The case against injecting polyethylene glycol into the human population

[roguemoon]

(PS: I have simplified a lot of the terminology below so please follow links for the unaltered text)

Polyethylene glycol or Macrogol is a common plastic allergen, it is something that 70% of people are allergic to, it being a component of laxatives, make up and even brake fluid (google DOT 3 brake fluid ingredients), it is also used in frozen foods to stop ice crystals forming making it an antifreeze. (PEG is made from multiple molecules of the toxic substance ethylene glycol linked together into a long strand).

According to the pubmed website polyethylene glycol is toxic when injected and can cause potentially life-threatening iatrogenic complications. Case studies included.
https://pubmed.ncbi.nlm.nih.gov/16162774/

aacijournal.biomedcentral.com lists polyethylene glycol as a clear cause of anaphylaxis, case study included.
https://aacijournal.biomedcentral.co...223-016-0172-7

Allergic reactions to Polyethylene glycol can also cause rashes, a plummeting of blood pressure, a shortness of breath, a fast heartbeat and even death.

It is summarised by leading allergists and immunologists that an unknown percentage of people previously allergic to PEG may now have high levels of antibodies against it, putting them at risk of an anaphylactic reaction to both the Mrna vaccines and flu shots (Polysorbates –in both the Astrazenica and J & J shots - are similar in size to Polyethylene glycol molecules).
Side effects from PEG can begin anywhere from minutes after the jab to12 hours to 36 hours.

POLYETHELENE GLYCOL INJECTION EXPERIMENT 1
In April 2011 an experiment was conducted on 24 dogs to assess the animals reactions to an intravenous injection of Polyethylene Glycol 400.
The dogs were separated into 4 groups, a control group receiving a normal saline injection then three further groups receiving an injection once a day for 30 days of.
A; 4.23g (4ml)
B: 6,34g (6ml)
and C: 8.45g (8ml)
Dry mouth and dry nasal mucus membrane were observed in dogs treated with 6.34g and 8.45g, additionally the latter group experienced the swelling of kidney cells and an increased glomerular volume.
The animals were all sacrificed 24 hours after the last injection.
No significant histological changes were found 21 days later. Repeated dosing did not affect the toxicokinetic profile of PEG-400 in dogs.
This study has shown systemic toxicity and toxicokinetics of a high dose of polyethylene glycol 400 in dogs following intravenous injections
https://pubmed.ncbi.nlm.nih.gov/21314471/

POLYETHYLENE GLYCOL 400 INJECTION EXPERIMENT 2
Published eith July 9th or Dec 2013
The first trial conducted on mice involving the injection of PEG appears to have taken place sometime in either late 2012 or early 2013. Mice were injected with 4ml of Polyethylene glycol; the experiment caused liver damage, necrosis and inflammation to the mice.
https://pubmed.ncbi.nlm.nih.gov/23831209/

Voicing his concerns researcher Giovanni Pellegrini penned the following letter to ‘Toxicology.’

Liverpool, 07-Apr-2013
Dear Editor-In- Chief,
I am sending you our manuscript entitled

“Intraperitoneal administration of high doses of polyethylene glycol (PEG) causes hepatic subcapsular necrosis and low-grade peritonitis with a rise in hepatic biomarkers” by Giovanni Pellegrini et al.

I would appreciate if you could consider it for publication as a “Short Communication” type of manuscript in “Toxicology”.

To our knowledge, this is the first report showing liver necrosis and generalised peritonitis in mice receiving PEG-400, a vehicle commonly used as excipient in preclinical and in vitro studies.

This work is the result of a collaboration between two Departments at the University of Liverpool (Pharmacology and Veterinary Pathology), which are both part of our MRC Centre for Drug Safety Science, directed by Professor Kevin Park.

We thought that our findings would appeal to the readership of Toxicology, as they are new and concern a commonly used chemical entity.
As such, I would like to confirm that this manuscript is not currently under consideration by another journal. In addition, all authors have approved the manuscript, agree with its submission to Toxicology and declare that there are no conflicts of interest.

Please address all correspondence to: Giovanni Pellegrini, MRC Centre for Drug Safety Science, Sherrington Building, University of Liverpool, Ashton Street, Liverpool, L69 3GE, Tel: 0151 795 0382 (pellegg@liv.ac.uk)

We look forward to hearing from you at your earliest convenience.
Yours’ faithfully, Giovanni Pellegrini

POLYETHYLENE GLYCOL INJECTION EXPERIMENT 3
16th of September 2019
Mice were again injected with Polyethylene glycol, this time at a higher dose of 8 mL
The mice ended up in severe pain and half of the animals had to be euthanized.
https://pubmed.ncbi.nlm.nih.gov/31526095/

The results above demonstrate quite clearly that PEG can be toxic when injected.
The 2 studies above clearly revealed that the cell changes caused by Polyethylene glycol injection occurred at both high and low concentrations.
When administered at a high dose to mice without prior dilution, PEG had an immediate debilitating effect on the lining of cells and the chief functional cells of the liver immediately leading to the death of cells and a neutrophilic inflammatory response.

Except for intramuscular and slow intravenous injections for individuals with joint pain Polyethylene Glycol has never been injected into the masses and has never been used in a human vaccine that is intended for the entire global population.

So with the vaccine roll out of 2021under way a third approach was trialled in the fall of 2020.

POLYETHYLENE GLYCOL INJECTION EXPERIMENT 4
Results published March 16th 2021.
PEG was administrated by an injection once a week to mice.
After 4 months of injections, at the dose of 1.67 mL/kg, a surprising increase in the activity of the cells of the nervous system was observed and increasing neuro inflammation in areas of the brain.
These results show a dramatic increase in pro-inflammatory cytokine proteins that led to a rapid inflammatory process.
https://pubmed.ncbi.nlm.nih.gov/33715554/

Conclusion
It is important to communicate these results to the wider scientific community to provide awareness of this potential deadly effect when 0.3ml of PEG is injected into the population not only during the two step vaccine injection programme but the boosters (both vaccine and flu jabs) that are planned for the winter.

hope you all like and please correct, share as much as you like.
much gratitude to you all.