A subscriber to NFU has asked me to re-send this important item from April
7, as it's more relevant ever, what with Trump's
now-tight relationship with Bill Gates' GAVI,
and his initiation of Operation Warp Speed.

MCM

*These vaccines should be outlawed, the CDC vaccine schedule radically
> revised—**and the big rush to develop, and ultimately force on all of us,
> a COVID-19 vaccine **now seriously questioned.*
>
> *MCM*
>
> *"As a consequence, this vaccine should be considered defective and
> potentially *
> *dangerous to human health, **in particular for the pediatric population,
> which is *
> *much more vulnerable to genetic and autoimmune damage **due to the
> immaturity **of the immunity systems."*
> First peer-reviewed publication on MMRV vaccines (Priorix Tetra)
>
> https://www.corvelva.it/speciale-corvelva/vaccinegate-en/first-peer-reviewed-publication-on-mmrv-vaccines-priorix-tetra.html
> VACCINEGATE - EN
> <https://www.corvelva.it/speciale-corvelva/vaccinegate-en.html> STAFF
> CORVELVA
> <https://www.corvelva.it/component/contact/contact/4-uncategorised/1-corvelva-coordinamento-regionale-veneto-per-la-liberta-delle-vaccinazioni.html?Itemid=200>
>  31
> MARZO 2020
> [image: First peer-reviewed publication on MMRV vaccines (Priorix Tetra)]
>
> Finally here we are -after almost two years- the first peer-reviewed
> publication of our analyses is being released and many others are going to
> be published.
>
> The aim of this article is to summarize the following issues: what has
> been published, what is its validity, and why it is important for our
> investigation on vaccines. All these arguments will be treated in a
> colloquial and non-technical way in the first pages, while from page 3 on,
> there will be a technical study in order to allow the specialists of this
> sector to evaluate the article in itself.
>
> The article published on “F1000 Research”1 is the outcome of the initial
> study performed by one of the laboratories that Corvelva Association
> appointed to carry out the analyses. We remind you - because more than two
> years have passed since the beginning of this work and many other results
> have been added to the first ones – that the first major issue that we
> had to investigate was the abnormal amount of human DNA found within the
> vaccines analyzed.
>
> The initial analyses showed that both the quadrivalent MMRV vaccines
> analyzed contained from 1 to 2.7 microgram/ vial (as published in the
> present article) and we decided to report publicly and immediately such
> results because, simply, it was not expected that such an amount of DNA
> could be present within a vaccine.
>
> Apart from the considerations and conclusions achieved by the study, which
> are strictly technical and therefore comprehensible only to those who work
> in the field of metagenomic research, what is observed in the graphs is
> that the two vaccine samples contain a high percentage of human DNA
> readings in addition to those expected from the chickenpox virus genome
> (Human alphaherpes virus 3), the only detectable one among four, as a
> DNA-seq type of analysis was presented in the article.
>
> However, we would like to point out that the quantities of DNA that were
> found and confirmed by the same method that is now validated here were
> even higher: up to 3.7 micrograms per vial, leading to a considerable
> difference from batch to batch. In fact, in our report released on December
> 22 20182 the results obtained from the analysis of different batches from
> those discussed in the present article were reported, and then confirmed by
> interlaboratory analysis that are still in process of publication.
>
> Therefore, what should be considered as of major interest in the present
> publication is that it validates the method we used, gives an important
> point to the discussions on the "type" of analysis carried out, and as a
> consequence it confirms in a definitive way all the studies that have
> been subsequently carried out with the NGS method: the in-depth analysis
> on the type of genetic material, the presence of adventitious viruses, the
> great absence of attenuated viruses that should be present and the amount
> of human DNA that was completely out of control (also because very
> different from sample to sample), the mutant population, phages, DNA from
> other species, and so on. You can find all the results summarized on our
> web site3.
>
>  Everything we have denounced in recent years, from a biological point of
> view, reporting thoroughly the results to the control bodies, takes on a
> more relevant scientific connotation (even if, we repeat it again, it was
> not the peer-reviews that had to worry but the data presented, very serious
> in their content and their possible implications for human health).
> However, now that the publication of the method has been done, we will
> demand the answers that we have not yet been given.
>
> These results unquestionably confirm the presence of fetal DNA in Priorix
> tetra vaccines, in variable quantities from batch to batch, indicating poor
> quality control of these pharmaceutical products.
>
> We’d also like to remind the report on the entire MRC-5 genome sequencing
> published in Corvelva website on September 27 20194  showing the deep
> modification of this DNA even in genes linked to the development of tumor
> diseases (this data also will soon be published). The contaminating fetal
> DNA found in all the analysed samples in variable (i.e. 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, on the basis of a statistical calculation, while the
> precautionary limit is 100 pg/dose), a limit that must necessarily be
> applied also to fetal DNA  inevitably contaminating Priorix Tetra vaccine.
>
> As a consequence this vaccine should be considered defective and
> potentially dangerous to human health, in particular for the paediatric
> population which is much more vulnerable to genetic and autoimmune damage
> due to the immaturity of the immunity systems.
>
>  As anticipated, the following part of the article is a more "technical"
> and difficult to understand for non-experts, therefore we decided, even for
> transparency purposes, to attach to this document also the "EMA Dossier -
> NGS Dossier Discussion on the results of the vaccine quality survey ". We
> had to extrapolate only the part that could be published, that is 50 pages
> of the dossier compared to the 200 pages of the NGS, since much of the
> information contained and registered to the regulatory bodies must remain
> confidential. The strict law of science dictates that a piece of
> information can be published in a journal only if it is original and since
> we have other work in progress, we do not want to put it at risk.
>
> EMA - NGS Dossier Discussion on the results of the vaccine quality
> survey". -  <https://bit.ly/342XKi7>https://bit.ly/342XKi7
>
> Finally, to avoid misunderstandings, we would like to highlight the part
> of "Financing Declaration" from the above mentioned publication:
> *"The B1 and B2 metagenomic sequencing was funded by Corvelva (non-profit
> association, Veneto, Italy), under a service contract with the laboratory.
> No other contribution was involved in supporting the work. The funders had
> no role in the design of the study, the collection and analysis of data,
> the decision to publish or the preparation of the manuscript"*
>
> *Click on the link for the rest.*
>

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