Category Archives: Propaganda Room
STUDY SHOWS: 6X more shedding and spreading of flu from the vaccinated
6.3 (95% CI 1.9–21.5) times more aerosol shedding among cases with vaccination in the current and previous season compared with having no vaccination in those two seasons.
The latest addition to this growing body of literature is found in a newly published article titled, “Infectious Virus Exhaled In Breath Of Symptomatic Seasonal Flu Cases,” published in PNAS (Proceedings of the National Academy of Science).
The study found that flu carriers exhale significant quantities of infectious influenza virus, and that counter intuitively, sneezing is rare and not important for influenza virus aerosolization; nor is coughing required to transmit these particles. Simply breathing will do. Additionally, the study found that males shed influenza viruses in greater quantity than females through fine aerosols, and women cough more frequently. READ MORE..
“#WeWontRest…VACCINE TWITTER WAR with Big Pharma
Join us: Start Twittering with images: To post a photo or GIF in a Tweet. Type your Tweet into the box at the top of your Home timeline, or click the Tweet button. … Once a photo or GIF is selected, the image will attach to your Tweet in full size. You can select up to 4 photos to Tweet at once.
The Pledge Wall: Read about the pledges the vaccine industry experts have made to help make the world a healthier place for everyone:

#WEWONTREST
Either create your own or use the attached JPEGs and stay with the same MEME and #WeWONTREST “vaccine destroy lives”. If you want to start another hashtag concomitant with WEWONTREST, the you might use #WeWillNotRest “vaccines destroy lives”. This additional hashtag may confuse the vaccine apologists and they will be hashtaging to the wrong place.
VACCINE INJURED BARBIE
Busted!!!
BITCOIN EXPLAINED (must watch…whoa)
Physicians’ perks for vaccinating children
Blue Cross, Blue Shield, Blue Care Network of Michigan publishes online a shameless and bold report of how much cash they reward physicians for performing certain tests, and which apparently acts as an incentive to over-prescribe, thus inflating the costs of U.S. healthcare, which should be illegal. If MDs meet a target of 63% of eligible member patients, they will receive a payout of $400 per completed eligible member. Wow! Now you know one of the key reasons why parents are hounded to vaccinate their infants and toddlers.
Vaccine Panel: Paul Offit, Arthur Caplan-“We must lie to the people”
Sesame Street (ELMO) SURGEON GENERAL FIRED BY TRUMP
TRUMP YANKS DR. MURTHY, SURGEON GENERAL
READ MORE…
The Federal Trade Commission’s STATUTORY AUTHORITY
The Commission’s basic authority to regulate advertising and marketing practices derives from Section 5 of the FTC Act, which broadly prohibits unfair or deceptive acts or practices in commerce. The Commission “will find deception if there is a representation, omission or practice that is likely to mislead the consumer acting reasonably in the circumstances, to the consumer’s detriment.” The elements to this analysis are:
(1) the representation, omission, or practice must be likely to mislead the consumer
(2) the act or practice must be considered from the perspective of the reasonable consumer
(3) the representation, omission, or practice must be material, that is, likely to affect a consumer’s choice or conduct, thereby leading to injury
(4) When a representation or sales practice is targeted to a specific audience, such as children, the Commission will determine the effect on a reasonable member of that group.
(5) Thus, advertisements directed to children are considered from the standpoint of an ordinary child.
The U.S. Food and Drug Administration
“…in connection with consumer-directed broadcast advertisements for prescription drug and biological products. The approach presumes that such advertisements:
Are not false or misleading in any respect
Present a fair balance between information about effectiveness and information about risk
Include a thorough major statement conveying all of the product’s most important risk information in consumer-friendly language
Communicate all information relevant to the product’s indication (including limitations to use) in consumer-friendly language.
Children’s Advertising Review Unit (CARU)
CARU’s Self-Regulatory Guidelines are deliberately subjective, going beyond the issues of truthfulness and accuracy to take into account the uniquely impressionable and vulnerable child audience.
The Guidelines are based upon the following core principles:
Advertisers have special responsibilities when advertising to children or collecting data from children online. They should take into account the limited knowledge, experience, sophistication and maturity of the audience to which the message is directed. They should recognize that younger children have a limited capacity to evaluate the credibility of information, may not understand the persuasive intent of advertising, and may not even understand that they are being subject to advertising.
Advertising should be neither deceptive nor unfair, as these terms are applied under the Federal Trade Commission Act, to the children to whom it is directed.
Advertisers should have adequate substantiation for objective advertising claims, as those claims are reasonably interpreted by the children to whom they are directed.
Advertising should not stimulate children’s unreasonable expectations about product quality or performance.
Products and content inappropriate for children should not be advertised directly to them. Advertisers should avoid social stereotyping.
New Report: PATIENT ADVOCACY GROUPS-BIG PHARMA SCAM!

Money and pills in medicine bottle
New Report Exposes “Patient Advocacy” Groups as a Big Pharma Scam
A new study shows that nearly all of these patient advocacy groups are captured by the drug industry.
David Hilzenrath at the Project on Government Oversight (POGO) reports that at least 39 of 42 patient advocacy groups who participated in discussions with the FDA over agency review processes for prescription drugs received funding from pharmaceutical companies. And at least 15 have representatives of drug or biotechnology companies on their governing boards.
The study is particularly notable now because Congress is poised to pass the 21st Century Cures Act, which trades temporary additional funding for the National Institutes of Health and the FDA for permanent weakening of the FDA’s approval process. Over 1,400 lobbyists have been working on this bill, which would be a major financial boon to the drug and medical device industries.
Patient advocacy groups have factored heavily into the lobbying effort. According to an analysis from research group Avalere in December 2014, 43 percent of public comments on the House version of the bill were from patient advocacy groups. READ MORE…