COVID-19 Shots Linked To Autism In Vaccinated Rats: Study

A study from Turkey discovered that female rats injected with mRNA COVID-19 vaccines gave birth to offspring exhibiting symptoms of autism and lower neuronal counts in the brain.

The peer-reviewed study, published in the Neurochemical Research journal on Jan. 10, examined the links between COVID-19 mRNA vaccines and neurodevelopmental disorders, with a focus on autism. It analyzed the offspring of pregnant rats injected with Pfizer’s mRNA COVID-19 vaccines during gestation. Researchers found that the vaccines had a “profound impact on key neurodevelopmental pathways,” with the male offspring exhibiting “pronounced autism-like behaviors, characterized by a marked reduction in social interaction and repetitive patterns of behavior.”

“Furthermore, there was a substantial decrease in neuronal counts in critical brain regions, indicating potential neurodegeneration or altered neurodevelopment. Male rats also demonstrated impaired motor performance, evidenced by reduced coordination and agility.”

In the study, female rats were randomly assigned into two groups. Those in Group 1 received an intramuscular saline injection on the thirteenth day of gestation, while rats in Group 2 received Pfizer shots on the same day. There were seven female rats in Group 1 and eight in Group 2, totaling 15 rats.

A total of 41 offspring were born—20 among the saline group and 21 among the vaccinated. The offspring were subjected to multiple behavioral tests 50 days after their birth, with researchers noting down their performances:

  • Open Field Test, which tested for general locomotor activity and anxiety.
  • Novelty-Induced Rearing Behavior, which evaluated the offspring for their exploratory behaviors.
  • Three-chamber Sociability and Social Novelty Test, which assessed the offspring’s sociability.
  • Rotarod Test, which analyzed the offspring’s motor skills and endurance.

Researchers found a “significant difference” between males and females in the vaccine group in terms of motor coordination and balance, with the male offspring exhibiting “more pronounced” impaired abilities.

However, no such sex-based differences in motor coordination and balance were observed in the offspring born from rats administered with saline.

In sociability tests, the male offspring in the vaccine group were seen spending “significantly less time” with rats who were strangers to them compared to the male offspring of the saline group.

This difference did not exist when comparing the vaccine group’s female offspring with the saline group’s female offspring.

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Doctor is stripped of his medical license after selling bogus $15,000 fecal transplants he claimed could treat AUTISM in toddlers

A Canadian doctor has been stripped of his medical licence after conning families out of thousands of dollars for bogus autism cures.

Charlatan Jason Klop charged $15,000 for fecal transplants which involved taking bacteria from the poop of healthy patients and transferring them to autistic children as young as two.

He claimed the treatment – carried out either with pills or enemas – caused ‘dramatic improvements’ in autism symptoms and offered them at clinics in MexicoHungary, Australia and Panama.

Klop admitted that his business violated multiple Health Canada rules as well as those standards set by the College of Naturopathic Physicians and will pay a meager $7,500 fine.

A notice by the College of Naturopathic Physicians of British Columbia said Klop was removed from the institution on Wednesday. He will have the right to apply for reinstatement in five years.

As well as admitting to promoting and selling fecal transplants that are not approved for autism, he admitted making ‘unverifiable statements’ in his advertising.

He has claimed to have seen ‘dramatic improvements’ in autism symptoms of young children he has treated at his clinics in Mexico, Hungary, Australia and Panama, for a measly $15,000. 

Klop also claimed to have met donor screening requirements from the Food and Drug Administration and American Gastroenterology Association. But it was later revealed that his lab had no protocols for screening donors or analyzing product, and disposed of fecal waste with household garbage.

Court documents reveal that he had ‘treated’ at least 60 children in this way.  

Fecal transplants are only approved in Canada and the US for the treatment of C.diff – a nasty and recurrent stomach infection. 

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Drinking Tap Water Containing Lithium While Pregnant Could Raise Autism Risk For Children

Pregnant women who drink tap water containing high levels of lithium are more likely to have children with autism, a new study warns. Researchers analyzed data from Denmark and found that mothers-to-be drinking water with the highest lithium levels were almost 50 percent more likely to have autistic children.

The team from UCLA found that the higher the lithium levels in the water supply, the more likely women were to give birth to babies with autism. Study authors warn that lithium levels in water could become more widespread in the near future due to lithium battery use and disposal in landfills — which could lead to an increase in developmental disabilities such as autism.

Researchers say this is one of the first ever studies to identify naturally-occurring lithium in water as a potential risk factor for autism. The team studied data collected from Denmark over 16 years, between 1997 and 2013. They chose to use the Danish data due to the country having the lowest consumption of bottled water in Europe, meaning most of the population drinks tap water.

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Virginia Teacher Reveals The Left’s Next Public School Quest: Convincing Autistic Kids They’re Trans

During a county school board meeting in Arlington, Virginia, on Oct. 13, Carly Hughes, a teacher in Long Branch Elementary School’s Multi-Intervention Program for Students with Autism (MIPA), spoke against Virginia Gov. Glenn Youngkin’s proposed public school policies for transgender-identifying students. Her reason? She believes her autistic students “may experience gender queerness more than other students.”

“I did my master’s study in queer inclusion in public schools,” Hughes told the school board. “My study told me that including trans students in all spaces is best practice. It also told me there are trans kids of every age — one I actually worked with in my student teaching. He was in the third grade.” 

Youngkin’s model policies specify that taxpayer-funded public schools cannot facilitate a child’s so-called “transition” without written consent from a parent. Additionally, the guidance prescribes that bathroom and locker room access and sports participation should be based strictly on a student’s sex. These policies are a reversal of previous guidance from former Democratic Gov. Ralph Northam, which asked schools to hide a student’s “gender identity” from his or her parents. 

Hughes herself identifies as a “queer” special education teacher. “I found that autistic students, the population I work with, may experience gender queerness more than other students,” she said. “These students … have helped me learn so much about myself as well.” 

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One in 44 U.S. children diagnosed with autism, new data suggests

New autism numbers released Thursday suggest more U.S. children are being diagnosed with the developmental condition and at younger ages.

In an analysis of 2018 data from nearly a dozen states, researchers at the Centers for Disease Control and Prevention found that among 8-year-olds, 1 in 44 had been diagnosed with autism. That rate compares with 1 in 54 identified with autism in 2016.

U.S. autism numbers have been on the rise for several years, but experts believe that reflects more awareness and wider availability of services to treat the condition rather than a true increase in the number of affected children.

A separate CDC report released Thursday said that children were 50 percent more likely to be diagnosed with autism by age 4 in 2018 than in 2014.

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CDC senior scientist: ‘We trashed data showing vaccine-autism link in African-American boys’

Here is the full statement by current CDC Senior Scientist on Vaccine-Autism questions: Dr. William Thompson. Stay tuned to this website for an update on the story, soon.

I regret that my [CDC] coauthors and I omitted statistically significant information in our 2004 article published in the Journal of Pediatrics.

My primary job duties while working in the immunization safety branch from 2000 to 2006 were to lead or colead three major vaccine safety studies. The MADDSP MMR-Autism Cases 
Control Study was being carried out in response to the Wakefield Lancet study that suggested an association between the MMR vaccine and an autism-like health outcome.
There were several major concerns among scientists and consumer advocates outside the CDC in the fall of 2000 regarding the execution of the Verstraeten study.

One of the important goals that was determined upfront in the spring of 2001 before any of these studies started was to have all three protocols vetted outside the CDC prior to the start of the analyses so that consumer advocates could not claim that we were presenting analyses that suited our own goals and biases.
       
We hypothesized that if we found statistically significant effects at either 18- or 36-month thresholds, we would conclude that vaccinating children early with MMR vaccine could lead to autism-like characteristics or features.
       
We all met and finalized the study protocol and analysis plan. The goal was to not deviate from the analysis plan to avoid the debacle that occurred with the Verstraeten Thimerosal study published in Pediatrics in 2003.
       
At the September 5 meeting, we discussed in detail how to code race for both the sample and the birth certificate sample. At the bottom of table 7, it also shows that for the 
nonbirth certificate sample, the adjusted race effect statistical significance was huge.
       
All the authors and I met and decided sometime between August and September 2002 not to report any race effects for the paper. Sometime soon after the meeting, where we decided to exclude reporting any race effects, the coauthors scheduled a meeting to destroy documents related to the study.

The remaining four coauthors all met and brought a big garbage can into the meeting room and reviewed and went through all the hard copy documents that we had thought we should discard and put them in a huge garbage can.
       
However, because I assumed it was illegal and would violate both FOIA and DOJ requests, I kept hard copies of all documents in my office, and I retained all associated computer files.

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Immunoexcitotoxicity as the central mechanism of etiopathology and treatment of autism spectrum disorders: A possible role of fluoride and aluminum

Our review suggests that most autism spectrum disorder (ASD) risk factors are connected, either directly or indirectly, to immunoexcitotoxicity. Chronic brain inflammation is known to enhance the sensitivity of glutamate receptors and interfere with glutamate removal from the extraneuronal space, where it can trigger excitotoxicity over a prolonged period. Neuroscience studies have clearly shown that sequential systemic immune stimulation can activate the brain’s immune system, microglia, and astrocytes, and that with initial immune stimulation, there occurs CNS microglial priming. Children are exposed to such sequential immune stimulation via a growing number of environmental excitotoxins, vaccines, and persistent viral infections. We demonstrate that fluoride and aluminum (Al3+) can exacerbate the pathological problems by worsening excitotoxicity and inflammation. While Al3+ appears among the key suspicious factors of ASD, fluoride is rarely recognized as a causative culprit. A long-term burden of these ubiquitous toxins has several health effects with a striking resemblance to the symptoms of ASD. In addition, their synergistic action in molecules of aluminofluoride complexes can affect cell signaling, neurodevelopment, and CNS functions at several times lower concentrations than either Al3+ or fluoride acting alone. Our review opens the door to a number of new treatment modes that naturally reduce excitotoxicity and microglial priming.

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