Covid Recovery: How can I manage GI issues?

Posted by sieb369 @sieb369, Jan 3, 2022

It has been 5 weeks since my COVID symptoms began. I am well past the isolation date. I had nausea and diarrhea during COVID along with the usual symptoms of cough, fatigue, rapid heartbeat and sinus issues. I have felt like I was over this, but I began having GI pain in the last week. I feel as if my intestines are sore on the inside. I guess it is inflammation. Has anyone else had this and is there anything I can do to help it? Probiotics maybe?

Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.

Profile picture for greg1234 @greg1234

Greetings, I had a breakthrough case of covid five months ago, all gastrointestinal symptoms. The symptoms still are recurring every few days. No gastrointestinal remedies seem to help: probiotics, prebiotics, Curing Pills, prevacid, all no help. Anyone having any success with gastro symptoms? Thank you!

Jump to this post

@greg1234 my doctors are still working with me but I have been helped by going on a low histamine diet, removing all sugar with the exception of fruit, reduce activity dramatically and I am dairy and gluten free. This helps if I do not walk too much and I mean 2 miles in a day is too much. D

REPLY
Profile picture for greg1234 @greg1234

Greetings, I had a breakthrough case of covid five months ago, all gastrointestinal symptoms. The symptoms still are recurring every few days. No gastrointestinal remedies seem to help: probiotics, prebiotics, Curing Pills, prevacid, all no help. Anyone having any success with gastro symptoms? Thank you!

Jump to this post

@greg1234 I have been helped by gluten, dairy free, no sugar and a low histamine diet. In addition no real activity.

REPLY
Profile picture for sunshinestateofmind @sunshinestateofmind

My husband is on day 7 of his 4th hospitalization for severe GI issues post Covid. He is 10 weeks out from Omicron. He was vaccinated w/ both Pfizer doses prior to contracting.

No prior history of diarrhea. 2 weeks post Covid he started having painful gas and diarrhea. It became so severe he was doubled over in pain and shaking. After the first CAT scan they said he had the worst case of diverticulitis they had ever seen, and admitted him with 3 different antibiotics and steroids.
Liquid diet, bowel rest, antibiotics, steroids.

We went home. Two days later after eating chicken soup, it all started again. He can’t leave the house w/o a diaper because the attacks are so frequent and so violent.

The colo/rectal surgeon was perplexed because when he scoped him, it wasn’t technically consistent with diverticulitis or even ulcerative colitis. The first 6” from the rectum in are in perfect shape, the next section is an angry inflamed nightmare, and the top looks fine as well.

He DOES have severe colitis and some ulcerations but that doesn’t mean us ulcerative colitis. 14 biopsies were taken. Most of the biopsies looked normal the biopsy of the small ulcers appeared to be either ischemia or infectious.
After 2 weeks of antibiotics the inflammation was unchanged so antibiotics were discontinued.

A fourth Angio CT showed no major blockages to the vessels but they can’t rule out a transient ischemic event in the colon.

When we tried to move back to soft foods yesterday a massive flare up ensued. He was basically having contractions every 60 seconds for 12-16hrs and not really producing much but shedding the mucosal lining I’m guessing. Just a brutal brutal experience. Hemoglobin is 12.7. Pinkish and some bright red blood in stool from time to time. White cells still elevated.

We are exactly where we were 4 weeks ago when we came to the ED the 1st time. It’s so discouraging. He has been on a liquid diet for 24 hours and after a stressful afternoon attacks have come back to every 20 minutes.

Still treating w/ 60mg steroids daily, back on antibiotics, and Mesalamine every 6hrs until we get him through the flare up. They are treating like ulcerative colitis until we can repeat the colonoscopy in 8 weeks.

I’m just scared there is something more we should be doing. I want to protect the integrity of his colon.

Any advice us greatly appreciated.

Kind regards,
H Kountanis

Jump to this post

@sunshinestateofmind what has worked for me is gluten and dairy free, no sugar except in fruit, no caffeine, low histamine diet, meditation, minimal activity. I got over it then it started when I went back to my old diet. Sleep is really important. I am also using gabapentin and now Ldn. If you do this for two months like I did it will help a lot. I am back to a two month process again. D

REPLY

I have been dealing with long Covid for 4+ years. I now have chronic constipation. My last Covid infection hit my GI tract very hard. I’ve had a colonoscopy and an endoscopy both came out clear. I now take daily meds to help me go. We are doing a gastric emptying study next. I wish you luck and I hope you get better soon!!

REPLY

My long covid constipation and diarrhea are all caused by specific foods and alcohol. I did an elimination diet after a year post covid and found I am now allergic to gluten, sugar, wheat, gluten free bread (don't yet know what ingredient I am reacting to), dairy, cheese with mold like blue cheese and red wine...probably the tannin. If I stay away from those foods, my digestive track is just fine but having a glass of red wine or a slice of bread will cause havoc! Low dose naltrexone has lessened some of these allergic reactions but they still continue 6 years post covid.

REPLY

I have a general question for folks who are dealing with gastrointestinal symptoms that are being identified as long Covid. Have you been able to actually get a diagnosis that relates your gastrointestinal issues to Covid? I had a mild case of Covid in 2022 that was congestion, sore throat and night sweats. Otherwise I felt fine. Shortly after, I experienced intestinal pain and cramping and on x-ray was told that I had constipation even though I didn’t think I had constipation. Since then, I’ve had endoscopy, MRI, CT, numerous x-rays. Those showed that I have mild gastritis and an esophageal stricture. I am fit, eat mainly vegetarian/vegan, don’t drink or smoke. Constipation has been chronic until recently. In 2025 I had a heart attack out of the blue!

I received a stent and was placed on the standard cocktail of medication. The original statin caused my liver enzymes to soar, and that has since been adjusted. My heart is healthy and I’m very grateful for that. I do take an aspirin every day so have been put on PPI to protect my stomach. This concerns me because I already have osteoporosis. I’m not interested in adding another medication for that. The constipation seems to be managed by regular MiraLAX most days of the week.

I guess my question is how does a person know if they have long Covid and does that change the way their symptoms are treated? I’ve got two cardiologists and a gastroenterologist, a lipidologist, and recently a hematologist because of low red blood and low ferritin. Iron messes with the GI so we are discussing infusion. Before 2022 I considered myself a very healthy person. I still consider myself a relatively healthy person, but I’m taking more medication than I ever imagined I would and honestly never feel great. I walk every day which I was doing prior to the heart attack anyway, I’m now 71 years old, my weight is good and always has been.

REPLY
Profile picture for sunshinestateofmind @sunshinestateofmind

My husband is on day 7 of his 4th hospitalization for severe GI issues post Covid. He is 10 weeks out from Omicron. He was vaccinated w/ both Pfizer doses prior to contracting.

No prior history of diarrhea. 2 weeks post Covid he started having painful gas and diarrhea. It became so severe he was doubled over in pain and shaking. After the first CAT scan they said he had the worst case of diverticulitis they had ever seen, and admitted him with 3 different antibiotics and steroids.
Liquid diet, bowel rest, antibiotics, steroids.

We went home. Two days later after eating chicken soup, it all started again. He can’t leave the house w/o a diaper because the attacks are so frequent and so violent.

The colo/rectal surgeon was perplexed because when he scoped him, it wasn’t technically consistent with diverticulitis or even ulcerative colitis. The first 6” from the rectum in are in perfect shape, the next section is an angry inflamed nightmare, and the top looks fine as well.

He DOES have severe colitis and some ulcerations but that doesn’t mean us ulcerative colitis. 14 biopsies were taken. Most of the biopsies looked normal the biopsy of the small ulcers appeared to be either ischemia or infectious.
After 2 weeks of antibiotics the inflammation was unchanged so antibiotics were discontinued.

A fourth Angio CT showed no major blockages to the vessels but they can’t rule out a transient ischemic event in the colon.

When we tried to move back to soft foods yesterday a massive flare up ensued. He was basically having contractions every 60 seconds for 12-16hrs and not really producing much but shedding the mucosal lining I’m guessing. Just a brutal brutal experience. Hemoglobin is 12.7. Pinkish and some bright red blood in stool from time to time. White cells still elevated.

We are exactly where we were 4 weeks ago when we came to the ED the 1st time. It’s so discouraging. He has been on a liquid diet for 24 hours and after a stressful afternoon attacks have come back to every 20 minutes.

Still treating w/ 60mg steroids daily, back on antibiotics, and Mesalamine every 6hrs until we get him through the flare up. They are treating like ulcerative colitis until we can repeat the colonoscopy in 8 weeks.

I’m just scared there is something more we should be doing. I want to protect the integrity of his colon.

Any advice us greatly appreciated.

Kind regards,
H Kountanis

Jump to this post

@sunshinestateofmind
I’ve had LC for six years now (only infection was early March 2020 nyc) and have had these symptoms on and off the entire time. I have also had almost every test imaginable (and some you don’t want to imagine). They all came back showing little to no evidence of damage. I’m in my 40s and was healthy and an athlete/dancer before. I’m now basically unable to work much and when the IBS hits I’m housebound until everything empties out.
Not much has worked for me to be totally honest. And sorry to say!! Stress reduction a little, but really I think it is dysautonomia for my case. I felt that way before all the tests and was both relieved and disappointed that there was no further guidance for me.
My GI person did give me cholestyramine 4 g packet
Commonly known as: Questran so maybe that’s an option to be asked about. Take good care, you aren’t alone 🙂

REPLY
Profile picture for ezjersey719 @ezjersey719

I have a general question for folks who are dealing with gastrointestinal symptoms that are being identified as long Covid. Have you been able to actually get a diagnosis that relates your gastrointestinal issues to Covid? I had a mild case of Covid in 2022 that was congestion, sore throat and night sweats. Otherwise I felt fine. Shortly after, I experienced intestinal pain and cramping and on x-ray was told that I had constipation even though I didn’t think I had constipation. Since then, I’ve had endoscopy, MRI, CT, numerous x-rays. Those showed that I have mild gastritis and an esophageal stricture. I am fit, eat mainly vegetarian/vegan, don’t drink or smoke. Constipation has been chronic until recently. In 2025 I had a heart attack out of the blue!

I received a stent and was placed on the standard cocktail of medication. The original statin caused my liver enzymes to soar, and that has since been adjusted. My heart is healthy and I’m very grateful for that. I do take an aspirin every day so have been put on PPI to protect my stomach. This concerns me because I already have osteoporosis. I’m not interested in adding another medication for that. The constipation seems to be managed by regular MiraLAX most days of the week.

I guess my question is how does a person know if they have long Covid and does that change the way their symptoms are treated? I’ve got two cardiologists and a gastroenterologist, a lipidologist, and recently a hematologist because of low red blood and low ferritin. Iron messes with the GI so we are discussing infusion. Before 2022 I considered myself a very healthy person. I still consider myself a relatively healthy person, but I’m taking more medication than I ever imagined I would and honestly never feel great. I walk every day which I was doing prior to the heart attack anyway, I’m now 71 years old, my weight is good and always has been.

Jump to this post

@ezjersey719 There is no diagnostic test for long covid. It is diagnosed by a process of elimination. If you feel sick, but every test says you are fine, then you are diagnosed with long covid. Sad, but true 🙁

REPLY
Profile picture for ezjersey719 @ezjersey719

I have a general question for folks who are dealing with gastrointestinal symptoms that are being identified as long Covid. Have you been able to actually get a diagnosis that relates your gastrointestinal issues to Covid? I had a mild case of Covid in 2022 that was congestion, sore throat and night sweats. Otherwise I felt fine. Shortly after, I experienced intestinal pain and cramping and on x-ray was told that I had constipation even though I didn’t think I had constipation. Since then, I’ve had endoscopy, MRI, CT, numerous x-rays. Those showed that I have mild gastritis and an esophageal stricture. I am fit, eat mainly vegetarian/vegan, don’t drink or smoke. Constipation has been chronic until recently. In 2025 I had a heart attack out of the blue!

I received a stent and was placed on the standard cocktail of medication. The original statin caused my liver enzymes to soar, and that has since been adjusted. My heart is healthy and I’m very grateful for that. I do take an aspirin every day so have been put on PPI to protect my stomach. This concerns me because I already have osteoporosis. I’m not interested in adding another medication for that. The constipation seems to be managed by regular MiraLAX most days of the week.

I guess my question is how does a person know if they have long Covid and does that change the way their symptoms are treated? I’ve got two cardiologists and a gastroenterologist, a lipidologist, and recently a hematologist because of low red blood and low ferritin. Iron messes with the GI so we are discussing infusion. Before 2022 I considered myself a very healthy person. I still consider myself a relatively healthy person, but I’m taking more medication than I ever imagined I would and honestly never feel great. I walk every day which I was doing prior to the heart attack anyway, I’m now 71 years old, my weight is good and always has been.

Jump to this post

@ezjersey719 Sadly diagnosis for Long COVID is symptom based. There is no consistent set of blood testing that will confirm it...for now. There do appear to be sets of long covid patients with similar sets of symptoms...last I heard they had identified something like 5 different sets of symptoms. For me, fatigue, overall pain from hyper inflammation, skin eruptions and slow healing due to lack of oil production, extreme allergies to food resulting in bloating/diarrhea/constipation, dry eyes/skin/mouth, post exertion malaise for days, sensitivity to smell/sound/heat/cold, sporadic shortness of breath/low blood pressure/pulse/palpitations, and dehydration. With my docs advice, I am getting slightly better using low dose naltrexone and daily vitamin d/b1. Also doing electrolytes in all of my fluid has helped.

REPLY
Profile picture for vostie @vostie

@ezjersey719 Sadly diagnosis for Long COVID is symptom based. There is no consistent set of blood testing that will confirm it...for now. There do appear to be sets of long covid patients with similar sets of symptoms...last I heard they had identified something like 5 different sets of symptoms. For me, fatigue, overall pain from hyper inflammation, skin eruptions and slow healing due to lack of oil production, extreme allergies to food resulting in bloating/diarrhea/constipation, dry eyes/skin/mouth, post exertion malaise for days, sensitivity to smell/sound/heat/cold, sporadic shortness of breath/low blood pressure/pulse/palpitations, and dehydration. With my docs advice, I am getting slightly better using low dose naltrexone and daily vitamin d/b1. Also doing electrolytes in all of my fluid has helped.

Jump to this post

@vostie thanks and best of luck to you, all of us I guess.

REPLY
Please sign in or register to post a reply.