Translate and edit by ：硫酸羟氯喹64
Since the global rollout of the COVID-19 vaccine last year, significant harm has been done to innocent victims. The damage caused by this vaccine is divided into three main phases: short-term (within one month): thrombosis, myocarditis, stroke, heart attack, spontaneous abortion, pulmonary embolism, anaphylaxis; mid-term (within one year): immune deficiency, antibody-dependent enhancement (ADE), impaired immune system, prion-like neurological damage; long-term (1-10 years): stinging protein-induced chromosomal damage, cancer, severe immunodeficiency, autoimmune diseases, infertility, etc.
Recently, a large number of vaccine recipients have been found to suffer from illness, permanent disability and even death due to early and mid-stage vaccine injuries, based on official clinical data, national databases of vaccine adverse events and exposure information from numerous media platforms. As vaccination rates increase, so does the incidence of cancer and may become the leading cause of death in the future.
According to Dr. EDDY BETTERMANN’s predictions, cancers caused by vaccines will arrive on schedule and most vaccinated Americans will be immunocompromised by Christmas. At the same time, cancerous tumors will begin to grow at an accelerated rate and will die within the next decade. From 1999 to 2019, the cancer death rate dropped from 2 in 1,000 to 1.5 in 1,000. but because full vaccination with the covid19 vaccine begins in 2021, the estimated number of cancer deaths will explode past 1 million by 2022 and the cancer death rate will remain high for the next decade. What’s even sadder is that we won’t see these real numbers until 2024.
Now that more than 204 million Americans have received more than two doses of the vaccine, this would be the greatest medical atrocity the government and drug companies have ever committed against humanity, and the sad thing is that no one is there to stop them. In fact, Big Pharma and crime syndicate leaders don’t want it to stop. The arrival of cancer then means they are in the final stages of their way through medical plunder and profiteering from chemotherapy and cancer surgery, while tens of millions of people are killed by the biological weapon of vaccines.
By the end of 2031, countless Americans will have their health severely compromised by cancer, and even if they don’t die from it, their deaths will be hastened by heart attacks, strokes and blood clots. All of this is due to government vaccination policies and the media’s false propaganda about “booster shots” from criminal pharmaceutical groups.
In Idaho, Dr. Ryan Cole of the Diagnostic Laboratory has reported a 20-fold increase in cancer among those who have been vaccinated.
According to the latest medical research, vaccines cause cancer and tumors for the following reasons:
First, studies have shown that the Pfizer vaccine alters the body’s innate immune response capacity and the production of inflammatory cytokines by immune cells.
Vaccination reduced the innate immune cell response to Toll-like receptor 4 (TLR4) TLR7 and TLR8. The vaccine also reduced the production of pro-inflammatory cytokines, tumor necrosis factor-α and interleukin-1β. Thus, the human immune system responds more to the fungal pathogen Candida albicans after vaccination)
Second, stinging proteins can inhibit DNA damage repair mechanisms to compromise systemic immunity.
Although there is no evidence that SARS-CoV-2 can infect thymocytes or bone marrow lymphocytes, spike-in proteins strongly hinder V(D)J recombination according to in vitro V(D)J reporter assays. Clinical observations also suggest that the risk of serious illness or death from COVID-19 increases with age, with the highest risk especially in the elderly, possibly because the spike protein of SARS-CoV-2 can weaken the DNA repair system in the elderly, thereby impeding V(D)J recombination and adaptive immunity. (V(D)J recombination is a mechanism of somatic cell reorganization that occurs only in developing lymphocytes in the early stages of T and B cell maturation. It leads to a highly diverse repertoire of antibodies/immunoglobulins and T cell receptors (TCRs) found in B cells and T cells, respectively. (This process is a defining feature of the adaptive immune system.)
In addition, the vaccine-generated stinger protein will bind to the p53 gene, known as the “guardian of the human genome”, rendering the p53 gene incapable of inhibiting cancer formation.
Coronaviruses (CoVs) are the largest RNA viruses ever discovered. SARS-nCoV-2 contains a spike (S) protein consisting of two subunits, S1 and S2. S1 helps the virus infect human cells by binding to human angiotensin-converting enzyme 2 (hACE2), and S2 mediates the membrane fusion process. There are strong interactions with p53 and BRCA. p53 and BRCA are well-known tumor suppressor proteins that regulate downstream genes in response to many cellular stresses and are frequently mutated in human cancers. Interestingly, we found that P53, BRCA-1 and BRCA-2 interact with the heptad repeat-2 region of the S2 subunit through the C-terminal structural domain. The PDB IDs of these proteins were extracted from the RCSB Protein Data Bank (PDB), which is more lethal for COVID-19 in people with underlying diseases, especially lung diseases, diabetes and cancer. Moreover, in terms of long-term side effects, the body will lose the ability to fight its own cancer, as has been demonstrated in current clinical case studies.
Latest clinical observation.
Lymph node enlargement at the injection site may be induced shortly after vaccination with an anti-SARS-CoV-2 mRNA vaccine. Although considered benign, according to the latest clinical study conducted in a series of 728 patients who received the BNT162b2 mRNA vaccine, 36% of subjects who received the first dose had hypermetabolic lymph nodes draining the vaccine injection site in the axillary and supraclavicular regions under PET/CT, and 54% in the study after the second dose had hypermetabolic 7% of the first dose vaccine recipients and 18% of the second dose vaccine recipients had enlarged hypermetabolic lymph nodes. Both differences were statistically significant, suggesting a greater effect on draining lymph nodes after the booster dose. Regarding the association with potential malignancy, hypermetabolic lymph nodes were considered malignant in 5% of patients, while no conclusion could be drawn regarding malignancy in 15% of vaccinees (including 16 patients with lymphoma). Interestingly, studies have also shown that AITL (angioimmunoblastic T-cell lymphoma) develops in the bodies of Pfizer vaccinated BNT162b2 recipients, and that half of the patients with this malignancy die within 5 years.
By observing vaccine-induced AITL progression in vaccinated patients, it was shown that AITL showed an alarming rate and magnitude of progression on two 18F-FDG PET-CT performed 22 days apart. Such rapid evolution is highly unexpected in the natural course of the disease. Since the mRNA vaccine is known to induce enlargement and hypermetabolic activity in the draining lymph nodes, it is reasonable to speculate that the vaccine was the trigger for the observed changes. Indeed, the axillary lymph nodes draining from the vaccine injection site showed higher increases in size and metabolic activity compared to the contralateral lymph nodes.
Vaccine-induced cancers will break out in a concentrated manner due to widespread mandatory vaccination, and as a result, countless families will be torn apart and many lives will be lost. The only solution once and for all is to turn grief into strength, stand up and fight, and hasten the demise of the Chinese Communist Party.
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