The data is in, yet nobody cares!
The data is in, yet nobody cares!
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I wouldn’t say nobody cares, I’d say there’s nobody that has real power to do something about and wasn’t in on it.
Incoming: more denial Gov'ts order social media to supress and censor Free Speech:
Judge Orders Fauci to Testify Under Oath on Social Media Censorship
In a 28-page order, U.S. District Judge Terry Doughty has ordered NIAID Director Anthony Fauci, former White House Press Secretary Jen Psaki, Surgeon General Vivek Murthy, and other leading federal officials in charge of the response to Covid to be deposed (testify under oath) in Missouri v. Biden
The case which NCLA Legal is representing plaintiffs including Jay Bhattacharya and Martin Kulldorff against the Biden administration for its coercion of social media companies to violate free speech during Covid.
Discovery documents in the case previously revealed a vast federal censorship army, with more than 80 federal officials across at least 11 federal agencies having secretly coordinated with social media companies to censor private speech, in what plaintiff Aaron Kheriaty described as potentially “the most ...
Discovery documents in the case previously revealed a vast federal censorship army, with more than 80 federal officials across at least 11 federal agencies having secretly coordinated with social media companies to censor private speech, in what plaintiff Aaron Kheriaty described as potentially “the most ...
This is how the FM/R/F mafia works!
The winter wave already goes down in Germany/Switzerland.
CH: https://www.covid19.admin.ch/de/overview
People don't want to vaxx anymore! So Pfizer decided to quadruple the EU prices of the heritage poison!
Bivalent Bombshell? BA.4/BA.5 mRNA Booster Dose Fails Comparative Antibody Titer Test: Could it be Antigenic Sin?
Prominent researchers at Columbia University represented by corresponding author Dr. David Ho, who heads up the Aaron Diamond AIDS Research Center (ADARC) and 1996 Time magazine Person of the Year, as well as University of Michigan epidemiologist Aubree Gordon, PhD report disappointing news about the bivalent Omicron BA.4/BA.5 vaccine booster recently released into the market by both the U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) without human clinical trials data. The well-known researchers note that despite their widespread use as a vaccine booster in the market, little is known about the antibody responses induced in humans—this this a laboratory experiment. Unfortunately, this targeted lab study didn’t instill more confidence. At about 3.5 weeks, the bivalent booster dose performed on par with the existing monovalent vaccine dose in the New York City-based laboratory experiments.
The Study
Collecting sera from a group of persons who received three doses of the original monovalent mRNA vaccines as well as the recent bivalent vaccines targeting BA.4 and BA.5, the prominent scientists compared virus neutralization by these sera to panels of sera from persons who received either three or four monovalent mRNA vaccines as well as to sera from persons with BA.4/BA.5 breakthrough infection post mRNA vaccination.
In the lab the team used pseudovirus neutralization assays to test the sera for neutralization against an ancestral SARS-CoV-2 strain, several Omicron sub-lineages, and several related sarbecoviruses. The findings were uploaded to the preprint server bioRxiv, meaning they still need to be peer reviewed.
The Findings
TrialSite reports what has to be considered disappointing news about these bivalent booster doses based on the laboratory examination set up at Columbia University. The bivalent booster vaccine failed to elicit higher NAB titers than a fourth dose of the original formula even against BA.5!
The authors report:
“At ~3-5 weeks post booster shot, individuals who received a fourth vaccine dose with a bivalent mRNA vaccine targeting BA.4/BA.5 had similar neutralizing antibody titers as those receiving a fourth monovalent mRNA vaccine against all SARS-CoV-2 variants tested, including BA.4/BA.5.”
Further the authors elaborated in the preprint:
“Those who received a fourth monovalent vaccine dose had slightly higher neutralizing antibody titers than those who received the bivalent vaccine against three related sarbecoviruses: SARS-CoV, GD-Pangolin, and WIV1. When given as a fourth dose, a bivalent mRNA vaccine targeting Omicron BA.4/BA.5 and an ancestral SARS-CoV-2 strain did not induce superior neutralizing antibody responses in humans, at the time period tested, compared to the original monovalent vaccine formulation.”
A truly surprising find, the study design seems sound, and the pedigree of the researchers cannot be disputed. They used a combination of Moderna/Pfizer for the primary series and the bivalent, so no brand-driven conclusions can be made.
Could this be the result of immune imprinting (aka: Original Antigenic Sin)? Perhaps, the inclusion of the ancestral sequence reinforced the immune system to respond with NABs against the original and similar antigen. To minimize imprinting, they need to only include the new antigen in order to gain a more targeted response. This was clear in the murine data they showed for the monovalent updated boosters.
Paul Elkins contributed to this article.
Lead Research/Investigator
David Ho, MD Professor of Microbiology & Immunology, Clyde '56 and Helen Wu Professor of Medicine and Director, Aaron Diamond AIDS Research Center
Member, National Academy of Medicine
Member, American Academy of Arts & Sciences
Fellow, American Association for the Advancement of Science
Aubree Gordon, PhD Associate Professor Epidemiology
Family Doctor, Mother of Five, Weighs in on Pediatric Immunizations for COVID-19
Dr. Katarina Lindley is a Croatian-born, American-trained, board-certified family physician practicing in the state of Texas. As a leader, Dr. Lindley is a member of the Pandemic Health Alliance and Global Covid Summit. More community engagement includes her roles as President-Elect of Texas AAPS, Board member of DPCAction, President-Elect of TOMA, and Immediate Past President of Texas ACOFP. Additionally, she’s authored several articles on healthcare and medicine, as well as worked on healthcare policy reform with legislators, and writing bills in Congress.
Dr. Lindley, a.k.a., “Dr. Kat,” spoke with TrialSite News about her concerns with the approval of COVID-19 vaccines for young children; in her opinion, (with a few exceptions) they are not worth the risk. Furthermore, she doesn’t believe that the public has received transparent information with which they could legitimately give informed consent.
She provides her reasons for questioning their necessity given the knowledge that has come through research and real-world data in the last two years.
Lindley’s Public Testimony to the FDA Panel
Many of her concerns were expressed in an open public hearing during the FDA’s evaluation meeting of COVID-19 vaccines for children 5 years and under. She asserted in her three allotted minutes that the mRNA vaccine platform is “only partially understood.” In comparison to the “over-simplistic and predictable picture projected by health authorities and vaccine manufacturers,” current study data reveals “a different picture” about vaccine side effects and effectiveness.
“To assume that the [mRNA-Lipid Nano Particles (LNPs)] platform is intrinsically safe and doesn’t require case-by-case safety assessment and regulatory scrutiny is, in my opinion, reckless and runs counter to the very purpose of a drug regulator.” The fact that this technology is new means the vaccines should be approached with “full regulatory scrutiny to test long-term safety.”
Lindley notes that LNPs are detected in unintended places, including various organs–especially reproductive organs– as well as tissue, bone marrow, adrenal glands, blood, and more. She asked the panel: “How can we move forward when pharmacokinetics studies have already shown there is spike production in regional lymph nodes for two months or longer?”
She raises the topic of VAERS safety signal data which are “being ignored,” with 1.3 million “injection harms.” (TrialSite reminds readers that adverse event reports to VAERS need to be investigated to determine if the vaccine was ultimately the culprit.)
Beyond the fact that VAERS is suspected to be underreported, Lindley says the “speedy rollout of the new technology” is causing “much graver concerns” with a “significant increase in complex neurological, endocrine, autoimmune, and cardiac issues.”
“You would have to be a gambler, or something much worse, to argue there is no risk of fertility issues – which could be catastrophic for our future generations.” Her worries about future health ramifications stem from the dangerous lessons learned from “regulatory disasters” when harmful drugs such as thalidomide and Vioxx had to be recalled.
She told TrialSite she questions what would be the “magic number," (the threshold of instances involving severe harm and death) that it will take before the regulators will halt these vaccines in America. “So, give us a target. When will [regulators] say enough is enough? And the fact that they're not saying it, honestly, is mind-boggling because they're not following signs for sure. And it's been really a disappointment to see where the medical community has gone and how much we have accepted and not pushed back.”
In terms of ignoring red flags, she said, “I can tell you that overall, we're not doing enough autopsies. It's almost as if they don't want to find out what's causing these people to suddenly die.”
She reminded listeners during her testimony that the FDA has a “deep responsibility” to protect our children and future generations. “My expectation is that the FDA will continue its mission of protecting public safety and best interest against any and all harm. Future framework with this new technology is an existential threat to public health and should not be approved.”
However, the assertive reminder she gave to the FDA about their mission statement made no difference. Regardless of her testimony, the FDA unanimously approved COVID-19 vaccine administration for the youngest cohort.
This week, the Center for Disease Control ( CDC) and the Prevention Advisory Committee on Immunization Practices ( ACIP) approved adding these vaccines to the recommended pediatric schedule. However, ACIP member Dr. Nirav Shah, insisted that there will be no “requirement,”--at least not from the CDC. Ultimately, each state will decide if the shots will be required for kids to attend school.
On October 23, the Kansas Attorney General, Derek Schmidt, announced he would join 13 other state attorneys general in an official objection to this recent recommendation.
Will More Colleagues Speak Out?
On her website, she explains how she escaped from a “violent and oppressive” communist country at the age of 18. After her hometown was attacked, her family urged her to escape. Ultimately, she found sanctuary in the US, where she was able to obtain her medical degree, start a practice, and utilize the blessings of American opportunity. Her “desire to make a difference” in her community stems from her belief that “medicine is also an opportunity to become a voice for patients and colleagues.”
“Americans are such good people, but very naive people in a sense. You've never had to fight for your freedom. That freedom is always like it's an abstract. I know what it is like not to be free. I think some of them are realizing what that is like now. We haven't woken up as a nation yet.”
The lack of activists willing to stand up against the medical tyranny drove her to mourn the dismal state of the apathetic American society, and the moral deterioration of the medical community. She said she needed to “grieve” through writing, specifically poetry. When she gave herself a few days to contemplate and reflect, she knew how she would move forward.
“That was the time when I kind of faced my own fear and realized that there's really no other path for me than this: to speak out because I see the damage. As physicians, we cannot accept one life being lost, and we've lost at least 29,000 lives in the United States” due to vaccine injury. (TrialSite reminds readers again, that these VAERS numbers are unconfirmed figures that are self-reported or registered by medical professionals, but as of October there are now some 34,000 reported deaths.)
Lindley said a good portion of Americans are waking up because of the illogical policies enacted by world health leaders and politicians. For instance, tennis champion Novak Djokovic withdrew from US Open because non-citizens cannot travel to the US without proof of vaccination; Djokovic publicly opposes the discriminatory policy. Also, many college students are still mandated to get vaccinations and boosters, even when enrolling in online courses. These are just a few among many examples of vaccination discrimination that still persists in public schools, employment, travel, hospital policies and more.
“It's really mind-boggling, and it's stupid. We need to start calling it for what it is: idiotic.”
Lindley’s Message to Concerned Parents:
Corruption in Regulation Should Be Considered
Lindley believes regulatory bodies are captured and compromised; one only needs to “follow the money.” Therefore, it is up to parents to take the time to truly understand the risks and benefits. She argued that the countries with the highest uptake of COVID-19 vaccinations such as the US, UK, Canada, and Israel, all have “huge ties to Big Pharma.”
In contrast, nations like Denmark, Finland, Norway, and Sweden have put a halt on mRNA vaccination for young people. “And they're doing the best for their own people. I would say that our own agencies are not following their own mission statement.” In contrast to the US, she said these nations “truly invest in the health of their people.” She mentions the alternative, prevention-based mindset of their societies, and government initiatives that aim to promote healthy, active lifestyles, as well as access to better nutrition.
Research on the Effectiveness for Children is Incomplete and Misleading
The data from Pfizer and Moderna that was used to evaluate these vaccines for kids was extrapolated from data on adults. “Their own trials on children actually show relatively negative data…So it's really clinically not indicated, and it's not safe and it's not effective in children.” She condemned the FDA approval without long-term safety data as “truly negligence.”
Lindley uses the story of one child, Maddie de Garay, to illustrate instances of glaring and egregious compromise regarding safety data on children. The teen was excited to be a participant in the Pfizer trial because she aspired to become a nurse. Unfortunately, she suffered life-altering injuries. She is now wheelchair-bound and must eat through a feeding tube. The de Garays said Pfizer removed Maddie (and her severe reaction results) from the trial and labeled it inaccurately as gastric distress.
Maddie’s abandonment by the trial physicians, Pfizer, and political leaders is an example of “crimes against children” says Lindley. To the physicians who dismissed de Garay: “that’s really the abandonment of your Hippocratic Oath,” she stated.
For the past two years, said Lindley, the public has complied with masks, isolation, lockdowns, 6-foot distancing, and vaccination. “I think it's really time for us to say to our leaders, the people who are supposed to be representing us, that now it's our time. We take our power back. We start owning our own lives. We start truly engaging in health.”
Vaccines are Not the Only Way to Treat and Protect Against Illness
"We need to realize that our bodies are a masterpiece. We were created in an image, and our bodies know what to do. So, it's past time to actually try to find medication for everything.” ---- Dr. Katarina Lindley
While she hasn’t lost faith in vaccine initiatives completely, she does question if every one of them is necessary. Furthermore, should we be administering the bulk of them to babies? She said she spaced them out for her daughter with the support of her pediatrician, “because I felt giving so many all at once was just insane.”
She referenced a recent article she read announcing a desire to develop a vaccine to prevent antibiotic-resistant illnesses. She's beginning to notice a growing "new trend' in which the public health community is looking to approach nearly every medical malady with a vaccine. "I'm sorry, we don't vaccinate our way through life."
Instead, she said public health leaders, legislators, and parents, should take a multifaceted approach to improve the health of the public. There are many steps parents can take to bolster the immune responses in their children.
“If we take care of our bodies, if we do our part, if you eat healthy, if you exercise, if you sleep, if you decrease stress, you take your vitamins, you drink your kefir every morning, or kombucha–I hate kombucha, but they have good bacteria, right? If you do all those good things, the immune system can handle most things. We need to realize that our bodies are a masterpiece. We were created in an image and our bodies know what to do. So, it's past time to actually try to find medication for everything.”
She also reiterates an important detail: the CDC reported in February that 75% of children already have natural immunity from prior infection. Lindley estimates the number could be as high as 90% to date with nine months of additional infections.
Steps to Hold Public Health Agencies and Vaccine Manufacturers Accountable
“So, there will come a time for all of us to look ourselves in the mirror and decide whether we are on the right side of this argument or not. But the biggest heartbreak is that we're going to lose children, and adults just because of agendas and money and everything that's going on in the world.”
Her solution is to put pressure on the legislators. “I honestly hope that these elections coming up make some waves because I would say that most people that are in DC do not represent us. I'm not sure what they represent, but they don't represent us.” She said that while a select few in congress are pursuing accountability for the harm caused by these vaccines–[Rep. Thomas Massie (R-KY 4th District), Rep. Chip Roy (R-TX 21st District), Sen. Ron Johnson (R-WI)] most legislators make excuses that there’s nothing they can do.
“And the thing that annoys me: [parents will rebut] ‘well, we're not in power, so we can't do this.’ You can make noise. You can have a press conference so that people feel that they're being heard.”
(Sen. Ron Johnson has held expert panel discussions that included testimony from vaccine-injured Americans and doctors who back their claims. Several public health leaders and COVID-19 vaccine executives –such as CDC Director Dr. Rochelle Walensky and Pfizer CEO Albert Bourla– were also invited, but not one of these leaders attended.)
Parents need a game plan to get their representatives' attention. “You can send letters. If there is a [drug manufacturing] company that's functioning in your state, put pressure on your governor to do something. There's so much [parents] can do. And the fact that Pfizer and different companies are still doing what they're doing despite their own data showing that this is damaging the lives of many people, it's incredible.”
Finally: Strokes and Myocarditis in Children Should Not Be Shrugged Off
Strokes in children are not normal, and the fact that doctors and public health leaders are trying to discount these signals of severity is worrisome to Lindley.
“I've read in medical books that children sometimes could possibly have a stroke at birth if they were born with some kind of genetic disorder, or something like that. Very rare. One of those zebras that you don't know much about, but they tried to normalize the fact that even children have strokes. No, I'm sorry, children don't have strokes.”
As far as “mild” myocarditis in children is concerned: “Yes, there are varying degrees of myocarditis, pericarditis, different degrees of damage, and sometimes it can be what we as physicians might call 'mild' because the damage to the muscle is not as extensive as others, but even 'mild' myocarditis carries risk.”
“So, if any of my three kids came to me in the middle of the night to say, ‘I have chest pain and shortness of breath,’ I can tell you that The Mama would freak out. But even as a doctor I would freak out because it's not normal. Children don't have suspended shortness of breath. And I think as parents, it behooves us to stop accepting that, to stop listening to this. I love my colleagues. I have lots of colleagues in pediatrics and family medicine. But I'm sorry, if you're willing to tell a parent that ‘myocarditis is mild, they'll get over it.’ You probably should rethink medicine and do something else.”
This week, the Center for Disease Control ( CDC) and the Prevention Advisory Committee on Immunization Practices ( ACIP) approved adding these vaccines to the recommended pediatric schedule.
A criminal gang of FM/R/F members provided Pfizer/Moderna with a new path for generating profit. Buddies help buddies. There is no more any sense of "we are united states". Instead there are highly criminals (the worst Nazi breed ever) that rule key parts of the states.
Independent Researchers Examining Pfizer mRNA Vaccines: Strange Reports
Manufacturers Must be Questioned on the Vial Contents and Manufacturing Practices.
In the US and abroad, Covid-19 vaccine manufacturers are not transparent about the ingredients in their products, claiming commercial secrecy. The vaccine vials are federal property in the US according to the vaccination provider contracts. They are ordered, shipped to, and distributed by the Department of Defense according to the DOD/BARDA-Pharma manufacturers' contracts. Even though the current demand for these vaccines is low, it is still expressly forbidden for any independent researcher to examine the contents of the vials or perform any independent study, claiming such effort would “divert” the vials from an “urgent” need. Internationally, similar prohibitions exist written into predatory contracts by the manufacturers. For example, contracts in the EU require the purchasers to suspend all laws and regulations applicable to quality control, good manufacturing or distribution practices that would apply to pharmaceutical products, and then also forbid testing the vials on import into the country. These contracts and lack of product integrity and transparent testing were questioned in a recent hearing in European Parliament and are now reportedly under investigation by the EU Public Prosecutor’s Office.
Despite the predatory contracts, prohibitions of transparency, gaslighting, and cover-up, many independent researchers worldwide have been investigating the contents of the vials using available equipment and skills. Most of the investigations are done under standard optical microscopes.
One such investigation has been conducted in Australia by Dr. David Nixon, a family physician. Dr. Nixon used examined several vials of Pfizer vaccines from a frozen state and up to several months of drying on a microscope slide. His findings are consistent with other published testing results and images. Overall, Pfizer's substance is a thin gel, not a clear liquid. It exhibits a snowy or “confetti-like” appearance under a microscope from a frozen state:
At some points, larger structures are visible right away, but many more appear after unfreezing. When left for several hours, structures grow and get larger. Characteristic structures include square and rectangular shapes as well as fibers or “ribbons”. These tend to grow to very large sizes by microscopic standards.
While slow, this growth and movement are clear when the multi-hour video is sped up to a few minutes.
Several experiments have shown that growth is inhibited when a sample is shielded from ambient electromagnetic fields by a Faraday bag. Some commentators have tried to dismiss the square-shaped structures as common salt, sugar, or cholesterol. However, a comparison with reference photos of these substances shows that the square shapes found in Pfizer vials are very different in symmetry and organization.
Image of cholesterol crystals:
Image of salt crystal:
Structures commonly found in Pfizer vials:
At any rate, cholesterol or salt crystals are not known to respond to electromagnetic fields.
Optical microscopy only shows micro, not nano-scale objects. The structures found in the vials are highly problematic due to their large size alone. The manufacturers of these products have not addressed any of these findings. The products should be deemed adulterated when any large shapes and contaminants are found. These products must be urgently stopped, recalled, and investigated properly.
New York Supreme Court reinstates all employees fired for being unvaccinated, orders backpay
State Supreme Court found that being vaccinated 'does not' stop the spread of COVID-19
A New York state Supreme Court ordered all New York City employees who were fired for not being vaccinated to be reinstated with back pay.
The court found Monday that "being vaccinated does not prevent an individual from contracting or transmitting COVID-19." New York City Mayor Eric Adams claimed earlier this year that his administration would not rehire employees who had been fired over their vaccination status.
NYC fired roughly 1,700 employees for being unvaccinated earlier this year after the city adopted a vaccine mandate under former Mayor Bill de Blasio.
Outbreaks of a highly pathogenic strain of avian influenza are leaving a path of destruction across Europe and North America, on a scale that has not been previously seen. Domestic bird culls once kept the virus in check, but sustained circulation in wild birds has become the norm since the early 2000s. Over the past year, transmission in wild birds has ramped up dramatically. “Something is quite different about this virus”, says wildlife-disease researcher Rebecca Poulson, but no one knows exactly what that is. It’s possible that mutations have enabled the virus to infect more bird species than previous strains; mammals such as seals, bobcats and skunks are also being infected. Researchers fear that the outbreaks could rage on.
Bivalent Bombshell? BA.4/BA.5 mRNA Booster Dose Fails Comparative Antibody Titer Test: Could it be Antigenic Sin?
Second Opinion confirms
Bird flu on the rampage
Outbreaks of a highly pathogenic strain of avian influenza are leaving a path of destruction across Europe
What's changed over last few years?
Wild birds the same, Lockdowned caged game birds released in spring the same
Poultry: chickens etc no longer in barns - they're outside Free Range
More 'be kind', 'be green' idiocy backfires and does more harm
Good article with indisputable facts - unless you're "three monkeys"
Excess deaths in UK homes alarmingly high:: https://www.ons.gov.uk/peoplep…l/weekending14october2022
The number of deaths was above the five-year average in private homes (26.8% above, 688 excess deaths), hospitals (14.3% above, 646 excess deaths), care homes (10.6% above, 232 excess deaths) and other settings (5.0% above, 41 excess deaths) in Week 41 in England and Wales.
These home deaths obviously are spontaneous and 100% likely due to vaccine damage.
LONG COVID TREATMENT CLINICAL TRIAL - AUSTRALIA
Registration number (1)
ACTRN12622001204730
Effectiveness of neutraceutical therapies on symptoms in adults with long-COVID-19: The Alliance Long COVID-19 Treatment Trial
Anticipated recruitment start - October 24, 2022.
2-staged intervention after baseline and 6 week assessments:
Stage 1 (1-6th week):
6-week nutritional supplement consisting of 35g pineapple powder + 2x3g ginger infused oil per day to be consumed at mealtimes with food as convenient; adherence monitored by diary.
Stage 2 (7-12th week):
3 groups: Allocation by location and referral by the trial doctor.
Group 1 will receive 30g of Intravenous Vitamin C twice weekly for 6 weeks, administered by a registered nurse
Group 2 will receive all the following oral supplements as capsules [Kyolic aged garlic extract (1.2 g) + Fish oil (2g) + Curcumin (500mg) + N-acetylcysteine (600mg) + Vitamin D (5000 IU) + Vitamin C (1g) + Zinc (15mg)] daily for 6 weeks, administered by the principal investigator; adherence will be monitored by return of unused supplements at the end of the 6-week period.
Group 3 will continue to receive the nutritional supplement consisting of 35g pineapple powder + 2x3g ginger infused oil per day to be consumed with food at mealtimes as convenient for 6 weeks; adherence monitored by diary.
Comparator / control treatment:
The patients are their own control. Treatment effectiveness will be assessed by comparison of symptoms before and after the intervention(s), Symptom assessment will be done at baseline, 6 weeks (after intervention 1) and 12 weeks (after intervention 2).
Outcomes
Primary outcome [1]
Symptom score assessed by online symptom questionnaire developed for this trial
Timepoint [1]
6 weeks after completion of intervention 1 and 12 weeks after completion of intervention 2 compared to baseline
Secondary outcome [1]
Composite Blood test results including Full blood cell count, D-Dimer, High-sensitivity C-reactive protein (hsCRP), erythrocyte sedimentation rate (ESR), histamine, thyroid function, Kidney/Liver function, Vitamin D levels
Secondary outcome [2]
Composite testing: Viral reactivation of EBV (Epstein-Barr-Virus), CMV (Cytomegalovirus) and/or HSV (Herpes simplex virus) assessed by inhouse developed Pathogen Blood Test - consisting of cytological analysis of isolated human cells followed by viral antibody Immuno-Cyto-Chemistry
Timepoint [2]
12 weeks after completion of both interventions 1 and 2 compared to baseline,
COVID-19 vaccine-induced encephalitis and status epilepticus
Learning points for clinicians
Convulsion/seizure may occur infrequently after mRNA-1273 vaccine (Moderna vaccine) administration, with an estimated risk of 285 events per million person-years. We report a rare case of coronavirus disease 2019 vaccine-induced encephalitis and status epilepticus. The patient recovered after pulse corticosteroid therapy administration. Clinicians should be aware of possible neurological complications post-vaccination.
Group 3 will continue to receive the nutritional supplement consisting of 35g pineapple powder + 2x3g ginger infused oil per day to be consumed with food at mealtimes as convenient for 6 weeks;
I would opt for the Kaviar champagne group with full shiatsu/tantra once a week...
I would opt for the Kaviar champagne group with full shiatsu/tantra once a week...
I'd stick to the stages but add vitamin b and Ganoderma lucidum, reishi mushroom every day for the whole trial and maybe add a shot of B12. Long COVID is the result of vitamin and mineral deficency, which science now points to Autoimmune disease from resulting infection
another bill of goods sold to the public! When Covid mutates mRNA vaccines are easy to tweak. It took 2 years for the first easy tweak and oh look, it's no better than original crap. ONE LIE AFTER AN OTHER!
Updated Covid-19 vaccines boost protection, but may not beat original formula against BA.4 and BA.5, early studies suggest
