the Complaint explains:

BonSens.org and AIMSIB have written numerous articles in order to alert the public authorities to the dangers linked to experimental genetically modified substances marketed by Pfizer, Moderna, AstraZeneca and Johnson & Johnson. The BonSens.org association has warned by all means (i.e. articles, open letters, registered letters) the members of parliament, and therefore in particular the members of parliament who are the main defendants, of the erroneous information they had concerning these pharmaceutical products.

The association BonSens.org and the AIMSIB have repeatedly warned that these products endangered the lives of others, involved serious risks of physical and psychological harm, and that these products were likely to lead to the death of thousands of citizens in the short and medium term. The letters were accompanied by factual evidence and international studies with a high level of scientific evidence.

In an interview the Plaintiff’s Lawyer Me de Araujo-Recchia elaborates:

It was a question of renewing the health pass (disguised vaccination obligation) and deciding on the vaccination obligation of many professionals (health professionals, firemen, soldiers among others).

In this way, the parliamentarians in question have condemned millions of French people to choose between their job/social life and their health. Indeed, it is not a question of submitting to a compulsory vaccination with a safe product for which there is ten years of hindsight and which is intended to protect against a fatal disease with no available treatment.

It is actually about forcing millions of French people to undergo a clinical trial of biological drugs (i.e. gene therapies that fall into the category of biological drugs under EU law), which had an impressive list of side effects even before they were put on the market.

The report of the Federal Drug Administration (FDA) of October 2020 shows this very well: there was already talk of myocarditis, Guillain-Barré syndrome, Creutzfeldt-Jakob disease etc.

These pharmaceutical products are the subject of millions of adverse reaction reports:
– 2,880,653 records reported on the WHO VigiAcces database,
– 19,387 deaths as of 18 December 2021 and 1,275,634 adverse reactions, 363,774 of which are serious, on the European pharmacovigilance website EudraVigilance.

These data are extremely alarming compared to the data from all conventional vaccination campaigns combined, bearing in mind that in the field of pharmacovigilance, reports actually concern 1-10% of actual effects according to internal studies by Health Human Services and Harvard).

Medical Rights

point 5 of the Nuremberg Code:

” 5. The experiment must not be attempted when there is a priori reason to believe that it will result in the death or disability of the subject.”

The International Covenant on Civil and Political Rights echoed this prohibition against involuntary experimentation in its 1966 text, which states: no one shall be subjected without his free consent to medical or scientific experimentation.” This prohibition is now so universally recognised that some courts and scholars have considered this right to informed consent as a matter of customary international law. (….). “

It is also important to note that France is a signatory to the International Covenant on Civil and Political Rights and the OVIEDO Convention and that these texts are binding.

Citizens are holders of rights, they make society, pay taxes and social charges and respect the laws.

If we only have duties, and freedoms are taken away, then this is modern slavery and totalitarianism.

Moreover, according to Article 16 of the Declaration of the Rights of Man and of the Citizen of 1789:

“Any society in which the guarantee of rights is not assured, nor the separation of powers determined, has no constitution.”

Defendant’s Argument

References

1. Contribution from the Plaintiff’s Lawyer Me de Araujo-Recchia
2. French Lawyer Files Complaint Against MPs Who Voted for Mandatory Injection of Workers