amidwesterndoctor | One mission of this Substack has been to bring the concept of zeta potential to the awareness of the general public as I believe it is critical for understanding many different diseases including COVID-19 and both spike protein and non-spike protein vaccine injuries. A detailed summary of the concept can be found here:
When a substance is mixed in water, it has three options, not mix with it (typically either floating to the top or settling to the bottom), dissolve like salt, or form a colloidal suspension. Stable colloidal suspensions are typically finely dispersed microparticles and as that stability is lost, the particles clump together in larger and larger agglomerations which eventually will separate out from the surrounding water.
The colloidal stability of biological solutions however is mostly overlooked in modern physiology (other systems like Chinese medicine through blood stasis hold a greater focus to it). When the colloidal stability of a living organism is sufficiently impaired, severe diseases, such as those created by blood cells clumping together and impairing circulatory function can occur (similarly early researchers showed malaria causes death by creating severe blood clumping in the largest blood vessels, something Pierre Kory has also observed occurs in critically ill patients via IVC ultrasound immediately preceding their deaths).
A key factor that determines if colloidal solutions clump together or remain dispersed is the balance of electrical charges present (positive charges agglomerate, negative charges disperse). Zeta potential provides a way to model this immensely complex balance and explains why tiny amounts of positive ions with high charge densities (e.g. aluminum) are capable of agglomerating colloidal suspensions (e.g. sewage or blood), and why microstrokes often follow injections of these substances (similarly, poor zeta potential increases the viscosity of the blood, and when it is improved, a variety of cardiovascular or circulatory disorders also improved).
When COVID-19 started, I realize that many of the unusual symptoms reported by colleagues were identical to what I would have associated with an agent severely impairing the zeta potential of the body as so many different fluid circulations appeared to be impaired or showing signs of agglomeration (e.g. the frequent blood clots). After some research, I concluded the spike protein had the most likely electrical composition to account for these facts, at which point I became extremely apprehensive over vaccine designs which mass produced spike protein within the body (much of what is now known about the spike protein’s toxicity was not known then).
In Fleming’s previously mentioned presentation which discussed the prion domain within the vaccine spike protein, he also provided one of the best examples I have seen of how a small amount of a zeta potential reducing agent can rapidly cause blood cells to clump together. This was done by showing the immediate effects of each of the spike protein vaccines on healthy blood.
The South African researchers quoted earlier in this article likewise observed the same phenomena:
Blood incubated with spike protein showed erythrocyte agglutination, despite the very low concentration of the spike protein. An increase in platelet hyperactivation, membrane spreading, platelet-derived microparticle formation were noted due to spike protein exposure.
Further as detailed here, this clumping is also consistently seen on the blood smears of vaccinated individuals:
This rapid clumping process is most likely what causes sudden
death immediately following vaccination in susceptible individuals, such
as this recent example where this ardent advocate of vaccination died 7 minutes after receiving the new booster in the pharmacy.
As
we circle back to Died Suddenly and the abridged version presented
here, consider the scenes where the blood of these deceased individuals
is shown (I am putting this video in again here so you don’t need to
scroll up).
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