The principal of a Waldorf school in Semily has been sacked for disregarding the government regulation on compulsory antigen testing in schools. He was dismissed in a unanimous vote by the town council. The school faces a three million crown fine for disregarding the regulation.
According to hygiene officers sent to investigate the case, the school principal allowed untested children into the classroom after their parents refused to have them tested. Some children underwent testing.
The principal of any school should be a human being who is aware of his responsibility to pass to the next generations wisdom, knowledge, and finest thoughts of past ages and to teach them to think independently while observing the objective laws of the universe. He is expected to be strong enough to stand up against the insanity of the world, not to conform to it. If all principals were like Ivan Semecky the governments would be forced to act differently and teach differently, certainly more like Waldorf schools than secular schools, twenty years after the completion human genome project.
Those, who have kept the most basic self-preservation drive do not have such dilema but for the rest there is a rational way to create an alternative opinion, based on one’s logic and undisputable professional facts like the composition of vaccines. Alphabetically first – Covid 19 AstraZeneka:
STATEMENT OF ACTIVE SUBSTANCE(S) One dose (0.5 ml) contains not less than 2.5 × 108 infectious units
ethanol, sucrose, sodium chloride, disodium edetate (dihydrate), water for injections.
PHARMACEUTICAL FORM AND CONTENTS Suspension for injection 10 multidose vials (8 doses per vial – 0.5ml per dose) 4 ml
METHOD AND ROUTE(S) O
Possible side effects Like all medicines, this vaccine can cause side effects, although not everybody gets them. If you notice any side effects not mentioned in this package leaflet, please tell your doctor, pharmacist or nurse. Get urgent medical attention if you get symptoms of a severe allergic reaction. Such reactions may include a combination of any of the following symptoms:
feeling faint or light-headed
changes in your heartbeat
shortness of breath
swelling of your lips, face, or throat
hives or rash
nausea or vomiting
stomach pain. The following side effects may occur with COVID-19 Vaccine AstraZeneca: Very Common (may affect more than 1 in 10 people)
tenderness, pain, warmth, itching, or bruising where the injection is given
feeling tired (fatigue) or generally feeling unwell
chills or feeling feverish
feeling sick (nausea)
joint pain or muscle ache Common (may affect up to 1 in 10 people)
swelling or redness where the injection is given
being sick (vomiting) or diarrhoea Uncommon (may affect up to 1 in 100 people)
sleepiness or feeling dizzy
enlarged lymph nodes
excessive sweating, itchy skin or rash
Hematologic Thrombocytopenia and coagulation disorders A combination of thrombosis and thrombocytopenia, in some cases accompanied by bleeding, has been observed very rarely following vaccination with AstraZeneca COVID-19 Vaccine. This includes severe cases presenting as venous thrombosis, including unusual sites such as cerebral venous sinus thrombosis, mesenteric vein thrombosis, as well as arterial thrombosis, concomitant with thrombocytopenia. The majority of these cases occurred within the first seven to fourteen days following vaccination. Some cases had a fatal outcome. Healthcare professionals should be alert to the signs and symptoms of thromboembolism and or thrombocytopenia. Those vaccinated should be instructed to seek immediate medical attention if they develop symptoms such as shortness of breath, chest pain, leg swelling, persistent abdominal pain following vaccination. Additionally, anyone with neurological symptoms including severe or persistent headaches or blurred vision after vaccination, or who experiences skin bruising (petechia) beyond the site of vaccination after a few days, should seek prompt medical attention. As with other intramuscular injections, AstraZeneca COVID-19 Vaccine should be given with caution to individuals with thrombocytopenia, any coagulation disorder or to persons on anticoagulation therapy, because bleeding or bruising may occur following an intramuscular administration in these individuals.
Breast-feeding It is unknown if AstraZeneca COVID-19 Vaccine is excreted in human milk. A risk to the newborns/ infants cannot be excluded. The developmental and health benefits of breast feeding should be considered along with the mother’s clinical need for immunization against COVID-19. 7.1.3 Pediatrics The safety and efficacy of AstraZeneca COVID-19 Vaccine in children and adolescents (under 18 years of age) have not yet been established. No data are available.
The side effects of the other vaccines are very similar.
WHAT ARE THE INGREDIENTS IN THE PFIZER-BIONTECH COVID-19 VACCINE? The Pfizer-BioNTech COVID-19 Vaccine includes the following ingredients: mRNA, lipids ((4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate), 2 [(polyethylene glycol)-2000]-N,N-ditetradecylacetamide, 1,2-Distearoyl-sn-glycero-3- phosphocholine, and cholesterol), potassium chloride, monobasic potassium phosphate, sodium chloride, dibasic sodium phosphate dihydrate, and sucrose
WHAT ARE THE INGREDIENTS IN THE MODERNA COVID-19 VACCINE? The Moderna COVID-19 Vaccine contains the following ingredients: messenger ribonucleic acid (mRNA), lipids (SM-102, polyethylene glycol [PEG] 2000 dimyristoyl glycerol [DMG], cholesterol, and 1,2-distearoyl-sn-glycero-3-phosphocholine [DSPC]), tromethamine, tromethamine hydrochloride, acetic acid, sodium acetate trihydrate, and sucrose.
PS: Regarding the ‘ape story’ – were we ready to intellectually grasp that human genes are not destined to be contaminated with those of lower order, on the contrary, that they carry the formula of the man¨s unique possible evolution, we would be in a different situation.
Jeden z nejsvědomitějších praktických lékařů této planety Dr. Thomas se podílel na vědecké studii očkovaných vs neočkovaných dětí, která byla právě publikována a jeho lékařská komora ho suspendovala z výkonu lékařské praxe. Když u nás dochází k nedůvěře laické veřejnosti k povinnému očkování, stává se to právě pro tyto skutečnosti, že slyšíme o faktech, která jsou vědecky průkazná a ortodoxní medicína je zcela bez zábran označuje za nebezpečná, aniž by byla schopná svůj postoj vědecky dokázat. Ty studie, které uvádí jako důkaz prospěšnosti vakcín, jsou publikovány ve vážených lékařských časopisech, ale nemusejí procházet žádnými nezávislými peer review. Následující rozhovor přímo volá po mezinárodní podpoře MUDr Thomase na poli, které se stará o budoucí lidstvo této planety. Ze sedmi episod videového pořadu The Truth About Vaccines je patrné, že Dr Thomas neříká, že vakcíny nesnižují výskyt onemocnění jako například spalničky. On vysvětluje , že se dětem vracejí v dospělém věku formou pásových oparů, které jsou mnohem horším onemocněním než spalničky v dětství a že imunní systém děti, očkovaných podle vládou sestavených očkovacích plánů není tak odolný jako u neočkovaných dětí. Časovou úpravou (hep.B po narození) snížil ve své praxi rizikovost následků prakticky k nule. Počet doporučených vakcín v USA je kolem sedmdesáti, ale ve většině států jsou dobrovolné, takže lze jejich počet regulovat podle dané situace. U nás jich je podstatně méně, ale zase jsou plošné a povinné.
Chápe ortodoxní medicína, jak je pro laiky snadné přestat věřit lékařům přinejmenším v otázce očkování, když se musejí potýkat celý život například s astma nebo herpesy a potom najdou takovouto studii? Autor recenze si ani nedá práci pozorně si přečíst tu část Kochovy studie, která je dostupná, jakou váhu má tedy recenze na studii Thomas/Weiler, když není navíc vůbec podložená desetiletími praxe s očkováním?
The universe has spiritual dimensions and Noah’s Ark should not be taken only as a myth, but as a warning that the Universe is created on the principle of “The General Cosmic Harmony-of-Reciprocal-Maintenance-of-All- Cosmic-Concentrations'” and if violated, its re-establishment must follow. We are under 48 universal laws, for us mostly clandestine as we cannot see even the parallel between the oceans full of plastic bags and synthetic biology. It is quite amazing. I wonder what the plastic holy grail will do in human bodies….
We are finally here, after almost two years the first peer review publication of our analyzes comes out and many others will follow.
Here we try to summarize in these first pages, in a very discursive and non-technical way: what has been published, what validity it has and why it is important for our investigation of vaccines.
(The following pages to 3 are instead dedicated to a technical in-depth analysis, finally leaving the evaluation of the article itself to the experts in the sector)
What was published in “F1000 Research” 1 is the result of the initial part of the work carried out on behalf of the Corvelva Association by one of the laboratories in charge of the analyzes. We remember – because more than two years have passed since the beginning of this work and many other results have been added to the initial ones – that the first major issue that we found ourselves having to investigate was the abnormal quantity of human DNA found inside of the vaccines analyzed.
In both quadrivalent MPRV vaccines analyzed, quantities of 1 to 2.7 micrograms / vial were initially found (as per publication in question), and this led us to publicly and immediately denounce this result because, simply, it was not expected that a this amount of DNA was present in a vaccine.
Apart from the considerations and conclusions reached by the work, which are strictly technical and therefore understandable only to those who research in the field of metagenomics, what is observed in the graphs is that the two vaccine samples were found to contain a high percentage of readings of human DNA in addition to those expected of the genome of the varicella virus (Human alphaherpes virus 3), the only one detectable among the four, having been presented in the article a DNA-seq type analysis. However, we would like to underline that subsequently the quantities of DNA found and confirmed with the same method that is now validated here were even higher: up to 3.7 micrograms per vial, leading to a notable difference between lot and lot. In fact, in our report released on 22.12.2018 2 the results for further batches analyzed after those discussed in the article were reported , then further confirmed by interlaboratory analyzes which are still being published.
Therefore, what most interests us about this publication is that it validates the method used , puts an important point on the discussions on the “type” of analyzes carried out, and consequently confirms decisively all the work carried out subsequently with the NGS method. : the in-depth analysis on the type of genetic material contained, the presence of adventitious viruses, the great absence of attenuated viruses that should instead exist and the quantity instead out of control (also because very different from sample to sample) of the human DNA present, the mutant population , phages, DNA deriving from other species, and gradually all the results that you find summarized on our site. 3
Everything that, from the point of view of biological content, we have denounced in recent years, slavishly reporting the results to the control bodies, takes on a more relevant scientific connotation (even if, we repeat again, it was not peer-reviews that had to worry but the data presented, very serious in their content and in their possible implications for human health). However, now that the publication of the method has been done, we will demand to obtain the answers that have not yet arrived.
These results unquestionably confirm the presence of fetal DNA in Priorix tetra vaccines, in variable quantities between the various batches, indicating a poor quality control of these pharmaceutical products.
We also recall the report on the sequencing of the entire genome of MRC-5 published on the Corvelva website on 27.09.2019 4 in which the profound modification of this DNA is evident also in genes associated with the development of tumor pathologies (another data in progress publication).
The contaminating fetal DNA present in all samples analyzed in variable (therefore uncontrolled) quantities is up to 300 times higher than the limit imposed by the EMA for carcinogenic DNA (10 ng / dose, corresponding to the DNA contained in about 1000 cancer cells, obtained on the basis of a statistical calculation, while the precautionary limit is 100 pg / dose) limit that must necessarily also be applied to the fetal DNA that inevitably contaminates the Priorix Tetra.
It follows that this vaccine must be considered defective and potentially dangerous for human health, in particular of the pediatric population much more vulnerable to genetic and autoimmune damage due to immaturity in shelter systems.
As anticipated, the following is a more “technical” part and difficult to understand for non-experts, therefore we have decided, also for transparency, to attach to this document also the “Dossier EMA – NGS Discussion of the results obtained from the survey on the quality of vaccines “ . We had to extrapolate only the disclosable part, over 50 pages of the dossier compared to the 200 of the NGS, since much of the information contained and registered with the regulatory bodies must remain confidential. The harsh law of science provides that a data can be published in a journal only if unpublished and we, having several other publications in the works, do not want to put them at risk.
Finally, for the avoidance of doubt, we would like to mention, from the publication, the part of the “Funding Statement”:
“B1 and B2 metagenomic sequencing was funded by Corvelva (non-profit association, Veneto, Italy), under a service contract with the laboratory. No other contributions were involved in supporting the work. Funders played no role in study design, data collection and analysis, decision to publish, or manuscript preparation. “
The authors address the technical-methodological question of whether it is possible to use a parallel massive metagenomics approach with low reading coverage to characterize complex biological matrices. Estimates of diversity and abundance of species are calculated and the ability to reconstruct the metagenome de novo in terms of length and completeness is evaluated, in order to understand how much the decrease in sequencing depth, varied by randomly sub-sampling the sequencing readings, can The results show that the diversity indices of prokaryotic, eukaryotic and viral complex communities can be accurately estimated with 500,000 reads or less, although particularly complex samples may require 1,000,000 reads. In reverse,
Among the various, and very different, complex matrices subjected to massive metagenomic analysis, two biological medicines were included, i.e. two different batches of live attenuated MPRV vaccine used for immunization against measles, mumps, rubella and chickenpox in children. DNA was extracted from the vaccines, genomic libraries were then built using standard commercial protocols and massive sequencing was carried out with Illumina technology.
Apart from the considerations and conclusions reached by the work, which are strictly technical and therefore understandable only to those who research in the field of metagenomics, what is observed in the pie charts contained in the ‘Extended data’ (https://osf.io/wq395/ samples B1 and B2) is that the two vaccine samples were found to contain a high percentage of human DNA readings in addition to those expected from the genome of the varicella virus (Human alphaherpes virus 3), the only detectable among the four, since a DNA-seq type analysis was presented in the article.
71% of the readings in one lot and 88% in the other are of human origin, presumably from the MRC-5 fetal cell line ( remember that subsequent analyzes confirmed that the line is MRC5 ) in which live attenuated rubella and chickenpox viruses are grown during vaccine preparation. Furthermore, as happened in the different batches of the same MPRV vaccine tested by Corvelva between 2017 and 2019, the amount of DNA extracted is of the order of a microgram.
In vaccine batches tested with the same protocols and technology reported in the materials and methods of the article, the quantities detected ranged between 1 and almost 3 micrograms per vial, quantities varying from one batch to another, but always significant.
In the report disclosed by Corvelva on 22.12.2018, the following results were reported for further batches analyzed after those discussed in the article , then further confirmed by interlaboratory analysis still being published:
Priorix Tetra lot. A71CB205A (June 2018) – DNA analysis
Priorix Tetra lot. A71CB256A (December 2018) – DNA analysis
The measurement of the DNA concentration with QuBit fluorometer showed that lot A71CB205A, contains a quantity of gDNA of 1.7 µg total per 0.5mL dose, calculated as follows: 9.41ng / µl (concentration determined at QuBit) x 45 (volume of resuspension DNA final after extraction, expressed in microliters) x 4 (the starting volume subjected to the extraction procedure is ¼ of the volume of the dose contained in the entire vial equal to 0.5mL).
The measurement of the DNA concentration with QuBit fluorometer showed that lot A71CB256A, contains a quantity of gDNA of 3.7 µg total per 0.5mL dose , calculated as follows: 40.8 ng / µl (concentration determined at QuBit) x 55 (volume of resuspension final DNA after extraction expressed in microliters) x 5/3 (the starting volume subjected to the extraction procedure was 300 µl on 500 µl of suspension).
The human DNA found in this lot is approximately 8 to 1 relative to chickenpox DNA (see results below of the DNA fragment classification-seq, which shows that 88% of the total sequenced DNA fragments are human origin, and 11% are from the varicella virus genome). Considering that NGS is a quantitative technology, the fluorimetric quantification of the total DNA extracted from the vaccine (e.g. lot. A71CB256A = 3.7 micrograms per dose), associated with the relative quantification consideration made above (8: 1), allows us to say that human DNA could be about 2.9 micrograms per dose , compared to about 740 nanograms of chickenpox DNA. It is also plausible thatat least a portion of the high molecular weight DNA that is seen on the gel may be high molecular weight human DNA.
The quantity of RNA contained in the vial of vaccine lot A71CB256A was found to be about 200ng .
The RIN equal to 8 indicates an excellent quality RNA and an intact eukaryotic RNA, being present both the 18S and 28S peaks typical of eukaryotic RNA.
The answers to our questions forwarded to the regulatory agencies over time are of great importance. Currently, the agencies have not yet answered the questions regarding the results of the full analyzes delivered to the EMA and AIFA.
Extract from the EMA’s answer to our question about the safety of mrc-5 residues in the priorix tetra vaccine (EMA request reference ask-43967 3 august 2018) – “Based on published information, Priorix Tetra contains viral strains produced separately in chicken embryo cells (mumps and measles) or human MRC-5 diploid cells (rubella and chicken pox). The cell lines used for Priorix Tetra include human diploid cell lines that cannot divide continuously. Note that, according to the European Pharmacopoeia, MRC-5 diploid cell lines are not tumorigenic, as demonstrated by decades of use and control, and therefore an upper limit for MRC-5 cell DNA does not apply “
To date we have not been provided with evidence (neither in terms of product quality analysis certificates, nor scientific reference literature for the EMA) of these controls ensuring that it is appropriate not to apply an upper limit.
In the FDA guideline “Guidance for Industry: Characterization and Qualification of Cell Substrates and Other Biological Materials Used in the Production of Viral Vaccines for Infectious Disease Indications” 6 it is reported that:
a diploid cell strain should always remain diploid. If these characteristics are not stable, it must be demonstrated that the instability does not adversely affect the production or conformity of the product.
for widely used human diploid cell strains, such as MRC-5 and WI-38 cells, measurement of residual DNA may not be necessary because we do not consider residual DNA from these human diploid cells to be a safety concern
residual DNA for non-tumorigenic continuous cells, such as low pass VERO cells, should be limited to less than 10 ng / dose for parenteral inoculation as recommended by WHO
And in the WHO guideline “Annex 3 – Recommendations for the evaluation of animal cell cultures as substrates for the manufacture of biological medicines and for the characterization of cell banks. Replacement of Annex 1 of the WHO technical report series, No. 878 ” 7 is added: (…) considerable experience has been accumulated on the cytogenetics of WI-38 and MRC-5 since the 1960s
and in support of this experience, the following articles are listed:
Jacobs JP. Updated results on the karyology of the WI-38, MRC-5 and MRC-9 cell strains. Developments in Biological Standardization, 1976, 37: 155–156.
Jacobs JP. et al. Guidelines for the acceptability, management and testing of serially propagated human diploid cells for the production of live virus vaccines for use in man. Journal of Biological Standardization, 1981, 9: 331–342.
Petricciani JC et al. Karyology standards for rhesus diploid cell line DBS-FRhL-2. Journal of Biological Standardization, 1976, 4: 43–49.
Schollmayer and et al. High resolution analysis and differential condensation in RBA-banded human chromosomes. Human Genetics, 1981, 59: 187–193.
Rønne M. Chromosome preparation and high resolution banding techniques: a review. Journal of Dairy Science, 1989, 72: 1363–1377.
It can be clearly observed that the reference literature, to argue that the diploid cells used for the production of vaccines are safe from the point of view of genetic stability, is obsolete . The first genetic anomalies were already found 40 years ago, considered negligible for the safety of vaccines, and from what is reported in the WHO guideline, since then no updates have been made with new sequencing technologies, in particular in NGS, which is also economical. and rapid, with the consequence that in the vaccines administeredfor decades the presence of DNA progressively more and more genetically modified and in uncontrolled quantities has been allowed by agencies. In this regard, see the report on the sequencing of the entire genome of MRC-5 published on the Corvelva website on 27.09.2019 8 in which the profound modification of this DNA is evident also in genes associated with the development of tumor pathologies. (data being published)
Below is an extract from the letter from Dr. T. Deisher, a world expert in the therapeutic use of stem cells and gene therapy, which underlines the concern of the risks associated with the use of vaccines contaminated with residues. of human fetal cells:
Dr. T. DEISHER (letter to the rulers – April 8, 2019) 9 – (…) injecting our children with human fetal DNA contamination carries the risk of causing two well-established pathologies:
insertional mutagenesis: human fetal DNA embeds itself into the baby’s DNA causing mutations. Gene therapy using homologous recombination of small fragments has shown that amounts as small as 1.9 ng / mL of DNA fragments result in genome insertion of stem cells in 100% of injected mice. Levels of human fetal DNA fragments in our children after vaccination with MMR, VARIVAX (varicella) or hepatitis A vaccines reach levels above 1.9 ng / mL.
autoimmune disease: fetal human DNA stimulates the immune system’s reaction to attack the body of the boy / girl.
Our results greatly reinforce the experimental observations of Dr. Deisher and above all the fact that the contaminating fetal DNA present in all the samples analyzed in variable (therefore uncontrolled) quantities is up to 300 times higher than the limit imposed by the EMA for Carcinogenic DNA (10 ng / dose, corresponding to the DNA contained in about 1000 cancer cells, obtained on the basis of a statistical calculation, while the precautionary limit is 100 pg / dose) limit that must necessarily also be applied to fetal DNA which inevitably contaminates the Priorix Tetra.
It follows that this vaccine must be considered defective and potentially dangerous for human health, in particular of the pediatric population much more vulnerable to genetic and autoimmune damage due to immaturity in shelter systems.
Russia won the race to develop the first vaccine against the novel coronavirus. The United States has responded by slapping sanctions on a Russian research facility involved in creating it.
The U.S. government has blacklisted several Russian scientific institutes, including the Russian Defense Ministry’s 48th Central Research Institute, which has worked with other non-military medical centers to develop and test the world’s first Covid-19 vaccine.
In April, a Russian company sent ventilators to the United States as a form of humanitarian aid, to help overwhelmed hospitals treat coronavirus patients. It was later revealed that this Russian firm had been under U.S. sanctions since 2014.
State-Led Research Beats US Model
The Russian government announced this August that it had registered the world’s first Covid-19 vaccine, called Sputnik V.
Sputnik V was developed by the Russian Health Ministry’s Gamaleya Research Institute of Epidemiology and Microbiology. This scientific facility created the vaccine in a joint research project with the Russian Defense Ministry’s 48th Central Research Institute.
On Aug. 27, the U.S. Commerce Department imposed sanctions on Russia’s 48th Central Research Institute, blacklisting the scientific body.
While Russia took a state-led approach to create a coronavirus vaccine, the Trump administration announced a “public-private partnership” in May. The program, called “Operation Warp Speed,” saw the U.S. government dole out billions of tax dollars to Big Pharma companies.
The Trump administration awarded massive contracts to private corporations like Novavax, Pfizer, and Moderna, while Trump reportedly offered “large sums of money” for exclusive rights to a vaccine being developed by a German firm so it could be sold for profit.
But the U.S. public-private partnership was unable to develop a vaccine before foreign countries with government-led research efforts did. Besides Russia, a state-owned Chinese company says its vaccine will be ready by the end of 2020, while Cuba is doing clinical trials for a vaccine of its own.
US Blacklists Russian Research Centers
The U.S. Department of Commerce’s Bureau of Industry and Security announced a series of new sanctions measures on Russian research centers in the U.S.government’s federal register on Aug. 27.
Washington accused the blacklisted institutes of being associated with Russian chemical and biological weapons programs. The Kremlin denied this, calling the accusation “absolute nonsense.”
Russian research institutions sanctioned by the U.S. government on Aug. 27, 2020.
A spokesperson for the Russian government called the decision “the sanctions theater of the absurd.” A Kremlin press release blasted Washington for being unable to “live without sanctions and without declaring restrictions for anyone every day.”
“Given the scientific research of one of the institutes [which is engaged in developing Russia’s coronavirus vaccine] we cannot rule out that this is another example of uncovered and rampant non-competitive struggle,” said the Russian government spokesperson, Dmitry Peskov.
The U.S. government’s media arm, Radio Free Europe / Radio Liberty (RFE/RL), accused these Russian research facilities of developing chemical and biological weapons.
RFE/RL explained, “Formally, the move imposes new licensing restrictions on U.S. companies that seek to do business with the blacklisted companies in Russia or elsewhere.”https://platform.twitter.com/embed/index.html?dnt=true&embedId=twitter-widget-0&frame=false&hideCard=false&hideThread=false&id=1298984519035318274&lang=en&origin=https%3A%2F%2Fconsortiumnews.com%2F2020%2F08%2F28%2Fus-sanctions-russian-research-institute-that-developed-covid-19-vaccine%2F&theme=light&widgetsVersion=223fc1c4%3A1596143124634&width=550px
Russian state media noted that, in addition to being used to conduct clinical trials for the Covid-19 vaccine, the Defense Ministry’s newly blacklisted 48th Central Research Institute is “where vaccines against Ebola and Middle East Respiratory Syndrome (MERS), as well as a universal flu vaccine, had been studied and successfully tested.”
The U.S. sanctions were imposed on the following Russian research institutions:
33rd Scientific Research and Testing Institute
48th Central Scientific Research Institute, Kirov
48th Central Scientific Research Institute, Sergiev Posad
48th Central Scientific Research Institute, Yekaterinburg
State Scientific Research Institute of Organic Chemistry and Technology
As the U.S. Commerce Department blacklisted these Russian research facilities, it imposed additional sanctions on two dozen Chinese institutions — mostly construction, technology, and communications companies — accusing them of “engaging in activities contrary to U.S. national security interests.”
Ben Norton is a journalist and writer. He is a reporter for The Grayzone, and the producer of the “Moderate Rebelspodcast,” which he co-hosts with Max Blumenthal. His website is BenNorton.com, and he tweets at @BenjaminNorton.
While our nation was busy spending a considerable amount of time discussing racial inequalities (as we should) or whether or not public schools and colleges were going to open or start online, or debating the upcoming national political conventions, our federal government, specifically, the Secretary of Health and Human Services (HHS) issued his 3rd amendment to The Public Readiness and Emergency Preparedness Act (PREP).
The Act was first enacted this year by a declaration from the Secretary of HHS on March 10, 2020.
The 3rd amendment, issued on August 24th, 2020, allows pharmacists to administer vaccines to children ages 3-18. Many states had previously established restrictions on who could administer childhood vaccinations.
I must admit that this announcement slipped past me last week. I was alerted to it when talking with a parent advocate one evening. I could not believe it and thought it must be just for a specific state.
Later, I searched the internet to find a few articles dated August 19th, 20th and 21st. The Federal Register listed the action on Monday, August 24, 2020. 
I remember my dad who was a pharmacist in North Dakota. In the 60’s and 70’s, he mastered the art of compounding pharmacy.
He was very busy preparing prescriptions for his customers, trying to interpret correctly the doctor’s handwriting.
He was very proud of his profession. Yet I doubt that he would enjoy today’s modern pharmacy. I would think that he would say vaccinations are for doctors, not for pharmacists.
This action by the Secretary of HHS allows certain licensed pharmacists to order and administer, and pharmacy interns (who are acting under the supervision of a licensed pharmacist) to administer, any vaccine that the Advisory Committee on Immunization Practices (ACIP) recommends to persons ages 3 through 18.
This amendment was prompted by a report from the CDC in which it found a significant decrease in rates of routine childhood vaccinations. 
Now with the federal announcement of this declaration, how will this play out in the states? How much weight does this declaration have regarding state law which traditionally regulates the activities of state licensed pharmacists?
So the question now to be answered, does this declaration by the Secretary of HHS supersede state law?
In the last couple of years, there were many proposed legislative bills introduced to allow pharmacists to administer childhood vaccines that did not go anywhere in state legislatures around the country.
Is this declaration a product of those legislative failures?
Or is this a flare shot high in the air to signal to state health departments to use their rule-making authority to modify statutes to allow pharmacies to enter the childhood vaccination arena?
Even my home state of Minnesota passed legislation in May, 2020 to allow pharmacists to administer any FDA-approved COVID vaccine to children as young as 6 years of age.
This is not a mandate, but rather setting up a horrible scenario for which pharmacists are clearly not trained to handle. The method of passing legislation during a Peacetime Emergency declaration by governors to circumvent public testimony is very troubling.
The PREP Act has been previously amended twice prior to this declaration.
Previous amendments of The PREP Act include:
The 1st amendment on April 10th to extend liability immunity to covered countermeasures authorized under the newly passed CARES Act.  This declaration provides limited immunity to manufacturers of masks, plastic shields, gloves and other protective equipment.
The 2nd amendment on June 4th for the purpose of clarifying that covered countermeasures include qualified countermeasures that limit the harm COVID-19 might otherwise cause.  Basically, allowing the use of therapeutics and other measures that were not designed for COVID, to be used if necessary.
Now comes the problem of allowing pharmacists to administer childhood vaccines.
In the Vaccine Court currently, the number one petition filed for compensation is for shoulder injury as the result of a vaccination (SIRVA). Most of the injured persons (adults) received influenza or Tdap vaccinations from their local retail pharmacy such as Walgreens, CVS, RiteAid or Target.
If these retail pharmacies cannot properly administer a vaccine to an adult, why would we allow this for children?
One of the biggest problems when filing a petition claiming shoulder injury is the failure of the retail pharmacies to accurately record in the medical records which arm the vaccine was administered in and who did it. These pharmacies can barely keep up with adults receiving one vaccine at a time.
What happens when a parent brings their child into the business to get several vaccines? Will the pharmacy tech or pharmacist record the date, time, which arm or leg?
Will they be able to obtain and examine a thorough review of medical records prior to administering the vaccine?
Most doctors lack any comprehensive training of what a vaccine injury is or adverse reactions in a child, let alone a pharmacist receiving this type of training.
This has all the makings for a disaster.
But why is our government transferring the responsibility of administering vaccines to retail pharmacies instead of doctors’ offices or clinics?
It just might be the pushback from doctors who claim it is not profitable or too costly to administer basic vaccinations in their office. From their point of view, it would be more cost effective in a pharmacy setting.
Or is it something more sinister? It does appear that our government, with pressure from Pharma, is trying to “gut” the NVICP and slowly move injury compensation into the CounterMeasures Injury Compensation Program (CICP).
This is clearly the landing spot for the COVID vaccine. And it is the black hole for those who are injured or have perished because of a vaccine.
If the public is withheld case decisions and information about CICP, then vaccine injury claims will no longer exist.
So many agendas by our government agencies and medical community have no regard for the best interest of the people.
The BIG problem here is The PREP Act being used as a vehicle to circumvent Congress. The real concern is will we see a federal mandate for COVID vaccine at some point in the future via The PREP Act?
They are adopting policy via fiat without proper and necessary public comments and testimony. Will the PREP Act become the vehicle to advance vaccine policy in the United States?
I believe that we will see a few more amendments to The PREP Act if Congress will not address the liability issue for businesses, schools, colleges to open up. There are lawsuits already filed by employees for wrongful death (WalMart) and hospitalizations of employees claiming being infected by COVID while employed.
We must remain vigilant, we must be prepared to act, and we must educate our elected officials on a federal level, state and local level as well.
The PREP Act is in force as declared in March, 2020 until October, 2024 unless revoked by the Secretary of HHS or POTUS, or another health care emergency emerges.
The similar, more general conclusion is to be found in BT of G.I.G:
“But from all the experiments conducted by this sage, it became evident that the most harmful vibrations for contemporary terrestrial three-brained beings are the ones produced in them by what they call ‘medical remedies.’