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

Sinus issues related to celiac?


Mikeymike93

Recommended Posts

Mikeymike93 Explorer

Anybody else have sinus problems as a main symptom of celiac? I went off gluten for over a year due to a positive blood test. Prior to that I had a lot of unknown sinus inflammation (thought it was seasonal changing allergies etc). It has been under control but I went on a gluten containing diet for the last week to get another celiac test. I have felt ok which surprised me, but now I have noticed the sinus problems returning yesterday like I haven't felt in a long time. How common is sinus inflammation a main sympton of celiac? Or does it sound more like an intolerance? Problem is winter is hitting and I am not sure if that is causing it instead. 


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



Celiac.com Sponsor (A8-M):



trents Grand Master

There could be a connection, at least indirectly through inflammatory processes being increased in general while back on gluten. And, as you say, you may also be allergic to wheat.

With something like that its hard to say what the trigger is given the fact that the cold and flu season is upon us and the heating season as well. 

Are you experiencing sinus inflammation apart from a sinus infection? Have you considered using one of those baking soda/saline sinus rinsing systems or a neti pot? 

Mikeymike93 Explorer

Ya I definitely have all the remedies down pat including a prescription sinus spray. I guess I am so curious whether this is a celiac symptom alot of people get that is coming back. I guess I could always go off gluten and if it goes away, go back on it for a week and see if it comes back again. 

trents Grand Master

I have suffered with chronic, low grade sinus infections/inflammation much of my life. I was dx with celiac disease in my early 50s, about 18 years ago. It has been much better in the last several years but that coincided with retirement and less exposure to UR infections that was previously the case. I have permanent damage now to my sinus cavity mucosa. Whenever I get a CT scan done it shows the mucosa lining the right maxillary sinus cavity is abnormally thick, even when I am asymptomatic. There has been erosion in that cavity in places such that the partitions have been eaten through and there are now holes where there shouldn't be. Having said all that, only in the last several years  years (since retirement) have I been able to be consistently avoid gluten and now my villi are healed. I am much healthier now in general as a result. I used to get about three upper respiratory infections a year, now almost never. Some of that probably is due to less exposure to infections.

GFinDC Veteran

Hi MM,

I have hayfever.  Before I went gluten-free I had much worse hayfever symptoms than I do now.  I was buying antihistamines every week basically.  My allergy symptoms backed way off after going gluten-free.  They aren't completely gone, but are much less of a problem and not a constant issue.   So I think there is definitely a link, at least in my case.

DJFL77I Experienced

I went to the ENT Dr like 3 weeks ago..   he said I have some inflammation up there in the nose when he looked.. causing some bleeding / nasal drip to the back of my throat..  he said allergies..   But I'm pretty sure it was caused by Celiac as I've never had this before until Celiac symptoms started...  I first noticed it about a week and a half after symptoms started...

I always thought it was coming from my stomach as reflux..  but since using a nasal spray I saw some blood being flushed out from the nose sometimes.. so it was definitely from the nose...

or he said might be a mild sinus infection.. have to do a X ray to check that though if after 3 weeks of nasal spray it isn't gone..

Mikeymike93 Explorer

That sounds similar to my issues. I actually had sinus and lymph nodes issues for 2 yrs and saw all the docs I could and nobody could figure it out. It was until wyrs later I started having digestive issues which caused them to look for and find celiac. I have been better since so I am guessing they were all related. Idk. 


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



Celiac.com Sponsor (A8-M):



Kate333 Rising Star

I moved to California in 2014.  I haven't stopped sneezing, suffering burning eyelids, nasal congestion/post-nasal drip/dry and sore throat ever since.  I have those symptoms 24/7, no matter what kind or how many antihistamines I take.

I think the increasingly severe air pollution from fire smoke, constant road and housing construction (which churns dust/debris into the air) has a lot to do with my symptoms.  When I first moved here, it was rare to have fire smoke and "fire season"--UGH!!--lasted "only" a few days or a week.   Now, CA has devastatingly long-lasting fires/smoke (lasting almost half a year!! from early summer through October) where fire smoke/ash descends over every part of the state and covers my car like snow.  Honestly, the air is so filthy during fire season, it looks like Beijing in the summers pre-pandemic!🤮

My New Year's resolution is to get the hell out of here (and avoid the entire Western US, as other western states have sadly also turned into an inferno like CA) as soon as it's safe to travel again (post-pandemic).😉

Kate333 Rising Star
20 hours ago, trents said:

I have suffered with chronic, low grade sinus infections/inflammation much of my life. I was dx with celiac disease in my early 50s, about 18 years ago. It has been much better in the last several years but that coincided with retirement and less exposure to UR infections that was previously the case. I have permanent damage now to my sinus cavity mucosa. Whenever I get a CT scan done it shows the mucosa lining the right maxillary sinus cavity is abnormally thick, even when I am asymptomatic. There has been erosion in that cavity in places such that the partitions have been eaten through and there are now holes where there shouldn't be. Having said all that, only in the last several years  years (since retirement) have I been able to be consistently avoid gluten and now my villi are healed. I am much healthier now in general as a result. I used to get about three upper respiratory infections a year, now almost never. Some of that probably is due to less exposure to infections.

Hi trents.  Just curious, you said you were first diagnosed with celiac disease almost 20 years ago, long before retirement, so did you mean that you could not maintain a strict gluten-free diet while still working??   Were you eating out a lot back then?  And how long did it take you to heal your gut (and any other symtpoms) after you went on a STRICT gluten-free diet in retirement?

notme Experienced

you can develop allergies as you age.  my husband never had hayfever/sinus allergies until he hit 55.  then he walked around sniffling and wondering if he was coming down with a cold until i made him try claratin 1x/day.  now he takes one per day and he's fine.  one of our friends developed allergies at about the same age - the difference was he didn't treat it immediately (he had no idea) and he ended up in the emergency room because the allergies had compounded into a severe sinus infection that needed to be drained immediately and if i recall, he stayed in the hospital while they made sure the antibiotics were working.  like, it was too close to his brain.  now, he takes his zyrtek religiously.  

if i get glutened, one of my symptoms is a runny nose.  i also have allergies that are under control, normally, unless i get glutened then they ramp up.  i am also on flonase and nasalcrom.  

DJFL77I Experienced

you can't get into the brain from the nose

trents Grand Master
33 minutes ago, DJFL77I said:

you can't get into the brain from the nose

It's not common but it can happen: https://health.clevelandclinic.org/sinus-infections-that-dont-quit-when-you-should-worry/#:~:text=Also in rare cases%2C sinus,from sinusitis%2C” he says.

docaz Collaborator
9 hours ago, DJFL77I said:

you can't get into the brain from the nose

I wonder what makes you think that. Here is a cross-section view that shows the proximity of the nasal cavity to the brain https://www.discovermagazine.com/mind/is-the-human-olfactory-bulb-necessary.

The cranial nerve that is responsible for smelling (olfactory bulb) is actually a direct extension of the brain and is separated from the upper nasal cavity by a very thin layer of bone that is perforated and called cribriform plate through which the smell nerve endings protrude. In fact, certain brain tumors are accessed through the nose such as tumors of the pituitary gland. That said, I only disagree with the above statement but I certainly do not want to cause anybody to panic because it is extremely rare for an infection to spread to the brain from the nose and I do not think that people with celiac disease are more prone to such infections to spread to the brain. 

DJFL77I Experienced

can allergies make you dizzy

Pat Jackson Apprentice

I used to think it was normal to get 2-3 sinus infections a year, until I finally saw an allergist when I was in my 30's.  She got me taking antihistamine daily, and had me use a nasal rinse regularly.  Since then, the infections have been once a year in the fall when we close up the house, and my asthma is much better, but it took constant work on my part to avoid allergens and rinse my sinuses after being outside in the summer.  Now, 30 years later, I discovered about 9 months ago that I have celiac and probably have had it for many years.  This fall is the first year that I didn't get a sinus infection that usually turns into bronchitis.  Coincidence?  I don't know.  But I've been struggling for a few weeks now, thinking I'm getting gluten somehow, and the sinus problem is back. 

One gluten incident was traced to a new brand of vitamin that I foolishly didn't research first.  I won't make that mistake again.  Another occurred after using the family toaster for some gluten free toast.  I was surprised both times that such a small exposure could cause such a major reaction.  That was 2 weeks ago, and I'm still not back to normal, whatever that is.

docaz Collaborator
3 hours ago, DJFL77I said:

can allergies make you dizzy

Nasal allergies can absolutely make you dizzy. The organ that controls balance is inside the inner ear which is right next to the middle ear. There is a tube that goes from pharynx to the middle ear that equalizes the pressure between the middle ear and the pharynx. When you are on a plane and are landing after flying at high altitude you feel that pressure equilibration. If the tube is blocked because the tissue is inflamed and swollen, then the pressure can not equilibrate and that can cause headaches and indirectly affect the vestibular organ and cause dizziness. This is all independent of celiac disease. I have not seen studies showing an increased incidence of sinus allergies associated with celiac disease but that does not mean that it does not exist. In general, celiac disease is a very different autoimmune reaction than celiac disease and the big question is if when they come together it is a coincidence or if they are related. I do not think that we have the answer at this time. 

CattyJay Newbie

Well i have chronic sinusitis, for many many years now. Celiac disease was only diagnosed a few weeks ago, so it wil lbe interesting to see if the chronic sinusitis eases, as i heal. We do live in the South African bush, so there is pollen and other allergens. But an interesting point, and something i will keep an eye on.

Scott Adams Grand Master

For most of my youth I had chronically clogged sinuses, the issue seemed to be magnified when I slept, and for years I was taking both pollen and food allergy shots to help deal with it. However, it wasn't until I was diagnosed with celiac disease in my mid-twenties and went gluten-free that my sinus issues began to improve. I suspect that my immune system was just overwhelmed at the time, and overreacting to everything.

trents Grand Master

This is pretty much my experience, Scott, except the celiac disease dx came much later in life.

DJFL77I Experienced
7 hours ago, CattyJay said:

We do live in the South African bush, 

they got internet there?

Scott Adams Grand Master

It's probably safe to say "yes!" to that, since they posted here. 😉

  • 1 year later...
N line Newbie

I am curious if anyone is having similar symptoms as me, I had a staph infection and got treated at ER drained, antibiotics… etc 

next day I come home take a shower and faint…weird… never fainted before, went to ER again everything checked out, about 4 weeks go by and I feel terrible brain fog, feeling drunk almost, not very coordinated, sinus headaches usually at night time right in between my eyebrows, and of course GI symptoms as well so during that 4 week period I was in and out of doc office doing several test and found out I had c diff and celiac disease, I got treated for c diff and began a strict gluten free diet and all was well after that for about 9 months… I am now having similar symptoms brain fog, uncoordinated, dizzy when standing too long, sinus pressure, and excessive thirst!!!

i did not consume gluten (that I know of)

I was just curious if this has happened to anyone else doctors don’t seem to know what’s going on and are testing me for a whole bunch of stuff but to no avail. 
please let me know if you’ve had something similar and what fixed it/made it better!

thanks all!!!

trents Grand Master

Sounds like you got glutened from some unknown source. Have you been eating out? Have you checked pills and supplements for gluten? Are you kissing someone who is not gluten-free?

 

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
×
×
  • 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.