…E, então, as trombetas da OMS anunciaram ao Mundo o advento de um novo Apocalipse, de seu nome gripe H1N1. Uma histeria colectiva percorreu o Globo. As previsões apontavam para milhões de infectados, grande parte dos quais condenados à morte.
Como no auge da guerra fria, fizeram-se listas dos “indispensáveis”, os quais, em vez de se refugiarem nos abrigos antiatómicos, tomariam a vacina imunizadora. Gente imprescindível (funcionários dos partidos políticos, por exemplo…) foi informada de que estaria na primeira linha para a recepção da vacina.
Os profissionais de Saúde, naturalmente, contavam–se entre os eleitos. Todavia, e infelizmente (já se verá para quem…), grande parte da classe recusou a benesse, argumentando que a gripe A não mataria mais do que a gripe sazonal. Em poucos meses, acabou-se o pânico – e hoje já quase ninguém fala na pandemia. Foi um “flop” positivo!
Mas, entretanto, os laboratórios farmacêuticos tinham posto as linhas de produção a trabalhar em pleno, a vacina não chegava para as encomendas, as acções dessas companhias subiam em flecha, os cofres estavam a abarrotar. E, agora, acaba-se nisto: a própria OMS vai pedir uma auditoria à gestão da gripe, pois há suspeitas de que os riscos da pandemia foram empolados, sob pressão dos laboratórios.
E, não sei porquê, ocorre-me outro “flop” – só que esse negativo. Falo da invasão do Iraque, decretada pela tríade Bush-Blair-Aznar, sob pretexto de que os seus arsenais estavam repletos de armas de destruição massiva. Não era verdade – só que, entretanto, alguém enchera os bolsos graças à ameaça de algo que não existia. Com a gripe A, suspeita a própria OMS, estará a passar-se coisa idêntica…
Novos purificadores de ar adaptados ao vírus pandémico. Empresa diz que conseguem evitar que o H1N1 infecte humanos
Chama-se “Virus Washer”, assemelha-se a um aparelho de ar condicionado e chega ao mercado apresentando-se aos consumidores como o primeiro produto que evita o contágio pelo vírus da gripe A. A japonesa Sanyo já comercializava purificadores de partículas e, quando surgiu a epidemia, percebeu que havia um novo mercado a explorar. Adaptou-os ao H1N1 e prepara-se agora para lançar este mês um modelo de uso doméstico e outro de uso industrial, destinado a espaços de maior dimensão. O director-geral da divisão de ar portuguesa, José Rodeia, diz que a estratégia é fechar negócio com “escolas, hospitais, salas de espera de consultórios e todos os locais com concentração de pessoas”.
A empresa garante ter testado esta tecnologia com ensaios feitos em colaboração com universidades e institutos japoneses e diz que o “Virus Washer” torna 99% dos vírus inactivos face a uma exposição de dez minutos. A tecnologia baseia-se no uso de água electrolisada – a água da torneira com que se abastece o aparelho contém iões de cloreto e, quando electrolisada, gera dois tipos de oxigénio activo: ácido hipocloroso e radicais OH. Os nomes são complexos mas têm uma missão simples: destruir a proteína que reveste o vírus da gripe (esporos), evitando que ele contamine células do hospedeiro. Mantém-se no ar, mas torna-se inactivo.
O virologista Mário Cunha, do laboratório do IPO de Lisboa, afirma que o vírus da gripe se transmite de três formas: contacto directo entre pessoas, contacto com objectos contaminados e inalação de aerossóis. No caso das superfícies, apenas o uso de álcool consegue destruir o H1N1 e, para evitar a transmissão por via respiratória, há os equipamentos de purificação de ar. “Qualquer um destrói o sobretudo que envolve o vírus, que fica inactivo e perde a capacidade de infectar”, refere Mário Cunha. O especialista diz ainda que o ar tem, em média, 12000 partículas por cm3 e, no interior dos edifícios, pode estar 2 a 5 vezes mais contaminado. “Quando tossimos e espirramos somos capazes de produzir até um máximo de 20 000 gotículas.”
José Rodeia refere que o equipamento já está a ser comercializado nos EUA e pretende agora entrar no mercado europeu, tendo já sido apresentado em Espanha. Chegará a Portugal a 15 de Dezembro com um preço de 399 euros na versão doméstica e 3999 na versão industrial (com capacidade de purificar salas até 100 metros quadrados com grande concentrações de pessoas).
Novye Izvestija Novye Izvestija
November 26, 2009 26 de novembro de 2009
Translated from Russian by Infowars Ireland Traduzido do russo por Infowars Irlanda
A pandemia de gripe suína que Novye Izvestija tem escrito sobre esre assunto, pode ser o embuste mais ambicioso e de corrupção do nosso tempo. Em qualquer caso, o aspecto comercial do enorme susto “gripe suína” é já evidente.
A mesma conclusão foi feita por jornalistas dinamarqueses que habilmente examinaram as relações entre a Organização Mundial da Saúde (OMS) e empresas farmaceuticas de todos o mundo, ganharam fortunas com a venda de drogas para combater a doença. Acontece, por exemplo, que muitos cientistas que se sentam em vários comitês da OMS, cuidadosamente ocultando o fato de que recebem dinheiro das empresas multinacionais farmacêuticas do mundo.
De acordo com o banco de investimento internacional da JP Morgan, a indústria farmacêutica vai fazer mais de 7 bilhões de euros este ano com a venda de vacinas contra H1N1. Os principais países ocidentais têm encomendado doses suficientes para vacinar toda a população, quer a sua (como a Austrália), ou um terço (Alemanha e em vários outros Estados-membros da UE).Fábricas de vacinas e comprimidos estão trabalhando dia e noite, em quatro rotações por turnos, com uma carteira de encomendas … eles não estão enfrentando a crise econômica mundial como pode acontece com outros.
Pela primeira vez em muitos anos de pandemia de gripe “o pânico” tem afetado a UE. A vacina foi produzida sem um número suficiente de exames clínicos e exames laboratoriais.
É um tal pânico justificado? um número crescente de especialistas está examinando a questão comparando as estatísticas de mortalidade do vírus da gripe suína e a “convencional”,que no Outono começam sua marcha por todo o planeta. Até agora, segundo a OMS, seis mil pessoas foram vítimas de H1N1, enquanto a taxa de mortalidade média anual durante as epidemias ‘tradicionais’ de gripe atinge meio milhão.
A principal causa da reação histérica à epidemia da gripe suína, de acordo com os repórteres do jornal dinamarquês ‘Informação’, não é porque ele é tão perigoso, mas por causa de uma forte campanha de relações públicas por especialistas da OMS. Alguns deles [especialistas da OMS], estão, literalmente, ao serviço dos fabricantes de vacinas.
“É preocupante que muitos dos cientistas que se sentam em vários comitês da OMS, são apresentados como” peritos independentes, mas escondem o fato de que recebem dinheiro das empresas farmacêuticas “, confessou o professor de epidemiologia, Tom Jefferson, que trabalha na do Centro Cochrane, em Roma, a repórteres.
A OMS anunciou a pandemia da gripe suína sob pressão de um painel de conselheiros, liderado por um médico holandês, Albert Ostenhaus, apelidado de “Dr. Flu’ (do nome ‘Tamiflu’), porque ele era activo na promoção da vacinação em massa da população através da OMS e dos média ocidentais. Agora, o governo da Holanda está a realizar um inquérito de emergência às actividades do “Doutor Flu”, tal se tornou conhecido que ele recebe um salário de várias companhias de fabricação de vacinas. Muitos outros conselheiros que se sentam nas duas cadeiras ‘(conflito de interesses) como Ostenhaus, e ao mesmo tempo a lidar com a pandemia da gripe suína, em nome da OMS, eles não gostam de anunciar que são pagos como assessores das gigantes farmacêuticas Roche, Johnson RW, SmithKline Beecham e Glaxo Wellcome, que receberam a maior parte das encomendas para a fabricação de vacinas. O resultado da pressão desses especialistas foi a resolução da OMS em 7 de julho deste ano, que apelou para uma campanha inédita de vacinação em massa.
“A OMS é tendenciosa em suas recomendações – diz o professor Tom Jefferson. – Medidas de higiene normal proporcionam efeitos muito maiores do que estas vacinas pouco estudadas, e ao mesmo tempo, a OMS refere-se ao uso de máscaras e lavar as mãos como um meio para combater a gripe suína apenas duas vezes em seus documentos. Vacinas e outros medicamentos são referidas 42 vezes! “Dr. Jefferson e vários de seus colegas acreditam que os assessores pagos pelas empresas farmacêuticas devem ser removidos de suas posições e não autorizados a dar recomendações à OMS, mas a própria organização não tem pressa para realizar essa reforma.Porta-voz da OMS, Gregory Hertl, comentando o artigo na ‘Informação’ (jornal dinamarquês) disse que é impossível negar os serviços dos maiores especialistas do mundo pela simples razão de que eles têm um interesse financeiro na promoção de uma estratégia para combater diversas doenças.
Refira-se que este não é o primeiro ano em que o tema da corrupção “em farmacologia tem sido o foco dos média ocidentais. The New England Journal of Medicine publicou “o denunciante” há vários anos. Em uma série de artigos do denunciante revelou a vida dentro da “máfia de branco”. Segundo eles, apenas 11-14% dos orçamentos das empresas farmacêuticas são gastos em pesquisa, mas 36% dos fundos são gastos no PR. Grande parte do dinheiro acaba nos bolsos dos médicos, cientistas, e as contas de várias organizações que trabalham em cuidados de saúde.
Morreu mais um feto no Hospital de Portalegre em que a grávida foi vacinada contra a gripe A.
A grávida residente em Ponte de Sôr deu entrada, nas últimas 24 horas, nesta unidade hospitalar, onde a 15 de Novembro morreu um outro feto com 34 semanas em que a mãe também foi vacinada.
O pai da grávida, Romão Catarino, confirmou o caso referindo que uma das possíveis causas poderá ter resultado do enrolamento do cordão umbilical à volta do pescoço do feto.
O Hospital de Portalegre promete, para o final da tarde, esclarecimentos sobre este caso, divulga a ‘Rádio Portalegre’.
No espaço de oito dias, sobe para quatro o número de grávidas vacinadas com a ‘Pandemrix’ que perderam os bebés. Além dos dois casos de Portalegre, ocorreu um em Lisboa e um outro em Leira.
Na Europa são conhecidos pelo menos mais três casos com grávidas que tomaram a vacina e perderam os bebés. Dois na Noruega e um em França.
Deu ontem entrada no Hospital de Santo André, em Leiria, mais uma grávida com um feto morto e que tinha sido vacina contra a gripe A (H1N1). É o terceiro caso em poucos dias, mas as autoridades não confirmaram até agora nenhuma relação causa-efeito entre a morte dos fetos e a inoculação.
A jovem de 27 anos estava grávida de vinte semanas e tinha sido vacinada no início do mês. Deu ontem entrada no Hospital de Santo André, em Leiria, que confirmou a morte do feto, que será autopsiado.
Ontem foi confirmada, no hospital CUF Descobertas, a morte de um feto de 34 semanas, cinco dias depois de a mãe ter sido vacinada contra a gripe A. A situação surgiu dois dias depois de uma outra mulher, vacinada em Portalegre, ter perdido a filha que esperava há também 34 semanas. A Direcção-Geral da Saúde recusa comentar o caso até serem conhecidos os resultados de análises e testes que só podem ser feitos depois do nascimento.
O director clínico do Hospital CUF Descobertas garantiu hoje que vai ser feita autópsia ao feto que morreu com 34 semanas. A autópsia poderá ser fundamental para encontrar a causa da morte, mas os médicos recusam estabelecer uma ligação entre a morte do bebé e a vacina para a gripe A.
Hospital de Portalegre diz que não há relação entre os dois factos
Uma mulher grávida de 34 semanas foi vacinada com a vacina contra a gripe A e o feto de oito meses acabou por morrer três dias depois, confirmou o tvi24.pt junto de fonte do Hospital de Portalegre.
A mesma fonte adiantou que até ao momento não está provada qualquer relação entre os dois factos. Em comunicado, o hospital esclarece que o nascimento do bebé já morto ocorreu este domingo e que a grávida dirigiu-se ao hospital no sábado «por diminuição dos movimentos fetais».
João Romacho, cunhado da mulher de 31 anos, natural de Alegrete, Portalegre, disse em declarações à Lusa, que depois de na quarta-feira ter sido vacinada contra a gripe A, a grávida começou a queixar-se de dores no corpo e mal-estar geral, estranhando que o bebé ora se mexesse mais do que o normal, ora não se mexesse.
«No sábado de manhã [a grávida] foi ao Centro de Saúde de Portalegre, onde a médica que a assistiu verificou que o batimento cardíaco do feto era baixo, mas existia, e aconselhou-a a ir para casa e a voltar no dia seguinte para ver como estava», disse João Romacho à Lusa.
A mulher acabaria por recorrer ao Hospital de Portalegre por volta do meio-dia de sábado, onde ficou a saber que o coração do feto tinha parado.
João Romacho disse à Lusa que os médicos afastaram desde logo a hipótese de a morte do feto estar relacionada com a vacina, mas os familiares da mulher desconfiam que possa haver uma ligação.
«Não podemos dizer que tenha sido da vacina até porque anteriormente já tinha havido um episódio em que o batimento cardíaco do bebé estava muito acelerado, mas claro que depois de ter tomado a vacina… deixa-nos intrigados e com interrogações. A realidade é que a partir daí [da vacinação] se desenvolveram uma série de reacções», disse o familiar.
O hospital confirma, no comunicado, que a mãe foi vacinada contra o vírus H1N1 na passada terça-feira, mas adianta que não é possível estabelecer uma relação causal entre a vacinação da grávida e da morte do feto».
A direcção hospital acrescenta também no comunicado que «a ocorrência de nados-mortos em Portugal, sem causa prévia, é em média de um por dia».
João Romacho adiantou ainda que os familiares aguardam agora pelos resultados da autópsia ao feto e reclamam explicações dos médicos que acompanharam a mulher ao longo da gravidez para apurar se houve responsabilidades. Só a autópsia, efectuada pelo Instituto de Medicina Legal, poderá revelar a causa de morte do bebé e se a morte estava ou não relacionada com a vacina contra o vírus H1N1.
Swedish boy, aged 4, close to death from “swine flu” vaccine
Kevin
The almost complete cover up in Sweden regarding deaths and other severe “side effects” from the poisinous Pandemrix “swine flu” vaccine is frightening. A few stories are getting out in spite of this, like the story of Kevin, aged 4 living in Stockholm with his mom Mia who is pregnant in her third trimester.
“- I was sure he was dead” she says in an article published at first only in the printed version of the news paper Aftonbladet and later added to their site after being “reminded” by readers to do so.
Kevin sat with his father in a café when he suddenly started to shake uncontrollably. His little body arched backwards in convulsions and his eyes rolled backwards exposing only white. His mom was not far away and someone quickly fetched her saying “Mia come quickly, Kevin is really bad”.
When she arrived to Kevin, a ring of people surrounded him as he was lying flat on the ground. “- His lips were completely white. I have never seen a person that white in my life. I took him in my arms and he was completely limp. My only thought was, ‘He is dead, He is no longer alive’ “, says his mom.
Kevin did no longer breathe. Two nurses happened to be there and they instructed Mia how to give CPR immediately. Mia started to do that while she at the same time felt she was starting to go into labor. She gave her son air as others called for an ambulance. “I lost the sense of time. But after a while his lips got their color back. He opened his eyes.”
During the ride to the hospital, Kevin only expressed one fear: “Mommy, I don’t want to have another shot…”
Doctors who cared for him at his arrival at the Hospital agreed that the only explanation to this was that he two days earlier got the poisonous Pandemrix “swine flu” vaccine. They also said “- He is the second one today, this is in no way unique.”
The news paper contacted The Medical Products Agency in Sweden and spoke with Professor Jan Liliemark who claimed he had never heard of similar cases. “- Children can come in to states of Coma from a variety of reasons. It could be connected to the vaccination but there could also be other reasons.”
Kevin’s parents chose to speak about their ordeal so that other parents would be better informed than they were. They never heard that things like this could happen after a vaccination.
Mia says “- What if this would have happened at home while playing alone in his room while I was cleaning downstairs?”
We have received unconfirmed reports that the number of vaccine “adverse effects” in sweden is now well over 500 including “severe adverse effects” which means life threatening conditions or death. The number of deaths is reported to us to be higher than 50 so far. This information is unconfirmed and the official numbers kept secret according to the also secret agreement between Sweden and GSK, GlaxoSmithKline who produces the poisonous Pandemrix vaccine.
I today spoke with a vaccine manufacturer (a supplier of the API, the active ingredient) at their plant here in Switzerland and they stated that they felt they had to play along in producing and supplying active ingredients to the larger “big” pharma companies since these companies are “so powerful”. The person I spoke with thought it was something seriously wrong with the way the whole “swine flu” scare has unfolded and the role of WHO. The same person also acknowledged that very much research in the medical field which does not support planned products or other businesses is hidden or buried. The two people I spoke with would “absolutely not” take the “swine flu” shot. They did say that the “swine flu” meant good business.
Child paralysed by Flu Mist in the US
“Our granddaughter, Jordyn, (Bobbi and Jeff’s daughter) received the nasal spray vaccine for H1N1 on Tuesday of this week and within a half an hour started feeling bad. She developed a fever of 103 and continued for most of Wednesday with it. She seemed better yesterday (Thursday), but was still not herself. She woke up this morning and could not walk (her legs were paralyzed). Bobbi and Jeff have taken her to Sparrow Hospital in Lansing and we are waiting word. We think she has Guillain Barre and, if so, the, paralysis can spread to her other limbs and her face. We are requesting prayer from you and as many believers as you have contact with.”
Nine students in the US rushed to hospital after swine flu jab
Nine Caledonia High students have reactions to H1N1 vaccine
All treated and released
by Brian Jones
Nine Lowndes County School District students were rushed to the hospital today after apparently having reactions to the H1N1 vaccine.
H1N1 shots are being made available at schools around the state by the Mississippi Department of Health. Nine students at Caledonia High School were transported to the emergency room after apparently having a reaction to the shot, said Lowndes County Superintendent Mike Halford.
“We had seven students transported by ambulance to Baptist Memorial Hospital-Golden Triangle,” Halford said. “Two more students were brought in by parents or family members.”
Of the nine, eight had been treated and released by 2:00 p.m. Wednesday, he said.
“The H1N1 vaccine was being administered [Wednesday] at New Hope High School, New Hope Middle School and all levels at Caledonia,” Halford said. “We had given the shots to the high school students, and about fifteen minutes after the shots were given we started having the issues.”
Halford said that students complained of symptoms including shortness of breath, itching and hives.
“We stopped giving the shots at that time,” he said.
According to Mississippi Department of Health District 6 Health Officer Rebecca James, two of the students who developed shortness of breath and hives did so because of a reaction to the shot. The others were “sympathetic reactions,” she said.
“There was no evidence of an allergic reaction in those six,” she said. “A sympathetic reaction is also called a ‘line of sight’ reaction. It’s similar to what happens when one person in a cafeteria throws up, and then suddenly people around them start feeling sick as well.
“Hives can be a sign of a reaction to the shot, but they can also be caused by stress,” she added. “Some of the hives could have been caused simply because the students were nervous about getting a shot. We may never know what caused those students to have those reactions.”
Counting the two reactions at Caledonia High School today, James said that there have been a total of three allergic reactions to the vaccine around the state.
“That is a very mild reaction rate,” she said. “I still feel very comfortable recommending that children be vaccinated against influenza, which can be deadly. I’d rather treat hives and itching that have to treat the flu.”
The vaccine that was given at Caledonia was the exact same vaccine that was given at other schools in Lowndes County, she said, and there had been no other reports of problems.
There have been 16 influenza-related deaths in Mississippi so far, she said.
James said that the LCSD will continue with the H1N1 vaccinations.
“Mike Halford has been very good about handling this,” she said. “He intends to offer the vaccinations at the middle and elementary schools to students who want them.”
A new permission form will be sent home to students before the vaccinations commence again, she said.
Vaccinations at New Hope Elementary School and West Lowndes are scheduled for a later date.
[At 5:00 p.m. yesterday afternoon an ambulance was dispatched to a residence on Mike Parra Road when one of the Caledonia High students treated earlier in the day began having “seizures” and fever. Ed.]
Teresa Forcades é freira no mosteiro de Sant-Benet, em Monserra-Barcelona. É médica especializada em medicina interna, PHD em saúde pública pela Universidade de Barcelona, especializada no E.U.A. da Universidade Estadual de Nova York. Fornece dados científicos verificáveis e as irregularidades perturbadoras relacionadas a este assunto. Isso é relevante para todos os países,para todas as pessoas.
Ela explica as consequências da declaração de uma pandemia, as consequências políticas desta declaração e faz uma proposta para manter a calma. Ela pede uma activação urgente de todos os mecanismos legais e a participação de todos os cidadãos nesta matéria.
Many Americans watch corporate-funded shills like ABC’s Doctor Oz tell them that the H1N1 swine flu vaccine is perfectly safe and then run out and allow themselves and their families to be injected with a dangerous mixture of ingredients that is so toxic that it does not even deserve to be called a “vaccine”. In case you do not know about what is in these “vaccines”, you need to read an earlier article that we published entitled “In Case You Were Wondering Why We Don’t Want To Take Your Swine Flu Vaccines”. The reality is that the big financial interests that own or have financial ties to ABC and the other big mainstream media outlets are the same big financial interests that own or have financial ties to the big pharmaceutical companies that are producing the swine flu vaccines. Do you actually think that the corporate owners that are making massive profits off of the vaccines are going to allow doctors to go on the television networks that they own and tell the American people that the vaccines are bad for them?
Fortunately, there are independent doctors like Dr. Leonard Horowitz and Dr. Sherri Tenpenny who are providing the American people with the other side of the vaccine safety debate. In the videos that you will view in this post, Dr. Horowitz rips apart ABC’s Dr. Oz and exposes the truth behind the H1N1 swine flu vaccine fraud. After you watch these videos you will not be so eager to run out and get your family shot up with toxic sewage.
Part 1 of the 3 part YouTube video series by Dr. Horowitz is posted at the top of this article. Parts 2 and 3 are posted below. After you have watched these videos, we would love to hear your opinions about them in the comments section below.
The truth is that you are NOT going to hear a balanced debate about swine flu vaccine safety on network television. The big pharmaceutical corporations buy millions upon millions upon millions of dollars worth of advertising on network television. Do you think that the networks are going to stick it to their biggest advertisers? In addition, as you saw in the videos above, the very same big money interests that control network television are very often the very same big money interests that own the big pharmaceutical companies.
You cannot just blindly rely on the television to make your decisions for you. Do your own research and make the best decisions for yourself and your family that you can.
For more coverage of the H1N1 swine flu and the dangers of the swine flu vaccines, we encourage you to visit our sister site: Organic Health
ALERT Canadians: Toxic Ingredients in the Arepanrix H1N1 Vaccine Harm Your Health
Health Canada has authorized the sale of Arepanrix™ H1N1 vaccine based on no conclusive clinical testing. The authorization is based on the Health Canada review of available data on the quality, safety and immunogenicity of similar vaccines, which established the benefit/risk profile in favour of inoculating the Canadian population.
Read the Notice of Decision issued by Health Canada. The decision by the Health Minister was based on a belief (not qualified or informed) that immediate action is required to deal with the H1N1 risk. The assertion that the decision is based on limited clinical testing is being misapplied. There has been NO conclusive results from any clinical trials on the Arepanrix H1N1 vaccine.
This report is designed to inform you how the risks outweigh the benefits of the vaccine. It will demonstrate how the Health Canada assessment is flawed and contradictory to established research on the detrimental health effects of the vaccine ingredients contained in Arepanrix.
Description and Composition
Arepanrix™ H1N1 (AS03-adjuvanted H1N1 pandemic influenza vaccine) is a two-component vaccine consisting of an H1N1 antigen (as a suspension), and an AS03 adjuvant (as an oil-in-water emulsion).
The virus is inactivated followed by formaldehyde treatment and disrupted with sodium deoxycholate.
Preservative content:
5µg (micrograms) Thimerosal USP per 0.5mL dose or 2.5 micrograms organic mercury (Hg) per 0.5mL dose
Adjuvant:
The AS03 adjuvant system is composed of DL-α-tocopherol, squalene and polysorbate 80 in a 3mL vial:
According to the Australian National Research Council, fewer than 20% but perhaps more than 10% of the general population may be susceptible to formaldehyde and may react acutely at any exposure level.
More hazardous than most chemicals in 5 out of 12 ranking systems, on at least 8 federal regulatory lists, it is ranked as one of the most hazardous compounds (worst 10%) to ecosystems and human health (Environmental Defense Fund).
Formalyn a 37 percent solution of gaseous formaldehyde which includes methano (used in vaccines as a tissue fixative) is considered a hazardous compound, and its vapor is toxic.
In the body, formaldehyde can cause proteins to irreversibly bind to DNA. Laboratory animals exposed to doses of inhaled formaldehyde over their lifetimes have developed more cancers of the nose and throat than are usual, as have workers in particle-board sawmills… Formaldehyde is classifed as a probable human carcinogen by the U.S. Environmental Protection Agency and as a known human carcinogen by the International Agency for Research on Cancer.
Sodium Deoxycholate
Sodium Deoxycholate is a water soluble ionic detergent/bile salt which causes cell death and symptoms such as burning, redness, and swelling. It has been shown to weaken the blood-brain-barrier (BBB) and subsequently activate seizures. It has demonstrated synergistic toxicity with antifungal drugs.
Detergents and emulsifiers promote tumors and cause cells to leak or explode by weakening their walls, with no mechanism for regulating destructive activity. These chemicals are not completely purified out of the final vaccine product, so they enter the body at the time of injection.
Detergents are used extensively in cell research precisely because of their ability to break cells open for further analysis. This catastrophically mimics the membrane attack complex (MAC). Detergents hit cells at random and continue destroying cells regardless of which call off the attack.
Sodium Deoxycholate is completely foreign to the relationships that define and make up the delicate balance of the immune system. It systematically disrupts these relationships to negate the optimal function and design of immune responses.
Thimerosal
Thimerosal has powerful and damaging effects on cells of the nervous and immune systems in mammals including humans. Its effect may vary depending on the dose, the genetics of the individual, and the timing of exposure. The mercury dose from thimerosal produces acute and often deadly ethylmercury blood levels.
Organic forms of mercury are well-known neurotoxic agents
and far more dangerous than inorganic mercury sources. Exposure to organic mercury produces predominantly central nervous system (CNS) effects that are commonly severe and can induce prolonged unconsciousness, coma and death. (See: Acta Chim. Slov. 2004, 51, 361-372)
After only 2 hour exposures, thimerosal at micromolar concentrations causes neuronal membrane damage and alterations leading to cell death in immune T-cells.
Thimerosal alters the functioning of critical neurotransmitters necessary for proper brain functioning.
Thimerosal causes DNA fragmentation of neuronal cells and disrupts
neuronal growth factor signaling at micromolar and even nanomolar concentrations. It also causes DNA methylation and attentional
pathways at nanomolar concentrations, leading to alterations in brain function.
Under microscopic magnification the following video presentation by the University of Calgary demonstrates the immediate damage mercury does to the structure of brain cells.
Too dangerous for human use, Squalene is not officially licensed for use in the United States or Canada. Oil adjuvants like squalene have been ordinarily used to inflict diseases in animals – for experimentation and study. According to anthrax vaccine expert Gary Matsumoto and other reliable sources, the US military used an unlicensed, experimental anthrax vaccination laced with squalene, with disastrous consequences, including Gulf War Sydrome.
“There are now data in more than two dozen peer-reviewed scientific papers, from ten different laboratories in the US, Europe, Asia and Australia, documenting that squalene-based adjuvants can induce autoimmune diseases in animals, observed in mice, rats, guinea pigs and rabbits. Sweden’s Karolinska Institute has demonstrated that squalene alone can induce the animal version of rheumatoid arthritis. The Polish Academy of Sciences has shown that in animals, squalene alone can produce catastrophic injury to the nervous system and the brain. The University of Florida Medical School has shown that in animals, squalene alone can induce production of antibodies specifically associated with systemic lupus erythematosus” writes Matsumoto.
Oil-based vaccination adjuvants like squalene have been proved to generate concentrated, unremitting immune responses over long periods of time according to a 2000 article in The American Journal of Pathology. The study demonstrated that a single injection of the adjuvant squalene into rats triggered a chronic, immune-mediated joint-specific inflammation, also known as rheumatoid arthritis. The researchers concluded the study raised questions about the role of adjuvants in chronic inflammatory diseases.
Polysorbate 80 is similar to Sodium Deoxycholate in its ability to increase cell permeability, damage, and bursting. After injection it can rapidly metabolize into sorbitol and ethylene oxide which is much more toxic than the original chemical. When Polysorbate 80 breaks down there are 20 moles of ethylene oxide for every mole of sorbitol. These polysorbates have been shown to cause dangerous, sometimes fatal effects, when given through a needle. Changes in heart function can occur immediately. The blood-brain-barrier (BBB) can be weakened and penetrated, followed by seizures and even death. Polysorbates demonstrate synergistic toxicity with a wide range of chemicals.
Polysorbate 80 has been found to negatively affect the immune system and cause severe anaphylactic shock which can kill. According to Annals of Allergy, Asthma and Immunology, Volume 95, Number 6, December 2005 , pp. 593-599(7), “it is of current relevance as a ‘hidden’ inductor of anaphylactoid reactions”, and “Polysorbate 80 was identified as the causative agent for the anaphylactoid reaction of nonimmunologic origin in the patient. The study included a pregnant woman who suffered anaphylactic shock after being given a IV drip of multi-vitamins containing polysorbate 80.
In addition to this, there have been studies in Food and Chemical Toxicology which showed that Polysorbate 80 causes infertility. Baby female rats were injected with polysorbate 80 at days 4-7 after birth. It accelerated the maturing of the rats and caused changes to the vagina and womb lining, hormonal changes, ovary deformities and degenerative follicles.
According to the World Intellectual Property Organization, which is part of the United Nations, scientists from the organization are developing vaccines specifically to damage fertility as a method of contraception. A suggested ingredient for the vaccine is Polysorbate 80 (also known as tween 80). As it is a preferred ingredient, scientists are obviously aware of its ability to cause infertility.
There are currently NO clinical trials or results which have validated the long-term safety and efficacy of the Arepanrix H1N1vaccine and its integrated AS03 adjuvant. Regulatory health agencies are refusing to acknowledge this fact or the nature of toxicity levels associated with Arepanrix and its ingredients. The well documented toxicity evidence for each ingredient presented above is simply being ignored.
A simple search on the ClinicalTrials.gov website shows that three “Rapid Evaluation” studies for Arepanrix H1N1vaccine have not even initiated recruiting as of the date this article was published.
One of the most critical elements which defines the toxicity potential of any vaccine are its pharmacokinetic properties. GlaxoSmithKline (GSK) and Health Canada do not consider the study, analysis or evaluatation of the pharmacokinetic properties of any vaccine including Arepanrix. This means that the bodily absorption, distribution, metabolism and excretion of ingredients within the Arepanrix vaccine are not known or even considered in safety assessments. This in itself is a highly suspicious and negligent behavior which leaves many questions on the credbility and reputability of GlaxoSmithKline and Health Canada and their motives for marketing this vaccine to the Canadian population.
Adults aged 18-60 years:
Dosage recommendations of 0.5ml are based on very limited clinical evidence of safety and immunogenicity data available from two 3-week studies. Neither study has validated the long-term immunogencity, safety, toxicity, or pharmacodynamics of the vaccine based on any dosage. Clinically, the shortest acceptable period to study the side effects of any vaccine is 6-8 weeks. The accepted studies noted by GSK and Health Canada are half this period.
Elderly (>60 years):
No clinical data are available for Arepanrix H1N1 in this age group including the effects of the AS03 squalene adjuvant. There is no data to justify any safe dosage in this age group.
Children and Adolescents aged 10-17 years:
No clinical data are available for Arepanrix H1N1 in this age group including the effects of the AS03 squalene adjuvant. No exact dosing recommendations can be made.
Children aged from 6-35 months:
No clinical data are available for Arepanrix H1N1 in this age group including the effects of the AS03 squalene adjuvant. No exact dosing recommendations can be made.
Pregnancy and Lactation
No data have been generated in pregnant or breast feeding women with Arepanrix nor with the AS03 adjuvant.
Fertility & Sterility
GSK suggests animal studies have not demonstrated harmful effects with respect to fertility which directly contradicts several scientific studies which show that Polysorbate 80 causes infertility.
Interactions With Seasonal Flu Vaccines
GSK claims that no data is available on the concomitant administration of Arepanrix H1N1 with other vaccines, including seasonal influenza vaccines.
Adverse Reactions
Solicited adverse reactions were reported more frequently in the H1N1+AS03 group compared to the H1N1 group based on 2 studies which evaluated the safety of another AS03-adjuvanted vaccine containing HA derived from A/California/7/2009 (H1N1)v-like (Pandemrix) in healthy subjects aged 18-60 years.
Since 48.6 of the 50.4 million doses of Arepanrix ordered by the Canadian government contain the AS03 adjuvant, we will focus on those adverse reactions documented which are as follows:
Pain
Redness
Swelling
Fatigue
Headaches
Arthralgia (joint inflammation)
Myalgia (muscle inflammation)
Shivering
Sweating
Swollen lymph nodes
Fever
Vomiting
Tingling or numbness of the hands or feet
Shortness of breath
Vasculitis (inflammation of the blood vessels) Serious adverse reactions are as follows:
Blood and lymphatic system disorders (lymphadenopathy)
Psychiatric disorders (insomnia)
Nervous system disorders (dizziness, paraesthesia, inflammation of the central nervous system, inflammation of nerves, autoimmune disorders affecting myelin sheaths of nerves such as Guillain-Barré Syndrome)
Ear and labyrinth disorders (vertigo)
Respiratory, thoracic and mediastinal disorders (dyspnoea)
Skin and subcutaneous tissue disorders (pruritus, rash)
Musculoskeletal and connective tissue disorders (back pain, musculoskeletal stiffness, neck pain, muscle spasms, pain in extremity)
General disorders and administration site conditions (bruising, asthenia, chest pain, malaise)
Disturbing Concentrations of Squalene
The average quantity of squalene injected into the US soldiers abroad and at home in the anthrax vaccine during and after the Gulf War was 34.2 micrograms per billion micrograms of water. According to studies, this was the cause of Gulf War syndrome in 25% of 697,000 US personnel at home and abroad.
The soldiers developed a cascade of reactions including arthritis, fibromyalgia, lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue, chronic headaches, abnormal body hair loss, non-healing skin lesions, aphthous ulcers, dizziness, weakness, memory loss, seizures, mood changes, neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR (erythrocyte sedimentation rate), systemic lupus erythematosus, multiple sclerosis, ALS, Raynaud’s phenomenon, Sjorgren’s syndrome, chronic diarrhea, night sweats and low-grade fever.
The AS03 adjuvant in the Arepanrix H1N1 vaccine contains 10.69mg per dose. This corresponds to approximately 2.136.0000 microgrammes pr. billion microgrammes of water, i.e. one million times more squalene per dose than the anthrax vaccine.
How much more evidence is necessary to convince public health officials that the risks of the Arepanrix H1N1 vaccine exceed any benefits?
Please do not play roulette with your health. Do not listen to the Public Health Agency of Canada or any public health or medical official that advises you to protect yourself from the flu with this vaccine. Its design and toxicity will only destroy your health.
Ron Paul Questions Why Obama Daughters Haven’t Taken Swine Flu Vaccine
Despite declaring national emergency in response to H1N1 outbreak, President refuses to allow his own children to be inoculated with controversial shot
Paul Joseph Watson
Prison Planet.com
Tuesday, October 27, 2009
Congressman Ron Paul has questioned why, despite his efforts to encourage the general public to get vaccinated against the H1N1 virus, President Barack Obama has refused to allow his own daughters to take the swine flu shot.
Despite the fact that Obama on Friday declared a national emergency in response to the H1N1 outbreak, he apparently doesn’t deem it enough of a threat to have his two daughters vaccinated against the virus.
Such double standards have led media pundits to call for Obama to get his daughters vaccinated on live television, in an effort to encourage American parents to do the same for their kids. The swine flu vaccination program, which was initially intended to be a “mass” inoculation covering the entire population, has been rejected by a majority of Americans who harbor deep suspicions about dangerous additives contained in the vaccine such as mercury and squalene.
In a Campaign For Liberty video message, former Presidential candidate Ron Paul labeled the vaccination program a “failure,” and slammed Obama for failing to follow the same advice he gave to the nation.
“It’s interesting to note that the President’s children have not gotten their shots and the explanation for this is it hasn’t been available to them – now that’s a little bit hard to buy when you think that probably anything the President wants can be available for their children,” said Paul, adding, “So in a way he’s made his decision not to give his children these inoculations – so if he has freedom of choice on this, I would like to make sure that all the American people have the same amount of freedom of choice.”
Others have echoed similar sentiments. “Surely if there is a national emergency and if the President and First Lady of the United States wanted flu shots for their daughters, they could get them. It is certainly connected to our national security right? I mean the president needs to have his wits about him 24/7 not worrying over sick children. Could this instead be yet another case of “do as I say, not as I do” from the Obama administration?” writes Cathryn Friar.
Paul compared Obama’s hypocrisy to politicians who lobby for the virtues of public education yet in every instance educate their own children privately.
“The biggest champions of public education make sure their kids never get public education, they always get private education where there’s a lot better choices than the kind of system they’re promoting,” said the Congressman.
Obama certainly isn’t stupid enough to inject his own kids with the same toxic soup that he encourages the idiot public to receive, and will probably be keen on getting access to the special additive-free swine flu shots produced by Baxter International that have been made available for the elite.
Employees of the Paul Ehrlich Institute in Germany also received the “green” inoculation after their president Johannes Löwer labeled the vaccine a greater threat than the virus itself. Löwer’s comment came after German lung specialist Wolfgang Wodarg said the vaccine increases the risk of cancer. The nutrient solution for the vaccine consists of cancerous cells from animals.
In the video update, Congressman Paul also warned that Obama’s emergency declaration on Friday was part of a plan to condition people to accept the notion of government as protector and coerce the public into complying with whatever they say, including forced quarantines.
Media in Sweden is having a tough time maintaining the propaganda as more and more people question the reasons for the mass vaccination. Now, authorities say that if not “80% of the population takes the shot, we risk 100 deaths from the swine flu”. Most Swedes know that a normal fly season see several thousand dead from complications from the seasonal flu so the proportions of the propaganda coming from media and the government has caused a growing revolt against the massive attempts to scare people to take the poisonous injection.
Today, Svenska Dagbladet reports that over 350 cases of side effects from the Pandemrix “swine flu” shot, have been recorded so far. It has also become clear that this shot contains the most deadly mix of substances of all the known vaccines manufactured against the so called “swine flu” H1N1 influenza. The official number of deaths from the “swine flu” vaccine is now five. And that is only those who have strong immediate reactons, the long term effects are usually never even investigated. If you would die from the shot two weeks after you took it, your death would not be considered to have anything to do with the vaccination. Severe healthproblems years after will of course be very had to link to the poisonous injection. Even if these five official cases died within days, the official story is of course as expected: “none of these deaths has been confirmed to be linked to the vaccine”.
As always with statistics like this, historically we know that very few of all real side effects are actually reported. Optimistically, up to ten per cent would be reported. It is also highly likely that deaths are being kept secret by the authorities so that the massive and hugely expensive vaccination program will not come to a complete stop. Too many have put their job, reputation and title at stake for the truth to be reported and published.
So far, three people have been reported dead from complications from getting the H1N1 virus. Five dead from the flu shot before the real vaccination campaign has even started should be an indication to question the vaccine and the strategy chosen but the authorities have so much prestige invested that it is unlikely it will ever happen – no matter how many will die from the poisonous injections.
The Swedish public are being kept in the dark about the most simple facts about the vaccinations. The questionable protection against the virus will only be for this present strain – any new mutations would immediately require a new vaccine for that strain. The new second wave of the new mutation is exactly what authorities warn about and use as an argument to take the poisonous injection.
Authorities are running out of arguments and completely idiotic arguments have been published the last week in Sweden. “There is less mercury in the shot than you get from eating mercury contaminated fish”, “You might get sick from the vaccine but you should take that risk to ´save” someone who could die from getting the H1N1 infection from you”, “It would be like killing someone to not take the shot out of solidarity” and “Mercury is not dangerous and also squalene is not dangerous, there is nothing called the Gulf War Syndrome and if there is, it has nothing to do with squalene because there was no squalene in the vaccines the US troops got”.
The number of flat out lies are so many, it is hard to keep track of them all.
The chief of The Swedish Institute for Infectious Disease Control (SMI), Annika Linde, says in the article: “- The Vaccine is principally natural to the body. The mercury was necessary but the amounts are very small. There are many who have been making statements without qualified knowledge. It is of course good that this type of mater is debated but some of the reporting is rather devastating for the possibility to vaccinate the whole population.”
The official line in Sweden is bordering to madness and the biggest medical scandal in the history of the nation has just started.
The news that a fourth person has died after taking the “swine flu” jab in Sweden is focussing attention on the failure of the Swedish Medical Products Agency (MPA) to halt the “swine flu” programme even as reports of serious side effects flood in.
The Swedish drug regulator has allowed the “swine flu” jab campaign to be launched even though there is no safety or efficacy data on the vaccine. GlaxoSmithKline’s Pandemrix with mercury and squalene has been given approval under new and lax European Union regulations formulated by the European Medicines Agency, (EMEA) for a “pandemic emergency” that do not require safety or efficacy data.
The EMEA derives three-quarters of its funding from pharmaceutical companies.
The “swine flu” jab has been authorised for use only on condition that governments and companies implement “post-authorisation” studies to check it is safe and effective. However, the MPA in Sweden appears to have limited its role in collecting data on death and damage to spontaneous reports from doctors and patients.
In addition, there appears to be no accurate data available on how many people have been given the “swine flu” jab in Sweden.
The MPA has said it has no such data and the SMI has said that its system for collecting data on vaccines is flawed.
EU’s own guidelines on “post authorisation” studies highlight the need to collect accurate data on “vaccine exposure”.
“The basis for the assessment of an association between A/H1N1 influenza vaccines and severe adverse events should be Observed-to-Expected analyses. For this purpose, data will be needed on vaccine exposure and the expected number of cases. It is therefore crucial that background incidence rates on AESIs are collected as early as possible, before the vaccine is introduced on the market. Vaccine manufacturers should actively liaise with public health and regulatory authorities in countries where its vaccine(s) will be used in order to explore the availability of such data. Use of large electronic databases could be used if available. If data are not available, they could be extrapolated from other countries. Background incidence rates should be provided with any specific signal evaluation. ”
MPA officials have given their view in the media that the deaths of Swedes directly after the “jab” were not linked to the “swine flu” vaccine but due to underlying medical condictions. Just how independent and effective will their investigation be if they are making this statement before conducting any inquiry or without adequate data?
Gunilla Sjölin-Forsberg from the MPA said in an email that the MPA was fulfilling all its requirements under the EMEA recommendations. She also revealed that there will be no study on the “swine flu” jab in Sweden. The only study on Pamdemrix (a mesma que foi adoptada em Portugal) will be carried out in the UK.
However, the question that needs to be to asked is whether there are personnel and financial links between the MPA officials and pharmaceutical companies. Have private or financial interests among MPA officials motivated them to allowed a drug classified as a bioweapon to come onto the market and to collude with pharmaceutical companies to evade responsibility for the harm this drug does to others by bending the regulations.
As a result of the gross negligence at a minimum of the MPA officials, millions of Swedes, especially children and maternity cases, are being exposed to death and damage from this jab.
These MPA officials must be held accountable.
This is Sjolin-Forsberg’s email:
“MPA has implemented all parts of the EMEA recommendations for agencies concerning the pharmacovigilance plan. Spontaneous reporting is encouraged and a standardized reporting form published on our website. Cases of adverse events of special interest are specifically searched for and we also receive reports directly from consumers.
To further clarify: the MPA has implemented all parts of the EMEA recommendations for agencies concerning the pharmacovigilance plan. Spontaneous reporting is encouraged and a standardized reporting form published on our website. Cases of adverse events of special interest are specifically searched for and we also receive reports directly from consumers. As for post-authorisation studies the EMEA request is that the MAH (marketing authorization holder) puts in place a prospective cohort study in at least one European Member state. This will be done in UK and for more information I suggest you contact the MHRA. These described actions summarizes the recommendations from EMEA.
In addition to this, a Swedish registry study is being implemented covering a significant portion of vaccinated people.
The first doses of the H1N1 swine flu vaccine are now being administered at clinics and hospitals across the United States, and many Americans are eagerly lining up to take their vaccine. But is the mainstream media accurately informing the public about what they are taking? The reality is that most Americans do not realize that all of the early batches of the H1N1 swine flu nasal vaccine (called FluMist) contain live swine flu. If you are trying to avoid the swine flu do you really think that it is a good idea to have live swine flu injected up your nose? Many health experts are expressing a grave concern about the safety of this FluMist vaccine, and many hospitals are rejecting this nasal spray vaccine altogether. In fact, several Denver area hospitals are rejecting the FluMist swine flu vaccine because “they don’t want to endanger patients”.
The mainstream media is reporting that the live swine flu in the FluMist vaccine has been “weakened”, but according to Dr. Sherri Tenpenny, between 10 million and 100 million swine flu viral particles are forcefully injected into the nostrils when FluMist is administered to a patient.
So millions of Americans will have live swine flu injected into their nasal passages over the coming weeks, and they will instantly become carriers of this deadly disease. Whenever these vaccinated Americans sneeze or whenever they exhale or whenever they wipe their hands on anything they risk spreading the swine flu to others.
The truth is that anyone who takes the FluMist vaccine can spread the disease for up to 21 (TWENTY-ONE) days.
In case you doubt this, just read FluMist’s own package insert: “FluMist® recipients should avoid close contact with immunocompromised individuals for at least 21 days.”
So, the question on everyone’s minds is this……
Will the live swine flu in the FluMist nasal spray vaccine cause a massive outbreak of the swine flu in the weeks ahead?
Let’s hope not.
But if you do happen to catch the swine flu there are some practical things that you can do…..
What can you do to prevent getting sick?
Many physicians and natural health experts recommend taking substantial doses of vitamins D & C to significantly boost your immune system.
If you do find yourself with the swine flu, many natural health experts are recommending oil of oregano and elderberry as ways to fight the disease naturally.
If all of that has not worked, some health experts suggest usingcolloidal silver as a last line of defense. They say to think of it as kind of a “silver bullet” that you don’t want to use every day, but that can come in quite handy when nothing else seems to work.
A maioria dos 200 enfermeiros que trabalham na Linha Saúde 24 recusa ser vacinado contra a Gripe A, noticiou hoje a TSF.
Fazem parte dos grupos prioritários, aqueles que têm primazia na vacinação contra a gripe A e deviam começar a ser vacinados na segunda-feira, mas não querem por considerarem que esta é uma vacina que levanta ainda algumas dúvidas.
A Direcção-geral de Saúde tem garantido que esta vacina contra a nova variante da gripe oferece todas as garantias.
The European Medicines Agency (EMA), based in London and responsible for reviewing the safety pandemic flu vaccine, has admitted a large-scale biological experiment is being conducted wilfully and deliberately by WHO and the vaccine companies on the people of Europe and the rest of the world by the use of a vaccine whose safety is not known.
Such biological experiments are forbidden under law.
In a June Q and A press release on the pandemic vaccines, the EMA states that the safety of the vaccine will not be known before it is issued to the general population and manufacturers will therefore be required to continue safety assessments during the administration of the vaccine.
Also, they will be required to put in place “special risk management plans”. There is talk of monitoring the safety of the vaccines but there is no mention of stopping the mass vaccination campaign.
The H1N1 Swine Flu Vaccine Is On The Way – Ready Or Not
The World Health Organization, the CDC and health authorities around the world are preparing for the largest and most comprehensive mass vaccination campaign in the history of humanity this fall. It appears that governments and health organizations around the world have virtually all decided to push forward with vaccinating their populations for the swine flu as quickly as possible – whether or not the vaccine have been sufficiently tested or proven to be safe.
The U.S. government is making unprecedented preparations to make sure that the vaccination program goes smoothly. According to the Department of Defense, even the U.S. military plans to “assist” civilian authorities in the event of a significant outbreak of the H1N1 swine flu in the fall.
So just how does the U.S. military plan to “assist” civilian authorities? Would they actually be involved with the vaccination program itself? After all, the World Health Organization is recommending that mandatory swine flu vaccinations be administered in almost 200 different countries.
And it now appears that a swine flu vaccine will be available in the fall – whether it is fully tested or not.
But governments around the globe seem to be ignoring any potential danger to rushing a swine flu vaccine out. In fact, the U.S. government is looking for several thousand volunteers to start rolling up their sleeves for the first swine flu shot trials.
Anybody want to volunteer?
Normally it takes months or even years to develop and fully test a vaccine.
The truth is that vaccines are not nearly as safe as they are portrayed to be.
Many vaccine activists are very concerned about this upcoming swine flu vaccination program, and the fact that the Washington Post has confirmed that the swine flu vaccine WILL contain mercury is not going to ease their fears.
In fact, U.S. health authorities are actually recommending that kids get FOUR flu shots this fall. Are you absolutely certain that it is healthy for your kids to be shot full of mercury? If not, then perhaps you should do some serious research.
In any event, health authorities around the globe are clearly extremely concerned about this swine flu pandemic, and they are determined to do something about it.
That is approximately one-third of the people on earth.
Wow! Those are eye-popping numbers.
Some cities have become so alarmed that they are taking their preparations to bizarre extremes.
For example, the Exeter City Council says that it is actually considering using the catacombs under the city to store the corpses of deceased swine flu victims if the pandemic worsens.
Now that is bizarre!
Hopefully we are not going to be facing a crisis that requires mass graves.
But in any event, are there rational things that the average person can do to prepare for this fall and winter?
Yes.
Some health experts are now claiming that Vitamin D is a “major weapon” against the swine flu. In fact, if you do some research there are a number of things that you can do to significantly boost your immune system, and there are a number of natural methods to fight the swine flu if you do end up contracting it.
But perhaps the biggest danger we will face is if the H1N1 virus seriously mutates. For example, scientists are now starting to wonder what will happen when the H1N1 flu encounters the H5N1 flu.
Will it create a super flu?
Will it create a flu that is easily transmissible from human to human like H1N1 but that also has a high death rate like H5N1?
Authorities are preparing to seize children from schools, set up quarantines and morgues, conduct mass vaccinations, and deal with riots and unrest, according to an international swine flu summit recently held in Washington DC which was attended by distinguished scientists, industry leaders and top health officials from all over the globe.
A conference first discussed by this website three weeks ago has now taken place, with health authorities meeting at the end of last week to finalize response plans to a swine flu pandemic that has been all but guaranteed to occur this coming fall.
According to a PDF information leaflet released before the meeting, attendees were briefed on how to “conduct morgue operations,” manage an interruption in food supplies and “manage panic caused by sudden disruption of services & interruptions in essential goods & services”.
During a swine flu pandemic, their duties would also include dealing with civil disturbances, controlling and diffusing social unrest and public disorder, carrying out mass vaccination programs and enforcing quarantines, according to the conference documentation.
One of the most shocking modules of the conference deals with “School/University Pandemic Planning” and strongly implies that authorities will usurp parental rights over children in the event of a swine flu pandemic.
“Concurrent Breakout Session #10″ outlines plans to “train teachers to screen for symptoms & know what
to do when students / teachers fall ill,” before then transporting ill students, which presumably means transporting them to quarantine zones with or without the consent of parents. The use of schools as “shelters” or quarantine centers is also mentioned.
As we have documented, authorities have been training to raid and remove children from schools during times of emergency for over a decade, mainly under the auspices of preparing for school shootings or during drug sweeps.
In October 2001, authorities swooped in to kidnap and remove 115 children from Heartland Christian Academy without a warrant. Children were forcibly loaded onto buses like criminals as they screamed for help in shocking scenes featured in Alex Jones’ Road To Tyranny documentary.
Earlier this month we reported on how a Maine high school was taken over by the National Guard in a drill focused around riots during a mass vaccination program. In this scenario, the rioters were begging for the vaccine, but obviously the opposite is likely to be the case if a mandatory vaccination program is announced, if there are riots then they will consist of people refusing to take the shot.
A You Tube user posted the following video which covers some of the issues raised by the swine flu conference.
Dr Wolfgang Wodarg is the chairman of the health committee in the German parliament and European Council
The swine flu vaccine has been hit by new cancer fears after a German health expert, Dr Wolfgang Wodarg, gave a shock warning about its safety. He has grave reservations about the firm Novartis who are developing the vaccine and testing it in Germany. Dr Wodarg has said that there are many risks associated with the vaccine for the H1N1 virus. The nutrient solution for the vaccine consists of cancerous cells from animals and “we do not know if there could be an allergic reaction”. People fear that the risk of cancer could be increased by injecting the cells. The vaccine – as Johannes Löwer, president of the Paul Ehrlich Institute, has pointed out – can also cause worse side effects than the actual swine flu virus.
Editorial, Bild.de, Germany
German health expert warning: Does virus vaccine increase cancer risk? –German health expert Wolfgang Wodarg has given a shock warning about the swine flu virus vaccine – does it increase the risk of cancer? 07 Aug 2009 Lung specialist Wolfgang Wodarg has said that there are many risks associated with the vaccine for the H1N1 virus. He has grave reservations about the firm Novartis who are developing the vaccine and testing it in Germany. The vaccination is injected “with a very hot needle”, Wodarg said. The nutrient solution for the vaccine consists of cancerous cells from animals and “we do not know if there could be an allergic reaction”. But more importantly, some people fear that the risk of cancer could be increased by injecting the cells. The vaccine – as Johannes Löwer, president of the Paul Ehrlich Institute, has pointed out – can also cause worse side effects than the actual swine flu virus. Wodrag also described people’s fear of the pandemic as an “orchestration”: “It is great business for the pharmaceutical industry,” he told the ‘Neuen Presse’. Swine flu is not very different from normal flu.
Portugal vai contar, a partir de meados de Setembro, com uma nova lei contra a propagação das doenças transmissíveis. A lei n.º 81/2009, publicada ontem em Diário da República, vem substituir um diploma que vigorava desde 1949.
“A nova lei estabelece princípios absolutamente inovadores no que toca à coordenação de medidas de saúde pública em situações de emergência”, congratulou-se o director-geral de Saúde, Francisco George, destacando a importância das novas regras no tocante à declaração obrigatória de doenças.
Até agora, os médicos ou laboratórios que falhassem o dever de notificação obrigatória de doenças transmissíveis e outros riscos em saúde pública arriscavam sanções irrisórias. “A lei de 1949 previa multas da ordem dos 200 escudos e, portanto, havia aqui um enorme vazio legal”, nota Paula Lobato de Faria, professora de Direito da Saúde. Quando a nova lei entrar em vigor (30 dias após a sua publicação), as sanções oscilarão entre os 100 e os 10.000 euros (singulares) e entre os 10.000 e os 25.000 euros (pessoas colectivas).
Desenhada para prevenir e conter a propagação das doenças transmissíveis, a nova lei institui um sistema nacional de informação de vigilância epidemiológica, denominado Sinave e cria o Conselho Nacional de Saúde Pública, ao qual competirá, por exemplo, solicitar ao Presidente da República a declaração do estado de emergência. Dentro daquele órgão funcionarão a Comissão Coordenadora de Vigilância Epidemiológica e a Comissão Coordenadora de Emergência. Numa situação de estado de emergência, a lei prevê a “restrição, suspensão ou o encerramento de actividades ou a separação de pessoas que não estejam doentes, meios de transporte ou mercadorias, de forma a evitar a eventual disseminação da infecção ou contaminação”.
Para Lobato Faria, a lei devia ter ido mais longe. “Devia prever o internamento compulsivo sem necessidade de mandado judicial”, aponta. Ao PÚBLICO, George sustentou apenas que “o internamento compulsivo não é contemplado por razões de coerência com os princípios constitucionais”. Lobato Faria lamenta ainda que a lei não tenha investido mais nos direitos e deveres dos cidadãos quanto a comportamentos que ponham em risco a saúde pública. “Ficaria mais fácil punir ou travar quem não cumprisse a obrigação de não contágio, por recusa de colocação de uma máscara”, exemplificou.
Da fronteira entre a Tailândia e o Camboja vêm terríveis notícias: o parasita da malária ali está a tornar-se resistente ao produto que o combate – o Artemisinin. É uma guerra esquecida, mas todos os anos a malária mata milhão e meio de pessoas em todo o mundo. Se o seu parasita resistir, matará muitos mais.
A malária não é erradicada porque não é um bom negócio como vai ser o vírus da Gripe A. Mas esta luta desigual não deixa de recordar os foguetes pelo fim da crise que foram lançados das sedes de alguns governos na Europa. Não é o fim da crise, como reconheceu Teixeira dos Santos. Porque há uma outra guerra perdida que vai continuar a minar a recuperação: o desemprego.
Joseph Schumpeter, com a sua tese da “destruição criativa”, dizia que o capitalismo tinha uma virtude: das cinzas do mundo empresarial existente nasce sempre um outro.
Não se duvida. Mas o desemprego mostra, desta vez, uma resistência como a da malária. O pesadelo ainda não se transformou num novo sonho. É óbvio que as notícias são boas para José Sócrates e piores para Manuela Ferreira Leite, mas para os desempregados pouco acrescentam. Portugal tem reumático económico estrutural e uns dias está melhor e outros está pior. Mas nunca está curado. Portugal irá à boleia da Europa e dos EUA, mas se se aplicasse a tese de Schumpeter a Portugal, esta seria a altura ideal para que da “destruição criativa”, que atirou centenas de empresas para a falência, nascessem outras, novas e pujantes, capazes de trazer o sonho aos que já não o vislumbram.
Cracks are beginning to appear in the UK’s mainstream media coverage over the “pandemic”, involving hyping Tamiflu and mass vaccinations while exaggerating the threat of the “swine flu”.
Check out this report:
Swine flu: TV presenter’s daughter ‘almost died’ after taking TamifluGMTV star Andrew Castle confronts health secretary, Andy Burnham, over policy of giving drug to children
Press Association guardian.co.uk, Tuesday 11 August 2009 10.40 BST Article history
Andrew Castle, right, with co-presenter Penny Smith confronted the health secretary, Andy Burnham, over giving Tamilflu to children during the swine flu pandemic.
The health secretary, Andy Burnham, today defended giving the antiviral drug Tamiflu to children for swine flu as TV presenter Andrew Castle said his daughter “almost died” after taking it.
Burnham was confronted by Castle on GMTV after researchers said the antiviral drug’s benefits did not outweigh its side-effects during the flu pandemic.
Castle said his older daughter, Georgina, had a “respiratory collapse” and “suffered very heavily” after being “just handed” the drug without a proper diagnosis.
The presenter said: “I can tell you that my child – who was not diagnosed at all – she had asthma, she took Tamiflu and almost died.”
Burnham sympathised with Castle, saying it must have been “very worrying”, but maintained that advice to parents to treat swine flu with Tamiflu remained unchanged.
The MP said Georgina would have been given Tamiflu during the earlier “containment” phase of swine flu.
He stressed that the research dealt with seasonal flu, not swine flu: “It’s very much a safety-first approach.”
Given that swine flu had a “disproportionate effect” on children, the minister maintained that the antiviral drug was “our only line of defence”.
Some 300,000 people in England, including children and adults, have received Tamiflu through the government’s National Pandemic Flu Service for England.
But yesterday, Oxford University researchers said children should not be given the antiviral drug to combat swine flu. They urged the Department of Health to rethink its policy on giving the drug to under-12s during the current pandemic.
The study, published in the British Medical Journal (BMJ), warned that Tamiflu could cause vomiting, which could lead to dehydration and the need for hospital treatment.
The researchers said children should not be given the drug if they had a mild form of the illness, although they urged parents and GPs to remain vigilant for signs of complications.
Parents of children with a compromised immune system or a condition such as cystic fibrosis should discuss the harms and benefits with their GP, they said.
But overall, the researchers said, children who were otherwise healthy could suffer more harm than benefit from taking Tamiflu or another antiviral, Relenza.
The researchers also found that using antivirals as a preventative measure had little effect – reducing transmission of flu by 8%.
The study was carried out in April and May, before the government decided to stop using Tamiflu preventatively.
Only those with suspected or confirmed swine flu were now getting the drug and are being urged to get access to Tamiflu through the pandemic flu service, which is accessed online or via a telephone helpline.
A Department of Health spokesman yesterday dismissed the researchers’ claims that their findings would also apply to swine flu.
“The BMJ review is based on seasonal flu and not swine flu,” he said.
“As the authors note, the extent to which the findings can be applied to the current pandemic is questionable – after all, we already know that swine flu behaves differently to seasonal flu, and past pandemics have hit younger people hardest.”
Georgina, 16, was given Tamiflu when five pupils at Alleyn’s school in south London were diagnosed with the illness in May.
“We saw a respiratory collapse through [the drug] and it almost cost my older child her life,” her father said on GMTV.
“Nobody checked that she had swine flu beforehand. The Health Protection Agency just handed it out … and a lot of kids suffered in the school very heavily.”
He went on: “The doctor’s surgery wouldn’t take her. The doctor said, ‘No, we can’t take her to A&E.’
“So she’s just on the floor having this nightmare of a situation. A lot of people are in this situation. They don’t know what to do.”
Burnham told the presenter: “It must have been a very worrying situation for you, but that was in a very different phase of the illness when we were seeing the scenes from Mexico and we were in what we call the containment phase, where we were trying to isolate every case and then give Tamiflu to those around those cases.
“We’ve got to keep things in proportion and people shouldn’t worry unnecessarily. People shouldn’t take Tamiflu unless they have got swine flu.”
Burnham said his message to parents was that they should not be worried if their child was taking Tamiflu for swine flu.”
Gripe A: Escolas devem prever substituição de professores e teletrabalho
Os planos de contingência das escolas devem prever a substituição dos professores infectados pela Gripe A e equacionar a utilização do teletrabalho e de actividades via e-mail, de acordo com a Direcção-Geral de Saúde.
Segundo o documento “Planos de Contingência para Creches, Jardins de Infância, Escolas e Outros Estabelecimentos de Ensino – Orientações para a sua elaboração”, o plano deve prever as formas de manter as actividades escolares consideradas essenciais no caso de um elevado absentismo dos seus profissionais.
“Perante um cenário de elevado absentismo dos professores ou outros profissionais, é fundamental planear a sua substituição de modo a minimizar o impacto desta situação nas actividades escolares”, lê-se no documento.
As escolas devem ainda equacionar “a possibilidade de utilização do teletrabalho”, bem como, no que se refere aos alunos, prever “actividades através de e-mail”, a fim de reduzir o impacto do absentismo dos professores ou de um eventual encerramento do estabelecimento.
Fonte do Ministério da Educação disse à Lusa que estas orientações já foram enviadas para as Direcções Regionais de Educação, que por sua vez as distribuem pelos estabelecimentos de ensino.
As orientações, datadas de 16 de Julho, indicam que deverá ser designado um “coordenador” e uma “equipa operativa”, que devem trabalhar em articulação com a Unidade de Saúde Pública do respectivo agrupamento de centros de saúde, pais e outras entidades pertinentes.
“É importante, igualmente, identificar os fornecedores de bens e serviços necessários para a manutenção das actividades consideradas essenciais e garantir que esses fornecedores estão igualmente preparados para responder em situações de crise […]. Se não for o caso devem ser encontradas soluções alternativas”, lê-se no documento, numa referência ao fornecimento de refeições ou transporte escolar, por exemplo.
É ainda recomendada, entre outras, a posse de “alguma reserva de água engarrafada e de alimentos não perecíveis”, bem como um aumento das “reservas de produtos de higiene e limpeza ou de materiais escolares”.
No caso de encerramento da escola ou absentismo dos professores, acrescenta, “poderão prever-se estratégias de informação e envolvimento dos pais que lhes permitam apoiar a realização de trabalhos escolares em casa, em articulação com os professores”.
Quanto a medidas de higiene no estabelecimento de ensino, o estado das instalações e equipamentos para lavagem das mãos deve ser avaliado, “no sentido de reparação de eventuais deficiências, de preferência antes do ínicio do ano escolar”.
“Deve ser feita uma identificação do equipamento que será necessário instalar, por exemplo dispositivos para fornecimento de toalhetes de papel nas casas de banho”, lê-se no documento, disponível no microsite da gripe da Direcção-Geral da Saúde.
Many Americans watch corporate-funded shills like ABC’s Doctor Oz tell them that the 
The first doses of the H1N1 swine flu vaccine are now being administered at clinics and hospitals across the United States, and many Americans are eagerly lining up to take their vaccine. But is the mainstream media accurately informing the public about what they are taking? The reality is that most Americans do not realize that all of the early batches of the H1N1 swine flu nasal vaccine (called FluMist) contain live swine flu. If you are trying to avoid the swine flu do you really think that it is a good idea to have live swine flu injected up your nose? Many health experts are expressing a grave concern about the safety of this FluMist vaccine, and many hospitals are rejecting this nasal spray vaccine altogether. In fact, several Denver area hospitals are rejecting the FluMist swine flu vaccine because 
So millions of Americans will have live swine flu injected into their nasal passages over the coming weeks, and they will instantly become carriers of this deadly disease. Whenever these vaccinated Americans sneeze or whenever they exhale or whenever they wipe their hands on anything they risk spreading the swine flu to others.
