Delayed Self Poisoning

October 10, 2021

DELAYED SELF-POISONING (OR A QUICK DEATH VIA MACROPHAGE ACTIVATION SYNDROME)

THE SPIKE PROTEIN OF SARS-CoV-2 IS AN ENGINEERED BIOWEAPON DESIGNED TO CREATE MASSIVE, ALMOST CERTAINLY LETHAL (DELAYED, AS IS THE CASE WITH EXTREME IRON OVERLOAD) IRON EFFLUX FROM MACROPHAGES AND RBCs. THE OBSERVED HYPOXIA IS PART OF THIS “PLAN.” THE BODY RELEASES YET MORE IRON UNDER HYPOXIC CONDITIONS: THE PARACRINE PARALLEL TO RADIATION POISONING.

A fascinating article appeared on ideas.ted.com in December of 2015. The chemist Rebecca Abergel realized the way to cure people of radiation poisoning was to remove it from the body, as it spreads in a PARACRINE fashion.

At high doses, radiation blasts through tissues, ruptures DNA strands and alters the rhythms of cell division. Disrupted cells cause nausea, diarrhea and fever, then dizziness, weakness and hair loss. Over time they may turn cancerous. For a person who has experienced high levels of radiation in a short period of time, from a nuclear weapon or a Chernobyl-scale nuclear power plant meltdown, treatment options are limited. Doctors can make a patient comfortable, treat burns and nausea, and try to keep the radiation from spreading. But an acute dose is usually fatal. The problem is, once radiation is in the body, IT CAN BE VERY HARD TO GET IT OUT.

What else is very hard to get out of the body?

You guessed it. IRON!

It is generally thought that no regulated pathway of iron excretion exists in the mammalian organism.

!

This is the point.

Just like radiation, the body HAS NO PATHWAY TO REMOVE IRON.

And, just as in radiation poisoning, the damage of Iron Poisoning spreads cell to cell.

PARACRINE COMMUNICATION BETWEEN DIFFERENT CELL TYPES TO SUSTAIN SYSTEMIC AND LOCAL IRON HEMOSTASIS
An increasing body of evidence shows that the maintenance of systemic iron homeostasis requires paracrine and endocrine communications between different cell types.

Back to the radiation poisoning parallel.

Nuclear weapons and accidents commonly release actinides, a group of radioactive elements at the bottom of the periodic table. Actinides such as plutonium, uranium and curium easily lock into our bones and organs, where they can emit radiation into our bodies for decades. Chemist Rebecca Abergel and colleagues at Lawrence Berkeley National Laboratory, in California, have created molecules that bind to actinides to form large, stable complexes that are easier for the body to expel.

And what does iron do when it is extremely overloaded? IT LOCKS INTO OUR BONES AND ORGANS.

The spike protein therapies must stop this instant. Observe iron biomarkers in the hours and days post dosage. You will find iron overload beyond anything previously observed. Because. It. Is. A. Weapon. Not. A. Goddamn. Virus.

Referenced/Related Papers

The Hyperferritinemic Syndrome: macrophage activation syndrome, Still’s disease, septic shock and catastrophic antiphospholipid syndrome

https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC3751883/

Cell-type-specific insights into iron regulatory processes

https://onlinelibrary.wiley.com/doi/full/10.1002/ajh.26001

“Pumping iron”—how macrophages handle iron at the systemic, microenvironmental, and cellular levels

https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC5362662/

Iron release from macrophages after erythrophagocytosis is up-regulated by ferroportin 1 overexpression and down-regulated by hepcidin

https://www.pnas.org/content/102/5/1324

This pill may be a cure for radiation poisoning

https://ideas.ted.com/how-were-making-a-pill-that-cures-radiation-poisoning/