Posted on 10/20/2022 7:43:21 AM PDT by Cercyon
Dr. Paul Marik, Front Line COVID-19 Critical Care Alliance(FLCCC) co-founder, said at an FLCCC conference on Oct. 15 that long COVID and injury from the COVID-19 vaccines share many overlaps in their symptoms and mechanisms.
Both diseases are systemic, affecting multiple organs, and tissues and are both driven by a high load of spike protein accumulated in these organs and tissues. These spike proteins trigger inflammation, mitochondrial dysfunction, and autoimmunity.
However, not everyone will experience these symptoms.
Whether a person will suffer from vaccine injuries is dependent on both permanent factors and temporal factors impacted by actions and choices.
Spike Protein Exposure Increases Risk, Severity
The best way to reduce spike protein injuries is to reduce opportunities of spike protein exposure through infections or vaccinations.
While early treatment can usually prevent spike proteins injury by quickly clearing the infection, a vaccine administer spike protein genetic material into the muscles and blood vessels.
There is a dose-response with the vaccine, such that the greater the number of vaccine doses, the higher the risk of spike protein injury.
“The more the patients are exposed to spike [proteins], the more severe the disease,” said Marik.
Both long COVID and injury from COVID-19 vaccines are driven by a prolonged exposure to spike proteins through infection and vaccination respectively, he explained.
Dr. Flavio Cadegianni hypothesized that receiving COVID-19 vaccines after having had COVID-19 increases one’s risk of spike protein injury. This is because vaccines likely trigger a higher amount of spike protein load in the bloodstream than a common COVID-19 infection.
In a common COVID-19 infection, it is difficult for the virus to enter the bloodstream through the lungs, but the vaccination gives spike protein mRNA and DNA a one-way ticket into the deltoid and then into the bloodstream.
The mRNA and DNA vaccines then enter the blood vessels and endothelial cells, these cells then produce spike proteins and present them on their cellular surface, resulting in an immune attack against these cells.
Spike proteins from vaccines can also be free-floating in the blood stream and the extracellular fluid. These spike proteins can trigger inflammatory pathways by binding to and reducing ACE2 receptors, forming complexes with antibodies, and affecting immune pathways, leading to pro-inflammatory responses.
Spike proteins from vaccination have been observed to be present even at 9 months (pdf) following vaccination, so subsequent shots and boosters could lead to more spike protein production, increased inflammatory complexes formation, and higher risk of symptom onset.
Dr. Pierre Kory, co-founder of FLCCC, who now has a clinic for treating long COVID and vaccine injury, said that he noticed his patients with either of these conditions would appear to worsen with subsequent spike exposures.
He said he recommended his long-haul and vaccine-injured patients to therefore avoid opportunities that may lead to spike protein exposure lest that their symptoms go out of control.
Varied Loads in Vaccines
Not all vaccine vials are made the same.
How Bad is My Batch is a website that compiles data on adverse events from the Vaccine Adverse Event Reporting System (VAERS) on COVID-19 vaccination.
By separating each adverse event into its corresponding vaccine batch, the website has shown that some vials were made different from others, as they are associated with a greater number of adverse events, deaths, and disabilities.
This could be due to impurities in the vaccines.
Leaked emails from staff in the European Medicines Agency (EMA) showed that the agency only asked for 50 percent mRNA integrity in their Pfizer vaccinations.
However, potential issues could also be due to the dosage; some vials may have a higher mRNA or DNA spike protein content than others.
Currently, doctors have no way to verify what is in the vials.
“We basically do not know what’s in these vaccines,” said Merryl Nass, an FLCCC-affiliated internal medicine specialist at the FLCCC conference. Doctors only know that some people are injured and that not all vials are made the same.
Nass had her medical license suspended by the Board of Licensure in Medicine (BOLIM), a state agency that regulates medical licensing in Maine. In January 2022 she received an order to submit to a neuropsychological evaluation by a psychologist selected by BOLIM to determine whether she was competent to practice medicine, citing her online criticism of COVID-19 policies as cause for concern. She filed a lawsuit and recently had a hearing.
Genetic Factors
“There’s a genetic predisposition,” said Marik. “If someone in the family is vaccine injured, it is very common that the brothers of that individual … [will also become] vaccine injured so there are genetic factors which we don’t understand.”
Marik has observed that certain genetic mutations may also put them at a greater risk of COVID-19 vaccine injury.
This included individuals with a methylenetetrahydrofolate reductase (MTHFR) gene mutation and those with Ehlers-Danlos type syndromes.
Around 40 percent of people in the United States carry or are affected by the MTHFR mutation. It is an enzyme responsible for transforming folate (vitamin B9) into its active form. Folate plays a role in breaking down homocysteine—an amino acid that is toxic in higher concentrations—to methionine, a useful amino acid.
Depending on the type of the MTHFR mutation and the number of copies a person carries, the function of MTHFR enzyme can be moderately or severely reduced, leading to folate deficiencies.
People with MTHFR mutations generally have a higher risk of cardiovascular diseases, diabetes, hypertension, blood clotting disorders, pregnancy loss, and certain types of cancer.
Folate deficiencies increase a person’s risk of severe COVID-19; homocysteine levels have been directly predictive for worsened COVID-19 outcomes.
There have been testimonies (pdf) from people with relatives who carry MTHFR mutations who have experienced adverse events following vaccination, though the actual mechanism behind this gene and elevated risk of COVID-19 and possible vaccine injury is not well understood.
Ehlers-Danlos type syndrome is a disorder of connective tissue primarily affecting skin, joints, and blood vessels. People with these conditions often report of joint dislocation, chronic pain, and chronic fatigue. This condition is also often associated with inflammation—a primary driver of long COVID and spike protein-induced disease.
Underlying Chronic Diseases and Immune Deficiencies
Metabolic diseases, especially high blood pressure and type 2 diabetes, have been associated with severe symptoms in COVID-19 infections and vaccination.
Dr. Aseem Malhotra, renowned cardiologist, wrote in his paper that even “a single high blood glucose reading in non-diabetics admitted to hospital [for COVID-19] has been shown to be associated with worse outcomes.”
Many metabolic diseases including obesity, diabetes, hypertension, and cardiovascular disease are driven by inflammation. The spike proteins also trigger many inflammatory pathways, which may be why people with these chronic diseases are at a greater risk.
Spike proteins both from the virus and the vaccine can bind to ACE2 receptors displayed on cells across any tissue it comes into contact with. ACE2 is responsible for reducing inflammation, but this binding reduces ACE2 receptors and therefore increases inflammation across the tissues.
“We’re talking about mononuclear cells in the brain, in the heart, in the liver, the spleen in the ovaries, so it results in a systemic disease,” said Marik.
Spike proteins are also highly autoimmune, meaning that it is able to trigger the immune system to mount attacks against self-tissues.
Studies led by Dr. Aristo Vojdani showed that antibodies made against SARS-CoV-2 spike proteins reacted “with various tissue antigens including the muscles, joints, thyroid, brain, skin, gastrointestinal tract, almost any antigen taken from different parts of the body,” said Vojdani to The Epoch Times.
A significant finding Marik and Kory observed was that individuals suffering from vaccine injury have a higher concentration of autoantibodies than those with long COVID.
Many studies have observed onset or a relapse of autoimmune diseases after COVID-19 vaccination. Documented cases include multiple sclerosis, neuromyelitis, arthritis, type 1 diabetes, and many more.
Those with a relapse of autoimmune diseases often experienced symptoms of greater severities.
These are all suggestive that people with underlying chronic diseases that compromise their health and immune system are at a greater risk of possible vaccine injury.
Vitamin Deficiencies
Deficiencies in folate, cobalamin (vitamin B12), vitamin D have been associated with an elevated risk of COVID-19 infection.
A pre-print study (pdf) authored by UK researchers funded by the National Health Service found that supplementation in vitamin D and vitamin B12 relieved neurological symptoms caused by COVID-19 vaccination.
Vitamin D is anti-inflammatory and can boost immune action, while vitamin B12 is critical for neural health as it helps to produce myeline, which is a fatty coat wrapped around neurons, that helps protect neurons against scarring and improves neural messaging.
“Vaccines, including the COVID-19 vaccines, are known to cause severe and/or chronic neurological reactions in rare cases. We support screening for vitamin B12 deficiency prior to vaccination in high-risk groups,” wrote the study authors.
Folate deficiencies have also been observed in patients hospitalized with COVID-19. The vitamin plays a role in the formation of DNA and RNA for cellular protein.
Data from VAERS also showed that women constituted around 65 percent of the adverse event reports; 41 percent of these reports came from women aged 18 to 49 at the time of the report.
Women in the 50 to 59 age bracket and the 65 to 79 age bracket also constituted a large fraction of the adverse event reports, taking up almost 35 percent of all reports in females.
Spike proteins trigger inflammation through many pathways. One pathway is through binding to ACE2 receptors on cell surfaces. This receptor is important for reducing inflammation, and a reduction of ACE2 through spike protein interaction thus increases inflammation.
Though ACE2 receptors are found across many organs, studies show that it is particularly abundant in the ovaries and the eggs.
Since the rollout of vaccines, many women have reported menstrual irregularities
The first main factor is whether or not you get the clot shot.
These 6 factors?:
1. Watching mainstream media
2. Voting for Biden
3. Using social media
4. Going to a liberal arts school
5. Being in the armed forces
6. Working in a job you can’t afford to lose
So, besides not being vitamin-deficient, does anyone here know how to ameliorate the effects of the spike proteins (or, better yet, how to clear them from one’s system)?
There is only 1 main factor. where dumb enough or pressured enough, or even forced to the clot shot. Everything else is just a contributor after that!
Ivermectin
Dr. Blaylock says to use curcumin - specifically the most bio-available one, from One Planet Nutrition that is nano-sized.
Dr. Blaylock says curcumin binds to the spike proteins and neutralizes them. Newsletter is behind a paywall, unfortuantely.
This is the one we buy - and use - every day.
https://www.oneplanetnutrition.com/shop#!/Nano-Curcumin-60-Caps-500-mg/p/100276443/category=27372415
Why is Novavax with dead, fragments of virus, and not an mrna vax also have heart problems?
Thanks for posting.
Bookmark
There is a dose-response with the vaccine, such that the greater the number of vaccine doses, the higher the risk of spike protein injury.
“The more the patients are exposed to spike [proteins], the more severe the disease,” said Marik.
Both long COVID and injury from COVID-19 vaccines are driven by a prolonged exposure to spike proteins through infection and vaccination respectively, he explained.
Dr. Flavio Cadegianni hypothesized that receiving COVID-19 vaccines after having had COVID-19 increases one’s risk of spike protein injury. This is because vaccines likely trigger a higher amount of spike protein load in the bloodstream than a common COVID-19 infection.
So the more vaccine doses you receive (two shots and two boosters, for example), the more likelihood of spike protein injury. That makes sense because you frequently hear of someone injured or dying after the second Covid shoot.
BK
I wonder if having more time between vacs and boosters reduces the risk of spike injury. Do spike protein numbers reduce over time? I took J&J May 2021 and the booster in Oct. Does J&J produce as much spike protein? Since a year has passed would I be less at risk if I boost this Nov. if I can find J&J?
You fall for marketing jive too easily.
“Do spike protein numbers reduce over time?”
Actually it’s S-protein antibodies vs N-protein antibodies being generated.
From what studies I have been able to read the answer is a conditional yes and that is a very conditional yes. The data seems to be minimal so far. The damage seems to vary.
The longer you go into to the cycle ie: initial doses with following “boosters “ there is more potential damage your body endures. Its now known that the spike producing Mrna package from the jab moves from the injection site to multiple locations and is dose dependent.
The Japanese found this out early on when Pfizer wanted access to their country for the jab.
Long story short. Yes maybe.
4 am bump!
Do you have any information on my question whether J&J produces as much spike protein as the mRNA vaccines?
Why would you even consider pulling the Russian Roulette trigger just one more time?
J&J used a 1 shot initial dose and then a booster. It was starting to get a reputation for causing problems and people started to get leery of it. The Public Health authorities said it was ok to mix n match Pfizer/Moderna with following boosters. Ask Gavin Newsome how that went. He did J&J then a Moderna booster.
As far as numbers re: spike protein amount goes I would have to look around my notes but don't know if I kept that info. What you really need to know is how much Mrna is delivered per dose.
I do know Pfizer introduces 30 micrograms of mRna per dose in the two initial doses and Moderna is 100 micrograms per dose and they are the 2 players left. That is why if you get “boosted” after a J&J jab it likely be Pfizer or Moderna.
At present a problem is the mRna “package” leaves the injection site and lodges in various systems such as the ovaries, testes liver etc. and does not clear. It even crosses the brain/blood barrier. A study showed the mrna was active in the body at least 60 days after injection.
Since you already went J&J and a booster and it is over a year and you have not said you had problems you seem to be lucky. I have seen vaccine injury within my family.
The choice is yours and yours alone to be “boosted”. I just offer my experiences and info I have gathered.
My SIL & BIL went J&J then a Pfizer booster. At ~ 5-6 mos. my SIL was fine, so far, but my BIL developed a Glioblastoma ( brain cancer tumor). It was taken out and luckily the surgeon believes they got it all. He seems to be recovering but his life is materially shortened. Survival median is ~15-16 mos. The occurrence of this in his ethnic group is very low He is Asian in his 50’s
Maybe he was really unlucky maybe not, Can I prove it definitively. No. He had no need to get Jabbed. Athletic and healthy as a horse. Lance Armstrong athletic. Covid was no threat to him. Just my 2cts.
Why not? 5 out 6 doctors say Russian Roulette is harmless/s
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