The test-to-enter is simply theatrics at this point. There is so much Covid everywhere right now, so many new variants cropping all over. Bizarre we aren’t doing things we know works (masks, ventilation, boosting), & now are back to square 1 with ineffective antics.
The test-to-enter is simply theatrics at this point. There is so much Covid everywhere right now, so many new variants cropping all over. Bizarre we aren’t doing things we know works (masks, ventilation, boosting), & now are back to square 1 with ineffective antics. https://t.co/VaWJQ4C7s5
That is like checking the fox (or wolves) after the fox has raided the hen house and left a them all dead...
100% BS Theatrics.... and click bait news. Testing only people flying in from China for covid after they infected the people on the flight, is a sick joke...
Alas there is no cure crack-pot moron ideas....and their sources...
All the more reason for the need for $RVVTF Bucci approval...
For one, it gets into the chronic illness history of the last 40 years, and the mental health, physical health, and medical system failures that are now growing exponentially with the now known as Long Haul Covid19, that I have been saying for months now basically just more autoimmune cases triggered by another virus. except in this case, there are so many the medical industry can no longer ignore it, and its mental health consequences...
Even the so called experts now have full blown evidence of the Brain x gut cross talk, and started to finally see how connected every thing is...
Check this part out, then read it all:
"The United States has a very different system of healthcare, which is largely private and insurance-based. That means the validity of diagnosis, what will and will not be accepted by insurance firms, is critical. If you suffer from an unrecognised condition, there’s a very good chance you won’t be able to receive any treatment. It’s a harsh environment, fraught with lawsuits, that has bred a tough kind of activist.
One of these is a man called David Tuller, a former HIV campaigner, who has become something of a hero to the ME/CFS community in the UK. He takes a highly detailed approach to medical papers, closely reading them to uncover any inconsistencies or potential flaws. He publishes his findings on a well-read blog called Virology.
It’s a development, says Sharpe, that has moved the conflict on to a “whole other level”. Such blogs and forums, he says, have become “a coordinating centre for actions against people getting the ‘wrong answers’”.
"Tuller has called the Pace trial a “piece of crap” and says that his goal is to “completely discredit” it. He describes researchers who conduct psychological tests for treatment of ME/CFS as “insane”, and he was instrumental in persuading the respected science journal Cochrane Database of Systematic Reviews to withdraw a paper that looked at eight randomised controlled studies of exercise therapy for ME/CFS. Sharpe says that the Cochrane editor “wilted badly… under direct pressure” from activists. The editor has since retired, and Sharpe understands that his decision is to be reversed."
"ME-like symptoms were noticed as far back as the 1930s, but it wasn’t until an outbreak in the 50s at the Royal Free hospital in north London that it earned the title of “benign myalgic encephalomyelitis”. In the 80s, the “benign” was dropped, but before that, a psychiatric review of major ME outbreaks concluded that they were psychological in nature. At around the same time, the condition became known as chronic fatigue syndrome.
Shepherd believes this was a “dreadful” mistake. As he has written: “The term CFS trivialised a serious medical condition – the equivalent of trivialising dementia by calling it a chronic forgetfulness syndrome – and shifted the focus from a ‘disease’ to a single symptom, ‘chronic fatigue’.”
" there is “growing evidence of a range of neurological abnormalities”, and there are neurologists who are “coming round to the idea that this is what we call a neuro-immuno disease”."
"At the moment there is such ill feeling on both sides that the fundamental process of improving health – the cooperation between patients and practitioners – has been damaged. Exactly how that will be fixed in a way that satisfies both medical science and sufferers of ME/CFS is a problem that has yet to be resolved." ------------------------------- My view on this, is that we are in the middle of a major evolution of the medical research and medical patient, care and drug fields, with social media self hacking and internet based collective networking on social media (Think early stages of the Star Trek Borg collective) becoming self aware and moving faster than the old school methods.
Access online to massive data, and AI technology, is already starting to eclipse the old mega millions dollar studies processes...
In part, because the autoimmune diseases are two complex for any one drug or one trial to solve the multi-facet problems that are involved.
Old school medical techniques and surgery, science based has its place and saves millions of lives. But most autoimmune diseases, including the new version named LHC Long Haul Covid, involves a huge amount of interconnected bio-chemical processes, and there is no one pill fits and solves all the problems.
I am speaking from personal and family and friends experience, having fought and more often than not beat RA/CFS for 40 years now, mostly on my own the first 32 years (by ignoring MDs, and doing my own research and trial and error testing, of diet, life style and supplements, and vitamins and nutraceuticals mix evaluations..