April 25, 2012 2 Comments
In a predictable reaction to American Airlines’ sound decision to pull her misinformation on vaccination, Meryl Dorey has launched her own petition.
The unsigned petition takes the reader on a journey of unfounded accusation and a synopsis of the original interview. It again makes the same striking distortions of truth managing to claim Ms. Dorey cites “peer-reviewed research”, when in fact she cites Wakefield’s officially retracted and fraudulent paper.
“Pharmaceutically funded organisations” have “blackmailed” American Airlines it claims. More so, removal of of the potentially lethal scheme is “un-American” and “a direct contravention to the First Amendment of the United States Constitution”.
Indeed the petition is actually worse than the interview, arguing that not only is the disproved link between vaccines and autism “verified” in the medical literature, but that vaccination:
… has contributed to a rate of autism in the United States that has increased from 1:10,000 20 years ago to 1:88 today
All that needs be stressed on this is that no peer reviewed literature supports this nonsense. Respected autism organisations across the globe agree the change in diagnostic frequency is just that – a change in diagnostic frequency. This is due to changing criteria and other factors increasing the likelihood of diagnosis. Which is vastly different to an increase in the incidence of autism as it was defined two decades ago.
Those scammed this way are playing Russian Roulette with measles according to a mother who didn’t vaccinate her son due to Wakefield’s fraud. The New Zealand Herald reported today on one person’s “informed decision”:
The theory [MMR linked to autism] was eventually retracted in 2010 and Wakefield was struck off the medical register, but not before triggering a worldwide health scare around the MMR vaccine.
Said Mrs Edwards-Lasenby: “It was one of those things where I had made the informed decision at the time not to do the MMR vaccine, with the information I had available to me. But where I went wrong was not going back to revisit that information and the advice available as time went on.”
She urged parents to reconsider immunisation, particularly if advice changes, to avoid playing “Russian roulette” with children’s lives.
It will take her son 12 months to fully recover from measles. He lost 7kg after not eating for 2 weeks, was on oxygen in isolation “fighting for his life” in hospital and even when well enough to return to school:
“Then he just caught anything,” Mrs Edwards-Lasenby said. “Any little scratch he had became an infection and he was constantly on antibiotics.”
Meryl Dorey is leading parents and innocent children toward this very suffering and potentially worse. Her proposed interview includes an entirely manufactured claim suggesting that measles vaccination is ineffective. If you’re wondering what our health regulators and authorities are doing you’re not alone.
The misguided line about new pertussis genomes was dealt with two posts ago, exposing Ms. Dorey’s intentional untruth about vaccine efficacy and infant fatality. Listen to your doctor – not Meryl Dorey.
Yet, the “trial myths” used by antivaxxers deserves noting. Whilst it’s thunderous hypocrisy for those who promote homeopathy, chiropractic treatment of disease and cancer “cures” to bemoan a lack of “the gold standard” in scientific testing (RCT), we also find more misinformation.
Firstly it is quite untrue that vaccines are not tested against a true placebo. Safety trials involve comparison to saline. Yet antivaxxers ignore this and attack efficacy trials as not being “placebo controlled”. These trials compare vaccine components minus the agent/s responsible for the immune response (in one sample), to the full vaccine (in another sample). Such trials are absolutely crucial to delineate a true immune response from other possible responses. This complaint is void and invalid.
Next is the rather amusing insistence of the need to test the overall health of the fully unvaccinated against the fully vaccinated. Exactly how we separate the former sample from protection, and thus good health, afforded by herd immunity and still preserve the integrity of this study has never quite been explained.
More so, how do we correct for fatalities from vaccine preventable disease in the unvaccinated who are no longer alive? If the notion is to begin studies at birth I am sure no ethics committee would pass such an absurdity. This is clear if we consider restrictions on Isaac Golden’s so-called “PhD in homeopathic immunisation”. He writes in the abstract:
The effectiveness of the program could not be established with statistical certainty given the limited sample size and the low probability of acquiring an infectious disease… Further research to confirm the effectiveness of the program is justified.
Of course the subtle suggestion is that vaccinated individuals will be of inferior health due to complications from the frogs and snails and puppy dog tails that wicked vaccines contain. I would suggest that as we’re witnessing the re-emergence of diseases and the fatality they cause as a consequence of lower immunisation levels that the long term and large scale outcome of this hypothetical trial is blindingly obvious.
Next is the complaint that pharmaceutical companies conduct trials and licence vaccines “with no independent oversight on the part of government regulators”. This is also entirely false. Good Manufacturing Practice is moderated by governments and the WHO. In relation to vaccines the WHO state [bold mine]:
WHO defines Good Manufacturing Practices (GMP) as “that part of quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization”. GMP covers all aspects of the manufacturing process: defined manufacturing process; validated critical manufacturing steps; suitable premises, storage, transport; qualified and trained production and quality control personnel; adequate laboratory facilities; approved written procedures and instructions; records to show all steps of defined procedures taken; full traceability of a product through batch processing records and distribution records; and systems for recall and investigation of complaints.
The guiding principle of GMP is that quality is built into a product, and not just tested into a finished product. Therefore, the assurance is that the product not only meets the final specifications, but that it has been made by the same procedures under the same conditions each and every time it is made. There are many ways this is controlled – controlling the quality of the facility and its systems, controlling the quality of the starting materials, controlling the quality of production at all stages, controlling the quality of the testing of the product, controlling the identity of materials by adequate labelling and segregation, controlling the quality of materials and product by adequate storage, etc. All of these controls must follow prescribed, formal, approved procedures, written as protocols, SOPs, or Master Formulae, describing all the tasks carried out in an entire manufacturing and control process.
The TGA (pages 10, 19, 20, 21, 22) and FDA have similar standards. Many Aussies will remember the visit and warning CSL received from the FDA following the Fluvax scare in W.A . The TGA overview is here. In Australia we have The Pharmaceutical Overview Inspection Scheme.
The petition raises a claim that must be expanded on:
The opponents of this interview cite a public warning issued by the NSW Health Care Complaints Commission (HCCC) against the AVN. What they have failed to inform you of is the fact that in February, 2012, the NSW Supreme Court found that the HCCC had acted illegally in issuing that warning and the warning has since been removed and costs were awarded against the HCCC in favour of the AVN.
Wrong. That was down to me and as I’ve pointed out already I cited the NSW HCCC findings, which Justice Christine Adamson ruled were still valid by not accepting the AVN submission that certiorari (quashing the HCCC findings), was warranted.
Thus whilst the warning and recommendation were outside of jurisdiction due to the HCCC failure to satisfactorily demonstrate Section 7(1)(b) of the HCC Act 1993 (“a health service which affects the clinical management or care of an individual client”), the investigation findings were not expunged in any manner whatsoever. The petition should thus rightly be amended.
Check the petition out further if you want, but I would suggest that both the interview and the petition have been fairly and honestly outed as scurrilous and dishonest attempts to force demonstrably false fringe beliefs onto a wider unsuspecting audience. Of course, the AVN maintain it’s a conspiracy and Dorey has been unfairly censored. American Airlines have capitulated to “druggies” according to one signatory.
Ultimately I do hope for someone who has had such a good run on the smell of an oily scam, Dorey has the decency to accept the outcome as fair and just.
- In a bit of a round up there’s ample to read from sites, bloggers and skeptics from the last few days: