AUTISM PREVENTION FATHER BABIES 24-34 PATERNAL AGE IS KEY IN NON-FAMILIAL AUTISMVaccines

"It is very possible that PATERNAL AGE is the major predictor of(non-familial) autism." Harry Fisch, M.D., author "The Male Biological Clock". Sperm DNA mutates and autism, schizophrenia bipolar etc. results. What is the connection with autoimmune disorders? Having Type 1 diabetes, SLE,etc. in the family, also if mother had older father. NW Cryobank will not accept a sperm donor past 35th BD to minimize genetic abnormalities.VACCINATIONS also cause autism.

Thursday, October 01, 2009

How U.S. Government Will Compel All Americans to Implant Positive I.D. Chip and Grave Concerns about H1N1 Vaccine
October 1, 2009 by captkarl



After watching the above video you know for a fact that you will not let the U.S. Government implant a chip in you or any member of your family right? Well that remains to be seen, my fellow American; because what if the U.S. Government and the Corporations that have, as Barack Obama himself stated on public TV; “fused in with the U.S. Government”, developed an implantable H1N1 detector Positive I.D. RFID chips which convince you to implant the device for what they will beguile you into believing is for your health and best interests and the health and best interests of “The Masses”?

Or, What if they legislate a law that requires you to implant the devise in yourself and every member of your family to protect Americans across our entire nation from some national terrorist emergency (or domestic terror; like Christians or Americans who believe in The Constitution and freedom) or pandemic like the Swine Flu?

Impossible you say? Here is a confirmed business news report:

Michael Barbe, Vice President of Sales at VeriChip Corporation which manufactures implantable RFIDs for human medical applications and which has just patented chips that can supposedly detect H1N1, was employed for Baxter managing their entire portfolio of sales of hospital products.
http://www.zoominfo.com/people/Barbe_Michael_1172882772.aspx
Unconfirmed reports say Baxter is planning to include nanochips in its “swine flu” vaccine.


If it turns out that Baxter has created nanite RFID chips and you get the swine flu vaccination, it may be possible that the U.S. Government could track you, “pinpoint you” as stated in the video, anywhere they would put up sensors like in door frames of buildings, telephone pole, traffic light poles, anyplace they could install super sensative RFID sensors. Unlike the old larger RFID chip shown in the video, nanites would flow around you body with your blood stream. They could not be removed like the RFID chip in the movie above because they would be racing around your whole body. Still want to get that H1N1 swine flu vaccine shot? Do you trust the U.S. Government and their cronies in BIG Corporations? Have you noticed how BIG Pharma has supported President Obama’s call for “The Public Option”? You had better ask yourself why. And, ask yourself; “What deal did they make with the U.S. Government to get them to lower their prices to save all that money Obama anounced?” And perhaps you better think twice about that vaccine shot.
UPDATE 1-VeriChip shares jump after H1N1 patent license win

Mon Sep 21, 2009 3:11pm EDT
Sept 21 (Reuters) – Shares of VeriChip Corp (CHIP.O)
tripled after the company said it had been granted an exclusive license to two patents, which will help it to develop implantable virus detection systems in humans. The patents, held by VeriChip partner Receptors LLC, relate to biosensors that can detect the H1N1 and other viruses, and biological threats such as methicillin-resistant Staphylococcus aureus, VeriChip said in a statement. The technology will combine with VeriChip’s implantable radio frequency identification devices to develop virus triage detection systems. The triage system will provide multiple levels of identification — the first will identify the agent as virus or non-virus, the second level will classify the virus and alert the user to the presence of pandemic threat viruses and the third level will identify the precise pathogen, VeriChip said in a white paper published May 7, 2009.
Shares of VeriChip were up 186 percent at $3.28 Monday late afternoon trade on Nasdaq. They had touched a year high of $3.43 earlier in the session.
(Reporting by Mansi Dutta in Bangalore; Editing by Mike Miller and Anil D’Silva)



Could the U.S. Government force you and your family to accept an injection of the RFID Positive I.D. Chip? What if the U.S. Government proves to some Federal Court that the injection of the RFID chip into all Americans will prevent thousands of people from dying from the “emergency”? Is it not possible, if not likely, that to protect many thousands of people from dying the court will find that it is Constitutionally legal to force the implantations under the (false) interpretation of the “General Welfare” clause? You better think about all of these things people BEFORE you are faced with this. What will you do when you are “under the gun” so to speak?

Public Health Emergency” and Martial Law: The John Warner Defense Authorization Act of 2007. H.R. 5122
New legislation is devised. The terms “epidemic”, and “public health emergency” are explicitly included in a key piece of legislation, signed into law by President Bush in October 2006.
Lost in the midst of hundreds of pages, Public Law 109-364, better known as the “John Warner Defense Authorization Act of 2007″ (H.R.5122) includes a specific section on the role of the Military in civilian affairs.
Section 1076 of this legislation entitled “Use of the Armed Forces in Major Public Emergencies” allows the President of the United States the deploy the armed forces and the National Guard across the US, to “restore public order and enforce the laws of the United States” in the case of “a natural disaster, epidemic, or other serious public health emergency”:
SEC. 1076. USE OF THE ARMED FORCES IN MAJOR PUBLIC EMERGENCIES.
(a) Use of the Armed Forces Authorized-
(1) IN GENERAL- Section 333 of title 10, United States Code, is amended to read as follows:
`Sec. 333. Major public emergencies; interference with State and Federal law
`(a) Use of Armed Forces in Major Public Emergencies- (1) The President may employ the armed forces, including the National Guard in Federal service, to–
`(A) restore public order and enforce the laws of the United States when, as a result of a natural disaster, epidemic, or other serious public health emergency, terrorist attack or incident, or other condition in any State or possession of the United States, the President determines that–
`(i) domestic violence has occurred to such an extent that the constituted authorities of the State or possession are incapable of maintaining public order; and
`(ii) such violence results in a condition described in paragraph (2); or
`(B) suppress, in a State, any insurrection, domestic violence, unlawful combination, or conspiracy if such insurrection, violation, combination, or conspiracy results in a condition described in paragraph (2).
`(2) A condition described in this paragraph is a condition that–
`(A) so hinders the execution of the laws of a State or possession, as applicable, and of the United States within that State or possession, that any part or class of its people is deprived of a right, privilege, immunity, or protection named in the Constitution and secured by law, and the constituted authorities of that State or possession are unable, fail, or refuse to protect that right, privilege, or immunity, or to give that protection; or
`(B) opposes or obstructs the execution of the laws of the United States or impedes the course of justice under those laws.
`(3) In any situation covered by paragraph (1)(B), the State shall be considered to have denied the equal protection of the laws secured by the Constitution.
`(b) Notice to Congress- The President shall notify Congress of the determination to exercise the authority in subsection (a)(1)(A) as soon as practicable after the determination and every 14 days thereafter during the duration of the exercise of that authority.’ (See ext of HR5122 http://thomas.loc.gov/cgi-bin/query/F?c109:6:./temp/~c109bW9vKy:e939907:http://www.govtrack.us/congress/bill.xpd?bill=h109-5122&tab=summary
These far-reaching provisions allow the Armed Forces to override the authority of civilian federal, state and local governments involved in disaster relief and public health. It also grants the Military a mandate in civilian police functions. Namely the legislation implies the militarization of law enforcement in the case of a national emergency.
“Catastrophic Emergency” and “Continuity of Government,”: The National Security and Homeland Security Presidential Directive NSPD 51/HSPD 20

Coinciding with the passage of the John Warner Defense Authorization Act, a National Security Presidential Directive was issued in May 2007, (National Security and Homeland Security Presidential Directive NSPD 51/HSPD 20) .
NSPD 51 /HSPD 20 is a combined National Security Directive emanating from the White House and Homeland Security. While it is formulated in relation to the domestic “war on terrorism”, it also includes provisions which allow for Martial Law in case of a natural disaster including a flu pandemic.
The thrust and emphasis of NSPD 51, however, is different from that of Section 1076 of HR 5122. It defines the functions of the Department of Homeland Security in the case of a national emergency and its relationship to the White House and the Military. It also provides the President with sweeping powers to declare a national emergency, without Congressional approval.
The directive establishes procedures for “Continuity of Government” (COG) in the case of a “Catastrophic Emergency”. The latter is defined in NSPD 51/HSPD 20 (henceforth referred to as NSPD 51), as “any incident, regardless of location, that results in extraordinary levels of mass casualties, damage, or disruption severely affecting the U.S. population, infrastructure, environment, economy, or government functions.”
“Continuity of Government,” or “COG,” is defined in NSPD 51 as “a coordinated effort within the Federal Government’s executive branch to ensure that National Essential Functions continue to be performed during a Catastrophic Emergency.”
The President shall lead the activities of the Federal Government for ensuring constitutional government. In order to advise and assist the President in that function, the Assistant to the President for Homeland Security and Counter terrorism (APHS/CT) is hereby designated as the National Continuity Coordinator. The National Continuity Coordinator, in coordination with the Assistant to the President for National Security Affairs (APNSA), without exercising directive authority, shall coordinate the development and implementation of continuity policy for executive departments and agencies. The Continuity Policy Coordination Committee (CPCC), chaired by a Senior Director from the Homeland Security Council staff, designated by the National Continuity Coordinator, shall be the main day-to-day forum for such policy coordination. (National Security and Homeland Security Presidential Directive NSPD 51/HSPD 20, emphasis added)
This Combined Directive NSPD /51 HSPD 20 grants unprecedented powers to the Presidency and the Department of Homeland Security, overriding the foundations of Constitutional government. NSPD 51 allows the sitting president to declare a ?national emergency? without Congressional approval The adoption of NSPD 51 would lead to the de facto closing down of the Legislature and the militarization of justice and law enforcement.
NSPD 51 grants extraordinary Police State powers to the White House and Homeland Security (DHS), in the event of a “Catastrophic Emergency”.
A flu pandemic or public health emergency is part of the terms of reference of NSPD 51. “Catastrophic Emergency” is broadly defined in NSPD 51 as “any incident, regardless of location, that results in extraordinary levels of mass casualties, damage, or disruption severely affecting the U.S. population, infrastructure, environment, economy, or government functions”
“The President shall lead the activities of the Federal Government for ensuring constitutional government. In order to advise and assist the President in that function, the Assistant to the President for Homeland Security and Counter terrorism (APHS/CT) is hereby designated as the National Continuity Coordinator. The National Continuity Coordinator, in coordination with the Assistant to the President for National Security Affairs (APNSA), without exercising directive authority, shall coordinate the development and implementation of continuity policy for executive departments and agencies. The Continuity Policy Coordination Committee (CPCC), chaired by a Senior Director from the Homeland Security Council staff, designated by the National Continuity Coordinator, shall be the main day-to-day forum for such policy coordination. (National Security and Homeland Security Presidential Directive NSPD 51/HSPD 20, emphasis added)
The directive acknowledges the overriding power of the military in the case of a national emergency: The presidential directive “Shall not be construed to impair or otherwise affect… the authority of the Secretary of Defense over the Department of Defense, including the chain of command for military forces from the President, to the Secretary of Defense, to the commander of military forces, or military command and control procedures”.
Since their enactment two years ago, neither the John Warner Defense Authorization Act nor NSPD 51 have been the object of media debate or discussion.
NSPD 51 and/or the John Warner H.R.5122 could be invoked at short notice following the declaration of a national health emergency and a nationwide forced vaccination program. The hidden agenda consists in using the threat of a pandemic and/or the plight of a natural disaster as a pretext to establish military rule, under the facade of a “functioning democracy”.
Vaccination: From H5N1 to H1N1
A nationwide flu vaccination program has been in the pipeline since 2005.
According to the Wall Street Journal (Oct 1, 2005), the Bush administration had asked Congress for an estimated $6-10 billion “to stockpile vaccines and antiviral medications as part of its plans to prepare the U.S. for a possible flu pandemic.” A large part of this budget, namely 3.1 billion was used under the Bush administration to stockpile the antiviral drug oseltamivir (Tamiflu), of which the intellectual property rights belong to Gilead Science Inc, a company headed by Don Rumsfeld prior to becoming Secretary of Defense under the Bush administration.
Consistent with its role as “lead agency”, more than half of the money earmarked by the Bush administration for the program was handed over to the Pentagon. In other words, what we are dealing with is a process of militarization of the civilian public health budget. Social sector budgets are now being transferred to the Department of Defense. The money for a public health program is controlled by the Department of Defense, under the rules of DoD procurement.

“The US Senate voted [September 3, 2005] yesterday to provide $4 billion for antiviral drugs and other measures to prepare for a feared influenza pandemic, but whether the measure would clear Congress was uncertain.
The Senate attached the measure to a $440 billion defense-spending bill for 2006, according to the Associated Press (AP). But the House included no flu money in its version of the defense bill, and a key senator said he would try to keep the funds out of the House-Senate compromise version. The Senate is expected to vote on the overall bill next week.
Almost $3.1 billion of the money would be used to stockpile the antiviral drug oseltamivir (Tamiflu), and the rest would go for global flu surveillance, development of vaccines, and state and local preparedness, according to a Reuters report. The government currently has enough oseltamivir to treat a few million people, with a goal of acquiring enough to treat 20 million”
(CIDRAP, http://www.cidrap.umn.edu/cidrap/content/influenza/panflu/news/sep3005avian.html)
The threat of the H5N1 bird flu pandemic in 2005 resulted in multibillion dollar earnings for the pharmaceutical and biotech industry. In this regard, a number of major pharmaceutical companies including GlaxoSmithKline, Sanofi-Aventis, California based Chiron Corp, BioCryst Pharmaceuticals Inc, Novavax and Wave Biotech, Swiss pharmaceutical giant Roche Holding, had already positioned themselves. In 2005,.a Maryland-based biotechnology company MedImmune which produces “an inhaled flu vaccine” had positioned itself to develop a vaccine against the H5N1 avian flu. Although it had no expertise in the avian flu virus, one of the major actors in the vaccine business, on contract to the Pentagon, was Bioport, a company part owned by the Carlyle Group, closely linked to the Bush Cabinet with Bush Senior on its board of directors.
Forced Vaccination under a Public Health Emergency? Multibillion Financial Bonanza for the BioTech Conglomerates
The 2005 bird flu hoax was in many regards a dress rehearsal. The 2009 H1N1 pandemic is a much larger multibillion dollar operation. A select number of biotech and pharmaceutical companies have been involved in negotiations behind closed doors with the WHO and the US Administration. Key agencies are the Atlanta based Center for Disease Control and the Food and Drug Administration (FDA) which have close ties to the pharmaceutical industry. The conflicts of interest of these agencies is brought to light in Robert F. Kennedy Jr.’s detailed study entitled Vaccinations: Deadly Immunity, June 2005:
“The story of how government health agencies colluded with Big Pharma to hide the risks of thimerosal from the public is a chilling case study of institutional arrogance, power and greed. I was drawn into the controversy only reluctantly. As an attorney and environmentalist who has spent years working on issues of mercury toxicity, I frequently met mothers of autistic children who were absolutely convinced that their kids had been injured by vaccines. … “The elementary grades are overwhelmed with children who have symptoms of neurological or immune-system damage,” Patti White, a school nurse, told the House Government Reform Committee in 1999. “Vaccines are supposed to be making us healthier; however, in twenty-five years of nursing I have never seen so many damaged, sick kids. Something very, very wrong is happening to our children.” Robert F. Kennedy Jr, Vaccinations: Deadly Immunity, June 2005.
The WHO is planning for the production of 4.9 billion dose, enough to inoculate a large share of the World’s population. Big Pharma including Baxter, GlaxoSmithKline, Novartis, Sanofi-Aventis and AstraZeneca have signed procurement contracts with some 50 governments. (Reuters, July 16, 2009). For these companies, compulsory vaccination is a highly lucrative undertaking:
“The WHO has refused to release the Minutes of a key meeting of an advisory vaccine group “packed with executives from Baxter, Novartis and Sanofi” that recommended compulsory vaccinations in the USA, Europe and other countries against the artificial H1N1 “swine flu” virus this autumn.
In an email this morning, a WHO spokesperson claimed there are no Minutes of the meeting that took place on July 7th in which guidelines on the need for worldwide vaccinations that WH0 adopted this Monday were formulated and in which Baxter and other Pharma executives participated.
Under the International Health Regulations, WHO guidelines have a binding character on all of WHO’s 194 signatory countries in the event of a pandemic emergency of the kind anticipated this autumn when the second more lethal wave of the H1N1 virus “which is bioengineered to resemble the Spanish flu virus” emerges.
In short: WHO has the authority to force everyone in those 194 countries to take a vaccine this fall at gunpoint, impose quarantines and restrict travel.” (Jane Burgermeister, WHO moves forward in secrecy to accomplish forced vaccination and population agenda, Global Research, July 2009).
On May 19th, the WHO Director General and senior officials met behind closed doors with the representatives of some 30 pharmaceutical companies.
“In a perfect world the planet’s leading pharmaceutical companies could produce 4.9 billion H1N1 swine flu vaccinations over the course of the next year. This is the World Health Organization’s latest assessment. WHO Director-General Dr. Margaret Chan met with 30 pharmaceutical companies on Tuesday and briefed reporters on a WHO plan to secure vaccinations for poor countries who lack sufficient infrastructure to fight a possible pandemic. (Digital Journal, 19 May 2009)
According to recent report in Business Week, “Wealthier countries such as the U.S. and Britain will pay just under $10 per dose, the same price for the seasonal flu vaccine. Developing countries will pay a lower price, (Business Week, July 2009). The WHO suggests that the 4.9 billion doses will not suffice and that a second inoculation will be required.
4,9 billion doses at about ten dollars ($10.00) a shot and somewhat less in the developing countries, represents a windfall profit bonanza for Big Pharma of the order of 400 billion dollars in a single year. And the WHO claims that one dose per person may not suffice…
Dangerous Life Threatening Vaccine: Who owns the Patent?
While the production has been entrusted to a select number of companies, it would appear that the intellectual property rights belong to Illinois based pharmaceutical giant Baxter. Baxter is central in the negotiations between the US Administration and the World Health Organization (WHO). Moreover, “a full year before any reported case of the current alleged H1N1″ Baxter had filed for a patent for the H1N1 vaccine:
Baxter Vaccine Patent Application US 2009/0060950 A1. (See William Engdahl, Now legal immunity for swine flu vaccine makers, Global Research, July 2009). Their application: states:
“the composition or vaccine comprises more than one antigen… such as influenza A and influenza B in particular selected from of one or more of the human H1N1, H2N2, H3N2, H5N1, H7N7, H1N2, H9N2, H7N2, H7N3, H10N7 subtypes, of the pig flu H1N1, H1N2, H3N1 and H3N2 subtypes, of the dog or horse flu H7N7, H3N8 subtypes or of the avian H5N1, H7N2, H1N7, H7N3, H13N6, H5N9, H11N6, H3N8, H9N2, H5N2, H4N8, H10N7, H2N2, H8N4, H14N5, H6N5, H12N5 subtypes.”
The application further states, “Suitable adjuvants can be selected from mineral gels, aluminium hydroxide, surface active substances, lysolecithin, pluronic polyols, polyanions or oil emulsions such as water in oil or oil in water, or a combination thereof. Of course the selection of the adjuvant depends on the intended use. E.g. toxicity may depend on the destined subject organism and can vary from no toxicity to high toxicity.”
With no legal liability, could it be that Baxter is preparing to sell hundreds of millions of doses containing highly toxic aluminium hydroxide as adjuvant? (Ibid)
The Los Angeles Times has reassured the US public with an article entitled: What are the odds that H1N1 will kill you? One might also ask, what are the odds that the H1N1 vaccine will kill you?
National Emergency Centers Establishment Act: H.R. 645
If Martial Law or a National emergency were to be adopted in the context of a Public Health emergency, what we would be dealing with is the “forced vaccination” of millions of people as well as the establishment of internment facilities for people who have been quarantined.
In this regard, it is worth noting that in January 2009, a piece of legislation entitled the National Emergency Centers Establishment Act (HR 645) was introduced in the US Congress.The bill calls for the establishment of six national emergency centers in major regions in the US to be located on existing military installations, which could be used to quarantine people in the case of a public health emergency or forced vaccination program.
The bill goes far beyond previous legislation (including H.R 5122). The stated purpose of the “national emergency centers” is to provide “temporary housing, medical, and humanitarian assistance to individuals and families dislocated due to an emergency or major disaster.” In actuality, what we are dealing with are FEMA internment camps. HR 645 states that the camps can be used to “meet other appropriate needs, as determined by the Secretary of Homeland Security.” (Michel Chossudovsky,Preparing for Civil Unrest in America Legislation to Establish Internment Camps on US Military Bases, Global Research, March 2009)
There has been virtually no press coverage of HR 645, which is currently being discussed by several congressional committees.
These “civilian facilities” on US military bases are to be established in cooperation with the US Military. Modeled on Guantanamo, what we are dealing with is the militarization of FEMA internment facilities.
Once a person is arrested and interned in a FEMA camp located on a military base, that person would in all likelihood, under a public health emergency, fall under the de facto jurisdiction of the Military: civilian justice and law enforcement including habeas corpus would no longer apply.
HR 645 could be used, were it to be adopted, in the case of public health emergency. It obviously bears a direct relationship to the economic crisis and the likelihood of mass protests across America. It constitutes a further move to militarize civilian law enforcement, repealing the Posse Comitatus Act.
In the words of Rep. Ron Paul:
“…the fusion centers, militarized police, surveillance cameras and a domestic military command is not enough… Even though we know that detention facilities are already in place, they now want to legalize the construction of FEMA camps on military installations using the ever popular excuse that the facilities are for the purposes of a national emergency. With the phony debt-based economy getting worse and worse by the day, the possibility of civil unrest is becoming a greater threat to the establishment. One need only look at Iceland, Greece and other nations for what might happen in the United States next.” (Daily Paul, September 2008, emphasis added)
The proposed internment camps should be seen in relation to the broader process of militarization of civilian institutions. The construction of internment camps predates the introduction of HR 645 (Establishment of Emergency Centers) in January 2009.
“Military Civil Support”: The Role of US Northern Command in the Case of a Flu Pandemic
US Northern Command has a mandate to support and oversee civilian institutions in the case of a National Emergency.
In addition to defending the nation, U.S. Northern Command provides defense support of civil authorities in accordance with U.S. laws and as directed by the President or Secretary of Defense. Military assistance is always in support of a lead federal agency, such as the Federal Emergency Management Agency (FEMA).
Military civil support includes domestic disaster relief operations that occur during fires, hurricanes, floods, and earthquakes. Support also includes counter-drug operations and consequence management assistance, such as would occur after a terrorist event employing a weapon of mass destruction.
Generally, an emergency must exceed the management capabilities of local, state and federal agencies before U.S. Northern Command becomes involved. In providing civil support, the command operates through subordinate Joint Task Forces.
(See US Northcom website at http://www.northcom.mil/index.cfm?fuseaction=s.who_civil ).
The Katrina and Rita hurricane disasters played a key role in shaping the role of US Northern Command in “military civil support” activities. The emergency procedures were closely coordinated by US Northern Command out of the Peterson Air Force Base, together with Homeland Security, which oversees FEMA.
During Hurricane Rita (September 2005), US Northern Command Headquarters was directly in control of the movement of military personnel and hardware in the Gulf of Mexico, overriding, as in the case of Katrina, the actions of civilian bodies. The entire operation was under the jurisdiction of the military rather than FEMA. (Michel Chossudovsky, US Northern Command and Hurricane Rita, Global Research, September 24, 2005)
Northern Command would, as part of its mandate in the case of a national emergency, oversee a number of civilian functions. In the words of Preident Bush at the height of the Rita hurricane, “the Government and the US military needed broader authority to help handle major domestic crises such as hurricanes.” Homeland Security Secretary Michael Chertoff subsequently classified Hurricane Rita as an “incident of national significance,” which justified the activation of a so-called “National Response Plan”(NRP). (For further details, consult the complete document athttp://www.dhs.gov/interweb/assetlibrary/NRPbaseplan.pdf
Within the broader framework of “Disaster Relief”, Northern Command has, in the course of the last two years, defined a mandate in the eventuality of a public health emergency or a flu pandemic. The emphasis is on the militarization of public health whereby NORTHCOM would oversee the activities of civilian institutions involved in health related services.
According Brig. Gen. Robert Felderman, deputy director of USNORTHCOM’s Plans, Policy and Strategy Directorate: “USNORTHCOM is the global synchronizer – the global coordinator – for pandemic influenza across the combatant commands”(emphasis added) (See Gail Braymen, USNORTHCOM contributes pandemic flu contingency planning expertise to trilateral workshop, USNORTHCOM, April 14, 2008, See also USNORTHCOM. Pandemic Influenza Chain Training (U) pdf)
“Also, the United States in 1918 had the Spanish influenza. We were the ones who had the largest response to [a pandemic] in more recent history. So I discussed what we did then, what we expect to have happen now and the numbers that we would expect in a pandemic influenza.”
The potential number of fatalities in the United States in a modern pandemic influenza could reach nearly two million, according to Felderman. Not only would the nation’s economy suffer, but the Department of Defense would still have to be ready and able to protect and defend the country and provide support of civil authorities in disaster situations. While virtually every aspect of society would be affected, “the implications for Northern Command will be very significant.”
“[A pandemic would have] a huge economic impact, in addition to the defense-of-our-nation impact,” Felderman said. The United States isn’t alone in preparing for such a potential catastrophe. (Gail Braymen, op cit)
It is worth noting that Northern Command (USNORTHCOM) has developed, over the past few years, a clearly defined mandate in the eventuality of a flu pandemic.
Also of relevance, was the repatriation of combat units from the war theater to assist US Northern Command in the case of a national emergency including a flu pandemic. In the last months of the Bush administration, the Department of Defense ordered the recall of the 3rd Infantry’s 1st Brigade Combat Team from Iraq.
The BCT combat unit was attached to US Army North, the Army’s component of US Northern Command (USNORTHCOM). The 1st BCT and other combat units would be called upon to perform specific military functions in the case of a national emergency or natural disaster including a public health emergency:
“The Army Times reports that the 3rd Infantry’s 1st Brigade Combat Team is returning from Iraq to defend the Homeland, as “an on-call federal response force for natural or manmade emergencies and disasters, including terrorist attacks.” The BCT unit has been attached to US Army North, the Army’s component of US Northern Command (USNORTHCOM). (See Gina Cavallaro, Brigade homeland tours start Oct. 1, Army Times, September 8, 2008, emphasis added).

HIN1 Pandemic: Mulitbillion Dollar bonanza for Big Pharma
GlaxoSmithKline: A Swine Flu Windfall?
Global Research, July 26, 2009
businessweek.com
GlaxoSmithKline: A Swine Flu Windfall? British drugmaker GlaxoSmithKline has orders for its swine flu vaccine from 16 countries and is in talks with 50 more By Kerry Capell
Europe Airlines Face Traveler Crash Fears Who Is New Porsche Boss Michael Macht? Intel Appeals EU Antitrust Ruling BP: Iraq Oil Deal is Start of Something Big Europe Issues New Bank Guidelines Story Tools post a comment e-mail this story print this story order a reprint suggest a story digg this save to del.icio.us linkedin connections British pharmaceutical giant GlaxoSmithKline (GSK) is set to reap billions as fear of the swine flu pandemic grows. The world’s second-largest drug company has secured orders from 16 countries for 195 million doses of the vaccine it is developing against the H1N1 virus, which has killed more than 740 people worldwide.
The Brentford (England)-based drugmaker began production of its new flu vaccine in June and is on track to begin shipping the first doses in September. At a July 22 briefing to announce the company’s second-quarter results, CEO Andrew Witty confirmed the number of orders is expected to be “substantially more” as the company currently is in discussions with 50 countries. While Britain has ordered 60 million doses of the vaccine, according to Witty, the U.S. has paid GSK $250 million to supply it with “pandemic products” such as the individual ingredients used in the vaccine. These include the antigen that prompts an individual’s immune response and GSK’s adjuvent technology, a sort of booster used to increase the vaccine’s yield and potency.
GSK also announced it expects to increase annual production of its inhalable anti-viral flu treatment Relenza threefold, to 190 million doses, by yearend. Relenza sales for the three months ended June 30 were $99 million, up from just $5 million in the second quarter of 2008. Since the beginning of 2006, GSK has invested $2.5 billion to put in place the technology and capacity needed to meet demand. “Short of putting beds in the labs, we are throwing just about every resource we have into this,” Witty says.
The Competition Heats Up Witty reckons continued demand for GSK’s flu drug and vaccine will likely boost sales in the second half of this year. GSK is one of several companies, including Novartis (NVS), Sanofi-Aventis (SNY), and Baxter International (BAX), racing to develop a swine flu vaccine.
While Witty says he is confident that GSK will meet its commitments, the company’s total production capacity is still unknown. That’s because the current strain of the swine flu virus is yielding less of the active ingredient or antigen needed to produce the vaccine than expected. (Because each flu virus varies, different strains produce varying levels of antigens.) Novartis also has conceded that the virus it’s growing for its swine flu vaccine is producing a lower-than-expected yield. But Witty says based on current production levels, GSK should still be able to meet its commitments to governments around the world by early 2010.
With countries stepping up efforts to combat the pandemic, GSK’s bottom line is likely to get a boost. However, Witty says that margins on both Relenza and the new vaccine are likely to be modest. GSK has a differentiated pricing structure for the new vaccine. Wealthier countries such as the U.S. and Britain will pay just under $10 per dose, the same price for the seasonal flu vaccine. Developing countries will pay a lower price, while GSK will donate 50 million doses of the vaccine to the World Health Organization for distribution to the world’s poorest countries.
Generics Hurt U.S. Sales Still, even the boost in sales of GSK’s flu treatment and vaccine were not enough to offset the rapid slowdown in U.S. prescription drug sales due to competition from generic drugs. In the three months ended June 30, GSK’s sales rose 15%, to $11 billion, on the back of the sterling’s weakness against major currencies such as the dollar. In constant currency terms, sales fell by 2% mainly due to the performance of the company’s U.S. pharmaceuticals business, where sales plummeted by 15%, to $3.8 billion, as former top sellers such as epilepsy treatment Lamictal faced generic competition. Net profits surged by 12%, to $2.5 billion.
The results, says Sanford C. Bernstein pharmaceuticals analyst Timothy Anderson, were slightly better than expected in large part thanks to the weakening of the British pound against the dollar. Witty acknowledged “there was still a lot more work to do” but claimed the company was “making progress in the right direction

Here is some light at the end of the tunnel. Hopefully the light won’t be ever turned off:

Preliminary Injunction to Halt Mandatory Flu Vaccination in the U.S. Has Been Issued

by Barbara Minton, Natural Health Editor
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(NaturalNews) A Preliminary Injunction to stop mandatory vaccinations has been issued in the United States District Court of New Jersey. This comes after a federal lawsuit opposing forced vaccines was filed in that court by Tim Vawter, pro se attorney, on July 31st with the federal government as defendant. When the judge signs the Preliminary Injunction, it will stop the federal government from forcing anyone in any state to take flu vaccine against their will. It will also prevent a state or local government from forcibly vaccinating anyone, and forbid any person who is not vaccinated from being denied any services or constitutional rights. Vawter’s filings included a Complaint, and several pages of evidentiary Exhibits.

Vawter’s legal papers have been written not only for filing in federal court, but additionally so they can be looked at by activists around the world for ideas on filing lawsuits in their own countries to help stop forced vaccinations. Vawter believes that as the truth of the dangers of flu vaccines continues to become known, banning the forced use of them will eventually succeed on a worldwide basis. He cautions people to avoid fear and keep themselves focused on the task of blocking forced vaccination.

Preliminary Injunction will immediately halt mandatory vaccinations in the U.S.

The Court, having heard the Motion for Preliminary Injunction and read the papers in its support, states in the Preliminary Injunction that it appears the federal government has engaged in some amount of negligence with regards to failure to properly investigate the safety of the flu vaccines scheduled for use in late 2009-2010, and the evidence submitted does warrant a more thorough investigation into the safety of the flu vaccines.

The Court ordered that the government shall be forbidden from forcing any person to be required to take any influenza vaccination against that person’s free will and free choice. The government will not allow any state or local government, or any party, to force any person to be required to take any influenza vaccination against that person’s free will and free choice.

It is further ordered that the government shall not deny any constitutional rights to any person who has not received a flu vaccine, nor allow any doctor, company, or other party to deny any of these people services such as medical care, attending school, or similar services or freedoms, nor can the government allow any doctors, companies, or other parties, to deny any of these people their constitutional rights. The only exception to this, where a person who does not get a flu vaccination might be denied certain services, shall be after it is shown in a court of law, with clear and convincing evidence, on an individual case-by-case basis, where due process and a right to a defense is allowed. Only then can a person be denied a particular service because the person did not receive a flu vaccine.

U.S. government sued for gross negligence and violation of the Constitution

In his Cause of Action, Vawter charged that the federal government has engaged in gross negligence by funding and promoting flu vaccines that are proven to be dangerous and manufactured with little oversight. The vaccines scheduled for use in late 2009 and 2010 contain heavy metals including thimerosal mercury, which have been proven to cause autism in children with lowered immune systems, and other dangerous and toxic ingredients. The federal government has stated it will force these flu vaccines onto the American public against their will, under a document signed by Health and Human Services Secretary Kathleen Sebelius.

He further charged that the vaccine makers stand to earn billions of dollars selling vaccines, and are already spending tens of millions advertising a “Phase 6 Pandemic” that the evidence shows does not really exist. The federal government has not required the World Health Organization (WHO) to show evidence of such a pandemic. There has been no collection of facts, sworn testimony, witnesses being questioned, hearings being held, or lie detector tests being given when preposterous statements have been made. The WHO declared a massive “Phase 6 Influenza Pandemic”, even though only a few hundred people worldwide had so far died of this swine flu virus, and when far more people die each year of regular flu.

Vawter noted there is a preponderance of evidence to show that the federal government so poorly trained its employees that they eagerly agreed with the unsubstantiated claims of the WHO in the face of evidence to the contrary.

Forced vaccination would violate the Fourth Amendment of the Constitution by allowing the government to enter homes and force people to be vaccinated, or to forcibly remove people to another location for vaccination. It would also violate Fifth Amendment Constitutional rights by depriving people of liberty without due process of law.

Vawter charged that the federal government has engaged in gross negligence by failing to properly investigate factual evidence submitted by esteemed medical professions over many years which proves flu vaccines have caused serious damage to people. The CDC has stated that thimerosal mercury is being used in the new flu vaccines being prepared.

The government has failed to investigate profiteering. Billions of dollars in vaccine sales can cause organizations to falsify threats so as to cause unwarranted public hysteria leading to forced vaccinations.

The government is guilty of gross negligence because its employees failed to properly investigate the release of a case of live swine flu virus. One of the main companies the government deals with, Baxter Vaccines, was apparently involved in the transporting of live bird flu virus that was released on a public train earlier this year. A lab technician with the Swiss National Center for Influenza in Geneva had traveled to Zurich to collect eight ampoules, five of which were filled with the H1N1 swine flu virus. However, failure of the dry ice in their container allowed pressure to build up, and the ampoules exploded as the train was pulling into a station.

The highly reputable UK newspaper “the Telegraph” reported on July 2nd that flu vaccines tested on homeless people caused twenty-one of them to die.

Vawter charged there is a preponderance of evidence to show that government will not provide people being vaccinated with a list of the vaccine ingredients and possible negative side effects before they are vaccinated. Most of the public will not know this flu vaccine contains thimerosal mercury.

Vawter submitted an Order to force the government to publish vaccine ingredients and side effects, and to give this information to everyone who takes a flu vaccine, and do so at least 3 days prior to their vaccination. A denial of this order would violate Plaintiff’s rights to demand the government obey the First Amendment of the U.S. Constitution by requiring it to engage in freedom of speech. The First Amendment not only allows a citizen to have freedom of speech himself, but it allows a citizen to demand his government engage in freedom of speech when it is promoting the use of such as these vaccinations to the public.

The government proclamation stating a person cannot sue for any damages he receives from the flu vaccine, completely bypasses the congress and the court system in violation of the Seventh Amendment of the Constitution which grants the right to sue to recover for damages. Vawter submitted an Order to deem unconstitutional any proclamation, rule or similar law that forbids people from suing for damages resulting from the vaccines of 2009 and 2010.

Vawter is seeking damages of $100,000.00 as the result of suffering depression, extreme anxiety and emotional duress when his nephew began life as a healthy, happy baby boy, only to come down with autism after being given baby vaccines that contained thimerosal mercury. For years his nephew has struggled with this incredibly debilitating, preventable condition. According to Vawter, a claim may be submitted not only by his nephew, but by others who have suffered damages from vaccinations.

Vawter claimed that several rules and proclamations detailed in the lawsuit are unconstitutional and claimed that if they are not stricken and amended, he and other people who may not be aware of the offenses or who may be unable to sue, will suffer pending “injury-in-fact” damages. As attorneys and law firms join this lawsuit, recovery requests will reveal the names of additional people who have suffered injuries so they can be contacted about recovering damages, as the law allows.

Motion for Preliminary Injunction claims some vaccines may contain live virus

Although much of the Preliminary Injunction is a reiteration of information contained in his lawsuit, there are a few additions of note. Vawter includes in his grounds the fact that since the manufacturing of flu vaccines involves first destroying a live flu virus, there is a possibility that live flu virus will be in some of the vaccines, causing even more damages to people who receive it, and spreading the virus.

He asked the Court to use federal law enforcement to initiate its own civil and criminal investigation into flu vaccine safety issue, as federal law allows for this.

He noted the days when Hitler’s Nazi doctors forcibly gave shots containing adjuvants to innocent people, and reminded that Nazi ideology was stamped out precisely because of those atrocities. He claims it is unwise for the U.S. government to follow in the same path as the Nazis. America is a nation of civil laws, not a dictatorship that gives proclamations bypassing the courts and congress to demand forced vaccinations containing hazardous ingredients known to cause damages.

The forced vaccination debacle of 1976 that the government had to halt because it was injuring more people than it was protecting shows vaccine makers should not be allowed to force their vaccines on people who have no recourse. The prohibition against lawsuits by the injured gives the green light to vaccine makers to include thimerosal mercury in their new flu vaccines. When the Order deeming the forbidding of lawsuits as unconstitutional is given, any defendant will have to present factual proof in federal court, not just hearsay or advertising slogans, as so why the Constitution says it is okay to forbid people from suing to recover damages resulting from flu vaccine.

Medical professionals argue flu vaccines harm not just certain people but almost everyone who receives them. Yet the government has ignored factual evidence proving this, and instead listens to a profit run group of vaccine manufacturers who stand to earn billions of dollars as the government orders forced vaccinations on the public for the coming flu season.

The government has published a chart listing the WHO’s “Phase 6 Influenza Pandemic” as being equal to an earthquake measuring 8.0 on the Richter Scale. This chart is preposterous because there are no factual criteria required for an “Influenza Pandemic” to be declared by the United Nations’ WHO. The United Nations is a collective of numerous nations, most of whom have very different laws than the U.S. has, and where their leaders can simply declare or proclaim things to be so without judicial review, and their population must obey.

Glaxo Smith Kline stands to make $4 billion from its two flu vaccine drugs. CEO Andrew Witty has said his company has been preparing for a flu pandemic for thee years and has spent over $1 billion to expand its factories. Executives from Glaxo, Baxter, Novartis, and Sanofi Pasteur had seats at the advisory group that on July 13th recommended mandatory H1N1 vaccination for everyone in all 194 countries belonging to the WHO.

The fear mongering involved with this Phase 6 alert has been intense. An example being spread by interested parties is the story of a girl in England purported by the WHO to have died of swine flu because she was not vaccinated. A more thorough investigation later revealed the girl actually died of septic shock due to tonsillitis. The WHO, CDC and numerous vaccine companies have been extensively advertising dire yet apparently concocted warnings of flu pandemics. Yet only a small number of people worldwide have died from the new flu virus.

When influential TV newscasters questioned the WHO proclaiming a “Phase 6 Influenza Pandemic” without factual evidence to prove it, the WHO responded by simply stopping their tracking of swine flu cases, a bizarre behavior on the part of an organization designated to be the main hub for information gathering on the disease.

Copies of the Vawter’s actual files can be viewed at:

http://www.safetylawsuits.com/compl…

http://www.safetylawsuits.com/motio…

http://www.safetylawsuits.com/preli…

About the author

Barbara is a school psychologist, a published author in the area of personal finance, a breast cancer survivor using “alternative” treatments, a born existentialist, and a student of nature and all things natural.

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