THERE are three Covid-19 vaccines in use in the UK, but none is causing more havoc than the Oxford/AstraZeneca jab, now known as the ‘clotshot’ because it can cause vaccine-induced thrombosis (VITT). By July 28, 73 VITT deaths had been reported to the Medicines and Healthcare products Regulatory Agency (MHRA), the body that makes sure new pharmaceuticals are safe. Deadly blood clots are not the only side-effects; there are many more affecting one in 110 people according to official figures. Some last for months and could be permanent even if they aren’t fatal.
Neurological occupational therapist Carla Freitas, 31, who works for the NHS, took part in the original AZ trial and is one of 11 women and men who reacted to the same batch of AstraZeneca Covid vaccine, batch number PV46671, earlier this year. The group are countrywide as it is common practice to distribute a batch to different areas. The PV46671 injured found each other on Twitter so there may be more victims not using social media out there. I talked to seven of them.
All seven received the jab before the MHRA began investigating adverse events reported to the Yellow Card Scheme, not originally flagged up by AstraZeneca. Carla said: ‘I was deemed fit enough to join the Oxford trial after thorough medical examinations. In December 2020, I was told I had been given the placebo and offered the jab once it was available, so I did not hesitate to take it. I was fine after the first injection but two weeks after the second one everything changed. I have been off work for five months since March trying to find solutions to my health problems. The doctors from the AZ trial have been unhelpful.’
BBC food broadcaster Jules Serkin, 63, from Canterbury, whose original tweet alerted the others, was ‘desperate for the vaccine’ but she has also suffered horrific side effects. She said: ‘My doctor agreed my reaction was from the vaccine. I contacted AstraZeneca and I’ve had five emails from them asking if they can contact my GP. I responded yes, of course. They never have.’
This close-knit, previously healthy group, aged from their early 30s to early 60s, have all developed chronic illnesses since vaccination. Some experienced symptoms within minutes of the jab being administered while others received PV46671 as their second jab. And while some are recovering slowly, others are getting worse.
Rachael Matthews, 31, and Claire Hibbs, 48, both developed heparin-induced thrombocytopenia (HIT) (blood clots usually caused by the anticoagulant drug heparin, typically used in the treatment of heart attacks but AZ victims seem to develop it despite the fact they are not taking heparin) and have tested positive for the heparin-PF4 antibody.
Other symptoms include heart problems, low blood platelets, palsy, excruciating headaches, insomnia, tinnitus, muscle pain, dizziness, disorientation, inflammatory autoimmune disease, pins and needles in hands, feet and face, fatigue, brain fog, difficulty swallowing, sore eyes and eye problems and stomach pains.
In the patient information leaflet, AZ, who have renamed their jab Vaxzervia, list many of the reactions the group have suffered but Serkin says: ‘Health professionals more often than not deny the connection.’
The leaflet says: ‘In clinical trials there were very rare reports of events associated with inflammation of the nervous system, which may cause numbness, pins and needles, and/or loss of feeling. However, it is not confirmed whether these events were due to the vaccine.
‘Following widespread use of the vaccine there have been extremely rare reports of blood clots in combination with low level of blood platelets. When these blood clots do occur, they may be in unusual locations, e.g. brain, liver, bowel, spleen.’
Both Matthews and Hibbs developed a clot in the portal vein which leads to the liver, while Serkin, Howard Griffiths, 52, and Dave McGuire are suffering numbness and pins and needles.
Despite their symptoms, some of those who reacted to their first dose are under pressure from GPs to have the second. This is inexplicable but one consultant suggested it could be because GP practices receive £25.16 for each double-jabbed person. With an average of 9,000 patients for each practice (although under-16s are not yet eligible for the jab) that could be a maximum £230,000 incentive. Patient health be damned!
Despite the MHRA’s denials – they say most adverse events are coincidental – logic suggests that if someone receives a vaccine that is designed to provoke an immune response and then develops autoimmune disease or other problems with their immune system, the jab should be first in the frame. However alleged vaccine damage seems to be rarely investigated or taken seriously.
Adverse reactions can be caused by a ‘hot lot’, a faulty batch of vaccine with too much of one ingredient. Big Pharma has known this for decades, and this problem was legally accepted in 1992 during an Irish court case involving Kenneth Best, 23. As a four-and-a-half-month-old baby, Kenneth suffered brain damage and seizures after he was given Wellcome’s diphtheria, tetanus, pertussis (DTP) vaccine in 1969. The Irish Supreme Court ruled: ‘The documentary evidence surrounding the particular batch out of which the vaccine given to the Plaintiff was taken indicates that it was excessively high in both potency and toxicity.’
It is hard to know if this happened in this case because the MHRA and AstraZeneca have not responded to repeated requests for information. Contacted on July 29, AZ has not responded (even after Oxford University press office contacted them on TCW’s behalf) while in an unsympathetic email the MHRA confirmed that they had not investigated the group’s concerns.
An MHRA spokesperson said: ‘We are sorry to hear of the health problems these people are experiencing. We are not aware of any batch-specific safety issues for the AstraZeneca vaccine. We are also not aware of any issues with individuals involved in Covid-19 vaccine AstraZeneca trials who subsequently received this vaccine outside of the trial but will follow this up with the investigator.’
Meanwhile those in the group who have been advised by medics not to have a second vaccine fear they will become victims of medical apartheid. Adele B, 57, worries that she will be labelled an antivaxxer because she linked her health problems to the jab. She said: ‘I’ve always believed in vaccines so nothing could be further from the truth.’
Serkin, Freitas and Hibbs would like to travel when they feel well enough, but worry they will not be allowed without vaccine passports. Hibbs says: ‘I so want to visit my son in Cyprus, I’m wondering if I should have the second jab just to go.’
Here are the stories of the seven in detail.
CLAIRE HIBBS, 48, works for easyJet, lives in Luton, and is married with two children.
‘I’ve been signed off work now since the end of March. I’m now concerned about returning to work if I’m vulnerable. Devastated with the travel rules that you have to be double vaccinated, and I cannot have the second dose. My son, 18, is in the Army and is moving to Cyprus. I planned to visit regularly, but not with blood clots in my lungs.’
1st jab date: March 31
2nd jab date: Advised not to have second jab
Health issues before the jab: None
Reactions: ‘I began feeling unwell on April 5 and developed blood clots in the vein leading to the liver (portal vein), also in my lungs. I’m suffering constant headaches, muscle, joint and neck pains, constant eye twitching. I’m off balance and have brain fog. Can’t get through the day without falling asleep.’
Tests done: Blood tests but liver scan cancelled due to staff shortages. D-dimer (checks for tiny clots), CT, ultrasound and MRV scans which detect VITT. Positive HIT test. Positive test for portal vein thrombosis. Appointment with gastro team. Official diagnosis: ‘Thrombocytopenia (low blood platelets) and portal vein thrombosis, pulmonary embolism (clot in the lung) induced by the AZ vaccine.’
Doctor’s response: ‘No luck with doctors, just keep getting fobbed off, mostly saying it’s stress. I’m feeling very let down.’
Time off work: Unable to work since March
Response from MHRA and AstraZeneca: ‘Filled in a Yellow Card. Acknowledgement but no other response. AZ have emailed me to ask for consent to contact my GP three times. I said yes but they have not contacted the GP.’
RACHAEL MATTHEWS, 31, an accountant from Norfolk, is married with one daughter.
‘I had my vaccine on my daughter’s first birthday at my GP surgery. I was apprehensive because I wanted to try for another baby in the spring. I’d had a complicated pregnancy, had a blood clot in my leg, but I was told I needed to have the jab to keep my daughter safe. Ironically, it nearly killed me which would have left my daughter without a mum. I’m now not well enough to consider having another baby. I’ve been told I was one of the first VITT cases in the UK.’
1st Jab: March 6
2nd Jab: ‘No second jab although I’ve been under pressure to take it.’
Health issues before jab: None, apart from pregnancy-related blood clot.
Reactions: ‘Started a week after the jab with stomach cramps, nausea and diarrhoea, very heavy legs. Struggled with everyday things I felt so weak. Couldn’t sleep, was struggling to walk, stopped being able to lift my daughter. Unable to get on to the doctor’s couch for a routine smear, a nurse insisted I went to A&E. I might have died otherwise. GPs had dismissed my symptoms. Blood clot found in the portal vein to my liver. VITT and HIT.’
Tests done: Two A&E visits, admitted to hospital for six days. Ultrasound, daily blood tests while in hospital. Endoscopy. Tests for HP4 heparin antibodies show HIT still present.
Time off work: ‘I work for my dad’s firm, so I fit in work when I’m well enough.’
GP’s response: ‘I asked about blood clots and was told it was fake news. Went to A&E and was told to take Gaviscon although routine blood tests showed very low blood platelets, around 50. When I was finally diagnosed with a blood clot I kept asking if it was the vaccine and no one would answer me.’
MHRA and AstraZeneca response: None.
HOWARD GRIFFITHS, 52, an events broadcaster for BBC, ITV and Channel 5, unmarried, lives in South Wales
‘I’m not Howard at the moment and I just want Howard back. I feel like my body has been hijacked, I’m desperate to get rid of the hijackers. I have always been highly motivated and full of energy. Before the jab I ran up Pen y Fan (highest peak in south Wales). After the jab I struggled to walk up hill to the shops.’
1st jab date: April 4
2nd jab date: ‘NHS say I cannot have second AZ but want to give me Pfizer.’
Health issues before the jab: None
Reactions: ‘Anaphylaxis. Within three minutes of the jab my lips and mouth became swollen, and I thought I was having a heart attack. My face went red. I have inflammation of the nervous system. I’m left with tingling and numbness in the hands, face, mouth and beneath the nose. Throbbing headache for ten days, changed to mild headaches but have now gone. Insomnia, which I never had before, dizziness, disorientation and fatigue. Tinnitus in left ear, throbbing in back of the neck and brain fog. Slight improvement but not back to normal.’
Tests done: Blood tests which showed low vitamin D. Three visits to GP and one to the hospital.
Time off work: Scaled down work at the beginning of pandemic anyway but would not have been able to carry on as normal
GP’s response: ‘Made no connection with the AZ.’
MHRA and AstraZeneca response: Filled in Yellow Card via phone call directly with MHRA but no contact since. Did not contact AZ.
JULES SERKIN, 63, freelance radio presenter for BBC specialising in food, married with three grown-up children and lives in Canterbury.
‘Too much stress at the moment. All I am doing is bouncing from pillar to post. Different GPs saying different things. Apparently, I’m a complex case.’
1st jab: March 5
2nd jab: Advised not to have second jab
Health issues before the jab: ‘Underactive thyroid. Initially, I was told it was safe to have the jab, but the advice has changed now for people with thyroid issues.’
Reactions: ‘Shivers were the first symptom, I felt like I had full blown flu. I was in bed for two days. Then blood clots came out of my nose for three weeks, I developed sinusitis. I began sleeping a lot, couldn’t look at a screen because my eyes were so sensitive. Developed a pain in my calf and headaches, which I’ve never had, with pains in my temples. Numbness in cheek and pins and needles in feet. Now my left eyelid has started to droop. I’m feeling tearful too.’
Tests done: Positive D-dimer test for blood clots. Blood tests show elevated liver enzymes which suggests liver damage. Ultrasound scan. MRI scan.
Time off work: ‘It’s affected my work for five months. I’ve been working but resting as often as possible.’
GP’s response: ‘You’re having a reaction to the vaccine.’
MHRA and AstraZeneca response: ‘AZ have sent five emails asking if they can contact my GP, but they haven’t yet. Filled in a Yellow Card in May, I’ve had an acknowledgment but that’s it.’
ADELE B, 57, is a retired communications co-ordinator, from Preston, who lives with her partner.
‘I’ve suffered weeks of weird symptoms. I feel it just can’t be coincidence that everything came at once. It also impacts on your family and friends. I feel like my partner is always checking on me. It’s put a cloud over my life. I cannot recall a day since I had the vaccine that I have felt completely well.’
1st jab: March 14
2nd jab: Advised not to have it while taking steroid medication to correct adverse reaction
Health issues before jab: None. Rarely went to the doctor.
Reactions: ‘Immediately after the vaccine I had chills, a sleepless night followed by a day with a headache and five days of feeling fatigued. The following week began with muscle aches and weakness in my shoulders, upper back, thighs and hips. Lack of sleep due to pain and I struggle to stand up after inactivity. These symptoms point to polymyalgia rheumatica (stiffness in neck and shoulders), an inflammatory autoimmune disease. My vision became blurry, and I had floaters in my right eye coupled with feeling disorientated when I sat down. I have heart palpitations, a strange rash behind my knee, dizziness and disorientation. Nerve pain and numbness in face, legs and feet and electric shock type sensations across my body. Health professionals are at a loss for a true diagnosis.’
Tests done: Several doctor’s appointments, seven blood tests, a 111 call, a visit to A&E, referral to rheumatology, referral to neurology, MRI scan of head, neck and spine, chest X-ray, eye examination.
Doctor’s response: ‘My doctor has advised me not to have the second AstraZeneca vaccine. Rheumatologist has indicated that she has seen several people reporting with autoimmune disorders since having their vaccine.’
MHRA and AstraZeneca response: Filled in Yellow Card, had a standard acknowledgement but nothing since. Didn’t contact AZ.
CARLA FREITAS, 31, highly specialist occupational therapist in neurology, neuro-cardiac and neuro-outreach at St George’s University Hospital, south London.
‘I was deemed fit enough to join the phase 1 Oxford Covid vaccine trials last April. I received the placebo and was offered the vaccine in January due to being an NHS worker. In the first few weeks of suffering nasty side effects and not understanding what was happening to my body I was in a very lonely place.’
1st jab: Jan
2nd jab: March 27
Health issues before jab: ‘None, 10-15-mile hikes at the weekend, scuba diving, travelling, you name it . . .’
Reactions: ‘No immediate side effects post second jab but after two weeks everything changed. I began getting headaches in the back of the head and pain in my neck. Stiff neck, pins and needles in my head and neck. Fatigue and short of breath during hikes. I had to stop after every lap when swimming. I tried to carry on as normal but couldn’t.’
Tests done: Four A&E visits and two admissions, one a suspected stroke the other because she couldn’t swallow, suspected VITT and Guillain-Barré syndrome (rapid onset muscle weakness), burning in hands and feet and leg weakness. Fifteen GP appointments, numerous blood tests, MRI of brain and spine, endoscopy, recorded heart rate for 24 hours, neurological physiotherapy, and exercises to help improve balance and reduce dizziness.
Time off work: Five months but hoping to return to work fulltime as feeling much better.
GP’s response: ‘I was told this is all stress and anxiety, in other words, all in my mind. Denial that the vaccine has anything to do with it. Doctors in the clinical trial have been unhelpful.’
MHRA and AstraZeneca response: Not known
DAVE McGUIRE, personal details not given. Dave provided three emails but has not been in contact since.
‘I’ve been talking to my best chum recently who had his first Pfizer jab a few weeks back. He’s now a fully-fledged member of the post vaccine headache world. What on earth is in these vaccines?’
1st jab: details not provided
2nd jab: not known
Health issues before jab: None
Reactions: Constant headaches, dizziness, abnormal heart rate, chest pain, reflux, fatigue, muscle pain and weakness in legs and arms, pins and needles and tingling in my right little finger, nausea, inflammation and stomach pains.
Tests done: Not known
Time off work: ‘Chest pain and muscle aches seem to be waning away and my heart is no longer racing like it used to.’
GP’s response: ‘One was hopeful that from her experience of seeing people with long-lasting effects from other vaccines that these should disappear with time.’
MHRA and AstraZeneca response: Not known
NOTE: By July 28, 24.8million people had received 48.4million doses of the AstraZeneca with one in 110 people reporting adverse reactions to the MHRA’s Yellow Card Scheme. A total of 20.46million have received 34.26million doses of the Pfizer with a reporting rate of one in 208 adverse events. Only 1.3million people have received 1.7million doses of the Moderna and 1 in 110 have reported serious side effects.
“Pfizer and BioNTech’s Covid-19 vaccine is just 39% effective in Israel where the delta variant is the dominant strain according to a new report from the country’s Health Ministry” we read in a CNBC report. Astonishment is one’s first reaction when coming across this piece of information, since it was not so long ago the vaccine manufacturers claimed their products were 92 to 98 percent effective.
The manufacturers’ initial claims, however, have been steadily revised down as real-world data has been coming in. In March of this year news came from South Africa that “AstraZeneca vaccine doesn’t prevent B1351 Covid.” A couple of months later, the Hill ran a piece by a Baylor School of Medicine virologist who observed:
“A new study published in the New England Journal of Medicine found that Pfizer-BioNTech vaccine provides only 51 percent protection against B.1.351 of South Africa.”
Just a couple of weeks ago, we learned that recipients of the Sinovac Biotech’s vaccine have no antibodies after six months. This effectually means that merely half a year after being injected into people’s bodies the vaccine has zero percent efficacy in protecting against Covid-19.
Even factoring for the variants, the hard data makes it quite clear that the initial claims of vaccine effectiveness were greatly exaggerated. This, of course, comes as no surprise to anyone familiar with the dynamic of the pharma industry. Drug manufacturers tend to wildly overstate the efficacy of their products, while doing their very best to understate their side effects. It is for this purpose they conduct trials that are manipulated to obtain the results they wish for. Sadly, they too often get away with it because of the corruption of the system by what is called regulatory capture. This is why the outcomes of manufacturers’ trials are almost never replicated by independent trials or real-world data.
This is what has apparently happened with the Covid vaccines. The manufacturers used the sense of emergency brought on by the Covid pandemic to conduct rushed and incomplete trials which were designed to yield the results they wanted to see. There is every reason to believe that the effectiveness of their injections was nowhere close to the 92-98% range they initially claimed even for the variants that were in circulation at that time.
Needless to say, one has a strong suspicion that even the meagre 39 percent figure is still overstated. This would only be natural, since everyone involved in the vaccination enterprise – the manufacturers, politicians, regulators, the medical establishment and corporate scientists – is trying their best to save face and reputation in the face of this fiasco. Bad though the data is, we can be quite sure that it has been massaged to soften the blow.
You can clearly observe this tendency at work in the CNBC piece which claims that even though Pfizer is only 39 percent effective, it still protects against serious disease. But this is simply not true, which you can easily see if you take the trouble to look into the data put out by the Israeli government. At roughly the same time that CNBC filed its report, the Israeli Ministry of Health published a bulletin which reported on Covid cases in the country. According to their data, there were 137 serious cases in Israel of which 95 were fully vaccinated and 42 unvaccinated or partially vaccinated (see here and here). In other words, the bulk of the serious cases was comprised of those who had received their shots. If the vaccine was as effective in protecting against heavy illness as the article claims, the numbers would look completely different. The figures published by the Israeli Ministry of Health shows that the claims of Pfizer’s efficacy of protecting against serious Covid are simply untrue.
This has been confirmed by the testimony of Dr Kobi Haviv, Director of Herzog Hospital in Jerusalem. In a recent TV interview, Dr Haviv stated that the fully vaccinated people account for about 90 percent of hospitalizations. Given that less than 90 percent of the Israeli population is fully vaccinated, it would appear that the vaccination not only does not prevent you from contracting the disease, but actually increases one’s chances of becoming a serious Covid case. Observes Dr Haviv: “yes, unfortunately, the vaccine… as they say, its effectiveness is waning.” And so it is, indeed. Dr Haviv’s interview is on YouTube so you can hear the truth straight from his mouth. It will be interesting to see how long it will take for the Establishment Censors to take it down.
Two days ago Merkel and the Bavarian minister announced stringent new measures directed against those who refuse to get their clot shot. For the past few weeks specific media have been inciting hatred against this group, based on lies, more specifically implicit premises that are untrue, as well as illogical or unwarranted conclusions:
• People who got the clot shot are immune to being infected.
• Hence, they are also incapable of infecting others.
• Asymptomatic viral transfer (with high viral load but no sickness) is very common.
• Nearly everyone with no clot shot is at equal risk to get acute viral symptoms.
• At least a 85% “vaccination rate” is required for herd immunity to end the pandemic.
• Those refusing the clot shot are guilty of prolonging the pandemic, harming society.
• These skeptics not going along are parasites who should be shunned from public life.
The recent graph from the central reporting authority in Berlin, the Robert Koch Institute, depicts a 26 week period that highlights the situation very well. The histogram data show gene sequencing information from sampling valid PCR test results, so all the false positives they got are not included here. The government pays labs 200 EUR to sequence a sample.
The gray shades represent the percentage per week that constitutes the derivatives of the virus that emerged in Wuhan, upon which the trial data associated with the clot shot temporary emergency use authorization are based. The blue shades refer to the British variant, and the red to the Indian variant, which have been renamed to get Greek letters. The South African and Brazilian variants barely play a role here.
From an epidemiological perspective it is clear that in Germany the original and British variants have essentially already been eradicated, what one would call “herd immunity” has been attained. Based on information from other countries farther along in the mass experiment, as well as recent admission by the CDC, the clot shot has no effect on the Indian (delta) variant.
Under these circumstances a plausible perception management approach could thus have been:
• Proclaim the experiment was a success because two key variants were wiped out.
• Acknowledge the clot shot is not effective against stemming the Indian variant.
• Discontinue any further inoculations, due to their potential adverse harm.
• Assert that the remaining variant has mild effects and can easily be dealt with.
• Declare an end to the so-called pandemic and the associated restrictive measures.
• Treat all people the same way, yet monitor possible viral spread with thermometers.
However, this was not done because the issue is not about public health but about instituting a totalitarian system that wants to deal harshly with those who are skeptical or critical about the false premises used to bring it on and staunchly refuse to go along with the clot shot experiment. Therefore, the consequences for those not already contaminated twice by the clot shot were instead, as follows:
• The threshold level to get an antigen test for basic activities (haircut, restaurant) was lowered from 50 to 35 (incidences per 100K population per week, based on flawed PCR test).
• People needing to get tested must pay for such tests out of their own pocket beginning October 11.
• In the future, they will likely be excluded altogether from participating in public life. It was suggested they should be shunned by private businesses (restaurants, hotels, cultural venues) as unwelcome customers.
The chosen policy is short-sighted. As the virtuous (obedient) people continue to spread the virus among each other, the skeptics will be blamed for the spread, while those newly infected who thought they were immune will be told that the clot shot is not quite 100% effective, so they will soon need to get a booster shot. Thus, another cycle of madness will be perpetuated, as the totalitarian grip tightens. Authorities want to get rid of the experimental control group consisting of those who did not consent.
Last week President Joe Biden told the coronavirus vaccines propaganda whopper that about 350 million Americans had taken shots of the experimental coronavirus vaccines. That number, of course, is greater than the United States population. Not content to leave the extreme overcounting of supposed vaccination success to her boss, White House Press Secretary Jen Psaki, in a Wednesday press briefing, claimed that we have “seen tens of millions of people’s lives saved who have gotten the vaccine; that data is clear across the country.”
Hmmm. Even the US government’s coronavirus death count, which is inflated by, among other things, the inclusion of people who died with coronavirus instead just people who died from it, shows well less than one million deaths since records began being kept early last year. We are supposed to believe that the giving of experimental coronavirus shots that only started rolling out in a limited fashion in December, and that tens of millions of Americans have chosen not to receive, has prevented many multiples of those deaths? Not a chance. We are not seeing that kind of coronavirus death rate anywhere in the world, including countries where comparatively very few people have taken experimental coronavirus vaccine shots.
Sure, Biden and Psaki may have just misspoken in providing these outrageously inflated numbers for people who have received or been saved by the shots. But, what do you expect? While they say to “trust the science,” what they dish out day after day is puffery dressed up as science. For example, Biden routinely touts the experimental coronavirus vaccines, some of which are not even vaccines under the normal meaning of the term, as being safe and effective for everyone, despite the reality being the shots can be both dangerous and ineffective. When people routinely say things so divorced from reality, they are bound to on occasion become carried away and make preposterous statements that can be exposed as indisputably false by the application of simple math.
When listening to politicians and their spokesmen hyping coronavirus danger and their grand plans for countering that danger, it is a good idea to keep in mind an old joke: How can you tell a politician is lying? His lips are moving.
We are not “anti-VAXers.” We were vaccinated because we believed we were being told the truth. Now we know better.
Unfortunately, the current gene-based vaccines (all vaccines on the US market today) were rushed to market without proper testing. They are dangerous and appear to have killed over 30,000 previously healthy Americans so far and disabled an equivalent number.
The Phase 3 trials were structured so that the results looked good because they were allowed to exclude unfavorable data (such as Maddie de Garay, a 12-year old girl who participated in the Pfizer trial and who is now permanently paralyzed due to the vaccine). People with a bad first reaction were allowed to drop out which doesn’t reflect the reality of “full vaccination” requirements of workplaces and schools.
We should stop the current gene-based vaccines ASAP. The risk/benefit justification isn’t there for any age group due to the poor safety profile of these vaccines compared with the alternatives.
Based on analysis of VAERS death data for vaccine deaths and CDC death data for COVID deaths, the younger you are, the less sense vaccination makes. If early treatments didn’t work at all, the toxicity of the current vaccines would only make sense for those over 30 (based data to date). However, the vaccines are too toxic and don’t meet the <50 deaths stopping criteria that we’ve used for the past 30 years, so they should never be used because we have better alternatives available today that can achieve the same goals.
We should never be giving vaccines that disable or kill previously healthy people in huge numbers if safer alternatives are available that can achieve all the same objectives.
Why would anyone in America choose to have lipid nanoparticles which deliver a toxic protein into your brain and where the long term effects are unknown, when safer alternatives are available? What parent would choose to experiment on their kids this way when safer and more effective options are available?
It is tragic that schools are requiring students to be vaccinated in order to attend classes. I’ve asked our top universities for the risk-benefit analysis to justify this action and have received nothing. If the vaccines were perfectly safe, no analysis would be needed. But they aren’t.
The rate of severe life-changing side effects appears to be well in excess of 25,000 people (the number reported disabled is comparable to the number dead). The fact that Facebook groups of vaccine victims had 200,000 users suggests that more than 1 in 1,000 are suffering from significant long-term impacts; people with minor temporary reactions have little incentive to seek out and sign up for a vaccine side-effects group.
People who claim “the clinical trials showed no significant side effects so it must be safe” have a tough time explaining how these facebook groups were so large before they were deleted. If you think the vaccines are so safe, show me the severity analysis of the 200,000 people there. These groups don’t appear with the influenza vaccine. You never see neurological effects like this in such high volume with a safe vaccine.
Some have cited the emergence of the Delta variant as changing the math to favor vaccination even if the vaccine is unsafe. But the case fatality rate (CFR) of the Delta variant is only 0.1 percent compared to the CFR of 1.9 percent for the original virus (alpha) according to UK government data. The argument that the lower CFR of delta is due to the higher number of vaccinated people isn’t very credible since the Eta variant has a 2.7 percent CFR.
Early treatments are a more effective and safer option than the current vaccines. We can achieve all of the objectives of the current vaccination program (herd immunity, eradication of the virus, re-opening our economy, ditching of masks) with fewer deaths and near zero serious side effects. In addition, we would have less problem with variants since variants are less likely to be generated if everyone is naturally immune. So why not promote early treatments? Why not give them a try for a month while we hit the pause button on the vaccines? Would that be so bad?
Allowing natural infection will impart broad natural immunity. We should instruct the population how to treat early with early treatment protocols as soon as they believe they are infected. People should have the drugs on-hand so that treatment can be started without delay after speaking with their doctor. This results in superior risk reduction in terms of fewer fatalities and side effects compared to the current vaccines.
There was never a need for masking or social distancing as COVID is very treatable when treated early. Nobody has to die or be hospitalized. We can get to herd immunity quickly this way. The key is to treat the virus early with a proven early treatment cocktail of repurposed drugs, adding novel antivirals if/when available.
Unfortunately, the NIH has unethically suppressed all early treatments in order to push the vaccine narrative. This is clear with the publication of a systematic review of ivermectin, the highest level of evidence possible. Yet the NIH and WHO pretend that it never happened. It isn’t even acknowledged that the systematic review came out. There has never been a peer-reviewed systematic review that was later overturned. This is why they are the top of the evidence pyramid.
Early treatments were never funded. When evidence came in they worked, the NIH ignored it. The corruption at the NIH and FDA should be corrected by Congress. Now.
If a safe sterilizing vaccine can be developed, we should test it adequately for safety before deploying it. We should not cut corners on safety again; with early treatments, there is no need to rush this.
Major medical journals have lost objectivity in publishing papers that go against the “safe” narrative. For example, the NEJM rejected a Letter to the Editor pointing out a flaw in a paper showing vaccines were safe for pregnant women. The Letter showed an alarming statistic. The NEJM refused to reveal their reasoning for the rejection. Three editors quit a journal after a peer-reviewed paper was published that showed that vaccination may cause more harm than good. Those who quit provided no evidence that the paper was in error.
The censorship of legitimate medical information on social networks must end. These networks are the new “public square” and should be regulated so that people are free to express their opinions to anyone who chooses to listen. There should be heavy monetary penalties for suppressing medical information that has the potential to save lives. Social networks should be required to compensate all those people who have been harmed by their actions.
Never again should we deploy a vaccine on the American public without proper testing and without informed consent. Databases such as V-SAFE that track safety data should be made transparent. Am I the only person who thinks that is a problem?
VAERS reporting should be required and the VAERS system should be modernized so that it is easy to use and results in records with consistent field coding. There should be a smaller lag time to get records into the database, all false reports should be 100% enforced as a criminal act, and the safety signal monitoring should be much stronger.
The cost-benefit analysis of the current gene-based vaccines for anyone of any age is at best a wash according to the scientific literature (new paper published June 24, 2021). This peer-reviewed paper looked at the real cost-benefit analysis and concluded that “This lack of clear benefit should cause governments to rethink their vaccination policy.” As far as I know, this is the most optimistic of all the papers looking at actual death rates of COVID vs. the vaccine. All the other ones are even worse for the vaccine.
Independent analysis by a statistician friend shows a similar effect. Like me, Mathew has no axe to grind here, just trying to get at the truth of the risk/benefit for the current vaccines. His conclusion: “More importantly, I also still disagree with the mass vaccination program. In particular, nearly all lives saved are in the high risk group. While vaccinating those in the low risk group might decrease spread into the high risk group, that’s asking young healthy people to act as human shields.
I also believe that when the vaccine deaths and adverse events are finally tallied and compared to either a ring vaccination strategy or combination ring vaccination and early treatment strategy, the current plan will look quite foolish and possibly even nefarious.”
Since the focus today is on getting kids vaccinated, I ran the numbers in the VAERS database for 20-24 year olds and 25-29 year olds. In both age ranges, the number of deaths caused by the vaccine outnumber the number of deaths saved. The vaccines caused 1.89 deaths per 100,000 (ages 25-29) and 1.74 deaths per 100,000 (ages 20-24).
This means the vaccines are net killing machines since they kill more people than they save (.3 to 1.0 lives per 100K saved according to the most recent CDC presentation). My calculations are in the body of this document and the calculations show no net benefit for any age group based on real-world data from the US and UK.
The comparison is even more extreme if we tell kids to ignore the current CDC advice and use an early treatment program. In that case, we can reduce the death rate by more than two orders of magnitude from COVID, so that the number of lives saved by the vaccine is fewer than 1 in 10M. This means the vaccines need to be less toxic than the influenza vaccine (which has a death rate of 1 in 10M) in order to be considered. They are not even close to that. Not by a country mile.
For older people, the numbers don’t work out either. We looked at the UK data for <50 and >50 and we found that the absolute death rate is very small for <50 group. There was a high relative risk reduction, but the absolute deaths were small. If the vaccine kills more than 1 in 1 million, it’s game over for the vaccine being useful. For age >50, the UK data shows that even if the vaccines killed nobody, it is not beneficial. So when you factor the death rate of the vaccines and early treatment as the other option, the case is extremely lopsided.
In short, because the current vaccines are so dangerous and early treatment is so effective (relative risk reduction of 100 or more with no permanent side effects), there is no reasonable case that can be made for vaccinating any age group.
Although we just looked at deaths in the analysis above, the same can be true for other side effects as well: the range and intensity of side effects from the vaccine dwarf anything seen in natural COVID. It’s even a more stark contrast when early treatment is added to the mix.
Long term, untreated vax patients and untreated COVID patients are virtually identical in terms of symptoms (thanks to Ram Yogendra for that insight). By vaccinating patients, we are essentially giving a portion of those vaccinated long hauler COVID.
The case numbers in the UK (one of the most heavily vaccinated countries) are now climbing. It suggests we should have listened to the arguments of Geert Vanden Bossche, one of the most famous scientists in the vaccine field, which are further clarified in this excellent video by Chris Martenson which points out that there are really only two ways out of the pandemic: a sterilizing vaccine (using the complete virus as the antigen) or allowing infection and treating with early treatment leading to natural immunity.
The Yellow Card system in the UK showed a similar safety signal. Independent analysis of that data by an expert in medical evidence concluded that the vaccines are unsafe for use in humans. It wasn’t a close call. The death rates from the vaccines are far greater than any absolute risk reduction.
This is taken from a very long article. Read the rest here: docs.google.com
Welcome to Vaccination Decisions Newsletter 280. This is my global newsletter sent from Perth, Western Australia that has enabled me to contribute my university research to the global debate on vaccines for the last eight years.
This came to an end on 10th October 2020 when MailChimp censored my newsletter by disabling my account. Did you know that Mailchimp has been in partnership with the US CDC since 2018?
In 2015 I completed a PhD investigating the reasons for the decline in deaths and hospitalisations (risk) to infectious diseases by 1950 in Australia – and in all developed countries. This included an investigation into the role that vaccines played in this decline.
I set up this newsletter in 2012 when I recognised that this public interest science was being suppressed from public debate in all the official channels. This is the result of powerful industry-lobby groups in Australia (and globally) that are influencing all media outlets and research institutions.
Due to this global newsletter my PhD has now been downloaded thousands of times and in March 2020 my book, “Vaccination: Australia’s Loss of Health Freedom”, became available just as everyone globally was being locked down.
This happened because in 2020-21 all the traditional measures for controlling infectious diseases were reversed for the first time in history by the World Health Organisation (WHO). This organisation, advised by the corporate-public partnerships in the GAVI alliance, including the Federation of Pharmaceutical Companies, falsely claimed that healthy (asymptomatic) people are a ‘risk’ to the community if the virus is identified in their body.
This was stated by the WHO scientists in March 2020 even though the WHO had no data to base this claim on in March 2020. Remember, this novel Coronavirus 2019 (SARS-Cov-2) only appeared in January 2020 and there was no evidence provided to support the statement that healthy people without symptoms were a risk to the community.
It was being assumed that a positive PCR result, a test that cannot diagnose disease, indicated an asymptomatic ‘case’ of disease.
This assumption has led to journalists and health departments reporting healthy people as a ‘case’ of disease in 2020-21, wildly inflating the risk from this alleged new flu virus in the media. This false assumption has led to healthy people being locked up in quarantine for two weeks as well as to the unnecessary masking of healthy people, social distancing and isolating of the elderly.
The mainstream media is not required to list the symptoms of the ‘cases’ of disease they are reporting, and this has enabled the government to hide this fact. This allows the media to frighten the public with cases of disease that are healthy people (no symptoms), and deaths that are elderly people with co-morbidity, that die with the flu every year. The difference is that this year, the media is reporting these deaths – normally you do not hear about them.
The fact that the WHO did not have any evidence in March 2020 to support the claim that ‘asymptomatic’ people are a risk to society, is provided by Dr. Maria Van Kerkhove, on 8 June 2020 – only three months after the ‘pandemic’ was declared. This WHO spokesperson appears to understand the traditional measures of controlling infectious diseases because she states that you isolate the people with symptoms and trace their contacts to prevent transmission.
However, even though she states that asymptomatic transmission is ‘very rare’, because the WHO doesn’t have any data to claim otherwise, she concludes that the WHO still advises that ‘some people without symptoms can still transmit the virus on.’
The flaw in this WHO statement is that there is a difference between transmitting the virus and transmitting disease. Whilst the virus can be passed on from a sub-clinical infection this does not lead to disease in the majority of cases in countries with good public health infrastructure.
Infection only leads to disease when there are poor environmental conditions or poor host characteristics. Hence, asymptomatic people do not transmit disease in the population, they transmit infection that is mostly beneficial when good conditions exist: asymptomatic ‘cases’ generate natural herd immunity.
This is the reason why the WHO changed the definition of ‘herd immunity’ in December 2020.
It was to claim that only vaccine created herd immunity would be successful with COVID19 disease. This was claimed without any risk-benefit data for the COVID19 vaccine: this drug had not been trialled in humans in December 2020.
The WHO changed this definition without providing any scientific evidence to support the claim that ‘vaccines can create herd immunity’ and without any scrutiny from the scientific community. Therefore, the claim has not been validated and it has been done to support the WHO’s desired outcome; to make the world reliant on vaccines.
Viruses are around us all the time and we do not need to eradicate them to live without disease. This is because viruses on their own cannot cause disease: the cause of disease from infectious agents is multifactorial.
This is where the GAVI/ WHO partnerships have deceived the public in 2020. Scientists have known since 1950 that viruses mostly cause sub-clinical infections, that never develop disease symptoms, due to improvements in public health infrastructure and nutrition.
It is these sub-clinical infections that resulted in herd immunity in the population of developed countries by 1950/60. This led public health officials to claim that ‘infectious deaths fell before widespread vaccination was implemented’ (Fiona Stanley, Australian of the Year for Public Health, 2003). Even smallpox of cases with symptoms was not controlled until after 1950 when isolation of cases with symptoms and case-tracing strategies played a significant role in the decline of this disease.
The fraudulent claims that are being made by the WHO are effectively manipulating public behaviour because the corporate-sponsored mainstream media and big tech companies are working together to censor public debate.
If this was a conspiracy theory, as the mainstream media would like you to believe, I would have hoped that the industry-lobby groups who petitioned to have my PhD removed in 2016 – after it was published on the University website – were successful. But they weren’t.
The University stood by this thesis because it provided the evidence to support the fact that global health policy is being designed by a collaboration of industry-partners. This is also supported by the extreme censorship of many doctors, scientists, and activists also providing this evidence to you in 2021. Science is only validated when it stands up to scrutiny from the community, so human health is at serious risk until we have this scientific debate.
DOCTORS, lawyers and other patient advocates around the world are challenging the legality, ethics and scientific basis of the global drive to vaccinate the entire population, including children, against Covid-19. But even as they raise their voices, the intensity of censorship is increasing.
The latest victim is cardiologist, internal disease specialist, epidemiologist and academic researcher Dr Peter McCullough, editor-in-chief of two medical journals and author of over 600 peer-reviewed publications in the US National Library of Medicine, more than 45 of them dedicated to Covid-19. He has managed the care of more than 100 Covid patients as well as advising on hundreds more worldwide.
When this top American doctor spoke out on the effectiveness of early treatment, and raised questions over the safety and effectiveness of the vaccines, he began to find himself a pariah among colleagues.
He now faces what he calls ‘a dark cloud of censorship and reprisal’, including a legal action against which his attorneys were filing a defence last week.
Google his name, and you find at the top of the list an outrageously biased stand-alone item about the lawsuit, in which the online journal Medpage Today accuses him of ‘Dishing Out Vax Falsehoods’.
An information war is under way, and though most of the weapons are in the hands of governmental and drug company-funded sources, the resistance movement is growing.
McCullough has prepared what he calls ‘five key messages of scientific truth that I want everybody to understand about the virus and the pandemic.’ He has all the necessary scientific back-up to support his claims.
If his messages were to be emblazoned across every media outlet in this land and abroad, there would be a chance of ending the socially and economically destructive policies that have so far cost UK taxpayers an incredible £400billion in additional public spending directly attributable to Covid-19.
The five messages are:
1. The virus is not spread asymptomatically. That is, only sick people give it to other people.
2. We should stop testing symptomless people. That just generates false positives – creating extra ‘cases’ and extra concerns. ‘There shouldn’t be a single person on Earth that should undergo an asymptomatic test or a test done on a routine basis. For any reason. People ought to just walk past these testing stations. They have absolutely no standing whatsoever.’
3. Natural immunity is robust, complete, and durable. It cannot be improved by vaccination, or any other method. A person who has developed immunity after exposure to the virus is at minimal risk of becoming seriously ill again from Covid. Where apparent cases of that kind have been reported, a misinterpretation in the test procedure has been responsible.
Even with loosely defined cases, 11 studies involving 650,000 individuals showed a long-term recurrence rate of only 0.2 per cent. ‘Someone who is naturally immune can walk up to someone who has Covid-19, get a big cough in the face, and they are not going to get the illness.’
4. Covid-19, no matter what the variant, is easily treatable at home with simple, available drugs. About 88 per cent of hospitalisation and death is avoidable with early treatment. ‘The only way people end up in hospital and have a miserable time is when they receive no treatment.’
It’s easy to treat the illness early on, when the symptoms are mild. It has three major components: Viral replication, inflammation, and thrombosis – blood clots. Once these develop, they lower oxygen levels in the lungs and are hard to reverse.
5. The current Covid vaccines – AstraZeneca, Johnson and Johnson, Pfizer, and Moderna – are obsolete. ‘They do not cover the new variants. Patients are being hospitalised and getting sick, despite having the vaccines.’ And because of the record levels of deaths and injuries reported after the jabs, they should be considered ‘unsafe and unfit for human use.’
McCullough delivers this message in a four-minute video posted on LifeSite News.
It could save many lives, and perhaps even avoid any further fall into lockdown lunacy, if the link were to be sent to every doctor and every home in the UK.
To all who come across this article, please take a look at the video and judge for yourself: Is this some anti-vax maniac pushing a self-serving agenda? Or a highly-experienced, concerned doctor offering valuable insights into Covid realities, and fighting for a more rational, science-based treatment approach?
This treatment guide, co-authored by McCullough and Dr Elizabeth Lee Vliet, president and CEO of the Truth for Health Foundation (THF), a Christian-based US charity founded by doctors, could also be widely distributed. Vliet is a past director of the Association of American Physicians and Surgeons.
Last week McCullough was among a team of physicians, scientists, clergy and patient advocates presenting ‘factual scientific and medical data previously kept from people around the world’ at the LifeSite-sponsored THF conference called Stop The Shot.
The foundation said the aim was ‘to help all of us be able to save lives and expose the threats to human health with these “shots” being forced on people without proper informed consent.’
Americans have not seen a single press briefing on vaccine safety, despite more than 100,000 people having died or been hospitalised in the wake of the jab, McCullough said.
‘My patients ask me: Doctor, am I going to be someone who dies after being hospitalised? I tell them: I don’t know, because our government is not telling us anything.
‘I had patients ask me today: Doctor, I hear the vaccine is failing. My friends have gotten the vaccine, but they’re getting sick with Covid, the Delta variant. Which vaccine is the best? Which one protects best against Delta? I say: I don’t know, because our government hasn’t told us anything.
‘So part of this conference is to have everyone start to really get on edge and demand of their government officials, their representatives, their hospital representatives, information – fair information.
‘If somebody gets on TV and says the vaccines are safe and effective, that’s misinformation. There’s nothing to suggest that these vaccines are safe and there’s nothing to suggest right now, based on the reports that we’re seeing, that they’re effective. We’re almost seeing a wholesale failure of the vaccine programme. So we have to take action now with early treatment.’
The situation is similar in the UK, where nearly 340,000 adverse reactions of varying severity, including 1,500 deaths, have been reported. With 84million shots administered, regulators insist that apart from local reactions to the jab, most of the deaths and injuries are coincidental.
That stand is highly questionable. In Germany, the Federation of Pathologists is urging that more autopsies should be conducted when people die in the wake of vaccination, to either exclude or prove a cause-and-effect link.
The call follows a study by Dr Peter Schirmacher, acting chairman of the German Society of Pathology, in which he performed autopsies on 40 people who had died within two weeks of the jab.
He found that 30-40 per cent of the deaths could be directly attributed to rare but serious adverse effects from the vaccine such as a blood clot in the brain, or autoimmune disease. He believes there may be many such cases in which the deaths go unnoticed, because doctors don’t make the link with the vaccine and certify the death as from natural causes.
After several dozen international publications, including The Washington Post and The Guardian, simultaneously reported in mid-July on a major investigation by Amnesty International and Forbidden Stories over Israel’s Pegasus spyware, another scandal over Israeli cyber-spying activities erupted.
According to the articles, not only Israel itself but also dozens of governments used Israeli technology to hack the phones of politicians, journalists, opposition activists, and human rights activists. Tens of thousands of phones were tapped. A direct trace is also evident in Israel’s complicity in the cyber-surveillance of the murdered Saudi journalist Jamal Khashoggi, hence the responsibility for the events that happened to him. The investigation contains a great deal of information about human rights abuses in many regions of the world through programs developed by Israel and, in particular, by the NSO Group, but this is only the tip of the iceberg. It has become apparent to everyone that not only government services are engaged in cyber espionage in Israel but, in addition to the NSO Group, there are other Israeli companies competing with each other: they manufacture similar products and supply them to those who commit similar crimes. There are also technologies possessed exclusively by the Israeli security and intelligence agencies, which provide their services to Israel’s close friends, including several Arab states.
As the British publication Al-Quds-Al-Arabistresses, “the current scandal could be much more severe if all information about Israel’s activities in providing repressive regimes with electronic and non-electronic means of espionage is made public, not to mention the scale of international involvement in its crimes. First, they are cybercrimes, later escalating into actual prosecution, abuse, and imprisonment, often to the point of intentional homicide.”
It is now clear to all: even by Israeli standards, Pegasus technology is a weapon since the license to sell it is a permit for “arms trade” issued by the Export Control Department of the Israeli Ministry of Defense. According to information published in recent years, Israeli security forces have used the program to spy on Palestinian and Arab residents and to control politicians inside Israel and in many countries worldwide. For instance, in the list of phone numbers tracked by the Pegasus spyware, one of the numbers of Emmanuel Macron, the numbers of former French Prime Minister Édouard Philippe and 14 ministers of the country have already been identified since 2017, as Le Monde wrote. According to The Washington Post, 14 heads of state were tracked through Pegasus, including South African President Cyril Ramaphosa, Iraqi President Barham Salih, King Mohammed V of Morocco, Imran Khan, Prime Minister of Pakistan, and others.
Accordingly, it is pretty understandable that in addition to whoever Israel sold a license to use the Pegasus spyware, the Jewish State also had every opportunity to control the behavior of foreign politicians using this spyware. And this justifies the natural demand of any foreign public for a detailed report from Tel Aviv on such illegal activities against foreign nationals.
However, there also have been other revelations of the use of cyber spyware to spy on foreign politicians before. So, in 2014, John Kerry, then serving as US Secretary of State, became a victim of unauthorized wiretapping during his Middle East tour, as reported by the German Spiegel, citing its own sources.
At the end of 2020, the Citizen Lab, University of Toronto, published a report that disclosed the hacking of the iPhones of dozens of Al Jazeera TV Channel employees using technology developed in Israel.
Modern warfare is increasingly moving into cyberspace. With its innovative and well-funded technology and active military intelligence apparatus, Israel is one of the most advanced players in cyber warfare. Israel’s energetic participation in these wars has long been no secret, as has the fact that it was Israel that was behind the Stuxnet, Duku, and Flame attacks on Iran a few years ago. According to articles published by The Washington Post, Israel had something to do with the May 2020 cyberattack on the Iranian port of Shahid Rajaee in Bandar Abbas, the Hormozgan Province, which disabled computers tracking ship and truck traffic at the port located in the strategic area of the Strait of Hormuz in the Persian Gulf.
The fact that Israel has become a leading exporter of civilian spying equipment was revealed back in 2018 by a Haaretz study covering 15 countries. This study showed that Israeli spyware allows almost total control and even command over cell phones: detecting their location, recording phone conversations, photographing areas near the phone, reading and writing text messages and emails, downloading applications, and infiltrating existing applications, accessing photos, clips, calendar reminders, and contact lists. And all this in complete secrecy.
Privacy International has been publishing research on the international trade in espionage technology since 1995. The latest report notes the tremendous growth of the industry, in which some three dozen Israeli firms are now very active. International data shows that Israel accounts for up to 20% of the global cyber market, and investments in Israeli startups in this industry account for more than 20% of the total amount in the world. The Israel Defense Forces (IDF), in turn, played the role of a business hothouse as their technology intelligence units grew and their graduates applied their knowledge to a multitude of startups.
Unit 8200, also known as the Central Collection Unit of the Intelligence Corps, sometimes referred to as the Israeli SIGINT National Unit (ISNU), covers the offensive spectrum of military use of cyber capabilities. It reports to the Israeli Military Intelligence (AMAN). It has rather strong operational capabilities and close ties with its US counterpart, the NSA. According to some estimates, more than 5,000 soldiers are assigned to Unit 8200, enabling the latter to conduct offensive cyber operations worldwide.
Tracking Israeli exports of spy devices is hampered by the fact that in many cases, they are not exported from Israel; many companies prefer to register abroad or work there for a variety of reasons: cheap labor, favorable taxation policies, greater secrecy, weak government regulation and the desire to disguise the Israeli origin of systems to penetrate markets in hostile countries.
For example, Circles Technologies, one of the leading companies operating in Europe, has created a product that uses the weakness of the cellular network to find devices. A phone number can be determined as to which cellular cell it is connected to and approximately where it is located.
Another system, widespread in the Israeli cyber industry, focuses on gathering information from social media. These are non-aggressive systems that are not under the control of the Ministry of Defense. They concentrate on open-source information and analyze it in a way that concludes big data. In Latin America, for example, there is little trace of Israeli activity. Still, AP news agency investigations show that in 2015 an Israeli company, Verint, set up a $22 million monitoring base in Peru capable of tracking satellite, wireless and fixed-line communications with 5,000 targets and recording conversations simultaneously.
Notably, Israel was a member of the fifth United Nations Group of Governmental Experts (UNGGE) on Information and Telecommunications and the Geneva Dialogue on Responsible Behavior in Cyberspace, thus establishing acceptable behavior norms for the cyberspace. Israel is also a signatory to the Convention on Cybercrime of the Council of Europe (2019) and has established bilateral cooperative relationships (e.g., with the United States in 2016, Bulgaria in 2018, and Australia in 2017). Therefore, the discovery of offenses using the Pegasus spyware imposes a special responsibility on Israel.
As the British Al-Quds-Al-Arabi publication stresses, Israel is committing cybercrimes, and it is time to bring it to justice. The latest scandal is the perfect opportunity to do just that.
International best-selling author, Dr Vernon Coleman MB ChB DSc FRSA, explains precisely what informed conset means, why it’s important and why vaccines are the only drugs given without informed consent.
This is not just scientific madness, it appears to be very intentional and purposeful.
The Moderna and Pfizer vaccine tests were conducted, as customary, with a control group; a group within the trial who were given a placebo and not the test vaccine. However, during the trial -and after the untested vaccines were given emergency use authorization – the vaccine companies conducting the trial decided to break protocol and notify the control group they were not vaccinated. Almost all the control group were then given the vaccine.
Purposefully dissolving the placebo group violates the scientific purpose to test whether the vaccine has any efficacy; any actual benefit and/or safety issues. Without a control group there is nothing to compare the vaccinated group against. According to NPR, the doctors lost the control group in the Johnson County Clinicial Trial (Lexena, Kansas) on purpose:
(Via NPR) […] “Dr. Carlos Fierro, who runs the study there, says every participant was called back after the Food and Drug Administration authorized the vaccine.
“During that visit we discussed the options, which included staying in the study without the vaccine,” he says, “and amazingly there were people — a couple of people — who chose that.”
He suspects those individuals got spooked by rumors about the vaccine. But everybody else who had the placebo shot went ahead and got the actual vaccine. So now Fierro has essentially no comparison group left for the ongoing study. “It’s a loss from a scientific standpoint, but given the circumstances I think it’s the right thing to do,” he says.
People signing up for these studies were not promised special treatment, but once the FDA authorized the vaccines, their developers decided to offer the shots. (read more)
Just so we are clear, the final FDA authorization and approval for the vaccines are based on the outcome of these trials. As noted in the example above, the control group was intentionally lost under the auspices of “the right thing to do”, so there is no way for the efficacy, effectiveness or safety of the vaccine itself to be measured.
There’s no one left within the control group, of a statistically valid value, to give an adequate comparison of outcomes for vaxxed -vs- non-vaxxed.
Whiskey – Tango – Foxtrot !!! This is nuts.
That NPR article is one to bookmark when people start claiming the vaccination is effective.
How can the vaccine not be considered effective when there is no group of non-vaccinated people to compare the results to?
Good grief, the entire healthcare system is operating on a massive hive mindset where science, and the scientific method, is thrown out the window in favor of ideological outcomes and self-fulfilling prophecies. The fact that the researchers and doctors, apparently under the payroll of the pharmaceutical companies that have a vested financial interest in the vaccine outcome, lost the control group on purpose is alarming.
Of course, Big Pharma will promote the vaccine as beneficial, and the controlled media will promote that message with a complete disconnect from the clinical trial details, and the FDA will grant approval on results that were intentionally constructed to produce only one outcome.
Back in early July I noted that data from the ZOE Covid Symptom Study was showing that new infections in the unvaccinated were peaking and falling while those in the vaccinated were still surging.
This was not a phenomenon noted elsewhere and prompted questions about whether it showed that the vaccines were delaying infection, or whether it was primarily an age-based phenomenon. Unfortunately, before anyone was able to investigate further, within a couple of weeks ZOE had ‘updated‘ their methodology and in their new data the phenomenon had oddly disappeared.
This left questions as to whether it had been entirely an artefact of problems with their previous methodology or whether it had been a real phenomenon.
PHE data from the three most recent technical briefings (18, 19 and 20) allow us now to answer this question. Above (top of page) are the Delta case counts for the period July 6th to July 19th and then July 20th to August 2nd, broken down by vaccination status and age. (Actually, it’s not clear whether the initial date is July 6th or another date around then as briefing 18 appears to have a typo and says its data runs up to June 21st, even though briefing 17 also had data up to June 21st and the figures in briefing 18 are higher. However, for the purpose of this analysis it’s not important exactly what the start date is, and I have used July 6th as that is what it would be assuming briefing 18 has the equivalent date to the other briefings.)
The key lines to look at in the chart are the grey and yellow lines. They show that in the under-50s, Delta cases in the unvaccinated dramatically declined between early July and late July whereas those in the vaccinated (at least 21 days after the first dose) were stable. In the second half of the month there were actually more infections in the vaccinated of all ages than in the unvaccinated (the blue and orange lines).
This was the period when new infections nationwide peaked (on July 17th, by report date) and dropped quickly. This new analysis allows us to see that this fast drop was entirely in the unvaccinated under-50s (presumably the result of reaching herd immunity for the Delta variant). Infections in the vaccinated of all ages (and the unvaccinated over-50s) did not fall at the same time but remained stable. This helps explain why the drop ended around July 28th (by report date) and new infections have currently plateaued. What we are experiencing now is the ‘wave’ of infections in the vaccinated (along with the unvaccinated over 50s).
We can’t be sure that the explanation of the phenomenon is that the vaccines delayed infection. Another possibility is that the early surge was in the younger, less vaccinated portion of the under 50s (i.e., people under 30). What we really need is a finer breakdown by age. Unfortunately, despite all the data published during this crisis, very little of it is properly broken down by both vaccination status and age to allow us to do this kind of analysis.
Nonetheless, this confirms that ‘old ZOE’ was right to show infections in the unvaccinated falling during July while those in the vaccinated did not. The fact that ‘new ZOE’ no longer shows this phenomenon once again leads to questions about what changes were made and why, and whether the new methodology is really more reliable, or just more politically acceptable.
She lies in the same sentence, claiming the vaccines still work “exceptionally well.”
If they don’t prevent transmission, you CANNOT USE PUBLIC HEALTH AND HERD IMMUNITY AS THE JUSTIFICATION FOR A MANDATE. At best, the vaccines might provide the recipient with some protection for a few months. But the downside is they might increase susceptibility or severity of disease later.
And when you add on the known and unknown short and long-term side effects, vaccination with an experimental product that went through minimal testing and poorly designed clinical trials just doesn’t make sense.
All the bluster about mandates was designed to trick the public into getting vaccinated before the truth came out. Now it’s out. Help your friends and family avoid these shots.
Remember: Your vaccine does NOT protect me, and it might not protect you either. Not for long. Then it might make things worse for you.
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