Long Covid doesn't exist, volume one zillion
A huge French study shows BELIEVING you had Covid is associated with many later symptoms. But ACTUALLY having had Covid isn't associated with any (except loss of sense of smell).
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The Journal of the American Medical Association has another stunning paper out, this one on post-Covid symptoms in almost 27,000 French adults.
Researchers asked people to report whether they had had Covid and whether they had any of 18 lasting symptoms like insomnia, fatigue, or cough. They found that self-reported Covid was very strongly associated with nearly every symptom.
But the scientists then went a step further.
They also had Sars-Cov-2 antibody test results for the people they had surveyed, so they didn’t have to depend on self-reported Covid. They knew who really had had Covid and who had not.
They then compared self-reported symptoms in people with antibodies - that is, people who had actually been infected and recovered from Covid - to the general population. And they found no difference in almost any symptom.
Covid was not a risk factor for chest pain, or breathing difficulties, or trouble focusing, or stomach pain, or any of the many, many other complaints that long Covid “patients” and interest groups say are real. There was one interesting exception; people with Covid antibodies did have a much higher rate of anosmia, losing one’s sense of smell. Because anosmia is a known and lasting side effect, it serves as a useful control of sorts.
The researchers also found that almost 60 percent of the people with antibodies HAD NO IDEA THEY HAD EVEN HAD COVID AT ALL. Meanwhile, while more than half the people who said they had had Covid had no antibodies. (Welcome to the plague so severe most halfway healthy adults don’t even know they’ve had it.)
The study strongly suggests that many people are using previous Covid diagnoses - either real or imagined - to help explain away common physical symptoms such as joint pain or cough. It also suggests that actually being infected Covid is far less risky than thinking you have been infected with Covid for many people.
The researchers concluded by explaining that people who claim they have long Covid may need help “to identify cognitive and behavioral mechanisms that may be targeted to relieve the symptoms.” Which is a very polite way of putting the truth.
This study should slow, if not stop, the rush to medicalize long Covid. It is yet more proof that the illness is a group of squishy (if painful and difficult) symptoms looking for a name - and more importantly a billing code.
But so many patients and physicians and public health experts are now invested (in some cases literally) in making long Covid real that the gravy train will likely roll on.
SOURCE: https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/2785832
Alex - I have been so grateful for all the work you’ve done these past 18mos and your courage and commitment in the face of so much resistance is inspiring.
Here comes “the but.” I just saw you on Tucker which led me to this and other pieces you’ve written on the topic of Long CoVid.
I have only my own experience and other anecdotal examples to go by and I can tell you that I am NOT interested in a check from the government or anyone else.
FACTS: I am not a hypochondriac, and am un-jabbed and prior to having CoVid in Feb 2020 (now with the T-cell immunity to prove it) the worst health-related issues I’ve ever had were mild seasonal allergies, an appendectomy 20+ years ago and a childhood bout of Hong Kong flu.
My parting gift from the vid: markedly diminished lung capacity (now at 70%) peripheral artery disease & fatigue (resulting from diminished lung capacity).
I did not go to my dr complaining of “long CoVid” - all I knew was that my left foot was purple from the ankle to the toes, I could no longer climb a flight of stairs without difficulty breathing and my pre-disease runs through the park have become brisk walks with frequent breaks. I would LOVE to participate in an investigative study but have been unable to find one. I see you reporting on such research but as for me, I have no choice but to say this is “FALSE.”
Based on ur comments this evening you would say I fit the “profile” of the person who abuses healthcare to pursue validation of my “disease.” I am not interested in a disability determination or a handout of my own tax dollars.
FEELINGS about your comments: it’s wrong for you (and Tucker) to shame people who are experiencing REAL long term (possibly life long) effects of the virus. I’m sure as with every other medical issues there are people who intentionally (or subconsciously) pursue a determination of disability for profit or due to mental health issues. I assure you I would pay to have my health status returned to what it was in January 2020.
Keep up the good work but you might want to do some more follow up on this topic. Maybe #1 billion and one will be more accurate.
Honestly I have no dog in this long COVID fight but it seems like small potatoes while there are tyrants dead set on maiming and killing children. That is giving me chest pains and trouble sleeping too