Long COVID and gluten sensitivity
So we got COVID twice within just about 5 months. The first time was bad. The second we were mostly asymptomatic. Since the second infection my 8 year old has gotten terrible stomach cramps every time she ate. Finally got her pulled off gluten, and since then only a few issues, and they were with heavy lactose foods, which we went ahead and cut as well. All fine since then.
Has anyone else had the same issue? Are you still going through it? Have your symptoms lessened at all? We're still waiting to see GI, the waiting time is so long. And her Dr has been helping as much as she can, but we just don't know what to expect anymore. This has been going on since January 22 for reference on time.
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I have Celiac and what you described is exactly what I experience immediately after consuming gluten. Most vegan meals and products are wheat based so I can’t imagine. Today I made a sandwich with Schar’s gluten free sour dough bread, it fell apart. ☹️
There are a few GF breads that are closer to "real" bread. Canyon Bakehouse loaves are good. It is best to toast GF breads before you use them in a sandwich; they are less crumbly. GF breads freeze well. Another option is to use GF waffles (toasted) for sandwiches. There are likely other brands, but I mostly make my own GF bread (even breadmaking machines have GF options now). The National Celiac Assoication has food options (and recipes).
We are in similar situation with my 13 yr old. Had covid in march 2022 and unsure if he caught it again but he is now severely intolerant to gluten with celiac testing negative. He gets stomach aches but also significant lethargy , weakness and headaches about 30 min after eating gluten . He also gets some vague shortness of breath and asthma like symptoms. For about 2 months this year he had anemia and low white blood cells but that has resolved although his symptoms are persisting. He has been tired, not himself, irritable and not able to gain weight . I am really worried. Doctors dont seem to know what is going on either.
That is scary. Not being able to eat what peers are is also emotionally isolating. If you haven't tried this, you could check with a nutritionist about an elimination diet to see if he is sensitive to any other foods. I was likely gluten intolerant for decades before it morphed into celiac, after I caught H1N1 flu 14 years ago. My pre-celiac symptoms were mostly bloating, rashes, reflux, fatigue, and neurologic problems . As with celiac, one needs to be gluten free, and gluten is hidden in so many things. If you have not, you might try things that are labeled gluten free for awhile, to see if he is getting cross contamination. I got a new toaster and cutting board after celiac; a small crumb of bread can cause an autoimmune reaction. The National Celiac Assoc site has info on gluten free foods, places to eat, and such for celiac and gluten intolerant people. The findmeglutenfree app also has places to eat. About 30-40% of people have the HLA-DQ2 and/or DQ8 gene, and in ~2% of them it triggers celiac, the majority of whom are undiagnosed.
Thank you so much for sharing. We have been doing gluten free as much as we can and he is significantly better. This weekend we were away for my daughters soccer tournament so are in restaurants and even though we avoided the easy stuff like bread etc I believe he had gluten somewhere significant and he crashed.
He also seems to get wheezing and dry cough in addition to fatigue when he has a lot of gluten. We have seen a naturopath and did some allergy sensitivity testing. He is also milk intolerant and intolerant to egg whites but gluten / wheat was more severe. M
I will keep working on this. Just happy to see that I am not imagining things..... and the link to Covid infection triggering all this could be true. Sometimes I feel we are imagining things.....😢
It takes a year or two to figure out what and where is safe to eat, or not. It takes time to get used to reading every ingredient. I tell the servers and chefs that I have celiac, and if it doesn't feel safe I don't eat (I always carry protein bars). If servers use the same utensils for a pot of wheat as gluten free pasta, that is enough for a reaction. Using the same pizza cutter as well. Some cities have celiac/gluten intolerance clubs that include kids/teens. It is nice to be able to eat out with others and not be afraid of getting sick. Gluten intolerance/celiac can be as hard emotionally as physically.
Yes, same. I was recently told or maybe they told me before. I don't remember very well either. Have you noticed any sort of difference?
If someone is gluten intolerant or has celiac, going GF makes a huge difference in how you feel and in your health, although a few people are asymptomatic with gluten exposure. Some people also have difficulty digesting the complex gluten molecules, particularly as we age. I noticed the change to my GI tract and arthritis a few days after going GF, but long-term damage such as reflux and skin rashes took a few months to disappear.
I became allergic to wheat. I have autoimmune disease which leaves me with multiple environmental sensitivities. I had covid three times last year. After the first I started breaking out in hives. I realized it was wheat. Also found out red meat causes problems. I’ve cut them out and have been much better especially after treatment for small intestine bacterial overgrowth.
Hello everyone, I am a doctor, I am 47 years old and after vaccines and 3 episodes of covid I began to have tachycardia, abdominal distention, gastric distention, minutes after eating, several times I had to go to the emergency room. They did an edoscopy where they only found moderate gastritis and duodenitis. As I began to follow a diet, I noticed that histamine-releasing foods were harmful to me, so I gradually eliminated them. This helped me reduce tachycardia. Foods such as shrimp, strawberries, apples, and bananas became intolerable, since they produced redness. in my face tachycardia of up to 160 per minute. I thought I had a deficiency of the enzyme diamine oxidase, and I bought supplements for that, I really don't know if it helped me, because I removed food at the same time as taking the enzyme. Afterwards I noticed a tolerance to milk and cheese, also an intolerance to almonds and peanuts, walnuts, cashews. I stopped eating them because they caused me abdominal, epigastric and mesogastric pain. Later I also noticed that gluten was causing me abdominal pain so I eliminated it little by little. I lost a lot of weight, but it helped me to increase my consumption of lean meat. I have noticed that corn does not produce symptoms, nor does avocado or egg. I already went to several gastroenterologists and the medications that worked for me were mirtazapine, esomeprazole, colchicine, and to reduce the anxiety and nervousness of helplessness because my other colleagues don't know much about it, I take 3 drops of clonazepam at night. I am also being treated with homeopathy, carbo vegetabilis, lycopodium clavatum, arasenicum album, nux vomica, china off, etc. I know that many doctors know things that they have seen in patients, but they just want to spread the word because there is a lot of economic benefit from what is happening. I hope that science and the great human values that still remain will end up coming out to defend the causes of those affected and everyone will move forward from these consequences.