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TRIM, COUNTY MEATH — Nine elderly residents are dead after a severe post-“vaccine” COVID-19 outbreak.
Eligible staff and residents received their first doses of mRNA on January 12 and 13, according to the Irish Times. It was either Pfizer or Moderna mRNA shots as those were the only two with emergency use authorization at the time. At least half of the 50 residents tested positive for COVID-19 by January 20.
Feber och huvudvärk är fortfarande de vanligaste biverkningarna av covidvacciner, men forskare noterar att allt fler patienter drabbas av nervskador som bland annat uttrycker sig i form av yrsel eller ansiktsförlamningar efter att de tagit Pfizers och Modernas kontroversiella mRNA-vaccin.
(NaturalHealth365) On February 26, 2021, the pharmaceutical company and COVID vaccine maker Johnson and Johnson (of Janssen Biotech, Inc.) held an advisory committee briefing with their sponsors. In the briefing (page 34), they outlined their plans to test their investigational viral vector vaccine, Ad26.COV2.S, in an upcoming cohort of participants.
(Natural News) Johnson & Johnson’s (J&J) rushed-to-market Wuhan coronavirus (COVID-19) vaccine was recently granted emergency use authorization (EUA) from the U.S. Food and Drug Administration (FDA), which means there is now a third Big Pharma contender vying for a piece of the Chinese virus fear pie. Not everyone is excited about the new jab, though, including the U.S. Conference of Catholic Bishops (USCCB)
The flaws of vaccine trials in general are really highlighted by current COVID-19 vaccine studies, one of the most egregious ones being the fact that vaccine makers rarely use inert placebos (such as a saline shot), which is the gold standard for drug trials.
As noted in a January 25, 2021, article in The Defender,1 vaccine developers typically assess the safety of a new vaccine against another vaccine, and by so doing, they effectively hide side effects as most vaccines have side effects and risks.
(NaturalHealth365) On a webpage about vaccine safety, the U.S. Centers for Disease Control and Prevention (CDC) states that while “clinical trials provide important information on vaccine safety, the data are somewhat limited because of the relatively small number (hundreds to thousands) of study participants. Rare side effects and delayed reactions might not be evident until the vaccine is administered to millions of people.” (Emphasis ours.)