MB Comment: There is a constant media barrage of stories urging everyone to get vaccinated against pertussis (whooping cough). Every such story castigates those who refuse the vaccine as endangering themselves and society by not vaccinating.
I previously ran an article discrediting that argument. The pertussis vaccine by definition is not bactericidal — it does not kill bacteria. Therefore, vaccinated individuals can carry and transmit pertussis bacteria just the same as the unvaccinated. Public health officials either don’t know this or are being dishonest when they blame minor pertussis outbreaks on the unvaccinated. They could be carrying the germ themselves and personally transmitting it to the reporter when they plant these pseudo-scientific stories.
What else are they not telling you? I took a close look at the Sanofi Pasteur DTaP vaccine (Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed) which is licensed by the FDA as the primary series in infants and children.
I was astonished to discover that Autism and Sudden Infant Death Syndrome (SIDS) are listed as ‘adverse events reported during post-approval use.’ ‘Events were included in this list because of the seriousness or frequency of reporting.’
The CDC, the FDA, Paul Offit and every public health flunky swear up and down the aisle that vaccines are perfectly safe and don’t cause autism or SIDS. Yet those conditions are listed on the DTaP package insert with the statement that they are included because such vaccine adverse reactions are serious and frequent.
At the same time the vaccine establishment is making a full court press with news stories everywhere to convince the public that vaccines are totally safe and it is our moral obligation to accept them, you find this evidence of harm. The defenders of vaccines are so far down the road of denial and dishonesty that they are incapable or unwilling to acknowledge the fact prominently displayed on the DTaP package insert: Autism and sudden infant death are associated with vaccination. This is a powerful indictment of the CDC, vaccine manufacturers and medical talking heads like Offit.
The DTaP package warning insert also includes these serious reported adverse events: convulsion/grand mal convulsion, encephalopathy and neuropathy. The Refusers Newsroom contains many articles on these subjects and my chapter in Vaccine Epidemic starts with the Merck Manual medical textbook definition of a vaccine adverse reaction – encephalitis. It is therefore no surprise that neurological damage is listed on the package insert. Anyone who takes the time to read FDA Vaccine Adverse Event Reporting System (VAERS) reports will find numerous rapid-onset cases of encephalitis, convulsions and sudden infant death. That is why those events are on the package insert, because they are happening.
In conclusion – the DTaP package insert reads like a cigarette package warning: Caution! This product can kill you or cause neurological damage. Thanks for the warning and as the American Medical Association (AMA) position on informed consent states: patients ‘can make an informed decision to proceed or to refuse a particular course of medical intervention.’ I will follow the AMA position on informed consent and refuse this vaccine.
Package Insert From FDA
‘Adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea. Events were included in this list because of the seriousness or frequency of reporting.’