Forwarded from Fiona Rose Diamond (Fiona CoviLeaks)
🌍WORLD WIDE RALLY FOR FREEDOM - LONDON🌏
📣SATURDAY 18TH SEPTEMBER📣
A meaningful March through central and residential London on a route that’s not been taken before!
We rise for freedom with over 40 countries and 100 cities worldwide and multiple U.K. regions, one day, everyone together.
On the 18th September we take a stand against vaccinating our children and against vaccine passports. We welcome ALL to come TOGETHER and stand in unity with millions across the world.
We will stop along the way for real community outreach and engagement.
For all updates, route, meeting location and live location on the day follow:
t.me/londonofficialworldwiderally
#TogetherWeAreFree
#UnitedNotDivided
#SaveOurChildren
#WeWillAllBeThere
📣SATURDAY 18TH SEPTEMBER📣
A meaningful March through central and residential London on a route that’s not been taken before!
We rise for freedom with over 40 countries and 100 cities worldwide and multiple U.K. regions, one day, everyone together.
On the 18th September we take a stand against vaccinating our children and against vaccine passports. We welcome ALL to come TOGETHER and stand in unity with millions across the world.
We will stop along the way for real community outreach and engagement.
For all updates, route, meeting location and live location on the day follow:
t.me/londonofficialworldwiderally
#TogetherWeAreFree
#UnitedNotDivided
#SaveOurChildren
#WeWillAllBeThere
Table above shows “positive” Covid cases have predominantly, per the Australian govt, been in younger age groups where there is a much lower risk of complications or death.
Over 32 million tests have been undertaken in Australia with around 0.2% showing a “positive” result
Link to data: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
Over 32 million tests have been undertaken in Australia with around 0.2% showing a “positive” result
Link to data: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
Australia
Out of over 32 million Covid-19 tests performed in Australia the govt has recorded just over 56k as being “positive” and from those has recorded deaths with Covid-19 of 1,019. Table above gives detail by region.
The Australian authorities have said that of the 466 deaths now being reported following the Covid-19 injections they have so far reviewed 460 of them and believe that only 7 are due to the Covid-19 injection.
Link: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
Link to the ADR data: https://apps.tga.gov.au/Prod/daen/daen-entry.aspx
Out of over 32 million Covid-19 tests performed in Australia the govt has recorded just over 56k as being “positive” and from those has recorded deaths with Covid-19 of 1,019. Table above gives detail by region.
The Australian authorities have said that of the 466 deaths now being reported following the Covid-19 injections they have so far reviewed 460 of them and believe that only 7 are due to the Covid-19 injection.
Link: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
Link to the ADR data: https://apps.tga.gov.au/Prod/daen/daen-entry.aspx
Australia
Table shows the “Covid-19 deaths” recorded by the Australian govt, shows that 74% have been in those aged 80 years and older and 91% in those aged 70 yrs and over
Link: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
Table shows the “Covid-19 deaths” recorded by the Australian govt, shows that 74% have been in those aged 80 years and older and 91% in those aged 70 yrs and over
Link: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
👍1
Australia
Table above shows survival rate across all age groups per Australian govt of the 56k people testing “positive” for Covid-19.
As we know younger age groups are at virtually no risk. No detail found on any pre-existing conditions these individuals may have suffered with.
Link: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
Table above shows survival rate across all age groups per Australian govt of the 56k people testing “positive” for Covid-19.
As we know younger age groups are at virtually no risk. No detail found on any pre-existing conditions these individuals may have suffered with.
Link: https://www.health.gov.au/news/health-alerts/novel-coronavirus-2019-ncov-health-alert/coronavirus-covid-19-case-numbers-and-statistics#covid19-summary-statistics
Forwarded from Robin Monotti
WHY THE COVID19 INJECTIONS DO NOT PREVENT EITHER SEVERE INFECTION OR DEATH
There is a simple explanation, and a clear scientific explanation to follow.
Of the 29 tested options the immune system's killer T-cells have to recognise and develop immunity to the virus, 26 of them, therefore the vast majority, are not part of the spike protein, therefore not part of what the gene therapy can do or is meant to do.
It is not possible to gain immunity to the virus by targeting 3 parts out of 29 of the immune system's targets of choice.
The injections are aimed towards a tiny fraction of what the immune system recognises of SARSCoV2, and therefore the gene therapy is never going to stop the virus even if the computer simulation of the spike in the mRNA/genetic code were to match the real spike protein, which is highly unlikely.
Remember killer T-cells are part of the first immune response to the virus. If they are not able to recognize enough of it, they are not able to defend you from an infection.
Antibodies generally come in much later, once you are already infected, and they can't enter the virus to destroy it because they are much bigger than the virus, T-cells are smaller and can recognise many virus proteins not just one and can destroy virus infected cells. Therefore for full immunity you always need to look at T-cells, not antibodies.
One of the big deceptions is the focus on antibodies instead of T-cells when it comes to preventing infection: it's the other way round: T-cells and NK cells prevent infection, not antibodies.
Even when it comes to antibodies, the injections only aim to create antibodies to a computer simulated early genetic code for a spike protein of the first virus dating to January 2020, which probably did not fully correspond to the real spike protein then, let alone now with the mutations.
This means that when the antibodies wane as they always do in time and the virus is able to either overcome them, or even be enhanced by them (Antibody-dependent enhancement or ADE), there is nothing there ready to recognise the virus apart from those spike antibodies to prevent severe infection or even death. The opposite is the case after natural infection: 29 out of 29 recognisable immune system targets will be recognised by the T-cells and severe infection and death will be avoided.
Robin Monotti
This is the referenced scientific research explanation:
Unbiased Screens Show CD8+ T Cells of COVID-19 Patients Recognize Shared Epitopes in SARS-CoV-2 that Largely Reside outside the Spike Protein
"We observed broad reactivity to many SARS-CoV-2 proteins, including ORF1ab, S, N, M, and ORF3a (Figure 4A). Notably, only 3 of the 29 epitopes were located in the S protein. Most epitopes (15 of 29) were located in ORF1ab, and the highest density of epitopes were located in the N protein."
https://www.cell.com/immunity/fulltext/S1074-7613(20)30447-7
There is a simple explanation, and a clear scientific explanation to follow.
Of the 29 tested options the immune system's killer T-cells have to recognise and develop immunity to the virus, 26 of them, therefore the vast majority, are not part of the spike protein, therefore not part of what the gene therapy can do or is meant to do.
It is not possible to gain immunity to the virus by targeting 3 parts out of 29 of the immune system's targets of choice.
The injections are aimed towards a tiny fraction of what the immune system recognises of SARSCoV2, and therefore the gene therapy is never going to stop the virus even if the computer simulation of the spike in the mRNA/genetic code were to match the real spike protein, which is highly unlikely.
Remember killer T-cells are part of the first immune response to the virus. If they are not able to recognize enough of it, they are not able to defend you from an infection.
Antibodies generally come in much later, once you are already infected, and they can't enter the virus to destroy it because they are much bigger than the virus, T-cells are smaller and can recognise many virus proteins not just one and can destroy virus infected cells. Therefore for full immunity you always need to look at T-cells, not antibodies.
One of the big deceptions is the focus on antibodies instead of T-cells when it comes to preventing infection: it's the other way round: T-cells and NK cells prevent infection, not antibodies.
Even when it comes to antibodies, the injections only aim to create antibodies to a computer simulated early genetic code for a spike protein of the first virus dating to January 2020, which probably did not fully correspond to the real spike protein then, let alone now with the mutations.
This means that when the antibodies wane as they always do in time and the virus is able to either overcome them, or even be enhanced by them (Antibody-dependent enhancement or ADE), there is nothing there ready to recognise the virus apart from those spike antibodies to prevent severe infection or even death. The opposite is the case after natural infection: 29 out of 29 recognisable immune system targets will be recognised by the T-cells and severe infection and death will be avoided.
Robin Monotti
This is the referenced scientific research explanation:
Unbiased Screens Show CD8+ T Cells of COVID-19 Patients Recognize Shared Epitopes in SARS-CoV-2 that Largely Reside outside the Spike Protein
"We observed broad reactivity to many SARS-CoV-2 proteins, including ORF1ab, S, N, M, and ORF3a (Figure 4A). Notably, only 3 of the 29 epitopes were located in the S protein. Most epitopes (15 of 29) were located in ORF1ab, and the highest density of epitopes were located in the N protein."
https://www.cell.com/immunity/fulltext/S1074-7613(20)30447-7
Forwarded from Mike Yeadon
Robin,
That’s pretty close. But to add a slight refinement, the gene based vaccines end up stimulating production of circulating antibodies of the IgG class in blood.
Generally, the virus isn’t in the blood, but inside cells, within tissues, away from the blood vessels.
Natural infection presents the virus to the lining of the nasopharynx & upper airways, and results in (1) locally secreted IgA type of antibodies which live in the secretions lining your entire airway (indeed all outward facing mucosal layers) & are designed to bind up viruses which have just landed. It also stimulates T-cells capable of killing own cells in they’re infected.
You’re quite right, the blood IgG antibodies are not only in the wrong location (blood not tissues) but are also more of less excluded from the insides of cells, because antibodies are too large to enter cells.
The way the “natural killer” or NKT-cells, kill infected cells is by recognising flags taken from the virus & placed outside, essentially saying “SOS, I’ve been infected, please destroy me”.
And that’s what the NKT cell does.
Cheers
Mike
Best wishes
Mike
That’s pretty close. But to add a slight refinement, the gene based vaccines end up stimulating production of circulating antibodies of the IgG class in blood.
Generally, the virus isn’t in the blood, but inside cells, within tissues, away from the blood vessels.
Natural infection presents the virus to the lining of the nasopharynx & upper airways, and results in (1) locally secreted IgA type of antibodies which live in the secretions lining your entire airway (indeed all outward facing mucosal layers) & are designed to bind up viruses which have just landed. It also stimulates T-cells capable of killing own cells in they’re infected.
You’re quite right, the blood IgG antibodies are not only in the wrong location (blood not tissues) but are also more of less excluded from the insides of cells, because antibodies are too large to enter cells.
The way the “natural killer” or NKT-cells, kill infected cells is by recognising flags taken from the virus & placed outside, essentially saying “SOS, I’ve been infected, please destroy me”.
And that’s what the NKT cell does.
Cheers
Mike
Best wishes
Mike
Mario Draghi getting everyone used to the idea of compulsory "vaccinations" for all. Italy is Europe's laboratory, what happens there is meant to serve as a model for other countries.
https://www.reuters.com/world/europe/italy-plans-third-covid-vaccine-shots-most-fragile-health-minister-2021-09-02/
https://www.reuters.com/world/europe/italy-plans-third-covid-vaccine-shots-most-fragile-health-minister-2021-09-02/
Reuters
Italy may eventually make COVID vaccine shots compulsory for all, Draghi says
Italy may eventually make COVID-19 inoculations compulsory for everyone of eligible age, and plans to start administering booster vaccine shots later this month to vulnerable people, Prime Minister Mario Draghi said on Thursday.
us_covid19_vaccines_proven_to_cause_more_harm_than_good_based_on.pdf
377.6 KB
US COVID-19 "Vaccines" Proven to Cause More Harm than Good Based on Pivotal Clinical Trial Data Analyzed Using the Proper Scientific Endpoint,
“All Cause Severe Morbidity”
“All Cause Severe Morbidity”
Country which did not implement lockdowns or mandate face masks bans visitors from country with highest rates of injections which implemented both.
"Sweden is the second European Union (EU) country to ban Israeli visitors because of an increasing number of infections.
Portugal on Wednesday prohibited Israelis from entering the country, including vaccinated individuals and those able to provide proof of a negative coronavirus test."
https://www.i24news.tv/en/news/coronavirus/1630608492-sweden-bans-entry-for-travelers-from-us-israel-due-to-rising-covid-19-rates
"Sweden is the second European Union (EU) country to ban Israeli visitors because of an increasing number of infections.
Portugal on Wednesday prohibited Israelis from entering the country, including vaccinated individuals and those able to provide proof of a negative coronavirus test."
https://www.i24news.tv/en/news/coronavirus/1630608492-sweden-bans-entry-for-travelers-from-us-israel-due-to-rising-covid-19-rates
Media is too big
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Dr. Merritt completed an Orthopaedic Surgery Residency in the United States Navy and served 9 years as a Navy physician and surgeon before returning to Rochester, where she was the only woman to be appointed as the Louis A. Goldstein Fellow of Spinal Surgery.
Dr. Merritt has been in the private practice of Orthopaedic and Spinal Surgery since 1995, served on the Board of the Arizona Medical Association, and is past president of the Association of American Physicians and Surgeons.
Dr. Merritt has been in the private practice of Orthopaedic and Spinal Surgery since 1995, served on the Board of the Arizona Medical Association, and is past president of the Association of American Physicians and Surgeons.
1974: National Security Council Document 20506: Implications of Worldwide Population Growth for U.S. Security and Overseas Interests
This 1974 memorandum drafted by Henry Kissinger led directly to the unleashing of experimental vaccines on the unsuspecting public. It sighted countries as targets for "initial population reduction experimentation to be implemented around the year 2000".
They identified India, Bangladesh, Pakistan, Nigeria, Mexico, Indonesia, Brazil, Philippines, Thailand, Egypt, Turkey, Ethiopia & Columbia for study.
3 million Filipinos ages 12-48 were given a test vaccine that ruined their health. North American Black & Native American Women were each given the same vaccine resulting in sterility rates of 25% & 35% respectively.
https://www.hli.org/resources/exposing-the-global-population-control/
➡️ https://pdf.usaid.gov/pdf_docs/Pcaab500.pdf
It followed a 1972 report (Bulletin #47) issued by the World Health Organization which referred to an immune virus which would selectively destroy the Human T Cell System
This coincided precisely with a polio vaccination program in central Africa - shortly preceding the outbreak of Aids in Africa, America & elsewhere. The determining factor most common in Aids victims is the breakdown of the T Cell System in the body. Another coincidence.
This 1974 memorandum drafted by Henry Kissinger led directly to the unleashing of experimental vaccines on the unsuspecting public. It sighted countries as targets for "initial population reduction experimentation to be implemented around the year 2000".
They identified India, Bangladesh, Pakistan, Nigeria, Mexico, Indonesia, Brazil, Philippines, Thailand, Egypt, Turkey, Ethiopia & Columbia for study.
3 million Filipinos ages 12-48 were given a test vaccine that ruined their health. North American Black & Native American Women were each given the same vaccine resulting in sterility rates of 25% & 35% respectively.
https://www.hli.org/resources/exposing-the-global-population-control/
➡️ https://pdf.usaid.gov/pdf_docs/Pcaab500.pdf
It followed a 1972 report (Bulletin #47) issued by the World Health Organization which referred to an immune virus which would selectively destroy the Human T Cell System
This coincided precisely with a polio vaccination program in central Africa - shortly preceding the outbreak of Aids in Africa, America & elsewhere. The determining factor most common in Aids victims is the breakdown of the T Cell System in the body. Another coincidence.
Human Life International
Exposing the Global Population Control Agenda
NSSM-200, or the Kissinger Report, shows that U.S. government population control isn’t about reducing poverty – the ulterior motive is explicitly...
'Scientists started Aids epidemic' BBC News,
A polio vaccine using tissue from primates could have been behind the leap made by the human immunodeficiency virus - HIV - from apes and moneys to humans, a new book claims.
Professor Bill Hamilton, of Oxford University's department of zoology, said: "This theory, rather sadly, has gone from strength to strength. It's not proven by any means, but it's looking very strong."
Dr Hilary Koprowski, a doctor in Philadelphia produced the vaccine in the 1950s when the race was on to prevent a disease that was as feared in its time as cancer or Aids now.
Edward Hooper, author of The River, points to a correlation between the sites of mass inoculations using Dr Koprowski's vaccine in the late 1950s and the first recorded cases of Aids in the 1960s.
Three parts of the Democratic Republic of Congo - at the time the Belgian Congo and subsequently Zaire - were particularly affected."
http://news.bbc.co.uk/1/hi/health/431167.stm
A polio vaccine using tissue from primates could have been behind the leap made by the human immunodeficiency virus - HIV - from apes and moneys to humans, a new book claims.
Professor Bill Hamilton, of Oxford University's department of zoology, said: "This theory, rather sadly, has gone from strength to strength. It's not proven by any means, but it's looking very strong."
Dr Hilary Koprowski, a doctor in Philadelphia produced the vaccine in the 1950s when the race was on to prevent a disease that was as feared in its time as cancer or Aids now.
Edward Hooper, author of The River, points to a correlation between the sites of mass inoculations using Dr Koprowski's vaccine in the late 1950s and the first recorded cases of Aids in the 1960s.
Three parts of the Democratic Republic of Congo - at the time the Belgian Congo and subsequently Zaire - were particularly affected."
http://news.bbc.co.uk/1/hi/health/431167.stm
WHO, Bulletin 47, 1972:
"Certain viruses, notably the leukaemia viruses and some of those causing persistent infections, depress the host's ability to mount an antibody response to antigens, while other viruses may enhance the antibody response.
Cell-mediated immunity may also be depressed.
Another immunopathological manifestation of virus infection is immune-complex disease. When viruses or their antigens persist in the circulation they combine with specific antibody, and the resulting complexes lodge in various sites, especially the kidney.
Further combination with complement leads to the release of tissue-damaging substances. A third condition associated with virus infection is antibody-mediated immunologic injury. Both oncogenic and non-oncogenic viruses frequently induce new antigens on the surface of the cells they invade. When antibody attaches to these antigens in the presence of complement, the cells are destroyed."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480894/
"Certain viruses, notably the leukaemia viruses and some of those causing persistent infections, depress the host's ability to mount an antibody response to antigens, while other viruses may enhance the antibody response.
Cell-mediated immunity may also be depressed.
Another immunopathological manifestation of virus infection is immune-complex disease. When viruses or their antigens persist in the circulation they combine with specific antibody, and the resulting complexes lodge in various sites, especially the kidney.
Further combination with complement leads to the release of tissue-damaging substances. A third condition associated with virus infection is antibody-mediated immunologic injury. Both oncogenic and non-oncogenic viruses frequently induce new antigens on the surface of the cells they invade. When antibody attaches to these antigens in the presence of complement, the cells are destroyed."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480894/
PubMed Central (PMC)
Virus-associated immunopathology: animal models and implications for human disease: 1. Effects of viruses on the immune system…
The tissue damage caused by virus infection has been traditionally explained by the ability of viruses to multiply in cells and thereby injure or destroy them. Recent evidence suggests, however, that lesions may also be caused by the host's immune ...
WHO, Bulletin 47, 1972
"Part 2 of this memorandum describes further mechanisms whereby the interaction of a virus with the host's immune system may lead to tissue damage.
Cell-mediated immunity plays a vital role in promoting recovery from virus infections, but under some circumstances tissue damage may be caused by the reaction of immune cells with viral antigens.
When mice are infected with lymphocytic choriomeningitis virus neonatally or as adults while receiving immunosuppressive drugs, widespread invasion of cells is seen but there is little overt disease. If, however, normal adults are infected or if immune cells are transfused into tolerant mice, cell injury and death follow.
Viruses have long been suspected of contributing to the pathogenesis of autoimmune diseases. Antibodies directed against normal cell constituents have been reported in several virus infections. Viruses may conceivably unmask or release host antigens, alter host antigens and act as “helper determinants”, or perhaps in other ways provoke immune responses against normal body constituents.
The immunopathological manifestations caused by viruses may also be influenced by the host's genetic makeup. Certain observations indicate that, in addition to controlling susceptibility to virus infection, genetic factors partly determine the effectiveness of the immune response. The memorandum calls attention to the possible implications of these concepts and findings for clinical research."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480896/
"Part 2 of this memorandum describes further mechanisms whereby the interaction of a virus with the host's immune system may lead to tissue damage.
Cell-mediated immunity plays a vital role in promoting recovery from virus infections, but under some circumstances tissue damage may be caused by the reaction of immune cells with viral antigens.
When mice are infected with lymphocytic choriomeningitis virus neonatally or as adults while receiving immunosuppressive drugs, widespread invasion of cells is seen but there is little overt disease. If, however, normal adults are infected or if immune cells are transfused into tolerant mice, cell injury and death follow.
Viruses have long been suspected of contributing to the pathogenesis of autoimmune diseases. Antibodies directed against normal cell constituents have been reported in several virus infections. Viruses may conceivably unmask or release host antigens, alter host antigens and act as “helper determinants”, or perhaps in other ways provoke immune responses against normal body constituents.
The immunopathological manifestations caused by viruses may also be influenced by the host's genetic makeup. Certain observations indicate that, in addition to controlling susceptibility to virus infection, genetic factors partly determine the effectiveness of the immune response. The memorandum calls attention to the possible implications of these concepts and findings for clinical research."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480896/
PubMed Central (PMC)
Virus-associated immunopathology: animal models and implications for human disease: 2. Cell-mediated immunity, autoimmune diseases…
Part 2 of this memorandum describes further mechanisms whereby the interaction of a virus with the host's immune system may lead to tissue damage. Cell-mediated immunity plays a vital role in promoting recovery from virus infections, but under some circumstances…
WHO, Bulletin 47, 1972
WHO coordinated research on the role of animals in influenza epidemiology: introduction.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480856/
WHO coordinated research on the role of animals in influenza epidemiology: introduction.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480856/
PubMed Central (PMC)
WHO coordinated research on the role of animals in influenza epidemiology: introduction.
WHO, Bulletin 47, 1972
"These findings suggest that Hong Kong virus did not arise by mutation from a pre-existing human strain and that it probably arose by the selection of a genetic recombinant in a partially immune population. It is postulated that the recombinant was formed as the result of the mixed infection of an animal or bird with an animal or avian influenzavirus and a human A/Asian strain."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480853/
"These findings suggest that Hong Kong virus did not arise by mutation from a pre-existing human strain and that it probably arose by the selection of a genetic recombinant in a partially immune population. It is postulated that the recombinant was formed as the result of the mixed infection of an animal or bird with an animal or avian influenzavirus and a human A/Asian strain."
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2480853/
PubMed Central (PMC)
The origin of pandemic influenza
Serological tests, using antisera specific to the surface subunits of the viruses (e.g., antisera to the haemagglutinin subunits devoid of any antineuraminidase or anti-host antigen activity) showed that the haemagglutinin subunits of the Hong Kong virus…
More articles from Volume 4 of WHO Bulletin 47:
https://www.ncbi.nlm.nih.gov/pmc/issues/169482/
https://www.ncbi.nlm.nih.gov/pmc/issues/169482/