With over 100 years combined experience and research of the Immune System; Professor's Ian Brighthope and Edward J (Ted) Steele explain how our TGA have set up Australia for catastrophe.
b) The Synthetic mRNA payload of these LNPS is ADDING a production process to the myriad of cell types using up resources, leaving debris and doin so in a manner never seen before by that cell type
Which of the following cell types will you guarantee has no impact on its other normal processes such as hormone, enzyme, protein etc.. tasks that it only EVER previously received from messenger RNA that originated from its species evolved DNA within its nucleus ?
Brain
Eyes
Spinal cord
Prostate (males)
Adipose tissue
Muscle
Stomach
Skin
Salivary glands
Testes (males)
Thymus
Bladder
Kidneys
Whole blood
Uterus (females)
Blood : plasma ratio
Heart
Pancreas
Bone (femur)
Pituitary gland
Lymph node (mandibular)
Plasma
Thyroid
Lung
Large intestine
Lymph node (mesenteric)
Small intestine
Bone marrow (femur)
Ovaries (females)
Adrenal glands
Spleen
Liver
c) From batch to batch there are varying spectroscopy readings indicating the presence of faulty, incomplete and fragmented Synthetic messenger RNA being encased in this cluster bomb delivery method; go knows what that will end up producing within the following cell types:
So its a nice brochure of what you might achieve invitro but its complete recklessness to put it into the arms of humans on a mass scale where 99.99% don't need it and 100% take on a massive risk profile
The known proclivity for uncontrolled bio distribution of LNP makes this technology a reckless and malfeasant path to take exposing nearly all vital cell types throughout the body to the effects of the LNP itself, the payload (SYNTHETIC mRNA),the bodies natural immune response to attack its own cells that appear to be producing foreign matter, partial and fragmented SYNTHETIC messenger RNA resulting in the production of completely unknowns... the scope of the recklessness is mind boggling. LNP SYNTHETIC messenger RNA technology must not only be stopped it should be outlawed and any business interests developing facilities to promote this technology shut down immediately
siRNA
What part of genome are they "knocking out?"
https://www.thermofisher.com/us/en/home/references/gibco-cell-culture-basics/transfection-basics/methods/cationic-lipid-transfection.html
You need to ask a lot more probing question than what's being knocked out and then put forward what looks like a sales brochure for LNP technology.
The problem is that when you can not control the biodistribution then you are left with
a) LNP (whether carrying a payload or not) that in of themselves are demonstrated to cause inflammation and reduce the innate immune system
See: https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1010830
Now imagine these LNPs entering
Brain
Eyes
Spinal cord
Prostate (males)
Adipose tissue
Muscle
Stomach
Skin
Salivary glands
Testes (males)
Thymus
Bladder
Kidneys
Whole blood
Uterus (females)
Blood : plasma ratio
Heart
Pancreas
Bone (femur)
Pituitary gland
Lymph node (mandibular)
Plasma
Thyroid
Lung
Large intestine
Lymph node (mesenteric)
Small intestine
Bone marrow (femur)
Ovaries (females)
Adrenal glands
Spleen
Liver
b) The Synthetic mRNA payload of these LNPS is ADDING a production process to the myriad of cell types using up resources, leaving debris and doin so in a manner never seen before by that cell type
Which of the following cell types will you guarantee has no impact on its other normal processes such as hormone, enzyme, protein etc.. tasks that it only EVER previously received from messenger RNA that originated from its species evolved DNA within its nucleus ?
Brain
Eyes
Spinal cord
Prostate (males)
Adipose tissue
Muscle
Stomach
Skin
Salivary glands
Testes (males)
Thymus
Bladder
Kidneys
Whole blood
Uterus (females)
Blood : plasma ratio
Heart
Pancreas
Bone (femur)
Pituitary gland
Lymph node (mandibular)
Plasma
Thyroid
Lung
Large intestine
Lymph node (mesenteric)
Small intestine
Bone marrow (femur)
Ovaries (females)
Adrenal glands
Spleen
Liver
c) From batch to batch there are varying spectroscopy readings indicating the presence of faulty, incomplete and fragmented Synthetic messenger RNA being encased in this cluster bomb delivery method; go knows what that will end up producing within the following cell types:
Brain
Eyes
Spinal cord
Prostate (males)
Adipose tissue
Muscle
Stomach
Skin
Salivary glands
Testes (males)
Thymus
Bladder
Kidneys
Whole blood
Uterus (females)
Blood : plasma ratio
Heart
Pancreas
Bone (femur)
Pituitary gland
Lymph node (mandibular)
Plasma
Thyroid
Lung
Large intestine
Lymph node (mesenteric)
Small intestine
Bone marrow (femur)
Ovaries (females)
Adrenal glands
Spleen
Liver
See: https://rumble.com/v230jdk-australian-covid-released.html
Watch it all but stop for a moment at 24:00 area
So its a nice brochure of what you might achieve invitro but its complete recklessness to put it into the arms of humans on a mass scale where 99.99% don't need it and 100% take on a massive risk profile
OMG; this so called vax is from hell
The vaccines must not simply be called mRNA vaccines
They are in fact
Lipid Nano Particle SYNTHETIC messenger RNA genetic vaccines
The known proclivity for uncontrolled bio distribution of LNP makes this technology a reckless and malfeasant path to take exposing nearly all vital cell types throughout the body to the effects of the LNP itself, the payload (SYNTHETIC mRNA),the bodies natural immune response to attack its own cells that appear to be producing foreign matter, partial and fragmented SYNTHETIC messenger RNA resulting in the production of completely unknowns... the scope of the recklessness is mind boggling. LNP SYNTHETIC messenger RNA technology must not only be stopped it should be outlawed and any business interests developing facilities to promote this technology shut down immediately