They are determined to make the “Omicron Variant” appear as frightening as possible, that means getting as many cases as possible, which means flipping all the way to the front of the Covid playbook.
For those of you feeling morbidly curious, here are the five signs of Omicron:
scratchy throat
Fatigue
mild muscle aches
dry cough
night sweats
The astute reader will no doubt pick up that these are the symptoms of every single one of the common cold viruses that infect millions of people all over the world every single year.
The odds are you’ve experienced these symptoms at least once or twice in the last year or so. This does not mean you had Omicron. It does not mean Omicron even exists.
Rather, it’s just a ploy to get you to follow government guidance and, in the words of the article:
“order a free PCR test as soon as possible”.
The government site for ordering PCR tests has already shut down due to millions of requests. We have repeated, ad infinitum, that these tests are scientifically meaningless, and return huge numbers of false positives.
Nevertheless, hundreds of thousands of PCR tests are being done on people with nothing but mild cold symptoms as we speak, and in these nasal swabs lies the incipient “Omicron wave”.
Then they’ll probably have the Prime Minister announce new restrictions… just after Parliament adjourns for the Christmas break, so they can’t be reviewed or voted on.
It’s the same old trick, again and again and again. Hopefully, people will stop falling for it soon.
Last week, I wrote about a second major study finding that natural immunity protects better against infection than the Pfizer vaccine. Both this study and the earlier one were from Israel, and while there’s every reason to believe the results generalise to other populations, it’s always good to have data from multiple countries.
We now have those data in the form of a study published by the Statens Serum Institut in Denmark. I can’t say the report itself is worth reading in full, since it’s written in Danish. But I’ve posted the key figure below. It shows protection against infection for three different groups – adjusting for age, sex, comorbidities, and time of year.
The orange line corresponds to people who’ve been previously infected but not vaccinated; the yellow line to those who’ve been previously infected and vaccinated; and the green line to those who’ve been vaccinated but not previously infected.
The y-axis gives the percentage reduction in the number of infections, compared to those who haven’t been vaccinated or previously infected. For example, a value of 90% means there would be only 10 infections for every 100 in the comparison group. The x-axis gives the number of days since the relevant event.
As you can see, vaccine-induced immunity wanes rapidly, beginning a few weeks after vaccination. And at the five month mark, protection is well below 50%. Natural immunity, by contrast, is robust: a full year after infection, protection is still above 70%.
Consistent with what the two Israeli studies found, hybrid immunity – conferred by the combination of vaccination and previous infection – is slightly better than natural immunity. However, the difference is small compared to that between natural and vaccine-induced immunity.
Evidence for the superiority of natural immunity is now robust. So while those who’ve already had Covid should be perfectly free to get vaccinated, there’s no obvious need for them to do so. The tricky part may be getting this message through to politicians.
The European Union database of suspected drug reaction reports is EudraVigilance, and they are now reporting 32,649 fatalities, and 3,003,296 injuries, following COVID-19 injections.
A Health Impact News subscriber from Europe reminded us that this database maintained at EudraVigilance is only for countries in Europe who are part of the European Union (EU), which comprises 27 countries.
The total number of countries in Europe is much higher, almost twice as many, numbering around 50. (There are some differences of opinion as to which countries are technically part of Europe.)
So as high as these numbers are, they do NOT reflect all of Europe. The actual number in Europe who are reported dead or injured following COVID-19 shots would be much higher than what we are reporting here.
The EudraVigilance database reports that through December 4, 2021 there are 32,649 deaths and 3,003,296 injuries reported following injections of four experimental COVID-19 shots:
From the total of injuries recorded, almost half of them (1,409,643) are serious injuries.
“Seriousness provides information on the suspected undesirable effect; it can be classified as ‘serious’ if it corresponds to a medical occurrence that results in death, is life-threatening, requires inpatient hospitalisation, results in another medically important condition, or prolongation of existing hospitalisation, results in persistent or significant disability or incapacity, or is a congenital anomaly/birth defect.”
A Health Impact News subscriber in Europe ran the reports for each of the four COVID-19 shots we are including here. It is a lot of work to tabulate each reaction with injuries and fatalities, since there is no place on the EudraVigilance system we have found that tabulates all the results.
Since we have started publishing this, others from Europe have also calculated the numbers and confirmed the totals.*
Here is the summary data through December 4, 2021.
Total reactions for the mRNA vaccineTozinameran (code BNT162b2,Comirnaty) from BioNTech/ Pfizer: 15,061 deaths and 1,399,513 injuries to 04/12/2021
38,170 Blood and lymphatic system disorders incl. 217 deaths
43,454 Cardiac disorders incl. 2,204 deaths
404 Congenital, familial and genetic disorders incl. 38 deaths
18,886 Ear and labyrinth disorders incl. 10 deaths
286,356 General disorders and administration site conditions incl. 1,544 deaths
971 Hepatobiliary disorders incl. 62 deaths
4,99 Immune system disorders incl. 30 deaths
33,416 Infections and infestations incl. 441 deaths
12,583 Injury poisoning and procedural complications incl. 180 deaths
23,958 Investigations incl. 159 deaths
12,472 Metabolism and nutrition disorders incl. 96 deaths
161,308 Musculoskeletal and connective tissue disorders incl. 114 deaths
650 Neoplasms benign malignant and unspecified (incl cysts and polyps) incl. 25 deaths
223,680 Nervous system disorders incl. 1,007 deaths
533 Pregnancy puerperium and perinatal conditions incl. 14 deaths
191 Product issues incl. 1 death
20,150 Psychiatric disorders incl. 60 deaths
4,093 Renal and urinary disorders incl. 63 deaths
15,594 Reproductive system and breast disorders incl. 2 deaths
38,722 Respiratory thoracic and mediastinal disorders incl. 817 deaths
49,877 Skin and subcutaneous tissue disorders incl. 53 deaths
1,533 Social circumstances incl. 6 deaths
1,499 Surgical and medical procedures incl. 26 deaths
27,179 Vascular disorders incl. 457 deaths
Total reactions for the COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson: 1,989 deaths and 105,819 injuries to 04/12/2021
1,029 Blood and lymphatic system disorders incl. 41 deaths
1,952 Cardiac disorders incl. 169 deaths
36 Congenital, familial and genetic disorders
1,080 Ear and labyrinth disorders incl. 2 deaths
72 Endocrine disorders incl. 1 death
1,415 Eye disorders incl. 7 deaths
8,743 Gastrointestinal disorders incl. 80 deaths
27,925 General disorders and administration site conditions incl. 533 deaths
130 Hepatobiliary disorders incl. 11 deaths
473 Immune system disorders incl. 9 deaths
4,676 Infections and infestations incl. 157 deaths
974 Injury, poisoning and procedural complications incl. 20 deaths
4,927 Investigations incl. 111 deaths
664 Metabolism and nutrition disorders incl. 50 deaths
15,331 Musculoskeletal and connective tissue disorders incl. 45 deaths
59 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 4 deaths
20,725 Nervous system disorders incl. 219 deaths
43 Pregnancy, puerperium and perinatal conditions incl. 1 death
32 Product issues
1,479 Psychiatric disorders incl. 17 deaths
443 Renal and urinary disorders incl. 26 deaths
2,249 Reproductive system and breast disorders incl. 6 deaths
3,799 Respiratory, thoracic and mediastinal disorders incl. 259 deaths
3,241 Skin and subcutaneous tissue disorders incl. 8 deaths
337 Social circumstances incl. 4 deaths
718 Surgical and medical procedures incl. 58 deaths
3,267 Vascular disorders incl. 151 deaths
*These totals are estimates based on reports submitted to EudraVigilance. Totals may be much higher based on percentage of adverse reactions that are reported. Some of these reports may also be reported to the individual country’s adverse reaction databases, such as the U.S. VAERS database and the UK Yellow Card system. The fatalities are grouped by symptoms, and some fatalities may have resulted from multiple symptoms.
Robert F. Kennedy, Jr.’s book attacking Anthony Fauci and the medical establishment has become a publishing sensation, spending more than a full week as the #1 Amazon bestseller and racking up over 2,600 reviews, 94% of them five-star.
Now after nearly a month of stunned silence, the American media is finally taking belated notice. This morning the Associated Press released a 4,000 word hit-piece harshly attacking the most prominent public figure in America’s much-vilified anti-vaxxing movement.
A great deal of effort had obviously been invested in this attack, and the byline of the named author was shared by five additional AP writers and researchers, underscoring the journalistic resources devoted to damaging the reputation of an individual who has obviously made such powerful enemies. But in reading the article, the phrase that came to my mind was “the Sounds of Silence” or perhaps the famous Sherlockian clue of “the Dog That Didn’t Bark.”
Almost half of the entire book under attack—around 200 pages—is devoted to the presenting and promoting the astonishing claim that everything we have been told about HIV/AIDS for more than 35 years probably amounts to a hoax. As I wrote last week:
Yet according to the information provided in Kennedy’s #1 Amazon bestseller, this well-known and solidly-established picture, which I had never seriously questioned, is almost entirely false and fraudulent, essentially amounting to a medical media hoax. Instead of being responsible for AIDS, the HIV virus is probably harmless and had nothing to do with the disease. But when individuals were found to be infected with HIV, they were subjected to the early, extremely lucrative AIDS drugs, which were actually lethal and often killed them. The earliest AIDS cases had mostly been caused by very heavy use of particular illegal drugs, and the HIV virus had been misdiagnosed as being responsible. But since Fauci and the profit-hungry drug companies soon built enormous empires upon that misdiagnosis, for more than 35 years they have fought very hard to maintain and protect it, exerting all their influence to suppress the truth in the media while destroying the careers of any honest researchers who challenged that fraud. Meanwhile, AIDS in Africa was something entirely different, probably caused mostly by malnutrition or other local conditions.
I found Kennedy’s account as shocking as anything I have ever encountered.
By any reasonable standard, Robert F. Kennedy, Jr. has now established himself as America’s #1 “HIV/AIDS Denier,” and prior to the Covid outbreak, AIDS had probably spent almost four decades as the world’s highest-profile disease, reportedly absorbing some two trillion dollars in research and treatment costs. So for someone to essentially claim that the disease doesn’t actually exist would seem the height of utter lunacy, on a par with Flat Earthism. Yet not a single word of this astonishing situation appears in the long AP article, that attacks Kennedy on almost all other possible grounds, fair or unfair. Did all six of the AP writers and researchers somehow skip over those 200 pages in Kennedy’s bestseller?
That large team of AP journalists seems to have spent at least ten days working on their lengthy article, mining Kennedy’s record for almost everything controversial they could possibly find, even highlighting a photograph that merely shows him standing next to Trump allies Roger Stone and Michael Flynn.
Surely these reporters consulted numerous leading figures in the medical establishment on the HIV/AIDS issue, yet not a single word on that incendiary topic was included in their 4,000 word denunciation.
Although ferocious attacks against Kennedy’s HIV/AIDS claims might naturally have been expected, perhaps certain aspects of the book caused the senior editors of the Associated Press to draw back and decide that discretion on this matter was the better part of valor. As I had explained:
However, the first endorsement on the back cover is from Prof. Luc Montagnier, the medical researcher who won a Nobel Prize for discovering the HIV virus in 1984, and he writes: “Tragically for humanity, there are many, many untruths emanating from Fauci and his minions. RFK Jr. exposes the decades of lies.” Moreover, we are told that as far back as the San Francisco International AIDS Conference of June 1990, Montagnier had publicly declared “the HIV virus is harmless and passive, a benign virus.”
Perhaps this Nobel Laureate endorsed the book for other reasons and perhaps the meaning of his striking 1990 statement has been misconstrued. But surely the opinion of the researcher who won a Nobel Prize for discovering the HIV virus should not be totally ignored in assessing its possible role.
I went on to note:
And he was hardly alone. Kennedy explains that the following year, a top Harvard microbiologist organized a group containing some of the world’s most distinguished virologists and immunologists and they issued a public statement, endorsed by three additional science Nobel Laureates, that raised the same questions:
It is widely believed by the general public that a retrovirus called HIV causes a group of diseases called AIDS. Many biomedical scientists now question this hypothesis. We propose a thorough reappraisal of the existing evidence for and against this hypothesis, to be conducted by a suitable independent group. We further propose that the critical epidemiological studies be designed and undertaken.
As Kennedy tells the story, by that point AIDS researchers and the mainstream media were completely in thrall to the ocean of government funding and pharmaceutical advertising controlled by Fauci and his corporate allies, so these calls by eminent scientists were almost entirely ignored and unreported. According to one journalist, some two trillion dollars has been spent on HIV/AIDS research and treatment over the decades, and with so many research careers and personal livelihoods dependent upon what amounts to an “HIV/AIDS industrial-complex,” few have been willing to critically examine the basic foundations of that empire.
Until a couple of weeks ago, I had never given any thought to questioning AIDS orthodoxy. But discovering the longstanding scientific skepticism of so many knowledgeable experts, including four Nobel Laureates, one of them the actual discoverer of the HIV virus, has completely shifted my perspective. I cannot easily ignore or dismiss the theories Kennedy presents… And in basic fairness to the author, he himself also repeatedly emphasizes that he can “take no position on the relationship between HIV and AIDS” but is simply disturbed that Fauci has successfully used his government funding and media clout to suppress an ongoing and perfectly legitimate scientific debate. According to Kennedy, his book is intended “to give air and daylight to dissenting voices.”
So the total silence of the article does certainly raise certain obvious suspicions. As I previously wrote:
Robert F. Kennedy, Jr. is a top figure in America’s much-vilified anti-vaxx movement and his book is becoming a major element of that cause. His strident attacks against pharmaceutical companies, medical orthodoxy, and Fauci have earned him numerous, powerful enemies. If his AIDS claims were really as ridiculous as they might seem, would they not have already become a lightning rod for attacks against him? Suppose that his anti-vaxx tome had devoted 200 pages to arguing that our world was secretly controlled by invisible 12-foot-tall Reptilians from another dimension. Surely Kennedy’s enemies would have unleashed a huge storm of media ridicule against him for that lunacy, thereby discrediting his critique of vaccination campaigns. Yet instead complete silence has greeted his AIDS claims, raising questions in my mind of whether the medical establishment suspects that it has a great deal to hide and that many of Kennedy’s accusations might be correct.
As an outside observer with no special expertise in these areas of medicine, I was impressed by much of the material that Kennedy marshaled in support of his unorthodox views on vaccines and Covid treatments, but found that the evidence he provided on HIV and AIDS was vastly more comprehensive and persuasive, while being backed by far more authoritative experts. But if as he argues, the truth about HIV and AIDS has been successfully suppressed for decades by the entire medical industry, we must necessarily become very suspicious about other medical claims, including those regarding Covid and vaccinations.
Unless the medical and media establishments swiftly and forthrightly challenges Robert F. Kennedy, Jr. on the issue of HIV/AIDS, any fair-minded observers must necessarily conclude they recognize that he is substantially correct. And if he is correct about AIDS, any shreds of remaining credibility in our public health authorities will surely be destroyed, while the longstanding theories of Berkeley Prof. Peter Duesberg will have been vindicated:
Angela Merkel’s successor in Germany has declared that there is nothing he won’t do to battle COVID, a stark statement given previous pledges to make compulsory vaccinations legal.
Chancellor Olaf Scholz used his first address to the nation in Germany to push vaccinations, declaring that they are the only way Germany can overcome the pandemic.
Scholz added that there would be “no red lines” in the battle against the current wave of COVID, which he declared to be fueled by unvaccinated citizens.
“We will pull every possible lever,” he continued, adding “It will get better. Yes, we will win the fight against this pandemic with the biggest determination. And, yes, … we will overcome the crisis.”
He added that “our society is not divided,” and referring to people opposed to vaccinations proclaimed “We will not put up with a tiny minority of uninhibited extremists trying to impose their will on our entire society.”
While claiming “We are listening. We are looking for debate,” Scholz stated “There is in Germany today . . . denial of reality, absurd conspiracy stories, wilful disinformation and violent extremism.”
“We will counter this with the means of our democratic constitutional state. Our democracy is a democracy capable of defending itself,” the Chancellor further warned.
On Sunday, Scholz stated that he supports vaccine mandates across Germany, noting that he intends to “vote for compulsory vaccination, because it is legally permissible and morally right.”
Germany recently recorded its highest COVID death toll for 9 months, despite having mask mandates and stringent rules in many regions that banned the unvaccinated from numerous venues.
The country is preparing to follow the example of Austria by imposing new lockdown measures that will exclusively apply to the unvaccinated.
It’s the 13th December 2021. In my video dated 11th December I detailed some of the health problems which face the gullible folk who have succumbed to the lies and misinformation shared so widely and enthusiastically by governments, the medical establishment and the mainstream media.
It has been established that there is much that no one yet knows about the covid-19 jabs and the eagerness of the Medicines and healthcare products regulatory agency in the UK to licence a product about which information appeared to be lacking has never been adequately explained. We do know however that, as I was the first to reveal, the MHRA received a huge sum of money from the Bill and Melinda Gates Foundation – which has financial links with jab producers such as Pfizer.
As far as the effect on the brain is concerned the big question is, can the lipid nanoparticles carry the mRNA jab across the blood brain barrier?
The blood brain barrier is a semi permeable barrier of cells which prevent some substances in the blood from crossing into the protective fluid around the central nervous system.
It is vital to know if this happens because if it does then all bets are off as to what might happen to the brain.
And after all, liquid nanoparticles are already used to deliver other drugs across the blood brain barrier.
If the LNPs carry the mRNA jab into the brain then the neurons, the brain cells, might be marked as foreign by the body’s immune system. And as more booster jabs are given the problem will get worse.
The worry is that brain cells might be targeted and killed by cytotoxic T cells.
It has now been established that mRNA has been found in all human tissues except the kidney. It has been found in heart, lung, liver, testicles – and brain. A Japanese study, for example, showed that the vaccine does end up in the brain.
Also worrying is the fact that researchers have called for studies to investigate any relationship between jabs and acute CNS demyelination.
How much damage will this do?
How long will it take before brain damage can be identified?
I don’t have the foggiest idea.
And nor does anyone else.
In a normal experiment with a new drug, doctors would be looking and checking all the possible problems before releasing the drug for widespread use.
But the covid-19 jabs are being rolled out to billions without any one having the faintest idea what will happen.
If you have been jabbed, the first certainty seems to be that the mRNA vaccine will enter your brain.
The second certainty is that the more covid jabs you have, the more dangerous this will be.
How many of your brain cells will die is something only time will tell. And children, of course, will be more vulnerable because they are more vulnerable anyway and because they are likely to live longer.
Some experts, advisors and regulators will tell you that the risks are small. But how can they know that? And what is small? They told us that the blood clotting problems were small.
In my view, having one of these jabs is the equivalent of taking a huge dose of LSD and waiting to see what happens. And hoping that you’re not going to end up like Peter Green for example.
And, remember, the covid-19 jabs don’t stop you getting covid-19 and they don’t stop you passing it on. According to the NHS’s own guidelines in the UK you can still get or spread covid-19 even if you have had three jabs.
The choice about whether or not to be jabbed should be yours.
But governments want to make these jabs compulsory.
If this jab were being given for a lethal disease with a 50% mortality rate then the risks might be worth taking. It’s not and they’re not.
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We all need to pray for the truth to be shared by the many, not just the few. Whatever your religion you need to pray because the people running this fraud respect only lies but, in the way that vampires fear sunlight, they fear the truth – it is your government’s greatest enemy and our only weapon. Finally, although it may feel like it at times, please remember that you are not alone. More and more people are waking up and once they are awake they don’t go back to sleep. – which means our numbers are growing daily.
If we are going to win this war then we have to fight hard and with determination and passion and the truth. Remember, this is primarily a propaganda and media war.
Distrust the government, avoid mass media and fight the lies.
Vernon Coleman’s no 1 bestselling book Endgame explains the awful truth behind the covid fraud and the global warming fraud – and explains where we are heading. Endgame is available from Amazon as a paperback and an eBook.
This strange and mildly disturbing illustration actually accompanies the article, one of many cases where the NYT betray the sinister undertones of their agenda via accompanying imagery.
Corona has vastly expanded the ranks of pandemic planners and public health botherers. Unless something is done, these people will destroy all of society in their radical pursuit of a few viruses.
Just a few words on “Omicron is a Dress Rehearsal for the Next Pandemic”, a New York Times article by Emily Anthes, a science journalist with ties to the World Economic Forum. It’s subtitled “America’s response to the variant highlights both how much progress we have made over the past two years — and how much work remains,” and it’s every inch as awful as you’d imagine.
In the piece, Anthes laments that the United States is “woefully unprepared for the challenges ahead, starting with the most fundamental of tasks: detecting the virus.” She quotes a microbiologist to complain that “We had a delay of one to two months before we were even able to identify the presence of [Omicron] … And by that time, it had already circulated widely between multiple states and from coast to coast.” She wastes many words on the necessity of “Testing, testing, testing”; here, apparently, America still needs vastly more capacity. She and her many scientist informants also want more gene sequencing to detect variants sooner. She’s sure that all of this is absolutely necessary, even though she doesn’t know why:
Scientists are finding more Omicron cases every day, and the variant could soon overtake Delta. What comes next — what we should aim for, even — is less clear. Should we spend the winter trying to stop every infection? Protecting the highest risk people from severe disease and death? Ensuring that hospitals are not overrun?
“One thing that we’ve lacked continuously through the pandemic is a goal,” said Emily Gurley, an epidemiologist at the Johns Hopkins Bloomberg School of Public Health. “We still don’t have that. Certainly, we don’t have that for Omicron.”
No realistic public health goal underpins this diagnostic mania, of course. People who test positive for Corona are sent home to suffer in untreated silence by themselves. Endlessly testing, tracing, sequencing, panicking and closing is, however, a goal in itself for people like Emily Gurley and all the other pandemicists Anthes gleefully quotes, from Eric Topol to Trevor Bedford to Ezekiel J. Emanuel. All of them want the Corona Circus to play on, and after it ends they hope for a sequel sometime soon. Never before have they enjoyed such personal and professional prominence.
Even if by some miracle all of this winds down tomorrow, this whole odious internationally networked enterprise of Virus Astrology, from virologers to sequencers to testers to planners to nudgers to vaccinators, won’t go away. They were a malign influence even before Corona, of course. In 2009, when we suffered under a small fraction of the Pandemicism that burdens us now, they succeeded in causing an international uproar over a mild strain of pandemic influenza. Now their ranks have been vastly expanded, and they are already hoping for the next opportunity to close our schools, lock us up at home and stick us full of needles.
The pandemicists are truly dangerous, and they will grind human civilisation into the dust unless we find some way of putting all of them out of work. They aren’t going to save anybody from the next pandemic; in the event it happens, they’ll just take advantage of the opportunity to expand their ranks still further and make all of our lives worse. And should novel viruses prove slow to materialise in the post-Corona era, they’ll get up to other tricks. Tricks like new and enhanced histrionics over every seasonal influenza outbreak. Tricks like the intentional release of more engineered viral pathogens to keep the grant funding flowing. Tricks like constant lunatic mass vaccination schemes against ever milder viruses. Still other tricks I haven’t considered. The pandemicists have to go.
Professor Lim, Chairman, JCVI COVID-19 subcommittee
Dr June Raine, Chief Executive, MHRARt
Hon Sajid Javid, Secretary of State for Health and Social Care
Professor Chris Whitty, Chief Medical Officer for England
Sir Patrick Vallance, Government Chief Scientific Adviser
Dr Jenny Harries, Chief Executive, UKHSA
Dear Professor Lim, Dr Raine, Mr Javid, Professor Whitty, Sir Patrick Vallance & Dr Harries,
URGENT RE:
(I) latest government guidance re myocarditis
(II) decision to offer a second dose of Pfizer to 12-15s
(III) reckless disregard for the benefits of natural immunity in children
As a group of senior scientists and clinicians, we wrote to you only two weeks ago regarding your decision to offer a second dose of the Pfizer COVID-19 vaccine to 16-17-year-olds despite lack of detailed safety data. We still await a reply, but are compelled to write again after this week’s UKHSA publication of guidance on myocarditis, coinciding with your latest unexpected advice to widen the age range for the second dose to include 12-15 year-olds. We also still awaiting a reply as to why the JCVI continue to recommend vaccination for those children who already have naturally-acquired immunity and for whom there is no possibility of any benefit from the COVID-19 vaccines.
I. Myocarditis guidelines
The following statements (in italics) from the UKHSA document require urgent clarification regarding our points (in red).
“myocarditis and pericarditis following vaccination is usually mild or stable and most patients typically recover fully without medical treatment”
This unsubstantiated assertion is not compatible with the statement made in the bullet point below. Unless these children had cardiac MRI scans and follow-up, it is impossible to state that they ‘typically recover fully’
“myocarditis – significant left ventricular (LV) fibrosis has been described in a high percentage of children admitted to hospital, with a small percentage of these having non-sustained ventricular tachycardia (VT)”
According to the authors, these children were not clinically distinguishable from children in other case series, also with an apparently ‘mild’ clinical course. The concerning findings on MRI were only discovered because the authors thoroughly investigated all children with serious VAEs.
“no follow-up data is available yet on hospitalised patients”
This point undermines the claim made in the first bullet point.
“the long-term consequences of this condition secondary to vaccination are yet unknown, so any screening recommendations need to be balanced against the frequency and severity of the disease with the aim to prevent complications, in particular of myocarditis (arrhythmias, long term myocardial damage or heart failure)”
As Pfizer have admitted, the children’s trials are too small to look for myocarditis, but long term studies are in progress due to report in 2025 Recommendations in paediatric patients: Why was there no consultation with the RCPCH?
“Where appropriate, thepatient should be seen face to face and this assessment should include their vital signs.”
When would it be ‘inappropriate’ to see face to face and check vital signs, in a child with any of the concerning symptoms listed?
“If patients have mild symptoms, they do not require referral to secondary care at this point.”
How would you expect a GP to determine whether myocarditis was ‘mild’ in the absence of an ECG and a Troponin level? How does such an approach match up with rigorous post-marketing surveillance of a vaccine still under emergency use authorisation?
(II) Decision to offer a second dose of Pfizer to 12-15s
There has been no new follow-up data disclosed since the JCVI decision to offer only one dose to 12-15s regarding the outcome for children with vaccine-induced myocarditis. The suggestion that the MHRA has seen no new adverse event reports of myocarditis, is perhaps not surprising given that the UK has not proceeded to a second dose known to be associated with a greatly increased risk. How does the JCVI look at the concerns outlined in the government’s own myocarditis guidance and reconcile them with their duty of care to First do no Harm?
A systematic study from Hong Kong linking all vaccinations to health records has revealed myocarditis occurring 1 in2,680 in young males after their second dose of Pfizer, and they have now dropped the second dose from their schedule. The latest FDA data similarly report 1 in 5000 for males age 16-17. How is it ethical to recommend a second dose to this cohort knowing the risks to the individual will far outweigh any benefits?
How will effective pharmacovigilance and real-time data be obtained on every child admitted with a diagnosis of myocarditis by vaccine status? How many child fatalities have you factored in as acceptable collateral damage resulting from your decision to recommend the second dose of this vaccine for a condition which poses no significant threat to this age group? The answer surely must be zero.
III. Naturally acquired immunity in children
Perhaps most pressing of all, why does the JCVI continue to disregard the obvious benefits of naturally acquired immunity? This has now been conclusively shown in adults to be much longer lasting and robust than that following vaccination . It is already known that children have good crossover immunity from previous coronaviruses, with excellent T-cell function. And it is widely recognised that their strong innate immune systems are the reason for Covid-19 being extremely mild in children. It is estimated that in England, 5.47 million 5-14-year-olds have already had SARS-CoV-2 infection (which represents 79% of the population of this age group). An international meta-analysis of re-infections post natural infection reported only 577 cases of reinfection from 22 countries over a 15-month period, including only 10 deaths, with not a single death in younger adults let alone in children. Numerous other publications have affirmed that naturally acquired immunity is robust, comprehensive and long-lasting.
Therefore, for the 80% of children who are already immune, there can be no benefit from vaccination and only the potential for serious or even life-threatening harm. For the 20% not yet infected, there are still unanswered questions about the potential for vaccination to interfere with the ability to mount a broad robust and long-lasting immunity and we risk committing these children to the theatre of ever more frequent boosters, each with its own risk of injury, which now seems to be the future for adults. Indeed, this becomes even more important with the new omicron variant. There is no point in vaccinating children with a vaccine which will cause immune imprinting to the Wuhan variant and will impede their ability to make antibodies to the new variants as they present.
We contend that any practitioner who chooses to vaccinate a child in the knowledge that they have recovered from SARS-CoV-2 infection, is in breach of their professional duty of care to put their patient’s best interest first. In addition. failure of the practitioner to disclose the full contents of the UKHSA Myocarditis guidance to the patient and parent would constitute a failure to obtain fully informed consent. See GMCGood Medical Practice Guidelines.
Yours sincerely,
Dr Rosamond Jones, MD, FRCPCH, retired consultant paediatrician
Professor Anthony J Brookes, Department of Genetics & Genome Biology, University of Leicester Professor David Livermore, BSc, PhD, Professor of Medical Microbiology, University of East Anglia
Professor Angus Dalgleish, MD, FRCP, FRACP, FRCPath, FMed Sci, Professor of Oncology, St Georges Hospital, London
Dr Theresa Lawrie, MBBCh, PhD, Director, Evidence-Based Medicine Consultancy Ltd, Bath
Dr Clare Craig, BMBCh, FRCPath, Pathologist
John Collis, RN, Retired specialist nurse practitioner
Professor Keith Willison, PhD, Professor of Chemical Biology, Imperial, London
Professor Richard Ennos, MA, PhD. Honorary Professorial Fellow, University of Edinburgh Professor John Fairclough FRCS FFSEM retired Honorary Consultant Surgeon
Lord Moonie, MBChB, MRCPsych, MFCM, MSc, House of Lords, former parliamentary under- secretary of state 2001-2003, former consultant in Public Health Medicine
Dr Roland Salmon, MBBS, MRCGP, FFPH, former Director, Communicable Disease Surveillance Centre, Wales
Dr John Flack, BPharm, PhD. Retired Director of Safety Evaluation, Beecham Pharmaceuticals 1980-1989 and Senior Vice-president for Drug Discovery 1990-92 SmithKline Beecham
Dr Alan Mordue, MBChB, FFPH. Retired Consultant in Public Health Medicine & Epidemiology
Dr Geoffrey Maidment, MD, FRCP, retired consultant physician
Dr Helen Westwood MBChB MRCGP DCH DRCOG, General Practitioner
Mr James Royle, MBChB, FRCS, MMedEd, Colorectal surgeon Dr Elizabeth Evans MA(Cantab), MBBS, DRCOG, Retired Doctor Dr Emma Brierly, MRCGP, General Practitioner
Dr Alan Black, MBBS, MSc, DipPharmMed, retired pharmaceutical physician
Mr Anthony Hinton, MBChB, FRCS, Consultant ENT surgeon, London
Dr Greta Mushet, MBChB, MRCPsych, retired Consultant Psychiatrist in Psychotherapy
Dr Kulvinder Singh Manik MBChB, MRCGP, MA(Cantab), LLM, Gray’s Inn
Dr Rohaan Seth, Bsc (hons), MBChB (hons), MRCGP, Retired General Practitioner
Mr Ian F Comaish, MA, BM BCh, FRCOphth, FRANZCO, Consultant ophthalmologist
Dr Sarah Myhill, MBBS, Dip NM, Retired GP, Independent Naturopathic Physician
Dr Christopher Exley, PhD, FRSB, Retired professor in Bioinorganic Chemistry
Dr David Critchley, BSc, PhD, 32 years in pharmaceutical R&D as a clinical research scientist. Dr Gerry Quinn, PhD. Postdoctoral researcher in microbiology and immunology
Dr Jonathan Engler, MBChB, LlB (hons), DipPharmMed
Dr Mark Bell, MBChB, MRCP(UK), FRCEM, Consultant in Emergency Medicine
Dr Zac Cox, BDS, LCPH, Holistic Dentist, Homeopath
Dr Elizabeth Burton, MBChB, retired general practitioner
Margaret Moss, MA (Cantab), CBiol, MRSB, Director, The Nutrition and Allergy Clinic, Cheshire
Julia Annakin, RN,
Dr Noel Thomas, MA, MBChB, DCH, DObsRCOG, DTM&H, MFHom, retired doctor
Immunisation Nurse Specialist
Dr Fiona Martindale, MbChB, MRCGP, GP in out of hours
Dr Branko Latinkic, BSc, PhD, Molecular biologist
Dr Jason Lester, MRCP, FRCR, Consultant Clinical Oncologist.
Dr Sam White, MBChB MRCGP, General Practitioner, Functional medicine practitioner
Dr Holly Young, BSc, MBChB, MRCP, Consultant Palliative Care Medicine
Dr David Bramble, MB ChB, MRCPsych, MD, Retired Consultant Child & Adolescent Learning Disability
Dr. Scott Mitchell, MBChB, MRCS, Associate Specialist, Emergency Medicine
Dr Peter Chan, BM, MRCS, MRCGP, General Practitioner, Functional medicine practitioner
Dr Stefanie Williams, Dermatologist
Dr Andrew Isaac, MB BCh, Physician, retired
Dr Christina Peers, MBBS, DRCOG, DFSRH, FFSRH, Menopause specialist
Dr Michael D Bell, MBChB, MRCGP, retired General Practitioner
Dr Livia Tossici-Bolt, PhD, NHS Clinical Scientist
Dr Carmen Wheatley, D Phil, Orthomolecular Oncology
Dr Ruth Wilde, MB BCh, MRCEM, AFMCP, Integrative & Functional Medicine Doctor
Dr David Morris, MBChB, MRCP(UK), General Practitioner
Dr Jayne LM Donegan, MBBS, DRCOG, DCH, DFFP, MRCGP, HMA, Integrative Medicine practitioner
Dr Franziska Meuschel, MD, ND, PhD, LFHom, BSEM, Nutritional, Environmental and Integrated Medicine
Governments around the world have encouraged and enforced a new form of segregation based on vaccine status. This is not only dangerously inhumane; there is no scientific basis for this.
There seems to be an underlying presumption here that the unvaccinated are unclean (regardless of natural immunity) and their presence will spread disease. What if, however, existing studies reveal that there is little to no difference between the COVID vaccinated and unvaccinated in terms of becoming infected, harboring the virus (viral load in the oral and nasopharynx), and transmitting it?
As it relates to Omicron, two recent small but interesting preliminary studies show that 80% of the omicron cases were double vaccinated. Wilhelm et al. reported on reduced neutralization of SARS-CoV-2 omicron variant by vaccine sera and monoclonal antibodies. “in vitro findings using authentic SARS-CoV-2 variants indicate that in contrast to the currently circulating Delta variant, the neutralization efficacy of vaccine-elicited sera against Omicron was severely reduced highlighting T-cell mediated immunity as essential barrier to prevent severe COVID-19.” Further, the CDC has reported on the details for 43 cases of COVID-19 attributed to the Omicron variant. They found that “34 (79%) occurred in persons who completed the primary series of an FDA-authorized or approved COVID-19 vaccine ≥14 days before symptom onset or receipt of a positive SARS-CoV-2 test result.”
As it relates to the vaccinated and unvaccinated being similar in terms of infection, viral load, and transmission capacity, and thus no underlying evidence to separate them societally, we specifically focus on and present (and based largely on Delta variant data) the body of evidence.
1) Salvatore et al. examined the transmission potential of vaccinated and unvaccinated persons infected with the SARS-CoV-2 Delta variant in a federal prison, July-August 2021. They found a total of 978 specimens were provided by 95 participants, “of whom 78 (82%) were fully vaccinated and 17 (18%) were not fully vaccinated…clinicians and public health practitioners should consider vaccinated persons who become infected with SARS-CoV-2 to be no less infectious than unvaccinated persons.”
2) Singanayagam et al. examined the transmission and viral load kinetics in vaccinated and unvaccinated individuals with mild delta variant infection in the community. They found that (in 602 community contacts (identified via the UK contract-tracing system) of 471 UK COVID-19 index cases were recruited to the Assessment of Transmission and Contagiousness of COVID-19 in Contacts cohort study and contributed 8145 upper respiratory tract samples from daily sampling for up to 20 days) “vaccination reduces the risk of delta variant infection and accelerates viral clearance. Nonetheless, fully vaccinated individuals with breakthrough infections have peak viral load similar to unvaccinated cases and can efficiently transmit infection in household settings, including to fully vaccinated contacts.”
3) Chia et al. reported that PCR cycle threshold (Ct) values were “similar between both vaccinated and unvaccinated groups at diagnosis, but viral loads decreased faster in vaccinated individuals. Early, robust boosting of anti-spike protein antibodies was observed in vaccinated patients, however, these titers were significantly lower against B.1.617.2 as compared with the wildtype vaccine strain.”
4) Israel, 2021 looked at Large-scale study of antibody titer decay following BNT162b2 mRNA vaccine or SARS-CoV-2 infection, and reported as “To determine the kinetics of SARS-CoV-2 IgG antibodies following administration of two doses of BNT162b2 vaccine, or SARS-CoV-2 infection in unvaccinated individuals…In vaccinated subjects, antibody titers decreased by up to 40% each subsequent month while in convalescents they decreased by less than 5% per month. Six months after BNT162b2 vaccination 16.1% subjects had antibody levels below the sero-positivity threshold of <50 AU/mL, while only 10.8% of convalescent patients were below <50 AU/mL threshold after 9 months from SARS-CoV-2 infection.”
5) In the UK COVID-19 vaccine Surveillance Report for week #42, it was noted that there is “waning of the N antibody response over time” and “that N antibody levels appear to be lower in individuals who acquire infection following 2 doses of vaccination.” The same report (Table 2, page 13), shows that in the older age groups above 30, the double vaccinated persons have greater infection risk than the unvaccinated, presumably because the latter group include more people with stronger natural immunity from prior Covid disease. See also UK PHE reports 43, 44, 45, 46 for similar data.
6) In Barnstable, Massachusetts, Brown et al. found that among 469 cases of COVID-19, 74% were fully vaccinated, and that “the vaccinated had on average more virus in their nose than the unvaccinated who were infected.”
7) Riemersma et al. found “no difference in viral loads when comparing unvaccinated individuals to those who have vaccine “breakthrough” infections. Furthermore, individuals with vaccine breakthrough infections frequently test positive with viral loads consistent with the ability to shed infectious viruses.” Results indicate that “if vaccinated individuals become infected with the delta variant, they may be sources of SARS-CoV-2 transmission to others.” They reported “low Ct values (<25) in 212 of 310 fully vaccinated (68%) and 246 of 389 (63%) unvaccinated individuals. Testing a subset of these low-Ct samples revealed infectious SARS-CoV-2 in 15 of 17 specimens (88%) from unvaccinated individuals and 37 of 39 (95%) from vaccinated people.”
8) Ignoring the risk of infection, given that someone was infected, Acharya et al. found “no significant difference in cycle threshold values between vaccinated and unvaccinated, asymptomatic and symptomatic groups infected with SARS-CoV-2 Delta.”
9) Gazit et al. out of Israel showed that “SARS-CoV-2-naïve vaccinees had a 13-fold (95% CI, 8-21) increased risk for breakthrough infection with the Delta variant compared to those previously infected.”
Dr Alexander holds a PhD. He has experience in epidemiology and in the teaching clinical epidemiology, evidence-based medicine, and research methodology. Dr Alexander is a former Assistant Professor at McMaster University in evidence-based medicine and research methods; former COVID Pandemic evidence-synthesis consultant advisor to WHO-PAHO Washington, DC (2020) and former senior advisor to COVID Pandemic policy in Health and Human Services (HHS) Washington, DC (A Secretary), US government; worked/appointed in 2008 at WHO as a regional specialist/epidemiologist in Europe’s Regional office Denmark, worked for the government of Canada as an epidemiologist for 12 years, appointed as the Canadian in-field epidemiologist (2002-2004) as part of an international CIDA funded, Health Canada executed project on TB/HIV co-infection and MDR-TB control (involving India, Pakistan, Nepal, Sri Lanka, Bangladesh, Bhutan, Maldives, Afghanistan, posted to Kathmandu); employed from 2017 to 2019 at Infectious Diseases Society of America (IDSA) Virginia USA as the evidence synthesis meta-analysis systematic review guideline development trainer; currently a COVID-19 consultant researcher in the US-C19 research group
Yesterday, in a statement to Parliament on the UK’s planned “vaccine passport”, Health Secretary Sajid Javid admitted the NHS Pass would require three shots for you to be considered “fully vaccinated”.
“Once all adults have had a reasonable chance to get their booster jab, we intend to change this exemption to require a booster dose,”
While many of us predicted this would be the case, it is the first time any British politician has actually said it out loud, and in front of parliament too.
All in all it seems pretty clear that, by the time 2022 rolls around, most of the Western world will require three shots in order to qualify as “fully vaccinated”.
It’s also clear that this won’t stop at three. Already, just last week, Pfizer were claiming they may need to “move up the timeline” for a fourth vaccine dose.
This change is being blamed on Omicron, with articles warning the “new variant” can “hit” the vaccinated. Fortune reports:
Omicron is making scientists redefine what it means to be ‘fully vaccinated’ against COVID
So, the third (and maybe fourth) doses are (allegedly) for Omicron…but that model can extend to perpetuity. In order to go to five, six or seven they’ll only need to “discover” more “new variants”.
It will just keep going and going.
But there is good news in all this, every time the powers-that-shouldn’t-be change the rules in the middle of the game, it’s a chance to knock people out of their media-induced hypnosis.
There are promising signs that millions of already-vaccinated will reject the booster. We can build on that.
So tell your single and double jabbed friends, try to open their eyes to the path they are starting down.
They may consider themselves “fully vaccinated”, but the government doesn’t, and never will.
mRNA vaccine protection from Covid is far weaker than natural immunity and declines very fast, according to a new study of almost 6 million people in Israel.
During the summer Covid wave, more than 140,000 Israelis who had been vaccinated but not received a booster shot became infected with Covid. Put another way, in just two months, about 1 out of every 20 vaccinated Israelis became infected with Sars-Cov-2.
Natural immunity – the protection following infection and recovery – lasts much longer, the study shows.
In fact, people who had already had Covid once had better protection from the virus more than a year later than people who had been vaccinated only three months before.
The gap was even larger in cases of severe infection.
Vaccinated people were more than five times as likely to develop severe infections than people with natural immunity. Only 25 out of roughly 300,000 Israelis with natural immunity developed severe Covid infections in the summer wave – compared to almost 1,400 vaccinated Israelis.
The difference did not result from gaps in age between vaccinated and recovered people. People over 60 benefitted even more from natural immunity relative to vaccination than did younger people.
The study also showed that giving people who had natural immunity a vaccine dose did little to lower rates of infection for them, raising the question of why they should ever be vaccinated.
Finally, the study offered a disturbing signal that vaccination may ultimately interfere with the development of lasting immunity in people who are infected after being vaccinated.
A booster shot did lower the risk of infection about to the level of peak protection from natural immunity – but because the study ended in September, it is impossible to know how long that protection may last.
All these findings come out of a database of Covid infections among almost 6 million Israelis in August and September, at the peak of the fourth Covid wave in Israel. The database contains information on essentially every Israeli over age 16 who was fully vaccinated or had previously had a Covid infection.
The paper, “Protection and waning of natural and hybrid COVID-19 immunity,” is currently available as a preprint at:
Oddly, the paper’s title does not mention waning of vaccine immunity, although the figures it presents make the severity of the problem clear. Such shyness is common among researchers presenting bad news about Covid vaccines – they will offer the data, but not highlight it.
Israel has exclusively used the Pfizer mRNA vaccine, began mass vaccinations before almost any other country, and has an excellent health care database. As a result, it has among the best information on the effectiveness of the shots. It offers far more complete data than the United States.
The vaccine failure over the summer in Israel – following apparent success in the spring – has presaged a similar pattern across the United States and Europe, and a similar desperate campaign for boosters.
In this paper, the researchers examined infection rates among five different groups of Israelis – those with natural immunity, those who had received boosters, those who were vaccinated but had not received boosters, those with natural immunity who had also received a vaccine, and those who had become infected after being vaccinated.
The researchers specifically excluded unvaccinated Israelis without natural immunity from the comparison because Israel has very few of them and they are “unrepresentative of the overall population.”
In other words, the researchers explicitly denied the validity of the comparison that vaccine advocates make when they compare Covid rates among vaccinated and unvaccinated people in places with high vaccination rates (a point I have been trying to make for months).
The researchers found that the highest rates of infection by far came in people who had been vaccinated at least six months before. They had a nearly 3 percent chance of being infected per month (the researchers present the figure as 89 per 100,000 “person-days.”)
Those people were four times as likely to be infected as newly vaccinated people. They were also seven times as likely to be infected as people who had natural immunity from an infection six to eight months before, and three times as likely as those who had natural immunity from an infection more than year before.
A single vaccination dose in people with natural immunity temporarily produced strong protection, the researchers found. But after six months, the advantage had faded to within the margin of statistical error. In other words, so-called hybrid immunity hardly appeared to exist after six months – natural immunity was once again providing the protection.
Nor did vaccination appear to stop severe disease.
Nearly every case of severe disease in the database – almost 1,400 of the roughly 1,600 cases – came in vaccinated but unboosted people. Boosters did appear to reduce severe disease significantly. Again, though, the study covered less than two months after the booster program began, when boosters should be at peak effectiveness.
Finally, the study showed that people who had been vaccinatedand then been infected and recovered were actually more likely to be infected again six months later than those who had only “pure” natural immunity.
That finding, though based on a small number of cases, adds to worrying data that mRNA vaccination may actually wrong-foot our immune systems in the long run and make it harder to build lifelong protection against Covid.
The label for Humira, once the best-selling drug in the world, lists its risks in plain print. One of them, in the label’s own words, is new “autoimmune” disease.
A drug prescribed for a condition labelled autoimmune carries a warning that it can cause a condition labelled autoimmune. That contradiction sits in every box, on a folded paper almost nobody reads.
My new book starts there.
No Autoimmunity: The Body Doesn’t Attack Itself
For seventy years, “your body is attacking itself, and we don’t know why” has ended the conversation for people diagnosed with multiple sclerosis, lupus, rheumatoid arthritis, Hashimoto’s, Type 1 diabetes, Crohn’s and psoriasis. More than eighty conditions now carry the autoimmune label. The diagnosis comes with a prescription for life. It almost never comes with a question about cause.
This book asks the question and answers it from the framework’s own records: its drug labels, its journals, its regulatory filings, and its own experiments. … continue
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