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Covid: US DoD and other world governments’ bioterrorism program confirmed by Twitterfiles releases
By Alexandra Bruce
According to Sasha Latypova, a retired pharma executive who started the websites, HowBad.Info and HowBadIsMyBatch.com, where you can check your vaxxine batch number to see if you got saline or if you got a Death Shot, she says that from a legal perspective, including the actual contracts signed by Pfizer with the DoD, as well as other internal documents that she’s acquired, Operation Warp Speed is a DoD project and the vaxx is under Emergency Use Authorization. Therefore, it is not subject to FDA regulation. Any pretense that we have seen of regulation is pure theater. It is a total PSYOP, because the vaxx is not a commercial pharmaceutical product.
This is why, in the face of all of the overwhelming evidence of injury and death, the FDA and its counterparts all over the world have not stopped this program. Legally, these shots are not clinical investigational products and they are not subject to any normal pharmaceutical regulations and there can be no other conclusion than that these are bioweapons that are intended to maim and kill.
Per contracts with the US Government, the product is shipped to the DoD, which retains ownership of the vials until the product is injected into people. These contracts are very detailed and they specify the manufacturing data to be delivered to the DoD but they don’t require any of the routine sampling that takes place per FDA regulations.
It is a regulatory requirement to retain samples of each batch produced, and these samples of vials should exist and be available for examination, for purposes of verification of their contents vs the label. However, the DoD contracts expressly forbid any such tests!
Despite the disturbing prohibition on independent vial testing, covert random testing of the mRNA vials has been ongoing worldwide – and the consistent finding among all is that there is yet to be a single vial found in full conformance to the manufacturer’s label.
Some batches which have tested as “blanks” have also been associated with those batches having almost no reported adverse events. This is why some people who’ve been injected are fine and why this was reported to be especially true of the earliest batches of 2021. They couldn’t have people dying suddenly, right off the bat.
According to Sasha Latypova, whose Substack is absolutely MUST-READ, she says that the American People and the peoples of the world have been subjected to a conspiracy to commit mass murder through bioterrorism and informational warfare operations by the DoD, HHS, other US government agencies – as well as other world governments, along their conspirators in the Mainstream Media and in Big Tech, who we’ve recently learned through the Twitterfiles have been enacting their unprecedented censorship on Americans, about the vaxx, about the elections, about transsexuals, etc. on the direct orders of our intelligence agencies.
Naomi Wolf was on with Steve Bannon yesterday and she echoed these thoughts but it looks like she isn’t quite ready yet to go on the record and say that large swathes of our own government – like many, many governments around the world – are committing genocide against their own people. This is not something that China is doing to us or that Big Pharma is inflicting on us and that our poor little government is asleep at the wheel. No.
My own source tells me that a big part of how this has occurred – not all of it but a big part of this infiltration of the US Government has been through the Senior Executive Service aka “The Keystone”, which is a kind of union for DC bureaucrats, where they’re not subject to the same degree of vetting, which is how we got Sam Brinton, the gender-fluid kleptomaniac in the Department of Energy and how it’s nearly impossible to fire them.
“It has been shown how deeply the son of the current US president, Hunter Biden, is involved in funding the US DoD-controlled company, Metabiota.
“However, some participants in closed projects remain in the shadows, although they are key players in Ukraine’s military-biological programme,” stated Major General Igor Kirillov, the head of the Russian military’s radiation, biological and chemical protection troops.Former AMA head Dr Kerryn Phelps lifts veil of silence over Covid vaxx adverse reactions and threats from regulators
by Frank Chung, senior reporter News.com.au
In an explosive submission to Parliament’s Long Covid inquiry, the former Australian Medical Association (AMA) president and politician Dr Kerryn Phelps has broken her silence about the “devastating” experience — emerging as the most prominent public health figure in the country to speak up about the taboo subject.
She suggested the true rate of adverse events is far higher than acknowledged due to under-reporting and “threats” from medical regulators.
“This is an issue that I have witnessed first-hand with my wife who suffered a severe neurological reaction to her first Pfizer vaccine within minutes, including burning face and gums, paraesethesiae, and numb hands and feet, while under observation by myself, another doctor and a registered nurse at the time of immunisation,” the 65-year-old said.
“I continue to observe the devastating effects a year-and-a-half later with the addition of fatigue and additional neurological symptoms including nerve pains, altered sense of smell, visual disturbance and musculoskeletal inflammation. The diagnosis and causation has been confirmed by several specialists who have told me that they have seen ‘a lot’ of patients in a similar situation.”
Dr Phelps married former primary school teacher Jackie Stricker-Phelps in 1998.
“Jackie asked me to include her story to raise awareness for others,” she said.
“We did a lot of homework before having the vaccine, particularly about choice of vaccine at the time. In asking about adverse side effects, we were told that ‘the worst thing that could happen would be anaphylaxis’ and that severe reactions such as myocarditis and pericarditis were ‘rare’.”
Dr Phelps revealed she was also diagnosed with a vaccine injury from her second dose of Pfizer in July 2021, “with the diagnosis and causation confirmed by specialist colleagues”.
“I have had CT pulmonary angiogram, ECG, blood tests, cardiac echogram, transthoracic cardiac stress echo, Holter monitor, blood pressure monitoring and autonomic testing,” she said.
“In my case the injury resulted in dysautonomia with intermittent fevers and cardiovascular implications including breathlessness, inappropriate sinus tachycardia and blood pressure fluctuations.”
Dr Phelps said both reactions were reported to the Therapeutic Goods Administration (TGA) “but never followed up”.
She revealed she had spoken with other doctors “who have themselves experienced a serious and persistent adverse event” but that “vaccine injury is a subject that few in the medical profession have wanted to talk about”.
“Regulators of the medical profession have censored public discussion about adverse events following immunisation, with threats to doctors not to make any public statements about anything that ‘might undermine the government’s vaccine rollout’ or risk suspension or loss of their registration,” she said.
The Australian Health Practitioner Regulation Agency (AHPRA), which oversees Australia’s 800,000 registered practitioners and 193,800 students, last year warned that anyone who sought to “undermine” the national Covid vaccine rollout could face deregistration or even prosecution.
AHPRA’s position statement said that “any promotion of anti-vaccination statements or health advice which contradicts the best available scientific evidence or seeks to actively undermine the national immunisation campaign (including via social media) is not supported by National Boards and may be in breach of the codes of conduct and subject to investigation and possible regulatory action”.
Earlier this year, Australian musician Tyson ‘tyDi’ Illingworth said he had been told privately by doctors that they feared being deregistered if they linked his neurological injury to the Moderna vaccine.
Dr Phelps said she had heard stories of vaccine injury from “patients and other members of the community”.
“They have had to search for answers, find GPs and specialists who are interested and able to help them, spend large amounts of money on medical investigations, isolate from friends and family, reduce work hours, lose work if they are required to attend in person and avoid social and cultural events,” she said.
“Within this group of vaccine injured individuals, there is a diminishing cohort of people who have symptoms following immunisation, many of which are similar to Long Covid (such as fatigue and brain fog), but who have not had a Covid infection. These people would be an important subset or control group for studies looking into the pathophysiology, causes of and treatments for Long Covid. It is possible that there is at least some shared pathophysiology between vaccine injury and Long Covid, possibly due to the effects of spike protein.”
She added that “in trying to convince people in positions of influence to pay attention to the risks of Long Covid and reinfection for people with vaccine injury, I have personally been met with obstruction and resistance to openly discuss this issue”.
“There has been a delay in recognition of vaccine injury, partly because of under-reporting, concerns about vaccine hesitancy in the context of managing a global pandemic, and needing to find the balance between risks and benefits on a population level,” she said.
“Reactions were said to be ‘rare’ without data to confirm how common or otherwise these reactions were. In general practice I was seeing cases, which meant other GPs and specialists were seeing cases too. Without diagnostic tests, we have to rely largely on clinical history.”
In July this year, the independent OzSAGE group of which Dr Phelps is a member issued a position statement calling for better systems and management of Covid vaccine adverse events and “recognition of the impact of vaccine injury”.
Dr Phelps, who was heavily involved in crafting the statement, wrote in her submission that the OzSAGE document “outlines the scope but not the scale of the problem because we do not know the scale of the problem”.
“This is partly because of under-reporting and under-recognition,” she said.
According to the TGA’s most recent safety update, there have been a total of 137,141 adverse event reports from nearly 64.4 million doses — a rate of 0.2 per cent.
There have been 819 reports “assessed as likely to be myocarditis” from 49.8 million doses of Pfizer and Moderna. Fourteen deaths have officially been linked to vaccination — 13 after AstraZeneca and one after Pfizer.
Cairns News: This data from the TGA is at odds with VAERS data from the US where there have been many thousands of reported deaths.
From the VAERS website: “From December 14, 2020, through December 7, 2022, VAERS (US) received 17,868 preliminary reports of death (0.0027%) among people who received a COVID-19 vaccine.”
The long term adverse affects are now beginning to emerge in Australia as emergency wards fill with those who have been injured by the mRNA vaxx. Many of these hospital admissions for vaccine damage are unreported or reported as Covid infections.
Parental online survey of child vaxx recipients is anecdotal and unfit for detailed, clinical analysis
From SMH
July 2022
Parents yet to vaccinate their children against COVID-19 are being urged not to wait amid a rise in cases among school students as new data shows side effects to the vaccine are overwhelmingly mild, and occur at lower rates than were predicted in clinical trials.
Children aged five to 15 are reporting fewer common side effects – which include a sore arm, fatigue, headaches and muscle pain – after their mRNA COVID vaccinations than those reported in clinical trials, data from national vaccine safety surveillance system AusVaxSafety shows.
An analysis of 392,268 survey responses from parents of children vaccinated between July 2021 and May 2022 showed roughly a quarter of five- to 11-year-olds reported at least one side effect within three days of their Pfizer vaccines (25 per cent following their first dose, and 28 per cent following their second).
Among 12- to 15-year-olds who received Pfizer, one in three reported at least one side effect by following their first dose (32 per cent), and half reported side effects after their second (49 per cent). One in three children in that age group who had the Moderna vaccine reported side effects after their first dose (34 per cent), and two in three following their second (64 per cent).
The survey responses were provided by parents via SMS or email.
A sore or itchy arm, redness and swelling at the injection site, fatigue, headaches and joint or muscle pain were the most common side effects among both age groups and usually faded away within a day, the researchers from the National Centre for Immunisation Research and Surveillance (NCIRS) reported.
Associate Professor Nick Wood, associate director of clinical services and vaccine safety at the NCIRS and lead author of the analysis, said the rate of side effects was “probably a third lower” than were observed during clinical trials.
“When you’re in a clinical trial, you’re more closely scrutinised … [but] this data shows how it is experienced in the real world,” Wood said.
Just 0.3 per cent of five- to 15-year-olds sought medical help for their side effects, and only 7 per cent reported that their routine activities were affected.
Side effects were slightly higher in children with chronic medical conditions, which might reflect closer observation by their parents. The researchers suggested the rate of side effects could be even lower, with parents more likely to complete the survey if they noticed side effects.
Wood said the reactions experienced by children were similar to those of adults, but incidences were fewer. For example, 53 per cent of adult Pfizer recipients reported an adverse event after dose two, and 21 per cent missed routine activities such as work or study.
About 2.2 million children aged five to 15 (53 per cent) have received at least one dose of a COVID vaccine and 1.9 million (40 per cent) have received their second. Wood said he hoped parents yet to vaccinate their children would use the survey data to inform their decision.
“Forewarned is forearmed … [so] here is data to support their decision making about the vaccine,” Wood said.
Professor Robert Booy, an infectious diseases paediatrician at the University of Sydney, said the results confirmed what was being seen abroad: that younger children were experiencing fewer side effects from the vaccines.
There were no reported cases of myocarditis (inflammation of the heart) or pericarditis (swelling of the tissue surrounding the heart) in the survey data, although the Therapeutic Goods Administration has received four reports of likely myocarditis and six of likely pericarditis in children aged five to 11 and about 700 likely myocarditis and 1050 likely pericarditis cases among the 12 to 17 age group, mostly in boys.
No child or adolescent has died from a COVID-19 vaccine in Australia, a statement that cannot be supported by this survey which flies in the face of contradictory VAERS medical data in the United States. The long-term effects of the experimental mRNA inoculation is totally unknown. The inventor of mRNA technology Dr Robert Malone has warned against its use. Cairns News
“The concern we had with older children and teenagers was myocarditis, but the reports are reassuring that this is considerably rare,” Booy said. Cairns News received anecdotal reports from the Atherton Tablelands last year that three separate adolescents two living on the same road and another nearby were all diagnosed with myocarditis (and remain permanently disabled) within weeks of getting a second vaxx.
The survey findings, which have not been peer-reviewed, were published on Thursday on medRxiv.
With the start of the school term, coronavirus infections have increased in children and teenagers, data from NSW Health’s latest surveillance report shows.
There were more than 4100 cases in children aged five to nine, up from 2600 the previous week, and more than 8500 cases in those aged 10 to 19, up from 5200.
The report also included data showing about 3 per cent of people infected with COVID-19 in January have now been reinfected.
According to NSW Health’s records, of the 639,000 cases reported in January, more than 10,000 had been reinfected within 90 days of their first positive test, 16,000 had been reinfected by the 120-day mark and 20,000 people (or 3.2 per cent) registered a positive COVID-19 test for a second time within 150 days of their first.
Cairns News: It should be noted that any diagnosed infection in this survey was performed by a PCR test, a notoriously inaccurate method described by its inventor Dr Kary Mullis as being “unfit for purpose” as a diagnostic tool for viral infections such as Covid 19.
A real statesman of the Australian Senate exposes the Covid scam – let the trials begin of those who killed or injured thousands of Australians by experimental vaxx
I have no doubt that, as the truth comes to light, history will judge those in this Parliament as cowards for failing to stand up against the COVID B.S.
Read the study, COVID-19 vaccines – An Australian Review by Conny Turni and Astrid Lefringhausen here.
Watch the COVID INQUIRY 2.0 videos here.
Hansard: As a servant to the people of Queensland and Australia, I note that at the European parliament inquiry into COVID two weeks ago, Janine Small, the President of International Developed Markets for Pfizer revealed that the Pfizer vaccine injection was never tested to see if it would prevent transmission—never tested. Small went on to say this was because Pfizer had to work at the speed of science. Well, it seems the speed of science and the velocity of money are the same thing. Shameful decisions were taken deliberately to facilitate big pharma getting their injections to market in time. The mouthpiece media have the same large investment funds on their share register as big pharma. It’s no surprise the mouthpiece media amplified the COVID scare, doubling down on fear porn and demonising anyone who clung to ‘my body, my choice’, just so the media’s shareholders could line their pockets with tens of billions of dollars in windfall profits.
I remember when the political left walked behind banners reading ‘my body, my choice’. Now real conservatives hold those banners high while the Left abuse us. How fast the Left abandon their principles when an opportunity to tell people what to do comes along, to control people. It was clear after just four months of COVID the scary Chinese videos of people dropping dead in the streets should not have been taken at face value. Measures taken out of an abundance of caution in March 2020 should have been re-examined just a few months later, as we requested and suggested. They never were. At the time, the data clearly showed COVID was no more deadly than a severe flu and well under anything the public would consider to be a pandemic. Let me support that statement.
The following data is from the Australian Bureau of Statistics published in part as a result of a One Nation document discovery a few weeks ago. In 2019, the year before COVID, the seasonal flu cost 4,126 lives. The next year, in 2020, Australia recorded 882 deaths from COVID and 2,287 deaths from the flu for a total of 3,196 deaths, 1,000 less than before COVID, almost a thousand less than the flu alone killed the previous year. In 2021, 1,137 deaths were recorded from COVID and 2,073 from the flu, for a total of 3,210. This means deaths from the flu including COVID across the first two years of the so-called pandemic were right on the long-term average of 3,255. There was nothing unusual about the Australian death rate in 2020 or 2021 yet the COVID substances—I won’t call them vaccines—the COVID injections, were given emergency approval. The only thing about our death rate in 2020 that was unusual was that it was at a seven-year low.
These are facts. This makes a joke of provisional approval granted for injections out of urgency. There was no urgency. It is not just the vaccines that were inappropriately approved; dangerous drugs like the antiviral Remdesivir were waved through using the same false urgency. Remdesivir’s side effects include respiratory failure and organ failure. The perfectly safe but out-of-patent antiviral ivermectin was banned to make way for remdesivir—banned, proven, banned. The UK has recently put ivermectin back into use. We must as well. The conclusion an increasing number of Australians are coming to is that our health technocrats tore up our tried and true health systems to shift products for their mates in the pharmaceutical industry, and now people are dying from those same products.
Once the injection rollout started, there was a spike in deaths. It must be noted correlation is not causation. The link between the cause—vaccines—and the effect—death, injury and suffering—must be proven. Well, it has now been proven beyond a shadow of a doubt. At my second COVID Under Question inquiry in August, many highly-qualified medical professionals from around the world established that link, providing evidence the injections were responsible for many more deaths than the health technocrats admit.
Late last month, the Clinical and Experimental Immunology journal published an article entitled ‘COVID-19 vaccines—an Australian review’. The authors are Conny Turni and Astrid Lefringhausen, from the University of Queensland. This article details the medical science behind the wide range of medical harms inflicted on Australians as a result of the hubris and the criminal negligence of health technocrats. I promised to hound you people down, and now science has done that for me. The issue of vaccine harm must be referred to a royal commission today. These criminals must be brought to justice. This report is reproduced on my website, and anyone who reads this report and still defends the fake vaccines is as guilty as the companies that made it.
It’s no surprise that COVID has spiked in correlation with the rollout of the fake vaccines. ABS data is not yet available for 2022, although Australian actuarial data is. In the first four months of 2022, death from all respiratory diseases—the flu, pneumonia and COVID taken together—is still at normal levels, yet deaths from cardiac and pulmonary events are up 11 per cent, and unexplained deaths are up 13 per cent. At this rate, an extra 10,000 Australians will die in 2022. Anyone reading the journal article I referred to will know exactly why this is happening. I refuse to believe our health technocrats do not know. A royal commission must ask what they knew and when.
In May 2020 I criticised fear-driven response to COVID in the Senate, within months of this mismanagement of COVID. At that time Senator Hanson and I were the lone voices of dissent in the Senate, and Craig Kelly and George Christensen were the lone voices in the other place, and Senators Rennick and Antic joined us—six representatives out of 227 people. Everyone else in both houses displayed an ignorance of proper scientific process, an inability to read empirical data and a misplaced trust of health bureaucrats. Health technocrats have spent their entire professional lives working closely with the pharmaceutical industry. And we expected them to be impartial. Come on! We delegated authority to the last people who should have been trusted with that authority.
The Senate is the house of review. Every aspect of our COVID response should have been scrutinised to the last detail. The Senate failed in that mission. COVID measures were beyond question, and it seems they still are. Rather than review, the Senate covered up. Senators Rennick and Antic, in company with myself and Senator Hanson, tried to draw out the truth and were demonised for doing so. Not one senator amongst the political Left entertained a moment’s thought that fear-driven response could be harming more people than it helped. ‘Resistance is futile’ was the message repeated at every press conference on every television in every house of parliament. New Zealand, Canada, the UK and America all joined in the circus of despair, designed to scare people into taking a substance they knew would cause serious harm and death.
Even today, vaccine mandates are still in place around Australia. The reality of a falling birth rate, unexplained increases in deaths and more than 130,000 cases of vaccine harm here in Australia is being ignored. Still, we are told the injection is safe and effective. Safe and effective is not one lie; it is two lies. The vaccine is neither safe nor effective. Medical practitioners who stood up for the rights of their patients were deregistered after action from big pharma’s enforcement arm, the Australian Health Practitioner Regulation Agency—under the direction, it seems, of CEO Martin Fletcher and Yvette D’Ath, as chair of the Health Ministers Meeting. They’re the ones who were in control. These technocrats decided they knew what was best for patients—better than the patient’s own doctor. AHPRA must be referred to the royal commission—and the TGA, ATAGI, the Chief Medical Officer, the secretary of the federal health department and Greg Hunt, the federal health minister at the time.
The vaccine emergency use authorisation expires early next year. An inquiry into how the vaccines went would normally be conducted, but they need to stop now. The emergency authorisation needs to stop. I do not have confidence the Therapeutic Goods Administration, the TGA, and the Australian Technical Advisory Group on Immunisation, ATAGI, will be honest and impartial in this inquiry. They have not been so far. Only a royal commission can decide all of the issues I have raised tonight. One royal commissioner will not be enough for the litany of legal and regulatory abuse, medical practice, financial malfeasance, conflict of interest, child abuse, human rights abuse and the shredding of international agreements Australia has endured for 2½ years.
The harm from our COVID response was foreseeable and preventable. If only the Senate, the ultimate house of review, had had the courage to stand up and call bullshit. The Senate did not.
The ACTING DEPUTY PRESIDENT ( Senator Chandler ): Order! Senator Roberts, that language isn’t parliamentary. I ask that you withdraw or find another word.
Senator ROBERTS: I retract that—the brown stuff.
The ACTING DEPUTY PRESIDENT: Thank you.
Senator ROBERTS: The Senate did not. As a result, the public has lost confidence in the medical profession, health administration and politicians. To his credit, member of parliament Dan Tehan publicly admitted his silence last year was wrong. This week a survey in the Daily Telegraph found that, based on the 50,000 respondents, 37 per cent of Australians who took the vaccine regret it. Only 43 per cent said they would do it again. The damage to the reputation of our once-trusted medical institutions can only be repaired with a royal commission to unravel the lies and get to the truth, and, in so doing, ensure this tyranny, this suffering and this loss of life never happens again.
I have no doubt that, when the truth comes to light, history will judge those in this place as being cowards all. We have one flag, we are one community, we are one nation, and Australians want justice.
Covid vaxx spike protein detox protocol
Glutathione (most important for body detoxification) or better
NAC = N-Acetyl-Cysteine 600-750mg (causes the body to produce glutathione itself)
Zinc
Astaxantin 5mg (also improves vision)
Quercetin
vitamin D3
Milk thistle (also liver and stomach protection)
Melatonin 1mg to 10mg (against 5G)
Alternatively CDS/CDL and zeolite
Dr. Zelenko’s Protocol contains Ivermectin, Hydroxychloroquine (HCQ), Zinc, Vitamin D3, and Quercetin.
Spike protein detoxification
David Wolf’s Shop, order here: http://bit.ly/SpikeProtein
This is the updated Nutrition protocol to protect those who’ve been injected with spike protein, graphene oxide and mRNA and the same protocol is useful to protect those concerned with the spike protein and graphene oxide shedding (transmission) coming off those who’ve been injected. We now have evidence of the latest injections containing: mRNA, spike protein, graphene oxide, SM-102, and numerous other potentially toxic substances (also: some—but not all—injections, appear to be higher in graphene oxide and some appear to be saline placebos).
If you know someone who has been injected and requires help, please provide them with this Nutrition Protocol:
Most Important Elements of the Protocol (Shortlist Summary)
Spike Protein: Shikimate neutralizes the Spike Protein
This is the Nutrition Protocol to Prevent Damage from Spike Protein and Derivatives due to Injection and to Protect from Spike Protein Shedding (transmission):
Shikimate Main Sources to Detox Spike Protein
• Pine Needle Tea for Shikimic Acid or Shikimate (from green edible pine needles) There are toxic pine needles, be careful! When drinking pine needle tea, drink the oil/resin that accumulates too!
And/Or
• Fennel and/or Star Anise Tea
And/Or
• Schizandra Berry Tea
• Iodine* (dosage depends on brand, more is not better). Iodine is a product you have to start with small dosages and build up over time.
• Vitamin D3* (10,000 IU’s per day)
Graphene Oxide Detox:
• C60 (1-3 droppers full per day): One of the issues we are seeing with those who have been injected is disturbances in their energetic field (magnetism) and hot spots of inflammation. C60 is a rich-source of electrons and acts like a fire extinguisher to inflammation and simultaneously (because it bio-distributes throughout the body) drives a normalization of electron flow throughout the body. In this category, we offer two products, the traditional C60 product* is made by yours truly and the C60 Super Concentrate* is made by a carbon scientist friend of mine and contains a higher concentration of electrons. C60 is recommended to neutralize spike protein, detoxify graphene oxide and SM-102.
• Kohlbitr Activated Charcoal: Take between 400-2000mg (1-5 capsules) a day with water.
• NAC: N-Acetyl Cystiene is the best precursor to glutathione in the body which has the best research for neutralizing graphene oxide. Take 900-1800mg a day. Get it while you can. The US Federal communist government is trying to make NAC illegal unless you have a doctor’s prescription.
• Enzymes (especially those containing serrapeptase and nattokinase such as VeganZyme— dosage for VeganZymes is 3 caps, twice daily):
Serrapeptase: Serrapeptase provides the anti-inflammatory breakdown of excess and unusual protein. Dosage: 100-200 mg on an empty stomach per day.
Nattokinase: Nattokinase has a long history of being used to prevent blood clots. 2000-4000 Fibrinolytic Units per day (2-4 capsules) with or without food.
Special Note: Ivermectin is showing great promise against hydrogels containing graphene oxide and found on PCR test swabs, but it is a pharmaceutical, so I do not include it.
Here is the Complete Protocol
•Coated Silver (1-6 drops per day, depending on degree of exposure) (Coated silver blocks the sulfur-bearing protein on the spikes from entering the cell. Sulfur-rich amino acids on the spike protein interact with silver causing them to fold incorrectly).
• NAC (N-acetyl cysteine) (accelerates detoxification and is considered a producer of the super detoxifier glutathione in the body) Dosage: 1200-2400 mg per day on an empty stomach. NAC is recommended to detoxify graphene oxide and SM-102. NAC is tough to find after the FDA recently made it illegal to purchase over the counter in the USA. Request NAC from your doctor!
• Zinc (30-80mg per day depending on immunological pressure)
• Vitamin D3* (10,000 IU’s per day)
• Lyposomal Vitamin C (30ml, twice daily)*
• Quercetin (500-1000 mg, twice daily)*
• Iodine* (dosage depends on brand, more is not better). Iodine is a product you have to start with small dosages and build up over time.
• PQQ* (20-40 mg per day)
Additional recommendations:
• Fennel and/or Star Anise Tea: These are also an excellent source of shikimate or shikimic acid (which is known to neutralize the spike protein)
Hesperidin sources to help disable spike protein:
• Citrus fruit (especially blood oranges, due to their high hesperidin content — hesperidin is a chalcone like quercetin that deactivates spike protein)
• Peppermint (very high in hesperidin)
Superherbs to help disable spike protein:
• Triphala formulations: In Sanskrit, the word Triphala means “three fruits”: a combination of Indian gooseberry (Emblica officinalis), black myrobalan (Terminalia chebula) and belleric myrobalan (Terminalia belerica). The terminalia fruits are rich in shikimate.
• St. John’s Wort (shikimate is found throughout the entire plant and in the flowers)
• Comfrey Leaf (rich in shikimate)
• Feverfew (leaves and flowers are rich in shikimate)
• Gingko Biloba Leaf (rich in shikimate)
• GiantHyssop or Horsemint (Agastache urtifolia) (rich in shikimate)
• LiquidAmbar (Sweet Gum tree) A tea of the spiky seed pods is rich in shikimate.
•Glycyrrhiza glabra (Chinese medicine’s licorice root): Glycyrrhizic acid is extracted from the root of the licorice plant inhibits spike protein.
New HIV super-strain is found in the Netherlands
from Alison Ryan
The UQ/CSL Australian COVID vaccine was scrapped because recipients tested positive for HIV after getting the jab
DECEMBER 11, 2020. How did the University of Queensland/CSL vaccine fail due to ‘false positive’ HIV tests? (medicalxpress.com)
However, news coming out now says:
*1 December 2021 Federal government announces that it will spend nearly $40 million ($50m) on HIV so more Australians can access HIV treatment.
https://7news.com.au/politics/federal-government-to-spend-50m-on-hiv-c-4768254
*New HIV super-strain is found in the Netherlands: Highly infectious variant makes people ill twice as quickly and has been spotted in at least 109 people – 4 February 2022
https://www.dailymail.co.uk/health/article-10473495/New-HIV-strain-Netherlands-Highly-infectious-variant-makes-people-ill-twice-quick.html
*Moderna launches early-stage clinical trial for HIV vaccine that uses mRNA technology. The biotechnology company has teamed up with the nonprofit International AIDS Vaccine Initiative to develop the shot, which uses the same technology as Moderna’s COVID-19 vaccine – 28 January 2022.
Moderna launches clinical trial for HIV vaccine that uses mRNA technology – ABC News (go.com)
Researchers Warn Some Covid-19 Vaccines Could Increase Risk of HIV Infection, Oct 20, 2020 – Some of the Covid-19 vaccines currently in development could increase the risk of acquiring HIV, warned a group of researchers in the The Lancet medical journal, potentially leading to an increase in infections as vaccines are rolled out to vulnerable populations around the world. The researchers warn of a “cautionary tale” from efforts to create an HIV vaccine over a decade ago, where a promising vaccine candidate actually increased the risk of some men catching the virus.
The vaccine made use of a modified virus — called adenovirus 5 (Ad5) — as a vector to transport some of HIV’s genetic material into the body.
Exactly how the vaccine increased the risks of HIV transmission is unknown, but a conference convened by the National Institutes of Health recommended against further use of Ad5 as a vector in HIV vaccines
(Dr. Anthony Fauci was lead author of the paper outlining this position.) Some of the leading candidates for a Covid-19 vaccine, including those from Johnson & Johnson and AstraZeneca, use adenoviruses as vectors.
Researchers Warn Some Covid-19 Vaccines Could Increase Risk Of HIV Infection (forbes.com)
WHO whistle-blower, Dr. Astrid Stuckelberger, is also a witness in the Grand Jury being chaired by Reiner Fuellmich. You can hear her testimonies “Perpetual pandemic. Perpetual fear” and “Grand Jury – Day 2 Part 6 – Dr. Astrid Stuckelberger and Dr. Sylvia Berendt Testimony”.
“These criminals have no limit… Now they say the Spike protein in the vax was designed with a “molecular clamp” made of an HIV protein and that everyone receiving the shot can give a “false positive” test for HIV… Do we need more mockery and deceit from the Controllers?”
It’s perpetual pandemania from the Jokers!
Big Pharma conducting lethal dose studies with experimental vaxx in a batch lottery for Australians and Americans
by Alexandra Bruce
Many are wondering why some geographic areas, such as those surrounding Silicon Valley are not seeing nearly as many adverse reactions to the vaxx as other areas, with Prudential reporting a 87% increase in death benefits paid out in the third quarter of 2021, compared the third quarter of 2020. Pacific Life and Annuity is reporting that claims are up by over 80% and other insurers reporting increases of between 12% and 40%.
According to Dr Jane Ruby, we the people of Planet Earth are being subjected to mass unethical drug testing, without informed consent, against all ethical and regulatory rules; tests that are supposed to be reserved for rats and mice.
ATTACK ON AMERICA: COMPANIES INTENTIONALLY DEPLOYING TOXIC BATCHES
Dr Ruby joins Stew Peters to relay how she spent 3 hours with researchers who have been painstakingly identifying the lot numbers of the most deadly vials that are now in circulation.
She says that hackers were able to break into the systems of Pfizer and Moderna and the researchers were able to put together a comprehensive list of all the lots and the code numbers of the most toxic batches.
According to the hackers, 5% of the batches have generated the 21,000 deaths reported to VAERS.
She says that in the Moderna analysis, the death rate in the United States was 10 times higher than in the EU and that the EU had ten times more disabilities, as compared with the US. She says it is clear that this was by design.
She says they’re not testing doses within the therapeutic range, they’re testing lethal doses. She says she will be coming back with a more in-depth report but says, “Before you let your child get in line for these bioweapon shots, if you don’t believe anything we’ve said, at least ask them for the lot numbers.” The lot numbers can then be checked on the researchers’ website, HowBad.Info.
Dr Ruby says, “What they’re telling us is that this is a worldwide human experiment, it’s intentional and there’s a subplot to this; that there is an attack on the American People.
“What they basically told me is that all three companies, Pfizer, Moderna and Johnson & Johnson – which is essentially Janssen – are testing. They’re actively testing and it’s worse than we thought, because there’s evidence that these companies are intentionally deploying toxic batches.
“They’ve also identified what they call ‘super toxic’ batches and they’ve released these lot numbers. And I felt like this was an emergency to get this to the American People and the people of the world.
“I want to show you what they found, in terms of most dangerous lots. And when we’re done with this segment, I urge everyone to go to HowBad.Info, where you can check the lots and you can know which lots are deadly and dangerous if you’re thinking or on the fence about getting any of these bioweapon injections.
“When you look at the first column here, for Pfizer, I want you to know that the most deadly, dangerous lot [for children] will begin with ‘EW’. Second to that is ‘FA’ and then ‘FC’…
“The most harmful lot for children, under this EW, FA, FC…the whole lot number is: EW0182 but you can go to HowBad.Info and look up the company and put your lot number in.
“Under Pfizer for adults, the most toxic, deadly batches begin with ‘EN’ and then, second to that is ‘ER’…
“Under Moderna [all ages]…their toxic, deadly batches end in ’20A’.
“Their ‘supertoxic’, under Moderna, have in the middle section – they got very clever…all companies coded their lot numbers so that they would know where the most toxic batches are and I’m going to share with you why that’s important in a little bit.
“But Moderna took it a step further, with a little cleverness, because they embedded their code for their most toxic amount, either in dose or chemical composition under the letters in the middle of that lot number, J, K, L, M.
“The analysts were a team that included the well-known [former Pfizer VP] Dr Michael Yeadon, Craig Partikooper from Africa, a woman named Alexandra Ladipova, who’s in California, our well-known Jessica Rose, who we’ve interviewed on the Stew Peters Show before and another analyst named Walter Wagner.
“Look, this ‘EW’ lot for children – anything that starts with ‘EW’ is responsible for almost all adverse events in children, all ER visits, all hospitalizations, all life-threatening events, disabilities and all deaths.
“This is serious. And here’s the kicker, Stew: All of these deadly lots that we’re going to show you are all already in circulation, remembering that there could be up to 1.5 million doses per lot.
This quantification is set by each company. And the way they know that is because they have looked at the companies and they’ve gotten into their systems to see how the companies have laid this out.
“They made the assertion, Stew – and this was shocking – that what these companies are doing is they’re exporting ‘disability’, as defined by the VAERS system, itself out to Europe; ex-USA. And what they’re doing is they’re exporting, if you will, death. More death, more lethal doses in the United States.
LETHAL DOSE STUDIES WITHOUT INFORMED CONSENT
“Now, let me share with everyone – there’s another chart with a scatter plot, it’s called ‘Pfizer Batches’. And when Pfizer batches were arranged alphanumerically along the X axis, the following patterns emerged. And you can see these dots, these vertical dots represent batch numbers.
“And again, there’s that ‘EW’, you can see the green stack of dots. Those are children’s doses. Even though the company claims that the amount is less than the adult dose, supposedly, we have no idea what’s in there…
“They are conducting what we call ‘lethal dose studies’. Now, in pharmaceutical drug development, lethal dose studies look at how much you need to cause death and obviously, they’re not done in humans, in people. They’re always done in animals, though they’ve slowed down in recent years, because people have become concerned. Even though they’re rats and mice; they’re ‘lower forms’, people are concerned about the cruelty to animals. But they’re never done in people.
“And what’s happening here is they are basically, from the analysis, these analysts tell us that these three companies are actively, right now conducting lethal dose studies.
“Let me explain ‘lethal dose’. They take the highest amount of chemical, in terms of dosage and chemical and what they do is that they determine what lethal amount to test half the population.
It’s one of the means to assess acute toxicity prior to going into human studies. And like I aid, it has been largely phased-out. They are conducting it without informed consent, it’s against all ethical and regulatory rules. In other words, we believe these companies are just proceeding with impunity, because there is nothing stopping them.
SIGNIFICANCE OF NUMBERS IN BATCH CODES
“I want to also show people something – before we get into a larger look at the lots and what’s happening and how these analysts are so sure that this is not by randomization, that this is not by chance, I want to take a look at the parts of a Moderna batch code.
“I mentioned earlier that Moderna got a little ore complex and clever. Remember, these companies, we now know are actually embedding into their lots a code to tell THEM which lots are toxic, which ones are causing disabilities and what types of disabilities! This is absolutely outrageous!
“When you look at the parts of a Moderna batch code, you see ‘011’, the letter ‘L’, and ’20A’.
“’20A’, as we mentioned before, in the first chart I showed…denotes the most lethal batch of lot codes in the Moderna program right now. And remember, all of these numbers I’m going to show you are from the middle of November, all the way up until s late as December 16, just a couple of weeks ago.
“So when you look at this number, 011-L-20A, what you’re looking at in the ‘011’ is the temporal batch order; so how it’s being developed over time and deployed by the company.
“The ‘L’ is the concentration. It tells he company the toxicity and number of adverse reactions.
“And then, the ’20A’ is qualitative; it’s the ingredient. And either ’20A’, which was the most toxic of their batch lots or ’21A’ came up, as well.
“So this is their clever scheme…The reason they’re not concerned with safety issues is because this is an a priori design. This is designed ahead of time to send out toxic batches and then, to gather their information.”
PROFESSIONAL HACKERS GOT INTO PFIZER & MODERNA
Dr Ruby explains that professional hackers got into Pfizer and Moderna’s systems and they were able to verify the whole lots. Dr Partikooper has a list of all the Moderna batches deployed so far and Moderna also has a web tool for checking the expiration dates for the batches and these computer guys hacked into the Moderna and Pfizer websites and got entire lists of all their batches and batch code numbers.
She says, “I just want to make something very clear: This exporting death to the USA and disability to the EU, what they found, for example, in the Moderna analysis. There was ten times the death rate in the United States than in the EU and in the Moderna group, there were ten times more disabilities in the EU group compared with the USA.”
Dr Ruby says they’re clearly not testing doses within the therapeutic range, they’re testing lethal doses. She says she will be coming back with a more in-depth report and says, “Before you let your child get in line for these bioweapon shots, if you don’t believe anything we’ve said, at least ask them for the lot numbers.” – Forbidden Knowledge TV
Deliberate Russian roulette with Pfizer, Moderna and Janssen Covid vaxxes targeting Red states
by Alex Bruce US correspondent
Ex-head of respiratory research at Pfizer, Mike Yeadon and researchers, including Craig Paardekooper have sourced VAERS data on vaccine death and injury in the US, database of over 700,000 adverse reactions caused by the Moderna, Pfizer and Janssen vaccines.
These vaccines have been deployed in different batches, officially referred to as “lots”.
This has allowed Yeadon’s team to back-engineer Big Pharma’s CoV-19 deployment agenda in the US.
All their information is published at HowBadIsMyBatch.com and HowBad.Info.
And what we learn is quite telling. About 0.5% of all batches are highly toxic, resulting in hospitalization, disability and death within days or weeks of injection.
Other batches cause minimal adverse reactions and most appear to be harmless placebos.
When plotting on a timeline, we can see that these three companies have been working together to quietly monitor the lethal effectiveness the deadly batches.
While one company is deploying a lethal batch, the other two deploy harmless ones, creating the scientific environment to perform dose range finding for the maximum tolerated dose for each specific batch.
The timeline shows that each lethal batch deployment is preceded and followed by a “quiet” period, allowing them time to establish their baseline, before the next deadly batch is deployed.
Private leaked documents from the CDC show a list of expiry dates and only certain lots are included – the very same lots found to be toxic in Paardekooper’s database, which makes sense.
There would be no reason to list expiration dates for saline placebo, only the deadly ones.
This mode of deployment allows governments to direct deadly batches into specific populations, such as Red States (Republican).
Analysis of deaths per 100,000 vaxxinated in 50 states shows us that the overwhelming majority of vaxxine deaths are happening in Red States. Some Red States are experiencing eleven times more vaxxine deaths than other states. On average, Red States are experiencing twice the amount of death and injuries as Blue States.
Ruling out other possibilities, Paardekooper concluded that this could only be due to the fact that Red States received twice as much of the lethal batches than Blue States did.
Among several other crimes, they are tipping the scales of the democratic process by killing people who voted against the New World Order’s woke Build Back Better Great Reset, while at the same time, endlessly flooding the borders with unvaxxinated foreigners.
And it’s happening right now.# Forbidden Knowledge TV
Investigations in Australia have revealed that some patients received a placebo jab having no adverse effect while the toxic vaxxed suffered badly and the death rates in hospital with ‘Covid’ are more than twice that of the unvaccinated according to health departments. – Editor
First CEO of Moderna was Anthony Fauci….?
Letter to the Editor
As the alleged history goes, there was a Company heavily involved in WW2 called IG Farben. This is believed to be a Company associated with George Soros who possibly even ran it.
George as a child was taken in by a Nazi family during the war despite being of Jewish descent.
After the war, George went to America.
It is claimed he eventually broke up with IG Farben and formed Moderna.
One of the main financial brokers of Moderna is believed to be Bill Gates.
The first CEO of Moderna is believed to have been a young Cornell Graduate by the name of …..Anthony Fauci.
For those who are holding out for the Novomax NVX-C0V2373 this is what can be found on the public record so far:
Novomax is a Biotechnology Company sponsored by the Bill Gates Foundation.
They have been given millions of dollars from CEPI for large scale manufacturing of vaccines.
This will be their first vaccine (if successful)
The President and CEO is Stanley Erck.
Novomax is a Company listed on the share market.
Novomax will be based on a genetically modified baculovirus.
Baculoviruses are viruses that infect insects.
The most common hosts are immature moths and butterflies, but also mosquitos.
These baculoviruses are not usually able to replicate in humans.
It is claimed Sf9 moth cells with be infected with a computer generated SARS Cov2 to produce a coronavirus spike protein, then harvested as a whole deactivated virus for injection.
The spike proteins harvested will be assembled onto a synthetic lipid nanoparticle displaying up to 14 spike proteins.
Novamax will be a recombinant protein injection from mixed sources.
A genetically modified nanoparticle technology.
The adjuvant that will be used for Novamax is code named QS-21 or “Matrix M”
An adjuvant is what is needed to get the immune system to respond.
The adjuvant in Pfizer has been Polyethelene glycol (PEG) and in AstraZeneca it was Polysorbate 80. The adjuvants used in some childhood vaccines have been primarily aluminium.
Pre 1990’s the adjuvant used in childhood vaccines was primarily mercury.
Novomax will have a saponin based adjuvant from the bark of the Chilean soap bark tree called quillaja saponaria.
Quillaja saponaria is an emulsifying foaming product.
This product is believed to have been used in lens cleaners, fire fighting foam and cosmetics.
Saponins are used to bind substances that would not normally mix, like water and oil.
Quillaja saponaria can allegedly cause liver damage if receiving high amounts of tannins.
It can reportedly cause breakdown of blood cells, respiratory failure, and convulsions.
It was claimed to have been used in Veterinary practice in the 1950’s but was considered “too toxic” for humans at the time because it caused the red blood cells to burst.
Phase 1 clinical trials for Novomax in healthy individuals already commenced in Australia way back in mid 2020.
The trials were mainly to see how people responded to the Matrix M saponin.
Phase 3 clinical trials are occurring overseas.
As always, do your own research as more information comes to light.
From
Seb
NSW
87% of kids aged between 12 and 17 are hospitalized after receiving the shot
Up to Nov 19, the US recorded 14,428 myocarditis cases in children – VAERS
by Dr Joe Mercola
Dr. Peter McCullough, a cardiologist, internist and epidemiologist, and editor of two peer-review journals, has been on the media and medical frontlines fighting for early COVID treatment. McCullough has also been outspoken about the potential dangers of the COVID shots, and the lack of necessity for them. Curiously, agencies that are currently calling the shots do not have the authority to dictate how medicine is practiced.
The U.S. Food and Drug Administration, for example, has no power to tell doctors what to do or how to treat patients. The National Institutes of Health are a government research organization and cannot tell doctors how to treat patients.
Ditto for the U.S. Centers for Disease Control and Prevention, which is an epidemiologic analysis organization. It is the job of practicing doctors to identify appropriate and effective treatment protocols, which is precisely what McCullough has been doing since the start of this pandemic.
In August 2020, McCullough’s landmark paper “Pathophysiological Basis and Rationale for Early Outpatient Treatment of SARS-CoV-2 Infection” was published online in the American Journal of Medicine.1
A follow-up paper, “Multifaceted Highly Targeted Sequential Multidrug Treatment of Early Ambulatory High-Risk SARS-CoV-2 Infection (COVID-19)” was published in Reviews in Cardiovascular Medicine in December 2020.2 It became the basis for a home treatment guide.
COVID Shots Are Dangerous and Ineffective
When it comes to the COVID injections, McCullough cites research showing those at highest risk of dying from COVID-19 are also at highest risk of dying from the COVID shot. Additionally, the shots are causing severe heart damage in younger people whose risk of dying from COVID is inconsequential.
He points out the safety signal is very clear, with 19,249 deaths having been reported to the U.S. Vaccine Adverse Events Reporting System as of November 19, 2021.3
The signal is also consistent both internally and externally. A number of side effects are reported in high numbers, and very close to the time of injection, that validate the suspicion that the shots are at fault. The U.S. data are also consistent with data from other countries, such as the Yellow Card system in the U.K.
Despite that, not a single safety review has been conducted to weed out risk factors and the like. “We’re almost a year into the program and there’s been no attempt at risk mitigation,” McCullough says. At the same time, there have been gross attempts to coerce Americans into taking the shots — everything from free beer or a free lap dance, to million-dollar lotteries and paid scholarships to state universities.
Such enticements are an undeniable violation of research ethics that strictly forbid any and all kinds of coercion of human subjects. As suspected and predicted, no sooner had bribery stopped working than government officials started talking about vaccine mandates.
President Biden infamously stated that his patience with “vaccine hesitancy” was “wearing thin.” The insinuation was that if people didn’t get the shot, they’d face serious repercussions, and we’re now seeing those repercussions play out day by day, as people are being fired and kicked out of school for refusing the jab.
Meanwhile, they haven’t even determined which vaccine is the most effective, which is remarkable. If government really wanted to end the pandemic with a vaccine, wouldn’t they determine which shot works the best and promote the use of that? But no, they tell us any shot will do.
“The fact that there’s no safety report, they’re not telling you if you’re taking the best vaccine, the fact that it’s kind of in a distorted way linked to your ability to work and go to school, that we’re violating the Nuremberg Code, violating the declaration of Helsinki — it’s just not adding up. It’s not looking good for those who are promoting the vaccine,” McCullough says.
Add to all that the now-clear finding that the shots offer only limited protection for a very short time — six months at best. According to McCullough, there are more than 20 studies showing efficacy drops to nothing at the six-month mark. They’ve also had very limited effectiveness against the Delta variant, which has been the predominant strain for several months.
Why Booster Treadmill Is Such a Health Hazard
I’ve often stated that, in all likelihood, your risk of side effects will rise with each additional shot. McCullough cites research showing your body will produce the toxic SARS-CoV-2 spike protein for 15 months.
If your body is still producing the spike protein — which is what’s causing the blood clots and cardiovascular damage — and you take an additional shot every six months, there will come a time when your body simply cannot withstand the damage being caused by all the spike protein being produced.
Also consider this: While you only get at most six months’ worth of protection from any given shot, each injection will cause damage for 15 months. If we continue with boosters, eventually, it’s going to be impossible to ever clear out the spike protein.
While the spike protein is the part of the virus chosen as the antigen, the part that triggers an immune response, it’s also the part of the virus that causes the worst disease. The spike protein is responsible for COVID-19-related heart and vascular problems, and it has the same effect when produced by your own cells.
It causes blood clots, myocarditis and pericarditis, strokes, heart attacks and neurological damage, just to name a few. As noted by McCullough, the spike protein of this virus was genetically engineered to be more dangerous to humans than any previous coronavirus, and that is what the COVID shots are programming your cells to produce. “They’re just grossly unsafe for human use,” McCullough says.
Myocarditis Will Likely Be Widespread
He goes on to discuss research from 2017,4 which showed myocarditis in children and youth occurs at a rate of four cases per million per year. Assuming there are 60 million American children, the background rate for myocarditis would be 240 cases a year. How many cases of myocarditis have been reported to VAERS following COVID injection so far? 14,428 as of November 19, 2021.5
“Doctors have never seen so many cases of myocarditis,” McCullough says, citing research showing that among children between the ages of 12 and 17, 87% are hospitalized after receiving the shot. “That’s how dangerous it is,” he says. “It is frequent, and it is severe.”
Yet the FDA claims myocarditis after the COVID shot is “rare and mild.” We’re now also getting reports of fatal cases of myocarditis in adults in their 30s and 40s. “Myocarditis right now looks like an unqualified disaster,” McCullough says, both for younger people and adults.
Children aged 12 to 17 are five times more likely to be hospitalized with COVID jab-induced myocarditis than they are to be hospitalized for COVID infection.
Sadly, children also reap no benefit from the shots, so it’s all risk and no benefit for them. McCullough points out there has been no recorded school outbreaks and no child-to-teacher transmission. He estimates 80% of school aged children are already immune, which would explain this.
Meanwhile, research cited in the interview found that children aged 12 to 17 are five times more likely to be hospitalized with COVID jab-induced myocarditis than they are to be hospitalized for COVID infection. These data counter the claim that COVID-induced heart problems are a far greater problem than “vaccine”-induced heart damage.
And let’s not forget, if you take a COVID shot, you have a 100% chance of being exposed to whatever risk is associated with that shot. On the other hand, if you decline the injection, it’s not 100% chance you’ll get COVID-19, let alone die from it. You have a less than 1% chance of being exposed to SARS-CoV-2 and getting sick.
So, it’s 100% deterministic that taking the shot exposes you to the risks of the shot, and less than 1% deterministic that you’ll get COVID if you don’t take the shot. (more p2)
Cairns News 