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

Air Hunger?


susieg-1

Recommended Posts

susieg-1 Apprentice

I keep hearing members mention having air hunger and I am not sure what they mean. Can someone describe what this feels like? I recently had a pulmonary function test and was told my small airways are not working efficiently, but not why. Got an inhaler to help with shortness of breath, is this the same as air hunger? I am soooo confused!!! :huh:


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

I have air hunger associated with Lyme Disease.

It's like I cannot get a full breath of air. No matter what, I feel like I'm not bringing in enough air. It has made me hyperventilate until I learned to not panic and breath out more completely.

I was tested for asthma and it came back negative.

Mine went away with Lyme (and babesia) treatment.

MELINE Enthusiast

well I googled it and Wikipedia is describing it like this:

From Wikipedia, the free encyclopedia

Air hunger is the sensation of the urge to breathe. It is usually caused by the detection of high levels of carbon dioxide in the blood by sensors in the carotid sinus and is one of the body's homeostatic mechanisms to ensure proper oxygenation. Natural chemicals in the blood such as epinephrine (adrenaline) can also induce an urge to breathe by a separate pathway. Insufficient pulmonary minute ventilation, a sustained breath-hold, constriction of the alveoli of the lungs as in asthma or high ambient levels of carbon dioxide in the air breathed can cause air hunger resulting in a respiratory distress condition characterized by dyspnea, labored breathing or gasping. Air hunger can be very distressing and triggers strong reactions to restore breathing.

In mammals (with the notable exception of seals and some burrowing mammals), the breathing reflex is triggered by excess of carbon dioxide rather than lack of oxygen, so asphyxiation progresses in oxygen-deprived environments, such as storage vessels purged with nitrogen or helium balloons, without the victim experiencing air hunger.

I don't know if that is any help for you.....

Meline

susieg-1 Apprentice

:D

well I googled it and Wikipedia is describing it like this:

From Wikipedia, the free encyclopedia

Air hunger is the sensation of the urge to breathe. It is usually caused by the detection of high levels of carbon dioxide in the blood by sensors in the carotid sinus and is one of the body's homeostatic mechanisms to ensure proper oxygenation. Natural chemicals in the blood such as epinephrine (adrenaline) can also induce an urge to breathe by a separate pathway. Insufficient pulmonary minute ventilation, a sustained breath-hold, constriction of the alveoli of the lungs as in asthma or high ambient levels of carbon dioxide in the air breathed can cause air hunger resulting in a respiratory distress condition characterized by dyspnea, labored breathing or gasping. Air hunger can be very distressing and triggers strong reactions to restore breathing.

In mammals (with the notable exception of seals and some burrowing mammals), the breathing reflex is triggered by excess of carbon dioxide rather than lack of oxygen, so asphyxiation progresses in oxygen-deprived environments, such as storage vessels purged with nitrogen or helium balloons, without the victim experiencing air hunger.

I don't know if that is any help for you.....

Meline

Thank you both this does help me to understand the term

RiceGuy Collaborator

This discussion reminded me of a radio commercial I sometimes hear, about something called lymphangioleiomyomatosis (LAM). So I looked it up, and though I don't know if it applies at all, I figured I should at least post a link: Open Original Shared Link

The site seems to suggest only women experience this, but I haven't dug into it. I'm guessing it's unrelated, but maybe it'll help someone reading this thread anyway.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - wellthatsfun posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      nothing has changed

    2. - trents replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

    3. - Charlie1946 replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

    4. - Charlie1946 replied to Charlie1946's topic in Related Issues & Disorders
      48

      Severe severe mouth pain

    5. - Jmartes71 replied to Jmartes71's topic in Related Issues & Disorders
      3

      New issue

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,102
    • Most Online (within 30 mins)
      7,748

    Dawn74
    Newest Member
    Dawn74
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • wellthatsfun
      i have been strictly gluten free for 7 months. this includes avoiding anything that may contain gluten and making sure surfaces and appliances are clean. i am 18 years old in australia and my tTG-IgA results were 69U/mL, pretty low compared to most people's, for reference. i feel the exact same as before. sure, i was pretty much asymptomatic/silent. the worst i'd get was occasionally bad stools and pitting of the nails/brittle hair since early childhood - and i was diagnosed with low iron and vitamin d which checks out due to easy bruising and such. but those symptoms have remained. maybe i'm jumping the gun, sure. i know it can take years to fully heal. but being over half a year in, i feel that i should be, y'know, healing. i'm nearly at my wits end and wondering if i should have a piece of bread or something to see how i go - to see if i possibly have refractory? my mental health is declining as i feel myself wanting to bang my head against a damn wall out of frustration every day. cravings haven't gotten better. look, i love the stuff i still can have, like salads and such. OH! i haven't lost any weight, which is mind boggling considering i eat very healthily now! i've always been on the chubbier side which is atypical of coeliac. i just don't know what's going on with me. i try to remain hopeful but i'm just so sad all the time. thanks for reading  
    • trents
      @Charlie1946There is a PM (Personal Message) tool built into the forum website that allows you to send a private message to other forum users. Just hover over their name with your mouse cursor and the menu containing that tool will pop up. This is useful if you want to communicate with an individual without everyone else involved in the thread seeing it.  Are you realizing that in my PPI taper down recommendations in an earlier post above, I was responding not to your posts but to @Caligirl57? If you must use a PPI, I certainly would advise taking the lowest dose that is effective for you.  
    • Charlie1946
      Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless! Hi everyone, I'm still trying to figure out how to each message individually. I saw one with some information on sebaceous hyperplasia but now I can't find it. I appreciate you all so much for all your responses and advice! God bless!
    • Charlie1946
      @trents thank you! I have only been taking 20mg 1x a day. Maybe I need to increase it.
    • Jmartes71
      Nope its just me because they can eat wheat and when we use same pans I found out last year thanks to you guys and the autoimmune website im learning,we are not to share though clean, same with sponge. I just wish doctors understood. I am with new gi and new pcp but im falling apart because blood work is fabulous.Im so ANGERY.I have reached out to my local representative, in Stanislaus but its just weekly stuff.Im going to need to physical go down there.Any recommendations on what to say and do because this is absolutely ridiculous. If I didn't have my husband though we are really hurting with one income, I would absolutely be one of the homeless population. Thats alarming begging to be heard about a diagnosis that was given as an adult and dealing with this, medical needs to stick to patients regardless of switching insurance or doctor. 
×
×
  • 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.