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Archive for May, 2011

Nine month old twins die just minutes after measles vaccination


(NaturalNews) A pair of nine-month old twin girls died within minutes of being given a measles vaccine at a private clinic in Ghaziabad, India.

The girls were taken by their uncle, Akhil Sharma, to receive a measles vaccine at the Divya Nursing Home.

“I took them for the vaccination around 6 p.m. on Wednesday,” Sharma said. “They were given the vaccination around 7:15 pm. In 15 minutes, the children started breathing heavily.”

When the first girl began to experience distress — breathing heavily and vomiting — her sister had not yet been vaccinated. Sharma asked the doctor to hold off on vaccinating the second girl, but he insisted on going ahead. The second girl went into distress, and both girls lost consciousness.

“Even as the condition of one of my daughters deteriorated, the doctor told us that we need not worry since it was a normal reaction to the vaccine,” the girls’ father, Sunil Sharma, said. “The deteriorating condition of the baby did not deter him from administering the vaccine to my other daughter.”

The doctor then transferred the girls to another hospital and vanished. The girls went into critical condition and their family rushed them to a third hospital.

“We took the twins to Ganesh Hospital in Nehru Nagar where doctors again declared them dead,” Sunil Sharma said. “Then we informed the police, and handed over the bodies and lodged the complaint at Kavi Nagar police station.”

“I have given orders to seal the hospital and take samples of the vaccine,” said SSP Raghubir Lal. “We have approached the Chief Medical Officer to probe the incident.”

The cause of death has not yet been determined.

“We have sent the viscera of both the babies for forensic examination and a central government team is also examining the case,” Chief Medical Officer A.K. Dhawan said.

Learn more:http://www.naturalnews.com/030712_measles_vaccination.html#ixzz1Nxb6s8ip

 

 

 

http://www.naturalnews.com/030712_measles_vaccination.html

Categories: Health/Pharma

Pfizer tested drugs on children

May 31, 2011 1 comment

THIS ARTICLE W

Pfizer - fail!

In April 2009, Pfizer reportedly reached a tentative agreement on lawsuits regarding the vaccine trials it had conducted in 1996. Pfizer tested Trovan, an oral antibiotic, on children of Nigeria’s Kano state. To avoid the lengthy clinical trial process required by the Food and Drug Administration, Pfizer decided to expedite the production of Trovan.

According to the cable 09ABUJA671, Pfizer tested its efficacy on Kano children during a meningitis epidemic, with the help of Doctors Without Borders. This bypasses national and international standards on medical ethics and put the lives of the Kano children in danger.

Since the testing, there has been one civil suit and one criminal case in both the Kano State and Federal High Courts. The Pfizer lawyers have worked closely with a former Nigerian Head of State on a $75 million settlement. The breakdown of the settlement would provide $10 million for legal fees; $30 million to the Kano State government; and $35 million to participants and families.

The US government was fully aware of the cases against Pfizer in Nigeria and helped Pfizer develop a new framework to conduct future testing in Nigeria. Pfizer considers Nigeria to be a major growth market and is working hard to restore its image there.

http://crowdleaks.org/pfizer_drug_test/

Categories: Health/Pharma

Commonly prescribed drugs containing fluoride or bromide

May 31, 2011 3 comments

Advair (fluticasone)
Alphagen (brimonidine) bromide
Atrovent (Ipratropium) bromide
Avelox (moxifloxacin)
Adovart (dulasteride)

Celebrex (celecoxib)
Celexa (citalopram) both fluoride and bromide
Cipro (ciprofloxacin)
Clinoril (sulindac)
Combivent (from the ipratropium)bromide
Crestor (rosuvastatin)

Diflucan (fluconazole)
DuoNeb (nebulized Combivent)
Enablex (darifenacin) bromide
Flonase (fluticasone)
Flovent (fluticasone)
Guaifenex DM (dextromethorphan) bromide

Lescol (fluvastatin)
Levaquin (levofloxacin)
Lexapro (escitalopram)
Lipitor (atorvastatin)
Lotrisone topical cream

Paxil (paroxetine)
Prevacid (lansoprazole)
Protonix (pantoprazole)
Prozac (fluoxetine)
Pulmicort (budesonide)

Razadyne (galantamine) bromide
Risperdal (risperidone)
Spiriva (tiotropium) bromide
Tobra Dex (from dexamethasone)
Travatan (travoprost)
Triamcinolone
Vigamox (moxifloxacin)
Vytorin (from eztimibe)
Zetia (eztimibe)

Categories: Health/Pharma

Study clearly demonstrates that aluminum found in vaccines can cause neurologic damage

May 31, 2011 1 comment

Randi Allaire was an Information Management Specialist in the military for almost four years. Three and one-half years were spent with the Air National Guard as Information Management, the previous five and half was with the Army Guard as a Flight Operations Specialist.

As part of the military’s program to protect their troops from chemical and biological weapons, Randi was required to take the anthrax vaccine. On March 14, 1999 she was given her fourth anthrax vaccine. It was after that shot that she has suffered chronic fatigue, memory lapses, migraines, pain in the forearms, and other aches and pains. She received no help with her condition and only denials that the anthrax vaccine could cause any of these problems and that the cause of her problems was likely the “flu” or too much “stress”. She was eventually thrown out of the military because she refused to take the fifth anthrax vaccine shot in fear for her own personal health.

Aluminum is the most commonly licensed adjuvant that is added to a large number of vaccines. An adjuvant is a substance added to a vaccine to amplify the immune response. Aluminum compounds, which were identified over 90 years ago as adjuvants, are considered by the pharmaceutical industry and various government agencies as safe. The FDA (Food and Drug Administration) has continued to approve the use of aluminum as an additive to vaccines for many years.

Despite these assurances that aluminum and all vaccine ingredients are safe, large numbers of military veterans who suffer from Gulf War Syndrome as well as parents of children who suffer from various neurologic conditions including Autism strongly believe that the vaccines were often at least in part a cause of their health problems.

A recent study in the Journal of Inorganic Biochemistry examined the possible neurotoxicity of aluminum. This new work builds on a previous study where the researchers had injected mice with a combination of aluminum and squalene, another vaccine adjuvant which is not licensed in North America.

In that study the investigators injected mice with adjuvants that mimicked the anthrax vaccine schedule set by the Anthrax Vaccine Immunization Program. The investigators concluded in that study”our data suggest that the aluminum hydroxide adjuvant induces both behavioral and motor deficits and the loss of motor neurons and increased presence of astrocytes [astrocytes are cells that express inflammatory markers] in spinal cord and neuronal apoptosis [cell death] in the primary motor cortex.” When Professor Shaw was asked in an article by Pieta Wooley about this research Professor Shaw replied “No one in my lab wants to get vaccinated. This totally creeped us out. We weren’t out there to poke holes in vaccines. But all of a sudden, oh my God-we’ve got neuron death!”

In this new study (also termed experiment 2), mice received 6 aluminum hydroxide injections over a 2 week period. These mice along with control mice were subjected to a more rigorous behavioral testing regime than the original experiment.

The investigators found “the multiple aluminum hydroxide injections of experiment 2 showed profound effects on motor and other behaviours… Multiple aluminum injections produced significant behavioural outcomes including changes in locomotion behavior, and induced memory deficits on water maze tasks.”

I asked Professor Shaw “To your knowledge have there been any autopsies performed on service men and women that had GWS [Gulf War Syndrome] and have died to examine if they have a similar pattern of aluminum contamination that you discovered in your research?” He responded “that it has not been done to my knowledge.” I also asked “Has there been an examination of people with autism to examine the obvious likely link between aluminum and mercury contamination and that condition?” Again he responded “Not to my knowledge.”

It is important to note that while this and their previous study showed “significant behavioural and neuropathological outcomes with aluminum hydroxide” that these results were achieved under minimal conditions and that the effect of multiple other factors in real situation such as “stress, multiple vaccinations, and exposure to other toxins” would more than likely make the outcomes worse. “A recent study examining some of these factors in combination showed that stress, vaccination, and pyridostigmine bromide (Pyridostigmine bromide has been FDA approved for military use during combat situations as an agent to be given prior to exposure to the nerve agent Soman in order to increase survival), may synergistically act on multiple stress-activated kinases in the brain to induce neurologic impairment in GWS.”

I asked Professor Shaw, “In your opinion why do various governmental agencies continue to insist that vaccines are safe when you clearly state in your research paper that ‘it also seems that there have been no rigorous animal studies of potential aluminum adjuvant toxicity. The absence of such studies is peculiar given the well known observation that aluminum in general can be neurotoxic under a number of conditions and adjuvants in particular have previously been implicated in neurological disease’?” Professor Shaw replied “A less charitable person than I would likely look at links between pharma and the regulatory agencies. I don’t know of any safe adjuvants. Aluminum is the one considered ‘safe’.”

The authors conclude, “Overall, the results reported here mirror previous work that has clearly demonstrated that aluminum, in both oral and injected forms, can be neurotoxic.” I followed up with Professor Shaw “knowing what you know about aluminum from your research would you personally use a vaccine that contains aluminum?” He responded “No, and I don’t.”

 

The following vaccines (vaccine name/trade name, manufacturer, and information from the product insert) contain aluminum adjuvant:

Anthrax Vaccine Adsorbed/Biothrax, Emergent BioDefense Operations Lansing, Inc., “The final product is formulated to contain1.2 mg/mL aluminum, added as aluminum hydroxide in 0.85% sodium chloride.”
Diphtheria & Tetanus Toxoids Adsorbed, Sanofi Pasteur Inc, “Each 0.5 mL dose is formulated to contain 6.7 Lf of diphtheria toxoid, 5 Lf of tetanus toxoid, and not more than 0.17 mg of aluminum.”

Diphtheria & Tetanus Toxoids & Acellular Pertussis Vaccine Adsorbed/Tripedia, Sanofi Pasteur, Inc., “Each 0.5 mL dose also contains, by assay, not more than 0.170 mg of aluminum and not more than 100 μg (0.02%) of residual formaldehyde.”

Diphtheria & Tetanus Toxoids & Acellular Pertussis Vaccine Adsorbed/Infanrix, GlaxoSmithKline Biologicals, “Each 0.5-mL dose contains 4.5 mg of NaCl and aluminum adjuvant (not more than 0.625 mg aluminum by assay). Each dose also contains ≤100 mcg of residual formaldehyde and ≤100 mcg of polysorbate 80 (Tween 80).”

Diphtheria & Tetanus Toxoids & Acellular Pertussis Vaccine Adsorbed/DAPTACEL, Sanofi Pasteur, Ltd., “Other ingredients per 0.5 mL dose include 1.5 mg aluminum phosphate (0.33 mg of aluminum) as the adjuvant, ≤5 μg residual formaldehyde, <50 ng residual glutaraldehyde and 3.3 mg (0.6% v/v) 2-phenoxyethanol (not as a preservative).”

Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed, Hepatitis B (Recombinant) and Inactivated Poliovirus Vaccine Combined/Pediarix, GlaxoSmithKline Biologicals, “Each 0.5-mL dose also contains 4.5 mg of NaCl and aluminum adjuvant (not more than 0.85 mg aluminum by assay). Each dose also contains ≤100 mcg of residual formaldehyde and ≤100 mcg of polysorbate 80 (Tween 80).”

Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed and Inactivated Poliovirus Vaccine/Kinrix, GlaxoSmithKline Biologicals, “Each 0.5-mL dose contains 4.5 mg of NaCl and aluminum adjuvant (not more than 210 0.6 mg aluminum by assay). Each dose also contains ≤100 mcg of residual formaldehyde and 211 ≤100 mcg of polysorbate 80 (Tween 80).”

Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed, Inactivated Poliovirus and Haemophilus b Conjugate (Tetanus Toxoid Conjugate) Vaccine/Pentacel, Sanofi Pasteur, Ltd, “Other ingredients per 0.5 mL dose include 1.5 mg aluminum phosphate (0.33 mg aluminum) as the adjuvant, polysorbate 80 (approximately 10 ppm by calculation), ≤5 μg residual formaldehyde, <50 ng residual glutaraldehyde, ≤50 ng residual bovine serum albumin, 3.3 mg (0.6% v/v) 2-phenoxyethanol (not as a preservative) and <4 pg of neomycin and <4 pg polymyxin B sulfate. ”

Haemophilus b Conjugate (Meningococcal Protein Conjugate) and Hepatitis B (Recombinant) Vaccine/Comvax, Merck & Co, Inc, “The individual PRP-OMPC and HBsAg adjuvanted bulks are combined to produce COMVAX. Each 0.5 mL dose of COMVAX is formulated to contain 7.5 mcg PRP conjugated to approximately 125 mcg OMPC, 5 mcg HBsAg, approximately 225 mcg aluminum as amorphous aluminum hydroxyphosphate sulfate, and 35 mcg sodium borate (decahydrate) as a pH stabilizer, in 0.9% sodium chloride. The vaccine contains not more than 0.0004% (w/v) residual formaldehyde.”

Hepatitis A Vaccine, Inactivated/Havrix, GlaxoSmithKline Biologicals, “Each 1-mL adult dose of vaccine consists of 1440 EL.U. of viral antigen, adsorbed on 0.5 mg of aluminum as aluminum hydroxide. Each 0.5-mL pediatric dose of vaccine consists of 720 EL.U. of viral antigen, adsorbed onto 0.25 mg of aluminum as aluminum hydroxide.”

Hepatitis A Vaccine, Inactivated/VAQTA, Merck & Co, Inc, “Pediatric/Adolescent Formulation (12 Months Through 18 Years of Age): each 0.5 mL dose contains approximately 25U of hepatitis A virus antigen adsorbed onto approximately 0.225 mg of aluminum provided as amorphous aluminum hydroxyphosphate sulfate, and 35 mcg of sodium borate as a pH stabilizer, in 0.9% sodium chloride. Adult Formulation (19 Years of Age and Older): each 1 mL dose contains approximately 50U of hepatitis A virus antigen adsorbed onto approximately 0.45 mg of aluminum provided as amorphous aluminum hydroxyphosphate sulfate, and 70 mcg of sodium borate as a pH stabilizer, in 0.9% sodium chloride.”

Hepatitis A Inactivated & Hepatitis B (Recombinant) Vaccine/Twinrix, GlaxoSmithKline Biologicals, “A 1.0-mL dose of vaccine contains 720 ELISA Units of inactivated hepatitis A virus and 20 mcg of recombinant HBsAg protein. One dose of vaccine also contains 0.45 mg of aluminum in the form of aluminum phosphate and aluminum hydroxide as adjuvants, amino acids, 5.0 mg 2-phenoxyethanol as a preservative, sodium chloride, phosphate buffer, polysorbate 20, Water for Injection, traces of formalin (not more than 0.1 mg), a trace amount of thimerosal (<1 mcg mercury) from the manufacturing process, and residual MRC-5 cellular proteins (not more than 2.5 mcg).”

Hepatitis B Vaccine (Recombinant)/Engerix-B, GlaxoSmithKline Biologicals, “Pediatric/Adolescent: Each 0.5-mL dose contains 10 mcg of hepatitis B surface antigen adsorbed on 0.25 mg aluminum as aluminum hydroxide. The pediatric formulation contains sodium chloride (9 mg/mL) and phosphate buffers (disodium phosphate dihydrate, 0.98 mg/mL; sodium dihydrogen phosphate dihydrate, 0.71 mg/mL). Adult: Each 1-mL adult dose contains 20 mcg of hepatitis B surface antigen adsorbed on 0.5 mg aluminum as aluminum hydroxide. The adult formulation contains sodium chloride (9 mg/mL) and phosphate buffers (disodium phosphate dihydrate, 0.98 mg/mL; sodium dihydrogen phosphate dihydrate, 0.71 mg/mL).”

Hepatitis B Vaccine (Recombinant)/Recombivax HB, Merck & Co, Inc, “All formulations contain approximately 0.5 mg of aluminum (provided as amorphous aluminum hydroxyphosphate sulfate, previously referred to as aluminum hydroxide) per mL of vaccine. In each formulation, hepatitis B surface antigen is adsorbed onto approximately 0.5 mg of aluminum (provided as amorphous aluminum hydroxyphosphate sulfate) per mL of vaccine.”

Human Papillomavirus Quadrivalent (Types 6, 11, 16, 18) Vaccine, Recombinant/Gardasil, Merck & Co, Inc, “Each 0.5-mL dose of the vaccine contains approximately 225 mcg of aluminum (as Amorphous Aluminum Hydroxyphosphate Sulfate adjuvant), 9.56 mg of sodium chloride, 0.78 mg of L-histidine, 50 mcg of polysorbate 80, 35 mcg of sodium borate, < 7 mcg yeast protein/dose, and water for injection. The product does not contain a preservative or antibiotics.”

Japanese Encephalitis Vaccine, Inactivated, Adsorbed (Military & Commercial)/Ixiaro, Merck & Co, Inc, “Each dose of vaccine contains approximately 6 mcg of purified, inactivated JEV proteins and 250 mcg of aluminum hydroxide.”

Pneumococcal 7-valent Conjugate Vaccine (Diphtheria CRM197 Protein)/Prevnar, Wyeth Pharmaceuticals, Inc, “Each 0.5 mL dose is formulated to contain: 2 μg of each saccharide for serotypes 4, 9V, 14, 18C, 19F, and 23F, and 4 μg of serotype 6B per dose (16 μg total saccharide); approximately 20 μg of CRM197 carrier protein; and 0.125 mg of aluminum per 0.5 mL dose as aluminum phosphate adjuvant.”

Tetanus & Diphtheria Toxoids, Adsorbed for Adult Use, Massachusetts Public Health Biologic Lab, “Each 0.5 ml dose contains by calculation not more than 0.45 mg aluminum and less than 100 μg (0.02%) of residual formaldehyde. The aluminum phosphate functions as an adjuvant to increase the immunogenicity of the toxoids in primary immunization.”

Tetanus & Diphtheria Toxoids Adsorbed for Adult Use/DECAVAC, Sanofi Pasteur, Inc, “Each 0.5 mL dose also contains a trace amount of thimerosal [mercury derivative, (≤0.3 μg mercury/dose) not as a preservative] from the manufacturing process, aluminum adjuvant (not more than 0.28 mg aluminum by assay), and not more than 100 μg (0.02%) of residual formaldehyde.”

Tetanus Toxoid Adsorbed, Sanofi Pasteur, Inc, “Each 0.5 mL dose is formulated to contain 5 Lf (flocculation units) of tetanus toxoid and not more than 0.25 mg of aluminum. The residual formaldehyde content, by assay, is less than 0.02%.”

Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Adsorbed/Adacel, Sanofi Pasteur, Ltd, “Other ingredients per dose include 1.5 mg aluminum phosphate (0.33 mg aluminum) as the 15 adjuvant, ≤5 μg residual formaldehyde, <50 ng residual glutaraldehyde and 3.3 mg (0.6% v/v) 16 2-phenoxyethanol (not as a preservative).”

Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Adsorbed/ Boostrix, GlaxoSmithKline Biologicals, “Each 0.5-mL dose also contains 4.5 mg of NaCl, aluminum adjuvant (not more than 0.39 mg aluminum by assay), ≤100 mcg of residual formaldehyde, and ≤100 mcg of polysorbate 80 (Tween 80).”


Source:

Aluminum hydroxide injections lead to motor deficits and motor neuron degeneration, Christopher A. Shaw, et al, Journal of Inorganic Biochemistry, 2009 Aug 20. [Epub ahead of print]

Aluminum adjuvant linked to Gulf War illness induces motor neuron death in mice, M.S. Petrik, et al, Neuromolecular Medicine, 2007, Vol. 1, No. 9, pp. 83-100

Conversation with Professor Christopher Shaw. Christopher Shaw is Professor of Neurology and Neurogenetics at the Institute of Psychiatry, King’s College London. He is also an Honorary Consultant Neurologist at King’s College Hospital and Neurogeneticist at Guy’s and St Thomas’ Hospitals.

An Interview with Staff Sergeant Randi Allaire in the Air Force National Guard available athttp://www.healthsentinel.com/joomla/index.php?option=com_content&view=article&id=2447:an-interview-with-staff-sergeant-randi-allaire-in-the-air-force-national-guard&catid=39:reports&Itemid=52

Vaccines Licensed for Immunization and Distribution in the US with Supporting Documents,http://www.fda.gov/BiologicsBloodVaccines/Vaccines/ApprovedProducts/ucm093830.htm

Categories: Health/Pharma

The emergence of Vaccine induced Diseases


On virtually every level, whether it is food, water, medications or the contamination of our environment across the board including the air we breathe, we, as human beings, are under attack.  The view of the worlds’ populations by corporate, scientific, pharmaceutical, military and even our respective governments is, one of contempt.  None view the populations of the earth as anything more than potential test subjects for a wide array of experimentations of all kinds.  We are the test rats in the maze. In fact, we are considered disposable and detested by the world’s elite.

Vaccines, disease, death:

What are we subjecting our infants, toddlers and young children to? And even ourselves, as adults?  Every jab of the vaccine needle injects a DNA altering soup and infects the new host with live and thought to be dead viruses supposedly because this will protect us from some infection or disease. The injections also contain carcinogens, heavy metals, wild viruses, mutated proteins, and the dna in the vaccine can be transfective and recombinant, meaning it can combine with human DNA and mutate.

While many parents routinely subject their infants and toddlers to more than 63 vaccinations before the age of five, these same parents many times will go ballistic at the thought of another parent refusing to allow their child to be infected with vaccines.  The chronic complaint of the vaccinating parent is that those not vaccinated somehow represent a threat to the vaccinated kids.  Excuse me…but if you believe vaccines work and are effective, what possible risk could you infer from an unvaccinated child?  Is not your child now protected because you had them vaccinated?

Actually, the reverse is true.  The vaccinated child is now virally active and for the next 21 days is shedding the virus every time he/she enters a room, coughs, sneezes or just breathes. And now, with their immune system compromised by the vaccine, and with the ability of recombinant DNA to mutate and create new viruses in their little bodies, your vaccinated child has become a viral incubator.

It seems that vaccinating a small defenseless baby or toddler with what you know to be harmful if not fatal concoction is nothing more than an opportunity to gather data.  You know….who died, who got sick, with what? How long were they sick? That kind of stuff.  The idea that hundreds of thousands of children are harmed or killed by what you have produced should not be used to interfere with corporate profits, so says SCOTUS and that is what we are talking about here.

The Rotarix vaccine, a GlaxoSmithKline vaccine for use on children anddocumented here :

“According to a PubMed.gov 2004 study, which just happens to be the NIH (U.S. National Library of Medicine National Institutes of Health),

“Infection of PCV1 was observed with 293, Hela and Chang liver cells, infection with PCV2 only in Rd cells. In addition, religated viral DNA of PCV1 and PCV2 has been used to transfect adherent human cell lines.”

The World Health Organization began recommending in 2009 that all Nations include this vaccination in their immunization program. Based on research during a clinical trial in which GlaxoSmithKline surprisingly enough participated in the funding.

******

Flu Shots:

A Global Research article dated August 28, 2009, Early and current Fears About Vaccine Dangers lists the ingredients found in most flu shots:

Flu shots contain 25 micrograms of mercury. One microgram is considered toxic. By age two, most US children have received around 237 micrograms of mercury through vaccines alone. Excerpted:

“Vaccines contain the following toxic and others substances:

– thimerosal (mercury);

– aluminum hydroxide and phosphate;

–ammonium sulfate;

– amphotericin B,

– animal tissues and fluids, including horse blood, rabbit brain, dog kidney, monkey kidney, chick embryo, chicken egg, duck egg, pig blood, and porcine (pig) protein/tissue;

– calf serum and fetal bovine serum;

– betapropiolactone;

– macerated cancer cells;

– formaldehyde;

– formalin;

– synthetic phenol;

– gelatin and hydrolyzed gelatin;

– glycerol;

– human diploid cells (from aborted human fetal tissue);

– MSG;

– the anti-biotics neomycin and neomycin sulfate;

– phenol red indicator disinfectant dye;

– phenoxyethanol (antifreeze);

– potassium monophosphate;

– polymyxin B;

– polysorbate 20 and 80;

– residual MRC5 proteins;

– sorbitol;

– sucrose;

– tri(n)butylphosphate;

– VERO cells, a continuous line of monkey kidney cells linked to the SV-40 virus known to cause leukemia; and

– washed sheep red blood cells.

One or a combinations of theses substances can play havoc with the human immune and neurological systems and cause deadly autoimmune and other diseases.”

+++++++

Plus you get a great big dose of the flu strain they are attempting to spread.

An attenuated (weakened) virus strain is used to infect the host with a reduced form of the disease or infection and this is supposed to prevent us from getting the full blown infection or disease.  I cannot reconcile being intentionally infected with a disease, with eradication of the disease, especially when you consider all the additional chemical, biological and tissue additives in each shot.  And even less understandable is the use of common table sugar, msg and antifreeze among many other things.  I can only conclude the only thing they are trying to kill off with these toxic injections is….us.

AIDS, SARS and other intended pandemics

The AIDs virus which has long been believed to have been lab created, is another of those pandemics meant to sweep the globe and reduce the global population. HR 15090 that became Public Law 91-213 established the intent of our own government to produce a genocidal virus.  $10 million was paid to MERCK to develop the virus in the early 50′s, which is a recombinant DNA virus using mycoplasma (a six-sided synthetic biological agent) and inserting it through a process called “viral insertion” into a selected “candidate human virus”.  The result is a new virus.  The intent was to create a virus for which the human body had no natural defenses.  During this time George W. Merck was the American Biological Weapons Industry Director and head of the Office of special Viruses.  The new virus was introduced into the worlds populations via vaccination.

Viral insertion has been used to create HIV/AIDS, and also SARS among other diseases.  During the 50′s also, Merck tested the SV40 vaccine on the Russians.  SV40 is a cancer producing virus.  The vaccine produced and used to supposedly treat Yellow Fever, contained a virus that produced leukemia. And now 60 labs have confirmed that many cancers appearing now are linked directly to the polio vaccines given during childhood.  But we still give polio vaccines.

Merck, the manufacturer of Gardasil, a vaccine they claim prevents cervical cancer, seems more to be about sterilizing young girls, if the vaccine doesn’t kill or permanently injure them first.  Every attempt has been made by state and federal governments to make this deadly vaccine mandatory.

Thousands of young girls are subjected to the Gardasil vaccine each year and suffer immediate adverse reactions to the first shot.  Now they are infecting young boys and men with this deadly vaccine, and several deaths have already resulted.

Here’s what we do know:

As the use of toxin riddled vaccines increased, so has the rate of autism; now one in every 110 children in those who have been vaccinated.  The rate of neurological disorders of all kinds is epidemic in children.

The increase in Alzheimers is now thought to be directly linked to early vaccines in the 60’s and 70’s, and an increase in this life robbing disease is anticipated with the constant admonishment to get vaccines of all kinds as we move through life.

The Gardasil vaccine is deadly but still being pushed as a safeguard against cervical cancer, anal warts, and whatever other excuse they can contrive to justify what is clearly a vaccine meant to sterilize.

The Rotarix vaccine that admittedly is a transfection which can cause spontaneous genetic mutations including mutations to cancer, is now recommended by the WHO and CDC for use around the world.

The flu vaccines have caused more deaths than the flu itself.

All of these vaccines and hundreds of others are administered to children and adults alike, all around the world all of which alter our DNA, mutate within our bodies and create life threatening diseases and side affects.

So how many have to die?  How many have to succumb to cancers later in life, caused by whatever is being injected into them now under the guise of preventing a childhood disease or in the case of Gardasil, supposedly to treat a non-threatening and short lived virus.

How many otherwise healthy infants will become autistic before this is stopped?  Ten years ago 1 in 220 children were autistic or suffering from mild to severe neurological damage after being vaccinated.  In 2005 the rate was 1-150 an increase that coincided with the increase in the number of vaccines given to infants and toddlers.  Its 2011, and now the rate is 1 in 110 children with autism or other neurological disorders; a dramatic increase that coincides with the 63 childhood vaccines now required before age five.

How much is enough?  How many of us have to end up with cancers, Alzheimers, strokes, heart disease or permanently injured children before this is stopped.  It is no longer acceptable to claim that vaccines are the answer in light of all the harm that is caused by them.  The idea behind vaccines might have been a good one, the implementation of vaccines and the obvious temptation to experiment with them…not so much.

___________________________________________________________

Congress funded over $550 million dollars for the development of HIV/AIDS, See, page 5, progress report #15, U.S. Special Virus program (1962 – 1978).

http://boydgraves.blogspot.com/2007/09/us-origin-of-hivaids-before-and-after-9.html

DEPARTMENT OF DEFENSE APPROPRIATIONS FOR 1970 : The funding of the Bio-terrorism AIDS virus HR 15090

HR 15090

http://www.scribd.com/doc/20272035/HB-15090

http://ppjg.wordpress.com/2010/03/25/are-glaxosmithkline-and-the-fda-lying-to-parents-about-the-rotarix-recall/

Vaccine Safety Manual

http://vacbook.com/vsm.htm

Early and current Fears About Vaccine Dangers

http://www.globalresearch.ca/index.php?context=va&aid=14937

http://en.wikipedia.org/wiki/Transfect

Cancer Linked to polio vaccine

http://articles.mercola.com/sites/articles/archive/2011/02/18/leading-vaccine-doctor-states-cancer-linked-to-polio-vaccine.aspx

 

 

Source: http://ppjg.wordpress.com/2011/04/08/the-emergence-of-vaccine-induced-diseases/

 

Categories: Health/Pharma

Expert calls for research into safety of anthrax vaccine in children


Nicole Lurie, the assistant secretary for preparedness and response at the U.S. Department of Health and Human Services, recently asked the National Biodefense Science Board to investigate the safety concerns of collecting data on the effects of the anthrax vaccine absorbed vaccine in children.

The U.S. government currently stockpiles AVA in order to potentially provide post-exposure care for at-risk populations in the case of an anthrax attack.

In a letter written to the chair of the NBSB, Dr. Patricia Quinlisk, and its members, Lurie said that recent national-level exercises highlighted the need to address particular questions regarding a lack of available data.

There is currently no safety, immunogenicity or efficacy data in pediatric and special populations that would allow the U.S. Food and Drug Administration to evaluate the drug for its utilization under an Emergency Use Authorization.

In the case of an emergency, adults could receive the countermeasures under the less stringent EUA status, while an investigational protocol would still need to be developed for its use in children and special populations. This would present an array of logistical, clinical and communication challenges during a public health crisis.

Lurie concedes that the simple solution is to gather the data in pediatric and special populations ahead of an urgent need, but acknowledges that there are legitimate concerns regarding the risk of testing AVA with no clear benefit at the time of conducting the study.

The NBSB has been asked for its recommendations on the best course of action to prepare for the use of AVA in a specifically pediatric population.

Lurie is primarily interested in the NBSB’s evaluation of the risks and benefits of conducting AVA safety studies in children before or after an emergency, to what extent there are ethical concerns regarding an attempt to gather enough data to permit the vaccine’s use under an Emergency Use Authorization, what planning needs to be in place to perform an investigational protocol after an attack and how the government should approach discussing the issue with parents and public health officials.

Categories: Health/Pharma

Scientists Create GM Corn Which Prevents Human Conception



Scientists have created the ultimate GM crop: contraceptive corn. Waiving fields of maize may one day save the world from overpopulation.

The pregnancy prevention plants are the handiwork of the San Diego biotechnology company Epicyte, where researchers have discovered a rare class of human antibodies that attack sperm.

By isolating the genes that regulate the manufacture of these antibodies, and by putting them in corn plants, the company has created tiny horticultural factories that make contraceptives.

“We have a hothouse filled with corn plants that make anti-sperm antibodies,” said Epicyte president Mitch Hein.

“We have also created corn plants that make antibodies against the herpes virus, so we should be able to make a plant-based jelly that not only prevents pregnancy but also blocks the spread of sexual disease.”

Contraceptive corn is based on research on the rare condition, immune infertility, in which a woman makes antibodies that attack sperm.

“Essentially, the antibodies are attracted to surface receptors on the sperm,” said Hein. “They latch on and make each sperm so heavy it cannot move forward. It just shakes about as if it was doing the lambada.”

Normally, biologists use bacteria to grow human proteins. However, Epicyte decided to use corn because plants have cellular structures that are much more like those of humans, making them easier to manipulate.

The company, which says it will not grow the maize near other crops, says it plans to launch clinical trials of the corn in a few months.

http://www.biotech-info.net/conception.html

 

Categories: Health/Pharma