Longer Healthy Life
© Copyright 2011 Ty Parr, Ph.D.(All Rights Reserved) Updated 30Apr2011
SMOKING- Please STOP if you are, DON'T start if you have not. This is a "no brainer"
ALCOHOL- not yet posted
COOKING CREATED DANGERS - not yet posted
TOXIC ELEMENTS AND DRUGS & TOXIC SYNERGY - not yet posted
IRRADIATED FOODS - not yet posted
Vaccines have in the past been the least costly and the most effective means of preventing highly pathogenic diseases. There were voluntary committees of citizens in each of the American colonies who gave time and resources to see that immunization against smallpox virus by early use of the relatively new Edward Jenner technique of using "cowpox" exposure to immunize against a much more deadly pathogen. Milk maids in the middle ages were visions of beauty because they apparently became immunized during the milking process and did not get smallpox with its disfiguring damage. That said, small pox like other diseases was declining due to ordinary public health measures like clean water, better (fresher) food, improved sewerage, less density of human habitation, and quarantine to limit the spread of diseases.
The Developing Bad
That said, the over use of vaccines and the new toxins that are used to hype immunological response (called adjuvant's) and the preservatives used are turning immunizations into nightmares now.
This is particularly clear with the rise of childhood autism, something very rare in the 1970's to be as common as 1 in 175 children now in the US and a similar elevation in Great Britain (as much as 1 in 60) Autism was only first described in 1943, some 12 years after childhood vaccinations included the poisonous mercury compound thiomersal. Thiomersal is an Ethyl mercury thiosalicylate compound, a compound much more toxic than the already highly toxic mercury ion (Hg++). This is due to the high bioavialability (ease of cell uptake) of the organic shielded ethyl mercury. A similar but gradual methyl mercury poisoning occurred when fish and shellfish were contaminated with mercury that was transformed biologically into methyl Mercury in Japan. Methyl mercury contamination in the Japanese town of Minamata was a source of grave and needless human misery .
Autism is not hard to diagnose as the child typically seeks no communication with others and usually shrinks from human touch.This is very unusual in a healthy young child. The Developed Countries (US,GB, France, Germany) have a historically recent rapid increase in childhood autism rates with the disease only recognized as a disease in 1943
For a long time, childhood immunizations were suspected, but proof was hard to obtain. An entrenched lobby of vaccine makers and "REGULATORY CAPTURE " of oversight agencies has made this a ever growing scandal.
What may cause this problem is the very high levels of Mercury (Hg++) and Aluminum (Al+++) that were present in vaccines. When the dose (total exposed to ) of each of these dangerous ions is adjusted to kill only one out of 100 rats, it has been found that the combination of both those low dose's kill 100% of all the rats. This is again an example of TOXIC SYNERGY were encountered earlier in the above section on TOXIC ELEMENTS AND CHEMICALS.
In the state of Illinois(USA), it is possible to opt out of childhood vaccination programs by choosing home schooling. Homefirst is a home schooling related medical service out of Chicago. Out of some 30,000-35,000 non-vaccinated children, Dr. Mayer Eisenstein with Homefirst Medical Services has never seen a single case of autism . The few cases of autism seen by Homefirst Medical service were from parents who had their children vaccinated before signing up with home first. A similar situation occurs among the Amish who also refuse vaccination of their children. Dr. Frank Noonan, a family practitioner in Lancaster County PA who has treated thousands of Amish for a quarter of a century has found no case of autism .
In open court proceedings, the US government has admitted in two separate cases that immunization was accepted as the cause of autism in these children . The suspicion is now great that the cause of the wide diversity of cases of autism may be mostly or almost entirely due to childhood vaccinations. The only thing that is worse about this situation is that autism can take place years after the triggering event. This is due to that cumulative poison combined with a tipping point of further insult that leads to massive stability. Thus we could see further rises in incidence. Below is a graph of rising incidence of autism in the USA.
Figure Rise of Autism Over Multiple Years (each line represents a cohort of children born a the same year that progresses with yet greater fraction of this same birth date population diagnosed as autistic. Note the huge (exponential) rise in cases with age. Realize that autism, despite its easy recognition by unusual social aversion and striking touch aversion, was not even recognized as a disease until 1943, twelve years after ethyl mercury (thiomersal) was first added to vaccines in the US. This absence of previous record and sudden massive rise has to have a more modern origin.
AUTISM PREVALENCE TREND US & OUTLYING AREAS ILLUSTRATION -REDUCE by 1/2 "
In a recent Huffington Post exclusive, Robert F. Kennedy Jr. and investigative journalist David Kirby reveal that in the recent case of Bailey Banks vs HHS, the Vaccine Court has ruled vaccines caused Bailey's autism and ordered compensation for his family. Banks is the second case where the government could not deny the overwhelming evidence showing vaccines caused a child's autism. The first was the case of Hannah Poling in March 2008. The government conceded the case and awarded awarded her family compensation.
The reasons for this horrific rise in autism rates are likely to be the increasingly toxic and dangerous adjuvant's (Aluminum ion) used and other toxic antimicrobial components like mercury . Additionally, too many vaccines given to a young developing immune system is very liable to bias the development of this system, possibly to the point of permanent injury.
What did the vaccine makers do when confronted with such evidence? They lie This is a replay of the tobacco industry knowing the dangers and stonewalling for all those years. Same reason - PROFIT MOTIVE ABOVE HEALTH.
This childhood vaccination may not only be about autism, it may well extend to Sudden Infant Death, Type 1 Diabetes and other possible unexplained infant fatalities and diseases.
It's Not Just the Children - Gulf War Syndrome
After the second Persian gulf war, a huge number of our 'volunteer' american soldiers came down with various ailments. At first the government blamed it on the conditions of war in Iraq. For a prolonged time, the Bush administration denied this problem. We know much more about some of these problems now.
Gulf War Syndrome is somewhat confusing as only some troops from the US, Canada, Australia, and Great Britain are reporting these initial diverse maladies of headaches, rashes, physical coordination problems, extensive non-viral cysts, physical weakness and many more. Only troops from the US, Canada, Australia, Great Britain received the anthrax vaccinations (some lots of which had squalene). The only reported Gulf War Syndrome suffers come only from the US, Canada, Australia, & Great Britain. None of the other coalition troops reported any such problems.
When talented and widely experienced academic and medical specialists began to study this phenomena, they were getting complaints from actual armed forces troops who were saying that they were being made sick by the vaccinations. This was actually before the war when a massive armed forces compulsive vaccination against Anthrax program was undertaken.
One of the difficult problems with a developing autoimmune condition is that the earlier stages often have non-specific complaints like the headaches, rashes, physical weakness, and so on. It usually takes years for the conditions to develop into the horrible crisis level autoimmune disease that alternates with recovery periods, only to repeat. A very smart scientist Dr. Pam Asa formulated an idea that these symptoms were the beginning of an autoimmune process. Since the Department of Defense was deeply involved in studying the use of squalene as a replacement for the only legal vaccine adjuvant in the US (Aluminum salts or alum), squalene was a real possibility. Adjuvants are compounds that get the immune system to become highly activated in what it thinks is a foreign substance in the body. Thus you would inject an antigen (say tetanus protein or the whole broken up tetanus bacteria) with the adjuvant (either legal Alum or the illegal squalene) . Then the body would react strongly and form a full immunological reaction to this foreign substance - hopefully giving you life long immunity. We'll have more to say about life long immunity later by vaccines later.
When you use the oil/water based squalene that is emulsified by Tween 80 (a particle sized so small and interrelated that oil does no separate as it does in a normal oil-vinegar mix) in place of only FDA approved (legal) US adjuvant of Aluminum salts, a further complication takes place. Squalene at vanishingly low doses (literally in parts per billions to parts per millions of the whole injection) causes almost 100% autoimmune diseases of a broad spectrum. It is as though the uniqueness of the animal determines what system is most easily affected first. Thus, squalene adjuvant can result in painful, incurable, autoimmune diseases like multiple sclerosis, rheumatoid arthritis or systemic lupus.
As you already know from the SUPPLEMENTS section, Vitamin D3 at relatively high levels of 5000 international units per day elevated immune function, but it also places a lid on the severity of immune reaction. This means that the too high immune activation that occurs during "cytokine storms" (ultrahigh levels of immune stimulants that trigger this over reaction) is blocked by high Vitamin D levels. Thus, the high lethality of such disease as the 1918 influenza world wide epidemic (50 million dead) and the more recent Sars epidemic in China would largely be prevented from killing most people. Both these cases had cytokine storms and then the immune system killed the lung tissues we need to deliver oxygen to our body. Thus, the virus was defeated and largely cleared, but the immune system kept attacking normal tissue until the lungs failed and the patient died. I hope this gives you added incentive to look at the Mercola and other videos suggested under Vitamin D section of the SUPPLEMENTS section. Just augmenting the immune system without this protection against over reaction would have and did kill many more in the Sars infection saga. This is an extremely important lesson - nature has multiple protective mechanisms that largely prevent these uncontrolled overreactions, our simple minded stimulation without understanding simply does not work when faced with this complexity of problem.
Autoimmunity can take years to diagnose" because early symptoms (headaches, joint pain, etc.) are so vague they can easily be from other causes. Different individuals advance toward disease at very different rates, but most progress
A substantial minority of the population suffers from these < autoimmune > diseases, which are often chronic, debilitating, and life-threatening. There are more than eighty illnesses caused by autoimmunity. It has been estimated that autoimmune diseases are among the ten leading causes of death among women in all age groups up to 65 years. Autoimmune Diseases Wikipedia <current author clarification>
In order to gain a 'molecular' handle on what was causing Gulf War Syndrome, scientists at the Tulane Medical School performed a study published in the peer reviewed journal "Molecular and Experimental Pathology 68(10, 55-64 (2000). Some 144 Gulf War Veterans including those injected with the squalene based anthrax vaccine and those not injected, and also including squalene based anthrax vaccine injected military personal who never went to Iraq or the theater of war as well as healthy and autoimmune suffering patient controls were included in this study. Some 95% of the military personal suffering from Gulf War syndrome that were in Iraq tested positive for self antibodies to squalene as did 100% of those suffering from Gulf War Syndrome who were injected with the squalene based vaccine but did not go to Iraq. Healthy controls tested negative (0% squalene antibodies) as did patients already suffering from unrelated autoimmune disease. Deployed and not deployed to Iraq soldiers that were injected with the anthrax vaccine (but not the squalene based lots) who did not have symptoms of Gulf War Syndrome tested negative for squalene antibodies. It is clear from extensive findings that only some lots of the vaccine had added squalene (verified by the FDA) , contrary to the military's assertion that no squalene was used in Anthrax vaccines).
This duplicity of the people running an illegal and immoral 'compulsive' experimental immune injection system on our service personal with squalene vaccinations (in an emulsified oil/water mix using the well established dangerous Tween 80 (polysorbate 80 -known to cause severe allergic reactions) as an emulsifier is only equaled by the 1950's & 1960's intentional irradiation of military personal from US, Russia, Great Britain, Canada, and Australia . While Great Britain , Canada, and Australia have admitted fault and offered reparations, neither the US nor Russia has taken any responsibility for these actions. This is just another example of the INHUMANE IMMORAL IRRESPONSIBILITY OF LARGE POWERFUL INSTITUTIONS that were not always this bad. It should be remembered that the post WW2 Nuremberg judgments found that it is a violation of law to compel people to take "medicine" or treatments that were not given with informed consent. The US Government has a long history of performing illegal and immoral tests on service personal as this is shielded from lawsuits and can be hidden by national security concerns.
"Our results strongly suggest that the production of anti-squalene antibodies is linked to symptoms of Gulf War illness and to the presence of squalene found in certain lots of anthrax vaccine.....human exposure to squalene in vaccines has been shown by others to cause immunological symptoms similar to those found in Gulf War illness patients. ......The absence of an association between the presence of Gulf War illness and deployment indicates that the causative agent or factor is not associated with the Persian Gulf. Consistent with this observation are the results of a recent epidemiological study finding that vaccinations that were given to both deployed and non-deployed personnel are associated with ill health. .......The presence of anti-squalene antibodies in ill people and the absence of the antibodies in healthy people is the first hard laboratory evidence that Gulf War illness is what some might refer to as a "real disease." ----Dr. Robert Garry Testimony January 24, 2002 to The House Subcommittee on National Security, Veterans Affairs, and International Relations http://www.whale.to/v/garry.html
In 1994, the U.S. Senate Committee on Veteran's Affairs staff published a report on its investigation into using U.S. soldiers by the Department of Defense (DOD) in federal research concluding:
"DOD incorrectly claims that since their goal was treatment, the use of investigational drugs in the Persian Gulf War was not research. DOD used investigational drugs in the Persian Gulf War in ways that were not effective. … DOD has demonstrated a pattern of misrepresenting the danger of various military exposures that continues today.” Part II: Squalene laced H1N1 vaccination 'pharmacological warfare'' August 18, 1:02 Peace Studies Examiner Deborah Dupre'
Oil adjuvant's are the most insidious chemical weapon ever devised. Dr. Pam Asa Adjuvant Index Page
The Yearly Flu Shot - A Real SCAM
The idea behind the annual flu shot is prevention, but to prevent a particular strain of influenza you must prepare you vaccine against that particular strain. The problem is that we simply don't know what particular strain of flu virus will dominate in the next winter season of high flu infection. This may seem a small quibble, after all, don't we just want all the protection we can get even if it is not against the particular strain? The answer to this is a definitive NO. Every immunization is a burden on your immune system in multiple ways. The reason is that vaccines introduce not only toxic poisons like thiomersal (ethyl mercury) and alum (and Aluminum containing salt) but they can disrupt and damage immune system function. We have clearly seen this in the sections on autism and Gulf War syndrome.
It's really much worse than that. There is just no strong evidence that flu vaccines are effective.
They must confer some protection. Don't they work?
Do flu shots work?
Not in babies. In a review of more than 51 studies involving more than 294,000 children it was found there was "no evidence that injecting children 6-24 months of age with a flu shot was any more effective than placebo. In children over 2 yrs, it was only effective 33% of the time in preventing the flu. Reference: "Vaccines for preventing influenza in healthy children." The Cochrane Database of Systematic Reviews. 2 (2008)...
Not in Adults In a review of 48 reports including more than 66,000 adults, "Vaccination of healthy adults only reduced risk of influenza by 6% and reduced the number of missed work days by less than one day (0.16) days. It did not change the number of people needing to go to hospital or take time off work. "Reference: "Vaccines for preventing influenza in healthy adults." The Cochrane Database of Systematic Reviews. 1 (2006).
Not in the Elderly In a review of 64 studies in 98 flu seasons, For elderly living in nursing homes, flu shots were non-significant for preventing the flu. For elderly living in the community, vaccines were not (significantly) effective against influenza, ILI or pneumonia. Reference: "Vaccines for preventing influenza in the elderly." The Cochrane Database of Systematic Reviews. 3(2006)
The belief that vaccinations, like flu shots, have eliminated death from infectious disease in the twentieth century is widespread. In fact, much of the reduction in death from infectious disease is due to public-health measures, including improved nutrition and sanitation. And vaccinations are not without potential danger. We still don't know the potential long-term effects of vaccination .Before you take that Pill: Why the Drug industry May be Bad for Your Health by J. Douglas Bremner
What do they contain that might injure you?
What's in the regular flu shot?
Egg proteins: including avian contaminant viruses
Gelatin: known to cause allergic reactions and anaphylaxis are usually associated with sensitivity to egg or gelatin
Polysorbate 80 (Tween80™): can cause severe allergic reactions, including anaphylaxis < this also causes infertility when injected >
Formaldehyde: known carcinogen
Triton X100: a strong detergent
Sucrose: table sugar
Resin: known to cause allergic reactions
Gentamycin: an antibiotic
thiomersal: mercury is still in multidose flu shot vials
The Truth About the Flu Shot Sherri Tenpenny
So now we are back to the suggestions in the IMMUNITY section. Doing the right things to elevate your own immunity (behaviorally, nutritionally, and with supplements). The Vitamin D3 suggestion is critically important. Our own immunity in a body that is getting enough Vitamin D is our greatest protection for influenza type diseases.
It's not just the Flu vaccine, the US CDC (Center for Disease Control) has suggested that adults take some 11 vaccines.
The Advisory Committee on Immunization Practices, a division of the Centers for Disease Control and Prevention (CDC), has released the 2007-2008 recommended immunization schedules for adults in the US. The schedule includes 11 different types of vaccines for adults, including:
• Tetanus, diphtheria, and acellular pertussis (Td/Tdap)
• Human papillomavirus (HPV)
• Measles, mumps, rubella (MMR)
• Herpes zoster (shingles)
Key changes in this year‘s recommendations include:
• Varicella (chickenpox) vaccination is recommended for all adults that have no apparent immunity to the virus
• Zoster (shingles) vaccination is advised for all adults 60 years of age and older, regardless of whether they have had a prior shingles episode
• HPV vaccine is recommended for women over the age of 26, who have not already completed the three-dose series
It is recommended that flu vaccination be administered to anyone with the following medical conditions:
• Chronic disorders of the cardiovascular or pulmonary systems, including asthma
• Chronic metabolic diseases, such as diabetes
• Renal or hepatic dysfunction
• Immunosuppression, including suppression caused by medications or HIV
• Pregnancy during flu season
Adult Immunization Schedule: United States, October 2007–September 2008 pubmed find
I don't know about you, but for me this is way overkill. When I see things like this, I suspect that this is more for the very high profit of vaccine companies than anything to do with human health. Pleas remember that this is the same government that puts Monsanto executives to run the
To put it clear, annual flu shots are a scam designed mainly to support the vaccine industry. This is just part of the too close relationships between regulators (FDA, etc) and the industries they are supposed to regulate. Again, REGULATORY CAPTURE. As we shall see later, it is also about something else. See also.
The Swine Flu Fiasco of 1976
In 1976, an outbreak of swine flu (type H1N1 much like the current Mexican Swine Flu type A H1N1) led to the death of a single soldier at Fort Dix in New Jersey. About 500 more were sickened by the same flu virus. Swine Flu outbreaks of this type were absent from 1957 to the 1976 outbreak. .As a consequence of this single death, the head of the CDC, David J. Sencer called for a massive nationwide vaccination program (for the entire nation). This was reasoned because the swine flu was believed to be like the 1918 influenza outbreak that killed so many americans. This was endorsed by President Gerald Ford and led to a crash program to prepare doses for the entire American population for the 1977 influenza season (fall through winter when Vitamin D production in the Northern Hemisphere was greatly depressed)..
Other experts were very doubtful of the wisdom of this rush to immunize the entire American population. Dr. Anthony Morris, the director of a branch of the FDA virus research stated: "There is no evidence that the swine flu is a killer. The swine flu vaccine is worthless".
Despite these doubts, the program went ahead and the vaccination program was begun before the fall/winter flu season. The first shots were given Oct. 1, 1976. By Dec. 14, 54 cases of Guillain-Barré syndrome were seen. Guillain-Barré syndrome is where the immune system attacks the nerves, causing paralysis. Immunization was suspended on Dec. 16, but by that time some40 million Americans had received them. Dozens of Americans died within 48 hours of receiving a swine flu vaccine In the fall of 1977. To allay the public fears that threatened to unravel the mass inoculation program, President Gerald Ford rolled up his shirtsleeve and received his shot in front of television cameras.
More than 40 million others followed his lead. But two months later, the campaign was abruptly stopped: More deaths had followed, and hundreds were reporting serious side effects, including paralysis. Naturally, the US Government was forced to pay out millions of dollars to those affected.
Recently, new examination of the historical evidence has been suggested that the virus involved was a laboratory strain.
Baxter Pharmaceuticals Near Pandemic Release of Live Bird Flu in a Vaccine
Baxter Laboratories, an Austrian subsidiary of the American vaccine company, was given by the UN WHO, a sample of supposed H3N2 flu virus (common usually non-lethal winter flu that is easily spread by sneezes). This was to be used for annual flu vaccine production. Baxter worked on the sample and expanded it and then sent it out a total of 72 kilograms (@ 160 pounds) of this sample to 19 countries around the world. these countries included Canada and many European countries. An analysis subcontractor laboratory in the Czech Republic, BioTest s.r.o, tested the sample for lethality in ferrets. When the ferrets died, something that does not happen with the H3N2 flu virus, the analysis laboratory blew the whistle and warned others of the the deadly nature of something in the supposed ordinary yearly flu sample vaccine was lethal. Tests subsequently showed that something to be the infectious asian bird flu H5N1 (just another sero group immunological subtyping of viruses so we can keep a catalogue). Had this material been used as an ordinary vaccine, the people vaccinated would be infected with the often lethal bird flu. This could cause a limited pandemic among the vaccinated as there is little evidence to show that the H5N1 virus in an infected human can easily infect other nearby humans. What makes the presence of the H3N2 a wild card is that H3N2 CAN and ROUTINELY DOES infect humans by sneeze droplets and such. If a reassortment of the viruses were to take place, you might get a easily (aerosol or airborne sneeze particle) infectious version of H5N1 bird flu. This could be a major concern.
No responsible vaccine company in the world would ever allow a sample of lethal bird flu to get anywhere near its production facility for yearly flu vaccine. This is BIOLOGICALLY INSANE or possibly EVIL INTENTIONED ( ? PROFIT INTENTIONED ? ). We may never know the real source of this contamination: the WHO?, Baxter?, intentional sabotage? In any case, the world missed a bullet here due to some responsible work at BioTest s.r.o, laboratory, and we should be grateful to them.
This event was reported by Blumberg news on 24 Feb 2009 (Feb 24, 2009) . The timing and context of this is important in light of the next occurrence of a major infectious outbreak of the "Mexican Swine Flu" that we will deal with next. As seems common place anymore, this was hardly even mentioned in the US press.
The Mexican Swine Flu & Vaccine
A novel flu strain infecting many Mexicans during April 2009 was termed the "Mexican Swine" Flu or Influenza A H1N1. The designation as H1N1 is a classification scheme of immunological reactivity types that science uses to characterize relatedness among a very large number of viruses by sorting into related groups. What at first seemed a massive news generated fear story of a profoundly lethal pandemic slowly faded into an awareness that this virus is not so deadly after all. Samples were obtained and scientists began the process of examining the molecular level details of this strain of flu. All (Influenza) Flu strains can be divide into three groups, A, B, & C. The A group infect both humans and animals and are the most common flu, while the B group are human infections only. The C group are without symptoms and generally disregarded.
A & B Flu viruses are composed of 8 separate but cooperative segments of single stranded RNA ( a single strand nucleic acid, unlike the double strand helix of DNA in our cells) packaged into a virion (viral) particle that has the 'cell attaching' hemagluttinin trimmer on the outside of the particle. Each of the 8 single stranded RNA segments has its own function. Once inside a human cell they are "reverse" transcribed into DNA which is then used to code for messenger RNA's. These new viral messenger RNA's (mRNA) use our cell synthesis machinery to vastly increase production of viral proteins. At the same time, the DNA sequences in the infected cell produces large numbers of complementary RNA that is packaged by these newly made viral protein - leading to a self assembly of new viruses that have to be released from the cell into the blood stream to infect yet more of the cells in our body. When scientists began examining the sequence of nucleic acid bases in this new virus, they encountered something not seen before.
"Mexican" Swine Flu" is a never-before-seen strain of influenza A virus that has elements of human binding, bird,origin, and swine origin "flu" genomes together despite those variants coming respectively from Asia and Europe and despite first appearing in Mexico on the north American continent. This makes it what is called a triple reassortment virus that are very very rare occurrence. These are mostly ONLY seen in laboratory experiments where growing tissue culture cells are simultaneously infected with multiple different viruses. This allows a single cell to be infected with two or more different viral types that permit the generation of a wide variety of different combinations to the typically 8 sequences making up an influenza genome. This was the first of several surprises. It is also important to realize that this virus type has never before been seen in the world since records of sequence structure were first collected (starting in the 1980's). Moreover, there are no clear set of evolutionary steps at intermediates that would explain the natural evolution of this VERY usual triple reassortment combination of genes from different continents that we usually only see when we do high titer multiple different virus infections of tissue culture cells in a laboratory. There are no series of steps that lead to this novel virus (THIS IS FOUL PLAY ALARM BELL #1)
One of these 8 pieces of RNA in each virus particle is called a hemagglutin (HA) gene whose protein binds to the carbohydrate (sialic acid) on the external surface of cells that fosters delivery of the viral RNA into cells for infection. This HA gene is of great importance as it is the primary source of virulence (dangerous infectious capability). Typically, HA genes of most flu's are restricted to the head and throat, and rarely can infect lung tissues. What was outstanding about the 1918 lethal influenza pandemic and the Sars (China) Pandemic is that their HA sequences allowed infection of the lungs. The high lethality of both the 1918 and the Sars viruses were due to this infection of lungs that caused a massive over reaction of the human immune system that cleared the lungs of virus, but kept attacking normal healthy lung tissue. Basically our immune system massively overreacted to the situation and killed both friend(lour healthy lung tissue) and foe(virus). This led to the second major surprise.The HA nucleic acid sequence in the Mexican Swine Flu has the lethality conferring mutations just discovered in the laboratory RECREATED deadly 1918 H1N1 virus published in 2005 . This 1918 H1N1 virus killed some 30-50 million people world wide in one of the worst world wide epidemics in the last century. There was considerable concern in academic circles about recreating the 1918 virus as an infectious and reproduction capable ("live or living") virus that might be capable of initiating a second wave of lethality at this time. Please understand that a virus is only "living" in the sense of reproducing when they infect a host animal whose cellular machinery is hijacked to produce the viral proteins and prepare new infectious virus particles that are then dumped into the blood stream to cause further cell infections. What makes this Mexican Swine flu virus so remarkable is that these lethality conferring mutations found in the 1918 killer flu have not been seen together in any recent potential parents for this Mexican Swine Flu virus. This Mexican Swine flu virus with a remarkable 1918 like HA sequence seems to spring fully formed some 5 years after the original sequence of the 1918 HA sequence was published in 2005. It has no history of evolution. It just appears with all these remarkably unlikely genes and with a HA sequence much like the 1918 lethal flu that has not been seen ever in our entire data base of thousands of influenza viruses. ( THIS IS FOUL PLAY ALAARM BELL #2 ). This alarm bell rings ever louder when you realize that the reconstitution of the 1918 lethal flu virus was done in a US military laboratory !
Most of the "normal lethality" from most Influenza infections is due to the 'secondary' or 'follow on' opportunistic bacterial infections in an immunologically stressed organism. These bacterial 'opportunistic" infections often attack lung tissues and kill the person due to bacterial pneumonia (lung infection). The 1918 virus was a major exception to this general rule. In the 1918 Pandemic, the virus infection triggered an immune system over reaction called a 'cytokine storm' (cytokines are immunological messengers to trigger and shape immune responses). This 'cytokine storm" triggered an over reaction so great that it can cross the normal limits of most immune reactivity (not attacking uninfected normal cells of our body ) and begin a life threatening attack on normal healthy (uninfected) tissues. In the case of the 1918 virus, this lead our own immune system to destroy normal lung tissue after defeating the virus. This and not the more common 'secondary' or 'follow on' opportunistic bacterial infection killed humans in the prime of life - and very rapidly. This was also unusual as most influenza (flu) deaths are typically in the elderly and the very young with weaker immune responses. This killing people in the early adult to young middle age was largely due to both their strong immune system responses and the uniqueness of the HA ( hemagglutin )sequence that allowed the 1918 virus to rapidly attack human lungs. Most normal influenzas are primarily head and nasal passage infections, rarely venturing into the lungs. it was also due to extremely low levels of sunlight UV-B light during winter that generates insufficient Vitamin D for protection. As you already know from the SUPPLEMENTS section, elevated intake of Vitamin D3 (some 5000 international units per day )leads to an activation of the immune system but ALSO PLACES A LIMIT ON HOW MUCH MORE THE SYSTEM MAY ACTIVATE. Thus, Vitamin D3 largely prevents a "cytokine storm" and the lethality associated with this 1918 virus. This is one of the many reasons I so strongly recommend high intake of Vitamin D to protect yourself. From the similar endorsements of the top researchers in the field quoted in the SUPPLEMENTS section, I am not alone.
The hemagluttinin sequence(HA) from the recreated 1918 flu is unique in the database of influenza sequences. That was until the "Mexican" Swine flu virus was found to have the lethal mutations of this same sequence, Again these have never been seen within our entire data base of RNA influenza sequences (these have only taken place from the 1980's and later when DNA sequencing made this possible, but some samples of virus were sufficiently well preserved that scientists have extensively sequenced earlier viral sequences. The Mexican Swine Flu suddenly reappears some 4 years after the recovery and sequencing of the unique 1918 virus that was published in 2005. This reconstitution and sequencing of the 1918 virus was only possible because of a recovery of the lung tissue of an Inuit woman who died and was buried in the permanently frozen tundra of Alaska. Incidentally, this reconstitution and extensive study of the important genes related to the lethality of the 1918 virus was done in a US military biowar facility. (Or rather in a biowarfare defense facility - a distinction without merit.). It would also be well to remember that the United States is a signatory (1975 President Ford signed) to the Biological Weapons Convention.
The combination of an extremely rare triple hybrid of human INFECTING HA sequence, bird, and swine sequences in the Mexican Swine flu from separate continents, a hemagluttinin sequence that exactly resembles the unique hemagluttinin sequence of the just recently rebuilt 1918 killer flu, and the absence of a series of isolated precursor steps from known existing flu strains that could explain the natural creation of this Mexican Swine flu begins to arise suspicions that this is a man made virus. The recent outbreak of a mutated version of the Mexican Swine Flu virus (Ukraine versions D225G) seen it Ukraine in Nov 2009 outbreak, seems to also have occurred in multiple world locations nearly simultaneously, something totally unexpected for the normally random process of mutation . An academic sequencing web site (Recombinomics ) following the Swine Flu sequence data pointed out the contrast to the more random and unpredictable (not exactly world wide coincident) timing of natural mutation changes in different population backgrounds and different locations around the world.
Given these very unusual and strikingly not consistent with our normal expectations for the evolutionary process, why are the academic virologists so quiet? Especially when this level of UNLIKELY NATURAL ORIGIN is painfully apparent? Academic scientist require grant funding mainly form the US government in the USA. How long do you think you are going to get grants after you bite the hand of the government that feeds you grant money? These conflicts of interest will be more completely explored in the MED CRITIQUE section.
What is ASTONISHING about the 2009 Mexican Swine Influenza A virus is that, while it readily infects human to human by normal sneeze droplets or contact with any bodily fluids, humans don't give it to pigs. Moreover, the only way we can infect a pig is by injecting HIM with the "live" virus. The infected pig does not infect other pigs or humans. This means that since it was not seen previously in pigs in the American continent (or any other continent), it would have to have grown somewhere else NOT IN PIGS.By this time, I hope that by this time, FOUL PLAY ALARM BELL #3 is ringing loudly in your brain. Very few things smell this bad as a "laboratory engineered viral plague" or equally fitting BIOLOGICAL WAR AGAINST HUMANITY.
In the testimony of USDA Secretary Vilsack in front of the Senate Subcommittee on Agriculture, Rural Development, Food and Drug Administration, this absence of pig to pig transmission was confirmed. If it did not develop over time in pigs, how was this able to spring full blown without any intervening steps to infect only humans landing first in Mexico ?
This last comment admits the absence of pig to pig transmission, but fails to explain the presence of a unique 1918 like lethal HA sequence that has not been seen in our entire data base of sequences, the presence of Asian and European H3N2 sequence, the appearance in Mexico without any record of occurrence anywhere else in the world. The absence of dealing with these questions by a representative of the US government begins to create a very unwanted sense that more is afoot here.
If this is a man made laboratory virus, naturally, the CREATORS could not use the whole 1918 virus as this was long lost and unknown until the just recently rebuilt1918 virus with the sequence published in 2005. The hemagluttinin (HA ) sequence and the other 1918 sequences from this was so unique that it would point the finger at those who sponsored the recreation of the 1918 "Spanish" flu. It could instead be due to those who used this information or were provided viral or DNA samples. Strangely enough, the lethality coffering critical mutations in the hemagluttinin (HA) sequence of the Mexican Swine flu virus share these lethality enhancing mutations of the 1918 sequence. The reasons given for such a recreation of the 1918 killer virus was to understand the critical mutations in sequence that were instrumental in the lethality. This is beginning to raise more than just suspicions. Like normal offspring, viruses generally have gradually changing lines of progenitors as mutations and rearrangements of their nucleic acid sequences occur. This Mexican Swine Flu has so many mutations that mimic the unique 1918 humanized (human infection specialized) hemaggutin sequence, but direct progenitors to this Mexican Swine Flu has never shown up in Nucleic Acid databases ! Viruses in nature rarely undergo such exquisite mimic of a long lost sequence, especially without a series of steps along the way - but laboratories can rapidly build such and assemble with the other members of the remaining 7 flu sequences to make a synthetic virus. Since these other sequences were constructed of bird and swine related sequences resulting in a EXTREMELY rare triple recombinant with it's swine and bird sequences coming from different continental regions of the world, It looks like "they" were a little careless about their choices to assemble a new completely novel virus. This one doesn't pass the smell test.
A better interpretation of this data is the hypothesis that the Mexican Swine Flu( A H1N1)it was designed in a laboratory to infect HUMANS. It was optimized to be optimally infectious and potentially lethal to humans by incorporating the critical HA ( hemagluttinin) sequences found in the recently reconstructed 1918 influenza HA sequence. Pigs were not involved or the object of the creation of this virus. This would explain a large amount of data that is inconsistent with a natural origin.
What About the Vaccine Against Mexican Swine Flu VIrus?
Responsible neurologists (study or treat brain problems) have issued a warning that the Mexican Swine Flu (A H1N1) vaccine may trigger a paralytic neurological disease called Guillain-Barre Syndrome (GBS . Neurologists in GB warned over the chance of a major increase in the neuroparalytic Guillain-Barre Syndrome (GBS) which also accompanied the 1976 Swine Flu vaccinations that were rapidly terminated when hundreds died and thousands were crippled by the vaccine. Only one death was ever attributed to the actual 1976 swine flu.
If all this is not bad enough for you, if you live in Europe there is much worse to come. European approved formulations of Influenza A (Mexican Swine Flu) vaccines have nanoparticles in them (see section on Nanotech above).
The problems with nanoparticles is that you never get rid of them and due to their size- they will interact and continually damage and destroy cells - one after another - in what the medical profession calls "a continuing infectious reaction". This has already killed workers exposed to methyacrylate (polyacrylamide) nanoparticles in Chinese factories. Do you think this is a safe vaccine?
Another particularly troubling aspect of the Mexican Swine Flu and then subsequent vaccine FEAR MONGERING that the United Nations World Health Organization has rushed to raise the alarm levels to unprecedented levels over a virus that just doesn't seem that dangerous. Not a complete 'dud', but not something to be massively fearful of.
The second disturbing aspect of the UN WHO behavior is insistence on vaccinating as many people on earth as possible. Worse yet, the WHO have described people who would not take this vaccination as "CRIMINALS". This seems wildly out of proportion to the real dangers seen so far.
Another troubling aspect is the laws that allow the US and Europe to force vaccinate their populations, especially in light of the relatively low lethality of this Swine Flu virus. In the US, the Model State Emergency Health Preparedness has been passed in various versions in some 38 states.
In the US, you and your children can be legally compelled to take a mandatory immunization:
Additionally, you have no right to any tort suit against the manufacturer in the event of injury from the vaccine.
Another frightening aspect is that the vaccines being prepared for this virus are ALL SQUALENE-WATER with the Tween80 emulsifier that we encountered in the Gulf War Syndrome.
Even worse, the WHO (World Health Organization of the United Nations) is now pushing for the these oil-water (squalene based ) adjuvants:
These are the same oil-in-water adjuvants that the UN previousl clearly warned as too dangerous for use on humans due to their dangerous auto-immune consequences:
The coy wording of this last quote ignores the autoimmune complications seen in the US soldiers in the Gulf War . Almost all of the small numbers tested that got the squalene based vaccine also now have autoimmune antibody responses to their own normal natural squalene, which is present on almost all cells. This includes soldiers who did not go to Iraq or even overseas. None of the tested soldiers that did not get the squalene based adjuvant showed these abnormal squalene antibodies.
Some of the 'off the shelf' sort of pre-made vaccines needing only addition of the specific antigen or virus (killed, injured, or live) to have a complete vaccine have another dirty little secret. They use squalene levels in the vaccines that are over a million times higher than those given to our service personal in the Gulf War. One of these is the GlaxoSmithKline Pandermix formulation. "Pandremix vaccine" from GlaxoSmithKline against influenza A (H1N1 Mex Swine Flu) is to have over a million times as much squalene as the lots of squalene containing vaccine given for Anthrax protection in the Gulf War. This has deeply alarmed physicians.
What is very disturbing about this whole mess is that autoimmune diseases have a gradual onset that may require months or years to arrive at a clear diagnosis of autoimmunity. Different individuals will progress to the disease each at their own rate, so we will only see a slow gradual rise in autoimmune diseases that the government can deny as a fault of the vaccine. This is what we saw in the gradual rise of cohorts of a birth age rise in autism. This is also exactly what the US government did for the military victims of atomic testing exposure and the Gulf War syndrome. Not seeing immediate autoimmune reactions is no protection. This is an insidious gradual process.
If the vaccine turns out to be more lethal then the "dud" swine flu, will it protect us? Not very well.
Data from Australia on the decline of Diseases Versus Vaccination or No Vaccination
However much one may believe in the wonder of medicine and vaccinations, this data is extremely clear. Vaccines against most diseases add very little in the way of improvement. Its really about public health in the form of clean water, good fresh food, personal hygiene, avoidance of infected persons when capable of disseminating disease, and good effective sewers as well as less crowed conditions. This another reason why good public health measures and a minimal level of medical services available to all is critical. Like it or not, we live as a community, and the health of that community with respect to communicable diseases is the health of each and every individual in it. No more rich person cant about 'we can't afford minimal care' to protect the community health. Ignore necessary public health and we will rapidly be back to high levels of communicable diseases, regardless of vaccines. Vaccines aren't magic bullets, they have become dangerous to you and your children.
One can classify different human contagious pathogens into three basic levels 1, 2, & 3.
Level 1 are the truly horrendous diseases like smallpox, cholera, ebola virus (and many other hemorrhagic (causing blood loss)viruses) ,typhoid fever, thypus, rabies etc. where the threat to health and indeed life is extreme. These have been primarily displaced by public health improvements that are mostly clean healthy food, fresh clean water,hygiene, well designed sewers to remove potential disease from us, and some minimal benefit from vaccination. Vaccination against even these horrible diseases usually lasts only a limited number of years instead of the lifetime protection that occurs when you survive them. Most of these diseases are not human restricted as they also have wild animal hosts, so failure of our public health protections will once again place us in grave danger. Since level 1 diseases are so dreadful, we may need to have both protections on occasions of extreme danger. We face VERY FEW OF THESE Level 1 diseases in the developed world and need to keep public health measures high to make sure we continue this. In the event of breakdown of public health measures and ability to rapidly reestablish them, we would be as vulnerable as third world countries. As these diseases generally have multiple hosts (unlike Smallpox which had only a human host), there are multiple natural animal reservoirs of them in the wild.
Level 2 can be fatal but is usually not. This comprises various diseases like influenza, tetanus, etc. The best way to deal with these things is to have considerable good health and a potential backup of drugs or medical support if needed. Using treatments as potentially dangerous as vaccines that have been made way too dangerous (to increase their potency) is proving unwise. This is a tremendous understatement of the degree vaccines here are nightmares.
Level 3 is ordinary minor infections such as the typical C virus colds, minor skin infections, etc. Again, public health, hygiene (like washing you hands, and avoiding exposures to infected individuals, etc.), and common sense as well as your good immune system is almost always enough to surmount or not even get these.
You already know from the section IMMUNITY that good nutrition, absence of simple sugars, sufficient Vitamin D3 (far above the RDA (Recommended Daily Allotment value of 400 International Units) and exercise & rest is critical to your healthy immune function.
The conclusion I have made is that vaccines can only be justified for extremely dangerous and deadly Level 1 pathogens and that only until we find what public health measures cause these to just disappear. Vaccines do not confer life long immunity like normal infections, where your body rejects them forever. Great age can complicate this as immune function declines substantially with great age. But even here, little benefit has been seen in the yearly flu vaccines for the elderly. Vaccines are much too dangerous for this 2nd and 3rd level pathogens. This is largely because vaccine manufactures are forced to aggravate our immune system while they also use very toxic poisons like high levels of mercury (Hg) preservatives to maintain sterility. It is no accident that the vaccine industry is now trying to use squalene (oil/water emulsions often using the allergy & fertility damaging Tween 80 emulsifier). They have to go so far as to deeply injure our immune system in order to get a reaction. This is very far from the normal process. The lack of long term (life long) immunity means we are not doing this protection in a manner that is close enough to the normal process to effect this result.
In the developed world we rarely ever experience the deadly Level 1 pathogens, primarily due to hygiene and public health measures as well as good diet. We rarely face the really deadly pathogens like smallpox or typhoid fever, etc. Vaccines are being used to damage children and adults. In general, this is just to extract more resources from people with little benefit. Our whole drug-pharmaceutical-vaccine system is failing to enhance our health. This is what health care should be about. Teaching what will lead to a longer healthy life. Right now, we are just being used to extract further wealth while not benefiting from this process and may actually be deeply or irreparably harmed.
Not only are vaccines not "safe" in the sense of often not preventing the disease they were designed to thwart, but they are especially not safe for all the extra cross species viral diseases they may carry live into your body when injected. The catalog of this horror story of cross species contamination with extremely dangerous animal viruses is well established in the scientific literature. What has not changed is the unreasonable unwillingness of the powers that be to rein in these uncontrolled biological experiments on you and your children. We are literally performing a huge uncontrolled experiment on human beings by submitting them to a very wide range of simian (apes & monkeys) and avian viruses that we would otherwise never be exposed to. This is one of many VERY DIRTY SECRETS OF VACCINES.
Vaccines are a garbage bag of unknown viruses as well as including many known cancer causing viruses, is it possible that the huge rise in cancer in the short period of mass vaccination is due to vaccinations?
While the current author does not believe that all cancers were the result of vaccination (ancient history has descriptions of these as well), it is clear that there may be a greater frequency and severity of cancers due to this contamination.This may seem like some sort of science fiction horror novel, but the real life consequences are tragic.
A recognized simian cancer virus, SV40 (Simian virus 40) has been confirmed to have been in Salk (injected) polio vaccinations given in the 1955 to 1963. This vaccine was administered to some 98 million Americans and an large number of overseas people. This vaccine employed monkey kidney cells to allow production of enough of the polio virus to enable a vaccine production. What makes this virus so particularly bad is that it contains the most carcinogenic protein known. This protein is called "Large T antigen", and is effective at taking over the machinery of a cell at almost unbelievable low concentrations of the virus. Good scientific studies have now confirmed that SV40 virus is present in many slow developing cancer types: mesothelioma (soft connective tissue cancer), osteosarcomas, pituitary and thyroid cancers, several types of bone tumors, and is also found in a high percentage of brain cancers like glioblastomas, astrocytomas, ependyomas, and some paillomas. Several researchers have suggested this may be the cause of rapidly rising brain turmors.
"SV40 is known to be far more tumorigenic than HPV (Herpes virus) in animals. One copy of SV40 per cell is enough to transform a cell." John Lednicky, of Baylor University
When Dr. Bernice Eddy found that injecting hamsters with a mixture of the cells used to culture the polio antigen for the Salk vaccine caused caused tumors, there was no effort to remove this deadly carcinogen. At that time, it was well established fact that simians had a whole group of cancer causing viruses (SV40 is #40 in the list). Dr. Eddy was demoted for her discovery and NIH successfully kept this secret for many years although they did order vaccine manufactures to screen for this in their production by 1961. Subsequent work led to the isolation of SV40 and characterization of how it causes cancers. This virus is so effective at cancer creation that is was routinely used to generate cancers in laboratories (for continuing unlimited cells in culture, albeit cancer cells). At this time, a cancer called "mesothelioma" was thought to arise from exposure to asbestos, but it has later been learned that asbestos mostly suppresses immune function rather than directly causes cancers. When foreign countries test their samples of mesotheliomas, Turkey and Finland both found no SV40 in their samples; neither country used vaccines that contain SV40. Finland has one of the world's lowest incidences of mesotheliomas.
It is now wide scientific understanding that SV40 is widely distributed in human beings, while that has never been shown to be prior to the Salk vaccine. It has been found in 45% of male sperm samples and some 23% of blood samples. It may be possible to contaminate another human with blood or biological fluids (like semen or mother's milk). This is the legacy of allowing the biologically sloppy creation of vaccines containing viruses we as humans would never encounter or be infected with. This is BIOLOGICAL INSANITY .
It is also clear that this small virus (SV40) manages to suppress the host's immune and intracellular (p53 gene) 'DNA-monitoring cell suicide' mechanism that our cells use to prevent cancer occurrence. It seems to do this by having large T antigen bind to the p53 system, inactivating it and other mechanisms that prevent cell division. It also damages our normal DNA structure in the infected cell and may even do a "hit and run" infection that is cleared except for the fact that the cell has sustained large levels of DNA translocations that may render the now "SV40 free" cell ready to go on to cancer status. Some of these now SV40 empty but DNA translocation damaged cells turn out to be much more malignant (tending to grow out of control) than the SV40 containing ones (that are strong immunogenic targets). This may be due to the fact that the SV40 large antigen strongly stimulates an immune response, that may not occur when SV40 makes a "hit and run" attack on the cell - leaving a transformed protocancer cell that no longer contains SV40.
Arnold Levine, the president of The Rockefeller University, in New York City, and the discoverer of p53, says that 60 percent of all cancers involve some sort of p53 damage, mutation, or inactivation. "The p53 gene is central to human cancers," he says, describing it as "the first line of defense against cancer formation".
What can you do to protect yourself, even if you were injected with the Salk or Sabin vaccines ? The critical element here is to have a robust immune system (reread the suggestions in the IMMUNITY section) and avoid any exposure to asbestos (an immunosuppressant) or any other immunosuppressant (like high consumption of simple sugars!).
What can we learn from this horrible history of INNOVATIVE IGNORANCE? Mainly no testing was done - much like the current Swine Flu vaccine - no real safety testing and especially no longer term testing. So what we have is Vaccine company ILLICIT & IMORAL PROFIT MOTIVE coupled with BIOLOGICAL INSANITY? Unfortunately, we may have already contaminated a large fraction of the gene pool of human beings on this planet by this hideous and evil idiocy of injecting live monkey (and bird) viruses into our bodies in the form of VACCINES. This does not even account for possible new viral creation by reassortment or recombinations between distant animal viruses that could form and entirely new pathogen(s). Can the vaccine companies that use monkey cells in vaccine production be certain that EVEN NOW no viruses are present (even as DNA integrated provirus)? The simple and clear answer to that is they cannot. Nor can anyone else. Federal regulations do not even include requirement to use the very sensitive PCR DNA amplification technique to screen for known virus in current vaccines. There certainly are a huge number of not yet known cancer causing viruses we simply have not yet found. BIOLOGICAL INSANITY is another MAJOR source of needless human misery.
FOR THE PRESENT, DON'T TAKE ANY VACCINES AND WARN ALL YOUR LOVED ONES AND FRIENDS TO AVOID THEM - ALL OF THEM. (SEE the SUPPLEMENT section on Vitamin D3)
Do not think that you are alone in this rejection of dangerous 'vaccines'. More and more of the medical community is opting out of this disaster as well. Half of Great Britain's doctors won't take Swine Flu Vaccine for reasons related to safety and inadequate testing. A third of British nurses will refuse to have the swine flu jab British Nurses refuse to have the swine flu vaccination by Daniel Martin Global Research, August 18, 2009)
Not only the medical profession, but the general public in the US and else where are now rejecting various vaccinations. In a poll of 1,678 US parents conducted b by the University of Michigan's C.S. Mott Children's Hospital, 46% said they will not have their children vaccinated against th Mexican Swine Flu (Influenza A H1N1). Only 40% said they will have their children vaccinated for this. Numbers count here, the authorities cannot compel what is deeply resisted by the majority. How could you face your grown children who would then know that the vaccination you authorized caused sickness or sterility? Would you want to be in that position?
Resources for more information
RFK, Jr. Article on Corruption of Vaccine Process http://www.globalresearch.ca/index.php?context=va&aid=14510
Dr. James Howenstine - vaccines don't work, refuse worldvisionportal.org/wvpforum/viewtopic.php?t=621
Other People With similar Opinions (Don't take any vaccination with squalene, avoid all/most vaccines altogether!)
Dr. William W Miller Vitamin D Better than Flu Shot William W Miller, Jr., MD Rock Creek Free Press Vol2,#11 Nov 2008
Dr. Mercola......... www.drmercola.com then search vaccine
Dr. Blaylock ..........What to Do if Forced to take the Swinde Flu vaccine
Dr. Tenpenny........ http://drtenpenny.com/the_truth_about_the_flu_Shot.aspx
Catherine Austin Fitts http://solari.com/blog/?p=3532
AUTOIMMUNITY TO REPRODUCTION - A UNITED NATIONS GENOCIDE INITIATIVE SINCE 1976
If you are in a "shell shocked" state from this vaccine information and think this vaccine story cannot get any worse, you are mistaken. The slow evolution of opinion in a wide variety of knowledgeable individuals now identify the laboratory created Mexican Swine Flu (A H1N1) a biowar assault on the human race. Unfortunately, this was proceeded by a prolonged covert sterilization program of the United Nations World Health Organization. This is a story of blocking conception by vaccine.
human "Choronic Ganadotropin" (hCG) is a hormone present in both women and men, but hCG is called the "pregnancy hormone" as it is first synthesized on fertilization by the embryo and then by the placenta. This hormone is to keep the lining of the uterus producing another hormone called "leutinizing hormone". Leutinizing hormone is needed so that the ovulated/fertilized embryo can implant and grow in a woman's uterus. In men it stimulates testosterone production but this is less well characterized. Without the production and action of this hormone, the uterus is not kept ready for implantation and development of an implanted growing embryo is not possible.
If you were a woman wishing to become pregnant, the last thing you would want is to have an autoimmune reaction to your own human choronic ganadotrophin. That condition would prevent pregnancy - permanently. So anyone putting a sample of human choronic gonadotrophin in a vaccine would be committing an act of GENOCIDE according to the United Nations definition of genocide. This would be a direct violation of the Genocide Convention of the United Nations Article 2(d) which states "imposing measures intended to prevent births within the group" falls under the category of genocide. The evidence for this is trickling in with more and more third world regions becoming outraged at the inhumanity of this group of eugenic criminals acting to make their women sterile. Imagine the United Nations committing genocide by their own definition.
During the early 1990s, the World Health Organization (WHO) had been overseeing massive vaccination campaigns against tetanus in a number of countries, among them Nicaragua, Mexico, and the Philippines. In October 1994, HLI (Human Life International, Pro-life Missionaries to the World, < current author has no association with this group > ) received a communication from its Mexican affiliate, the Comite' Pro Vida de Mexico, regarding that country's anti-tetanus campaign. Suspicious of the campaign protocols, the Comite' obtained several vials of the vaccine and had them analyzed by chemists. Some of the vials were found to contain human chorionic gonadotrophin ( hCG), a naturally occurring hormone essential for maintaining a pregnancy.
human Choronic Ganadotropin (hCG) Auto-Antibodies
In nature the hCG hormone alerts the woman's body that she is pregnant and causes the release of other hormones to prepare the uterine lining for the implantation of the fertilized egg. The rapid rise in hCG < human chorionic gonadotrophin > levels after conception makes it an excellent marker for confirmation of pregnancy: when a woman takes a pregnancy test she is not tested for the pregnancy itself, but for the elevated presence of hCG.
However, when introduced into the body coupled with a tetanus toxoid carrier, antibodies will be formed not only against tetanus but also against hCG. In this case the body fails to recognize hCG as a friend and will produce anti-hCG antibodies. The antibodies will attack subsequent pregnancies by killing the hCG< actually inactivating it, not killing > which naturally sustains a pregnancy; when a woman has sufficient anti-hCG antibodies in her system, she is rendered incapable of maintaining a pregnancy.(1)
HLI reported the sketchy facts regarding the Mexican tetanus vaccines to its World Council members and affiliates in more than 60 countries.(2) Soon additional reports of vaccines laced with hCG hormones began to drift in from the Philippines, where more than 3.4 million women were recently vaccinated. Similar reports came from Nicaragua, which had conducted its own vaccination campaign in 1993.
The Known Facts
Here are the known facts concerning the tetanus vaccination campaigns in Mexico and the Philippines
* Only women are vaccinated, and only the women between the ages of 15 and 45. (In Nicaragua the age range was 12-49.) But aren't men at least as likely as young women to come into contact with tetanus? And what of the children? Why are they excluded?
* Human chorionic gonadotrophin ( hCG ) hormone has been found in the vaccines. It does not belong there -- in the parlance of the O.J. Simpson murder trial, the vaccine has been "contaminated."
* The vaccination protocols call for multiple injections -- three within three months and a total of five altogether. But, since tetanus vaccination < a single vaccination > provide protection for ten years or more, why are multiple inoculations called for?(3)
* WHO has been actively involved for more than 20 years in the development of an anti-fertility vaccine utilizing hCG tied to tetanus toxoid as a carrier -- the exact same coupling as has been found in the Mexican-Philippine-Nicaragua vaccines.(4) ...
When the first reports surfaced in the Philippines of tetanus toxoid vaccine being laced with hCG hormones, the WHO and the Philippine Department of Health (DOH) immediately denied that the vaccine contained hCG. Confronted with the results of laboratory tests which detected its presence in three of the four vials of tetanus toxoid examined, the WHO and DOH scoffed at the evidence coming from "right-to-life and Catholic" sources. Four new vials of the tetanus vaccine were submitted by DOH to St. Luke's (Lutheran) Medical Center in Manila -- and all four vials tested positive for hCG!
From outright denial the stories now shifted to the allegedly "insignificant" quantity of the hCG present; the volume of hCG present is insufficient to produce anti- hCG antibodies.
But new tests designed to detect the presence of hCG antibodies in the blood sera of women vaccinated with the tetanus toxoid vaccine were undertaken by Philippine pro-life and Catholic groups. Of thirty women tested subsequent to receiving tetanus toxoid vaccine, twenty-six tested positive for high levels of anti- hCG! If there were no hCG in the vaccine, or if it were present in only "insignificant" quantities, why were the vaccinated women found to be harboring anti- hCG antibodies? The WHO and the DOH had no answers
New arguments surfaced: hCG's < human chorionic gonadotrophin > apparent presence in the vaccine was due to "false positives" resulting from the particular substances mixed in the vaccine or in the chemicals testing for hCG. And even if hCG was really there, its presence derived from the manufacturing process.
But the finding of hCG antibodies in the blood sera of vaccinated women obviated the need to get bogged down in such debates. It was no longer necessary to argue about what may or may not have been the cause of the hCG presence, when one now had the effect of the hCG. There is no known way for the vaccinated women to have hCG antibodies in their blood unless hCG had been artificially introduced into their bodies! Are New Vaccines Laced with Birth Control Drugs? < current authors clarification >
I should state that I do not endorse the Human Life Organization, but I will look for truth from any source. A crime of genocide is too inhumane a crime to refuse to consider because the accusation comes from a group with its own agenda.
If this is not bad enough for you, then you may be surprised to find that this project of sterilization was supported by the Rockefeller Foundation and the human chroronic gonadotropin ( hCG ) was supplied by the US National Institute of Child Health and Human Development (part of NIH, the National Institute of Health). Before recombinant human choronic gonadotropin (r- hCG) was produced in 2005, the only human choronic gonadotrophin hormone available came from concentrating it from human female urine.
Allied with the WHO in the development of an anti-fertility vaccine (AFV) using hCG with tetanus and other carriers have been UNFPA, the UN Development Programme (UNDP), the World Bank, the Population Council, the Rockefeller Foundation, the All India Institute of Medical Sciences, and a number of universities, including Uppsala, Helsinki, and Ohio State.(5) The U.S. National Institute of Child Health and Human Development (part of NIH) was the supplier of the hCG hormone in some of the AFV experiments.(6)
The WHO begain its "Special Programme" in human reproduction in 1972, and by 1993 had spent more than $356 million on "reproductive health" research.(7) It is this "Programme" which has pioneered the development of the abortificant vaccine. Over $90 million of this Programme's funds were contributed by Sweden; Great Britain donated more than $52 million, while Norway, Denmark and Germany kicked in for $41 million , $27 million, and $12 million, respectively. The U.S., thanks to the cut-off of such funding during the Reagan-Bush administrations, has contributed "only" $5.7 million, including a new payment in 1993 by the Clinton administration of $2.5 million. Other major contibutors to the WHO Programme include UNFPA, $61 million; the World Bank, $15.5 million; the Rockefeller Foundation, $2.5 million; the Ford Foundation, over $1 million; and the IDRC (International Research and Development Centre of Canada), $716.5 thousand. Are New Vaccines Laced with Birth-Control Drugs? http://www.thinktwice.com/birthcon.htm < current authors emphasis >
In case you are surprised by the presence of Sweden as a supporter here, Sweden has long had a compulsory sterilization program like that of California in the 30's and 40" only the Swedish program went till the 1950's.
Contrary to popular opinion, sterilization and eugenics was not just a stigma of Nazi Germany on the continent in the twentieth century. Sweden once exercised a strong sterilization program from the early 1930s until the mid 1950s. 21,000 were forcibly sterilized, 6,000 were coerced into a ‘' voluntary’' sterilization while the nature of 4,000 cases could not be determined. The program was an attempt to prevent mental illness and disease. Eugenic legislation was enacted in 1934 and was formally abolished in 1976 before a government report looked into the issue in 2000 following news stories of the policy. Alva and Gunnar Myrdal, founders of the Swedish Racial Hygiene Society, argued that sterilization was the best solution for the Swedish welfare state and was help eliminate the transmission of undesirable hereditary characteristics. Canada and the USA have also had a history of sterilization programs. NSSM 200 and Swedish Sterilizaion Sunday 19 July 2009
Further evidence of the validity of these assertions is found in the published scientific papers that include some UN scientists as authors. Please note that these papers come from 1976 forward. This was a long planned endeavor.
"Clinical profile and Toxicology Studies on Four Women Immunized with Pr-B-hCG-TT," Contraception, February, 1976, pp. 253-268.
"Observations on the antigenicity and clinical effects of a candidate antipregnancy vaccine: B-subunit of human chorionic gonadotropin linked to tetanus toxoid," Fertility and Sterility, October 1980, pp. 328-335.
"Phase 1 Clinical Trials of a World Health Organisation Birth Control Vaccine," The Lancet, 11 June 1988, pp. 1295-1298. "Vaccines for Fertility Regulation," Chapter 11, pp. 177-198, Research in Human Reproduction, Biennial Report (1986-1987), WHO Special Programme of Research, Development and Research Training in Human Reproduction (WHO, Geneva 1988).
"Anti- hCG Vaccines are in Clinical Trials," Scandinavian Journal of Immunology, Vol. 36, 1992, pp. 123-126.
...in 1995, the Catholic Women's League of the Philippines won a court order halting a UNICEF anti-tetanus program because the vaccine had been laced with B- hCG, which when given in a vaccine permanently causes women to be unable to sustain a pregnancy. The Supreme Court of the Philippines found the surreptitious sterilization program had already vaccinated three million women, aged 12 to 45. B- hCG-laced vaccine was also found in at least four other developing countries UNICEF Nigerian polio vaccine contaminated with sterilizing agents scientist finds LifeSiteNews.com Canada/USA March 11, 2004
By their own admission in a patent for this anti-pregnancy vaccine, the United Nations have virtually hanged themselves.
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 tween 80 (polysorbate 80): “In a preferred embodiment the vaccine comprises oil, preferably a biodegradable oil such as squalene oil. Typically, the vaccine is prepared using an adjuvant concentrate which contains lecithin in squalene oil. The aqueous solution glycoprotein is typically a phosphate-buffered saline (PBS) solution, and additionally preferably contains Tween 80.” (Fertility Impairing Vaccine And Methods of Use. This application claims the benefit of U. S. Provisional Application No. 60/070,375, filed January 2,1998, U. S. Provisional Application No. 60/071,406, filed January 15,1998.) Exploring Vaccines
This effort is no a new direction. Since at least 1973, the UN has been not just exploring these techniques, but putting then in practice mainly against the black and brown people of the world.
The World Health Organization also has a Task Force on Vaccines for Fertility Regulation. An article in Human Reproduction (Human Reproduction, Vol. 6, No. 1, pp. 166-172, 1991 1991 European Society of Human Reproduction and Embryology) called “The WHO Task Force on Vaccines for Fertility Regulation. Its formation, objectives and research activities” by P.D. Griffin of the Special Programme of Research, Development and Research Training in Human Reproduction, World Health Organization 1211 Geneva 27, Switzerland summarized its work this way: Over the past 18 years, the WHO Task Force on Vaccines for Fertility Regulation has been supporting basic and clinical research on the development of birth control vaccines directed against the gametes or the preimplantation embryo. These studies have involved the use of advanced procedures in peptide chemistry, hybridoma technology and molecular genetics as well as the evaluation of a number of novel approaches in general vaccinology. As a result of this inter national, collaborative effort, a prototype anti-HCG vaccine is now undergoing clinical testing, raising the prospect that a totally new family planning method may be available before the end of the current decade." That means that since 1973 the World Health Organization has been looking for ways to use vaccines and injections to control the world's fertility. If those methods are offered to men and women so that they can make a choice about their reproductive lives, well and good. If, however, they are hidden in smallpox vaccines (Africa) with the avowed purpose of “ ' eliminating 150 million excess Sub Saharan Africans'” as they were in vaccines distributed by the WHO starting in 1985, or in tetanus vaccines which would cause abortions in South and Central America women starting in the 1990's, we are not dealing with reproductive options, but reproductive genocide... The FDA approved the same sterility vaccine in the US within the last 18 months. For what purpose? Which group will receive it in which vaccine, hidden in a syringe supposedly offered to “protect” patients?... Is the World Health Organization empowered to decide which group of people may reproduce and which must become sterile? And if so, by whom is it so empowered? How about the FDA? GM Files: GM corn to make men sterile Already a Reality < current author's emphasis >
These anti-pregnancy vaccines are published in scientific journals and attempts to take out a patent on this method was conducted. The UN's own definition of GENOCIDE in section 2d states: "Imposing measures intended to prevent births within the group". This is much like the suggestions in a paper published during Henry Kissinger's tenure as Secretary of State of the US that suggested that genocide could be very profitable.
During the late 60s/early 70s, Dr. Archie Kalokerinos was administering vaccines to Australia's aboriginal children. Dr. Kalokerinos describes how half the aboriginal children died from the vaccines until he began giving them large doses of vitamin C. He reported his findings to the Australian government. Instead of taking a humanitarian interest in the simple, inexpensive procedure, the government's reaction "was one of extreme hostility," said Dr. Kalokerinos. "My final conclusion after 40 years or more in this business is that the unofficial policy of the World Health Organization and the unofficial policy of the Save the Children's Fund and almost all those organizations is one of murder and genocide. They want to make it appear as if they are saving these kids, but in actual fact they don't," said Dr. Kalokerinos. Vaccine Weapons for the 21st Century. By Don Harkin
This is the ultimate REGULATORY TAKEOVER. The United Nations at best has been "used" to commit GENOCIDE and potentially on a much greater scale than that of Adolph Hitler. It clearly appears that the controllers of the developed world have already carried out a sustained program of population genocide by sterilizing women in the third world. Funny how the people eugenists want to most exterminate seem to be black and brown. This forces ever more concern about vaccinations to this man made Mexican Swine Influenza farce. This sterilization is to be done not by the virus, but by the vaccine. Remember, "The FDA approved the same sterility vaccine in the US within the last 18 months". Fortunately, I think the people in the First world will strongly object when this is turned on them - their only problem is that they won't know for years after the vaccination that sterilization and progressive autoimmunity has occurred.
Do any of these actions fit with a lawful limited government organization of life on this planet? Do they fit with the UN definition of health: "The United Nations' World Health Organization defines health as "a state of complete physical, mental and social well-being and not merely the absence of disease or infirmity."" . You already know that this falls into the UN definition of GENOCIDE under section 2d : "Imposing measures intended to prevent births within the group" (http://www.hrweb.org/legal/genocide.html) . Additionally it is a violation of our own government's adherence to agreed upon international standards such as the the NUREMBURG CODE (voluntary consent of the human subject is absolutely essential).
This is AGAIN one more of many VERY DIRTY SECRETS OF VACCINES. They are being used TO COMMIT GENOCIDE (by the above definition 2d of "imposing measures intended to prevent births within the group") and to VIOLATE THE NUREMBERG CODES established to prevent such immoral medical practices as the Nazi's (voluntary consent of the human subject is absolutely essential). Adolph Hitler would have been DELIGHTED IF HE COULD HAVE DONE THIS ! Moreover, it is being done through the offices of the UNITED NATIONS World Health Organization (WHO). Worse yet, this has been going on from probably the late 1970's in multiple third world countries The whole purpose of a United Nations WORLD HEALTH ORGANIZATION (UN WHO ) requires TRUST - that "trust" is routinely given and not examined until after profound MISBEHAVIOR. Don't blame your doctors for participating in this misbehavior, they have no way to ascertain what the labels say is all that is in the vaccines. The UNITED NATIONS desperately needs to prosecute this continuing ATROCITY immediately! Otherwise, the UN WHO will be rejected by the first world much as it has been in the Islamic world, much of Africa, and much of the southern hemisphere catholic world. Doing nothing when you know about genocide is explicitly defined as complicity in GENOCIDE. This is directly written the UN definition of Genocide.
Do not imagine for a second that the UN WHO could or would do these things without backing and support if not directions and demands for it from powerful countries in the UN. This evil power cartel will not go away by itself. The people of the world deserve a just end to this and punishment of people who engaged in this GENOCIDE. We are talking of as few as 5 million women to possibly 100 million sterilized women. After you cover the ECOLOGY section, you will understand that this was needless even if it was due to fears of overpopulation. Leaders already understood this and still conducted this atrocity.
What should really set your hair on fire is a patent for another immunity based anti-reproduction technique.
(WO/1999/034825) FERTILITY IMPAIRING VACCINE AND METHOD OF USE
This application claims the benefit of U. S. Provisional Application No. 60/070,375, filed January 2,1998, U. S. Provisional Application No. 60/071,406, filed January 15,1998
"The vaccine of the invention preferably additionally includes an immunological adjuvant to enhance the immunological response of the subject to the glycoprotein antigen. Examples of adjuvants include Freund's Complete Adjuvant, Freund's Incomplete Adjuvant, and an adjuvant comprising an immunostimulant such as synthetic trehalose dicorynomycolate (STDCM) and an oil such as squalene oil" (see P. Willis et al., J. Equine Vet. Sci., 14,364-370 (1994)). An adjuvant comprising synthetic trehalose dicorynemycolate, squalene oil, and a surfactant such as lecithin is preferred. Lecithin typically includes phosphatidyl choline. In a preferred embodiment the vaccine comprises oil, preferably a biodegradable oil such as squalene oil. Typically, the vaccine is prepared using an adjuvant concentrate which contains lecithin in squalene oil. The aqueous solution glycoprotein is typically a phosphate-buffered saline (PBS) solution, and additionally preferably contains Tween 80.
A vaccine comprising an antigen derived from a zona pellucida glycoprotein is effective to impair fertility in animals, preferably carnivores. The vaccine can be used as an immunosterilant or an immunocontraceptive.
What has been learned is that injecting just squalene and Tween80 with the relatively inexpensive synthetic trehalose dicorynomycolate (STDCM) can lead to an autoimmune block to conception !
Remember our presentation of the components in the Swine Flu Vaccine? Yes, Squalene and Tween80 in relatively high doses. All you have to add is this relatively inexpensive synthetic trehalose dicorynomycolate which mimics carbohydrate residues on tissues required for reproduction. Thus, the vaccine alone without any more evil additions of live viruses will sterilize women (and men! ) . Do you really think that the people who have already perpetrated this grotesque evil on a large number of third world people, will inform you or your doctors of this consequence of these vaccines? These genocidal scum bags hide in the shadows.
We have the basic and universal right not to be deliberately harmed by our own government, or used as unwilling laboratory subjects for completely untested and dangerous vaccines. It is inhuman and in total contravention of all international laws to deliberately cause grave harm or death to citizens. This is what the Nazis did. The United States is now a rogue country that ignores basic universal human rights. Massive greed and collusion-to-cause-untold-grave-harm have taken its place. Where our own innocent, young children are used as test subjects, where our government puts us all in harm's way, where we are threatened with internment in FEMA concentration camps, if we refuse to be compliant and be injected with poisons, while nothing of basic humanity remains from any public official... Whatever lies are being promulgated by a corporate-controlled and compliant media, there is no real investigative journalism left. There is no search for the truth. What we have now every day is Orwellian Doublespeak, while the entire population of the United States is at grave risk of enormous physical harm. Dangers in the Shots - Components Of H1N1 Vaccines -They are considered a biodefense agents. By Dr. Ilya Sandra Perlingieri
Welcome to the NEW WORLD ORDER, where hidden powers in the shadows will decide sterilization or life or death for your children and yourself. This is so far beyond the conception of a common human dignity, it boggles the mind to realize how far we have fallen.. We need to end this and severely punish the offenders, NO MATTER WHERE THIS LEADS. This should confirm your rightful suspicions of the hype and con-man pitch for the Mexican Swine Flu Vaccine (A H1N1). Something very evil is among us !
UNTIL THIS NIGHTMARE IS CLEARED AWAY, I WILL TAKE HIGH DOSES OF VITAMIN D3 (5000 International Units/day) and AVOID ALL VACCINES. You will have to decide what you wish to do
SPECIAL IMMUNOLOGICAL PROTECTIONS
There are a few concentrates of natural substances that can MASSIVELY augment our avoidance of becoming infected and others that strongly stimulate our immune systems to respond if we do become infected. Most medical doctors have never even heard of this. One of these can be used daily (I do) and the other two are strictly for situations where one is in danger from a serious infection. All are covered in the SUBSCRIBER only IMMUNE ENHANCEMENT PDF.
A potent safe natural substance creates a safe "FIREWALL PROTECTION" for our mucus membranes. This is covered in the SUBSCRIBER only IMMUNE ENHANCEMENT PDF. If you use this safe and inexpensive "FIREWALL PROTECTION" daily, you may never become infected*. Also covered in this IMMUNE ENHANCEMENT PDF are two extremely potent methods to enhance your T & B-cell responses and directly kill pathogens by augmenting your bodies own naturally produced antibiotics. This is for any infection that gets through the FIREWALL protection. Naturally this is only used when you have become infected. This is defense in depth. What I have found is that I just never get the colds and flu that are all around me with sick and sneezing students. Try it, you will not regret the absence of colds and flu.