They’ve known since 2005 how to screen children for vulnerability to some types of vaccine-caused autism before injecting them, but they’re not doing it. ( http://www.phschool.com/science/science_news/articles/blood_hints_autism.html ) Can you guess why? Even if our satanic overlords weren’t eugenicists (this is naked eugenics whether you choose to believe that it’s deliberate or not), the medical establishment isn’t about to lose all respectability and face legal liability for what they’ve already done to thousands of children and their families. Medicine is up to its ears in similar conflicts of interest, not just about vaccines, but also about circumcision and obstetrical abuse, and their profitable offshoot: psychiatry: http://thoughtcrimeradio.net/2011/04/burstow-on-shock-as-violence-against-women/ http://thoughtcrimeradio.net/2014/06/cia-mind-control-project-financed-circumcision-psychological-research/ http://thoughtcrimeradio.net/2017/03/obstetrical-abuse-circumcision-and-psychiatry-a-profitable-collaboration/ https://web.archive.org/web/20010607215244/http://www.stopshrinks.org/winkel/2nader080100.htm
“Notably, only 2% of children with ASD (autism spectrum disorder) in our study presented without at least one polymorphism in the MTHFR gene.”— Association of MTHFR Gene Variantswith Autism, Journal of American Physicians and Surgeons Volume 9 Number 4 Winter 2004
Increased Risk of Noninfluenza Respiratory Virus Infections Associated With Receipt of Inactivated Influenza Vaccine
We randomized 115 children to trivalent inactivated influenza vaccine (TIV) or placebo. Over the following 9 months, TIV recipients had an increased risk of virologically-confirmed non-influenza infections (relative risk: 4.40; 95% confidence interval: 1.31-14.8). Being protected against influenza, TIV recipients may lack temporary non-specific immunity that protected against other respiratory viruses. …
There was no statistically significant difference in the risk of confirmed seasonal influenza infection between recipients of TIV or placebo, although the point estimate was consistent with protection in TIV recipients (relative risk [RR], 0.66; 95% confidence interval [CI], .13–3.27). TIV recipients had significantly lower risk of seasonal influenza infection based on serologic evidence (Supplementary Appendix). However, participants who received TIV had higher risk of ARI (acute respiratory infection) associated with confirmed noninfluenza respiratory virus infection (RR, 4.40; 95% CI, 1.31–14.8). Including 2 additional confirmed infections when participants did not report ARI, TIV recipients had higher risk of confirmed noninfluenza respiratory virus infection (RR, 3.46; 95% CI, 1.19–10.1). The majority of the noninfluenza respiratory virus detections were rhinoviruses and coxsackie/echoviruses, and the increased risk among TIV recipients was also statistically significant for these viruses (Table 3). Most respiratory virus detections occurred in March 2009, shortly after a period of peak seasonal influenza activity in February 2009 (Figure 1)….
This child is being dissociated with trauma for the purpose of making him a slave, MK-Ultra style. The colored flashing lights and weird vocal changes indicates the child has probably been given an hallucinogenic drug. The programmer might be Podesta. For more on the political uses of child abuse, pedophilia and blackmail for political control, see http://thoughtcrimeradio.net/2015/05/interview-with-mind-control-victim-used-to-blackmail-politicians-as-a-child/ and http://thoughtcrimeradio.net/2014/12/franklin-coverup-the-white-house-call-boy-ring/
Dear Bloggers: Thousands of published studies you cite and praise are wrong, useless, irrelevant, deceptive—and the medical journals know it, and they’re doing nothing useful about it.
The issue? Cell lines. These cells are crucial for lab research on the toxicity of medical drugs, and the production of proteins. Knowing exactly which cell lines are being studied is absolutely necessary.
And therein lies the gigantic problem.
Statnews.com has the bombshell story (July 21, 2016):
“Recent estimates suggest that between 20 percent and 36 percent of cell lines scientists use are contaminated or misidentified — passing off as human tissue cells that in fact come from pigs, rats, or mice, or in which the desired human cell is tainted with unknown others. But despite knowing about the issue for at least 35 years, the vast majority of journals have yet to put any kind of disclaimer on the thousands of studies affected.”
“One cell line involved are the so-called HeLa cells. These cancerous cervical cells — named for Henrietta Lacks, from whom they were first cultured in the early 1950s — are ubiquitous in labs, proliferate wildly — and, it turns out, contaminate all manner of cells with which they come into contact. Two other lines in particular, HEp-2 and INT 407, are now known to have been contaminated with HeLa cells, meaning scientists who thought they were working on HEp-2 and INT 407 were in fact likely experimenting on HeLa cells.”
“Christopher Korch, a geneticist at the University of Colorado, has studied the issue. According to Korch, nearly 5,800 articles in 1,182 journals may have confused HeLa for HEp-2; another 1,336 articles in 271 journals may have mixed up HeLa with INT 407. Together, the 7,000-plus papers have been cited roughly 214,000 times, Science reported last year.”
“And that’s just two cell lines. All told, more than 400 cell lines either lack evidence of origin or have become cross-contaminated with human or other animal cells at some point in their laboratory lineage. Cell lines are often chosen for their ability to reproduce and be bred for long periods of time, so they’re hardy buggers that can move around a lab if they end up on a researcher’s gloves, for example. ‘It’s astonishingly easy for cell lines to become contaminated,’ wrote Amanda Capes-Davis, chair of the International Cell Line Authentication Committee, in a guest post for Retraction Watch. ‘When cells are first placed into culture, they usually pass through a period of time when there is little or no growth, before a cell line emerges. A single cell introduced from elsewhere during that time can outgrow the original culture without anyone being aware of the change in identity’.” …