New study will examine irritable bowel syndrome as long Covid symptom
healthsciences.arizona.edu
healthsciences.arizona.edu
(This is not a political statement. I am honestly interested in what the state of empirical evidence on the issue is and I found it hard to find out anything definite about it as a layman.)
I have not heard of people saying they contracted long covid is response to the vaccine (without getting covid) - though I will admit I've tried to stay away from long covid news these days.
I didn't say either/or.
Then it took me more then half a year to get back to that point. It was a very slow recovery but most importantly, it could be quantitatively measured first from how far until I had to disembark my bike to walk up the rest of the hill to eventually the lowest gear I had to to shift into to get to the top without ever disembarking.
I’ve never had any other flu-like sickness cause me to be weak for so long.
One should remember that the flu has been around forever, so the flus you are comparing to were probably the 10th exposure - recovering from a new illness - and not being a small child - may take much longer.
Out of all these it's quite simple to dismiss the psychological explanations of LC. There are obvious physical changes found in various tissue and blood in LC patients. Changes that we can be reasonably certain aren't caused by mental issues.
Could it be caused by vaccinations? Probably not. There seem to be plenty of unvaccinated people with long covid. The politicization of things might make it hard to study in general. Many of the people who were not vaccinated will insist they just had the flu, or a bad cold and would have avoided any sort of official diagnosis.
Could vaccines have made it worse? This is probably even harder to answer definitivel
For this to be logical, you need to state that vaccinated people do not have long covid.
If Group A and Group B have similar outcomes, then the outcome would seem to not be correlated to the difference between Group A and B.
Whether or not the vaccine is a cause of long covid symptoms is not the same as whether the vaccine prevents long covid symptoms.
What do your groups represent?
Both groups can catch COVID. Both groups can develop long COVID symptoms.
This fits with "There seem to be plenty of unvaccinated people with long covid."
You said:
"For this to be logical, you need to state that vaccinated people do not have long covid."
Which I don't follow.
- If long COVID is unrelated to being vaccinated, but is caused by having a COVID infection, you would expect both vaccinated and unvaccinated groups to develop long COVID symptoms because they can both have COVID infections.
- If the vaccine causes long COVID (but a COVID infection itself does not) then you would expect non-vaccinated people to not get long COVID.
So if both groups get long COVID symptoms, it seems unlikely that the vaccine causes it while COVID does not. You also can't expect the vaccinated group to report 0 cases of long COVID since they can still have COVID infections.
Perhaps the long COVID rates would be different between the two groups. Or the severity of initial infection and symptoms. Maybe vaccinated people are more likely to have a COVID infection but not report any symptoms or a positive test result at the time of infection because their symptoms are milder.
My point is not to provide evidence or make a claim one way or the other, but just to say that the presence of long COVID in both groups is not evidence that the vaccine itself is causing long COVID.
And I'm happy to amend my statement to "For this to be logical, you need to state that vaccinated people (who never had covid) do not have long covid."
Right, but it does provide insight into the vaccine being the primary cause of long COVID, rather than an actual COVID infection.
So it depends on how you interpret “the vaccine causes long COVID” meaning exclusive to or inclusive of COVID also causing long COVID.
"vaccinated people (who never had covid) do not have long covid."
seems very difficult to study in the general population given the prevalence of COVID infections among the population and the ability for people to not know or test whether they have had COVID, even if they did have a mild infection.
I don't really understand how that is relevant in this context? Aren't there plenty of people who never suffered from long covid, but suffer from irritable bowel syndrome, both vaccinated and unvaccinated as well?
We also now know that the manufacturing process for some brands was different from the trial groups to general availability, the latter of which contained much more varied biological material.
So, what could a bunch of unpure mRNA, RNA, and DNA strands coated in an immune system-evading 'nano-coating' do to your body? God only knows at this point, we didn't do the science to find out.
Point 1 was in a Pfizer document first leaked from Japan's government in mid 2021, officially released a year or more later.
Point 2 (ish) was in a footnote in Pfizer's FDA approval notice, there were formulation changes in the inactive ingredients between the EUA and brand version for (IIRC) shelf-life stability. I don't remember details on the exact difference being in there though, and I don't remember differences between the trial and EUA versions (but scaling up can cause this by accident).
I can't find the reference at the moment, but I believe they used PCR to replicate the mRNA during the trials, and used the bacteria replication for the subsequent versions.
Here's a professor giving testimony to his findings: https://www.youtube.com/watch?v=IEWHhrHiiTY
I would say my flare ups have increased over the past three years, I assume now that I must be fighting off a repeat variant occasionally.
I would not at all be surprised if this just exposes existing IBS in people, maybe experiencing their first noticible flare up
To any new sufferers of IBS, I would highly recommend Metamucil or any psyllium husk product. I regret not trying it sooner.
I may not have been, but it is the first time I've had symptoms like this.
It's definitely a disease we need to learn more about.
Which is the tricky thing about diagnosis that a lot of people don't really get. Symptoms are sexy, symptoms get the headlines, symptoms get treated. But sometimes multiple diseases present with similar symptoms. And for all we know about medicine and the human body, there is still a lot we are unsure about. So a lot of the time, symptoms are all we have to go on.
And it sucks for you while we're figuring it all out, and I do sympathize, but I can't help but be fascinated by medicine and biology when I run into these situations.
yeah, I dont get much joy from life these days.
The symptom profile of long covid is very close to lyme disease, another disease people actually get but also many more people claim to have without evidence.
I'd like to see the overlap between long covid sufferers, IBS, lyme disease, people with a gluten allergy, PCOS etc and the level of evidence that they actually have those diseases.
I've long been curious what the ratio is in various situations like this. It seems the lynchpin for any argument for withholding support. I've only ever seen the equivalent of "well obviously" on both sides and never any data
As people understood what long covid was and does, people generally came around to the idea, but still (mainly online) people have this opinion that 'people must be making it up' - despite SARs being known to cause similar long term issues for some of those infected, and some people having long term impacts from Spanish Flu 100 years ago.
So if I'm not hyperchondriac, but am frustrated and stressed by (x) random symptom or covid related (y), or being off sick w/ "normal" Covid & struggling to regain energy, then if I'm emotionally distressed by it, then may develop IBS and fatigue symptoms on top of that - which then feeds into the loop...
(Said as someone for the last several months currently struggling with a whole bunch of symptoms and not managing to get any helpful diagnosis or area I can work on to improve things...)
I think a part of this is online communities spring up around these diseases and a doctor telling you that you don't have it is basically them telling you they don't get to hang out with your friends anymore.
Better data exists for IBS on this line of thinking:
> The Illness Attitudes Scales (IAS) and the Beck Depression Inventory (BDI) were administered to 40 patients with irritable bowel syndrome (IBS) and these were compared with 35 patients with organic gastrointestinal (GI) disease, 37 depressed patients, and 40 healthy volunteers.
> All the patient groups had abnormal IAS scores compared with the healthy group, but these were most marked among the IBS patients with elevated scores on six out of the eight subscales. Three of these were specific to the IBS patients: bodily preoccupation, hypochondriacal beliefs and disease phobia.
Also - given medical developments in gut health on GABA, the gut-brain link is not so crazy. So your study could be a reverse causation.
After no physical ailments are detected, they should be treated by psychologists rather than physicians.
The body is a pretty complex thing, it can be difficult to determine the underlying cause of a symptom even if we do have an underlying understanding of what the body is doing (and sometimes we don't!).
Lyme disease can actually be detected. For IBS and long covid, you are making the "no true Scotsman" argument. Diagnosing those is basically filling a questionnaire asking in so many ways "do you feel like you have it?" The same is true for many mental illnesses, by the way. Not to discount people's experience of having these problems - they definitely are real - but since the "official" diagnose is very close to just people telling the doctor that they feel like they have it, self diagnosing is not as bad as you make it sound.
> people claim to have without evidence.
Bit of a technical note. Patients claim is the evidence on its own. Patient may be undiagnosed, but there is an evidence for such claim.
IBS, lyme disease, all sorts of allergies are very hard (and expensive) to diagnose. Some people have no money for doctors, and may not be even registered with GP.
If customer at restaurant says they have a peanut allergy, you better to believe them. Saying "there is no evidence for such claim" may get you in troubles very fast...
The idea of a hypochondriac making a spurious claim to IBS is pretty ludicrous. You know if you have the symptoms or not, and IBS is probably the best possible outcome for someone with chronic bowel symptoms.
Lumping PCOS in with gluten allergy is giving "shit men believe about women's health." Maybe try listening to some women before forming opinions on their reproductive health.
She didn't get IBS per se; however, we have noticed a few changes with respect to her digestive system: she seems to have developed a recent sensitivity to wheat gluten and dairy/lactose. Both now make her gassy and uncomfortable.
The timing of it seems to be coincidental with COVID. Whereas we used to get pizza once or twice a month, it's basically been removed from our diet because it causes digestive issues.
So it's possible that some folks might not be having severe IBS, but a spectrum of digestive issues related to lingering effects that trigger inflammation with certain proteins/sugars?
I suspect the cycle is <something triggers GI inflammation> -> certain foods exacerbate the condition -> until inflammation or underlying cause of inflammation has resided, condition continues.
She has mostly returned to normal after losing many types of foods, but still can't eat beef or eggs in any quantity.