My response

Dear Dan

You do realise it’s a clinical trail until 2023 so what you are suggesting is that we subject children to a medical experiment for a virus that kills people with an average age of 82.4 which is above the life expectancy of men in this country alone without the virus. You can not sit there in all good conscience and tell me it’s safe nobody can because the experiment is happening live and you are supporting it not exposing it. It’s very disturbing for me to see someone in your position advocating for the potential harm to children for a virus that they are at very little risk of you are either very ignorant incredibly sinister or extremely corrupt. Even the governments own yellow card data shows the harm this vaccine can course and you want to expose this risk to children? I hope I’m wrong and everything will be ok but if any children get harmed from this experiment I hope it comes back to haunt you..

Regards Robert

⬆️ Email to Dan Jarvis MP

Anybody who says "vaccines work" without saying they killed more than 10,000 people in the West alone is complicit in Crimes Against Humanity and will be brought to justice at Nuremberg 2.0. EVERY SINGLE ONE.

Tiananmen Square: 300 deaths

Srebrenica: 8,000 deaths

Vaccines: 15,000+ deaths & counting

Spot a pattern?

In the UK alone, the official number of "vaccine" deaths is more than 1,200. Real adverse reaction figures are always considered to be 10-100 times greater than reported figures. This applies to deaths too.
https://yellowcard.ukcolumn.org/yellow-card-reports

"The lockdown should continue indefinitely"..
https://twitter.com/talkRADIO/status/1402157941550206977

DR PETER MCCULLOUGH: "In the trials of 2300 children aged 12-15 in the US 18 “cases” of sniffles were prevented and 60-80% of children were harmed."

MAGNETOFECTION: "Dr. Jane Ruby joined Stew Peters with a horrific revelation regarding the 'magnetism' videos circulating the world of social media in self-recorded videos of people sticking metal objects to themselves."
https://rumble.com/vi6vfp-exposed-magnetism-intentionally-added-to-vaccine-to-force-mrna-through-enti.html

MAGNETOFECTION (2019)
"Improving Magnetofection of Magnetic Polyethylenimine Nanoparticles into MG-63 Osteoblasts Using a Novel Uniform Magnetic Field (2019): This study aimed to improve the magnetofection of MG-63 osteoblasts by integrating the use of a novel uniform magnetic field with low molecular weight polyethylenimine modified superparamagnetic iron oxide nanoparticles (PEI-SPIO-NPs). The excellent characteristics of PEI-SPIO-NPs such as size, zeta potential, the pDNA binding and protective ability were determined to be suitable for gene delivery. The novel uniform magnetic field enabled polyethylenimine-modified superparamagnetic iron oxide nanoparticles/pDNA complexes (PEI-SPIO-NPs/pDNA complexes) to rapidly and uniformly distribute on the surface of MG-63 cells, averting local transfection and decreasing disruption of the membrane caused by the centralization of positively charged PEI-SPIO-NPs, thereby increasing the effective coverage of magnetic gene carriers during transfection, and improving magnetofection efficiency."
https://pubmed.ncbi.nlm.nih.gov/30874913/

MAGNETOFECTION (2011)
"Magnetofection is an efficient new physical gene transfection technology. Despite its effective gene delivery capability, till now relatively little work has been conducted on the mechanism of magnetofection, especially the intracellular fates of the components of magnetofectins and their effects on magnetofection. In this study, we investigated the mechanism of magnetofection using magnetofectins that were prepared via electrostatic self-assembly of the three components: polyethyleneimine (PEI)-coated magnetic nanoparticles (MNPs-PEI), plasmid DNA (pDNA) and PEI in the free form (free PEI). TEM observation and agarose gel electrophoresis assays have indicated MNPs play the role of driving magnetofectins to the cell surface without entering into the nucleus."
https://pubmed.ncbi.nlm.nih.gov/21807084/

MAGNETOFECTION AS VACCINE DELIVERY SYSTEM (2014) 🧲💉🩸

"The efficiency of delivery of DNA vaccines is often relatively low compared to protein vaccines. The use of superparamagnetic iron oxide nanoparticles (SPIONs) to deliver genes via magnetofection shows promise in improving the efficiency of gene delivery both in vitro and in vivo. In particular, the duration for gene transfection especially for in vitro application can be significantly reduced by magnetofection compared to the time required to achieve high gene transfection with standard protocols. SPIONs that have been rendered stable in physiological conditions can be used as both therapeutic and diagnostic agents due to their unique magnetic characteristics. Valuable features of iron oxide nanoparticles in bioapplications include a tight control over their size distribution, magnetic properties of these particles, and the ability to carry particular biomolecules to specific targets. The internalization and half-life of the particles within the body depend upon the method of synthesis. Numerous synthesis methods have been used to produce magnetic nanoparticles for bioapplications with different sizes and surface charges. The most common method for synthesizing nanometer-sized magnetite Fe3O4 particles in solution is by chemical coprecipitation of iron salts. The coprecipitation method is an effective technique for preparing a stable aqueous dispersions of iron oxide nanoparticles. We describe the production of Fe3O4-based SPIONs with high magnetization values (70 emu/g) under 15 kOe of the applied magnetic field at room temperature, with 0.01 emu/g remanence via a coprecipitation method in the presence of trisodium citrate as a stabilizer. Naked SPIONs often lack sufficient stability, hydrophilicity, and the capacity to be functionalized. In order to overcome these limitations, polycationic polymer was anchored on the surface of freshly prepared SPIONs by a direct electrostatic attraction between the negatively charged SPIONs (due to the presence of carboxylic groups) and the positively charged polymer. Polyethylenimine was chosen to modify the surface of SPIONs to assist the delivery of plasmid DNA into mammalian cells due to the polymer's extensive buffering capacity through the "proton sponge" effect."
https://pubmed.ncbi.nlm.nih.gov/24715289/

magnetofection_2_4.pdf

Cover of pdf above

"#Magnetofection is a novel, simple and highly efficient method to transfect cells in culture. #CombiMAGis a #magnetic particle preparation designed to be combined with any commercially available transfection reagent such as polycations and #lipids"
https://web.archive.org/web/20191231104325/http://www.chemicell.com:80/products/magnetofection/docs/magnetofection_2_4.pdf#

MY EDUCATED GUESS: THE INJECTIONS ARE MAGNETIC BECAUSE OF MAGNETOFECTION. WHAT ARE THE LONG TERM EFFECTS ON THE HUMAN BODY? MANUAL FROM MANUFACTURER LINK & PDF ABOVE. THEY DID NOT TELL US DID THEY? 🧲💉🩸

They lied about EVERYTHING so far but somehow they would be truthful about what's in the injections? Why? That's not how they work. I would suggest the opposite: the whole operation began with the ingredients of the injections and the lies around them. The vaccine ingredients are most likely the ORIGIN of the big lie. It's where the Minotaur lives.