COVID19 ASSEMBLY TAKE LEGAL ACTION AGAINST MHRA TO HALT CHILD VACCINATIONS

The Covid19 Assembly are spearheading a legal case against the MHRA to challenge the temporary authorisation of Covid-19 vaccines for children aged 12 to 15.

On behalf of many extremely concerned parents the Covid19 Assembly is taking legal action to challenge the Medicine and Healthcare products Regulatory Agency (MHRA)’s decision to approve the Pfizer/BioNtech vaccine for use in 12-15 year olds.

We have assembled a world class group of experts doctors and scientists, including renowned Canadian pathologist Dr Roger Hodkinson MA, MB, FRCPC, FCAP, the US specialist in mRNA vaccines Dr Robert Malone MD, MS,  South African-born medical doctor and research design analyst residing in the UK Dr Tess Lawrie MBBCh DFSRH PhD,  British paediatrician Dr Ros Jones MD FRCPCH and many others. We now need, without delay, to fund preparations for Judicial Review of the MHRA’s decision.

We have a strong case

We have substantial evidence we are satisfied clearly establishes that there is no legal, moral or medical justification for children to receive this treatment. There can be no argument that this ‘vaccine’ is novel and comes with associated risks. It has not yet completed clinical trials to demonstrate efficacy beyond a few months and therefore there simply can be no long-term safety data.

SOURCE.

https://www.covid19assembly.org/2021/07/take-back-control/

SARS-CoV-2 Spike Protein Impairs Endothelial Function via Downregulation of ACE 2

SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) infection relies on the binding of S protein (Spike glycoprotein) to ACE (angiotensin-converting enzyme) 2 in the host cells. Vascular endothelium can be infected by SARS-CoV-2, which triggers mitochondrial reactive oxygen species production and glycolytic shift. Paradoxically, ACE2 is protective in the cardiovascular system, and SARS-CoV-1 S protein promotes lung injury by decreasing the level of ACE2 in the infected lungs. In the current study, we show that S protein alone can damage vascular endothelial cells (ECs) by downregulating ACE2 and consequently inhibiting mitochondrial function.

We administered a pseudovirus expressing S protein (Pseu-Spike) to Syrian hamsters intratracheally. Lung damage was apparent in animals receiving Pseu-Spike, revealed by thickening of the alveolar septa and increased infiltration of mononuclear cells. AMPK (AMP-activated protein kinase) phosphorylates ACE2 Ser-680, MDM2 (murine double minute 2) ubiquitinates ACE2 Lys-788, and crosstalk between AMPK and MDM2 determines the ACE2 level. In the damaged lungs, levels of pAMPK (phospho-AMPK), pACE2 (phospho-ACE2), and ACE2 decreased but those of MDM2 increased. Furthermore, complementary increased and decreased phosphorylation of eNOS (endothelial NO synthase) Thr-494 and Ser-1176 indicated impaired eNOS activity. These changes of pACE2, ACE2, MDM2 expression, and AMPK activity in endothelium were recapitulated by in vitro experiments using pulmonary arterial ECs infected with Pseu-Spike which was rescued by treatment with N-acetyl-L-cysteine, a reactive oxygen species inhibitor

https://www.ahajournals.org/doi/10.1161/CIRCRESAHA.121.318902

VigiAccess Database

This database allows you to browse and view data on suspected side-effects from various medicinal products (also known as suspected adverse drug reactions (“ADRs”)). All data contained herein is sourced from VigiBase®, the World Health Organization’s (the “WHO”) global database for ADRs, maintained by the Uppsala Monitoring Centre (the “UMC”).

To access the database follow the link below and type into the search box “comirnaty”.

Comirnaty contains the active ingredient(s): Covid-19 vaccine.

http://www.vigiaccess.org/

COVID Vaccines: Necessity, Efficacy and Safety

Covid-19 vaccines are exposing populations to serious, unnecessary and unjustified medical risks.

Abstract: COVID-19 vaccine manufacturers have been exempted from legal liability for vaccine-induced harm. It is therefore in the interests of all those authorising, enforcing and administering COVID-19 vaccinations to understand the evidence regarding the risks and benefits of these vaccines, since liability for harm will fall on them.
In short, the available evidence and science indicate that COVID-19 vaccines are unnecessary, ineffective and unsafe.


Necessity: immunocompetent individuals are protected against SARS-CoV-2 by cellular immunity. Vaccinating low-risk groups is therefore unnecessary. For immunocompromised individuals who do fall ill with COVID-19 there is a range of medical treatments that have been proven safe and effective. Vaccinating the vulnerable is therefore equally unnecessary. Both immunocompetent and vulnerable groups are better protected against variants of SARS-CoV-2 by naturally acquired immunity and by medication than by vaccination.

Efficacy: Covid-19 vaccines lack a viable mechanism of action against SARS-CoV-2 infection of the airways. Induction of antibodies cannot prevent infection by an agent such as SARS-CoV-2 that invades through the respiratory tract. Moreover, none of the vaccine trials have provided any evidence that vaccination prevents transmission of the infection by vaccinated individuals; urging vaccination to “protect others” therefore has no basis in fact.


Safety: The vaccines are dangerous to both healthy individuals and those with pre-existing chronic disease, for reasons such as the following: risk of lethal and non-lethal disruptions of blood clotting including bleeding disorders, thrombosis in the brain, stroke and heart attack; autoimmune and allergic reactions; antibody-dependent enhancement of disease; and vaccine impurities due to rushed manufacturing and unregulated production standards.


The risk-benefit calculus is therefore clear: the experimental vaccines are needless, ineffective and dangerous. Actors authorising, coercing or administering experimental COVID-19 vaccination are exposing populations and patients to serious, unnecessary, and unjustified medical risks.

COVID Vaccine Necessity, Efficacy and Safety

COMIRNATY

This post is in relation to COVID-19.

This database allows you to browse and view data on suspected side-effects from various medicinal products (also known as suspected adverse drug reactions (“ADRs”).

All data contained herein is sourced from VigiBase®, the World Health Organization’s (the “WHO”) global database for ADRs.

http://vigiaccess.org

Enter search database
Type in COMIRNATY
Search ADR database

Stop Coerced Vaccination

Coerced vaccination, no jab – no pay – no job, is not a thing of the future. The ‘vaccine hesitant’ are being sacked and it is happening now.

Barchester Healthcare Ltd employ a staff of approximately 17,000. Over several months they have conducted a campaign successfully to ‘persuade’ all their workforce to have a Covid-19 vaccine. They say about 90% have been vaccinated. They have written to the rest to say that, unless they can provide evidence of medical exemption, then their employment will be terminated.

Their campaign of persuasion has been nothing less than coercion. Barchester have offered a vaccine bonus for the vaccinated but for employees who do not agree to be vaccinated, they have repeatedly and expressly threatened.

The legal case

The law has not changed. The Human Rights Act is still in place, as is the legal requirement for informed consent.

Coerced injection of any substance is an interference with fundamental human rights that must be justified as necessary and proportionate. In circumstances where the government keeps repeating that the vaccines do not stop transmission and that the vulnerable have been vaccinated already, it is difficult to see any justification whatsoever.

Irrespective of your thoughts about these treatments – who may or may not benefit from any Covid vaccine, their efficacy, the adverse events, their experimental nature, unknown medium or long term harms or whether they should be regarded as unlawful because there is no longer an emergency – everyone still has the right to their personal and bodily autonomy.

Lawyers against lockdown.

https://www.crowdjustice.com/case/stop-coerced-vaccination/

Notices of Liability for COVID-19 Vaccine Harms and Deaths Served on All Members of the European Parliament

On April 20, all following Members of the European Parliament were served with notices of liability, advising that they may be held personally liable for harm and death caused by implementation of a Digital Green Certificate (Vaccine Passport), to be voted upon in the European Parliament on April 28, 2021.

https://doctors4covidethics.medium.com/notices-of-liability-for-covid-19-vaccine-harms-and-deaths-served-on-all-members-of-the-european-a1f81f57216f

COVID-19 vaccine adverse reaction reporting

As of 14 April 2021, for the UK, 50,022 Yellow Cards have been reported for the Pfizer/BioNTech vaccine, 145,994 have been reported for the Oxford University/AstraZeneca vaccine, 44 for the Moderna vaccine and 516 have been reported where the brand of the vaccine was not specified.

For a medicine or vaccine to be considered safe, the expected benefits will be greater than the risk of having harmful reactions.

Vaccine Analysis Profile – Pfizer/BioNTech

Vaccine Analysis Profile – Oxford University/AstraZeneca

Vaccine Analysis Profile – Moderna

Vaccine Analysis Profile – brand unspecified

Doctors and Scientists Accuse Medical Regulator of Downplaying COVID-19 Vaccine Dangers

On April 1st the experts issued a rebuttal letterto the EMA, following the regulator’s dismissal of their earlier warnings regarding COVID-19 vaccine dangers from clotting and bleeding.

Within days of the EMA receiving the group’s original letter on March 1st, outlining risks of blood disorders from COVID-19 vaccines, over a dozen countries suspended the AstraZeneca vaccine following deaths from clotting and bleeding, as the doctors had warned.

https://doctors4covidethics.medium.com/re-issued-press-release-doctors-and-scientists-accuse-medical-regulator-of-downplaying-covid-19-5960665964c7

Our mRNA Medicines – The ‘Software of Life’

Our Operating System

Recognizing the broad potential of mRNA science, we set out to create an mRNA technology platform that functions very much like an operating system on a computer. It is designed so that it can plug and play interchangeably with different programs. In our case, the “program” or “app” is our mRNA drug – the unique mRNA sequence that codes for a protein.


When we have a concept for a new mRNA medicine and begin research, fundamental components are already in place.

Generally, the only thing that changes from one potential mRNA medicine to another is the coding region – the actual genetic code that instructs ribosomes to make protein. Utilizing these instruction sets gives our investigational mRNA medicines a software-like quality. We also have the ability to combine different mRNA sequences encoding for different proteins in a single mRNA investigational medicine.

We are leveraging the flexibility afforded by our platform and the fundamental role mRNA plays in protein synthesis to pursue mRNA medicines for a broad spectrum of diseases.

Source:

https://www.modernatx.com/mrna-technology/mrna-platform-enabling-drug-discovery-development