It seems that the Covid mRNA vaxxes just keep on giving, as far as adverse effects go. The one for this week, last week being that the mRNA spike protein was found in breast milk, is that the spike proteins have a neurological effect. As the researcher Philip Oldfield noted in a recent article in the journal Vaccines: “This mini-review focuses on the mechanisms of how SARS-CoV-2 affects the brain, with an emphasis on the role of the spike protein in patients with neurological symptoms.
“Following infection, patients with a history of neurological complications may be at a higher risk of developing long-term neurological conditions associated with the alpha-synuclein prion, such as Parkinson’s disease and Lewy body dementia.
“Compelling evidence has been published to indicate that the spike protein, which is derived from SARS-CoV-2 and generated from the vaccines, is not only able to cross the blood–brain barrier but may cause inflammation and/or blood clots in the brain.
“Consequently, should vaccine-induced expression of spike proteins not be limited to the site of injection and draining lymph nodes there is the potential of long-term implications following inoculation [vaccination] that may be identical to neurological complications seen in patients who were infected with SARS-CoV-2.”
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8780773/
“The list of complications, conditions, and diseases resulting from the COVID shots is nearly endless and can affect any organ system in the body. Pfizer knew. Here’s their document.
Look at the last 8 pages, which lists more than 1100 serious side effects and life-threatening illnesses Pfizer knew would happen from the first shot. We posted an article on The Tenpenny Reports about it: They All Knew.
Neurologic Injury
This study published by Philip Oldfield in January 2022, is eye-opening. Here is the abstract, edited lightly for clarity:
“This mini-review focuses on the mechanisms of how SARS-CoV-2 affects the brain, with an emphasis on the role of the spike protein in patients with neurological symptoms.
“Following infection, patients with a history of neurological complications may be at a higher risk of developing long-term neurological conditions associated with the alpha-synuclein prion, such as Parkinson’s disease and Lewy body dementia.
“Compelling evidence has been published to indicate that the spike protein, which is derived from SARS-CoV-2 and generated from the vaccines, is not only able to cross the blood–brain barrier but may cause inflammation and/or blood clots in the brain.
“Consequently, should vaccine-induced expression of spike proteins not be limited to the site of injection and draining lymph nodes there is the potential of long-term implications following inoculation [vaccination] that may be identical to neurological complications seen in patients who were infected with SARS-CoV-2.”
It is important to mention, we now know the spike proteins do not remain localized in the arm.
Let’s drill down on this article, starting with some definitions:
Alpha-Synuclein: These are the major component of Lewy bodies, which are characteristic of Parkinson’s disease and Lewy body dementia. There is much speculation on what the primary function of alpha-synuclein may be under healthy conditions. However, the accumulation of this protein when it has folded abnormally seems to be central to neurodegeneration. Since the culprit of chronic illness has been widely described as being the spike protein, a 2021 study of monkeys provided compelling evidence that the spike protein associated with SARS-CoV2 is responsible for Lewy body formation.
Parkinson’s disease: A long-term degenerative disease of the central nervous system, affecting the motor system. The most obvious early signs are resting tremor, rigidity, slowness of movement, and difficulty walking.
Lewy body dementia: This type of dementia is associated with difficulty thinking, slowed movement along with changes in behavior and mood. Lewy body dementia is one of the most common causes of dementia, affecting more than 1 million individuals in the United States and millions more around the world.
Both Parkinson’s disease and Lewy body dementia are characterized by groups of misfolded alpha-synuclein proteins in brain. The two diseases together are the second most common cause of neurodegenerative dementia, only surpassed by Alzheimer’s disease.
The Oldfield article goes on to say:
“…many of the serious neurological symptoms associated with COVID-19 are due to hypoxia, cytokine storms, and blood clots, all of which contribute to damaging neurons in the brain. Some of the symptoms of brain injury include loss of smell and taste (anosmia), severe headaches, debilitating fatigue, trouble thinking clearly (brain fog), seizures, strokes, and various degrees of paralysis.”
We know that these symptoms can be attributed to the spike protein, which can enter the brain by two primary entryways:
- Through the Vasculature: All of the blood vessels in the brain have ACE2 receptors. The spike protein binds to this receptor, which essentially ‘opens the door’ and allows the spike protein to enter. Once inside the cell, the spike proteins promote and contribute to micro-thrombi, leading to small and large blood clots.
- By directly damaging the blood brain barrier: The blood–brain barrier (BBB) is part of the microvasculature of the central nervous system. The tight junctions in these specialized blood vessels control what is allowed to pass from the general circulation into the brain. The BBB protects the central nervous system from toxins, pathogens, and other pro-inflammatory molecules. Spike proteins tested in vitrocaused significant changes to the properties of the BBB with loss of barrier integrity. When the BBB is destabilized, the spike protein—and many other destructive substances—can freely pass into the brain, leading to the neurological complications seen in both those who have experienced the infection and those who have received a COVID vaccine.
A separate mouse study showed that spike (S1) proteins tagged with iodine (I-S1) crossed the BBB very quickly. In fact, more than 50 percent of I-S1 proteins crossed the capillary wall and entered into the brain and interstitial fluid spaces within 30 minutes of the IV injection. The spike protein was taken up by all 11 areas of the brain that were tested, which could explain the wide variety of different neurological symptoms that are observed clinically.
“These data show that S1 antigen production after the initial vaccination can be detected by day one and is present beyond the site of injection site and the associated regional lymph nodes.”
“It was observed that the spike protein S1 subunit was detectable in the systemic circulation up to approximately two weeks post-injection in eleven out of thirteen healthcare workers. Although concentration of the S1 subunit was low, this study provides proof-of-principle that spike proteins can get into circulation following inoculation.”
Can it be any clearer that the pathology observed after a COVID injection is from the spike proteins produced by the mRNA, gene-modification technology that came through that needle?
Will those who had the shots and experienced now immediate side effects be at greater risk of Parkinson’s disease or Lewy body dementia in 10 or 20 years? Is brain dysfunction already starting to appear?
Although it seems we’ve been talking about this pandemic and its shots forever, the Pfizer and Moderna shots were unleashed on the world December 2020; the J&J and AstraZenca shots were released in February 2021. In reality, it’s been less than two years. We are in the middle of a great experiment, and the final results will not be known for many years.”