The Origin of Vaccine Harm, By Brian Simpson

The Mid Western Doctor blogger, who always writes insightful articles debunking the ruling myths of medicine, has updated a piece he did some months back on why vaccine harms exist. The harms from the Covid-19 mRNA vax are the best known, being the most extensive of any vaccine, but the problem goes right across the board. It is by means of medical hypotheses, which will require empirical testing, but be sure the funds for doing this will not be coming from Big Pharma.

The main hypotheses, based around impaired circulation and related problems, which are not mutually exclusive, are that, as neurologist Andrew Moulden thought, vaccines frequently trigger micro-strokes, leading to numerous ill-health effects. As well, and this has been observed with the Covid mRNA vax, blood cell clumping and blood clots can occur, which can also lead to strokes and heart attacks. In addition, there is immune dysfunction, where chronic inflammation causes immune suppression of various degree. Overall, the invasion of a vaccine puts the body into a threat mode, which can impair normal cell functioning, such as with the mitochondria. Outside of the mainstream, this has been suggested as one cause of autism, but the claim is controversial. Autism was thought by the Andrew Moulden a Canadian neuroscientist and doctor specializing in neuropsychiatry, to be the result of micro-strokes children had after vaccinations, but which went unnoticed.

If Trump survives and becomes president, he said he will set up a commission to study vaccine harms, headed by Robert Kennedy Jr, which should be ground breaking. Hopefully research funding will become available to test these hypotheses.

https://www.midwesterndoctor.com/p/why-do-all-vaccines-cause-harm

"Many medical problems stem from the diagnostic approach of physicians, especially with complex illnesses, which are often misdiagnosed and lead to ongoing patient struggles.

Complex conditions can present with varied symptoms across patients and resemble other illnesses (e.g., fibromyalgia vs. chronic fatigue syndrome). In turn, poorly trained physicians often default to psychiatric explanations, overlooking the true causes.

Vaccine injuries have a wide range of symptoms and hence have confused doctors for over 200 years (with many doctors in the past labelling them as "encephalitis"). Presently, I believe three main mechanisms underlie the myriad of vaccine injury:

Immune Dysfunction: Vaccines frequently cause chronic autoimmune disorders and varying degrees of immune suppression.

Cell Danger Response: Cells can enter a primitive state under threat, stopping normal mitochondrial function. This temporary state can become chronic, underlying many severe conditions. Treating this response has resolved conditions linked to vaccination, like autism.

Impaired Circulation: Vaccines can impair fluid circulation by affecting the body's zeta potential. This causes fluid clumping (i.e. micro blood clots and blood thickening) and obstructs blood flow in capillaries.

My focus was drawn to the zeta potential concept once I realized that many of the mysteries of COVID-19 (and later the COVID-19 vaccines) were due to the spike protein being extremely disruptive to the body's zeta potential. I now believe that patient outcomes would significantly improve if the medical system prioritized the zeta potential.

Andrew Moulden was a Canadian neuroscientist and doctor specializing in neuropsychiatry. During his clinical training, he noticed young children showing subtle neurological signs of strokes that his colleagues missed. Over time, he found these strokes often occurred soon after vaccination and could lead to severe neurological disorders like autism.
Note: vaccine injury reports as far back as the early 1800s contain the same signs Moulden noticed.

Moulden realized that the subtle stroke signs doctors look for in adults should also be assessed in children. Because these strokes in infants are often missed, many conditions are misdiagnosed or attributed to unknown causes. One scientific challenge is making "invisible" issues visible. In neurology, disruptions in brain function, often due to impaired blood flow, can reveal stroke locations through careful physical examination.

Moulden found that cranial nerves in the brainstem, particularly in watershed areas with less redundant blood supply, were vulnerable to strokes. These strokes, caused by impaired blood flow, often due to increased blood thickness, were missed in infants, leading to conditions misdiagnosed or attributed to unknown causes.

Key cranial nerves indicating vaccine-caused microstrokes include:

Cranial Nerve VI: Controls eye movement; damage causes inward eye resting or jerky side-to-side movement.

Note: often, you will see multiple cranial nerve issues on the same face (which suggests more parts of the brain lost their blood supply and hence that deeper neurological damage is also present).

Once you know how to look for these symptoms (e.g., a loss of smooth eye motion), they are very easy to spot, and you will gradually become aware of how far reaching the neurological damage that results from vaccination can be (as any part of the brain can be affected).

Moulden's work also suggested strokes were also occurring in other watershed areas of the body, such as internal organs and speech centers. Evidence included:

Autopsy studies showing strokes in internal organs of children with congenital rubella.

Similar disease processes in teenagers and adults after HPV or anthrax vaccination.

One of the most striking examples was the children of soldiers who received the anthrax vaccine and were born without limbs (thalidomide was also notorious for doing this by blocking the formation of new blood vessels).

Neurodegenerative processes in the elderly and psychiatric disorders being linked to cranial nerve damage.

Note: a major issue in conventional medicine is the failure to recognize that neurological damage can lead to psychiatric issues. Consequently, emotional changes in patients with nervous system injuries are often misattributed as the cause rather than a symptom of their illness.

Moulden thus began exploring what universal response was leading to these microstrokes and how they could be treated. From this, he produced three videos describing the problem (which can be viewed here). Unfortunately, shortly before releasing a second series on the solutions for these injuries, he died under suspicious circumstances. However, we now have many clues as to what Moulden discovered.

In the medical world, a long-standing puzzle revolves around how small insults to the body can lead to widespread illness or even death. One key factor in this equation is blood sludging, a phenomenon observed for centuries where the blood clumps together and thickens under certain disease conditions. Melvin Knisely, Ph.D., in the mid-20^th century made critical discoveries about this phenomenon.

Knisely's research, particularly with malaria-infected monkeys, revealed that certain severe illnesses could trigger significant blood sludging, starting in small vessels and eventually spreading to larger ones, which was typically fatal (unless prevented with the anticoagulant heparin). This thickening of blood can be likened to traffic jams, disrupting the body's natural blood-flow, and eventually leading to gridlock (death).

Additionally, he discovered that this sludging could be seen externally through the eyes, providing a non-invasive way to assess this process throughout the body.

From this, he discovered the greatest blood sludging was seen in critically ill hospital patients—something Pierre Kory MD also observed with point-of-care ultrasound, as once micro clots within the IVC became echogenic (visible), patients died shortly after).

Knisely's grading scale for blood sludging severity correlated with disease prognosis, highlighting its clinical significance.

After learning of this, we attempted to replicate Knisely's microscope and have been able to see the same sludging he observed 80 years ago in his patients.'