by Rhoda Wilson, Daily Expose:
Confidential documents reveal that within months of receiving the initial doses of the COVID-19 vaccine, some individuals are developing Antibody-dependent enhancement (ADE) and Vaccine-Associated Enhanced Disease (VAED).
And as if that weren’t alarming enough, official documents also prove that a mysterious form of Acquired Immune Deficiency Syndrome is also appearing in a disturbing number of recipients just five months after their initial injections.
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This may explain why, tragically, official Government records confirm that millions of people have mysteriously died suddenly in countries around the globe, including the United States, United Kingdom, Australia, Canada, and Europe, in the wake of the widespread distribution of the COVID-19 vaccines.
Antibody-dependent enhancement (ADE) and Vaccine-Associated Enhanced Disease (VAED). are serious adverse events that can occur after vaccination.
ADE and VAED can occur when an individual is exposed to a pathogen, such as the alleged Covid-19 virus, after receiving a vaccine that does not provide full immunity.
In these cases, the vaccine-induced antibodies may actually enhance the ability of the pathogen to infect cells, leading to more severe illness than if the individual had not received the vaccine.
When a vaccine causes ADE or VAED, it can have significant public health implications.
First and foremost, individuals who receive the vaccine and develop ADE or VAE may suffer from severe illness, and in some cases, even death.
One example of a previous vaccine that has been associated with ADE is the dengue vaccine. In many cases, individuals who received the dengue vaccine and were subsequently infected with the dengue virus experienced more severe illness and an increased risk of hospitalization and death.
Similarly, ADE has been reported in individuals who received vaccines for respiratory syncytial virus (RSV) and HIV.
One example of a bacterial infection that could potentially be worsened by ADE or VAE is streptococcus A (strep A) infection. Strep A is a type of bacteria that can cause a wide range of illnesses, including sore throat, pneumonia, and sepsis. You will have most likely seen in the mainstream news that Strep A infection is killing children left, right and centre this winter.
Covid-19 vaccination is the most likely reason for this, and the most important piece of evidence to support this fact is official Government reports that prove Covid-19 vaccination damages the immune system and has the potential to cause some new form of acquired immunodeficiency syndrome.
It is entirely possible that ADE and VAED can lead to immense immune system damage similar to that seen in acquired immune deficiency disorder (AIDS).
In individuals with AIDS, the immune system is severely compromised, making them more susceptible to infections and other diseases. Similarly, the occurrence of ADE or VAED can lead to damage to the immune system, potentially leading to a higher risk of infections and other diseases.
In addition to the risk of severe illness comparable to AIDS, ADE and VAED may also increase the risk of developing certain cancers. For example, some studies have suggested that ADE may increase the risk of developing certain types of lymphoma.
The occurrence of these adverse events has had devastating consequences for the individuals who develop them and confidential and official documents prove that ADE and VAED have occurred due to COVID-19 vaccines, leading to a new form of Acquired Immune Deficiency Syndrome and millions of excess deaths around the world.
Pfizer, the company hit with the largest healthcare fraud settlement and criminal fine to date in 2009; which also happens to be the same company behind the first ever mRNA gene therapy injection administered to the general public under emergency use authorisation in the name of Covid-19, has admitted in confidential documents, that it desperately tried to keep from going public, that its Covid-19 mRNA gene therapy may cause Vaccine-Associated Enhanced Disease.
The US Food and Drug Administration (FDA) attempted to delay the release of Pfizer’s COVID-19 vaccine safety data for 75 years despite approving the injection after only 108 days of safety review on December 11th, 2020.
The FDA originally said that they were prepared to release 500 pages per month in a response to the Freedom of Information (FOI) request filed on behalf of Public Health and Medical Professionals for Transparency (PHMPT) requesting the safety data.
Instead, in early January 2022, Federal Judge Mark Pittman ordered them to release 55,000 pages per month. They released 12,000 pages by the end of January.
Since then, PHMPT has posted all of the documents to its website.
One of the documents contained in the latest data dump is ‘reissue_5.3.6 postmarketing experience.pdf’. Table 5, found on page 11 of the document shows an ‘Important Potential Risk’, and that risk is listed as ‘Vaccine-Associated Enhanced Disease (VAED), including Vaccine-Associated Enhanced Reporatory Disease (VAERD)’.
Pfizer claimed in their confidential document that up to 28th Feb 2021, they had received 138 cases reporting 317 potentially relevant events indicative of Vaccine-Associated Enhanced Disease. Of these 71 were medically significant resulting in 8 disabilities, 13 were life-threatening events, and 38 of the 138 people died.
Of the 317 relevant events reported by 138 people, 135 were labelled as ‘drug ineffective’, 53 were labelled as dyspnoea (struggling to breathe), 23 were labelled as Covid-19 pneumonia, 8 were labelled as respiratory failure, and 7 were labelled as seizure.
Pfizer also admitted that 75 of the 101 subjects with confirmed Covid-19 following vaccination, had severe disease resulting in hospitalisation, disability, life-threatening consequences or death.
But Pfizer still definitively concluded, for the purposes of their submitted safety data to the Food and Drug Administration (FDA), the very data that was needed to gain emergency use authorisation and make them billions and billions of dollars, that ‘None of the 75 cases could be definitively considered as VAED’.
But Pfizer then went on to confirm that based on the current evidence, VAED remains a theoretical risk.
This confidential data proves that the Covid-19 injections should never have been granted emergency use authorisation, and should have been pulled from distribution by the FDA as soon as they sighted the figures.
And here’s how we know the ADE and VADE caused by Covid-19 vaccination have led to immune system damage comparable to AIDS.
