#ActualScience
IVM circulates in the plasma latching things in the way, 'cleaning' and coating. Plasma is not a vacuum, IVM coats cells helping the lymph transport inbound unnatural pathogens out of the body. It does this because it has superior binding power ESPECIALLY PROXIMAL TO ACE2 RECEPTORS. Think of the AC2 Receptor as a cell's front door entry.
What is the mechanism of action?
First, understand a little current context about spike proteins (SP)
And we don't know which batches of mRNA Vaxx are benign and which are generational bombs designed by FrankenFauci.
The idea is that SP2 will cause an immune response similar to SP1, BUT like SP1, SP2 IS ALSO STICKING AROUND THE ACE2 RECEPTOR. SP1 is there to deliver a payload to the cell interior. BUT BOTH SP1 and SP2 CAN STAY HUNG UP TO THE ACE2 RECEPTOR AND DISTURB ITS FUNCTION <== INFLAMMATION.
In theory, SP2 occupies the ACE2 Receptor as do IVM and HCQ but the latter do not disturb the receptor's normal function but SP2 does <== INFLAMMATION
In theory, if we get the vaxx, we develop an immune response to these SPs. We expect our immune response to take out SP1 and SP2 because they are structurally similar. They just have different interior content (payload), we hope. Batches of mRNA Vaxx product might be disturbingly different. Quality control anyone?
If our immune response keeps taking out these SPs, what happens? In the case of SP2, WE NEED BOOSTERS. Because our immune response will deplete SP2.
IVM/HCQ are blocking SPs from binding to the ACE2 Receptor without disturbing the ACE2 Receptor's normal functioning. IVM is safe, safer than Vitamin C. It has the highest binding energy, it is a more powerful molecular magnet, it is going to repel the SPs from cell receptors creating a prophylaxis environment.
IVM like HCQ covers ACE2 receptacles preventing entry by pathogens. IVM repels SP1, the SARS-COV-2 spike protein. It also repels SP2, the mRNA Vaxx spike protein.
Here are some key excerpts:
It has also been suggested that large amounts of spike protein are just binding ACE2 receptors and not proceeding any further into the cell, effectively blocking or disabling normal ACE2 function in a given tissue. Additionally, when the spike protein binds a cell wall and "stops" there, the spike protein serves as a hapten (antigen) which can then initiate an autoimmune (antibody or antibody-like) response to the cell itself, rather than to the virus particle to which it is usually attached. Depending on the cell types to which such spike proteins bind, a wide variety of diseases with autoimmune qualities can result.
The above is the tip of an iceberg. What is also disturbing is the compromise of science content. There is more knowledge of scrubbing, distorting scientific findings, fabricating others; much more will be revealed over time. Along with getting rid of the rigged voting machines, we need to be rid of these mRNA Vaxx mandates. They are two heads of the same Hydra.
Yes. Well aware.
Have a dear friend who unwillingly took the jabs (family pressure), then had a bad case of china flu, a few months later.
Her family doc would not prescribe Ivm....told her to wait until symptoms worsened (more than they were!), and to then go to ER.
She luckily went to a nearby urgent care, and that doc did prescribe Ivm.
She continued taking it, for several weeks, afterward, as she was having residual pain in ther (shot) arm.
It seems to have cleared up/is much better. She is now on an ongoing maintenance regimen of NAC and Quercetin.
#ActualScience