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descriptionمصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى Emptyمصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى

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قرأت فى احد المواضيع عن الكلام ده
و بالمقال و المصادر تأكدت من الأمر
المصل الشافى من أنفلونزا الخنازير ما هو إلا سلاح بيولوجى للقضاء من عدة نواحى على دول العالم التالت
فالمصل يحتوى على تسريع عمليات الوفاة أو إنهيار الجهاز التناسلى أو إنعدام الذكاء لدى البشر و أخيرا عدد من الوفيات

لمراجعة المقال بالمصادر
أتفضلوا الرابط
http://www.jimstonefreelance.com/squalene.html

و سأنقل ما هو مكتوب هنا
لأن ممكن لتعتيم الحقيقة بيوم
يلغوا الموقع أو ماكتب

Date: Monday, August 10, 2009, 3:58 AM
Tainted nightmare


Dr. Sarah Stone, Pharm-D
Jim Stone, Freelance Journalist
Russ Clarke, Editor

"The H1N1 vaccination program, when put into the same frame as the engineered virus to go with it, appears to be a clear effort to divide humanity into two groups; those who have lost their intellect, health and sexuality via a tainted vaccination, and those who have not and are therefore superior."

I met the story about the swine flu with great skepticism; it played like a story line in a B movie - Students go abroad for spring break. Students get the virus. Students bring it home. Worldwide pandemic starts. The story line was unbelievable, and I knew from day one that there was either no virus at all, and that it was just a "wag the dog", or that a manufactured outbreak was intentionally released and underway.
Unfortunately the latter was true, and now we have an entirely new bug on our hands. It has never been seen before, and virologists have been quoted saying "where the hell it got all these genes from we don't know." Extensive analysis of the virus has revealed genes from the original 1918 flu, the avian flu, and two new H3N2 viruses from Eurasia. All evidence points to the fact that the swine flu is indeed a genetically engineered virus.
This article is the result of a team effort intended to explore what the motive for releasing it may be, to warn you in advance of things to come.


The first attempt

In Feb 2009, Baxter, a major manufacturer of vaccines, sent the seasonal flu shot to 18 different countries with live unattenuated H5N1 bird flu. When the Czech company Biotest was assigned to test the vaccine on live animals for the Czech government, they realized something was wrong when the test animals died. The alarm went out to all others who had received it, fortunately before it was administered. Upon follow up examination of the vaccine the live virus was revealed, had no one caught Baxter's tainted batch, we would now be in the midst of a pandemic with massive numbers of dead.
Baxter was not prosecuted or punished in any way for this, even though their operational BSL3 (bio safety level 3) protocol would have stopped such contamination from being possible. The safety protocol, combined with the potency and volume of the virus in the shots clearly shows that the contamination was intentional, and that indeed an attempt to kill millions was stopped simply because ONE country paid attention to what it was getting. The protocol made it technically impossible for the virus to make the leap from the research department to the vaccine manufacturing department, which could never have had H5N1 show up there due to any reason other than willful intent.
One would think that Baxter would have been put out of business for making such an "error" but the opposite is true, which begs many questions, such as how did the live bird flu end up in millions of doses of vaccine? Why were the ingredients of the vaccine formulated to allow the virus to survive fully potent en route? Why was Baxter not prosecuted or punished in any way? Instead of rightfully blackballing the company, the World Health Organization has rewarded Baxter with a contract to make a large portion of the "Swine flu" vaccinations set to be distributed world wide this fall. How on earth could that be?


The main focus

Let's switch to another aspect of vaccines, the real focus of this article, which is the plan to destroy our intellect, our health and our sexuality via a mass world wide vaccination campaign. With the use of special additives called adjuvants, manufacturers are able to increase the number of possible doses that can be made on time for the fall flu season. But though there are many safe adjuvants which can be added, they are adding one - squalene, which has been shown to cause prolonged systemic immune response against the squalene itself, which results in reduced fertility, reduced intellect and reduced life span.
Squalene is an important molecule in the body. It is a precursor to many different oils and hormones, and is needed for proper brain function, fertility and also plays an important role in protecting cells from aging and mutation. Anything which affects your natural squalene can have a major negative impact on your health.
Because the squalene will be injected in the presence of a pathogen during the H1N1 vaccination, it will cause an immune response against not only the pathogen, but to the squalene itself. Squalene is a precursor molecule which is essential for the production of many hormones including all of the male and female sexual hormones. Squalene is also a precursor to many of the neurochemical receptors prevalent in the nervous system and when the immune system is programmed to attack squalene, it causes irreversible neuronal and neuromuscular damage which can range from a loss of intellect and autism to more serious disorders such as Lou Gehrig's disease and systemic autoimmune diseases and possibly brain tumors.
In independent studies where squalene laced vaccines were injected into guinea pigs, the resultant autoimmune disorders killed 14 out of 15. A later test, to verify the results had the same outcome.
When first injected via the anthrax vaccine in Gulf War 1, it permanently disabled many of the soldiers who received it, due to the effects now known as the Gulf War Syndrome. 95 percent of the soldiers who recieved the anthrax vaccine have been found to have antibodies to squalene. Few of the soldiers who recieved the vaccine remained healthy and do not have the antibodies whether or not they were deployed. None of the soldiers who did not receive the vaccine have the antibodies, even those who fought in Iraq. Squalene antibody related deaths total 6.5 percent of the vaccinated group.
It takes approximately a year for the effects to fully manifest themselves because that much time passes before the nervous system and brain deplete the reserves of Squalene that are out of the reach of the immune system and only after the reserves are gone will cell injury begin. This takes the pressure off vaccine manufacturers who deny any wrongdoing for a response so delayed. And with Congress passing legislation granting immunity to any corporations who cause damage with their vaccines, the outlook is evermore dark.
After examining the components of the H1N1 flu vaccine we can only conclude that it is not intended to treat the flu at all, quite differently, it is intended to:
1. Reduce intelligence
2. Reduce life span
3. Reduce fertility
4. Cause numerous deaths
For if it was intended for any other purpose, Squalene and other adjuvants beyond the scope of this article would not be present. Furthermore, the scope of this article only covers squalene, and we believe that because there are so many ways to induce autoimmune responses equally devastating via other injectable formulations coupled with the obviously intentional shipment of a pandemic by Baxter that the credibility of vaccines is forever tainted and the trust in the greater medical community may have been irreparably broken. Baxter should be out of business, the fact that they are not is damning.


The trust is broken

Through a manufactured pandemic and damaging vaccine the world health organization along with major manufacturers in the pharmaceutical industry have demonstrated clear intent to damage all of mankind. For what purpose is difficult to determine, but it would be safe to assume that there will be those who have been told and know better than to take one of these tainted vaccines, and as a result they will be of superior intelligence and health when put in perspective with those who receive them. The H1N1 vaccination program, when put into the same frame as the obviously engineered virus to go with it, appears to be a clear effort to divide humanity into two groups, those who have lost their intellect, health and sexuality via a tainted vaccination, and those who have not and are therefore superior. It can now be reasoned that it is no longer safe to take ANY vaccination for any reason; please, do not let them get your children.


If you ever see a video of major figures getting theirs, keep in mind that not all shots will be created equal!</STRONG>


References
</STRONG>
The most valuable reference for this article by far was Dr. Sarah Stone, Pharm-D. Thank you so much, you helped sort fact from fiction and made this article possible
Newsmax.com "Vaccine May Be More Dangerous Than Swine Flu"
Mercola.com "Squalene: The Swine Flu Vaccine's Dirty Little Secret Exposed"
Chiroweb.com "Vaccines May Be Linked to Gulf War Syndrome"
The Unify Coalition "Experimental Vaccines / Adjuvants / Squalene:"
Health Freedom Alliance Read this to item 122, it returns to English half a page down!
Rense This is an excellent report on the Gulf War Syndrome and Autism, by Neurosergeon Dr Blaylock

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المصدر الأول باتقرير

Vaccine May Be More Dangerous Than Swine Flu



By: Dr. Russell Blaylock
An outbreak of swine flu occurred in Mexico this spring that eventually affected 4,910 Mexican citizens and resulted in 85 deaths. By the time it spread to the United States, the virus caused only mild cases of flu-like illness.

Thanks to air travel and the failure of public health officials to control travel from Mexico, the virus spread worldwide. Despite predictions of massive numbers of deaths and the arrival of doomsday, the virus has remained a relatively mild disease, something we know happens each year with flu epidemics.

Worldwide, there have only been 311 deaths out of 70,893 cases of swine flu. In the United States, 27,717 cases have resulted in 127 deaths. Every death is a tragedy, but such a low death rate should not be the basis of a draconian government policy.

It is helpful to recall that the Centers for Disease Control with the collusion of the media, constantly tell us that 36,000 people die from the flu each year, a figure that has been shown to be a lie. In this case, we are talking about 300 plus deaths for the entire world.

This virus continues to be an enigma for virologists. In the April 30, 2009 issue of Nature, a virologist was quoted as saying,“Where the hell it got all these genes from we don’t know.” Extensive analysis of the virus found that it contained the original 1918 H1N1 flu virus, the avian flu virus (bird flu), and two new H3N2 virus genes from Eurasia. Debate continues over the possibility that swine flu is a genetically engineered virus.

Naturally, vaccine manufacturers have been in a competitive battle to produce the first vaccine. The main contenders have been Baxter Pharmaceuticals and Novartis Pharmaceuticals, the latter of which recently acquired the scandal-ridden Chiron vaccine company. Both of these companies have had agreements with the World Health Organization to produce a pandemic vaccine.

The Baxter vaccine, called Celvapan, has had fast track approval. It uses a new vero cell technology, which utilizes cultured cells from the African green monkey. This same animal tissue transmits a number of vaccine-contaminating viruses, including the HIV virus.

The Baxter company has been associated with two deadly scandals. The first event occurred in 2006 when hemophiliac components were contaminated with HIV virus and injected in tens of thousands of people, including thousands of children. Baxter continued to release the HIV contaminated vaccine even after the contamination was known.

The second event occurred recently when it was discovered that Baxter had released a seasonal flu vaccine containing the bird flu virus, which would have produced a real world pandemic, to 18 countries. Fortunately, astute lab workers in the Czech Republic discovered the deadly combination and blew the whistle before a worldwide disaster was unleashed.

Despite these two deadly events, WHO maintains an agreement with Baxter Pharmaceuticals to produce the world’s pandemic vaccine.

Novartis, the second contender, also has an agreement with WHO for a pandemic vaccine. Novartis appears to have won the contract, since their vaccine is near completion. What is terrifying is that these pandemic vaccines contain ingredients, called immune adjuvants that a number of studies have shown cause devastating autoimmune disorders, including rheumatoid arthritis, multiple sclerosis and lupus.

Animal studies using this adjuvant have found them to be deadly. A study using 14 guinea pigs found that when they were injected with the special adjuvant, only one animal survived. A repeat of the study found the same deadly outcome.

So, what is this deadly ingredient? It is called squalene, a type of oil. The Chiron company, maker of the deadly anthrax vaccine, makes an adjuvant called MF-59 which contains an ingredient of serious concern--squalene. A number of studies have shown that squalene can trigger all of the above-mentioned autoimmune diseases when injected.

The MF-59 adjuvant has been used in several vaccines. These vaccines, including tetanus and diphtheria, are the same vaccines frequently associated with adverse reactions.

I reviewed a number of studies on this adjuvant and found something quite interesting. Several studies done on human test subjects found MF-59 to be a very safe immune adjuvant. But when I checked to see who did these studies, I found—to no surprise—that they were done by the Novartis Pharmaceutical Company and Chiron Pharmaceutical Company, which have merged. They were all published in “prestigious” medical journals. Also, to no surprise, a great number of studies done by independent laboratories and research institutions all found a strong link between MF-59 and autoimmune diseases.

Squalene in vaccines has been strongly linked to the Gulf War Syndrome. On August 1991, Anthony Principi, Secretary of Veterans Affairs admitted that soldiers vaccinated with the anthrax vaccine from 1990 to 1991 had an increased risk of 200 percent in developing the deadly disease amyotrophic lateral sclerosis (ALS), also called Lou Gehrig’s disease. The soldiers also suffered from a number of debilitating and life-shortening diseases, such as polyarteritis nodosa, multiple sclerosis (MS), lupus, transverse myelitis (a neurological disorder caused by inflammation of the spinal cord), endocarditis (inflammation of the heart’s inner lining), optic neuritis with blindness and glomerulonephritis (a type of kidney disease).

Because squalene, the main ingredient in MF-59, can induce hyperimmune responses and induce autoimmunity, a real danger exists for prolonged activation of the brain’s immune cells, the microglia. This type of prolonged activation has been strongly associated with such diseases as multiple sclerosis, Alzheimer’s disease, Parkinson’s disease, ALS and possibly vaccine-related encephalitis. It has been shown that activation of the systemic immune system, as occurs with vaccination, rapidly activates the brain’s microglia at the same time, and this brain inflammation can persist for long periods.

What most people do not know, even the doctors who recommend the vaccines, is that most studies by pharmaceutical companies observe the patients for only one to two weeks following vaccination—these types of reactions may take months or even years to manifest.

It is obvious that the vaccine manufacturers stand to make billions of dollars in profits from this WHO/government-promoted pandemic. Novartis, the maker of the new pandemic vaccine, recently announced that they would not give free vaccines to impoverished nations—everybody pays.

One must keep in mind that once the vaccine is injected, there is little you can do to protect yourself—at least by conventional medicine. It will mean a lifetime of crippling illness and early death.

There are much safer ways to protect oneself from this flu virus, such as higher doses of vitamin D3, selective immune enhancement using supplements, and a good diet.











©️ 2009 Newsmax. All rights reserved.

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المصدر الثانى بالتقرير

Squalene: The Swine Flu Vaccine’s Dirty Little Secret Exposed


مصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى 8.4vaccine

By Dr. Mercola

According to Kathleen Sebelius, Secretary of the U.S. Department of Health and Human Services, your children should be the first target for mass swine flu vaccinations when school starts this fall.
This is a ridiculous assumption for many reasons, not to mention extremely high risk.
In Australia, where the winter season has begun, Federal Health Minister Nicola Roxon is reassuring parents the swine flu is no more dangerous than regular seasonal flu. "Most people, including children, will experience very mild symptoms and recover without any medical intervention," she said.[ii]
Sydney-based immunization specialist Robert Booy predicts swine flu might be fatal to about twice as many children in the coming year as regular influenza. Booy estimates 10-12 children could die from the H1N1 virus, compared with the five or six regular flu deaths seen among children in an average year in Australia.[iii][/url
Cure the Disease, Kill the Patient

Less than 100 children in the U.S. die each year from seasonal flu viruses.[url=http://articles.mercola.com/sites/articles/archive/2009/08/04/Squalene-The-Swine-Flu-Vaccines-Dirty-Little-Secret-Exposed.aspx#_edn4][iv] If we use Australia’s math, a very rough estimate would be another 100 children could potentially die of swine flu in the United States in the coming year.
If children are the first target group in the U.S. per Sebelius, that means we’re about to inject around 75 million children with a fast tracked vaccine containing novel adjuvants, including dangerous squalene, to prevent perhaps 100 deaths.
I’m not overlooking the tragedy of the loss of even one child to an illness like the H1N1 flu virus. But there can be no argument that unnecessary mass injection of millions of children with a vaccine containing an adjuvant known to cause a host of debilitating autoimmune diseases is a reckless, dangerous plan.
Why are Vaccinations Dangerous?
The presumed intent of a vaccination is to help you build immunity to potentially harmful organisms that cause illness and disease. However, your body’s immune system is already designed to do this in response to organisms which invade your body naturally.
Most disease-causing organisms enter your body through the mucous membranes of your nose, mouth, pulmonary system or your digestive tract – not through an injection.
These mucous membranes have their own immune system, called the IgA immune system. It is a different system from the one activated when a vaccine is injected into your body.
Your IgA immune system is your body’s first line of defense. Its job is to fight off invading organisms at their entry points, reducing or even eliminating the need for activation of your body’s immune system.
When a virus is injected into your body in a vaccine, and especially when combined with an immune adjuvant like squalene, your IgA immune system is bypassed and your body’s immune system kicks into high gear in response to the vaccination.
Injecting organisms into your body to provoke immunity is contrary to nature, and vaccination carries enormous potential to do serious damage to your health.
And as if Vaccines Weren’t Dangerous Enough on Their Own …
… imagine them turbocharged.
The main ingredient in a vaccine is either killed viruses or live ones that have been attenuated (weakened and made less harmful).
Flu vaccines can also contain a number of chemical toxins, including ethylene glycol (antifreeze), formaldehyde, phenol (carbolic acid) and even antibiotics like Neomycin and streptomycin.
In addition to the viruses and other additives, many vaccines also contain immune adjuvants like aluminum and squalene.
The purpose of an immune adjuvant added to a vaccine is to enhance (turbo charge) your immune response to the vaccination. Adjuvants cause your immune system to overreact to the introduction of the organism you’re being vaccinated against.
Adjuvants are supposed to get the job done faster (but certainly not more safely), which reduces the amount of vaccine required per dose, and the number of doses given per individual.
Less vaccine required per person means more individual doses available for mass vaccination campaigns. Coincidentally, this is exactly the goal of government and the pharmaceutical companies who stand to make millions from their vaccines.
Will There Be Immune Adjuvants in Swine Flu Vaccines?
The U.S. government has contracts with several drug companies to develop and produce swine flu vaccines. At least two of those companies, Novartis and GlaxoSmithKline, are using an adjuvant in their H1N1 vaccines.
The adjuvant? Squalene.
According to Meryl Nass, M.D., an authority on the anthrax vaccine,

[i]“A novel feature of the two H1N1 vaccines being developed by companies Novartis and GlaxoSmithKline is the addition of squalene-containing adjuvants to boost immunogenicity and dramatically reduce the amount of viral antigen needed. This translates to much faster production of desired vaccine quantities.”
[v]
<BLOCKQUOTE></BLOCKQUOTE>
Novartis’s proprietary squalene adjuvant for their H1N1 vaccine is MF59. Glaxo’s is ASO3. MF59 has yet to be approved by the FDA for use in any U.S. vaccine, despite its history of use in other countries.
Per Dr. Nass, there are only three vaccines in existence using an approved squalene adjuvant. None of the three are approved for use in the U.S.

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المصر الثالث

-During the GW Era, experimental vaccine(s) with equally experimental adjuvant(s) were administered. At least one of the vaccines given contained a highly experimental synthesized polymer adjuvant known as squalene. It has been reported, the same adjuvant was used in, at least, several lots / batches of the anthrax vaccine recently being given. And the most recent malaria vaccine being administered is reported to contain squalene as an adjuvant.
-Natural squalenes, as found in food sources, ingested and digested are changed to sterols in our bodies and are not normally problematic, nor do they produce anti-bodies to squalene. Digestion somehow creates the molecular changes / conversions, modifying the squalene into useful sterols.
-Laboratory synththetic polymer (processed) squalene, for vaccine adjuvants, differs somewhat in composition and greatly in body reactivity.
-Adjuvant activity is enhanced by the addition of other adjuvants, (e.g.. MDD, MTPE, Etc.) and, to some extent, by the processing itself.
-Body reactivity and antibody production comes primarily as a result of route of administration other than oral ingestion / digestion. To administer IV, IM, SQ is not natural and does not convert and assimilate squalene into sterols. It appears this un-natural administration establishes the ability to produce immune antibody reactivity to squalene.
-The molecular weight of squalene is 410.71 Large molecule and is C30H50 Identified as Hexamethyltetracosane. The polymer squalene is double bonded and generally unstable.
-Squalene, as an adjuvant, is capable of initiating antibody production to itself and initiating autoimmune disease, both neurological and rheumatological, by itself. The addition of the derivatives (MDD, MTPE, Etc) of mycobacterial cell walls enhances these effects.
-In oral ingestion/digestion route, the mucosal epithelium of the intestines modifies the squalene as it is absorbed from food materials into sterols and other molecular structures to which the body does not generate immune reactions.
-Injected squalene is not seen as normal by the immune system, hence, it does initiate immune reactivity to itself. The body synthesizes squalene in the Golgi apparartus of hepatocytes and is further processed into chylomicrons covered by lipoproteins containing triglycerides and cholesterol esters, considered to be poorly immunogenic molecules. Antibodies to cholesterol have been generated only by the addition of lipid A as an adjuvant or by the injection of silicone or silicone oil intraperitoneally (indicating its ability to act as an adjuvant and initiate autoimmunity). PB/DU/Chemicals-Insecticides, etc.
-I think it important to mention here, that not all got the same vaccines/adjuvants. It is also important to note that not all were deployed, but large numbers of non-deployed are ill with GWS illnesses.
-Equally important, for those who were deployed, not all were exposed to all of the same environmental contaminants, e.g.; DU, chemicals & insecticides, oil well fires, etc.
-Use of PB tabs is of significant concern. Probably more deployed, ingested PB tabs than were exposed to all of the environmental contaminants.
-DU exposure is also of very serious consideration, especially where quantities entered and continue to reside in the body.
-There are many possible equations for those who deployed, but only one common denominator, for the largest numbers, of both deployed and non- deployed. That was the use of experimental vaccines/adjuvants. It is interesting to note, the DOD continues to vehemently deny use of same, even in the face of mounting evidence to the contrary.
I hope this is of some help. Best wishes to you and your loved ones.
Sincerely,
Rick Shuster
Viet Nam Era Vet
Father of 3 GW Era Vets

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المصدر الرابع

Vaccines May Be Linked to Gulf War Syndrome


DOD to Review Possible Use of Illegal Additive



By Michael Devitt
Less than four months after its publication, the Department of Defense (DOD) has agreed to review a controversial study that appears to link Gulf War syndrome (GWS) with a banned substance used in experimental vaccines.

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The study, conducted by scientists at Tulane University Medical School, found that an overwhelming majority of sick veterans who had served in the Gulf War, and had received at least one vaccination, tested positive for antibodies to a naturally occurring substance called squalene. None of the healthy veterans in the study tested positive for squalene antibodies.
DoD officials originally dismissed the study as flawed and asserted that none of the vaccines administered during the Gulf War contained squalene. In response to pressure from Congress, however, the department has asked the Armed Forces Epidemiological Board (AFEB) to re-examine the study. The Institute of Medicine is also reviewing the research to see what role squalene may play in Gulf-related illnesses.1
Squalene Adjuvant: Friend or Foe?
A naturally occurring molecule, squalene is produced by the human liver and plays a role in the metabolism of cholesterol. It is most commonly found in vegetable oils, shark liver oil, cosmetics and various health supplements.
Under normal circumstances, squalene is released into the blood to help combat physical injuries. However, people don't usually have enough squalene in their blood to prompt the production of detectable levels of antibodies.
Since the late 1980s, squalene has been studied by the DoD and the National Institutes of Health as a possible adjuvant in vaccines. Because adjuvants boost the immune system's response to foreign antibodies, the subtance has sparked the interest of researchers. Drug manufacturers, for their part, have incorporated adjuvants into vaccines in the belief that the substance will render the vaccine more effective.
Adjuvants, however, can sometimes trigger unwanted immune responses. While large-scale studies have yet to be conducted in humans, animal studies have shown that squalene adjuvants may generate autoimmune versions of arthritis and multiple sclerosis type-conditions that attack the body from within.2
Although they have been used in a number of vaccines worldwide, only one adjuvant - aluminum hydroxide - has been approved by the Food and Drug Administration for use in vaccines in the United States. And although squalene-adjuvant vaccines have been used on laboratory animals and in experimental human tests, the FDA has not approved the general use of any vaccine containing squalene in the U.S.
"We Never Used Squalene in Vaccines"
Military officials have said all along that no Gulf War vaccines contained squalene. In August 1997, spokespersons for the DoD claimed that squalene "was not an adjuvant that was in any of the vaccines that were used by the Department of Defense,"3 and that "we never used squalene in vaccines" during the Gulf War. However, in a report4issued in March 1999, the General Accounting Office (GAD) - the investigative arm of Congress - stated:

<BLOCKQUOTE>We cannot say definitively whether or not Gulf War-era veterans were given vaccines with adjuvant formulations containing squalene for a number of reasons. Although DoD officials told us they did not administer such vaccines, they stated they did not have documentation on the process and results of decision-making related to the administration of vaccines at the time of the Gulf War. Also, some officials involved in the decisions were no longer employed with DoD at the time of our review, and we were either unable to locate them, or they declined to be interviewed.</BLOCKQUOTE>

A month after the GAO issued its 1999 report, the first hint that squalene might be linked to Gulf War syndrome appeared in an article in New Scientist magazine.5 Robert Garry, a virologist at Tulane University, tested more than 400 Gulf War veterans for antibodies to squalene and found that 95 percent of those with GWS had high levels of squalene antibodies.
Garry also tested a pair of volunteers who had received experimental herpes vaccines containing squalene in trials conducted by the National Institutes of Health. Both had high levels of squalene antibodies and also suffered from GWS-type symptoms.
In February, the peer-reviewed journal Experimental and Molecular Pathology6 published a study written by Garry's team at Tulane University and Dr. Pamela Asa, an immunologist from Tennessee. Dr. Asa was one of the first health professionals to advance the theory that Gulf War syndrome might be an autoimmune disorder caused by experimental vaccinations.
The research included blinded and unblinded studies. In the blinded study, 56 Gulf War-era veterans and military personnel who were on active service in 1990-91 were tested for squalene. Of those 56, 38 had been deployed to the Persian Gulf and had GWS-type symptoms; 12 had been deployed but were healthy; and six had not been deployed but were nevertheless ill.
The researchers found that among the 38 ill veterans who had been deployed, 36 (94.7 percent) tested positive for squalene antibodies. None of the deployed healthy individuals, however, tested positive.
Furthermore, all six subjects who were ill, but had not been sent to the Gulf, also had squalene antibodies. While they did not serve in the war, they had received the same type and number of vaccinations given to Gulf War troops.
To see whether squalene antibodies might be a marker for other types of autoimmune diseases, the researchers also tested groups of patients with lupus and chronic fatigue syndrome, as well as a small sample from the general population. Only 15 percent of those with chronic fatigue tested positive for squalene; only 10 percent of those with lupus tested positive; and only five percent of the general population had squalene antibodies.
The Tulane study made no conclusion about whether Gulf War vaccines contained squalene, what may have produced the antibodies, or what role they play in Gulf War syndrome. Still, it is hoped that the research conducted by Garry and Asa will prompt others to investigate the role of vaccinations in Gulf War syndrome and the safety of vaccines that contain squalene.
"We don't know what caused the immune system to produce anti-squalene antibodies in the Gulf War veterans, but this study shows that the antibodies are indeed there," observed Dr. Russell Wilson, president of Autoimmune Technologies, which helped market the study. Dr. Wilson does not believe that the antibodies were the result of a reaction to squalene added to vaccines. "That possibility must still be formally ruled out,"7 he concluded.
Approximately 700,000 Americans served in the Gulf War between 1990-91. One hundred and forty-eight Americans were killed in action; 467 were wounded. The Department of Veterans Affairs estimates that as many as 100,000 veterans may be suffering from Gulf War syndrome or related symptoms, and that approximately 6,500 soldiers have died since the war's conclusion, including more than 1,300 soldiers between the ages of 18-24.8


  1. Hughes J. Scrutinizing squalene: government to review study linking gulf illness, antibodies. Associated Press, April 14, 2000.
  2. What is squalene? Associated Press, April 14, 2000.
  3. Rodriguez PM. The Gulf War mystery. Insight Magazine, September 8, 1997.
  4. Gulf War Illnesses. Questions about the Presence of Squalene Antibodies in Veterans Can Be Resolved. United States General Accounting Office, March 1999.
  5. Mackenzie D. Victims of vaccines. New Scientist April 10, 1999.
  6. Asa PB, Cao Y, Garry R. Antibodies to squalene in Gulf War syndrome. Experimental and Molecular Pathology February 2000;68(1):55-64.
  7. New antibodies discovered in Gulf War syndrome patients. AutoImmune Technologies (www.autoimmune.com ), January 31, 2000.
  8. Turner A. Death ruling raises issue of Gulf War ills. Houston Chronicle April 15, 2000.

مصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى Dingbat

descriptionمصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى Emptyرد: مصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى

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المصدر الخامس
Evidence as to the Role of Baxter in Producing and Releasing Pandemic Virus Material in Austria.

97. Baxter Pharmaceutical http://www.baxter.com/ has been chosen by the WHO to lead the efforts in finding a vaccine cure for the swine flu H1N1 virus.
98. This in spite of the fact that Baxter AG, headquartered in Vienna, and the Austrian subsidiary of the pharmaceutical company Baxter International, headquartered in Deerfield, IL, USA, sent vaccine material contaminated with deadly live H5N1 bird flu virus to 16 laboratories in four countries in winter 2009 before a technician caught the mistake. (See Attachment (A) for criminal charges filed at the Vienna City Prosecutor’s office on April 8th, now being investigated by the police).
99. According to Austrian Health Minister Alois St&ouml;ger , 72 kilograms of vaccine material was contaminated.
http://www.parlament.gv.at/PG/DE/XXIV/AB/AB_01457/fnameorig_158854.html
Parliamentary answers 1457/AB (XXIV. GP) May 20th, 2009,
Fragen 14 und 15:
Das für Forschungszwecke bestimmtes Material -72 kg waren als kontaminiert anzusehen - wurde in die Firma zurück geholt und kontrolliert vernichtet.“
100. It is still not clear how 72 kilograms of the world’s deadliest bioweapon can be sent by accident from a high biosecurity facilities, not irradiated and under a false label.
101. However, we know from Baxter itself that it produced the 72 kilograms contaminated material using a wild type live bird flu virus obtained from the WHO reference center.
http://www.promedmail.org/pls/otn/f?p=2400:1001:53103::NO::F2400_P1001_BACK_PAGE,F2400_P1001_PUB_MAIL_ID:10001,76322
A statement on behalf of Baxter
——————————-
I would like to provide the following update to a posting on ProMED dated 25 Feb 2009 (Avian influenza, accidental distribution - Czech Rep. ex Austria: RFI).
The H5N1 strain was the A/Vietnam/1203/2004 strain, received from a WHO reference centre. All information concerning this incident has been provided to the involved national authorities and appropriate international bodies such as ECDC and WHO.

Christopher Bona
Director,
Global BioScience Communications
Corporate
Communications
Baxter
International Inc.
One Baxter Parkway
Deerfield,
IL 60015
christopher_bona@baxter.com
102. Also, Baxter is the only flu vaccine manufacturer to work with wild type flu viruses, felt to be more dangerous than the altered and attenuated (weakened) viruses other manufacturers use.
http://chealth.canoe.ca/channel_health_news_details.asp?news_id=27436&news_channel_id=1020&channel_id=1020
103. The Austrian police have launched an investigation into the incident that almost triggered a global pandemic. The mixture of the deadly H5N1 virus with a mix of H3N2 seasonal flu viruses is classified as one of the most deadly bioweapons in the world with a mortality rate of 63 per cent.
104. So, with the Baxter incident in Austria, there is proof that Baxter not only created the disease producing microorganisms with help from WHO, but also distributed them in large quantities to trigger a pandemic, while positioning themselves to produce the vaccine allegedly to “protect” against the virus they created and released, but which,so it is alleged, is actually a disguised way of spreading the biological agent and creating a pandemic.
105. In criminal charges filed against Baxter on April 8th, 2009 at the Vienna City Prosecutor’s office, Landesgerichtstr 11, 1080 Vienna, Austria by Jane Burgermeister,a resident of Vienna, Austria, it was alleged that Baxter unlawfully, wilfully and knowingly, in the period between December 2008 and February 2009, employed manipulative and deceptive devices and contrivances in violation of national and international laws on the manufacturing, possession, release and dissemination of biological weapons of mass destruction and on organised crime, to manufacture and distribute a biological agent that is classified as a bioweapon among the population in order to profit from the pandemic.
106. First, Baxter manufactured influenza material contaminated with a bird flu virus in its biomedical research laboratories in Orth on the Danube in December 2008.
107. Baxter uses BSL 3 (Biosafety Level 3) precautions in its laboratories, a system for the safe-handling of toxic substances, which makes an accidental contamination of ordinary flu material with the dangerous bird flu virus virtually impossible.
108. The 72 kilograms of contaminated vaccine material contained a mixture of a seasonal H3N2 human influenza virus and the deadly bird flu H5N1 virus. By adding a virus of the type H5N1 to an ordinary flu virus of the type H3N2, The H5N1 virus is restricted in its human-to-human transmissibility, especially because it is less airborne. However, when it is combined with seasonal flu viruses, which are airborne and easily spread, a new bioweapon is created.
109. Second, Baxter distributed via Avir this contaminated vaccines using false concealment and a false label to 16 laboratories in Austria and in other countries at the end of January/beginning of February, potentially infecting at least 36-37 laboratory staff, who had had to be treated preventively for bird flu and ordinary flu in hospital.
110. A total of 18 laboratory staff belonging to Avir had to undergo preventative treatment for the bird flu and ordinary flu at the Otto Wagner Hospital in Vienna on February, 9th, 2009, because of their exposure as part of their work to the highly pathogenic bird flu virus.
111. This indicates that, in the opinion of medical experts, there was a risk that the staff of Avir had contracted bird flu, and, unknowingly, acted as carriers of a pandemic virus into the population of a densely built up Vienna city district and in winter time.
112. The material was only discovered when staff working for Biotest (in Konarovice in the Czech Republic), tested the vaccination on ferrets, who then died.
113. Biotest was supposed to test anti-flu vaccination that should serve Europeans during the next flu season, and the labels on the material sent to them from Baxter via Avir gave no indication of the lethal contents.
114. The 13 BioTest staff were treated with Tamiflu and were placed in quarantine for fear they had been contaminated with the bird flu virus, which is on the list of the possible biological weapons and one of the most dangerous biological agents on the Earth with more than 60% death rate.
115. Subsequently the same problem of the Baxter vaccine contamination with H5N1 was found in the laboratories in Slovenia, Austria and Germany, who had received the material from Baxter.
116. First the company Baxter evoked the ‘trade secret” and refused to explain how exactly how a Level 3 biological warfare pathogen found its way into H3N2 material, regardless whether or not this experimental vaccine material was ‘intended’ for eventual use in humans or not.
117. Baxter representatives have said that the material sent to the Czech republic, Austria, Slovenia and Germany was in fact a pure H5N1 sent by accident - maybe to mask the previous assumption, that it was in fact an ordinary flu vaccine, which was contaminated. It is still not clear whether it was in fact the pure H5N1 or contaminated vaccine.
118. The Austrian Health Minister Alois St&ouml;ger confirmed on May 20th 2009 that the 72 kilograms of contaminated vaccine material has been destroyed, but no information has been released as to the genetic sequences of the contaminated material or what Clade was Baxter’s H5N1 vaccine from, whether from Clade 1? Clade 2? Clade 3? Other?
119. Therefore, it is not possible to know whether H5N1 resembles the strains circulating in waterfowl.
Was the contaminated H5N1 strain genetically engineered? If so, by whom? Does the NS protein in Baxter’s H5N1 material contain polymorphisms which suppress human interferon production? Was Baxter’s H5N1 a full set of influenza genes? Or was it just the hemaglutanin and neuraminidase? Did Baxter’s H5N1 contain a poly-basic cleavage
site on the Hemaglutanin surface protein? Why were the samples of experimental vaccine material not irradiated?
120. Coinfection of H5N1 and H3N2 would not produce simple reassortment but a complex in vivo recombination of many competing strains in the infected host.
121. Furthermore the complex coinfection of H5N1 and H3N2 in a human would produce natural selection pressure for maximum virulence.
122. The book “Evolutionary Dynamics” suggest that viral coinfection selects for both maximum virulence and infectivity.

descriptionمصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى Emptyرد: مصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى

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القاهرة: اثار إصرار مسئولي وزارة الصحة المصرية على عدم مسئوليتهم تجاه اي آثار جانبية قد تظهر نتيجة تناول المصل الجديد لفيروس إنفلونزا الخنازير، خوف وذعر المواطنين المصريين خاصة الذين يعتزمون أداء فريضة الحج هذا العام، وذلك في ظل إعلان السعودية بأنها سوف تسمح بأداء فريضة الحج فقط لمن حصل علي المصل الخاص بالمرض.
وكان الدكتور حاتم الجبلي وزير الصحة المصري أعلن في أكثر من مناسبة عدم مسئوليته من مخاطر استيراد لقاحات وأمصال ضد إنفلونزا الخنازير، مؤكدا ان وزارته غير مسئولة عن الآثار الجانبية التي قد تحدث للأشخاص الذين سوف يتعاطون المصل الجديد الخاص بالمرض والذي سيتم توريده لمصر خلال منتصف شهر أكتوبر الحالي.

وأضاف الجبلي أن الشركة المنتجة لهذا المصل طلبت أخذ إقرار علي كل من يحصل علي المصل الجديد لعدم تأكدها من آثاره الجانبية.
وحسبما ذكرت جريدة "الوفد" المصرية المعارضة، أكد الدكتور محمد حسن خليل عضو "الدفاع عن الحق في الصحة" أن العالم في ورطة لأن أي مصل جديد لابد أن يمر بثلاث مراحل هي: الدراسة علي الحيوانات ثم المتطوعين ثم مرحلة الدراسة البدائية علي المرضي، لكننا في سباق مع الزمن إذا تمت مراجعة المصل خلال 6 شهور سيكون الوباء قد انتشر ويصبح المصل لا فائدة منه.
اضاف: الشركات تأخذ إقراراً علي كل من يحصل علي المصل بمسئوليته الشخصية عن الأضرار الجانبية حتي تخلي مسئوليتها ولا يعود عليها أحد بدعاوي وقضايا، وبالتالي لم يعد أمامنا سوي الاختيار بين نارين ألا نأخذ المصل ونصبح معرضين للإصابة بالمرض أو نأخذ المصل مع احتمال وجود مخاطر وهذا واقع فيه العالم كله.
من جانبه، قال الدكتور حمدي السيد نقيب الأطباء المصريين أن المشكلة أن السعودية أصرت علي تطعيم إجباري للحجاج والمصل لن يبدأ استخدامه إجبارياً إلا السنة القادمة بعد تجربته وخلوه من الآثار الجانبية.
وأضاف: تصريحات الجبلي خاصة بالأفراد الواجب عليهم أخذ التطعيم مبكراً قبل أن يكون هناك وقت كاف للاطمئنان من خلوه من الآثار الجانبية.
وأشار السيد الى ان هناك اطمئناناً نسبياً من قبل المنظمات الدولية تجاه المصل وأنا ما يشاع من تحذيرات مضادة له ليس صحيحاً لأنه لم يستخدم حتي الآن.
بدوره، أكد الدكتور عبدالمنعم عبيد وكيل وزارة الصحة سابقاً أنه لا يجب أن ننتظر حتي تحدث الأعراض الجانبية بل ينبغي الاستعداد السريع من مراكز البحث وكليات الطب في مصر لإجراء بحوث علي هذا المصل بمجرد الحصول عليه ولا مانع من المشاركة مع الهيئات العلمية لإخضاع المصل للبحث العلمي.
وأضاف عبيد لابد من توقع الآثار الجانبية للمصل ومحاولة معالجتها مبكراً، وأشار إلي أن كل الأدوية بصفة عامة لها آثار جانبية والمهم ألا تكون هذه الآثار مساوية لخطورة المرض فيصبح المصل فائدته أقل من عدمه.
وطالب عبيد إذا كان من الضروري أخذ هذه الأمصال فيجب المتابعة الكاملة لكل من أخذ هذه الأمصال في الخارج والمشاركة في البحوث من الآن وأن نقيم مشروعاً لإنتاج أمصالنا بأنفسنا.
من ناحيته، أكد مصطفي أورخان مدير مركز العلوم للمصل واللقاح أنه لا يجب علينا إعطاء تطعيم للمواطنين قبل أن تنتهي الشركة المنتجة من جميع التجارب الإكلينيكية ومعرفة الآثار الجانبية للمصل لأنه عند طرح أي لقاح لابد أن يرافقه نشره بآثاره الجانبية وليس عقلاً الأخذ من شركة لم تنته من دراساتها وأقول: أنا غير مسئول، وكأنني أقوم بتجارب علي البشر.
وأضاف أورخان أن هذه الإنفلونزا ليست مخيفة لدرجة أخذ مصل بدون معرفة آثاره الجانبية، فهي مثل الإنفلونزا العادية يغشي منها علي ضعاف الصحة ومرضي القلب والسكر والحساسية الصدرية.
قلق دولي
كانت منظمة "هيلث كروسيدرز"، المعنية بمحاربة أخطاء الممارسات الطبية لشركات الأدوية العالمية، شككت في أهداف برامج التطعيم ضد الفيروس، لافتة إلى أن الفيروس ربما لا يوجد من الأساس، أوأنه تم تخليقه مخبرياً لتنفيذ أجندة سرية عالمية للسيطرة على تزايد أعداد سكان الكرة الأرضية.
وجاء تشكيك المنظمة في إطار حملة يشنها أطباء وصيادلة وأخصائيون في الكيمياء الحيوية ضد لقاح الفيروس، الذي عهدت بإنتاجه منظمة الصحة العالمية إلى ثلاث شركات دوائية هي: "نوفارتس"، "وروشه"، و"باكستر"، ومن المتوقع أن تنتج كميات كبيرة منه في غضون الأسابيع المقبلة.
وانضمت إلى الحملة صحف ومجلات عالمية، سعت إلى التشكيك في أهداف الشركات العالمية، في حين قابلت المنظمة كل ذلك بمصل أنفلوانزا الخنازير طلع مضروب و عبارة عن سلاح بيولوجى 439258 كامل، ولاسيما "التاريخ الأسود" لشركة "باكستر".
كما يأتي تشكيك المنظمة بعد أيام قليلة من القنبلة المدوية التي فجرتها صحفية نمساوية متخصصة في الشؤون العلمية والتي قالت ان ما بات يعرف بفيروس أنفلونزا الخنازير، الذي اجتاح بلدان العالم في ظرف قياسي، ما هو إلا مؤامرة يقودها سياسيون ورجال مال وشركات لصناعة الأدوية في الولايات المتحدة الأمريكية.
وحسبما ذكر موقع "الامارات اليوم" الالكتروني، تساءل خبير الأمصال الدولي الدكتور أيه تروت، والذي يقود حملة دولية لمعارضة برامج التطعيم الإجباري، عن الكيفية التي تمكّن بها الفيروس من تغيير تركيبه الجيني ليضم مكونات من فيروس أنفلونزا الطيور "إتش5 إن1"، وفيروس أنفلونزا الخنازير، بالإضافة إلى المكونات البشرية لفيروس الأنفلونزا العادية "إتش3 إن1"، مشيراً إلى أن هذا التحوّر لا يمكن أن يتم بصورة عادية في الطبيعة، ويحتاج إلى تجارب مخبرية معقدة لحدوثه.
وقال تروت إنه تلقى نسخة من خريطة التركيب الجيني للفيروس، التي تم رسمها باستخدام برمجيات كمبيوتر متطوّرة، وأظهرت أن ست سلالات، من بين ثماني سلالات رصدها، تعرضت لنحو 66 تحوّراً جينياً مخبرياً، لتغيير التركيب الكروموسومي للفيروس حتى يتمكن من إصابة بلازما الخلايا البشرية.
واعتبر تروت أنه "لا توجد أدلة طبية تثبت أن الفيروس له فاعلية تبرر تطعيم مليار شخص في مختلف أنحاء العالم بصورة متزامنة ضد فيروس لا تزيد خطورته على خطورة البرد العادي".
ولفت إلى أن "51 دراسة مخبرية أُجريت على نحو 294 ألف طفل في مختلف أنحاء العالم أثبتت أن المصل ليس له أي تأثير في الأطفال الذين تتراوح أعمارهم بين سنتين وست سنوات"، مشيراً إلى أن "المصل يحمل أخطاراً شديدة على الأطفال المصابين بالربو والأزمات التنفسية".
وحذّر تروت من الأخطار التي تنطوي عليها برامج الأمصال الإجبارية التي تشمل فشل الأعضاء والخلايا، ومرض التوحّد لدى الأطفال، والتهاب المفاصل الروماتيزمي، وفقدان الذاكرة، والحكة الجلدية، والإجهاد المزمن، وتساقط الشعر.

أنفلونزا الخنازير.. مؤامرة أم وباء؟



مع زيادة المخاوف من تحول مرض أنفلونزا الخنازير لوباء غير قابل للعلاج مع حلول فصل الخريف، ومع الاتهامات التي تطول سياسيين ورجال مال وشركات لصناعة الأدوية في الولايات المتحدة الأمريكية بأنهم يروِّجون لمرض غير موجود لكسب المال وأيضًا لاستخدامه كعامل ضغط سياسي، بين هذا وذاك زادت حيرة شعوب العالم بين الاهتمام من أجل إيقاف المرض أو ترك الأمر لرد الصاع الصاعين على الشركات المتآمرة للترويج له وإخراجها من الأمر بلا مكاسب.

ففي الوقت الذي تنادي فيه الأمم المتحدة بضرورة الاهتمام بالحصول على مصل لقاح المرض، ظهر العديد من العلماء والخبراء والمحللين الذين يؤكدون أن الحديث عن أنفلونزا الخنازير ما هو إلا استغلال لفقراء العالم، وأن أنفلونزا الخنازير ليست إلا كـ "موَّال" آخر من المحاولة لنشر الذعر والفوضى بين السكان والمحاولة لإجبارهم على التطعيم، الذي ينبغي على كل شخص أن يعلم باحتوائه على الزئبق الذي يدمر الجهاز العصبي ويسبب الإصابة بالسرطان.

وفي الوقت الذي تسعى فيه دول العالم الثالث الحصول على لقاح المرض بصعوبة، فإن تقديرات منظمة الصحة العالمية تشير إلى أن قدرة العالم الإنتاجية من مصل أنفلونزا الخنازير ستناهز في أفضل الأحوال خمسة مليارات جرعة في العام تقريبًا.
مؤامرة أمريكية يهودية



يبدو أن القضية لا تقف عند حد انتشار مرض ومحاولة صده؛ إذ أن الصحفية النمساوية يان بيرجرمايستر اتهمت منظمة الصحة العالمية، وهيئة الأمم المتحدة، والرئيس الأمريكي باراك أوباما، ومجموعة من اللوبي اليهودي المسيطر على أكبر البنوك العالمية، وهم ديفيد روتشيلد، وديفيد روكفيلر، وجورج سوروس، بالتحضير لارتكاب إبادة جماعية، وذلك في شكوى أودعتها لدى مكتب التحقيقات الفدرالي الأمريكي (إف بي آي)، حسبما ذكرت جريدة "الشروق" الجزائرية.

وتزامنت الشكوى الجديدة مع شكاوى أخرى رُفعت في إبريل الماضي ضد شركات الأدوية "باكستر" و"أفير جرين هيلز وتكنولوجي"، والتي ترى الصحفية أنها مسئولة عن إنتاج لقاح ضد مرض أنفلونزا الطيور، من شأنه أن يتسبب في حدوث وباء عالمي، من أجل البحث عن الثراء في نفس الوقت.

وترفع الصحفية في شكواها جملة من المبررات تراها موضوعية، تتمثل في كون المتهمين ارتكبوا ما أسمته "الإرهاب البيولوجي"، مما دفعها لاعتبارهم "يشكلون جزءًا من "عصابة دولية" تمتهن الأعمال الإجرامية، من خلال إنتاج وتطوير وتخزين اللقاح الموجَّه ضد أنفلونزا، بغرض استخدامه كـ "أسلحة بيولوجية" للقضاء على سكان الكرة الأرضية من أجل تحقيق أرباح مادية".

واعتبرت بيرجر مايستر "أنفلونزا الخنازير" مجرد "ذريعة"، واتهمت من أوردت أسماءهم في الشكوى، بالتآمر والتحضير للقتل الجماعي لسكان الأرض، من خلال فرض التطعيم الإجباري على البشر، على غرار ما يحدث في الولايات الأمريكية، انطلاقًا من يقينها بأن "فرض هذه اللقاحات بشكل متعمد على البشر، يتسبب في أمراض قاتلة"، مما دفعها إلى تكييف هذا الفعل على أنه انتهاك مباشر لحقوق الإنسان، والشروع في استخدام "أسلحة البيوتكنولوجية".

ومن هذا المنطلق ترى يان بيرجرمايستر في عريضة الشكوى، أن مثل هذه الأفعال لا يمكن تصنيفها إلا في خانة "الإرهاب والخيانة العظمى".

وتحوَّل موضوع هذه الشكوى، إلى قضية حقيقية رفعتها منظمات حقوقية ومهنية في مختلف دول العالم، وفي مقدمتها "جمعية آس أو آس عدالة وحقوق الإنسان" الفرنسية، التي سارعت بدورها إلى المطالبة بفتح "تحقيق جنائي بهدف منع وقوع أزمة صحية خطيرة". وشددت على ضرورة وضع حد للتطعيم واسع النطاق المخطط للشروع فيه بداية من فصل الخريف الجاري.

ووفقًا لمتخصص ألماني بأمراض الرئة فإن اللقاح أو التطعيم يحتوي على خلايا سرطانية من الحيوانات، كما تم إثبات أن لقاح أنفلونزا الخنازير الذي يُتوقع طرحه في شهر أكتوبر يزيد من خطر الإصابة بالسرطان.

وقد أضاف الدكتور الألماني د. ودارج: "إنها تجارة كبيرة للصناعة الدوائية، فأنفلونزا الخنازير لا تختلف كثيرًا عن الأنفلونزا العادية، وعلى العكس تمامًا، إذا نظرت إلى عدد الحالات فإنها لا تساوي شيئًا مقارنة بموسم الأنفلونزا العادية"، ولا تسبب إلا العوارض العادية للأنفلونزا، ولا تستلزم إلا بضعة أيام من الراحة.

ويقول الباحث د. بلايلوك: إن لقاح أنفلونزا الخنازير لشركة باكستر، الذي يسمى Celvapan ، يحتوي على خلايا من القردة الأفريقية الخضراء التي تم تورطها من قبل بنقل العديد من لقاحات ملوثة بفايروسات أخرى مثل فايروس HIV ، بالإضافة لأنها تسبب العديد من الأمراض السرطانية.

في هذه الأثناء، قال عدد من أخصائيِّي علم الفيروسات: "إن برنامج التطعيم الإجباري ضد مرض أنفلونزا الخنازير عندما يُنظر إليه يتأكد أن فيروسH1N1 هو المسبب للمرض من الفيروسات المركبة جينيًا وأنه تم إطلاقه عن عمد لتبرير التطعيم.

ويتساءلون : من أين حصل هذا الفيروس على كل هذه الجينات؟!.. ويقولون: إن التحليل الدقيق للفيروس يكشف عن أن الجينات الأصلية للفيروس هي نفسها التي كانت في الفيروس الوبائي الذي انتشر عام 1918م، بالإضافة إلى جينات من فيروس أنفلونزا الطيورH5N1 ، وأخرى من سلالتين جديدتين لفيروس H3N2 ، وتشير كل الدلائل إلى أن أنفلونزا الخنازير هو بالفعل فيروس مركب ومصنَّع وراثيًا.
مؤامرة ضد فقراء العالم



"ما يحدث ليس سوى مؤامرة لاستغلال فقراء العالم".. بهذه الكلمات فسَّر عالم الاجتماع السويسري يان تسيجلر، المستشار في مجلس حقوق الإنسان التابع للأمم المتحدة، اهتمام الولايات المتحدة ومعاونيها من اللوبي اليهودي بخطورة انتشار المرض ومحاولة نشر المصل الخاص بصده وتوقيفه.

ويقول تسيجلر: "إن أنفلونزا الخنازير تُستغل على حساب فقراء العالم، وأنه بينما يستنفر الإعلام من أجل 45 شخصًا توفوا بالفيروس خلال الأسابيع الأولى منه فإن مائة ألف شخص يموتون يوميًا من الجوع وتداعياته المباشرة".

وأضاف أنه من "التبجح" أن يظهر مسئول من منظمة الصحة العالمية أمام وسائل الإعلام المختلفة قائلاً: إن فيروس إتش 1 إن 1 يهدد ملياري إنسان، مشيرًا إلى أن مسئولي المنظمة يتعاملون "بشكل غير مسئول" مع التصريحات حول خطورة الفيروس.

وتابع أنه لا ينكر أن منظمة الصحة العالمية ملزَمة بمراقبة الصحة العالمية "ولكن عليها ألا تبالغ في تصوير الأشياء"، وأن تعطي كل حدث قدره الضروري من الاهتمام، وألا تُدخل الخوف في قلوب الناس؛ لأنها تعرف أكثر مما يعرفه الناس من الحقائق عن المرض.

وأوضح أن نحو 953 مليون إنسان يعانون بشكل دائم من نقص التغذية، كما أن العالم يشهد وفاة طفل تحت سن عشر سنوات كل خمس ثوان، مضيفًا: "نحن نقبل ذلك وكأنه أمر طبيعي للغاية".

وأكد أنه "ليست هناك مؤتمرات صحافية عن هؤلاء الناس ولا استنفار دولي من أجلهم، في حين أن منظمة الصحة تدعو وسائل الإعلام يوميًّا لمقرها الرئيس في جنيف لإطلاعها على آخر المستجدات الخاصة بأنفلونزا الخنازير". وقال تسيجلر: "عندما يتعلق الأمر بالكبار فإن الضمير العالمي يهتز، إن هذا يدل على العمى الذي أصابنا وعلى برودة عواطفنا المتدنية للغاية وتهكمنا من الواقع".

كما يرى البروفيسور السويسري أنه من المثير للدهشة أن يتم توجيه الإعلام في التعامل مع أزمة الخنازير، وقال: إنه لن يستغرب لو تبيَّن فيما بعد أن شركات الأدوية الكبرى هي الممسكة بدفة هذا التوجيه الإعلامي في ضوء الركود الذي أصابها جراء الأزمة المالية والاقتصادية العالمية.

وأضاف تسيجلر أن أنفلونزا الطيور عادت على شركات الأدوية العملاقة بالمليارات من بيع الأدوية بعد "تكدس" براءات الاختراع التي تمتلكها والخاصة بالعقاقير المضادة للأنفلونزا.
خطة لتدميرنا



وتأكيدًا لما سبق، فإنه صدرت تقارير إعلامية عربية تؤكد أن لقاح أنفلونزا الخنازير الذي تعمل شركات الأدوية الكبرى على قدم وساق لإنتاج كميات كبيرة منها خلال أشهر تكفي لتطعيم سكان العالم، ما هو إلا خطة لتدمير فكرنا و صحتنا وقدراتنا الجنسية عبر حملة تطعيم عالمية واسعة وذلك باستخدام مواد إضافية خاصة تسمى المواد المساعدة، الهدف النظري من إضافتها هو زيادة قوة التطعيم.

وتضيف التقارير أنه على الرغم من أن هناك العديد من المواد المساعدة الآمنة التي يمكن أن تضاف للتطعيم، فقد قرروا إضافة مادة السكوالين، وهي مادة هامة ومنتشرة بشكل كبير في الجسم ويستمدها من الغذاء , إنها المادة الأساسية التي ينتج منها الجسم العديد من الزيوت والأحماض الدهنية المختلفة المهمة لأداء الوظائف الحيوية الهامة في مختلف أعضاء الجسم، وهي المادة الأم التي تنتج منها كافة الهرمونات الجنسية، سواءً في الرجل أو المرأة، وبالتالي المسئولة عن خصوبة الذكور والإناث، كما أنها مهمة لخلايا المخ لتقوم بأداء وظائفها بشكل صحيح، وأيضًا تلعب دورًا مهمًا في حماية الخلايا من الشيخوخة والطفرات الجينية، وقد ثبت أن حقن السكوالين كمادة مساعدة مع التطعيمات يسفر عن حدوث استجابة مناعية مرضية عامة ومزمنة في الجسم بأكمله ضد مادة السكوالين.

فيما تؤكد التقارير أن الأعداد المهولة التي تذكرها منظمة الصحة العالمية WHO حول إصابات أنفلونزا الخنازير ليست دقيقة.. فالحقيقة شيء آخر تمامًا، وهنا يبرز السؤال.. لماذا كل ذلك؟

وتأتي الإجابة، لأن بعض الدول مثل بريطانيا تسجل الآن جميع حالات الأنفلونزا على أنها أنفلونزا خنازير.. وذلك اعتمادًا على استفتاءات تقوم بها على الانترنت لا أكثر!!! فلا عجب إن كانت أغلب هذه الحالات مجرد أنفلونزا عادية.

وتكشف تقارير صحية عالمية أن هناك مؤامرة تقف وراءها دول بعينها تخطط لتقليل الانفجار السكاني المتزايد في العالم بطريقة جماعية وسريعة، كما يريدون الوصول إلى داخل الجسم البشري للتحكم فيه عقليًّا وعاطفيًّا وجسديًّا... وهذا ما يبرر هذا الانفجار الهائل للتطعيمات للأطفال في السنوات الأخيرة.

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