising Star

 

I have had this same problem for years and I finally found out what was going on. I (and I imagine everyone in this discussion) have something called "Hyperventilation Syndrome." Basically, over the years, we have learned to stop breathing deep in our bellies, as all newborns do, and learned to breathe in our chest's. Most of the time this is completely unconscious. Anxiety CAN exacerbate this, but most likely would go completely unnoticed. 
 
Before you say "Its not anxiety! I've tried every antidepressant and gotten all of the tests and nothing came back!" I would tell you that I did the same thing, and it all came back clear. Not being able to breathe and not knowing why is probably one of the most terrifying feelings there is and there have been many times where I have just wanted to take a swan dive over a high bridge. But believe me, there is a solution. First of all, realize that you absoloutely are getting enough air. That is not the problem. You will not die from this. The reason you feel like you are constantly out of breathe is because you are expelling too much carbon dioxide. Carbon dioxide is essential for maintaining oxygen levels; so when you don't have enought CO2, your brain realizes this, and attempts to take in more air, giving you that "air hunger" feeling. All you have to do to cure yourself of this is to relearn how to do belly-breathing. Google "Buteyko Method". It is excellent. Also check out the book Hyperventilation Syndrome by Dinah Bradley. Believe me when I tell you that it works and once you learn how to do this you will be fine. Sorry to everyone who is going through this horrible feeling. When it was at its worst, I literally felt like I was suffocating. If you find yourself panicking, just remember - you're expelling too much CO2. The best way to fix this is to breathe "low and slow". Lie on your back and breathe deep into your belly, as slowly as you can. Your chest shouldn't move at all. At first, it will feel very incomfortable; this is because your brain still feels like it needs more air. But what you are doing is slowly restoring the CO2, which will in turn modulate your oxygen. As I am writing this it sounds like a bunch of mumbo jumbo, but believe me it works. If you can't trust some random dude posting on this forum, and who would blame you if you couldn't, then just google "Hyperventilation syndrome" and try the deep belly breathing. You should also go for brisk walks and ONLY breathe through your nose. Never your mouth. Every time you breathe through your mouth you are expelling more CO2 and thus receiving less oxygen. I hope this works. It did for me. 

 

 

Just an FYI.  The Original Poster you quoted has not been active since January of 2011.  You may not get a response.  If you want to start a new discussion on the topic, feel free to do so.

 

Colleen

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,079
    • Most Online (within 30 mins)
      7,748

    Geraldine Selenne
    Newest Member
    Geraldine Selenne
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.6k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      @KRipple, thank you for the lab results from your husband's celiac disease blood antibody testing. The lab result you share would seem to be the tTG-IGA (Tissue Transglutaminase IGA) and the test result is in excess of 10x normal. This is significant as there is an increasing tendency for physicians to grant a celiac disease diagnosis on the basis of antibody testing alone when the scores on that particular test exceed 10x normal. This trend started in the UK during the COVID pandemic when there was tremendous pressure on the medical system over there and it has spread to the USA. The tTG-IGA is the centerpiece of celiac disease blood antibody testing. All this to say that some doctors would grant a celiac disease diagnosis on your husband's bloodwork alone and not feel a need to go forward with an endoscopy with biopsy. This is something you and your husband might wish to take up with his physicians. In view of his many health issues it might be wise to avoid any further damage to his small bowel lining by the continuing consumption of gluten and also to allow healing of such to progress. The lining of the small bowel is the place where essentially all of our nutrition is absorbed. This is why celiac disease when it is not addressed with a gluten free diet for many years typically results in additional health problems that are tied to nutritional deficiencies. The millions and millions of tiny finger-like projections that make up the nutrient absorbing surface of the small bowel lining are worn down by the constant inflammation from gluten consumption. In celiac disease, the immune system has been tricked into labeling gluten as an invader. As these finger-like projections are worn down, the efficiency of nutrient absorption becomes more and more compromised. We call this villous atrophy.   
    • KRipple
      Thank you so much! And sorry for not responding sooner. I've been scouring the hospital records and can find nothing other than the following results (no lab info provided): Component Transglutaminase IgA   Normal Range: 0 - 15.0 U/mL >250.0 U/mL High   We live in Olympia, WA and I will be calling University of Washington Hospital - Roosevelt in Seattle first thing tomorrow. They seem to be the most knowledgeable about complex endocrine issues like APS 2 (and perhaps the dynamics of how APS 2 and Celiacs can affect each other). His diarrhea has not abated even without eating gluten, but that could be a presentation of either Celiac's or Addison's. So complicated. We don't have a date for endoscopy yet. I will let my husband know about resuming gluten.    Again, thank you so much for sharing your knowledge with me!
    • Jmartes71
      Ginger is my best friend, it helps alot with tummy issues..
    • aattana
      Hi Phosphone, did you ever figure out what elevated your DGP?  I am in the same boat. 
    • trents
      Scott makes a good point about the prednisone. It has a general suppressing effect on the immune system. Don't misunderstand me. In view of your husband's several autoimmune afflictions, it would seem to be an appropriate medication therapy but it will likely invalidate endoscopy/biopsy test results for celiac disease.
×
×
  • Create New...