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

Coughing A Lot


macallen

Recommended Posts

macallen Newbie

I was just diagnosed with celiac 6 days ago, and have had a cough that seems to get worse in the evenings, and was wondering if anyone else had experienced this. I don't have a cold, and it doesn't seem to be allergies, at least not like any I've ever had before. I have been on the gluten free diet since the day I was diagnosed, but worry that I am being cross contaminated by the pots and pans and cooking utensils that I have been using. The food I've been eating is definitely gluten free, but could I possibly be getting glutened by my cookware? I have been totally fatigued, with absolutely no energy, and it doesn't seem to be getting any better. My husband thinks I am just paranoid, but I think he's wrong. Anyone have any similar experience, especially with the coughing.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

Cookware that is scratched or items made of a porous material like wood or cast iron should be replaced. If you have a cast iron skillet that you love you can put it in a selfcleaning oven and set the oven on the 'clean' then scrub well and reseason. You also need to get a new dedicated toaster and strainers.

Since you are very new to the diet it is quite possible that you are going through withdrawl which would lead to the fatigue and perhaps even some moodiness. I don't know if the coughing is related but celiac inflammation has recently been linked to asthma.

Welcome to the board and ask any questions you need to.

cO-ol Explorer

I used to cough after eating all the time. There were a few times when I'd cough a lot for no apparent reason and the doc gave me antibiotics and steroids (a short course) when I went to make sure that I wasn't dying or something. Is it a dry cough? At any rate, for me, that was the first thing to go when I went gluten-free. And I don't cough much anymore at all.

So you possibly could be getting glutened still (Dear Firefox: GLUTENED IS A WORD DANGIT :P). I always thought the cough was related to my reflux because I almost always coughed aftrt eating, but I still deal with reflux but not the cough. So maybe it was inflammation-related. And maybe yours is too?

GFinDC Veteran

I cough some lately too. Been on the gluten-free diet for a little over 3 years. I really just think life is inappropriate right now. little Cough cough, Kidding!

Anyhow, I was drinking a lot of peppermint tea over the winter. I had developed (sounds impressive eh?) an ongoing sinus infection since last December. So, it's warm now (kinda) so I stopped drinking the peppermint tea. My sinuses stopped bleeding and my congestion reduced dramatically. I still have this little cough thing but it is spring and I always did have hay fever in spring.

I guess my point is you can be allergic (react) to anything your body decides to be allergic to. Stink about it, and maybe you find something that is possibly a problem for U.

Sloopy Newbie

Coughing was my only symptom -- I coughed for years for no apparent reason that I could find. It's still my only indication that I've been glutened. I start the dry, gagging cough almost immediately. Otherwise, it's gone -- cleared up within a week of going gluten-free.

macallen Newbie

Cookware that is scratched or items made of a porous material like wood or cast iron should be replaced. If you have a cast iron skillet that you love you can put it in a selfcleaning oven and set the oven on the 'clean' then scrub well and reseason. You also need to get a new dedicated toaster and strainers.

Since you are very new to the diet it is quite possible that you are going through withdrawl which would lead to the fatigue and perhaps even some moodiness. I don't know if the coughing is related but celiac inflammation has recently been linked to asthma.

Welcome to the board and ask any questions you need to.

So, I really should replace my pots and pans and wood and plastic utensils to avoid cross contamination. I am very overwhelmed by all this. I have been out of work since the beginning of December, when I had a herniated disk and had sciatica so bad that I couldn't walk or sit, and then after I had surgery I started being nauseous all the time, and it never seemed to get better. At first I just thought it was due to the anesthesia, but then after two weeks when it didn't go away I was thinking it had to be something else. I ended up getting a CT scan, and they told me I had gall stones and would need to have my gall bladder removed, so I had that removed exactly four weeks after the back surgery. I thought that would cure me, and yet I was still feeling awful, no energy, and couldn't eat more than a few bites of food at a time. I finally went to see a gastro specialist, and he had me get an MRCP and an endoscopy, because they thought maybe I had an ulcer. Turns out that the biopsy and the blood tests showed that I have celiac. I was not expecting that diagnosis, since I had always been able to eat just about anything before my back surgery and never had any problems. Then all of a sudden WHAM, they drop the celiac diagnosis on me. Told me if I just started eating food without gluten I'd be fine in a few weeks. It's been one week exactly today, since my diagnosis, and I still feel horrible, and was wondering how long it might be before I start to notice an improvement. (if I can keep from being cross contaminated) I have been out of work for three months, and would really like to have my life back.

ravenwoodglass Mentor

You will get your life back. It has only been a week and it can take some time to heal. Be sure to check any meds you take with the maker and if you take supplements be sure to read all ingredients as they can be labeled gluten free but still have wheat or barley grass and those are not something you want.

Hang in there, I know it is rough right now and the diagnosis may have hit you by surprise but you will feel better. Do stay away from dairy for a little while also, if your not already, as the same areas that are damaged by celiac are the areas that produce the enzymes we need to digest dairy.

I hope you feel better soon but we can have some ups and downs at first, especially moodwise. It will get better.


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



Celiac.com Sponsor (A8-M):



glutenfreesavvy Rookie

macallen,

Bless your heart! I can see how frustrating it is for you right now. It will get better, even if it doesn't seem likely at this moment. :) Do you have someone or a group of support nearby? It's so much easier to take the first steps of your gluten-free journey with a supportive friend/spouse or group.

Imho, you should replace most, if not all of your kitchen cookware, utensils & such. I did keep some glass & stainless steel bowls & such but cleaned & sterilized repeatedly, then threw away the cleaning cloths. Also, I cleaned every square inch of my kitchen - cabinets, drawers, etc. Don't forget your oven & dishwasher. Over the first few months of eating gluten-free, I learned how VERY sensitive I am to any gluten cross contamination, so I ended up cleaning everything out of my kitchen. There were lots of sentimental things in my kitchen, so giving up my grandmother's cast iron skillet was kind of a bummer. :(

If you think something has glutened you & it's supposedly gluten-free, listen to your body. Don't eat it. :) Gluten cross contamination is a real issue & it's far more prevalent than most realize. Trust your body & listen to its' cues. It's usually right on the money. :)

I can relate to wanting your life back. I've felt that way too. While this road of healing is tough right now, you can look forward to improved health in the future, no matter how dark it seems now. Be prepared though, your life will be forever changed & for the best, in my opinion. You'll eventually get your life back, in a new & improved version. :D I'm thankful the doctor found the issue when he did. Having celiac disease symptoms surface after severe stress, like surgery, is not uncommon. I'm so glad you now know! That's a blessing. It sounds like your doctor acted quickly.

If you're not physically able to do a lot of the sorting & "gluten cleaning", do you have friends or family that can help you? Just take each moment, each step, each day at a time - easier said than done sometimes - but vital if you're feeling overwhelmed.

I wish you all the best!!!

Warmly,

Faydra

So, I really should replace my pots and pans and wood and plastic utensils to avoid cross contamination. I am very overwhelmed by all this. I have been out of work since the beginning of December, when I had a herniated disk and had sciatica so bad that I couldn't walk or sit, and then after I had surgery I started being nauseous all the time, and it never seemed to get better. At first I just thought it was due to the anesthesia, but then after two weeks when it didn't go away I was thinking it had to be something else. I ended up getting a CT scan, and they told me I had gall stones and would need to have my gall bladder removed, so I had that removed exactly four weeks after the back surgery. I thought that would cure me, and yet I was still feeling awful, no energy, and couldn't eat more than a few bites of food at a time. I finally went to see a gastro specialist, and he had me get an MRCP and an endoscopy, because they thought maybe I had an ulcer. Turns out that the biopsy and the blood tests showed that I have celiac. I was not expecting that diagnosis, since I had always been able to eat just about anything before my back surgery and never had any problems. Then all of a sudden WHAM, they drop the celiac diagnosis on me. Told me if I just started eating food without gluten I'd be fine in a few weeks. It's been one week exactly today, since my diagnosis, and I still feel horrible, and was wondering how long it might be before I start to notice an improvement. (if I can keep from being cross contaminated) I have been out of work for three months, and would really like to have my life back.

etta694 Explorer

I had a chronic cough for about 5 months before going on a gluten free diet. I would erupt in coughing after I ate any carbs. It has taken a while to disappear but it has. Sometimes I still cough a little if I eat a lot of carbs now but it is a miniscule problem and goes away quickly.

IrishHeart Veteran

I cough some lately too. Been on the gluten-free diet for a little over 3 years. I really just think life is inappropriate right now. little Cough cough, Kidding!

Anyhow, I was drinking a lot of peppermint tea over the winter. I had developed (sounds impressive eh?) an ongoing sinus infection since last December. So, it's warm now (kinda) so I stopped drinking the peppermint tea. My sinuses stopped bleeding and my congestion reduced dramatically. I still have this little cough thing but it is spring and I always did have hay fever in spring.

I guess my point is you can be allergic (react) to anything your body decides to be allergic to. Stink about it, and maybe you find something that is possibly a problem for U.

Hi DC

I had developed this sinus/throat.burny mouth thing --back in July '09 (pre- Diagnosis)..always feel like I am in a "histamine" response 24/7. It's awful! I had a dry cough, even my lungs feel sore. I was drinking peppermint tea for nausea and took a ton of herbal supps over the course of 3 years, like tumeric, willow bark, etc....(lots of "helpful" advice from an ND and an MD) :huh:

Turns out, someone on here suggested that you can develop a sensitivity to salicylic acid (great, I love grapes, dates, honey--bummer!!) and I am guessing maybe that's what it is??

Don't know if that's why giving up the pep tea stopped your symptoms? Just a thought! I gave up all foods with SA--as was suggested (I'll try anything to feel better) and in a few days, it is a bit less!!...here's hoping.

You are right--seems as if anything can bite us on the butt.....sigh....

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,859
    • Most Online (within 30 mins)
      7,748

    Lesley-Anne
    Newest Member
    Lesley-Anne
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • 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    
×
×
  • 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.