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

Celiac And The Flu


RP276

Recommended Posts

RP276 Newbie

Hello all.

I've been diagnosed with Celiacs Disease, not sure that is the correct terminology though. The diagnosis was about 30 days ago with a blood test, and I will have an edoscopy in the next week or so. So the question I have is this. I have been diligent with my diet and started to feel better and stronger immediately. My sleep improved, depression lessened and as I stated I almost immediately started to feel stronger and honestly about 5 years younger. Now for the bad news. The flu swept through our home about a week ago. When I first had a sysmptom I assumed I had been glutened. When my son started throwing up and subsquently his sisters, I knew that the flu had arrived. After about 6 days of flu related diareha I had about 2 days when I felt fine again. I thought OK I rallied and I'll be fine again shortly. The weird thing is that I have not felt well. I had the 2 days of reprieve and then the diareha started again and has been with me for 3-4 days. I finally gave up and took an Amodium AD and it helped, but I fear it is just masking the symptoms. Is this normal?

In the past 5-6 years I have never had the flu or even a difficult cold. I'm healthy other than Celiacs and hereditary heart disease. Ironically I always ate really well and had plenty of whole grains in my diet. I guess I just had the wrong ones. :unsure:


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



Celiac.com Sponsor (A8-M):



sandsurfgirl Collaborator

It may be that your body is taxed by trying to repair celiac damage and you're worn down a bit. Flu happens. It can last quite awhile sometimes.

If you are already gluten free for over a month, your endoscopy is likely to be negative because your body may have healed the damage in the spots they take biopsies from. That does NOT mean you aren't celiac. If you had a positive blood test then you have celiac. There are no false negatives.

There are some threads about the problems with endoscopies in this forum you may want to read. Honestly if you got a positive blood test and are responding well to the gluten free diet, why are you getting the endoscopy? It's likely to be negative and it's an invasive procedure. I chose not to have one. I didn't want a surgical procedure just so they could tell me what I already knew and put some more money in their pockets.

Macbre Explorer

Hello all.

I've been diagnosed with Celiacs Disease, not sure that is the correct terminology though. The diagnosis was about 30 days ago with a blood test, and I will have an edoscopy in the next week or so. So the question I have is this. I have been diligent with my diet and started to feel better and stronger immediately. My sleep improved, depression lessened and as I stated I almost immediately started to feel stronger and honestly about 5 years younger. Now for the bad news. The flu swept through our home about a week ago. When I first had a sysmptom I assumed I had been glutened. When my son started throwing up and subsquently his sisters, I knew that the flu had arrived. After about 6 days of flu related diareha I had about 2 days when I felt fine again. I thought OK I rallied and I'll be fine again shortly. The weird thing is that I have not felt well. I had the 2 days of reprieve and then the diareha started again and has been with me for 3-4 days. I finally gave up and took an Amodium AD and it helped, but I fear it is just masking the symptoms. Is this normal?

In the past 5-6 years I have never had the flu or even a difficult cold. I'm healthy other than Celiacs and hereditary heart disease. Ironically I always ate really well and had plenty of whole grains in my diet. I guess I just had the wrong ones. :unsure:

One thing you need to consider about the endoscopy is that it may not be accurate since you have been 30 days gluten free. I chose not to have the endoscopy because my doctor told me to stop eating gluten immediatly when the blood test came back positive and they had me scheduled for the endoscopy for 3 weeks later, but after talking with "veteran celiacs" I was told numerous times that the results might not be accurate since I had already started healing. Just keep this in mind.

Regarding your flu symptoms lingering....that is not unusual. When I first went gluten free (11 months ago) I had days when I would feel great and other days I felt like nothing had improved. It's a rollercoaster ride in the beginning. You might still be getting gluten and not even realize it. I was getting it from my mouthwash and body lotion. It's trial and error in the beginning. I'm just now starting to have more good days then bad....there is light at the end of the tunnel, but you have to be very strict in avoiding all gluten produts.

red island Newbie

I was always able to fight off stomach flu's, while others around me got really sick, I only ever had mild symptoms - until last winter. Then the flu would hang on for weeks. I've been off gluten for 3 months now and hopefully my poor gut has healed enough that I wont be sick as much.

And why do the docs tell you to stop eating gluten immediately only to tell you that you have to start again for the endoscopy? I just had my scope this week, my GI doc told me he would not ask me to do the gluten challenge because my reaction to being cc'd was so severe - he says if it turns out to be non-diagnostic we can decide where to go from there, but at least he will know how things look in there.

sa1937 Community Regular

And why do the docs tell you to stop eating gluten immediately only to tell you that you have to start again for the endoscopy? I just had my scope this week, my GI doc told me he would not ask me to do the gluten challenge because my reaction to being cc'd was so severe - he says if it turns out to be non-diagnostic we can decide where to go from there, but at least he will know how things look in there.

You have a smart doctor!!! In spite of the fact that you may have a negative biopsy, he can still test you for other things.

My doctor was also ready to diagnose me after a high positive celiac panel. I did stay on gluten until I had the endoscopy because I knew my adult daughter had a problem with gluten so I felt I should go the full route hoping I'd get a positive diagnosis...and I did.

Several months later she had the blood tests and also had high positives on her celiac panel. However, she just went gluten-free and skipped the endoscopy.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.