Some vaccine facts to ponder upon.

March 25, 2008

QUICK FACTS

USA population has 90% of the world's neurologically damaged population. Autism has increased from 1 in 10,000 in 1978 to 1 in 137 today, because of several things in various vaccines...China had no Autism until 1999...when the DPT vaccine arrived from America,now they have 1.8 million of them! Japan had their first Autistic children appear when vaccines arrived from America after WWII.At that time these children had been given the DPT and they discovered about the lack of myelin sheath being the vulnerability in infants, and made laws to wait 2 years before vaccinating... but today, immunization in Japan is voluntary... and their minds work great!

DTaP safer than DTP a myth!In making the batches of Pertussis bacteria into the vaccine, they grind up the Whole Cells into smaller pieces (thus, the name 'A-Cellular'), and rinse them with formaldehyde, which is used in every single vaccine as the one chemical that either "stuns" viruses for the living viral vaccines or "kills" bacteria for the dead bacterial vaccines. It's like making Decaffeinated Coffee, which is done by rinsing out the caffeine, just wash what they can away! Today, when making the DTaP, they ADD BACK IN pertussis toxin, to make up for washing it out, adding more than DOUBLE the toxins back in! This is the major cause of Autism - the pertussis increase - but, also, there is diptheria, tetanus, and the MMR, causing a regressive autism (destructive of myelin in brain by immune system killing colonizing measles virus). Pertussis Vaccines has always been BANNED (contra-indicated) by the

manufacturers for anyone over the age of 6 !

SIDS (Sudden Infant Death Syndrome) is caused by the toxins in the dead-bacterial vaccine Pertussis (DTaP)As declared by the manufacturer of the vaccine, "85% of SIDS cases occur at ages 1-6 months, with the peak occuring at 6 weeks- 4 months of age." This is because they lack Myelin Sheath to protect their nerves and brain from pertussis poisons!

Viral Vaccines (living to colonize)Measles - grown in Chicken Eggs. Polio - grown in Monkey Kidneys. Chicken Pox - grown in Human Embryonic Lung Cells, and embryonic guinea pig cells. HepB - grown in Yeast (fermented) - purified for surface antigen (protein/DNA) - absorbed onto Aluminum. Bacterial Vaccines

(dead but poisonous)HIB (haemophilus influenzae) - grown in Yeast (fermented yeast) - filtered - Aluminum added. Pertussis (DTP)- grown in Nutrient Medium - killed with formaldehyde - absorbed onto aluminum phosphate.Diptheria - grown in Bovine nutrients (cow) - steamed, filtered, de-toxified with Formaldehyde - absorbed onto aluminum.Tetanus - grown in Casein (milk/cheese) - killed with Formaldehyde - absorbed onto aluminum phosphate. Researchers call

Vaccines, "Designer Diseases."

Allergies are made during the hours following vaccination, when immune systems are launched into full scale response, into such a battle frenzy that EVERY FOREIGN PROTEIN that enters the body will be considered an enemy... confused with the enemy, so by de-facto an enemy. There are foreign proteins in dust from dust mites, peanut butter has protein, so does the dairy that we used to raise our children on so well in the past. Thus, the immune system does it's job well, attacking all the foreign proteins, which unfortunately, makes it so that everything, especially common foods, or spores in the air, or microbial colonies in dander, are all forms of proteins that are mistaken as enemies while in the heat of battle against the true enemy within the 'designer disease' of the vaccine... so, pets at home, dust in the air, milk from the cup will be

marked as enemies forever, for Allergies are just immune system responses to common things. Vaccinating immature immune systems creates most of the Allergies that exist today...

The history of studies on vaccines began in 1922 when a smallpox vaccination program caused an outbreak of encephalitis, with a secondary result of Guillain-Barre Syndrome, an ascending paralysis ending in death. The polio virus produces a breakdown of the myelin sheath, called poliomyelitis, which results in paralysis. Encephalitis, whether caused through disease or as a result of vaccination, can cause demyelination of the nerves.. For more information, see The Mechanism of Encephalitic Damage from Vaccines. General paralysis is rare in regions where no organized vaccination of the population exists. It is impossible to deny a connection between vaccination and the encephalitis which sometimes follows it. [Reference: Wise RP, Kiminyo KP, Salive ME. Hair loss after routine immunizations. J Am Med

Assoc 1997; 278: 1176-8.]

Mercury Neurotoxicity (There is mercury in vaccines)

At high exposure levels, mercury causes neurotoxicity in humans, especially in fetuses and small infants whose brains are still developing. The major toxicity of mercury is manifested in the central nervous system. Forty years ago, when women at Minamata Bay, Japan, ate fish contaminated with methylmercury from pollutants, their children were exposed to high levels in utero and were born with developmental and neurologic disorders. Methylmercury poisoning also occurred in Iraq following consumption of seed grain that had been treated with a fungicide containing methylmercury. In both the Japanese and Iraqi episodes, exposures to methylmercury were high. Two population-based studies are often cited as the basis for calculations on the neurotoxicity of mercury in utero. In the first, a study from the Seychelles, infants were exposed to mercury in utero when their mothers ate a high daily consumption of methylmercury-containing fish. The mothers had mean mercury levels in hair of 6.8 ppm. No developmental defects were detected. In the second, a study from the Faroe Islands, infants were born to mothers with mean hair levels of 4.3 ppm. In contrast to the Seychelles mothers, these mothers were exposed to mercury through intermittent "bolus" consumption of pilot whale meat. Lower scores on memory, attention, and language tests were associated with methylmercury exposure in the children (see the Mercury Study Report to Congress, EPA, 1997).

The Centers for Disease Control and Prevention (1,2,3,4 ) and the vaccine manufacturers (5,6,7) have always warned against the administration of live virus vaccines during pregnancy, and shortly prior to conception.

This report describes six mothers who received live virus vaccines and one who received a Hepatitis B vaccine during pregnancy (8) after having received an MMR booster

five months prior to conception.

All the children who resulted from these pregnancies have had developmental problems, six out seven (85%) were diagnosed with autism, and the seventh seems to exhibit symptoms often associated with autistic

spectrum disorders.

The routine administration of a live virus vaccine booster, during the postpartum period, to previously vaccinated women who have remained rubella-susceptible, should be

reconsidered.

It is likely that continued rubella susceptibility in these women, is not due to a problem with the vaccine, but with the woman herself, and therefore it seems reasonable not to attempt to correct it by the administration of

more boosters.

Some re-vaccinated mothers are developing unusual problems, and many remain rubella-susceptible. Their children also appear to have an inordinate number of difficulties of their own. Twenty out of twenty five families (80%) in

this study have children with autism.

Large-scale independent investigations on the possible link between live virus vaccines, MMR, and autism should be undertaken.

Two studies, published in late December 1999, described the very high incidence of autism in children whose mothers had received live virus vaccines in the postpartum period (1), prior to conception and during pregnancy. (2)

In the following weeks, twenty two more mothers reported having been vaccinated in those same periods. Every one of them (100%) subsequently had at least one child who developed Autism/PDD.

All three studies clearly demonstrate that the administration of a live virus vaccine booster to a mother, around conception, pregnancy, or delivery, may carry certain risks and merits immediate review.

There is crucial need for large-scale independent investigations of a vaccineâ€“autism connection.

Conflict of Interest and Vaccine Development

In August 1999, the Committee on Government Reform initiated an investigation into Federal vaccine policy.1 This investigation focused on possible conflicts of interest on the part of federal policy-makers. The Committee conducted an extensive review of financial disclosure forms and related documents, and interviewed key officials from the Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC). In the course of the investigation, the committee discovered that many individuals serving on two key advisory committees had financial ties to the pharmaceutical companies that manufacture vaccines. Often, these individuals were granted waivers to fully participate in the discussions that led to recommendations on vaccine licensing and adding vaccines to the Childhood Immunization Schedule.. Under federal law, members of advisory committees are required to disclose any financial conflicts of interest and recuse themselves from participating in decisions in which they have an interest. The Committee's investigation determined that conflict of interest rules employed by the FDA and the CDC were weak, enforcement was lax, and committee members with substantial ties to pharmaceutical companies had been given waivers to participate in committee proceedings. The Committee noted several specific problems, including:

The CDC routinely granted waivers from conflict of interest rules to every member of its advisory committee.

CDC advisory committee members who were not allowed to vote on certain recommendations due to financial conflicts of interest were allowed to actively participate in committee deliberations and advocate specific positions.

The Chairman of the CDC's advisory committee until recently owned 600 shares of stock in Merck, a pharmaceutical company with an active vaccine division.

Members of the CDC's advisory committee often left key details out of their financial disclosure statements, and were not required to provide the missing information by CDC ethics officials.

Regarding the FDA and CDC approval of the controversial rotavirus vaccine in 1998 and 1999:

3 out of the 5 FDA advisory committee members who voted to approve the rotavirus vaccine in December 1997 had financial ties to the pharmaceutical companies that were developing different versions of the vaccine.

4 out of the 8 CDC advisory committee members who voted to approve guidelines for the rotavirus vaccine in June 1998 had financial ties to pharmaceutical companies that were developing different versions of the vaccine.

The rotavirus vaccine was pulled from the market one year after approval, after it was found to cause severe bowel obstructions.

Taken from the websites:

http://www.trackingvaccinations.com/

http://healing-arts.org/children/vaccines/

http://www.garynull.com/Documents/autism99b3.htm