Showing posts with label h5n1. Show all posts

Monday, 16 November 2009

Investigation of Baxter Swine Flu Vaccine

Many questions surround a vaccine that’s rushed into the human bloodstream

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The New Zealand Minister of Health, Hon Tony Ryall, has asked Ministry of Health officials to urgently advise him on issues raised about a "swine flu" vaccine produced by Baxter International Inc. This follows his receipt of a letter raising concerns about whether vaccines produced by Baxter for "swine flu" can be trusted.

In an open letter to all members of the New Zealand House of Parliament, Penny Bright, Media Spokesperson for Water Pressure Group, a judicially recognized Public Watchdog for Metrowater, water and Auckland regional governance matters, raises a series of questions and concerns about the safety of the vaccine. She demands to know whether Baxter products are currently being used in New Zealand for the "swine flu", "bird flu" or any other type of flu.

Bright highlights the fact that Baxter is currently facing criminal charges for producing contaminated "bird flu" vaccine that date back to February of this year when it became known that the company had sent out 72 kilos of live "bird flu" virus supplied by the World Health Organization in the winter of 2009 to 16 laboratories in four countries. These charges were filed by journalist Jane Burgermeister of Austria and were exclusively reported by Natural News http://www.naturalnews.com/026503_p...

Burmeister's allegations claim that clear evidence exists that the pharmaceutical company and international government agencies actively conspired in producing, developing, manufacturing and distributing biological agents classified as the most deadly bioweapons on earth in order to trigger a pandemic and cause mass death.

Last December, the Austrian branch of Baxter sent a batch of ordinary human H3N2 flu, altered so it could not replicate, to Avir Green Hills Biotechnology, also in Austria. In February, a lab in the Czech Republic working for Avir alerted Baxter that, unexpectedly, ferrets inoculated with a sample from the shipment had died. It was discovered that the sample contained live H5N1, which was to be used by Baxter to make vaccine. Baxter claims the two mixed by error, and called the incident a simple "accident".

According to an article appearing in The Times of India on March 6, Markus Reinhard of Baxter said no one was infected because the H3N2 was handled at a high level of containment. But world renowned virologist Ab Osterhause of Erasmus University in the Netherlands has stated emphatically that great lengths must be taken to make sure this kind of thing does not happen again. In May, Osterhaus told participants at Europe's largest conference on infectious diseases that the outbreak of influenza A H1N1 is without question the most important event of the past 40 years in human influenza. He stressed that the current H1N1 threat is serious.

Accidental release of the mixture of live H5N1 and H3N2 virus subtypes could have resulted in extremely dire consequences. Although H5N1 does not easily infect people, H3N2 does. Anyone exposed to a mixture of the two strains and simultaneously infected with both could serve as a human incubator for a hybrid virus able to transmit easily to other people and their communities. This is the outcome feared by many scientists in the U.S. for the fall flu season, and the stated reason for the push to get everyone vaccinated, even if by force.

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In her open letter, Bright asks members of the New Zealand Parliament to consider whether they would consent to being injected with a "swine flu" vaccine produced by Baxter while it is under investigation for charges it produced contaminated "bird flu" vaccine. She asks Parliament members if they would consent to having their own children and grandchildren vaccinated with Baxter's product which is slated to appear on the market this month [last July – Ed].

She also asks them to consider a situation in which their consent to vaccination or lack thereof was overridden under emergency legislation arising from the New Zealand Epidemic Preparedness Act 2006, and to consider their response to mandatory or forced vaccination.

Under the Epidemic Preparedness Act 2006, broad powers are granted to the Medical Officer of Health in response to the threat or emergence of a new epidemic. These powers include the ability to require a person to undergo a medical examination (section 70(1)(e)); require persons, places, buildings, ships, vehicles, aircraft, animals, or things to be isolated, quarantined, or disinfected (section 70(1)(f)); require people to remain in quarantine until they have been medically examined and found to be free from infectious disease, and until they have undergone any prescribed preventive treatment (section 70(1)(h); close any premise (section 70(1)(la) or all premises within a certain area (section 70(1)(m)(i)-(ii); forbid people to congregate in outdoor places of amusement or recreations, whether public or private (section 70(1)(m)(iii)-(iv); and take possession of personal property including land, buildings, vehicles, medicines, and other things, and for purposes including the accommodation or treatment of patients, disposal of bodies, transportation of patients, medical personnel, medicine etcetera (section 71(1)).

These powers are automatically engaged when an epidemic notice is issued, much like the setup in the U.S. which allows for similar powers to automatically come into effect with the declaration of Pandemic Level 6. A Pandemic Level 6 alert was declared on June, 11th.

The powers of the Medical Officer of Health include ordering the removal of any person to a hospital for isolation if he or she has reason to believe or suspect that the person, whether suffering from an infectious disease or not, is likely to cause the spread of any infectious disease (section 79).

For additional information:
http://www.naturalnews.com/025760.html
http://www.naturalnews.com/026503_p...
http://www.chenpalmer.com/WhatsNew/...

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From – NaturalNews.com, 8^th July 2009

Friday, 21 April 2006

Avian Flu or Mycoplasma Pandemic?

Germ Theory – What Is Mycoplasma?

Mycoplasma fermentans
“…What we fear is another opportunity the world is being given to exchange an ancient disease (a viral influenza) for something new: a ‘flu-like illness’ caused by a Mycoplasma species. In fact, if our worst fears are realised, a large part of the human family has already been contaminated with this deadly new pathogen. It has been engineered from its earlier and natural antecedent by the US government’s biowarfare weapons research, development, testing and deployment agencies and their university and commercial partners…

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“Mycoplasma is now acknowledged by a patent, held by the US Government, to be a factor in ‘…AIDS or ARC, Chronic Fatigue Syndrome, Sarcoidosis, respiratory distress syndrome, Kibuchi’s disease, autoimmune diseases such as Collagen Vascular Disease and Lupus and chronic debilitating diseases such as Alzheimer’s Disease.’ This dramatic list of Mycoplasma-related diseases is taken from the 1991 US Patent #5,242,820, with its ‘inventor’ cited as Shyh-Ching Lo, who assigned the patent rights to the American Registry of Pathology, Washington, DC. In other words, the US Government holds a patent upon a death and disease weapon of mass destruction in the form of a patent on ‘Pathogenic Mycloplasma’. And this Mycoplasma causes a ‘flu-like illness’ which can be fatal.

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“…suppose something were to kill [a} bacterium – something such as a variant of penicillin which opens a rupture in the bacterial wall. The draining of the cytoplasm will kill the life-form, but there is still a will to live in parts of the DNA and RNA. Thus, particles of the DNA and RNA cluster together and quickly assemble a protein protective coat around themselves. Here you have the essential virus; a particle of genetic information with a protein coat.

“Take a further look at the bacterium and note the ribosomes… the cytoplasm is full of them – the nucleic acids called ribonucleic acid (RNA) are assembled when it is necessary for the bacterium to manufacture proteins and enzymes for the bacterium to function. As with particles of the DNA, certain bacterial RNAs have the capacity to seek to survive when their original life-form is threatened, by clustering together and self-assembling a protein protective coat.

“Somehow or other, the life-force which motivates the bacterium has an inherent sense of which nucleic particles it need to save when the original life-form is threatened. Thus, the various species of virus are select particles of genetic code which have sheltered themselves with a protein coat until they can access another living cell and get on with the business of life.

“Unfortunately, in seeking to save their life-particles, the viruses often have to destroy other life-forms such as human cells. When the latter happens, the destroyed cells present as disease-ravaged remnants of earlier life-forms…

“Even though the WHO and other ‘health’ agencies would have you believe that you should fear the avian flu virus, species H5N1, it is the mycoplasma that humanity has to fear… the world of official medicine apparently doesn’t want the average citizen even to know that such an organism exists.

“Allow us to give you a thumbnail sketch of the mycoplasma. Start by taking a look at the bacterium. Note that the bacterium has ribosomes which, as we have seen, are involved in the manufacture of RNA, and note further that sometimes particles of the RNA get loose due to bacterial death and are preserved by being gathered together into groups of eight RNA fragments which are then enclosed in a protective matrix and a cell membrane, and voila: there you have the influenza virus!

“…If the bacterium is killed…particles of DNA will also seek to continue as living organisms by creating themselves a membrane and setting off within their environment to find another host cell which will let them inside and give them a refuge. Again, voila: this cell-wall-less DNA particle becomes a self-replicating but somewhat incomplete life-form known as a species of Mycoplasma!…

“So, you start off with some species of ‘walled bacteria’and it all falls apart (degenerative evolution) for one of a variety of reasons, such as the operation of penicillin. Then, select particles of the bacterial DNA quickly start a search for some other cell within which it can take up residence. It is almost a virus, without the protective protein coat that we noted above…

“When the mycoplasma finds a cell which will allow it to cross the cellular membrane, the mycoplasma will generally lie peacefully, doing no harm to its new host until it is subjected to some kind of trauma.

“The body of which the cell is a part may be subjected to a rear-end automobile accident, or it may be traumatized by a fall on the ice. Even the news that a dear and valued friend has died can produce a trauma sufficient to rouse the dormant mycoplasma into life.

“When so roused into activity, certain species of the DNA mycoplasmal particle will begin to up-take pre-formed sterols from its new host, ultimately killing the host. The totality can be called a ‘mycoplasmal infection’ and can present as, for example, pneumonia, wherein the cells in the lungs begin to degenerate and release fluid which floods the alveoli, or air-containing cells of the lungs.

“…there may well be a worldwide pandemic and it may well kill thousands of people a day over a period of time. But the chances of it being the consequence of a sole, mutating H5N1 species of avian flu virus are miniscule or totally unlikely, and the chances of it being a mycoplasmal infection are very high…

“we returned to Dr Shyh-Ching Lo’s Uniformed services University of the Health Sciences course on Mycloplasma and read it for the tenth time… and suddenlywe realized what one paragraph of that unit was really saying. Here is the paragraph:

“’The most serious presentation of M[ycoplasma] fermentans infection is that of a fulminant systemic disease that begins as a flu-like illness. Patients rapidly deteriorate, developing severe complications including adult respiratory distress syndrome, disseminated intravascular coagulation, and/or multiple organ failure.’ (The Journal of Degenerative Diseases, vol. 5, no. 2, p. 28)

“Now, please note: this is not influenza, but is a ‘flu-like illness’ which anyone could honestly mistake for the influenza – but it is not the flu, and it is not caused by the H5N1 strain of the avian flu virus. It is caused by a pathogen patented by the United States government!

- From Avian Flu or Mycoplasma Pandemic

NEXUS New Times Magazine, vol. 13 no. 3, pp27-83

By Donald W. Scott, MA, MSc and William L.C. Scott

The Common Cause Medical Research Foundation

images - http://images.tutorvista.com/content/kingdoms-living-world/mycoplasma-cell-structure.jpeg

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