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Bernie,

When we spoke at the gun show I expressed my concerns about the Swine Flu vaccine. Despite the fact that the virus has proven far less potent than the common flu, governments across the world have been preparing to roll out mass vaccination campaigns. I also shared my concern that these shots will contain mercury and squalene and have also been linked with autism in children and killer nerve diseases like Guillain-Barre Syndrome and Gulf War Syndrome in adults.

Now I have more info to share with you. I am angered, and very concerned that children and expectant mothers are the prime targets for this untested and potentially unsafe vaccine. I became aware of this when I read an article in the Wall Street Journal titled ‘Flu Vaccine Panel Creates Priority List’ which disclosed “some of the vaccine will be stored in multi-dose vials containing thimerosal, an antibacterial additive that contains mercury. But there will also be single-dose syringes without thimerosal, a substance that some assert is harmful to children.”

This WSJ news article would also seem to confirm the story that nurse told me at the gun show about two batches of the vaccine being sent to her hospital and how she witnessed the Doctors take the batch without the mercury for themselves, leave the rest for everyone else. When I told you that story the nurse told me, you seemed to get upset and even suggested an investigation should be called for. I agree, but after doing some digging I have found that is a lot more to this story.

Going back to early days of the swine flu outbreak in late April, Ret. Army General Russell Honoré was on CNN and he said this: “How did it start in Mexico, where did it eminate from? We’ve been able to find that out in all previous pandemics, the question now is to get at the heart of how this started - did it start from the occasion of viruses coming together or did it come out of a lab? All those questions have to be answered.”

The H1N1 virus is an odd duckling with a suspicious composition: it contains genes from birds, humans, and pigs from many different continents. It seems that the new strain of swine flu is a synthetic structural recombinant, it therefore is reasonable to assume it came out of a laboratory, specifically a bioweapons laboratory.

Now consider this statement by the WHO published on their own website: "some manufacturers have conducted advance studies using a so-called 'mock-up' vaccine. Mock-up vaccines contain an active ingredient for an influenza virus that has not circulated recently in human populations and thus mimics the novelty of a pandemic virus. Such advance studies can greatly expedite regulatory approval."

In order words, the WHO admits vaccine manufacturers have been testing these mock-up vaccines, using live flu viruses in order to “mimic the novelty of a pandemic virus” because doing so would “greatly expedite regulatory approval.” Did you get that? Their motive is money, and WHO claims we can trust them. Yes, influenza viruses are secretly being introduced into human populations so Big Pharma can make money, nothing to worry about.

Now consider this testimony from a woman who knows firsthand from a nurse (her friend) working on clinical vaccine trials in Mexico, that the original swine flu deaths in that country were caused by an experimental vaccine. Here is the video.

I would like you to investigate this further.

/mark

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This "confession" by the WHO is a smoking gun.

Go look at the link, the WHO admits right on their own website that "mock-up" vaccines were being tested to "expedite the regulatory approval." How is this not a crime? But we are told they do this to make money, so nothing to worry about, right? Right!

According to Rima E. Laibow, MD, head of the Natural Solutions Foundation, a citizen watchdog group monitoring the pharmaceutical industry states, "Our best intelligence estimate is that pandemic Avian Flu has already been created through genetic engineering in the United States, fusing the deadly genome of the 1918 Pandemic, misnamed the ‘Spanish Flu’, with the DNA of the innocuous H5N1 virus in a growth medium of human kidney cells, according to the National Institutes of Health and the vaccine’s manufacturer. Some virologists believe that this would insure that the man-made mutant virus recognizes human cells and knows how to invade them." 1

This was written over a year ago!

Laibow also points out, "A basic virological fact that the public has not been told is that it is impossible to make a vaccine against a virus that does not yet exist. Public relations efforts to the contrary, IF a vaccine is being made against the Avian Flu virus in its pandemic form, that means that the pandemic virus must already exist, period, end of discussion."2

If I understand this correctly, that means before a "mock-up" vaccine is tested, a novel virus (against which it is to be tested) would have to be created in the same lab first. Logic tells me that novel lab virus would have to be released into a human population before any test could be conducted. what am I missing here? Looks like a smoking gun to me.


-----------------------
1) Rima E. Laibow, M.D., Weaponized Avian Flu Intelligence Report (July 19, 2008)
2) Ibid.
Vaccins, The W.H.O. , Dr Robertson , and the World's Collective Death Sentence !Posted by luggnutz on May 20, 2009 at 1:30pm

http://snardfarker.ning.com/profiles/blogs/vaccins-the-who-dr-rober...

http://royalsociety.org/downloaddoc.asp?id=3521
Summary of oral evidence: Dr John Wood and Dr James Robertson, National Institute for Biological Standards and Control (NIBSC) 27 April 2006

Dr John Wood and Dr James Robertson are Principal Scientists in the Division of Virology at NIBSC. Dr Wood and Dr Robertson lead the NIBSC’s influenza group and their responsibilities include the control and standardisation of influenza vaccines. On behalf of the World Health Organisation (WHO) the NIBSC is involved in the serological testing of vaccine trials; the PREPARATION and DISTRIBUTION of INFLUENZA VIRUSES TO VACCINE MANUFACTURERS; and the COORDINATION of EU STRAIN SELECTION PROCESSES.

Back to the summary. Drs Robertson and Wood consider development slow in EU due to limited public funding. EMEA have helped persuade industry to invest in pandemic vaccines with introduction of the "mock up files" and by waiving regulatory fees and several pandemic vaccines are now in clinical trials.

So since public won’t consent to dogma or needs to be forced with freak outbreaks like SARS was in Toronto ( you might want to rethink how that all went down now in review of this!), which is even stated in the report when they claim it has gone better in North America than it has in Europe, they turn to Pharma to do initial investment by easing profit restrictions and fast tracking research publications from Pharma Doctors to later supply investors a Pandemic payoff!

Drs Wood and Robertson were ASKED their OPINION on PRIMING the POPULATION for a PANDEMIC USING LIVE VACCINES and if they consider it to be a good idea. However the timing is critical; if LIVE H5N1 VACCINES are used now it would be CONSIDERED too DANGEROUS,but IF a PANDEMIC is IMMINENT the RISK may be JUSTIFIED. A STOCKPILE OF LIVE VACCINES,with the cleavage site removed,could be USED to PRIME the POPULATION IN ADVANCE of the PANDEMIC REACHING the UK. Even without an exact match in virus strain, it is predicted that this would provide a broad immunity to the population.

What are live vaccines??? http://en.wikipedia.org/wiki/Live_vector_vaccine
A live vector vaccine is a vaccine that uses a chemically weakened virus to transport pieces of the virus in order to stimulate an immune response.
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