Nope. As of Jan-23:
- Of people with self-reported long COVID, 142,000 (7%) first had (or suspected they had) COVID-19 less than 12 weeks previously, 1.8 million people (89%) at least 12 weeks previously, 1.2 million (61%) at least one year previously and 687,000 (35%) at least two years previously.
Sauce:
https://www.ons.gov.uk/peoplepopula...onaviruscovid19infectionintheuk/2february2023
Of course in the post truth world Bill Gate might be pulling the strings behind the ONS.
Edit - hmm it's self-reported long-covid? Can't give the values too much credit then. A pinch/shovel of salt required.
IIRC at the moment it takes a long time for a doctor to even start to consider "long covid" as a diagnosis. For example you've got to have been clear of covid for several months (no reinfection) and still have symptoms of it for something like 3-6 months, and i'm not sure if there is a proper clinical criteria for it yet.
It's similar in some regards to CFS/ME both of which seem to share some symptoms with "long covid" and are also possibly/probably triggered by viral infections (although genetics and environment may or may not also play a part) maybe even with some of the same results, and to put that in perspective there are thought to be about 100-200k people with that in the UK, but only a handful of doctors who specialise in it, and it's usually only diagnosed after you've had the symptoms for about 6 months minimum and pretty much every other test has been run to rule out other things (so in reality a year+ of being ill before you've got a chance at diagnosis*).
In the US there are thought to be over a million people with CFS/ME, but I was reading a while back (in relation to long covid**) that the number of specialists wouldn't fill a mini bus.
So to put things in a short form, if long covid is real (and it looks to be, we know covid does damage, and there is research showing persistent micro clots in some people), you could have hundreds of thousands of people who have the signs of having it, but only a trickle getting diagnosed because it's not immediately life threatening (so no rush) and a condition where they can't do a test that will show something specific, and it can take weeks/months between each of the tests so you could be looking at a lag of well over a year, especially with the health system struggling.
It's also worth noting that with the decrease in testing finding out who has some od, lingering illness and being able to link it to covid or something is going to get a lot harder, so you'll potentially have a number of people with something that can no longer be traced back to a known specific cause.
*And with that time frame it was no wonder so many people with it were misdiagnosed as "depression" at one point, as if you went from being active and fit to having some odd debilitating illness depression isn't going to be uncommon (it happens to some people who've had an injury or illness that they know about and know they'll recover from it, but maybe not for 6+ months).
**As basically the best people to know about how to deal with it in the short term are potentially those already familiar with dealing with similar symptoms.