Read this oaks!
Go to this link for all the details:
The vaccine study designs do not test if the vaccine reduces severe covid-19 symptoms, including hospital admissions, ICU or death.
The tests are not designed to determine if the vaccine can interrupt virus transmission, either.
The tests are designed to see if the vaccine acts as prophylactic or therapeutic, but uses unreliable tests to manufacture fraudulent end points.
Even if the vaccine was an efficacious prophylactic, it carries risk of injury; administering the vaccine to healthy, uninfected people doesn’t make sense because there are better prophylactic and therapeutic strategies that do reduce actual symptoms if the need arises, preventing complications and death.
The worst part of the study design is that it is based on fraudulent diagnoses of SARS-CoV-2.
The doctors warn that “High cycle thresholds, or Ct values, in RT-qPCR test results have been widely acknowledged to lead to false positives.”
They instruct the vaccine makers to fix the study design to properly confirm infection.
“RT-qPCR-positive test results used to categorize patients as ‘COVID-19 cases’ in the trials and used to qualify the trial’s endpoints should be verified by Sanger sequencing to confirm that the tested samples in fact contain a unique SARS-CoV-2 genomic RNA,” the doctors wrote.
The vaccine makers are using fraudulent false positive diagnosis of covid-19 in the control group to make the vaccine look more efficacious. PLEASE NOTE OAKS.
Since high cycle PCR tests have been ruled to be 97 percent false positive, the end points collected in the Pfizer/ BioNTech studies could ultimately show that the vaccine is less than 3 percent efficacious, with potential to cause severe and lasting health effects, including but not limited to: infertility of women.(PLEASE NOTE OAKS!)
Maybe eugenics was the goal of these vaccines after all. Isn’t that right, Mr. Bill Gates?
By Lance D Johnson / References: 2020News.ed [PDF]; NCBI.NLM.NIH.gov
Vaccines have been proposed as one of the strategies for population control. Immunocontraceptive vaccines can be designed to inhibit: (1) production of gametes (sperm and egg); (2) functions of gametes, leading to blocking of fertilization; and (3) gamete outcome (pregnancy). Immunization with gonadotropin?releasing hormone coupled to different carriers has shown curtailment in the production of sperm with concomitant infertility in various species. Immunization of nonhuman primates and men with ovine follicle stimulating hormone has also resulted in reduced sperm output. Various spermatozoa?specific proteins such as FA1, PH?20, LDH?C4, SP?10, SP?17, sp56, SPAG9, and Izumo have been proposed as candidate antigens to develop contraceptive vaccines, which have shown efficacy in inhibiting fertility in different animal models. Immunization with zona pellucida glycoproteins?based immunogens also results in curtailment of fertility in a variety of species. However, ways to overcome the observed oophoritis associated with zona proteins immunization have yet to be discovered, a necessary step before their proposal for control of human population. No netheless, this is a very promising approach to control wildlife animal population. Phase II clinical trials of ??human chorionic gonadotropin?based vaccine in women have established the proof of principle that it is possible to inhibit fertility without any untoward side?effects by vaccination. Further scientific inputs are required to increase the efficacy of contraceptive vaccines and establish their safety beyond doubt, before they can become applicable for control of fertility in humans.Keywords: Fertilization, Hormones, Immunocontraception, Spermatozoa, Vaccine, Zona pellucida