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Hepatitis A - Inventing A Market For Another Superfluous Vaccine
By Tim O'Shea
www.thedoctorwithin.com
2-6-2
They finally did it. After years of lobbying and angling, GlaxoSmithKline
finally got their new vaccine for Hepatitis A tacked onto the
mandated schedule as of Jan 2002, with no public fanfare. (http://www.aap.org/) The vaccine is called
Havrix, and is delineated on p.1544 of the 2002 Physicians Desk
Reference, which incidentally was printed much earlier last year.
Merck also has a hepatitis A vaccine - Vaqta.
The CDC's mandated schedule is the brass ring that all vaccine manufacturers
are going for - approval of a vaccine can mean annual revenues
of $1 billion or more, which is about what Merck pulls in for
their current Hepatitis B vaccine.
Hepatitis A vaccine appears in a brand new category on the mandated
schedule called the 'high risk' category. The significance of
this new category will soon become apparent. But before we get
into that, let's take a look at Hepatitis A the disease and assess
the necessity for a mandated vaccine.
WHAT IS HEPATITIS A?
As every doctor knows, Hepatitis A is an acute viral disease of
the liver.
Hepatitis A virus (HAV) has supposedly been isolated:
"a 27-nm RNA picornavirus (enterovirus) with only one serotype..."
- American Academy of Pediatrics, Dec 1996
The infectious agent is passed from human to human either through
- the oral - fecal route, waterborne, often from raw shellfish or
dirty water
- blood and body secretions
Hepatitis A is a mild, self-limiting disease, resolving on its own
with no treatment in 4-8 weeks. Most infections are subclinical,
meaning that most people who get the disease never even know
it because they never manifest symptoms. (Merck Manual, p 377)
The journal Pediatrics agrees:
"Most HAV infections in young children are asymptomatic... Clinical
hepatitis occurs in fewer than 10% of infected children."
This disease is so mild that 90% of kids who get hepatitis A never
even know it. Even the National Institutes of Health states that:
"Most people who have Hepatitis A get well on their own after a
few weeks." - NIH Manual: What I Need To Know About Hepatitis
A
Most cases of hepatitis A are found in Third World areas, outside
the US. The question pops up: then why are we the only country
in the world who recommends the vaccine on a mass scale?
That billion dollars hanging in the balance wouldn't be in the equation,
now would it?
Diagnosis of hepatitis A is supposedly by IgM antibody. But more
often, diagnosis is by symptoms alone.
SYMPTOMS OF HEPATITIS A
According to Merck Manual, the chief symptoms of hepatitis A are
- loss of appetite
- NVD
- hives
- joint pain
- dark urine
p 382
Hardly life-threatening situations. Jaundice may also occur, but
it usually indicates the beginning of recovery. By the time these
symptoms appear, the disease is no longer infectious.
Unlike hepatitis B, Type A hepatitis disappears completely after
acute infection, and does not contribute to chronic liver disease
or to cirrhosis. It is important to note that after the patient
recovers, he has lifetime immunity. True immunity.
Hepatitis A is a disease of poor personal hygiene, bad sanitation,
poverty, overcrowding - Third World scenario. Even well-groomed,
well-fed junkies are not high risk for Hepatitis A. They're more
apt to get Type B. Medline indicates the lack of sewers in Third
World locales as the biggest contributor to Hepatitis A. Again
from the journal Pediatrics we find that: "The major method for
prevention of HAV infections is improved sanitation and personal
hygiene" Bottom line here: Hepatitis A is not common in most
of the United States.
OTHER CAUSES
It's shocking to discover that hepatitis can be caused by both hepatitis
B and hepatitis C vaccines! This fact is found in a disclaimer
that GlaxoSmithKlein makes about Havrix, that it can't cure the
hepatitis caused by these other 2 vaccines. So can we infer from
this that Havrix itself also causes hepatitis? We don't need
to infer it. The manufacturer states it on p 1545 of the 2002
PDR: a possible side effect of Havrix is hepatitis!
Another source of hepatitis A for children is nososcomial infection.
That means infants in hospital intensive care units pick it up
there. We never hear about it because the new literature is leaving
it out.
(AAP Policy Statement, 1996)
SO THEN WHAT'S THE VACCINE FOR?
The question arises - did we really need another vaccine beyond
the 40 already mandated for schoolkids, and specifically did
we need a vaccine for a rare disease that resolves by itself
in a few weeks?
To answer the first, we must ask were there any studies done which
prove that the new vaccine is safe when Havrix is added to the
other 40 mandated vaccines? No, there are none. This concept
of the cumulative viral load is discussed at length in the 2002
edition of The Sanctity of Human Blood.
Secondly, to substantiate the necessity for any vaccine, we must
look at two criteria: Incidence of disease severity HOW MANY
CASES REALLY ARE THERE?
This is tricky - research roulette. In the 2002 Physicians Desk
Reference, the manufacturer of Havrix cites 13-year old studies
which supposedly show the incidence of hepatitis A and state
that the case death rate is six-tenths of one per cent. (p 1545)
This is claiming that about six out of a thousand who get hepatitis
A die from hepatitis A. It seems like a rather high death rate
until one realizes that these are not US figures, but global
figures, meaning that they were taken primarily from Third World
countries because that's where the majority of hepatitis A is
found! So that means that these patients are trying to recover
from a disease of poverty, filth, and malnutrition in an environment
of poverty, filth, and malnutrition. Hardly applies in the rare
instance of a patient in most of America. But these are the studies
and figures that the vaccine manufacturer has used to convince
the FDA that Hepatitis A is such a serious disease in the US
that a vaccine is necessary.
Numbers, numbers, numbers. Different sources, different stats. From
the American Academy of Pediatricians website we see only half
the death rate reported by the PDR:
"Mortality is rare, especially in children. The case-fatality rate
has been estimated as 3 per 1000 clinical cases in the United
States.." - http://www.aap.org/policy/01207.html
Looking at the true incidence of the Hepatitis A in the US is an
academic artifice, a daunting challenge indeed. A standard government
reference for epidemiology is Statistical Abstracts. On p 137
of the most recent edition (2000), we find that the overall incidence
of Hepatitis A has been declining for the past 2 decades:
1980 --- 29.1 cases per 100,000
1998 --- 23.2 cases per 100,000
This decline is good news, and of course has nothing to do with
the vaccine. The vaccine just came out.
But the figures still seem a little high, don't they? On closer
inspection, getting out the magnifying glass and reading the
microprint footnote on that same page, we read:
"Includes cases imported from outside the United States"
Huh? 'Cases imported from outside the United States'? We're not
talking Pinot Noir here. No one doubts that the vast majority
of hepatitis A cases are foreign. It's a disease of poverty,
filth, and malnutrition.
Unfortunately, in a disease which only manifests symptoms less than
10% of the time, and with the immense amount of immigration and
international travel going on, there is simply no way to separate
foreign from domestic origin.
To further illustrate the low credibility of government figures
for hepatitis A cases, we need only look at a CDC report which
claimed more than 10 times higher incidence: 30,000 cases, which
is about 300 cases per 100,000. (Hepatitis Surveillance Report
No. 55)
That's a little different from 23 cases per 100,000. So which study
is right?
Who knows? Results depend on who funded it, who wrote it, and who
was responsible for verification.
The truth is no one can really say with authority how many cases
of hepatitis A occur in the US annually.
THE REAL NUMBER OF DEATHS
In an earlier part of that same reference - Statistical Abstracts,
p 90 - we find that the total number of annual US deaths from
all 3 types of viral hepatitis put together (Types A, B, and
C) in 1998 was only 4700.
Remember this 4700 also includes complications of autoimmune diseases,
terminal infectious diseases, and other serious illnesses, most
in communities of poverty and malnutrition, alcoholics, drug
addicts - individuals of this nature. This lowest common denominator
of life supposedly represents the necessity of a vaccine for
all.
Looking at the PDR's global figures above - a mortality of 6 out
of 100,000 - we see the usual attempt by the vaccine manufacturers
to grab the credit for saving us from an already declining disease.
As we learned from the Michael Alderson figures cited in The
Sanctity of Human Blood (p 45), virtually every infectious disease
of the past century had almost disappeared by the time vaccines
came on the market.
This is the perfect time to make the same claim for Hepatitis A,
before it disappears completely on its own. Masterful PR in action,
a la The Doors of Perception - http://www.thedoctorwithin.com/
We may be sure that future studies on US hepatitis A incidence will
show vast decreases, for which the vaccine will doubtless be
given credit. Just remember the virtual impossibility of determining
incidence at this time, when the vaccine is being introduced.
Stats game aside, almost all sources agree that children are not
the group dying from hepatitis A: "hepatitis with mortality occurs
mostly in people with underlying conditions, such as chronic
liver disease, and in older age groups" - http://www.aap.org/policy/01207.html
THE VACCINE ITSELF
This is fun. Hepatitis A vaccine is made from infected human connective
tissue cells. Not kidding. Not from just one guy, but rather
each batch of vaccine is made from an infected mass of cells
which had 1000 donors. (Pediatrics) Imagine that party. They
are infected with hepatitis A virus, the causative vector presumed
to be present in every case of hepatitis A disease.
The agents are filtered, and attenuated with aluminum, formaldehyde,
and phenoxyethanol - a synonym for ethylene glycol - a component
in antifreeze. Someday we're gonna pay for this.......
ALUMINUM AND FORMALDEHYDE
Just for the sake of argument, let's make the colossally irresponsible
concession that the attenuated viral agent in this vaccine is
necessary to stave off the "epidemic" of Hepatitis A about to
sweep through our children's bloodstreams. All right, we'll concede
that unlikely situation. So do the science wizards then want
to explain the additional presence of one of the most potent
of all human neurotoxins and also of a well known carcinogen
in this supposed life-saving elixir? Of course I am now referring
to the aluminum and formaldehyde which GlaxoSmithKline thought
so vital to the composition of Havrix. (PDR, p 1544) As Drs.
Russell Blaylock and Theo Colburn have well explained, it is
not just the connection with Alzheimer's that makes aluminum
such a danger to human physiology. It's that aluminum can interfere
with the formation, development and survival of virtually any
human nerve tissue in an unpredictable fashion, beyond any timetables
yet devised. (Excitotoxins, Our Stolen Future) We simply don't
know.
As for formaldehyde, let's just ask how much danger of cancer is
an acceptable risk in the pure, perfect blood of a newborn? Cancer
occurs first in just one cell. So where are the studies that
prove that this "trace" of formalin or antifreeze will not be
sufficient to cause that first cell mutation that develops into
cancer? Where are they?
As long as we're talking about scientific probability here, let's
take the discussion one step further. This single causative viral
agent that has been identified for hepatitis A is a presumption.
Remember - diagnosis is often by symptoms and by the presence
of IgM in the blood. Viral infections are not cultured for diagnosis
- it's largely theoretical. So then doesn't the isolation, concentration,
and dissemination of an infectious viral agent seem at least
a little presumptuous if not enormously reckless, especially
when we're talking about the unformed immune systems of the newborn
infant population?
That seems like a reasonable question, doesn't it?
MASS DISSEMINATION OF AN UNPROVEN AGENT
Here's the key point -- is it really necessary to introduce an attenuated
infectious vector into our entire population of children in order
to theoretically prevent a disease which is extremely rare in
the vast majority of US communities, and getting rarer? And is
self limiting, does not contribute to chronic liver disease,
and confers lifetime immunity to the ones who get it? What are
we doing?
Even the manufacturer does not claim that the vaccine confers immunity,
but only delay of the disease. Thus the need for boosters. Get
the idea - if the vaccine worked, we wouldn't need boosters after
6 months or a year. Following this shaky logic, if the immunity
only lasts a year, the child should get boosters every year for
the rest of his life. Now, the booster shot and the first vaccination
shot are identical. So why does the first shot supposedly last
for a year but the last one is going to be effective for the
rest of the patient's life?? Anybody ever think of that??
The other big issue is that the Hepatitis A virus is supposedly
a specific agent that has been photographed, sequenced, and catalogued,
and occurs the same in every case of the disease. Classical diagnosis
is by symptoms and the presence of the antibody, remember? IgM.
But acute viral liver infections can be of a variety of completely
different agents and disease scenarios. To pretend that they
can all be cured by the dissemination of one single type of attenuated
viral agent is disingenuous at best and scientifically ludicrous,
even criminal, at worst. Mass inoculation must be absolutely
proven to be necessary, beneficial and free from side effects,
or else it shouldn't even be considered. Havrix meets none of
these criteria.
THE NEW HIGH RISK CATEGORY
The most disconcerting - make that horrifying - aspect of the new
Mandated Vaccine Schedule that has just sneaked up on us will
prove to be the creation of this new High Risk category, in my
opinion. As we would expect, this ingenious addition was tacked
onto the program with no fanfare, no general public attention.
Suddenly the most vaccinated children in the history of the world
are still not getting sufficient injections, even at 40 vaccines
now mandated. So for further protection, the CDC has now created
the new High Risk category which they'll christen with just 2
vaccines: Hepatitis A and influenza.
Now folks, these extra shots aren't really part of the mandated
schedule, but are intended for the child who needs that extra
protection because he is what we doctors call 'high risk.' Which
according to the American Pediatrics Association means any child
who seems to have a tendency to get colds, asthma, allergies,
the flu, or is generally sick.
What percentage of kids does that include? Like, all of them?
Step right up. It's such a slick set-up. The script will go something
like, well, little Johnny and little Suzie just got their regular
shots, so they should be fine. By the way, Mrs. Jones, do these
children have a tendency to get allergies, colds, or the flu?
Oh, they do? Well, then the newest recommendations, just to be
on the safe side, are that for extra protection for Johnny and
Suzie we should add just two more shots today, while they're
here. And that's the new Hepatitis A shot and the flu shot. Yes,
and then they should be good for a year. Yes, all the other kids
are getting the 2 extra shots. You can't be too careful these
days, you know.
Who's going to argue with a rap like that? Only the most informed.
SET-UP FOR FUTURE VACCINES
The most insidious consequence of the new High Risk category, however,
is the door that it opens up for future vaccines. With all the
hysteria surrounding bioterrorism and anthrax, we've certainly
been inundated with beaucoup worries about coming vaccines:
anthrax AIDS smallpox and a whole string of others waiting in the
wings. That's where Hepatitis A vaccine was last year. Don't
miss the implication here: the High Risk Category is now providing
the infrastructure for any new vaccine that has to be rushed
to the population in a hurry because of supposed bioterrorist
threats. This is the set-up for the administration of the edicts
which may come down if the draconian Health Emergency Powers
Act should ever pass through Congress.
(www.mercola.com/2001/dec/26/mehpa.htm)
As you may have read, by this Act the governor of any state would
be given absolute, dictatorial powers to proclaim virtually any
situation a terrorist emergency, and to summarily decree that
all or any part of the population must submit to whatever health
measures are deemed necessary, including experimental vaccines.
Those who refuse may be quarantined, prosecuted, imprisoned,
or forced to submit, and property may be burned or confiscated.
Why not toss in the guillotine?
It seems unlikely that legislation this extreme would ever pass
through Congress. But just the fact that it is being considered
at all should make us ask ourselves - who is behind these totalitarian
proposals and at what point we might actually want to become
involved in state politics... Given these two options, Nazis-R-Us
or Terrorists Might Pop Up Here and There, give me the threat
of terrorism any day of the week. We've seen how well the government
can protect us from anything. The answer is obviously not to
give them another bigger chance, in this writer's opinion.
THE ILLUSION OF HIGH RISK
The big trouble with the High Risk Category is that it doesn't target
high risk groups - it hoses down everybody. In a semantic bait-and
switch, typical of organized medicine, they will call the category
High Risk, and then proceed to hustle every possible individual
into it by the absurdly overbroad and indiscriminate criteria
of anyone with a tendency towards allergies colds the flu
Very selective. There are true high risk groups for hepatitis A,
including those living in overcrowded, unhygienic surroundings,
improper diet, and certain racial selections as well. But here's
where politics controls science - imagine the furor that would
emerge if the vaccine were mandated according to living environment
and race. That would be interesting - trying to convince those
groups that the vaccine was for their own good. But if the CDC
recommends it for almost everybody, hey then everybody's equal
- the American way, right? And no one whines.
PROPAGANDA VS. INFORMATION
With uncharacteristic foresight, in 2000 the National Institutes
of Health published a booklet whose goal was to prepare the public
for the addition of Hepatitis A vaccine to the 2002 Schedule.
As a study in language alone, the book is a frightening representation
of the NIH's presumptions about the public's intelligence, which
are probably accurate. Written in Basic Retard, What I Need To
Know About Hepatitis A spoonfeeds the ninth grade mentality some
idiotically simplistic propaganda, dumbing them down in the most
patronizing and condescending manner. Some excerpts:
"A vaccine is a drug that you take when you are healthy that keeps
you from getting sick." Really? First of all vaccines aren't
drugs, nor do people "take" them. As for keeping people from
getting sick, perhaps we should ask the hundreds of VAERS parents
whose children have suffered fatal injury or permanent damage
from vaccines about how well vaccines kept their child from getting
sick. This is classic Edward L Bernays (Propaganda, 1928)
Or this gem:
"Vaccines teach your body to attack certain viruses, like the hepatitis
A virus."
This myth has survived intact since Jenner first propounded it in
1799. If it were true we would not have the ridiculous situation
where the only cases of diseases for the last 35 years have occurred
in the vaccinated population, as with smallpox and polio. (Salk,
Sabin)
Here's another excerpt from the same NIH booklet:
"Children can get the vaccine after they turn 2. Children age 2-18
will need 3 shots. The shots are spread out over a year.... Adults
get 2 shots over 6 -12 months. ... You need all of the shots
to be protected." Yes, 2 years is the recommended age for the
vaccine. And where are the studies showing the absolute safety
of injecting aluminum and formaldehyde into the unformed neurophysiology
of a 2 year old?
Where?
CALL IT IN THE AIR
What is shocking about these statements is the cavalier, arbitrary
fashion in which dosages are recommended. I mean, reading it
like this, it seems so scientific, doesn't it, and you assume
that an enormous amount of scientific study is behind this very
sober recommendation for "3 shots over a one year period." So
why is it that in the PDR, the manufacturer has a totally different
dosage recommendation and the AAP still another?? (Policy Statement)
On p 1545 of the new PDR, the manufacturer of Havrix states that
the child may get an initial dose, and then get one booster 6-12
months later.
What is this - Spin the Bottle?
Yes, actually it is. That's exactly what it is. These dose recommendations
are just guesswork - not the result of clinical trials. A year
from now they may change completely, as we just saw with other
vaccines on the new schedule. That's why different sources recommend
different dosages.
Nothing is more obvious is studying government publications than
inconsistency and ignorance of the most fundamentally pertinent
literature and policies of related health offices, even within
the same office. The classic left hand and right hand thing.
There's no real "oversight" which is a bureaucratic word that
means "watching over" an entire field of inquiry. Each office
just sort of says what it wants, and then the doctors or lawyers
or health officials quote the parts they can use. There's really
no such thing as objective science when it comes to legislated
health policies. Either you know this or you don't. The unfortunate
thing for those who don't is that they follow blindly what they
assume to be health policies and decisions made with the physical
welfare of the child in mind. Discovering their mistake too late,
the consequences can be physically disastrous.
Some other arbitrary, unscientific recommendations by the AAP for
the new experimental hepatitis A vaccine include just-in-case
shots for
· travelers to practically any destination that doesn't have a US
zip
code
· military personnel
· Persons living in or moving to areas that have a high rate of
HAV
infection.
· Persons who may be exposed to the hepatitis A virus repeatedly
due
to a high rate of hepatitis A disease, such as Alaskan Eskimos and
Native
Americans.
· Persons engaging in high-risk sexual activity, such as homosexual
and bisexual males.
· Persons who use illegal injectable drugs.
· Persons living in a community experiencing an outbreak of hepatitis
A.
· Persons working in facilities for the mentally retarded.
· Employees of child day-care centers.
· Persons who work with hepatitis A virus in the laboratory.
· Persons who handle primate animals.
· Persons with hemophilia.
· Food handlers.
· Persons with chronic liver disease.
Again, this is just guesswork and does not have to make any particular
sense. No special studies of these groups with the vaccine were
done. If the vaccine doesn't confer true lasting immunity, then
why would it be good for any of the above groups? If the disease
itself is mild and self limiting and confers true lasting immunity,
wouldn't it be better for that very low number of people just
to get the disease and forego the addition of carcinogens and
neurotoxins into their bloodstream?
Another question about the persons using illegal injectable drugs
- how would a virus know whether or not the injections were illegal?
With all the serious side effects from prescription drugs and
vaccines, legal - illegal: why would one be higher risk than
the other? This is nonsense.
Why on earth would someone who already has chronic liver disease
want to take a risky vaccine that only claims to protect him
from a mild, temporary type of liver disease? Especially one
which has a hepatitis as a possible side effect and one which
is going to further stress the liver with toxic adjuvants? Even
though the above bullets are pure conjecture, they do represent
groups that are being designated as High Risk. The question then
becomes - why isn't the vaccine recommended ONLY for these groups
instead of for the majority of the childhood population? What
was that - one billion...?
PREGNANT? DON'T EVEN THINK ABOUT IT
Under no circumstances should Hepatitis A vaccine be given in pregnancy.
The manufacturer states that pregnancy studies simply have not
been done. (www.aap.org/policy/01207.html) So unless you want
to be in the experimental group, when that doctor who has not
read the manufacturer's insert tries to give you this vaccine "just
to be on the safe side" - pass.
WRAP UP
So what have we learned? Well, there's a new vaccine for hepatitis
A being recommended for most children over 2 years old, as part
of a brand new category in the Vaccine Schedule. And the disease
itself - hepatitis A is not a big problem because in the vast
majority of cases the individual never even knows the disease
is present. And even if he gets the disease, it almost always
resolves in a few weeks with no permanent after effects whatsoever.
And there are a few problems with the vaccine:
- aluminum
- formaldehyde
- ethylene glycol
- many
side effects, including hepatitis itself
- the
dosages are best guesses
- the
manufacturers can pull in a billion new dollars per year
- the
vast majority of hepatitis A occurs outside the US, yet no
other country has mass vaccines
- the
mass dissemination of an infectious agent in to the childhood
population
- adding
to the cumulative viral load of the most vaccinated children
in world history
Outside of that, everything should be fine.
SOMEWHERE MACHIAVELLI SMILES
Perhpas the darkest consequence of all the foregoing is that most
of us have lost our confidence in the inner curative power of
Nature - the body's inborn wisdom. A hundred media snippets a
day, week after week, year after year, have undermined our ability
to even consider the notion that 99.9% of infants may be perfect
as they are. Or that their pure blood is the most sacred medium
in the universe, the crucible in which the human genome itself
was meant to be safeguarded and passed on from age to age. Or
that the immune system can only develop to its full potential
if left to its own devices, largely unknown to human science.
Such natural, vital postulates as these sound foreign to our ears,
even fanatical, cultist. Clear, rational independent thinking
has become so rare, so unwelcome, so feared in this world where
Conventional Wisdom on all topics of consequence is locked down
tight, top to bottom. Adrift in this gallery of manufactured
illusion, no effort is spared to keep one idea from surfacing:
that we have all but lost the ability to trust our own instincts,
to find the truth, and then to act on it.
REFERENCES
NIH - What I Need To Know About Hepatitis A 2000
US Dept of Commerce - Statistical Abstracts of the United States,
p .137 2000
Medical Economics - Physicians Desk Reference 2002
Beers & Berkow, MD - The Merck Manual, Centennial Edition 1999
National Library of Medicine
http://www.nlm.nih.gov/medlineplus/druginfo/hepatitisavaccineinactivatedsy202902
.html#Brands
Blaylock, R MD - Excitotoxins: The Taste That Kills --- Health Press
1997.
Colburn, T, PhD - Our Stolen Future - Plume 1997.
O'Shea, T - The Sanctity of Human Blood - New West 2002.
American Academy of Pediatrics - Policy Statement: Prevention Of
Hepatitis
A Infections: Guidelines For Use Of Hepatitis A Vaccine And Immune
Globulin
Pediatrics, vol 98 no 6, p.1207-1215 Dec 1996.
Committee on Infectious Diseases - Centers for Disease Control and
Prevention. Hepatitis Surveillance Report No. 55. p 1-34 1994.
Bernays, E. Propaganda --- Liveright, New York 1928.
Micromedex - National Library of Medicine
Sabin, Albert MD - La Stampa, Torino Italia 8 Dec 1985.
Model Emergency Health Powers Act (MEHPA) Turns Governors into Dictators
http://www.mercola.com/2001/dec/26/mehpa.htm
Salk, Jonas, MD quoted in Science Abstracts 4 Apr 1977.
Copyright 2002
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