Covid Science Library

With 2.8% annual population cull, we can calculate the time taken to reach 25% 0.75 = (1 -0.028)^t log 0.75 = t x log 0.972 t = log 0.75 / log 0.972 t = 10.12 years If the cull began in January 2021, then at an estimated fall of 2.8% per year, it will reach 75% by February 2031 This assumes a constant rate with no further exposure to toxins.

Rough outline of an adverse reaction database

I have compressed the V-Safe Cardiac file to 25% to enable easier sharing

There should be measurable consistency between the three V Safe data releases concerning the frequencies of each symptom. So what I plan to do next is to do a symptom count (word count) for each data release and for each symptom related to the nightmare phenomenon. I will see if they correlate together - showing consistency.

13. INDIVIDUAL INFORMED CONSENT : Full informed consent must always be respected 14. PARENTAL CONSENT : Application of any drug to a child must require both parental and child consent, and show evidence that the child was not coerced and evidence that both the parent and the child received accurate information. 15. STATE CONSENT : The consent of local or state governments must be obtained before a drug can be administered. Federal consent is insufficient. 16. NATIONAL or FEDERAL CONSENT: The consent of a nations elected leaders must be obtained before a drug can be administered. International consent by unelected bodies is insufficient 17. INTERNATIONAL POLICIES : Any policy proposed by the UN or WHO must be subject to open review by member nations, states, individual experts and individual members of the public.

13. INFORMED CONSENT : Full informed consent must always be respected 14. PARENTAL CONSENT : Application of any drug to a child must require both parental and child consent, and show evidence that the child was not coerced and evidence that both the parent and the child received accurate information.

Vaccines are no more important for health than other medicines and so should not be exempt from the same safety testing as other medicines . To argue that they should be free of liability is to remove all responsibility for their safety . Millions have developed thrombosis when coerced into taking the Covid shot to keep their jobs. If liability protection had been removed then this rollout of a dangerous vaccine would never have occurred . Instead people would have used ivermectin and good hospital protocols. The danger is that in the event of future fabricated or deliberately created pandemics another dangerous vaccine will be pushed onto the public resulting in another round of mass deaths. Constitutional rights demand that the American people have full information rather than blank inserts, have full safety testing for gene editing vaccines instead of blank trial results ( aka Pfizer myocarditis trials) and liability for manufacturers and administrators of products that cause severe adverse effects. The people of America have a right and an expectation to be protected by their appointed government. However post injury liability is too late for the deceased or disabled victims, since their affliction is severe, irreversible and lifelong - what price can you put on being able to walk or see? So Constitutional rights also demand that full informed consent be maintained so that people can never again be coerced into taking or being injected with dangerous drugs . It must be made clear to employers that making any drug compulsory for employment is both illegal and also makes them responsible for the effects of that drug (as a condition of employment). PRE-MARKET TESTING 1. SAFETY TESTING : Vaccines must be subject to the same safety testing as regular medicines 2. EFFECTIVENESS TESTING : Any test used to detect a disease must first be assessed to determine its % of false positive results. This testing must be open to review and criticism - so censorship of any reviewer is forbidden 3. PEER REVIEW : Trial results must be reviewed critically, so censorship of any reviewer is forbidden. INFORMATION 4. INSERTS : Full information must be provided on drug inserts - including full ingredients, full RNA sequence and all reported adverse effects with their relative incidences (PRR scores). The ingredients must be made public - no trade secrets allowed. No publicly administered drug can be classified as a military countermeasure or military secret. And random samples of the drug must be made available for independent analysis - without foreknowledge of the manufacturer or distributor. 5. TRIAL RESULTS : Full trial results must be made public 6. SCIENTIFIC PAPERS : All papers concerning the effects of the drug should be made available in one place online, so the public can decide. There must be no censorship. Ongoing research must be made available, easy to find and easy to read. 7. PERSONAL TESTIMONIES : Censorship of sharing of personal testimonies on social media must be forbidden 8. INDEPENDENT MONITORING : Post marketing adverse event records must be independently collected (i.e. not under the control of anyone financed by pharma or in public private-public partnership with pharma) 9. REGULAR MONITORING UPDATES : Post marketing adverse events must be made known to the public on a regular monthly basis, so timely decisions can be made by the public. LIABILITY 10. MANUFACTURER LIABILITY : Manufacturers must be held liable for vaccine injuries just as they are held liable for injuries from any regular drug 11. EMPLOYER LIABILITY : Employers who make any drug a condition for employment must be subject to fines and/or prison, and made to compensate for injuries caused. 12. MEDICAL LIABILITY : Any administrator of the drug must provide evidence that they have fully informed the recipient of the adverse effects - including items listed in the INFORMATION section above. Failure to do so will render them liable to fines, loss of license. INFORMED CONSENT

Vaccines are no more important for health than other medicines and so should not be exempt from the same safety testing as other medicines . To argue that they should be free of liability is to remove all responsibility for their safety . Millions have developed thrombosis when coerced into taking the Covid shot to keep their jobs. If liability protection had been removed then this rollout of a dangerous vaccine would never have occurred . Instead people would have used ivermectin and good hospital protocols. The danger is that in the event of future fabricated or deliberately created pandemics another dangerous vaccine will be pushed onto the public resulting in another round of mass deaths. Constitutional rights demand that the American people have full information rather than blank inserts, have full safety testing for gene editing vaccines instead of blank trial results ( aka Pfizer myocarditis trials) and liability for manufacturers and administrators of products that cause severe adverse effects. The people of America have a right and an expectation to be protected by their appointed government. However post injury liability is too late for the deceased or disabled victims, since their affliction is severe, irreversible and lifelong - what price can you put on being able to walk or see? So Constitutional rights also demand that full informed consent be maintained so that people can never again be coerced into taking or being injected with dangerous drugs . It must be made clear to employers that making any drug compulsory for employment is both illegal and also makes them responsible for the effects of that drug (as a condition of employment). PRE-MARKET TESTING 1. SAFETY TESTING : Vaccines must be subject to the same safety testing as regular medicines 2. EFFECTIVENESS TESTING : Any test used to detect a disease must first be assessed to determine its % of false positive results. This testing must be open to review and criticism - so censorship of any reviewer is forbidden 3. PEER REVIEW : Trial results must be reviewed critically, so censorship of any reviewer is forbidden. INFORMATION 4. INSERTS : Full information must be provided on drug inserts. 5. TRIAL RESULTS : Full trial results must be made public 6. SCIENTIFIC PAPERS : All papers concerning the effects of the drug should be made available in one place online, so the public can decide. There must be no censorship. Ongoing research must be made available, easy to find and easy to read. 7. PERSONAL TESTIMONIES : Censorship of sharing of personal testimonies on social media must be forbidden 8. INDEPENDENT MONITORING : Post marketing adverse event records must be independently collected (i.e. not under the control of anyone financed by pharma or in public private-public partnership with pharma) 9. REGULAR MONITORING UPDATES : Post marketing adverse events must be made known to the public on a regular monthly basis, so timely decisions can be made by the public. LIABILITY 10. MANUFACTURER LIABILITY : Manufacturers must be held liable for vaccine injuries just as they are held liable for injuries from any regular drug 11. EMPLOYER LIABILITY : Employers who make any drug a condition for employment must be subject to fines and/or prison, and made to compensate for injuries caused. 12. MEDICAL LIABILITY : Any administrator of the drug must provide evidence that they have fully informed the recipient of the adverse effects - including items listed in the INFORMATION section above. Failure to do so will render them liable to fines, loss of license. INFORMED CONSENT 13. INFORMED CONSENT : Full informed consent must always be respected 14. PARENTAL CONSENT : Application of any drug to a child must require both parental and child consent, and show evidence that the child was not coerced and evidence that both the parent and the child received accurate information.