Tag Archives: CDC

“ANTIGENS IN EUROPE,” bringing “high passage” G39/40 plus recombinant OspA from B31:Documentation

 

Both the Steere-in-Europe and the Dressler/Steere Dearborn reports are scanned in on this
page. See also Chapter 3 on What Steere Did to falsify the testing for Lyme…

The CDC’s old standard, performing serial Western Blots to look for changing and expanding IgM and IgG antibodies, was Steere’s old standard. This is the 1990 CDC standard criteria for Lyme. This all changed in 1994 at the CDC’s Dearborn Conference, where, actually no one has any idea why we still got stuck with Steere’s new bogus method, since no one agreed with Steere at the conference, as I told the FDA Vaccine Committee in Jan 2001 because no one agreed with the proposal among the attendees.

Steere’s original observations published in 1986 (diagnose Lyme as is if is Relapsing Fever):
http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=423723&blobtype=pdf

Steere said OspA and B were prominent antibody bands, originally, but later he said they weren’t.
How did that happen?

Steere illegally used high-passage strains since Yale, Imugen and L2 Diagnostics wanted a monopoly on vaccines and testing and recombinant OspA and B without the lipid attached (no lipid = no antibodies):

No one is allowed to have “Lyme disease,” unless they have the genes for the arthritis or inflammatory presentation, due to the scientific fraud committed by Yale and Allen Steere. 

How did Allen Steere end up leaving OspA and B out of the CDC’s diagnostic standard?
He used a high-passage strain of borrelia that he knew would have dropped the OspA and B plasmid- which is a crime. 
Steere originally said “Lyme disease is a genetically linked condition of a high antibody response to OspA !!!”  And then suddenly OspA and B are left out of the CDC’s standard testing for Lyme???

“ANTIGENS IN EUROPE,” bringing “high passage” G39/40 plus recombinant OspA from B31:

This is the CDC’s Dearborn method:

http://www.cdc.gov/mmwR/preview/mmwrhtml/00038469.htm

Notice there is no band 31 (OspA) or 34 (OspB)

After saying Lyme was a condition of a high antibody response to OspA and B, Steere deliberately invented a standard where OspA and B were not present as diagnostic antigens so Yale could pass off a bogus Lyme vaccine and also have a monopoly on all the national testing for Lyme, by being the only labs (Imugen and L2 Diagnostics) licensed to use Dave Persing’s test with the Borrelia burgdorferi bug that had dropped the OspA-B plasmid.

That was the scientific fraud and RICO part of the scientific fraud and racketeering in Lyme disease.  That was the monopoly on testing.  It all happened as a result of Steere fraudulently using high-passage strains of borrelia to determine that OspA and B should be left out of the standard testing for Lyme- yet OspA is the vaccine?

The following is the CDC’s IgG method developed by Steere in Germany with Frank Dressler (and you cannot obtain this online):

Here is the bogus part about high concentration (ROC area) equaling greater accuracy.  It does not.  This is where Steere claims that high antibody concentration associated with Lyme arthritis is a validation of the method, when we know the specificity of each antibody is the accuracy of the test in a human.  If a person has OspA antibody, they have a 100% chance of having Lyme, and the goal in Methods Development and Validations is to validate a method that detects the LOWEST concentration of something, reliably.

These idiots say this Lyme test is “sensitive” when obviously is does not detect LOW concentrations of antibody, if the area of the darkened (absorbance) means MORE AREA EQUALS MORE (higher) CONCENTRATION OF ANTIBODY.  This Dressler/Steere article is the exact opposite of the truth!  This is a bogus validation and “a bogus article.”


The following is from the Congressional Record on Dual-Use Bioweapons exported to Iraq

 

Source

The following is from the Congressional Record on Dual-Use Bioweapons exported to Iraq:

Click to access US_SELLS_IRAQ_BIOWEAPONS.pdf

“Lyme” and OspA were time bombs or Trojan horses that detonate Epstein-Barr/similars and tolerize to fungal infections in the blood resulting in chronic fatigue.

Exposure to borrelial antigens (blebbing) turns off the antibody response, meaning “Lyme” could not possibly be an “autoimmune disease” – it’s the reverse. It belongs in the cancer and AIDS class.

Did someone day “Lyme Disease” wasn’t an accidental release from Plum Island?

1) Firstly, there is no such thing as “Lyme Disease” it’s just Relapsing Fever and officially serologically so in 1990:

Uncoordinated phylogeography of Borrelia burgdorferi and its tick vector, Ixodes scapularis.
Humphrey PT, Caporale DA, Brisson D.
Source

Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Abstract

Vector-borne microbes necessarily co-occur with their hosts and vectors, but the degree to which they share common evolutionary or biogeographic histories remains unexplored. We examine the congruity of the evolutionary and biogeographic histories of the bacterium and vector of the Lyme disease system, the most prevalent vector-borne disease in North America. In the eastern and midwestern US, Ixodes scapularis ticks are the primary vectors of Borrelia burgdorferi, the bacterium that causes Lyme disease. Our phylogeographic and demographic analyses of the 16S mitochondrial rDNA suggest that northern I. scapularis populations originated from very few migrants from the southeastern US that expanded rapidly in the Northeast and subsequently in the Midwest after the recession of the Pleistocene ice sheets. Despite this historical gene flow, current tick migration is restricted even between proximal sites within regions. In contrast, B. burgdorferi suffers no barriers to gene flow within the northeastern and midwestern regions but shows clear interregional migration barriers. Despite the intimate association of B. burgdorferi and I. scapularis, the population structure, evolutionary history, and historical biogeography of the pathogen are all contrary to its arthropod vector. In the case of Lyme disease, movements of infected vertebrate hosts may play a larger role in the contemporary expansion and homogenization of the pathogen than the movement of tick vectors whose populations continue to bear the historical signature of climate-induced range shifts.

© 2010 The Author(s). Journal compilation © 2010 The Society for the Study of Evolution.

2) We have scientific evidence that “Lyme” did not naturally evolve
UNCOORDINATED PHYLOGEOGRAPHY OF BORRELIA BURGDORFERI AND ITS TICK
VECTOR, IXODES SCAPULARIS:

Evolution of a focus of Lyme disease.
Schulze TL, Shisler JK, Bosler EM, Lakat MF, Parkin WE.
Abstract

Epidemiological investigations were initiated in 1984 when significant Lyme disease activity was observed within a 5-km radius of an area previously used as a non-endemic control site for Lyme disease research in New Jersey. Through 1983, collections of Ixodes dammini from vegetation and feral rodents were infrequent and no human cases were identified within a 16-km radius of the control site. In 1984, 4 human cases and 3 serologically reactive canines (greater than or equal to 1:512) were recognized within the area and adult I. dammini populations were over 3-fold greater than those at our primary study location where Lyme disease has been endemic since 1981. Using darkfield microscopy, 53.4% of adult I. dammini were infected with Borrelia burgdorferi as compared to 50.0% of adults collected during the same period at the known endemic study site. These data indicate that a focus of Lyme disease has recently become established at the previously non-endemic control site and that the establishment of new foci may occur more rapidly than once thought.
“Despite the intimate association of B. burgdorferi and I. scapularis, the population structure, evolutionary history, and historical biogeography of the pathogen are all contrary to its arthropod vector.”

3) We have scientific evidence that the original outbreak area was indeed the area of Plum Island/Lyme

4) They happen to perform that kind of vector-pathogen competence studies on Plum Island (Durland Fish)

5) Govt Goons tried to silence Willy Burgdorfer (who was recruited from Switzerland in the first place to work at the NIH Rocky Mountains Bioweapons lab specifically because he was an expert in spirochetes)

6) No one from the NIH, CDC, Yale or IDSA will answer the question as to what OspA is and they threatened me with jail (again) if I persisted in reporting to Francis Collins that no one to whom I was referred by Collins’ office (Fauci and NIAID) could tell me what OspA was

because if anyone ever told us what OspA was, they would have to admit it could never have been a vaccine and was therefore falsely qualified (they would have to admit the Dearborn criteria was fraud). And to date, no one at MIT or Stanford or Princeton or Duke or any of the other formerly respected institutions of higher learning can tell you what OspA is either. (Because why? This is an IQ test: Why won’t anyone from mit.edu or berkeley.edu or stanford.edu etcetera et al report the truth about Lyme as Relapsing Fever or what OspA is/does?)

7) The “science” of “Lyme” is about attacking the victims and calling them crazy and this has been the case since 1990 when the ALDF.com a commercial entity supported by the likes of Mort Zuckerman (CFR) and the AIG Greenbergs (CFR) was founded at New York Medical College (http://www.actionlyme.org/CONNOLLY_FISH_WEINSTEIN.htm)
Ever since the imaginary vaccine trials, the only other so-called study performed by these crooks was Klempner’s bogus long term retreatment study of people 2/3 of whom never were treated according to the protocol before, and half of whom tested positive to the Dearborn protocol when no one knows what Dearborn means. The testing schema was research fraud committed by CDC officer/draft dodger Allen Steere alone in Europe.

None of the participants invited to the Dearborn conference in 1994 agreed with Allen Steere’s proposal:

8) The CDC deliberately falsified their mycoplasma/Chronic Fatigue Syndrome study by throwing out the red blood cells, to which the mycoplasma adhere, resulting in fatigue without the anemia:

1992; [The effect of Eperythrozoon suis infection on the osmotic fragility of erythrocytes]

Osmotic fragility of erythrocytes was tested in weaned pigs experimentally infected with Eperythrozoon (E.) suis. Acute eperythrozoonosis of splenectomized pigs led to an increase of osmotic fragility. It is supposed that E. suis infection causes a structural change in erythrocyte membrane. Possible mechanisms of this cell membrane injury are discussed.

And you can see more images of mycoplasma adhering to erythrocytes here:
http://www.actionlyme.org/PAM3CYS_IMMUNE_SUPPRESSION.htm
http://www.actionlyme.org/BIOMARKERS2.htm

The process by which people become tolerized to mycoplasma (bearing TLR2-agonists) is due to the chronic exposure of persons with Lyme Relapsing Fever to shed antigen (blebbing) as demonstrated by UConn’s Justin Radolf, here:
http://www.actionlyme.org/PIIB.htm
Blebbing, by Alan Barbour
http://www.actionlyme.org/BARBOURS_STEALTH_BOMBERS.htm

9) Durland Fish admitted he writes “bogus articles” when planning to stalk, wiretap, and harass Karen Forschner of the Lyme Disease Foundation

10) IDSA fellas have referenced the “cysts are vi

 


Big Pharma Vaccines: Brain Damaged Children

 

SOURCE

 

Why don’t we know why Tb is so hard to treat and why is there no vaccine for it?

Because MYCObacteria tuberculosis is a fungal type infection, bearing the same antigens as LYMErix (TLR2 agonists), which did not prevent Lyme, but gave people an immuno suppression – like AIDS – outcome, just like Lyme.

Yale and UConn lied about the definition of Lyme and they lied about the outcome of LYMErix. (And now they have been defunded by the NIH.)

See more about how Yale and UConn lost all their funding, but the university that employs the man who discovered all mechanisms/outcomes of Lyme and LYMErix (arthritis to enhancing opportunistics like Epstein-Barr and CMV) was given a 65 million dollar grant to “translate” this research,… further down on this homepage.

We’d like to thank the Wall Street Journal for bringing this fiasco to the world’s attention.

Why don’t we know why infections like MRSA, Tb, and Lyme are so tough to treat?

What are the mechanisms of the reactivation of latent viruses?

Why is there no HIV, Tuberculosis or “Lyme” (real name, Relapsing Fever) vaccine?

Why did all the vaccines for these – Tb, Lyme, and HIV – all fail?

What happens to the immune system with chronic exposure to fungal antigens like the chronic shedding of Osps by Borreliae (known as blebs) in their typical Relapsing Fever-like mechanisms of relapse?

Why did all those vaccines end up to be the same thing and no one knew they all were the same thing and especially that they all failed in the same way?

[Because Yale and UConn lied about the outcome of LYMErix and the definition of Lyme to the FDA in 1994 and again in 1998. And they are lying still.]

But why does everyone at the CDC, NIH, Yale and IDSociety.org still say they don’t know what OspA is?

Maybe they refuse to admit what OspA is because that info betrays the mechanisms of vaccines-induced brain damage.

The reasons there are no Lyme, HIV, and TB fungal “vaccines” are the same reasons childhood immunizations fail and end up giving children the very viruses the vaccines were intended to prevent.

The CDC staff has recently been detected going around to the colleges recruiting from the chemistry and biochemistry undergraduates.

It’s too late. Because of this crime, USA has no competitive technoglobal edge. The whole world looks at this crime. Brazilian scientists flat out make fun of Americans and “Lyme Disease.”

The Tuberculosis global fiasco is a headline article in the Wall Street Journal – not a rag usually associated with moral issues. Clue. USA lost its technoglobal edge. American biotech and Pharma companies are sucking global wind.

THE FOLLOWING IS A LETTER OF COMPLAINT ABOUT THE INCOMPETENCE OF IDSA AND THE NIH, (See more at 101016.htm, or the Immunology of Epstein-OspA-Borreliosis).

This is evidence that it is known why children acquire the brain damage we call Autism and the mechanisms by which that damage occurs is similar to Lyme- and LYMErix-Disease:

To: sr393d@nih.gov, francis.collins@nih.gov, AllenM1@mail.nih.gov, zach_dann@blumenthal.senate.gov, francis.collins@nih.gov, ras8@cdc.gov, olib@od.nih.gov, afauci@niaid.nih.gov, joseph.breen@nih.gov, michael.greenwood@yale.edu, richard.horton@lancet.com, astrid.james@lancet.com, m.zecevic@lancet.com, ideditorial@lancet.com, Lawrence.Tabak@nih.gov, pgauwaerter@gmail.com
Cc: spinlyme@yahoogroups.com

Subject: A 5-points rule on fungal vaccines and brain-damaged children (failed TB and Lyme fungal vaccines notwithstanding)
Date: May 1, 2012 6:00 AM

Greetings,

I would like to propose a rule on fungal antigens and vaccines
which is related to the OspA outcomes:

1) “Finally, there is the risk that the virus may not be fully or completely inactivated or attenuated and thus, the vaccine may actually cause disease.”
http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=7%2C632%2C510.PN.&OS=PN%2F7%2C632%2C510&RS=PN%2F7%2C632%2C510

2) Measles, Mumps, and Rubella — Vaccine Use and Strategies for Elimination of Measles, Rubella, and Congenital Rubella Syndrome and Control of Mumps: Recommendations of the Advisory Committee on Immunization Practices (ACIP)
http://www.cdc.gov/mmwr/preview/mmwrhtml/00053391.htm

“Updated information on adverse events and contraindications, particularly for persons with severe HIV infection, persons with a history of egg allergy or gelatin allergy, persons with a history of thrombocytopenia, and persons receiving steroid therapy [are immunosuppressed- KMD].”

3) CDC: Human Exposure to Brucella abortus Strain RB51 — Kansas, 1997
http://www.cdc.gov/mmwr/preview/mmwrhtml/00051495.htm

An ^^^ immunosuppressed pregnant cow was given a Brucella (LYMErix-like) “live attenuated” vaccine and the baby cow ended up with the disease, which then was transferred to the humans handling the cow and her dead baby. This parallels what is happening to children who are vaccinated while immunosuppressed, or who receive mycoplasmally (LYMErix-like) contaminated vaccines.

4) in the case of pandemic MRSA, as we have seen, the vaccine didn’t work because TLR2 agonists (lipoproteins) suppress the immune system. We also learned from the MRSA vaccine patent, that:

“Several established vaccines consist of live attenuated organisms where ***the risk of reversion to the virulent wild-type strain exists. In particular in immunocompromised hosts this can be a live threatening scenario.*** Alternatively, vaccines are administered as a combination of pathogen-derived antigens together with compounds that induce or enhance immune responses against these antigens (these compounds are commonly termed adjuvant), since these subunit vaccines on their own are generally not effective.”
http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=7,771,728.PN.&OS=PN/7,771,728&RS=PN/7,771,728

5) The effect of exogenous corticosterone on West Nile virus infection in Northern Cardinals (Cardinalis cardinalis) http://7thspace.com/headlines/410671/the_effect_of_exogenous_corticosterone_on_west_nile_virus_…

Do not ^^ cause immunosuppression/stress as
it causes increased mortality from existing
infections and especially do not cause stress to
humans by treating them to *ABUSE* instead
of medicine when they don’t the special “controversial”
disease that fits the commercial (unknown) vaccine model:
http://www.ncbi.nlm.nih.gov/pubmed/20466055

Because ^^ that – the abuse – activates Epstein-Barr.

———————————

RULE: Don’t give immunosuppressed mammals live attenuated vaccines, and especially don’t give them vaccines that contain fungal or mycoplasmal antigens like LYMErix or OspA.

What do you say? Do you like that rule?
Especially if we added the OspA/MS/Roland Martin
“Immunosuppression>> MS Outcome of Lyme” data
to that data set?

What about if we added the 1918 Spanish
Flu data to the rule: “People with strong
(Steere-HLA-like, Dearborn definition-like)
immune responses are likelier to choke to death
on the pneumonia (fungal) that follows the influenza,
whereas immunosuppressed people won’t produce a
hyperinflammatory response and thereby survive the
pandemic.”

We haven’t had any new Rules in a while.

All we ever hear is that “Lyme causes nothing”
and “no disease outcomes happen from Lyme”
and “nothing causes anything” and “Lyme victims
are looney” and “Lyme victims have paranoid
delusional wannabee diseases” and the latest:
“Lyme victims are terrorists !!!”:
http://www.ncbi.nlm.nih.gov/pubmed/21867956

“But get the mysterious unknown OspA vaccine.”

– – – – – – –

??

What do you think?

How about that for a rule?

You might have to find out what OspA is, first.

No hurry. It was ordered removed by the FDA
in Feb, 2002 for producing “chronic Lyme-like”
illness (clue).

And that was the last time Uncle Sam said
anything *TRUE* about “Lyme Disease.”

10 years….

Kathleen M. Dickson
former Pfizer Analytical Methods Development
and VALIDATION chemist

 


VACCINE-AUTISM link suppressed by Big Pharma, FDA, CDC – From LoadsOf RedPills

 

FROM LOADS OF RED PILLS. Please Visit The Original Blog
I recently posted an article about how 52 officials from FDA, CDC, WHO and big pharma experts met in secret to hide the results of a dramatic study exposing that since 1991, the estimated number of CASES OF AUTISM HAD INCREASED FIFTEEN-FOLD, from one in every 2,500 children to one in 166 children DUE TO MERCURY IN THE VACCINES. They couldn’t care less about hurting your kids, and worked together to suppress the article exposing them, so I am reposting it here in full.

Please read this article, it is APPALLING, they are just a big mafia, and send it to as many people as you can.

I gave this link towards the article on Rolling Stones, but it has ‘mysteriously disappeared’ without a trace. They have been caught red-handed because I usually save those articles on my disk, fully aware of their tactics. So, here is a copy of the full article, with my comments in brackets. They can try to delete this post behind my back, I will repost it again and again, because I also back-up my posts.

Read the following article and learn how they couldn’t care less about human life, but only big pharma profits. FDA, CDC have been working together for a century to increase big pharma profits.

PARENTS, you MUST read this to understand what they are up to! They work for big pharma, not you. Your kids are their property. They want to turn them into their lifelong customers. You are there to raise and feed them, and pay for their drugs until they are able to do it themselves. Go ahead, read the article, and prove me wrong.

The article starts here …

Deadly Immunity / Rolling stones

Robert F. Kennedy Jr. investigates the government cover-up of a mercury/autism scandal

ROBERT F. KENNEDY JR. Posted Jun 20, 2005 12:00 AM

In June 2000, a group of top government scientists and health officials gathered for a meeting at the isolated Simpsonwood conference center in Norcross, Georgia. Convened by the Centers for Disease Control and Prevention, the meeting was held at this Methodist retreat center, nestled in wooded farmland next to the Chattahoochee River, to ensure complete secrecy. The agency had issued no public announcement of the session — only private invitations to fifty-two attendees. There were high-level officials from the CDC and the Food and Drug Administration, the top vaccine specialist from the World Health Organization in Geneva and representatives of every major vaccine manufacturer, including GlaxoSmithKline, Merck, Wyeth and Aventis Pasteur. All of the scientific data under discussion, CDC officials repeatedly reminded the participants, was strictly “embargoed.” There would be no making photocopies of documents, no taking papers with them when they left [that’s how those who you ‘trust’ to protect you conspire against you].

The federal officials and industry representatives had assembled to discuss a disturbing new study that raised alarming questions about the safety of a host of common childhood vaccines administered to infants and young children. According to a CDC epidemiologist named Tom Verstraeten, who had analyzed the agency’s massive database containing the medical records of 100,000 children, a mercury-based preservative in the vaccines — thimerosal — appeared to be responsible for a dramatic increase in autism and a host of other neurological disorders among children. “I was actually stunned by what I saw,” Verstraeten told those assembled at Simpsonwood, citing the staggering number of earlier studies that indicate a link between thimerosal and speech delays, attention-deficit disorder, hyperactivity and autism. Since 1991, when the CDC and the FDA had recommended that three additional vaccines laced with the preservative be given to extremely young infants — in one case, within hours of birth — the estimated number of cases of autism had increased fifteen-fold, from one in every 2,500 children to one in 166 children.

Even for scientists and doctors accustomed to confronting issues of life and death, the findings were frightening. “You can play with this all you want,” Dr. Bill Weil, a consultant for the American Academy of Pediatrics, told the group. The results “are statistically significant.” Dr. Richard Johnston, an immunologist and pediatrician from the University of Colorado whose grandson had been born early on the morning of the meeting’s first day, was even more alarmed. “My gut feeling?” he said. “Forgive this personal comment — I do not want my grandson to get a thimerosal-containing vaccine until we know better what is going on” [oh yeah, but please do not warn the other parents, they deserve to see their kid turned into a vegetable because of your actions].

But instead of taking immediate steps to alert the public and rid the vaccine supply of thimerosal, the officials and executives at Simpsonwood spent most of the next two days discussing how to cover up the damaging data. According to transcripts obtained under the Freedom of Information Act, many at the meeting were concerned about how the damaging revelations about thimerosal would affect the vaccine industry’s bottom line. “We are in a bad position from the standpoint of defending any lawsuits,” said Dr. Robert Brent, a pediatrician at the Alfred I. duPont Hospital for Children in Delaware. “This will be a resource to our very busy plaintiff attorneys in this country.” Dr. Bob Chen, head of vaccine safety for the CDC, expressed relief that “given the sensitivity of the information, we have been able to keep it out of the hands of, let’s say, less responsible hands.” Dr. John Clements, vaccines advisor at the World Health Organization, declared that “perhaps this study should not have been done at all.” [this tells all you need to know about the criminality of the WHO, whose sole purpose is to expand big pharma profits and reduce the population by harming kids as much as they can]. He added that “the research results have to be handled,” [sir, research results are PUBLISHED, that’s how science moves forward, you are a criminal] warning that the study “will be taken by others and will be used in other ways beyond the control of this group.”

In fact, the government has proved to be far more adept at handling the damage than at protecting children’s health. The CDC paid the Institute of Medicine to conduct a new study to whitewash the risks of thimerosal, ordering researchers to “rule out” the chemical’s link to autism [that’s how big pharma does science these days, they order people to come up with the results they want, it has nothing to do with safey or healing people]. It withheld Verstraeten’s findings, even though they had been slated for immediate publication, and told other scientists that his original data had been “lost” and could not be replicated. And to thwart the Freedom of Information Act, it handed its giant database of vaccine records over to a private company, declaring it off-limits to researchers. By the time Verstraeten finally published his study in 2003, he had gone to work for GlaxoSmithKline and reworked his data to bury the link between thimerosal and autism.

Vaccine manufacturers had already begun to phase thimerosal out of injections given to American infants — but they continued to sell off their mercury-based supplies of vaccines until last year. The CDC and FDA gave them a hand, buying up the tainted vaccines for export to developing countries and allowing drug companies to continue using the preservative in some American vaccines — including several pediatric flu shots as well as tetanus boosters routinely given to eleven-year-olds.

The drug companies are also getting help from powerful lawmakers in Washington. Senate Majority Leader Bill Frist, who has received $873,000 in contributions from the pharmaceutical industry, has been working to immunize vaccine makers from liability in 4,200 lawsuits that have been filed by the parents of injured children. On five separate occasions, Frist has tried to seal all of the government’s vaccine-related documents — including the Simpsonwood transcripts — and shield Eli Lilly, the developer of thimerosal, from subpoenas. In 2002, the day after Frist quietly slipped a rider known as the “Eli Lilly Protection Act” into a homeland security bill, the company contributed $10,000 to his campaign and bought 5,000 copies of his book on bioterrorism. The measure was repealed by Congress in 2003 — but earlier this year, Frist slipped another provision into an anti-terrorism bill that would deny compensation to children suffering from vaccine-related brain disorders. “The lawsuits are of such magnitude that they could put vaccine producers out of business and limit our capacity to deal with a biological attack by terrorists,” says Dean Rosen, health policy adviser to Frist [terrorism again, the perfect excuse to do anything they want under that banner…yeah, let’s be afraid of bearded cavemen !].

Even many conservatives are shocked by the government’s effort to cover up the dangers of thimerosal. Rep. Dan Burton, a Republican from Indiana, oversaw a three-year investigation of thimerosal after his grandson was diagnosed with autism. “Thimerosal used as a preservative in vaccines is directly related to the autism epidemic,” his House Government Reform Committee concluded in its final report. “This epidemic in all probability may have been prevented or curtailed had the FDA not been asleep at the switch regarding a lack of safety data regarding injected thimerosal, a known neurotoxin.” The FDA and other public-health agencies failed to act, the committee added, out of “institutional malfeasance for self protection” and “misplaced protectionism of the pharmaceutical industry.”

The story of how government health agencies colluded with Big Pharma to hide the risks of thimerosal from the public is a chilling case study of institutional arrogance, power and greed. I was drawn into the controversy only reluctantly. As an attorney and environmentalist who has spent years working on issues of mercury toxicity, I frequently met mothers of autistic children who were absolutely convinced that their kids had been injured by vaccines. Privately, I was skeptical.

I doubted that autism could be blamed on a single source, and I certainly understood the government’s need to reassure parents that vaccinations are safe; the eradication of deadly childhood diseases depends on it. I tended to agree with skeptics like Rep. Henry Waxman, a Democrat from California, who criticized his colleagues on the House Government Reform Committee for leaping to conclusions about autism and vaccinations. “Why should we scare people about immunization,” Waxman pointed out at one hearing, “until we know the facts?”

It was only after reading the Simpsonwood transcripts, studying the leading scientific research and talking with many of the nation’s pre-eminent authorities on mercury that I became convinced that the link between thimerosal and the epidemic of childhood neurological disorders is real. Five of my own children are members of the Thimerosal Generation — those born between 1989 and 2003 — who received heavy doses of mercury from vaccines. “The elementary grades are overwhelmed with children who have symptoms of neurological or immune-system damage,” Patti White, a school nurse, told the House Government Reform Committee in 1999. “Vaccines are supposed to be making us healthier; however, in twenty-five years of nursing I have never seen so many damaged, sick kids. Something very, very wrong is happening to our children.” [that’s good for big pharma, those will be lifelong customers]

More than 500,000 kids currently suffer from autism, and pediatricians diagnose more than 40,000 new cases every year. The disease was unknown until 1943, when it was identified and diagnosed among eleven children born in the months after thimerosal was first added to baby vaccines in 1931.

Some skeptics dispute that the rise in autism is caused by thimerosal-tainted vaccinations. They argue that the increase is a result of better diagnosis — a theory that seems questionable at best, given that most of the new cases of autism are clustered within a single generation of children. “If the epidemic is truly an artifact of poor diagnosis,” scoffs Dr. Boyd Haley, one of the world’s authorities on mercury toxicity, “then where are all the twenty-year-old autistics?” Other researchers point out that Americans are exposed to a greater cumulative “load” of mercury than ever before, from contaminated fish to dental fillings, and suggest that thimerosal in vaccines may be only part of a much larger problem. It’s a concern that certainly deserves far more attention than it has received — but it overlooks the fact that the mercury concentrations in vaccines dwarf other sources of exposure to our children.

What is most striking is the lengths to which many of the leading detectives have gone to ignore — and cover up — the evidence against thimerosal. From the very beginning, the scientific case against the mercury additive has been overwhelming. The preservative, which is used to stem fungi and bacterial growth in vaccines, contains ethylmercury, a potent neurotoxin. Truckloads of studies have shown that mercury tends to accumulate in the brains of primates and other animals after they are injected with vaccines — and that the developing brains of infants are particularly susceptible. In 1977, a Russian study found that adults exposed to much lower concentrations of ethylmercury than those given to American children still suffered brain damage years later. Russia banned thimerosal from children’s vaccines twenty years ago, and Denmark, Austria, Japan, Great Britain and all the Scandinavian countries have since followed suit.

“You couldn’t even construct a study that shows thimerosal is safe,” says Haley, who heads the chemistry department at the University of Kentucky. “It’s just too darn toxic. If you inject thimerosal into an animal, its brain will sicken. If you apply it to living tissue, the cells die. If you put it in a petri dish, the culture dies. Knowing these things, it would be shocking if one could inject it into an infant without causing damage.”

Internal documents reveal that Eli Lilly, which first developed thimerosal, knew from the start that its product could cause damage — and even death — in both animals and humans. In 1930, the company tested thimerosal by administering it to twenty-two patients with terminal meningitis, all of whom died within weeks of being injected — a fact Lilly didn’t bother to report in its study declaring thimerosal safe. In 1935, researchers at another vaccine manufacturer, Pittman-Moore, warned Lilly that its claims about thimerosal’s safety “did not check with ours.” Half the dogs Pittman injected with thimerosal-based vaccines became sick, leading researchers there to declare the preservative “unsatisfactory as a serum intended for use on dogs.”

In the decades that followed, the evidence against thimerosal continued to mount. During the Second World War, when the Department of Defense used the preservative in vaccines on soldiers, it required Lilly to label it “poison.” In 1967, a study in Applied Microbiology found that thimerosal killed mice when added to injected vaccines. Four years later, Lilly’s own studies discerned that thimerosal was “toxic to tissue cells” in concentrations as low as one part per million — 100 times weaker than the concentration in a typical vaccine. Even so, the company continued to promote thimerosal as “nontoxic” and also incorporated it into topical disinfectants. In 1977, ten babies at a Toronto hospital died when an antiseptic preserved with thimerosal was dabbed onto their umbilical cords.

In 1982, the FDA proposed a ban on over-the-counter products that contained thimerosal, and in 1991 the agency considered banning it from animal vaccines. But tragically, that same year, the CDC recommended that infants be injected with a series of mercury-laced vaccines. Newborns would be vaccinated for hepatitis B within twenty-four hours of birth, and two-month-old infants would be immunized for haemophilus influenzae B and diphtheria-tetanus-pertussis.

The drug industry knew the additional vaccines posed a danger. The same year that the CDC approved the new vaccines, Dr. Maurice Hilleman, one of the fathers of Merck’s vaccine programs, warned the company that six-month-olds who were administered the shots would suffer dangerous exposure to mercury. He recommended that thimerosal be discontinued, “especially when used on infants and children,” noting that the industry knew of nontoxic alternatives. “The best way to go,” he added, “is to switch to dispensing the actual vaccines without adding preservatives.”

For Merck and other drug companies, however, the obstacle was money. Thimerosal enables the pharmaceutical industry to package vaccines in vials that contain multiple doses, which require additional protection because they are more easily contaminated by multiple needle entries. The larger vials cost half as much to produce as smaller, single-dose vials, making it cheaper for international agencies to distribute them to impoverished regions at risk of epidemics. Faced with this “cost consideration,” Merck ignored Hilleman’s warnings, and government officials continued to push more and more thimerosal-based vaccines for children. Before 1989, American preschoolers received eleven vaccinations — for polio, diphtheria-tetanus-pertussis and measles-mumps-rubella. A decade later, thanks to federal recommendations, children were receiving a total of twenty-two immunizations by the time they reached first grade.

As the number of vaccines increased, the rate of autism among children exploded. During the 1990s, 40 million children were injected with thimerosal-based vaccines, receiving unprecedented levels of mercury during a period critical for brain development. Despite the well-documented dangers of thimerosal, it appears that no one bothered to add up the cumulative dose of mercury that children would receive from the mandated vaccines. “What took the FDA so long to do the calculations?” Peter Patriarca, director of viral products for the agency, asked in an e-mail to the CDC in 1999. “Why didn’t CDC and the advisory bodies do these calculations when they rapidly expanded the childhood immunization schedule?”

But by that time, the damage was done. At two months, when the infant brain is still at a critical stage of development, infants routinely received three inoculations that contained a total of 62.5 micrograms of ethylmercury — a level 99 times greater than the EPA’s limit for daily exposure to methylmercury, a related neurotoxin. Although the vaccine industry insists that ethylmercury poses little danger because it breaks down rapidly and is removed by the body, several studies — including one published in April by the National Institute of Health — suggest that ethylmercury is actually MORE toxic to developing brains and stays in the brain longer than methylmercury [in other words, they chose the most toxic of the two, and still brag about its inocuity].

Officials responsible for childhood immunizations insist that the additional vaccines were necessary to protect infants from disease and that thimerosal is still essential in developing nations, which, they often claim, cannot afford the single-dose vials that don’t require a preservative. Dr. Paul Offit, one of CDC’s top vaccine advisers, told me, “I think if we really have an influenza pandemic — and certainly we will in the next twenty years, because we always do — there’s no way on God’s earth that we immunize 280 million people with single-dose vials. There has to be multidose vials.”

But while public-health officials may have been well-intentioned, many of those on the CDC advisory committee who backed the additional vaccines had close ties to the industry. Dr. Sam Katz, the committee’s chair, was a paid consultant for most of the major vaccine makers and was part of a team that developed the measles vaccine and brought it to licensure in 1963. Dr. Neal Halsey, another committee member, worked as a researcher for the vaccine companies and received honoraria from Abbott Labs for his research on the hepatitis B vaccine.

Indeed, in the tight circle of scientists who work on vaccines, such conflicts of interest are common. Rep. Burton says that the CDC “routinely allows scientists with blatant conflicts of interest to serve on intellectual advisory committees that make recommendations on new vaccines,” even though they have “interests in the products and companies for which they are supposed to be providing unbiased oversight.” The House Government Reform Committee discovered that four of the eight CDC advisers who approved guidelines for a rotavirus vaccine “had financial ties to the pharmaceutical companies that were developing different versions of the vaccine.”

Offit, who shares a patent on one of the vaccines, acknowledged to me that he “would make money” if his vote eventually leads to a marketable product. But he dismissed my suggestion that a scientist’s direct financial stake in CDC approval might bias his judgment. “It provides no conflict for me,” he insists. “I have simply been informed by the process, not corrupted by it. When I sat around that table, my sole intent was trying to make recommendations that best benefited the children in this country. It’s offensive to say that physicians and public-health people are in the pocket of industry and thus are making decisions that they know are unsafe for children. It’s just not the way it works.”

Other vaccine scientists and regulators gave me similar assurances. Like Offit, they view themselves as enlightened guardians of children’s health, proud of their “partnerships” with pharmaceutical companies, immune to the seductions of personal profit, besieged by irrational activists whose anti-vaccine campaigns are endangering children’s health. They are often resentful of questioning. “Science,” says Offit, “is best left to scientists” [when you hide studies exposing the dangers of thimerosal, you are not a scientist anymore, but a freaking criminal who deserves life sentence. Offit goes as far as saying that vaccines are ‘so safe, that you could inject 1,000 into a kid].

Still, some government officials were alarmed by the apparent conflicts of interest [they faked to be alarmed because this has been going on for a century, and it is only getting worse]. In his e-mail to CDC administrators in 1999, Paul Patriarca of the FDA blasted federal regulators for failing to adequately scrutinize the danger posed by the added baby vaccines. “I’m not sure there will be an easy way out of the potential perception that the FDA, CDC and immunization-policy bodies may have been asleep at the switch re: thimerosal until now,” Patriarca wrote. The close ties between regulatory officials and the pharmaceutical industry, he added, “will also raise questions about various advisory bodies regarding aggressive recommendations for use” of thimerosal in child vaccines.

[what about making it unlawful to have ties to big pharma when you are in a committee for a start?]

If federal regulators and government scientists failed to grasp the potential risks of thimerosal over the years, no one could claim ignorance after the secret meeting at Simpsonwood. But rather than conduct more studies to test the link to autism and other forms of brain damage, the CDC placed politics over science [why do ‘more’ studies, only ONE study is enough when it exposes a danger]. The agency turned its database on childhood vaccines — which had been developed largely at taxpayer expense — over to a private agency, America’s Health Insurance Plans, ensuring that it could not be used for additional research [when people do things like that, it is a proof that what they are hiding is true, otherwise they wouldn’t bother – they are pure criminals]. It also instructed the Institute of Medicine, an advisory organization that is part of the National Academy of Sciences, to produce a study debunking the link between thimerosal and brain disorders. The CDC “wants us to declare, well, that these things are pretty safe” [as Offit said, it’s better to leave science to scientists … who are paid by big pharma]. Dr. Marie McCormick, who chaired the IOM’s Immunization Safety Review Committee, told her fellow researchers when they first met in January 2001. “We are not ever going to come down that [autism] is a true side effect” of thimerosal exposure. According to transcripts of the meeting, the committee’s chief staffer, Kathleen Stratton, predicted that the IOM would conclude that the evidence was “inadequate to accept or reject a causal relation” between thimerosal and autism. That, she added, was the result “Walt wants” — a reference to Dr. Walter Orenstein, director of the National Immunization Program for the CDC.

[See, this is a GIGANTIC error of logic because ONE study proving something is harmful destroys a trillion studies who can’t put the evidence to light, but they do it all the time, and the gullible public doesn’t see the trick.]

For those who had devoted their lives to promoting vaccination, the revelations about thimerosal threatened to undermine everything they had worked for [which means they had worked towards harming people, and they wanted it to keep it like that]. “We’ve got a dragon by the tail here,” said Dr. Michael Kaback, another committee member. “The more negative that [our] presentation is, the less likely people are to use vaccination, immunization — and we know what the results of that will be. We are kind of caught in a trap. How we work our way out of the trap, I think is the charge.”

Even in public, federal officials made it clear that their primary goal in studying thimerosal was to dispel doubts about vaccines [in science, we call that ‘bias’ and unscientific because you are not trying to find the truth, just to look away from it]. “Four current studies are taking place to rule out the proposed link between autism and thimerosal,” [in other words, they make studies ‘knowing’ the results in advance, which is only possible when you have decided to lie, it’s a show] Dr. Gordon Douglas, then-director of strategic planning for vaccine research at the National Institutes of Health, assured a Princeton University gathering in May 2001. “In order to undo the harmful effects of research claiming to link the [measles] vaccine to an elevated risk of autism [you cannot ‘undo’ the fact that mercury causes autism, they are just trying to confuse people with results from studies who search where there is nothing to find], we need to conduct and publicize additional studies to assure parents of safety” [no, you don’t, the study mentioned at the beginning of this article is the ‘black swan’ of vaccination, it’s game over for vaccine defenders because the link has been exposed]. Douglas formerly served as president of vaccinations for Merck, where he ignored warnings about thimerosal’s risks.

In May of last year, the Institute of Medicine issued its final report. Its conclusion: There is no proven link between autism and thimerosal in vaccines. Rather than reviewing the large body of literature describing the toxicity of thimerosal, the report relied on four disastrously flawed epidemiological studies examining European countries, where children received much smaller doses of thimerosal than American kids [as I said, by not looking on purpose where the danger is, you won’t find it, it is utterly non scientific]. It also cited a new version of the Verstraeten study, published in the journal Pediatrics, that had been reworked to reduce the link between thimerosal and autism [this is outright criminal … someone bring the electric chair]. The new study included children too young to have been diagnosed with autism and overlooked others who showed signs of the disease [no respect for humanity …]. The IOM declared the case closed and — in a startling position for a scientific body — recommended that no further research be conducted.

The report may have satisfied the CDC, but it convinced no one. Rep. David Weldon, a Republican physician from Florida who serves on the House Government Reform Committee, attacked the Institute of Medicine, saying it relied on a handful of studies that were “fatally flawed” by “poor design” and failed to represent “all the available scientific and medical research.” CDC officials are not interested in an honest search for the truth, Weldon told me, because “an association between vaccines and autism would force them to admit that their policies irreparably damaged thousands of children. Who would want to make that conclusion about themselves?” [well, true scientists for a start …]

Under pressure from Congress and parents, the Institute of Medicine convened another panel to address continuing concerns about the Vaccine Safety Datalink Data Sharing program. In February, the new panel, composed of different scientists, criticized the way the VSD had been used in the Verstraeten study, and urged the CDC to make its vaccine database available to the public.

So far, though, only two scientists have managed to gain access. Dr. Mark Geier, president of the Genetics Center of America, and his son, David, spent a year battling to obtain the medical records from the CDC. Since August 2002, when members of Congress pressured the agency to turn over the data, the Geiers have completed six studies that demonstrate a powerful correlation between thimerosal and neurological damage in children. One study, which compares the cumulative dose of mercury received by children born between 1981 and 1985 with those born between 1990 and 1996, found a “very significant relationship” between autism and vaccines. Another study of educational performance found that kids who received higher doses of thimerosal in vaccines were nearly three times as likely to be diagnosed with autism and more than three times as likely to suffer from speech disorders and mental retardation. Another soon-to-be published study shows that autism rates are in decline following the recent elimination of thimerosal from most vaccines.

As the federal government worked to prevent scientists from studying vaccines, others have stepped in to study the link to autism. In April, reporter Dan Olmsted of UPI undertook one of the more interesting studies himself. Searching for children who had not been exposed to mercury in vaccines — the kind of population that scientists typically use as a “control” in experiments — Olmsted scoured the Amish of Lancaster County, Pennsylvania, who refuse to immunize their infants. Given the national rate of autism, Olmsted calculated that there should be 130 autistics among the Amish. He found only four. One had been exposed to high levels of mercury from a power plant. The other three — including one child adopted from outside the Amish community — had received their vaccines.

At the state level, many officials have also conducted in-depth reviews of thimerosal. While the Institute of Medicine was busy whitewashing the risks, the Iowa legislature was carefully combing through all of the available scientific and biological data. “After three years of review, I became convinced there was sufficient credible research to show a link between mercury and the increased incidences in autism,” says state Sen. Ken Veenstra, a Republican who oversaw the investigation. “The fact that Iowa’s 700 percent increase in autism began in the 1990s, right after more and more vaccines were added to the children’s vaccine schedules, is solid evidence alone.” Last year, Iowa became the first state to ban mercury in vaccines, followed by California. Similar bans are now under consideration in thirty-two other states.

But instead of following suit, the FDA continues to allow manufacturers to include thimerosal in scores of over-the-counter medications as well as steroids and injected collagen. Even more alarming, the government continues to ship vaccines preserved with thimerosal to developing countries — some of which are now experiencing a sudden explosion in autism rates. In China, where the disease was virtually unknown prior to the introduction of thimerosal by U.S. drug manufacturers in 1999, news reports indicate that there are now more than 1.8 million autistics. Although reliable numbers are hard to come by, autistic disorders also appear to be soaring in India, Argentina, Nicaragua and other developing countries that are now using thimerosal-laced vaccines. The World Health Organization [another criminal organization started by Rockefeller] continues to insist thimerosal is safe, but it promises to keep the possibility that it is linked to neurological disorders “under review” [yeah, and in the meantime, let’s keep using African and developing nations as lab rats and also keep their depopulation agenda on track].

I devoted time to study this issue because I believe that this is a moral crisis that must be addressed. If, as the evidence suggests, our public-health authorities knowingly allowed the pharmaceutical industry to poison an entire generation of American children, [ON PURPOSE = ELECTRIC CHAIR] their actions arguably constitute one of the biggest scandals in the annals of American medicine. “The CDC is guilty of incompetence and gross negligence,” says Mark Blaxill, vice president of Safe Minds, a nonprofit organization concerned about the role of mercury in medicines. “The damage caused by vaccine exposure is massive. It’s bigger than asbestos, bigger than tobacco, bigger than anything you’ve ever seen.”

It’s hard to calculate the damage to our country — and to the international efforts to eradicate epidemic diseases — if Third World nations come to believe that America’s most heralded foreign-aid initiative is poisoning their children. It’s not difficult to predict how this scenario will be interpreted by America’s enemies abroad. The scientists and researchers — many of them sincere, even idealistic — who are participating in efforts to hide the science on thimerosal claim that they are trying to advance the lofty goal of protecting children in developing nations from disease pandemics [who wants a protection like that]. They are badly misguided. Their failure to come clean on thimerosal will come back horribly to haunt our country and the world’s poorest populations.

NOTE: This story has been updated to correct several inaccuracies in the original, published version. As originally reported, American preschoolers received only three vaccinations before 1989, but the article failed to note that they were innoculated a total of eleven times with those vaccines, including boosters. The article also mis-stated the level of ethylmercury received by infants injected with all their shots by the age of six months. It was 187 micrograms – an amount forty percent, not 187 times, greater than the EPA’s limit for daily exposure to methylmercury [oh yeah, I am feeling better for those kids now, because you know you can trust that daily exposure limit after all we have seen, you can be confident it has been developed with the kids interest in mind]. Finally, because of an editing error, the article mis-stated the contents of the rotavirus vaccine approved by the CDC. It did not contain thimerosal. Salon and Rolling Stone regret the errors.

[you can feel the hand here of big pharma criminal lawyers who would protect any misdemeanor and crime to make money – shame on them – they are probably responsible for the disappearance of this article from the website]

An earlier version of this story stated that the Institute of Medicine convened a second panel to review the work of the Immunization Safety Review Committee that had found no evidence of a link between thimerosal and autism. In fact, the IOM convened the second panel to address continuing concerns about the Vaccine Safety Datalink Data Sharing program, including those raised by critics of the IOM’s earlier work. But the panel was not charged with reviewing the committee’s findings. The story also inadvertently omitted a word and transposed two sentences in a quote by Dr. John Clements, and incorrectly stated that Dr. Sam Katz held a patent with Merck on the measles vaccine. In fact, Dr. Katz was part of a team that developed the vaccine and brought it to licensure, but he never held the patent. Salon and Rolling Stone regret the errors.

CLARIFICATION: After publication of this story, Salon and Rolling Stone corrected an error that mis-stated the level of ethylmercury received by infants injected with all their shots by the age of six months. It was 187 micrograms, an amount forty percent, not 187 times, greater than the EPA’s limit for daily exposure to methylmercury. At the time of the correction, we were aware that the comparison itself was flawed, but as journalists we considered it more appropriate to state the correct figure rather than replace it with another number entirely.

Since that earlier correction, however, it has become clear from responses to the article that the forty-percent number, while accurate, is misleading. It measures the total mercury load an infant received from vaccines during the first six months, calculates the daily average received based on average body weight, and then compares that number to the EPA daily limit. But infants did not receive the vaccines as a ?daily average? ? they received massive doses on a single day, through multiple shots. As the story states, these single-day doses exceeded the EPA limit by as much as 99 times. Based on the misunderstanding, and to avoid further confusion, we have amended the story to eliminate the forty-percent figure.

Correction: The story misattributed a quote to Andy Olson, former legislative counsel to Senator Bill Frist. The comment was made by Dean Rosen, health policy adviser to the senator. Rolling Stone and Salon.com regret the error.Loads Of Red Pills


Vaccines' Genocide

 

Are Vaccines Causing More Disease Than They are Curing?

By Alan Cantwell Jr., M.D.

Vaccines help keep us safe from infectious diseases. Smallpox and polio epidemics have been wiped out by mass vaccine programs. People rush to get flu shots every autumn, and kids are bombarded with a barrage of 22 required vaccinations before the age of six. Even pets need their shots. The manufacture of vaccines is a giant industry and what you pay for – inoculations and doctor visits – is big business for pediatricians, family practitioners and veterinarians. So why are more and more people worried about vaccines, especially the ones for kids?

Vaccine-induced Illness

Barbara Loe Fisher, president of the National Vaccine Information Centre, a consumer’s group based in Virginia, USA, claims vaccines are responsible for the increasing numbers of children and adults who suffer from immune system and neurologic disorders, hyperactivity, learning disabilities, asthma, chronic fatigue syndrome, lupus, rheumatoid arthritis, multiple sclerosis, and seizure disorders. She calls for studies to monitor the long-term effects of mass vaccination and Fisher wants physicians to be absolutely sure these vaccines are safe and not harming people.

No one can deny the dangers of vaccines. The measles, mumps, rubella (German measles) and polio vaccines, all contain live but weakened viruses. Although health officials tell you that polio has been wiped out in the US since 1979, they often fail to mention that all recorded cases of polio since that time are actually caused by the polio vaccine.

Vaccine investigator Neil Z. Miller questions whether we still need the polio vaccine when it causes every new case of polio in the USA. Before mass vaccinations programs began fifty years ago, Miller insists we didn’t have cancer in epidemic numbers, that autoimmune ailments were barely known, and childhood autism did not exist.

Vaccine Contamination

There is also the problem of contamination that has always plagued vaccine makers. During World War II a yellow fever vaccine manufactured with human blood serum was unknowingly contaminated with hepatitis virus and given to the military. As a result, more than 50,000 cases of serum hepatitis broke out among American troops injected with the vaccine.

In the 1960s it was discovered that polio vaccines manufactured in monkey kidney tissue between 1955 and 1963 were contaminated with a monkey virus (Simian Virus, number 40). Although this virus causes cancer in experimental animals, health authorities insist it does not cause problems in humans. But evidence of SV40 genetic material has been popping up in human cancers and normal tissue. Researchers are now connecting SV40-contaminated polio vaccines to an increasing number of rare cancers of the lung (mesothelioma) and bone marrow (multiple myeloma). In a 1999 report, SV40 DNA was detected in tissue samples from four children born after 1982. Three were kidney transplant patients, and a fourth had a kidney tumour. Could SV40 be passed on from parents to their children? No one knows for sure.

Covert Vaccine Experiments

Using kids as guinea pigs in potentially harmful vaccine experiments is every parents’ worst nightmare. This actually happened in 1989-1991 when Kaiser Permanente of Southern California and the US Centres for Disease Control (CDC) jointly conducted a measles vaccine experiment. Without proper parental disclosure, the Yugoslavian-made “high titre” Edmonston-Zagreb measles vaccine was tested on 1,500 poor, primarily black and Latino, inner city children in Los Angeles. Highly recommended by the World Health Organisation (WHO), the high-potency experimental vaccine was previously injected into infants in Mexico, Haiti, and Africa. It was discontinued in these countries when it was discovered that the children were dying in large numbers.

Unbelievably, the measles vaccine caused long-term suppression of the children’s immune system for six months up to three years. As a result, the immunodepressed children died from other diseases in greater numbers than children who had never received the vaccine. Tragically, African girl babies in the experiment were given twice the dose of boys, and therefore suffered a higher death rate. The WHO pulled the vaccine off the market in 1992.

Ironically, the E-Z measles vaccine tested by Kaiser on minority babies was supposed to increase immunity in younger infants. Instead, the vaccine produced the opposite effect. A Los Angeles Times editorial (June 20, 1996) assured readers that “none of the 1,500 was injured by the unlicensed vaccine” and called upon the CDC to ensure that experiments like the E-Z measles vaccine could never occur again.

One wonders how many secret vaccine experiments are conducted by health authorities that never come to the attention of the public. During the two-year measles experiment I was employed by Kaiser and I never knew anything about it until I read the report in The Times five years later, in 1996.

In the poor inner cities across the United States the number of asthma cases is exploding and health officials don’t know why. According to the CDC, 5000 asthma deaths occur annually; and it is estimated that 17.3 million people (4.8 million are children) suffer from the disease, up from 6.7 million in 1980. Asthma usually begins before age 6, and blacks are two to three times more likely to die from asthma than whites. In the Bronx and Harlem sections of New York City, the hospitalisation rate for asthma is 21 times higher than in the more affluent areas of the city.

Could the sharp rise in asthma in poor children be connected with immunosuppression caused by a barrage of vaccines, as well as a lack of quality medical care and insurance, poor diet, and environmental factors? The possible connection of immunosuppressive vaccines to diseases like asthma has never been raised by health officials.

With vaccine experiments frequently performed in Africa and now on black Americans, no wonder one out of every four African-Americans believes AIDS was developed as a genocide program by the US government to exterminate the black population.

But vaccine experiments in the 1990s have not been limited to blacks. Millions of female Mexicans, Nicaraguans and Filipinos have been duped into taking tetanus vaccines, some of which contained a female hormone that could cause miscarriage and sterilisation. In 1995, a Catholic human rights organisation called Human Life International accused the WHO of promoting a Canadian-made tetanus vaccine laced with a pregnancy hormone called human choriogonadotropic hormone (HCG).

Suspicions were aroused when the tetanus vaccine was prescribed in the unusual dose of five multiple injections over a three month period, and recommended only to women of reproductive age. When an unusual number of women experienced vaginal bleeding and miscarriages after the shots, a hormone additive was uncovered as the cause.

Apparently the WHO has been developing and testing anti-fertility vaccines for over two decades. Women receiving the laced tetanus shot not only developed antibodies to tetanus, but they also developed dangerous antibodies to the pregnancy hormone as well. Without this HCG hormone the growth of the fetus is impaired. Consequently, the laced vaccine served as a covert contraceptive device. Commissioned to analyse the vaccine, the Philippines Medical Association found that 20 percent of the WHO tetanus vaccines were contaminated with the hormone. Not surprisingly, the WHO has denied all accusations as “completely false and without basis,” and the major media have never reported on the controversy. For further details on this issue, consult the Human Life International website (www.hli.org).

Newly approved vaccines may also pose serious risks. In October 1999 a vaccine against “rotavirus” infection (which causes most cases of childhood diarrhea) was pulled off the market. One year after the RotaShield vaccine was inoculated into over a million infants, it was found to increase the risk of bowel obstruction. Almost 100 cases of bowel obstruction were reported to the government, and twenty infants developed bowel obstructions within one or two weeks after receiving the vaccine.

Vaccine Manufacture and Associated Dangers

Although the public has heard about side effects of vaccines, most people are clueless about the manufacture of vaccines. Few people know that viruses used in vaccine production need to be grown on animal parts like monkey kidneys, or in chicken embryos, or in human and fetal “cell lines.” Harvesting viruses in human cell-lines can be perilous because some human cell lines are derived from cancer cells.

In AIDS & The Doctors of Death I wrote about the development of the first human “HeLa” cell line – an “immortal” cell line used extensively in cancer and vaccine research for decades. Henrietta Lacks was a young black woman from Baltimore who died from a highly malignant cervical cancer in 1951. Small pieces of her tumour were donated to a laboratory specialising in tissue cell culture. In those days most attempts to grow human cells outside the body failed. But for some unknown reason Henrietta’s cancer cells grew vigorously and became known as the first successful human tissue cell line in history – the now famous HeLa cell line commemorating the legendary HEnrietta LAcks.

Henrietta’s cells were kept alive by feeding them a witches’ brew of beef embryo extract (the ground-up remains of a three-week-old, unborn cattle embryo); fresh chicken plasma obtained from the blood of a live chicken heart; and blood from human placentas (the placenta is the sac that nurtures the developing fetus and contains powerful hormones).

It is now suspected that a sexually-transmitted papilloma virus is the cause of cervical cancer. And it is anybody’s guess how many other chicken, cattle, and human viruses are incorporated into the HeLa cell line, but none of this possible viral contamination seems to bother scientists who have extensively used the cells in cancer research. What laboratory scientists did eventually discover was that HeLa cells proved so hardy that they frequently contaminated other tissue cell lines used in cancer and cancer virus research.

In the late 1960s when widespread HeLa cell contamination problems were uncovered, scientists were shocked and embarrassed to learn that millions of dollars worth of published cancer experiments were ruined. “Liver cells” and “monkey cells” that were used in cancer experiments turned out to be Henrietta’s cancer cells in disguise. Benign cells that supposedly “spontaneously transformed” into malignant cells were found to be cells contaminated with cancerous HeLa cells.

The serious problem of HeLa cell contamination in cancer and vaccine research is revealed in Michael Gold’s A Conspiracy of Cells: One Woman’s Immortal Legacy and the Medical Scandal It Caused. Even Jonas Salk, who developed the legendary Salk polio vaccine, was fooled when HeLa cells contaminated his animal cell lines. He admitted this years later in 1978 before a stunned audience of cell biologists and vaccine makers. In experiments performed in the late 1950s on dying cancer patients, Salk tried injecting them with a cell line of monkey heart tissue – the same cell line he used to harvest polio virus for his famous vaccine. He hoped the monkey cell injections would stimulate the immune system to fight cancer. However, when abscesses developed at the site of injections, Salk began to suspect that he might be injecting HeLa cells rather than monkey cells, and he stopped the experiment.

Mark Nelson-Rees, a HeLa cell expert and one of the 1978 conference attendees, offered to test Salk’s line if it was still available. Salk graciously agreed and the monkey cells indeed proved to be HeLa cells which had invaded and taken over the monkey cell line. According to author Gold, Salk thought there were adequate ways to separate viruses from the tissue cell lines they were harvested in, so that it really didn’t matter what kind of cells were used. Even if vaccines weren’t filtered, and even if whole cancer cells were injected directly into a human, Salk believed they would be rejected by the body and cause no harm. In those days doctors didn’t much believe in cancer-causing viruses. Nowadays, no researcher would dare try injecting cancer cells into a human being. But in the 1950s Salk had done it accidentally. He had injected HeLa cells into a few dozen patients and it hadn’t bothered him a bit.

Is There a Vaccine Contamination
Connection to AIDS?

Most people assume vaccines are “sterile” and germ free. But sterilising a vaccine can destroy the necessary immunising protein that makes it work. Thus, contaminating viruses or viral “particles” can sometime survive the vaccine process.

Animal viruses are also contained in fetal calf serum, a blood product commonly used as a laboratory nutrient to feed various tissue cell cultures. Vaccine contamination by fetal calf serum and its possible relationship to HIV was the subject of a letter by J. Grote, published in the Journal of the Royal (London) Society of Medicine in October 1988. Bovine visna virus (which looks similar to HIV) is a known contaminant of fetal calf serum used in vaccine production and virus-like particles have been detected in vaccines certified for clinical use. Grote warns that “It seems absolutely vital that all vaccines are screened for HIV prior to use, and that bovine visna virus is further investigated as to its relationship to HIV and its possible role in progression towards AIDS.”

Could virus-contaminated vaccines lie at the root of AIDS? A few researchers, including myself, believe HIV was “introduced” into gays during the experimental hepatitis B vaccine trials when thousands of homosexuals were injected in Los Angeles, San Francisco, and New York, during the years 1978-1981.

The AIDS epidemic first erupted in gays living in those cities in 1981. In 1980, one year before, already 20% of the gays inoculated in Manhattan with the experimental vaccine were already HIV-positive. This was several years before definite AIDS cases were diagnosed in Africa. In the early 1970s the hepatitis B vaccine was developed in chimpanzees, now wildly accepted as the animal from which HIV supposedly evolved.

Hepatitis B vaccine was developed to protect people from the sexual spread of the hepatitis B virus. Now the government recommends that all newborn babies be given the vaccine [this is also the case in Australia]. Such recommendations do not make sense to many parents. And people are still fearful of the hepatitis B vaccine because of its original connection to gay men and AIDS. The original experimental vaccine was made from the pooled blood serum of hepatitis-infected homosexuals and, as mentioned, serum-based vaccines cannot be sterilised.

Another theory of AIDS is that HIV originated from polio vaccines contaminated with chimp and monkey viruses, and administered to Africans in the late 1950s. In The River: A Journey to the Source of HIV and AIDS, published in 1999, Edward Hooper details how polio vaccine was made using monkey (and possibly chimp) kidneys and how the ancestor virus of HIV could have jumped species (via the vaccine) to produce the outbreak of AIDS in Africa. Hooper’s well-researched book greatly expands the polio vaccine theory of AIDS first reported by Tom Curtis in Rolling Stone magazine in 1992, and The River is a must-read for anyone interested in the possible man-made origin of AIDS.

Other researchers think it more likely that the various WHO-sponsored vaccine programs (particularly the smallpox program) in Africa in the 1970s are responsible for unleashing AIDS in Africa in the 1980s. Hooper, who has worked as a United Nations official, has discounted the research pointing to AIDS as a man-made disease, as proposed by Dr. Leonard Horowitz in Emerging Viruses, and in my two books AIDS & The Doctors of Death: An Inquiry into the Origin of the AIDS Epidemic and Queer Blood: The Secret AIDS Genocide Plot.

Horowitz and I both suspect contaminated smallpox vaccines as the source of HIV in Africa. Certainly the smallpox (vaccinia-cowpox) virus is an excellent virus to use for the genetic engineering of new, multipurpose vaccines. By splicing into the DNA genes of the vaccinia virus, scientists can add on parts of disease-producing viruses like influenza, hepatitis, and other viruses. The safety of this technique has not been fully evaluated, prompting one vaccine maker at a Vaccinia Virus Workshop in 1984 to ask if this could lead to another form of AIDS.

Vaccine Connection to Gulf War Illness and Huntsville Mystery Illness

The cause of Gulf War Illness (GWI) is unknown. For years this debilitating illness (which now affects one-half of the Gulf War vets) has been ignored by Pentagon officials who claim the disease does not exist and that vets are simply reacting to stress. GWI is also thought to be contagious. Vets insist their disease has been passed on to spouses, other family members, and even pets.

Some people suspect multiple vaccines, particularly the experimental anthrax vaccine, are implicated in the disease. Currently, soldiers who refuse to take the mandatory anthrax vaccine are being court-martialled and dismissed from the service.

Researchers Dr. Garth Nicolson and his wife Nancy have found a tiny bacterial microbe (a “mycoplasma”) in the blood of nearly half the ill vets with GWI. Amazingly, this infectious agent has a piece of HIV (the AIDS virus) attached to it. This microbe could never have occurred naturally. On the contrary, the composition of the microbe suggests a man-made and genetically-engineered biological warfare agent.

Garth Nicolson’s scientific credentials are impeccable. For 16 years he was a professor of medicine at the University of Texas M.D. Anderson Cancer Centre in Houston, as well as professor of pathology and laboratory medicine at the University of Texas Medical School, also in Houston. Nancy Nicolson, a molecular biophysicist, was on the faculty at Baylor College of Medicine.

Six months after returning home from the Gulf War, the Nicolson’s daughter contracted GWI. Her mother Nancy had contracted a similar illness in 1987 when she was working with Mycoplasma incognitus in infectious disease research. Finally suspecting that this research had biowarfare implications, Nancy Nicolson became a whistle-blower and angered officials. As a result, she believes she was deliberately infected with the mycoplasma. After partial paralysis and a long illness, she finally regained her health with the antibiotic Doxycycline.

The Nicolson’s discovery of a similar mycoplasma (but without the attachment of HIV) in a mysterious illness that erupted in the Huntsville, Texas area among prison guards and their families has all the drama of a ‘Movie of the Week’. Although the Huntsville disease broke out in the late 1980s (shortly before the Gulf War), it has many of the same signs and symptoms of GWI. Many locals are convinced the sometimes deadly disease originally spread from prisoners incarcerated in several large prisons around Huntsville.

In experiments conducted during the 1970s and 80s, the prisoners were inoculated with flu vaccines containing genetically engineered viruses and mycoplasma. It is suspected that vaccines were being covertly developed and deployed as biological warfare weapons. Nobel prize winner James Watson, world famous for his discovery of the molecular structure of DNA and a leading researcher of the still ongoing Human Genome Project, was involved in these prison experiments. The guards are convinced the Huntsville mystery illness is intimately connected to these experiments, jointly conducted by the Medical School and the military. Like GWI, health officials deny the disease exists.

The Nicolsons continue to developed antibiotic treatments, which have helped some vets. But they have paid a heavy price for their controversial research and unprecedented discoveries. Garth Nicolson was forced to resign from M.D. Anderson in 1996. His career and reputation destroyed, the Nicolsons have since moved to California and head The Institute for Molecular Medicine in Huntington Beach.

Dangerous Animal and Human Cell Lines
in Vaccine Manufacture

In an effort to quell concerns about the safety of vaccines, scientists are finally taking another look at the “non-infectious” particles of bird-cancer viruses (avian leukosis virus) in the mumps/measles/rubella vaccines routinely given to kids. Could this be the reason the US Federal Drug Administration held a meeting in September, 1999, to reconsider using human tumour cell lines (like HeLa) rather than monkey kidneys and chicken embryos which are no longer guaranteed 100% safe?

Writing in Science, Gretchen Vogel admits public trust in vaccines is a bit shaky. In Wales anti-vaccine parents are holding “measles parties” to infect their children with the disease rather than vaccinate them. She cites the danger of using immortal cell lines for live vaccine production because cancer genes or other hazardous factors might be transferred to people receiving vaccines. But manufacturers also realise vaccine critics are becoming more wary of vaccines made in animal and bird tissue. And vaccine makers want to use immortal cell lines to grow their viruses because obviously viruses can’t grow on their own.

The big question everyone seems to avoid is: Can vaccines cause cancer? There is certainly evidence connecting contaminated vaccines to AIDS. And HIV is a cancer-causing virus. Robert Gallo, the co-discoverer of HIV in 1984, has clearly stated AIDS is an epidemic of cancer.

Animal and avian viruses can contaminate vaccines and have all been studied as cancer-causing agents. And cancer and vaccine research would be much more difficult without the use of cell lines, some of which are derived from cancer.

Vaccines and Public Paranoia

Is the fear of vaccines justified? It is clear that vaccines can be dangerous. The contamination of vaccines is a reality, and vaccine experiments can be hazardous to one’s health. AIDS, unknown two decades ago, is now an increasing worldwide epidemic with millions of death predicted for the next decade. Could vaccines contaminated with cancer-causing and immunosuppressive viruses unleash new plagues in the New Millennium? If so, the new plagues may be far worse than the diseases we eradicated by vaccine programs in the twentieth century.

References

“Anti-diarrheal vaccine for babies recalled,” Los Angeles Times, October 16, 1999.

Butel JS, Arrington AS, Wong C, et al.: Molecular evidence of simian virus 40 infections in children. J Infect Dis 180:884-887, 1999.

Cantwell A: AIDS & the Doctors of Death. Aries Rising Press, Los Angeles, 1988.

Cantwell A: Queer Blood. Aries Rising Press, Los Angeles, 1993.

Gold M: A Conspiracy of Cells. State University of New York Press, Albany, 1986.

Hooper E: The River: A Journey to the Source of HIV and AIDS. Little, Brown and Company, Boston, 1999.

Horowitz L: Emerging Viruses: AIDS & Ebola. Tetrahedron, Inc, Rockport, MA, 1996.

Jaroff Leon: “Vaccine Jitters,” TIME, September 13, 1999.

Likoudis P: “Gulf war illness probe to advance with new study,” The Wanderer, January 21, 1999.

“Measles, government and trust ” (Editorial), Los Angeles Times, June 20, 1996.

Miller NZ: Immunization: Theory vs Reality. New Atlantean Press, Santa Fe, 1996.

Miller NZ: Immunizations: The People Speak! New Atlantean Press, Santa Fe, 1996.

Quinnan GV: Vaccinia Viruses as Vectors for Vaccine Antigens. Elsevier, New York, 1985.

Stolberg SG: “Poor fight baffling surge in asthma,” New York Times, October 18, 1999.
Source

 


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