It looks like you're using an Ad Blocker.
Please white-list or disable AboveTopSecret.com in your ad-blocking tool.
Thank you.
Some features of ATS will be disabled while you continue to use an ad-blocker.
originally posted by: Ksihkehe
originally posted by: DAVID64
I have a question for all those rabid Pro Vaxxers, who called those of us who refused it "anti science" "anti vaxxers" and tried to shame us into getting an experimental drug. Told us it was our moral duty to shut up, line up and roll up our sleeves like a good little soldier.
My question is this : How does it feel now, to know you were lied to, tricked and used like a $2 hooker on payday ?
Probably feeling more than a bit foolish right about now, huh ?
Well......we tried to warn you.
The ones that felt foolish have stopped being vocal about it, as any rational person does when recognizing there has been fraud perpetrated against them.
Those that are still doing it have been provided more than enough real information to know better, yet still support killing kids to maintain a collapsed political narrative and further authoritarian violations of basic human rights.
I still support their freedom of speech though virtually all remaining vaccine supporters were very much on the side of silencing my accurate statements and my removal from society. I believe in people being able to make their own decisions, even when them doing so is evidence of the enormous harm ignorance can do to society.
COVID should be a lesson in why the government should never be allowed anywhere near our freedom of expression. I have two years of state funded attacks against me for being right, never exaggerating, and making statisticslly conservative estimates. Once they start censoring the fringe they next come for anything that contradicts their lies.
originally posted by: Albert999
originally posted by: Ksihkehe
originally posted by: DAVID64
I have a question for all those rabid Pro Vaxxers, who called those of us who refused it "anti science" "anti vaxxers" and tried to shame us into getting an experimental drug. Told us it was our moral duty to shut up, line up and roll up our sleeves like a good little soldier.
My question is this : How does it feel now, to know you were lied to, tricked and used like a $2 hooker on payday ?
Probably feeling more than a bit foolish right about now, huh ?
Well......we tried to warn you.
The ones that felt foolish have stopped being vocal about it, as any rational person does when recognizing there has been fraud perpetrated against them.
Those that are still doing it have been provided more than enough real information to know better, yet still support killing kids to maintain a collapsed political narrative and further authoritarian violations of basic human rights.
I still support their freedom of speech though virtually all remaining vaccine supporters were very much on the side of silencing my accurate statements and my removal from society. I believe in people being able to make their own decisions, even when them doing so is evidence of the enormous harm ignorance can do to society.
COVID should be a lesson in why the government should never be allowed anywhere near our freedom of expression. I have two years of state funded attacks against me for being right, never exaggerating, and making statisticslly conservative estimates. Once they start censoring the fringe they next come for anything that contradicts their lies.
They also may be continuing to champion the vaxine because they are paid to đ§
irrefutable evidence and simple logic that proves kids will be hurt and killed for no benefit
Despite Eddyâs warnings, an estimated 120,000 children that year were injected with the Cutter vaccine, according to Paul A. Offit, director of the Vaccine Education Center at Childrenâs Hospital of Philadelphia. Roughly 40,000 got âabortiveâ polio, with fever, sore throat, headache, vomiting and muscle pain. Fifty-one were paralyzed, and five died, Offit wrote in his 2005 book,
A year later, on April 12, 1955, when officials announced the results at a news conference at the University of Michigan, there was jubilation. Reporters hollered: âIt works! It works!â Offit wrote. The news made front-page headlines across the country. âPeople wept,â Offit said. âThere were parades in Jonas Salkâs honor. ⌠Thatâs what contributed to the tragedy of Cutter more than anything else ⌠the irony.â
That same day, licenses were hurriedly granted to several drug companies, including Cutter Laboratories, to make the vaccine. But the officials granting the licenses were never told of Eddyâs findings, Offit wrote. The year before, Eddyâs scrutiny of the Cutter vaccine had continued through the summer and fall.
She had started at NIH in 1937, had headed testing of vaccines for influenza, and in 1954 was asked to help test the Salk polio vaccine. The pressure was intense. âFor weeks she and her staff worked around-the-clock, seven days a week,â OâHern wrote.
âThis was a product that had never been made before, and they were going to use it right away,â Eddy had said.
She began testing Cutterâs samples in August 1954 and continued through November, according to a later report in the Congressional Record. She found that three of the six samples paralyzed test monkeys. âWhat do you think is wrong with these monkeys?â
she asked a colleague, Offit recounted. âThey were given polio,â the colleague replied. âNo,â Eddy said. âThey were given the ⌠vaccine.â
A new polio outbreak in Sudan has been linked to the oral polio vaccine that uses a weakened form of the virus. News of the outbreak comes a week after the World Health Organization (WHO) announced that wild polio had been eradicated in Africa.
The WHO linked the cases to a strain of the virus that had been noted circulating in Chad last year and warned that the risk of spread to other parts of the Horn of Africa was high.
In a statement on the new cases, the WHO said two children in Sudan, one from South Darfur state and the other from Gadarif state, close to the border with Ethiopia and Eritrea, were paralysed in March and April.
Both had been recently vaccinated against a different strain of polio. The WHO said initial outbreak investigations showed the cases were linked to a continuing vaccine-derived outbreak in Chad that was first detected last year and is now spreading in Chad and Cameroon.
Panic spread in the state following the death of a two-year-old child hours after he was given polio vaccine near Chennai on Sunday. But doctors have reassured parents that the death wasn't related to the vaccine.
The child, A Joshua, was administered the oral vaccine at 8.30am at an anganwadi centre in Padapai on Sunday as part of the pulse polio programme. He died at his house two hours later.
His mother A Dhanalakshmi, 20, alleged that the child died due to the vaccine. As the news spread, many other children, who received the vaccine from the same centre, were rushed to a nearby government hospital in Chrompet, where doctors assured the parents that the vaccine was safe.
A boy has died from polio in Papua New Guinea in the first fatal case since an outbreak of the disease in June.
The World Health Organisation said on Tuesday that the boy died in Enga province, one of 14 confirmed cases across the country .
Speaking at the launch of a nationwide polio vaccination campaign on Monday, the WHO representative in the country, Luo Dapeng, said that there had been five confirmed cases in Eastern Highlands province, three in Morobe, two in Enga, two in Madang, one in Port Moresby and one in Jiwaka, the Papua New Guinea Post Courier website said.
The countryâs health department said the child died when the muscles around their lungs became paralysed by the virus, Radio NZ said.
The South Sudanese government says 15 young children have died as a result of a botched measles vaccination campaign.
All of the children who died were under the age of five, said the Health Ministry, which blamed the deaths on human error.
One syringe was used for all the children over four days, it said, and the vaccine was not stored properly â with children as young as 12 years old administering injections.
Two health workers have been suspended after three toddlers died following the administration of the MMR (measles-mumps-rubella) vaccine in the Belagavi district of Karnataka. Health and Family Welfare Minister K Sudhakar told the media on Monday that an auxiliary nursing midwife (ANM) and a pharmacist were suspended and a report was sought from the district health officer and a state-level immunisation programme officer.
The deceased children from Ramdurg taluk have been identified as Pavitra Hulagur (13 months) and Madhu Umesh Karagundi (14 months), of Bochabal village, and Chetan Pujari (12 months), of Mallapur village.
One child died in the Ramdurg taluk hospital the same day and another after returning home the next day. As the condition of the other two children also worsened, they were referred to Belagavi Institute Of Medical Sciences (BIMS), where one died at the intensive care unit (ICU) on Saturday. The fourth child has since then recovered.
Over the same period, Pfizer, a U.S. pharmaceutical company, tried to launch a new antibiotic drug, Trovan. While Pfizer had tested the drug on adults, it had not yet been tested on children. Additionally, early testing on adults had shown some serious side effects of the drug, including liver problems and cartilage abnormalities.
After learning of the meningitis epidemic, Pfizer decided to use it as an opportunity to test the efficacy of Trovan in pediatric settings. Pfizer set up a site beside the Doctors Without Borders testing area and over two weeks, selected a sample of 200 children between 3 months and 18 years old to participate.
A month later, 11 of the children that had participated were dead. Additionally, numerous parents of children involved in the trials reported disabilities among their children, including paralysis and liver failure.
In December 2000, The Washington Post published a series of exposĂŠs, alleging Pfizerâs fault in the deaths and disabilities of multiple children and accusing Pfizer of conducting unethical experimental trials without attaining informed consent from the participants.
Parents alleged that they had not been informed of the experimental nature of the trials, with many reporting that they thought they were receiving the standard medication issued in the neighboring Doctors Without Borders area. The reporting sparked a series of protests in Muslim states in northern Nigeria in 2001.
Protesters, led by Muslim religious leaders, highlighted the deaths of Muslim children and the fact that the trials had been conducted in a Muslim state as evidence for the claim that Pfizer and its associated âWesternâ institutions were targeting and trying to kill Muslims with vaccines.
Pfizer denied any wrongdoing, stating that the children died of meningitis rather than their drug.
An investigation by a panel of experts hired by the Nigerian government found Pfizer at fault in the childrenâs deaths and guilty of conducting human trials without informed consent.
In subsequent years, several lawsuits were filed against Pfizer by parents and the Kano state government. An out-of-court settlement was reached for, allegedly, $75 million to Kano state and $175,000 to four families of dead children in 2009.
While Pfizer settled out of court for $75 million, how do these costs compare to the costs of reduced child vaccination in the country? Being unvaccinated increases an individualâs risk of infection from disease. The significant costs to treat these illnesses can incur large financial burdens on households. We conduct simple back-of-the-envelope calculations on the potential costs of treatment from an increased number of unvaccinated Muslim children as a result of the negative news about the Pfizer drug trials.
Using our most conservative estimates of direct medical costs of treatment only, and without factoring in any potential deaths from disease, the reduced vaccination of Muslim children in the aftermath of the disclosure of the Pfizer drug trials incurred a total potential cost of treatment of over $94 million over the counterfactual scenario. This cost is more than $19 million higher than the Pfizer settlement to the Nigerian government of $75 million.
MUMBAI: A two-month-old died this week after taking the BCG (Bacille Calmette Guerin) vaccine, given to prevent childhood tuberculosis, TOI has learnt.
The yet-to-be-named infant, the son of Chembur Naka resident Geeta Mane, was administered the BCG vaccine at a health post in Abhudaya Nagar on Tuesday.
���BCG is usually given at birth, but health workers who had gone for a polio immunisation round realised that the child hadn���t taken his BCG and he was subsequently given the shot at the health post,������ said a source, adding that the child died the next day.
Public doctors said it was the first time the infant was being immunised, and that the entire batch of BCG vaccines as well as the diluent in which it is mixed had been seized.
But the vaccine has significant limitations, Feinberg said, and hasnât stopped the disease from being the second-leading cause of death among infectious diseases globally in 2020, following COVID-19.
âThe vaccine surely saved many people's lives, but it is far from an optimal vaccine,â he said. âTB killed half as many people as COVID did in the past year. ⌠It's kind of remarkable how little the world has prioritized the development of a TB vaccine.â
While vaccines typically aim to replicate a natural immune response, there are still unknowns around what an effective natural response to TB is and around the bacteriaâs ability to evade the immune system.
But 90% of people who have evidence of past infection do not develop the disease, suggesting that most can mount an immune response.
Tuberculosis is similar to HIV in that people may develop disease years after infection and researchers donât have âimmunologic guideposts,â making vaccine development a challenge, Feinberg said.
While the BCG vaccine can prevent severe disease in infants, it doesnât protect older people at risk of developing pulmonary tuberculosis, which represents the majority of the disease burden and is responsible for TBâs spread, Feinberg said.
So even though a significant portion of the worldâs population has been immunized with BCG, a high disease burden remains.
The USâs health protection agency has reduced the number of deaths it is attributing to covid-19 by more than 70â000 after what it referred to as âcoding logic errorsâ were highlighted on social media.
On 15 March the Centers for Disease Control and Prevention (CDC) removed 72â277 deaths, including those of 416 children, from its Covid-19 Data Tracker, which has been posting real time data collected from more than two dozen state health departments since April 2020.1 The tracker is one of two sources used to report deaths from covid-19 in the US.
The other is the National Center for Health Statisticsâ website, which is also run by the CDC but relies on death certificates for its data.2 By mid-March the figures presented by the two sites differed substantially. For example, the Covid-19 Data Tracker put the number of deaths among infants and children aged 0-17 at 1700, while the statistics site stated 900.
The figures have been widely used by media outlets to report on deaths in the US. The UKâs Guardian newspaper, for example, carried an article on 11 March with the headline, âOne-third of all US child Covid deaths occurred during Omicron surge.â3 This cited CDC data to say that 550 children had died from covid-19 in the US in 2022, compared with 1017 children in the preceding 22 months.
The Guardian later amended the story using figures from the American Academy of Pediatrics, which put child deaths at 179 during 2022, with 735 deaths in the preceding 20 months.4
The inaccuracies were picked up by Kelley Krohnert, a former IT programmer from Atlanta, Georgia, on 23 February. âHelp needed!!!â she tweeted.5 âIt appears [CDCâs] Data Tracker has major issues when it comes to pediatric death reporting. We deserve accurate data when so much is on the line for our kids!â
Bob Anderson, chief of the mortality statistics branch at the National Center for Health Statistics who also served on covid-19 response task forces, told The BMJ that this was essentially a case of accidentally capturing deaths âwithâ rather than âfromâ covid.
The tracker draws from case reports submitted to local health departments. Any hospital patient with a positive covid result would generate a case reportâeven a patient with a head trauma, for example. If that patient died the date would be noted and the case report checked to see whether the death was caused by covid-19, to screen out such cases.
But the data tracker was capturing any death recorded on these case reports as a covid-19 death. The tracker is based on the National Notifiable Disease Surveillance System, which âwas built mainly to deal with rare diseasesâ such as measles, explained Anderson. âPeople at the state and federal level did their best to pull it together, but the fact is the system wasnât built to handle hundreds of thousands of deaths,â he said.
The CDCâs Estimated Covid-19 Burden page is another source of errors in the 0-17 age bracket. On 1 March, Krohnert pointed to a calculation error in the proportion of estimated child deaths.8 It was listed as 4%, but Krohnert calculated the CDCâs raw numbers in a thread on Twitter as less than 1%. On 4 March the CDC revised the calculation to 0.07%.
Mercury (Hg) is a toxic element that can cause profound damage to the nervous system as was observed following methyl-Hg poisonings in Japan [7] and Iraq [8] and ethyl-Hg poisonings in Iraq [9] and China [10]. It was previously published that most Hg exposure in the US today is characterized as occurring from three primary sources: methyl-Hg in fish, Hg vapor from dental amalgam tooth fillings, and ethyl-Hg in the form of Thimerosal added as a preservative to some vaccines [11]. The potential for low-dose Hg toxicity in adults is a controversial subject and there is little agreement as to whether a threshold dose exists below which no damage is likely to accrue to the central nervous system
This cross-sectional study provides the first epidemiological evidence linking increasing blood ethyl-Hg levels with cognitive decline in older adults and elderly Americans. It is recommended that future longitudinal cohort studies be conducted for consistency with the observations made in the present study and to determine the persistence of cognitive decline symptoms associated with ethyl-Hg exposure in older adults and the elderly.
The main route of human exposure to MeHg is oral ingestion of seafood; for ethylmercury, human exposure is mainly by injection of thimerosal-containing vaccines. Compared with inorganic mercury salts, organic mercury is absorbed more effectively. There are clear differences in the toxicokinetics of oral MeHg and intramuscular injection of ethylmercury as assessed in infant monkeys. After a single acute dose, both organic mercury salts show peak total blood Hg concentration at 48 h, but the half-life (T1/2) of MeHg is âź20 days compared with ethylmercury, which has a T1/2 of âź7 days. This trend was also observed in premature newborns with low birth weights treated with thimerosal-containing vaccines. In the infant monkeys, oral MeHg was three times more likely to enter the brain parenchyma compared with the ethylmercury salt
Mercury exists in nature primarily as elemental mercury or as a sulfide and is found in the earth's crust at approximately 0.5 parts per million. Atmospheric exposures occur from outgassing from rock or through volcanic activity.
Human sources of atmospheric mercury include coal burning [9] and mining (mercury and gold in particular). Atmospheric elemental mercury settles in water, where it is converted by microorganisms into organic (methyl or ethyl) mercury, which is ingested by smaller creatures which are eventually consumed by larger fish. Fish at the top of the food chain (e.g., tuna, swordfish, or shark) may concentrate considerable mercury in their tissues.
Human mercury exposures occur chiefly [7, 8] through inhalation of elemental mercury vapor via occupational or dental amalgam exposure or through ingestion of mercury bonded to organic moieties (methyl, dimethyl, or ethyl mercury), primarily from seafood.
Most human metallic mercury exposure comes from mercury vapor outgassing from amalgam fillings, at a rate of 2 to 28 micrograms per facet surface per day, of which about 80% is absorbed, according to the World Health Organization [7, 8] and Berglund et al. [10].
A less common source of mercury vapor is spilled mercury [11], and there is a report in the literature of Idiopathic Thrombocytopenic Purpura [12] caused by vacuuming spilled mercury (thereby producing a major acute exposure to mercury vapor).
Mercury toxicity is not often included in the differential diagnosis of common subjective complaints such as fatigue, anxiety, depression, odd paresthesias, weight loss, memory loss, and difficulty concentrating, but these are the symptoms of low-grade chronic mercury exposure described by the investigators cited previously.
Given the ability of the various forms of mercury to deposit in most parts of the human body, the range of symptoms potentially caused by mercury is quite large. Animal studies linking mercury toxicity to neurodegenerative diseases [117, 118] raise clinical concern, as do a series of associations between mercury and neurodegenerative diseases in humans [119â123].
Mercury exposure is not insignificant according to WHO, as cited previously, and the NHANES reports suggest widespread exposure in the United States, especially among women [124, 125]. Diagnosis of mercury overload is difficult.
The commonly used modalities (blood, urine, and/or hair levels) do not correlate with total body burden and offer little diagnostically useful information.
Provocation with DMPS appears to offer a more accurate assessment of body burden. Since provocation is safe and inexpensive, indications for provocation must rest on clinical grounds: does the patient have multiple, vague symptoms similar to those described in the mercury literature, without other plausible, and potentially reversible, explanation?
Is there a significant history of mercury exposure: multiple amalgam fillings, high seafood intake, and history of multiple thimerosal-containing vaccinations or significant occupational exposures? Is there a family history of Alzheimer's, Parkinson's, or other diseases with postulated links to mercury exposure? Is there a history of known glutathione transferase (GST) polymorphisms, which decrease the body's ability to clear heavy metals like mercury?
originally posted by: thethinkingman
Mercury (Hg) is a toxic element that can cause profound damage to the nervous system as was observed following methyl-Hg poisonings in Japan [7] and Iraq [8] and ethyl-Hg poisonings in Iraq [9] and China [10]. It was previously published that most Hg exposure in the US today is characterized as occurring from three primary sources: methyl-Hg in fish, Hg vapor from dental amalgam tooth fillings, and ethyl-Hg in the form of Thimerosal added as a preservative to some vaccines [11]. The potential for low-dose Hg toxicity in adults is a controversial subject and there is little agreement as to whether a threshold dose exists below which no damage is likely to accrue to the central nervous system
This cross-sectional study provides the first epidemiological evidence linking increasing blood ethyl-Hg levels with cognitive decline in older adults and elderly Americans. It is recommended that future longitudinal cohort studies be conducted for consistency with the observations made in the present study and to determine the persistence of cognitive decline symptoms associated with ethyl-Hg exposure in older adults and the elderly.
ohhhh
But apparently ...mercury is fine to inject into people. One of the most toxic substances there is....but when we use it magically its fine because it would be real bad if it wasnt right??? so thats why its fine because that makes you feel better
The main route of human exposure to MeHg is oral ingestion of seafood; for ethylmercury, human exposure is mainly by injection of thimerosal-containing vaccines. Compared with inorganic mercury salts, organic mercury is absorbed more effectively. There are clear differences in the toxicokinetics of oral MeHg and intramuscular injection of ethylmercury as assessed in infant monkeys. After a single acute dose, both organic mercury salts show peak total blood Hg concentration at 48 h, but the half-life (T1/2) of MeHg is âź20 days compared with ethylmercury, which has a T1/2 of âź7 days. This trend was also observed in premature newborns with low birth weights treated with thimerosal-containing vaccines. In the infant monkeys, oral MeHg was three times more likely to enter the brain parenchyma compared with the ethylmercury salt
dumb
Literally somehow trying to claim its better ...because its not AS toxic.......its still #ing toxic!!???
Yeah injecting new borns with several doses of mercury, viruses and aluminum directly into their arms is a magical idea..........
originally posted by: thethinkingman
Mercury exists in nature primarily as elemental mercury or as a sulfide and is found in the earth's crust at approximately 0.5 parts per million. Atmospheric exposures occur from outgassing from rock or through volcanic activity.
Human sources of atmospheric mercury include coal burning [9] and mining (mercury and gold in particular). Atmospheric elemental mercury settles in water, where it is converted by microorganisms into organic (methyl or ethyl) mercury, which is ingested by smaller creatures which are eventually consumed by larger fish. Fish at the top of the food chain (e.g., tuna, swordfish, or shark) may concentrate considerable mercury in their tissues.
Human mercury exposures occur chiefly [7, 8] through inhalation of elemental mercury vapor via occupational or dental amalgam exposure or through ingestion of mercury bonded to organic moieties (methyl, dimethyl, or ethyl mercury), primarily from seafood.
Most human metallic mercury exposure comes from mercury vapor outgassing from amalgam fillings, at a rate of 2 to 28 micrograms per facet surface per day, of which about 80% is absorbed, according to the World Health Organization [7, 8] and Berglund et al. [10].
A less common source of mercury vapor is spilled mercury [11], and there is a report in the literature of Idiopathic Thrombocytopenic Purpura [12] caused by vacuuming spilled mercury (thereby producing a major acute exposure to mercury vapor).
Mercury toxicity is not often included in the differential diagnosis of common subjective complaints such as fatigue, anxiety, depression, odd paresthesias, weight loss, memory loss, and difficulty concentrating, but these are the symptoms of low-grade chronic mercury exposure described by the investigators cited previously.
Given the ability of the various forms of mercury to deposit in most parts of the human body, the range of symptoms potentially caused by mercury is quite large. Animal studies linking mercury toxicity to neurodegenerative diseases [117, 118] raise clinical concern, as do a series of associations between mercury and neurodegenerative diseases in humans [119â123].
Mercury exposure is not insignificant according to WHO, as cited previously, and the NHANES reports suggest widespread exposure in the United States, especially among women [124, 125]. Diagnosis of mercury overload is difficult.
The commonly used modalities (blood, urine, and/or hair levels) do not correlate with total body burden and offer little diagnostically useful information.
Provocation with DMPS appears to offer a more accurate assessment of body burden. Since provocation is safe and inexpensive, indications for provocation must rest on clinical grounds: does the patient have multiple, vague symptoms similar to those described in the mercury literature, without other plausible, and potentially reversible, explanation?
Is there a significant history of mercury exposure: multiple amalgam fillings, high seafood intake, and history of multiple thimerosal-containing vaccinations or significant occupational exposures? Is there a family history of Alzheimer's, Parkinson's, or other diseases with postulated links to mercury exposure? Is there a history of known glutathione transferase (GST) polymorphisms, which decrease the body's ability to clear heavy metals like mercury?
ohhhh
They know alot of # harms people but do they give a f-u-c-k????
originally posted by: AaarghZombies
a reply to: Ksihkehe
irrefutable evidence and simple logic that proves kids will be hurt and killed for no benefit
Can you find a single identifiable child, who has been proved to exist pre covid, who actually died of the vax?
And I don't mean some friend of a friend who you won't name, an actual verifiable person with a name and a face and parents screaming and shouting about how the vax killed their child.