H1N1 Hoax - Interesting Facts

This is what WHO said on Monday, May 11th 2009 - 5:15 am UTC

"H5N1 taught the world to expect a pandemic, and to plan for this event,. The world is better prepared for an influenza pandemic than at any time in history, thanks, in part, to your vigilance and diligence. Years of alert and expectation mean that most countries now have preparedness plans. Vaccine manufacturing capacity has increased sharply. Large stocks of antiviral drugs have been produced and procured. Right now, treatment courses from the WHO stockpile are being shipped to more than 70 countries in the developing world. We are, right now, gaining experience in the use of non-medical interventions, such as social distancing, to delay spread of the H1N1 virus. WHO and its regional offices have tested their alert and response plans, also in operational exercises. We are prepared." said Dr. Margaret Chan , WHO Director-General.

This is what I ask: Do you believe what Dr. Margaret Chan said?

This is the real fact, a news report on Thursday, April 30th 2009 - 12:31 am UTC

Vaccine against H1N1 virus could be ready for September

United States health officials said Wednesday that a vaccine against the H1N1 virus, also known as the swine flu, could be ready for human use by early September. The announcement was made at a joint press conference held by the Department of Health and Human Services, the Centers for Disease Control, and the Food and Drug Administration.

This is what I realized: Dr. Margaret Chan is a big time bullshitter! She is expecting governments from all over the world to buy a non-exist vaccine.

This is what scientists believe:

The top official warned that scientists did not believe that vaccines against seasonal influenza, which kills 36.000 people each year in the US, would protect against the "novel" virus now making headlines.

"We don't expect there to be protection. Based on the laboratory testing that's been done so far, we don't expect there to be cross-protection" said Anne Schuchat, acting deputy director for science and public health program at the US Centers for Disease Control and Prevention before US senators

Asked why experts worried about swine flu given the annual havoc wreaked by regular, seasonal influenza, Schuchat said "we are dealing with a novel virus" and that the general population had not built up resistance to the illness.

"It's a virus that hasn't been around before," she said. "The general population doesn't have immunity to this virus. With seasonal flu, a good proportion of the population has some immunity."

(source: http://en.mercopress.com/2009/05/11/world-is-better-prepared-for-influenza-pandemic-says-dr.-chan)

This is what I ask: Does it matter?

“So far, most of the infections are relatively mild. We’re hoping it’s going to stay that way, but we don’t really know. With the large number of people who are predicted to become infected, the number of serious health complications and even deaths could soar.” said Robert Belshe, M.D., director of the Center for Vaccine Development at Saint Louis University School of Medicine and a co- investigator for several of the national research studies.

Evidence mounted through May 2009 that the symptoms were milder than health officials initially feared. As of May 27, 2009, most of the 342 confirmed cases in New York City had been mild and there had been only 23 confirmed deaths from the virus. Similarly, Japan has reported 1,048, mostly mild flu cases, and no deaths, with the government reopening schools as of May 23, stating that the "virus should be considered more like a seasonal flu." In Mexico, where the outbreak began in April, Mexico City officials lowered their swine flu alert level as no new cases had been reported for a week.

"New York City officials struggle for balanced response to swine flu". Los Angeles Times. 21 May 2009.
"Spread of Swine Flu Puts Japan in Crisis Mode". New York Times. 21 May 2009.

"Mexico City ends swine flu alert, no cases in week". Associated Press. 21 May 2009.

This is what I know: The vaccine is not ready.

" This round of research studies will recruit thousands of healthy volunteers nationally to test the safety and measure the body’s immune response to an investigational H1N1 flu vaccine. They will include adult, pediatric and elderly volunteers.

Eight Vaccine and Treatment Evaluation Units (VTEUs) which are funded by the National Institute of Allergy and Infectious Diseases (NIAID), part of the NIH, will participate in these trials. In addition to the VTEU at Saint Louis University, the VTEU sites are Baylor College of Medicine; Emory University; University of Maryland School of Medicine in Baltimore; Children’s Hospital Medical Center in Cincinnati; Group Health Cooperative in Seattle; University of Iowa; and Vanderbilt University. They will be joined by Duke University Medical Center and Children’s Mercy Hospital in Kansas City. " said Sharon Frey, M.D., professor of infectious diseases at Saint Louis University School of Medicine and lead investigator for one of the national research studies.

My conclusion: The governments are buying untested vaccines based on fear mongering which scientists are not sure whether it is effective or not.

Want to know what non-medical expert said about H1N1.

A market analysis make the following comment:

It may be a bad time to be vulnerable to the flu, but it's a good time to be a vaccine maker. Glaxo, for example, could rake in $2.1 billion in sales next year on its H1N1 vaccine.

Know how much monies drug company is making on unproven vaccine?

The drugs giant has already taken 128m orders for its Relenza treatment in deals worth approximately £600m.

As the disease gathers pace, analysts forecast windfall orders for Glaxo's H1N1 swine flu vaccine, which they expect to generate at least £1.3bn in sales next year.

It is thought that chief executive Andrew Witty will comment on progress in developing the vaccine and sales of Relenza when Glaxo announces its quarterly results on Wednesday.

The company is expected to post a 10pc increase in earnings from sales up 14pc, boosted by the effect of the weak pound.

If you still do not understand why all the fear mongering and spin doctors are all out to create the media hype about H1N1.Take a look at this article:

The U.S. government and soon here in Canada, is about to unleash a sweeping new vaccination program that claims to protect people from swine flu. The vaccines, which are of course completely useless against any mutated strain of the H1N1 influenza virus, are nevertheless quite useful at suppressing the immune function of those who receive them. Well-designed medical studies conducted over the years have consistently shown that the people who catch the flu (influenza) with the greatest frequency are precisely those who get the most flu shots. The answer, of course, is that swine flu vaccines have nothing to do with public health and everything to do with generating billions of dollars in profits for Big Pharma. For the drug companies to rake in all this money manufacturing vaccines, they obviously have to give the shots to somebody — just to create the illusion that something productive might be going on in order to justify the government expenditures. It’s a lot like war budgets: You gotta drop bombs on somebody in order to justify making new ones. So the vaccines are dropping little viral bombs on precisely those citizens least able to fend for themselves: Children, pregnant women, senile seniors and adults suffering from chronic disease… these are the new “targets” of the government’s mass vaccination program. One last item worth mentioning. Take A Look.

Meanwhile, the pharmaceutical factories are churning out huge doses of the swine flu vaccine: 100 million doses will reportedly be available for injection into victims by mid-October.

Curiously, one of the companies being contracted to manufacture this vaccine is Baxter International, the very same company, caught late last year inserting live influenza viruses into vaccine materials that was distributed to 18 countries. Apparently, this company has already perfected the techniques for infecting vaccines with live viruses, and now the U.S. government has contracted with Baxter to help manufacture hundreds of millions of doses of swine flu vaccines to be injected into infants, pregnant women and chronically diseased adults. So……………………….for those that believe the flu shot is a good thing, you just keep rolling up your sleeve and I will stick to the good old fashioned natural medicine of yesteryear that I know of and that has proven results with no side effects or deadly long range effects.

If you still not convince by my write-up, please read this:

Fast-tracked Swine Flu Vaccine under Fire

The vaccines far more deadly than the swine flu; mass vaccinations a recipe for disaster Dr. Mae-Wan Ho and Prof. Joe Cummins

This report has been submitted to Sir Liam Donaldson, Chief Medical Officer of the UK, and to the US Food and Drugs Administration

Please circulate widely, with all the hyperlinks included, to your elected representatives, wherever you are

A swine flu outbreak occurred in Mexico and the United States in April 2009 and spread rapidly around the world by human-to human transmission. The new type A H1N1 influenza virus is unlike any that had been previously isolated [1, 2], judging from the first data released in May. It is a messy combination of sequences from bird, human and swine flu virus lineages from North America and Eurasia. A senior virologist based in Canberra, Australia, told the press he thought that the virus could have been created in the laboratory and released by accident [3]. Some even suggest it was made intentionally as a bioweapon [4], while others blame the intensive livestock industry and extensive trafficking of love animals over long distances, which provide plenty of opportunity for generating exotic recombinants [5]. But what worries the public most is the mass vaccination programmes governments are putting in place to combat the emerging pandemic, which could well be worse than the pandemic itself.

Watchdog opposes fast-track vaccine for school children

The US government is intending to vaccinate all children in September when school re-opens, and the country’s vaccine watchdog National Vaccine Information Center (NVIC) has called on the Obama Administration and all state Governors to provide evidence that the move is [6] “necessary and safe”, demanding “strong mechanisms for vaccine safety screening, recording, monitoring, reporting and vaccine injury compensation.”

The US Departments of Health and Homeland Security had declared a national public health emergency in April soon after the swine flu outbreak. As a result, some schools were closed, people quarantined, and drug companies were given contracts worth $7billon to make vaccines that are being fast tracked by the Food and Drugs Administration [7]. That means they will only be tested for a few weeks on several hundred children and adult volunteers before being given to all school children this fall.

Furthermore, under federal legislation passed by Congress since 2001, an Emergency Use Authorization allows drug companies, health officials and anyone administering experimental vaccines to Americans during a declared public health emergency to be protected from liability if people get injured. US Secretary of Health and Human Services Kathleen Sebelius has granted vaccine makers total legal immunity from any lawsuits that may result from any new swine flu vaccine. And some states may make the vaccination mandatory by law.

The NVIC is asking whether the states are prepared to obey vaccine safety provisions in the 1986 National Childhood Vaccine Injury Act, which include: 1. Giving parents written information about vaccine benefits and risks before children are vaccinated; 2. Keeping a record of which vaccines the children get, including the manufacturer’s name and lot number; 3. Recording which vaccines were given in the child’s medical record; and 4. Recording serious health problems that develop after vaccination in the child’s medical record and immediately making a report to the federal Vaccine Adverse Event Reporting System.

NVIC also wants to know if the states are prepared to provide financial compensation to children injured by the swine flu vaccines, whether parents will be given “complete, truthful information about swine flu vaccine risks”, and have the right to say “no” to vaccination.

Co-founder and president of NVIC Barbara Loe Fisher said [6]: “Parents and legislators should be asking themselves right now: Why are children the first to get experimental swine flu vaccines? Are schools equipped to get signed informed consent from parents before vaccination, keep accurate vaccination records and screen out children biologically at high risk for suffering vaccine reactions? Will people giving these vaccines know how to monitor children afterwards and immediately record, report and treat serious health problems that develop? And will states have the financial resources to compensate children who are injured?”

WHO and mass vaccination fever

The mass vaccination order has come from the World Health Organization (WHO) [8]. In early July 2009, a group of vaccination experts concluded that the pandemic is unstoppable, and Marie-Paul Kieny, WHO director on vaccine research said all nations will need access to vaccines, and that a vaccine should be available as early as September.

Critics point out that the ‘vaccination experts’ are dominated by the vaccine makers standing to gain from the enormously lucrative vaccine and antiviral contracts awarded by governments. But the decisive argument against mass vaccinations is that flu shots simply don’t work and are dangerous [9].

Flu shots ineffective and increase risks of asthma

There are widely acknowledged reasons why flu vaccines won’t work, as already pointed out with regard to the much touted vaccines against the ‘pandemic bird flu’ that has yet to materialize [10] (How to Stop Bird Flu Instead, SiS 35). The flu virus changes quickly - even without the help of genetic engineering in the laboratory, and especially with the help of the intensive livestock industry - whereas the vaccines target specific strains. Furthermore, flu vaccination does not give permanent protection, and must be repeated annually; the vaccines are difficult to mass-produce, and some strains won’t grow at all under laboratory conditions.

Numerous studies have documented that flu shots give little or no protection against infection and illness, and there is no reason to believe that swine flu vaccines will be different.

A review of 51 separate studies in 2006 concluded that flu vaccines worked no better than a placebo in 260 000 children ranging in age from six months to 23 months [11]. A report published in 2008 found flu vaccines in young children made no difference in the number of flu-related doctor and hospital visits [12].

On the other hand, a study of 800 children with asthma found that those receiving a flu vaccine had a significantly increased risk of asthma-related doctor and emergency room visits [13]; the odds ratios were 3.4 and 1.9 respectively. This was confirmed in a report published in 2009, which showed children with asthma who received FluMist had a 3-fold increased risk of hospitalization [14]

Flu vaccines are equally useless for adults, including the elderly, giving little or no protection against infection or illnesses including pneumonia (see [9]).

Toxic adjuvants in flu vaccines

Vaccines themselves can be dangerous, especially live, attenuated viral vaccines or the new recombinant nucleic acid vaccines [10], they have the potential to generate virulent viruses by recombination and the recombinant nucleic acids could cause autoimmune diseases.

A further major source of toxicity in the case of the flu vaccines are the adjuvants, substances added in order to boost the immunogenicity of the vaccines. There is a large literature on the toxicities of adjuvants. Most flu vaccines contain dangerous levels of mercury in the form of thimerosal, a deadly preservative 50 times more toxic than mercury itself [9]. At high enough doses, it can cause long-term immune, sensory, neurological, motor, and behavioural dysfunctions. Also associated with mercury poisoning are autism, attention deficit disorder, multiple sclerosis, and speech and language deficiencies. The Institute of Medicine has warned that infants, children, and pregnant women should not be injected with thimerosal, yet the majority of flu shots contain 25 micrograms of it.

Another common adjuvant is alum or aluminium hydroxide, which can cause vaccine allergy, anaphylaxis, and macrophage myofascitis, a chronic inflammation syndrome, In cats, alum also gives rise to fibrosarcomas at the site of injection [15]. Numerous new adjuvants are no better, and could be worse. According to a recent review in a science and business pharmaceutical publication [15], most newer adjuvants including MF59, ISCOMS, QS21, AS02, and AS04 have “substantially higher local reactogenicity and systemic toxicity than alum.”

Current status of swine flu vaccines

Five different companies have been contracted to produce vaccines worldwide: Baxter International, GlaxoSmithKline, Novartis and Sanofi-Aventis and AstroZeneca [16]. Already stretched beyond capacity, there is every intention to make smaller vaccine doses go further with a range of new adjuvants [17], with the blessing of the WHO (see later).

Flu vaccines are traditionally produced from non-virulent (attenuated or weakened) influenza viruses (see Box for a description of the viruses). To be effective, the genes of the non- virulent virus used must match those of the viral strain spreading in the population. Activation of the immune system by exposure to the non pathogenic form of the circulating pathogenic strain leads to the production of antibodies that will confer protection against the pathogenic strain. Producing the non-virulent virus involves first identifying and then recreating the subtypes of two of the virus’s surface proteins, haemagglutinin (H) and neuraminidase (N), which determine the strain’s virulence and ability to spread, and are also the target proteins for vaccine production.Influenza viruses

There are 3 types of influenza viruses, A, B and C. The influenza A type virus is the main one that cause diseases in birds and mammals. Its genome consists of 8 segments of RNA coding for 11 proteins, and the viruses are further classified by subtype on the basis of the two main surface glycoproteins (proteins with complex carbohydrate side chains): haemagglutinin (H) and neuraminidase (N) [18]. The segmented genome enables the virus to’ reassort’ (shuffle) segments as well as recombine within segments, thereby greatly increasing the rate of evolution and generation of new strains. Reassortment is also widely exploited in the laboratory in the process of creating vaccine strains. To-date, 16 H and 9 N subtypes have been detected in numerous combinations circulating in wild birds [19].


Seed viruses are first made to provide the starting material for large scale production of live non-virulent flu viruses. The seed viruses are approved by the WHO or the United States Food and Drug Administration (USFDA). The usual method of seed virus production is reassortment (see Box). Fertilized chicken eggs are injected with both a standard non-pathogenic influenza strain known to grow well in eggs and the strain that carries the genes expressing the desired vaccine H and N protein subtypes. The two viruses multiply, and their eight genome segments reassort with 256 possible combinations. The resulting recombinant viruses are then screened for the desired virus with the six genome segments that allow the standard strain to grow so well in eggs and the H and N genes from the circulating strain. The seed virus is then injected into millions of eggs for mass production of vaccine. This conventional method of seed stock production takes about one to two months to complete [20].

Cell culture systems may eventually replace chicken eggs. Baxter International applied for a patent on a process using cell culture to produce quantities of infecting virus, which are harvested, inactivated with formaldehyde and ultraviolet light, and then detergent [21]. Baxter has produced H5N1 whole virus vaccines in a Vero cell line derived from the kidney of an African green monkey, and conducted phase 1 and 2 clinical trials with and without aluminium hydroxide as adjuvant [22, 23]. The main finding was that the toxic adjuvant did not increase neutralising antibodies against the vaccine strain. Baxter has agreed to ship H1N1 vaccine by the end of July or early August 2009 but details of the production of that vaccine have not yet been released to the public [16].

In December, a Baxter facility in Austria sent a human flu vaccine contaminated with the deadly H5N1 live avian flu virus to 18 countries, including the Czech Republic, where testing showed it killed the ferrets inoculated [24]. Czech newspapers questioned whether Baxter was involved in a deliberate attempt to start a pandemic.

Norvatis, another big pharma, announced on 13 June that it, too, has produced a swine flu vaccine using cell-based technology and the proprietary adjuvant MF59®. The MF59® adjuvant is oil based and contains Tween80, Span85, and squalene [25]. In studies of oil-based adjuvants in rats, the animals were rendered crippled and paralyzed. Squalene brought on severe arthritis symptoms in rats, and studies in humans given from 10 to 20 ppb (parts per billion) of squalene showed severe immune system impact and development of autoimmune disorders [26].

Novartis was in the news in 2008 for a clinical trial of a H5N1 vaccine in Poland. The trial was administered by local nurses and doctors who gave the vaccine to 350 homeless people, leaving 21 died; and were prosecuted by the Polish police [27, 28]. Novartis claimed the deaths were unrelated to the H5N1 vaccine [29], which had been “tested on 3500 other people without any deaths.”

GlaxoSmithKline’s vaccine will be made up of antigens of the recently isolated influenza strain, and also contains its own proprietary adjuvant system AS03 that has been approved in the EU along with its H5N1 bird flu vaccine in 2008. According to the European Public Assessment Report [30], AS03 adjuvant is composed of squalene (10.68 milligrams), DL-α-tocopherol (11.86 milligrams) and polysorbate 80 (4.85 milligrams). The H5N1 vaccine also contains 5 micrograms thiomersal, as well as Polysorbate 80, Octoxynol 10, and various inorganic salts. The company is aggressively promoting various adjuvant systems as its ‘adjuvant advantage’ that reduces the dose of vaccines [31].

A recent WHO survey of primary vaccine producers concluded that the potential output of 4.9 Billion doses of H1N1 vaccine per year is a best-case scenario, assuming among other factors that the most dose-sparing formulation (that will include toxic adjuvants) be selected by each manufacturer and that production will take place at full capacity. WHO Director-General, Dr .Margaret Chan, and the United Nations Secretary-General, Mr Ban Ki-moon, met with senior officials of vaccine manufacturers on 19 May and asked them to reserve part of their production capacity for poor countries that would otherwise have no or little access to vaccine in the case of a pandemic [32].

The last mass-vaccination in the US was a disaster. In 1976, cases of swine flu were found in soldiers at Fort Dix, New Jersey, and one of them died, most likely of physical overexertion rather than from the infection [7]. This led to the launch of a mass vaccination of 40 million against a pandemic that never materialized. Thousands filed claims for injury. At least 25 died and 500 developed paralyzing Guillain-Barre syndrome [33, 34].

Swine flu syndromes mostly mild

As of 22 July 2009, the CDC listed a total of 40 617 cases in the US, with 319 fatalities, giving a fatalites/case ratio of 0.8 percent [35]; though the real death rate – among all cases of infection including the mild ones that go unreported – is probably much lower. Experts estimate that only 1 out of 20 cases are reported [36].

The UK is the worst affected European country, and the pandemic is in the headlines everyday in July. A new telephone helpline was set up on 23 July to let people get advice and tamiflu without seeing a doctor. In that week, there has been a record rise in cases to 100 000 and a total of 30 deaths so far [37], giving a fatalities/case ratio of 0.03 percent, a more accurate reflection of the actual death rate.

UK’s chief medical officer Sir Liam Donaldson has ordered the NHS to plan for as many as 65 000 deaths, with 350 a day at the peak [38]. There has been no plan as yet for mass vaccination; but the UK government has advance orders for 195 million doses of vaccine with GlaxoSmithKline (GSK).

The vaccine that GSK is developing will be tested on a limited number of people as the UK drug company reportedly [39] “weighs the pandemic danger against the risks of an unsafe shot.” This was criticized as “risky” by Prof. Hugh Pennington, a retired microbiologist at the University of Aberdeen, Scotland. “By limiting clinical trials, Glaxo raises the danger that the vaccine dose isn’t properly calibrated, and could lead to shots that don’t protect people from the virus or at worse are unsafe,” Pennington said.

Pennington added that the shot’s ability to trigger the body’s defences is crucial and requires tests to determine the best dose and whether an adjuvant is needed to bolster the immunity. (As we know, GSK is definitely promoting its new range of toxic adjuvants.) He also referred to the Fort Dix incident in 1976 (see earlier).

France has ordered vaccines from Sanofi, GSK and Novartis, but sees no reason to ask vaccine makers to shorten or skip clinical trials [16]. Sanofi-Aventis, the French drug maker developing its own swine flu vaccine will begin testing the product in early August, and estimates it will need as much as two and a half months of tests before having a shot that’s “both safe and protective”, according to Albert Garcia, speaking for the company’s vaccine unit, “the vaccine will be ready in November or December, he said.

Baxter, however, will produce a vaccine by early August for clinical tests.

Glaxo also said it is developing a face mask coated with antivirals to prevent infection and boosting production of its Relenza drug for patients already suffering from swine flu.

There are obviously safer and more effective ways to combat the pandemic than mass vaccinations: washing hands often, sneezing into a tissue that can be safely disposed of, avoiding unnecessary gatherings, and delay opening schools – all advised by governments - and we would add, eating healthily, exercise, and getting enough vitamin D to boost your natural immunity [10].
References

1. New details on virus’s promiscuous past”, Jon Cohen, Science 2009, 324, 1127.

2. Garten RJ, Davis CT,Tussell CA et al. Antigenic and genetic charaatcteristics of swine-origin 2009 A (H1N1) influenza viruses circulating in humans. Science 2009, 325, 197-201.

3. Virologist to make his case for lab origin of swine flu”, Peter Duveen, Opednews.com, 4 July 2009

4. Is swine flu a biological weapon?”, Paul Joseph Watson, PrisonPlanet.com 27 April 2009

5. CDC confirms ties to virus first discovered in U.S. pig factories” Michael Greger, 3 May 2009

6. “Swine flu vaccine should not be given to children in schools”, Barbara Loe Fisher, National Vaccine Information Center, 22 July 2009

7. “Now legal immunity for swine flu vaccine makers” F, William Engdahl, Global Research 20 July 2009

8. Swine flu pandemic now ‘unstoppable’: WHO official”, Agence France-Presse 13 July 2009, Calgary Herald

9. What are the dangers of mandatory swine flu vaccination? Dr. Mercola, June 2009

10. Ho MW. How to stop bir flu instead of the vaccine-antiviral model. Science in Society 35. 40-42, 2007.

11. Smith S, Demicheli V, DiPietrantoni C, Harnden AR, Jefferson T, Matheson NJ and Rivett A. Vaccines for preventing influenza in healthy children. Cochrane Database Systematic Review 2006, Jan 25: CD004879.

12. Szilagyi PG, Fairbrother G, Griffin MR et al. Influenza vaccine effectiveness among children 6 to 59 months of age during 2 influenza seasons: a case-cohort study. Arch Pediatr Adolesc Med 2008, 162, 943-51.

13. Christy C, Aligne C, Auinger P, Pulcino T and Weitzman M. Effectiveness of influenza vaccine for the prevention of asthma exacerbations. Arch. Dis Child 2004, 89, 734-5

14. Flu vaccination may triple risk for flu-related hospitalization in children with asthma, 25 May 2009

15. Petrovsky N, Heinzel S, Honda Y, Lyons AB. New-age vaccine adjuvants, friend or foe? BioPharm International 2 August 2007,

16. “Update: 1-Baxter can take no more H1N1 flu vaccine orders”, Bill Berkerto, 16 July 2009, Reuters.

17. H1N1 ‘swine flu’ vaccine, postnote, May 2009, number 331

18. Avian Influenza (Bird Flu) CDC, 18 November 2005,

19. Olsen B, Munster VJ, Wallensten A, Waldenstrom J, Osterhaus ADME and Fouchier RAM. Global patterns of influenza A virus in wild birds. Science 2006, 312, 384-8.

20. Hood E. Environews Innovations 2006 Environmental Health Perpectives 114,A108-111.

21. Kistner,O,Tauer,C, Barrett,N. Mundt,W. Method for Producing Viral Vaccines 2009 Patent application US2009/0060950A1

22. Ehrlich HJ, Müller M, Oh HM, Tambyah PA, Joukhadar C, Montomoli E, Fisher D, Berezuk G, Fritsch S, Löw-Baselli A, Vartian N, Bobrovsky R, Pavlova BG, Pöllabauer EM, Kistner O, Barrett PN; Baxter H5N1 Pandemic Influenza Vaccine Clinical Study Team. A clinical trial of a whole-virus H5N1 vaccine derived from cell culture. N Engl J Med. 2008 Jun 12;358(24):2573-84.

23. Ketel.W,Dekker,C,Mink,C,Campbell,J,Edwards,K,Patel,S,Ho,D,Talbot,H,Guo,K,Noah,D,Hill,H.Safety and immunogenicity of inactivated, Vero cell culture-derived whole virus influenza A/H5N1 vaccine given alone or with aluminum hydroxide adjuvant in healthy adults Vaccine 2009 in press doi:10.1016/j.vaccine.2009.03.015

24. “Bird flu mix-up could have spelled disaster”, NewScientist 6 March 2009

25. Kenney RT and Edelman R. Survey of human-use adjuvants. Expert Review of Vaccines April 2003; 2(2):167-88

26. “Vaccines may be linked to Gulf War Syndrome”, Chiroweb.com, June 12, 2000

27. “Homeless people die after bird flu vaccine trial in Poland”, Mathew Day, Telegraph, 2 July 2008

28. “Homeless people die after trials of bird-flu vaccine”, 10 July 2008, Pharmaceutical Portal for Poland

29. “Polish industry not dented by deaths”, Emma Dorey, Entrepreneur, 21 July 2008

30. Pandermrix = European Public Assessment Report [EMEA] 27 September 2009,

31. Vaccine adjuvant system technology background information. GlaxoSmithKline, accessed 25 July 2009

32. Collin N, de Radiguès X, Kieny MP; the World Health Organization H1N1 Vaccine Task Force.New influenza A(H1N1) vaccine: How ready are we for large-scale production? Vaccine. 2009 Jun 26 in press doi:10.1016/j.vaccine.2009.06.034

33. 1976 swine flu outbreak, Wikipedia, 22 July 2009,

34. Haber P, Sejvar J, Mikaeloff Y and DeStefano F. Vaccine and Guilaain-Barre syndrome. Drug Saf 2009, 32, 309-23.

35. 2009 flu pandemic in the United States”, Wikipdeia, 22 July 2009

36. 2009 flu pandemic, Wikipedia

37. “Swine flu website overwhelmed by demand as new cases double in a week”, Owen Bowcott and Severin Carrell, The Guardian, 23 July 2009

38. “Swine flu: medical chief orders NHS to prepare for 65 000 deaths – with a toll of as many as 350 a day”, Daniel Martin, The Daily Mail, 17 July 2009

39. “Glaxo to limit tests of flu vaccine, citing urgency”, Jason Gale and Trista Kelley, Bloomberg Press, 22 July 2009

If you are really so afraid about H1N1, let me teach you a way to get rid of the H1N1 flu. If you ever notice muscle pain, stiff neck, fever, afraid of cold. This is the symptom of flu attack. All you need to do is to make sure that you sweat. If you have a car off your air-con, keep the window shut and go for a mindless trip, make sure that you sweat. If you don't have a car, go for a mindless run, make sure that you sweat. If you still not sure it is effective, go and order a bowl of nice hot porridge, and a hot drink,make sure that you sweat. If you still not sure it is good enough go back home and take a nap, cover yourself with thick blanket,make sure that you sweat. you can sweat the virus out of your body without any medication.

More related info on H1N1 Hoax:

[1] Politico, Sebelius downplays swine flu threat, May 6, 2009

[2] World Health Organization, World now at the start of 2009 influenza pandemic, June 11, 2009

[3] World Health Organization, What is phase 6?, June 11, 2009,

[4] USAToday.com, Swine flu shots may go to kids first, Sebelius says, June 16, 2009

[5] CDC National Vital Statistics Reports, Deaths: Final Data for 2006, Volume 57, Number 14, April 2009

[6] PubMedCentral.nih.gov, Archives of Disease in Childhood, August 2004, Effectiveness of influenza vaccine for the prevention of asthma exacerbations

[7] Medscape Medical News, ATS 2009: Flu Vaccination May Triple Risk for Flu-Related Hospitalization in Children With Asthma, May 25, 2009

[8] PubMed.gov, Cochrane Database of Systematic Reviews 2007, Vaccines for preventing influenza in healthy adults

[9] Cochrane.org, Vaccines for preventing influenza in the elderly

[10] Mercola.com, Why Flu Shots for Kids Don’t Work


[11] The Times of India, Virus mix-up by lab could have resulted in pandemic, March 6, 2009

[12] Baxter.com, Baxter Receives Preparedness Contract From Austrian Ministry of Health for Pandemic Influenza Vaccine, November 2006

[13] Expert Review of Vaccines April 2003; 2(2):167-88

[14] Chiroweb.com, Vaccines May Be Linked to Gulf War Syndrome, June 12, 2000

[15] Executive Order 13295

[16] CBSNews.com, DHS Sets Guidelines For Possible Swine Flue Quarantines, April 28, 2009

[17] Project BioShield Act of 2004

[18] Executive Order 13375

[19] Division E – Public Readiness and Emergency Preparedness Act