Seekers of Truth Always Thinking, Searching…

(1) Moses was high on drugs when God appeared to him – Israeli researcher

Date: Fri, 7 Mar 2008 18:00:30 -0500 (EST)
From: IHR News <news@ihr.org>

http://afp.google.com/article/ALeqM5gEOpkeLopJixolK1-9AQ_zNeWe5g

Moses was high on drugs: Israeli researcher ==

Hebrew University researcher: Moses was tripping at Mount Sinai

By Ofri Ilani, Haaretz Correspondent

Last update – 23:15 04/03/2008

http://www.haaretz.com/hasen/spages/960403.html

“And all the people perceived the thunderings, and the lightnings, and
the voice of the horn, and the mountain smoking.” Thus the book of
Exodus describes the impressive moment of the giving of the Torah on
Mount Sinai.

The “perceiving of the voices” has been interpreted endlessly since
these words were first written. When Professor Benny Shanon, professor
of cognitive psychology at the Hebrew University of Jerusalem, reads the
verse, he recalls a powerful hallucinatory experience he had when he
visited the Amazon and drank a potion made from a plant called ayahuasca.

“One of the things that happens when you drink the potion is a visual
experience created via sounds,” he says.

Shanon presents a provocative theory in an article published this week
in the philosophy journal Time and Mind. The religious ceremonies of the
Israelites included the use of psychotropic materials that can found in
the Negev and Sinai, he says.

“I have no direct proof of this interpretation,” and such proof cannot
be expected, he says. However, “it seems logical that something was
altered in people’s consciousness. There are other stories in the Bible
that mention the use of plants: for example, the tree of the knowledge
of good and evil in the Garden of Eden.”

Shanon, former head of the Hebrew University psychology department, said
his first experience with ayahuasca was in 1991 when he was invited to a
religious ceremony in the northern Amazon in 1991 in Brazil.

“I experienced visions that had spiritual-religious connotations,” he says.

Since that time, he has used it hundreds of times, and has published a
book about the plant.

“Hypotheses have been around for 20 years connecting the beginning of
religions with psychoactive materials,” Shanon says. He believes the
Israelites used two plants in Sinai and the Negev: one of them is wild
rue, a hallucinogen used by the Bedoin to this day. However this plant
is not identified with any plant mentioned in the Bible.

The acacia tree also has psychedelic properties, Shanon says, which the
Israelites could have used. The acacia is mentioned frequently in the
Bible, and was the type of wood of which the Ark of the Covenant was
made. According to Shanon, he drank a potion prepared from a species of
acacia while he was in South America, which caused similar experiences
to those produced by the ayahuasca.

Shanon also sees signs of a hallucinogenic vision in the story of the
burning bush. “Moses ‘looked, and, behold, the bush burned with fire,
and the bush was not consumed,'” Shanon quotes from Exodus 3:2. Time
passes differently when under the influence of the plant, he notes.
“That’s why Moses thought the bush was not consumed. It should have been
burned in the time he thought had passed. And in that time, he heard God
speaking to him.”

“But not everyone who uses a plant like this brings the Torah,” Shanon
concedes. “For that, you have to be Moses.”

(2) “There never was a Jewish people, only a Jewish religion” –
Historian Shlomo Zand

Date: Wed, 5 Mar 2008 18:05:10 -0500 (EST)
From: IHR News <news@ihr.org>

An Invention Called `the Jewish People’

Tom Segev — Haaretz (Israel)

http://www.haaretz.com/hasen/spages/959229.html

Israel’s Declaration of Independence states that the Jewish people arose
in the Land of Israel and was exiled from its homeland. Every Israeli
schoolchild is taught that this happened during the period of Roman
rule, in 70 CE. The nation remained loyal to its land, to which it began
to return after two millennia of exile. Wrong, says the historian Shlomo
Zand, in one of the most fascinating and challenging books published
here in a long time. There never was a Jewish people, only a Jewish
religion, and the exile also never happened – hence there was no return.
Zand rejects most of the stories of national-identity formation in the
Bible, including the exodus from Egypt and, most satisfactorily, the
horrors of the conquest under Joshua. It’s all fiction and myth that
served as an excuse for the establishment of the State of Israel, he
asserts.

According to Zand, the Romans did not generally exile whole nations, and
most of the Jews were permitted to remain in the country. The number of
those exiled was at most tens of thousands. When the country was
conquered by the Arabs, many of the Jews converted to Islam and were
assimilated among the conquerors. It follows that the progenitors of the
Palestinian Arabs were Jews. Zand did not invent this thesis; 30 years
before the Declaration of Independence, it was espoused by David
Ben-Gurion, Yitzhak Ben-Zvi and others.

If the majority of the Jews were not exiled, how is it that so many of
them reached almost every country on earth? Zand says they emigrated of
their own volition or, if they were among those exiled to Babylon,
remained there because they chose to. Contrary to conventional belief,
the Jewish religion tried to induce members of other faiths to become
Jews, which explains how there came to be millions of Jews in the world.
As the Book of Esther, for example, notes, “And many of the people of
the land became Jews; for the fear of the Jews fell upon them.”

Zand quotes from many existing studies, some of which were written in
Israel but shunted out of the central discourse. He also describes at
length the Jewish kingdom of Himyar in the southern Arabian Peninsula
and the Jewish Berbers in North Africa. The community of Jews in Spain
sprang from Arabs who became Jews and arrived with the forces that
captured Spain from the Christians, and from European-born individuals
who had also become Jews.

The first Jews of Ashkenaz (Germany) did not come from the Land of
Israel and did not reach Eastern Europe from Germany, but became Jews in
the Khazar Kingdom in the Caucasus. Zand explains the origins of Yiddish
culture: it was not a Jewish import from Germany, but the result of the
connection between the offspring of the Kuzari and Germans who traveled
to the East, some of them as merchants.

We find, then, that the members of a variety of peoples and races, blond
and black, brown and yellow, became Jews in large numbers. According to
Zand, the Zionist need to devise for them a shared ethnicity and
historical continuity produced a long series of inventions and fictions,
along with an invocation of racist theses. Some were concocted in the
minds of those who conceived the Zionist movement, while others were
offered as the findings of genetic studies conducted in Israel.

Prof. Zand teaches at Tel Aviv University. His book, “When and How Was
the Jewish People Invented?” (published by Resling in Hebrew), is
intended to promote the idea that Israel should be a “state of all its
citizens” – Jews, Arabs and others – in contrast to its declared
identity as a “Jewish and democratic” state. Personal stories, a
prolonged theoretical discussion and abundant sarcastic quips do not
help the book, but its historical chapters are well-written and cite
numerous facts and insights that many Israelis will be astonished to
read for the first time.

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Disrupt the Cancer PROCESS…

The Body's Cure for Cancer?

Defending Against Cancer

by Mauris L. Emeka November 25, 2004


a self-help article about important dietary changes for preventing and
overcoming cancer — The Body’s Cure for Cancer —

It is often said that we
all get cancer from time to time, but that the body cures it and allows
us to go on living normal lives. What mechanism does the body use to
cure cancer in the course of our daily lives? That question was asked
roughly 100 years ago by a renowned Scottish embryologist named Dr.
John Beard.

Dr. Beard’s work has long been ignored by
conventional medicine, although in recent years his important findings
are being re-discovered. His research is documented in “The
Enzyme Treatment of Cancer and Its Scientific Basis”,copyrighted
in 1911. It explains that the body cures cancer with protein digesting
enzymes supplied by the pancreas.

Research shows that protein
digesting enzymes can dissolve the protein coating from around cancer
cells, and this enables white blood cells (which are part of the immune
system) to destroy the cancer cells. Cancer cells are actually
trophoblasts cells that are misbehaving– that is, they are trying to
do the wrong thing at the wrong time and place. Trophoblasts cells are
basic to the development of every newly conceived baby. But if out of
control trophoblast activity begins to occur in later life then cancer
is the result.

Thanks to Dr. Beard’s research he proved that if
there are enough enzymes, especially enzymes designed to digest
protein, then cancer cannot gain a foothold.

Food Enzymes, the First Line of Defense —

There
is a problem: Dr. Edward Howell, M.D. notes in his seminal work Enzyme
Nutrition, that the pancreas (which was just mentioned) has a limited
capability to produce enzymes. Add to that the fact that the pancreas
is almost always over worked trying to produce digestive enzymes to
digest the cooked food that we eat. Cooked, refined and processed foods
have no enzymes.

The body is at greatest risk of cancer when the pancreas can no longer produce an adequate supply of protein digesting enzymes.

But
there is good news! Through diet, we can do something about a scarcity
of protein digesting enzymes. It is possible to make it so the pancreas
does not have to work so hard. That can be done by significantly
decreasing the consumption of animal protein (because animal protein
requires lots of protein digesting enzymes), and by eating more raw
fruits, vegetables, and nuts, since they are rich in enzymes.

And
note this: the tropical fruits papaya (and their seeds) along with
pineapple are especially important, because their enzymes closely mimic
the protein digesting enzymes produced by the pancreas. (That’s
why meat tenderizers contain papaya). Our first line of defense against
cancer is therefore protein digesting enzymes (and other food enzymes)
all of which can be gotten from raw whole foods.

Nitriloside, a Little Known Food Factor —

We
are fortunate to have available to us a second line of defense against
cancer. It involves eating foods that contain a little known food
factor called nitriloside. Dr. Ernst Krebs, M.D. is a pioneer in cancer
research who in the 1920s discovered that nitriloside suppresses cancer
cells.

He demonstrated that this food factor was essential for
maintaining good health, and he called it vitamin B-17. It has shown to
be a kind of natural ‘chemotherapy’ because it kills cancer
cells while enhancing healthy cells, and produces no negative side
effects. Unfortunately, conventional medicine ignores the importance of
Dr. Krebs’ findings.

Where can the food factor,
nitriloside, be found? It occurs naturally in foods, and is found in
greatest abundance in apricot kernels. (Although apricot kernels are
hard to find, one can go online and locate companies in California that
sell them).

Nitriloside also occurs in lesser concentrations in
a host of other whole foods, including lima beans, lentil, millet,
sprouts, ginger root, turmeric, black eye peas, walnuts, avocados,
blackberries, cranberries, papaya, barley, cassava, to mention a few.

Unfortunately,
our Western diet no longer includes very many foods like the ones just
mentioned. The typical American diet is high in processed food, simple
carbohydrates, refined grains, and meat and pasteurized dairy from
grain fed animals. These foods are essentially devoid of nitriloside.
In Summary

Cancer
is a chronic metabolic disease, and no chronic metabolic disease has
ever been cured without involving certain food factors found in whole
natural foods. The evidence of this is seen in the fact that countries
around the world have all but wiped out other chronic metabolic
diseases such as scurvy, rickets, pellagra, and pernicious anemia by
including certain food factors.

But unlike most other chronic
metabolic diseases, cancer is a multiple variable deficiency disease.
For example, although nitriloside is crucial, it cannot get into the
tissues and do its work unless there is a sufficient level of zinc. In
addition, vitamin C is equally crucial.

That’s why whole foods
— like apricot kernels, raw fruits,deep green leafy vegetables, and
nuts — that come with vital trace minerals are preferable to
synthesized food supplements. The bottom line: cancer is held in check
by protein digesting enzymes supplied by the pancreas, and by the food
factor we now know as nitriloside.

Do you want to make your body
a place where cancer cannot survive? Then, instead of emphasizing drugs
that only treat symptoms, you can eat foods each day that disrupt the
cancer PROCESS — foods rich in enzymes and in nitriloside.

What
a blessing to know that there is something we all can do (on our own)
about preventing and overcoming what is arguably the most devastating
illness of our time!

And God said, Behold, I have given you
every herb bearing seed, which is upon the face of all the earth, and
every tree in which is the fruit of a tree yielding seed; to you it
shall be for meat.” — Genesis 1:29

Mauris Emeka is the
author of Cancer’s Best Medicine, copyright 2004, and also of the
book Fear Cancer No More, copyright 2002. Apollo Publishing. P. O. Box
1937. Port Orchard, WA 98366. Refer to: http://www.cancernomore.com

pad
pad Cancer No More
pad
LINK to Mauris L. Emeka’s site
pad
pad

Remember we are NOT Doctors and have NO medical training.

INOCULATIONS: THE TRUE WEAPONS OF MASS DESTRUCTION


    


CAUSING
VIDS (VACCINE INDUCED DISEASES)


(AN
EPIDEMIC OF GENOCIDE)


by Rebecca
Carley, M.D.


Court
Qualified Expert in VIDS and Legal Abuse Syndrome



                                                                                            
 
 Amended  January 21, 2007

“One basic truth can be used as a
foundation for a mountain of lies, and if we dig down deep enough in the
mountain of lies, and bring out that truth, to set it on top of the mountain
of lies; the entire mountain of lies will crumble under the weight of that
one truth.  And there is nothing more devastating to a structure of lies
than the revelation of the truth upon which the structure of lies was built,
because the shock waves of the revelation of the truth reverberate, and
continue to reverberate throughout the Earth for generations to follow,
awakening even those people who had no desire to be awakened to the truth.” 
(by Delamar Duvaris as written in the preface of “Behold the Pale Horse” by
William Cooper).

     The basic truth
that served as the foundation for the mountain of lies known as vaccinations
was the observation that mammals which recover from infection with microorganisms
acquire natural immunity from further infections.  Whenever
cytotoxic
T cells
(the little Pac man cells
which devour and neutralize viruses, bacteria, and cancer cells, thus conferring
cellular immunity and are also responsible for allograft
rejection) and
B
cells
(antibody producing cells
which confer humoral immunity by circulating in the body’s fluids
or “humors”, primarily serum or lymph) are activated by various substances
foreign to the body called antigens, some of the T and B cells become memory
cells.  Thus, the next time the individual meets up with that same antigen,
the immune system can be quickly triggered to demolish it.  This is the
process known as natural immunity.

     This truth gave birth to a
beLIEf that if a foreign antigen was injected into an individual, that
individual would then become immune to a future infection.  This beLIEf,
(you see the lie in the middle), was given the name, “vaccinations”. 
What the promoters of vaccination failed to realize is that secretory
IgA (an antibody found predominately in saliva and secretions of the
gastrointestinal and respiratory tract mucosa) is the initial
normal antibody response to all airborne
and ingested pathogens. IgA helps protect against viral infection, agglutinate
bacteria, neutralize microbial toxins, and decrease attachment of pathogens
to mucosal surfaces. What this author has realized is that bypassing
this mucosal aspect of the immune system by directly injecting organisms
into the body leads to a corruption in the immune system itself whereby
IgA is transmuted into IgE, and/or the B cells are hyperactivated to
produce pathologic amounts of self-attacking antibody as well as suppression
of cytotoxic T cells (as explained shortly).  As a result, the pathogenic
viruses or bacteria cannot be eliminated by the immune system and remain
in the body, where they cause chronic disease and thus
further grow and/or mutate as the individual is exposed to ever more
antigens and toxins in the environment.  This is especially true with
pathogens grouped under the term “stealth adapted“. 

These are formed when vaccine viruses combine with viruses from tissues
used to culture them, or when bacteria lose their cell walls when a
person takes antibiotics and transform into “L forms”, leading to
a lack of some critical antigens normally recognized by the cellular
immune system. Another example is stealth adapted (mutated) cytomegaloviruses
which arose from African green monkey (simian) kidney cells when they
were used to culture polio virus for live polio virus vaccines.  Thus,
not only was the vaccinee inoculated with polio, but with the cytomegalovirus
as well.

     The mechanism
by which the immune system is corrupted can best be realized when you understand
that the two poles of the immune system (the cellular
and humoral mechanisms) have a reciprocal relationship in that
when the activity of one pole is increased, the other must decrease. Thus,
when one is stimulated, the other is inhibited.  Since vaccines activate
the B cells to secrete antibody, the cytotoxic (killer) T cells are subsequently
suppressed.  (In fact, progressive vaccinia (following vaccination with
smallpox) occurs in the presence of high titers of circulating antibody to
the virus1 combined with suppressed cytotoxic T cells, leading
to spreading of lesions all over the body).  This suppression of the
cell mediated response is thus a key factor in the development of cancer and
life threatening infections.  In fact, the “prevention” of a disease
via vaccination is, in reality, an inability to expel organisms due to the
suppression of the cell-mediated response.  Thus, rather than preventing
disease, the disease is actually prevented from ever being resolved

The organisms continue circulating through the body, adapting to the hostile
environment by transforming into other organisms depending on acidity, toxicity
and other changes to the internal terrain of the body as demonstrated by the
works of Professor Antoine Béchamp.  He established this prior
to the development of the “germ theory” of disease by Louis Pasteur. 
Pasteur’s “germ theory” was a plagiarist’s attempt to reshape the truth from
Béchamp into his own “original” premise – the beLIEf that germs are out to
“attack” us, thereby causing dis-ease. Thus, treatment of infection with antibiotics
as well as “prevention” of disease with vaccines are both just corrupted attempts
at cutting off the branches of dis-ease, when the root of the cause
is a toxic internal environment combined with nutritional deficiency. 
However, since Pasteur’s germ theory was conducive to the profits of the burgeoning
pharmaceutical cartels that only manage dis-ease, no mention of the work of
Professor Béchamp is made in medical school curricula.

     To make matters worse than
the suppression of cellular immunity which occurs when vaccines are
injected, adjuvants (which are substances added to vaccines to
enhance the antibody response) can actually lead to serious side effects
themselves. Adjuvants include oil emulsions, mineral compounds (which
may contain the toxic metal aluminum), bacterial products, liposomes
(which allow delayed release of substances), and squalene.  The
side effects of adjuvants themselves include hyperactivity of B cells
leading to pathologic2 levels of antibody production,  as
well as allergic reaction to the adjuvants themselves (as demonstrated
in Gulf War I soldiers injected with vaccines containing the adjuvant
squalene, to which antibodies were found in many soldiers). Note that
the pathologically elevated hyperactivity of antibody production caused
by adjuvants also results in a distraction from the other antigens that
the immune system encounters “naturally”, which must be addressed
to maintain health.

       In addition to the transmutation
of IgA into IgE leading to allergic reactions described shortly, the
overall hyperactivity of the humoral (antibody producing) pole of the
immune system is, in this author’s opinion, the sole cause of all

autoimmune diseases; where the auto-antibodies produced
activate functioning T cells to then attack self; and both the activated
B & T cells also produce cytokines (which further enhance inflammation
and immunological involvement).
The
only thing which determines which autoimmune disease you develop is
which tissues in your body are attacked by auto-antibodies3.
PLEASE NOTE THAT THIS FINDING HAS NOW BEEN CONFIRMED BY DR. JEFFREY
BROWNING SENIOR DIRECTOR, DEPARTMENT OF IMMUNOBIOLOGY, BIOGEN-IDEC,
IN HIS SCIENTIFIC PAPER ENTITLED “B CELLS MOVE TO CENTRE STAGE: NOVEL
OPPORTUNITIES FOR AUTOIMMUNE DISEASE TREATMENT” PUBLISHED IN
NATURE REVIEWS DRUG DISCOVERY 5, 564-576 (JULY 2006)
; AVAILABLE
ON THE INTERNET AT:
http://www.nature.com/nrd/journal/v5/n7/full/nrd2085.html#a1
.

Read the rest of this article at: http://www.drcarley.com/

It’s Not the Mercury…

 

It’s not the mercury,
it’s the vaccine itself
that causes autism!

http://www.drcarley.com

http://www.wealthshare.wordpress.com

…see posts below to find out more about this vital data…

1918 flu gives clues to stopping next pandemic

The following MSNBC report has been removed from the MSNBC site.

1918 flu gives clues to
stopping next pandemic

1 February – MSNBC reported that two little
changes in the virus that caused the 1918 Spanish flu pandemic stopped it
from spreading from one animal to another, a finding that may help determine
what will cause the next pandemic. Researchers who have been studying a
reconstructed version of the 1918 virus found it very easy to stop the virus
from spreading from one infected ferret to another — although the
altered viruses still quickly killed the animals. Researchers made a modest
change of two amino acids in the hemagglutinin protein that stopped
transmission of the virus between ferrets.
View Article

Editors Note:

Even after this data was known those who are suppose to protect us are predicting massive Bird Flu Pandemic, even though they know how to stop it.

sovereignjohn

Cause of Autism Discovered…and it’s Not the Mercury !!!


Cause Of Autism Discovered……And It’s Not The Mercury!

Posted by: “Eric WhoRU”
ewrbn@yahoo.com


ewrbn

Mon Mar 10, 2008 7:31 pm (PDT)

SPECIAL REPORT!
Cause Of Autism Discovered……
And It’s Not The Mercury!
By: Dr. Rebecca CarleySource: http://www.drcarley.comMarch 8, 2008

This is the update that has gone out to the thousands of people on my
list. I await the response of David Kirby and Dr Boyd Haley, who are
receiving this e-mail as well.

The following is the ammo by which Big Pharma can be brought to its
knees. I ask you to circulate it widely. It is time for you to
DEMAND that those promoting mercury as the cause of autism respond to
what I have written below. If the true intention of these people is
to stop this epidemic in our children, then they should let go of
their egos and admit that I have figured out the true cause. Let me
first encourage all of you to go to
http://www.drcarley.com/the_big_picture.jpg you will see that I have
ALWAYS said it is the BIG PICTURE of assaults to our immune systems
(and mercury is there) which combine to cause disease, including
autism. But it is the corruption of the immune system caused by the
inoculation of viruses which is the root cause of all autoimmune
diseases and cancer…and once this information is in the hands of a
critical mass of the people, we will put a stop to the biggest
epidemic the world has ever known…VIDS (Vaccine Induced Diseases).
And the individuals who continue to promote mercury as the root cause
in the face of this information will be exposed for being INTENTIONAL
disinformers.

Below is a verbatim copy of the US Government concession filed last
November in a Court of Federal Claims case brought by a family
claiming that mercury containing vaccines were the cause of the
child’s autism that is posted on David Kirby’s blog at
http://www.huffingtonpost.com/david-kirby/the-vaccineautism-court-
_b_88558.html. David Kirby, author of “Evidence of Harm”, is one of
the individuals who is distracting the public that it is “all about
the thimerosol”. The take home message therefore is that if the
mercury were removed, vaccines would be safe. A BIGGER LIE HAS NEVER
BEEN TOLD; and my document “Inoculations the True Weapons of Mass
Destruction” posted on www.drcarley.com describes the corruption of
the immune system caused by the injection of viruses directly into
the body, bypassing secretory IgA (an antibody in the upper GI and
respiratory tracts critical for the processing of the germ by the
immune system for natural immunity to occur).

I was a guest with David Kirby on a radio show which is posted on my
website at http://www.drcarley.com/kirby_vs_carley_autism.mp3, on
which I confronted him with the fact that autism is actually a non-
fatal case of subacute sclerosing panencephalitis caused by
demyelination following vaccine induced encephalitis, and that the
name of the condition was changed to autism to hide this self evident
fact. I have sent Mr. Kirby copies of the documents on my website,
and asked him multiple times to be a guest on one of my internet
shows to discuss the “mercury vs demyelination” theories of autism.
He will not do so.

What is truly amazing is that he is now mentioning live viruses
amongst a plethora of other potential problems (see # 6 at
http://www.huffingtonpost.com/david-kirby/government-concedes-
vacci_b_88323.html)….but is he discussing the live viruses
bypassing secretory IgA, causing vaccine induced encephalitis and
subsequent demyelination? NO…he is mentioning live viruses as a
cause of mitochondrial damage. So once again, we will now be
distracted with this genetic mitochondrial defect…perhaps develop a
test to find the children with this problem before they are
vaccinated, when in fact genetic defects can also be caused by
vaccines. More confusion and distraction…rather than admitting
that there is no such thing as a safe vaccine…and the practice
should be abandoned altogether, and attention placed on strengthening
the immune system. Of course, since population reduction is the true
agenda of the powers that be, not only will the vaccine push
continue…but viruses are being developed to cause disease and
cancer. The mad scientists have to be stopped…and this WILL happen
once enough people have opened their eyes.

I urge all of you to carefully read this decision dated 11/9/07, in
which this young girl won her case claiming vaccines caused her
autism. Note these important points:

1. 2 days after multiple vaccines (which included the MMR, which has
NEVER had mercury), she developed a high fever, high pitched
screaming, and was lethargic and irritable. these are symptoms of
VACCINE INDUCED ENCEPHALITIS, an inflammation of the brain caused by
injection of LIVE VIRUSES (not from mercury).

2. She also began to arch her back when she cried (a sign of vaccine
induced encephalitis, NOT mercury poisoning).

3. She developed a POST-VARICELLA VACCINATION RASH (which proves
that the vaccination GAVE HER THAT DISEASE).

4. She was diagnosed with vaccine induced ENCEPHALOPATHY
(degenerative disease of the brain)…as you will see below, mercury
is involved in causing the degenerative disease Alzheimer’s, NOT
autism).

5. She developed a SEIZURE DISORDER later on (go to the CDC website
and look for the vaccine information statement on the MMR vaccine
(which has never had mercury), and you will see that one of the side
effects is LONG TERM SEIZURES.

6. You will also note that they did genetic testing of the child and
found that she has a genetic defect in her cellular energetics (Note
that vaccines are known to cause GENETIC MUTATION due to insertion of
plasmids of DNA from the viruses or tissues used to culture them; in
fact, this is the whole basis on which DNA vaccines are designed).

7. You will notice that although the white coat in this case went as
far as to do genetic testing in this child, there were NO ANTI MYELIN
OR ANTI NEURONAL FILAMENT LEVELS DONE; this IS the test that
demonstrates demyelination before it is massive enough to show up on
MRI’s; and this IS the test that proves that autism is actually a non-
fatal form of subacute sclerosing panencephalitis (which is why this
test is almost never done).

Here is the decision (but please be sure to also read what I have
written after it)…

IN THE UNITED STATES COURT OF FEDERAL CLAIMS
OFFICE OF SPECIAL MASTERS

CHILD, a minor,

by her Parents and Natural Guardians,

Petitioners,

v.

SECRETARY OF HEALTH AND HUMAN SERVICES,

Respondent.

RESPONDENT’S RULE 4(c) REPORT

In accordance with RCFC, Appendix B, Vaccine Rule 4(c), the
Secretary of Health and Human Services submits the following response
to the petition for compensation filed in this case.

FACTS

CHILD (“CHILD”) was born on December –, 1998, and weighed eight
pounds, ten ounces. Petitioners’ Exhibit (“Pet. Ex.”) 54 at 13. The
pregnancy was complicated by gestational diabetes. Id. at 13. CHILD
received her first Hepatitis B immunization on December 27, 1998.
Pet. Ex. 31 at 2.

From January 26, 1999 through June 28, 1999, CHILD visited the
Pediatric Center, in Catonsville, Maryland, for well-child
examinations and minor complaints, including fever and eczema. Pet.
Ex. 31 at 5-10, 19. During this time period, she received the
following pediatric vaccinations, without incident:

Vaccine Dates Administered

Hep B 12/27/98; 1/26/99

IPV 3/12/99; 4/27/99

Hib 3/12/99; 4/27/99; 6/28/99

DTaP 3/12/99; 4/27/99; 6/28/99

Id. at 2.

At seven months of age, CHILD was diagnosed with bilateral otitis
media. Pet. Ex. 31 at 20. In the subsequent months between July 1999
and January 2000, she had frequent bouts of otitis media, which
doctors treated with multiple antibiotics. Pet. Ex. 2 at 4. On
December 3,1999, CHILD was seen by Karl Diehn, M.D., at Ear, Nose,
and Throat Associates of the Greater Baltimore Medical Center (“ENT
Associates”). Pet. Ex. 31 at 44. Dr. Diehn recommend that CHILD
receive PE tubes for her “recurrent otitis media and serious otitis.”
Id. CHILD received PE tubes in January 2000. Pet. Ex. 24 at 7. Due to
CHILD’s otitis media, her mother did not allow CHILD to receive the
standard 12 and 15 month childhood immunizations. Pet. Ex. 2 at 4.

According to the medical records, CHILD consistently met her
developmental milestones during the first eighteen months of her
life. The record of an October 5, 1999 visit to the Pediatric Center
notes that CHILD was mimicking sounds, crawling, and sitting. Pet.
Ex. 31 at 9. The record of her 12-month pediatric examination notes
that she was using the words “Mom” and “Dad,” pulling herself up, and
cruising. Id. at 10.

At a July 19, 2000 pediatric visit, the pediatrician observed that
CHILD “spoke well” and was “alert and active.” Pet. Ex. 31 at 11.
CHILD’s mother reported that CHILD had regular bowel movements and
slept through the night. Id. At the July 19, 2000 examination, CHILD
received five vaccinations – DTaP, Hib, MMR, Varivax, and IPV. Id. at
2, 11.

According to her mother’s affidavit, CHILD developed a fever of 102.3
degrees two days after her immunizations and was lethargic,
irritable, and cried for long periods of time. Pet. Ex. 2 at 6. She
exhibited intermittent, high-pitched screaming and a decreased
response to stimuli. Id. MOM spoke with the pediatrician, who told
her that CHILD was having a normal reaction to her immunizations. Id.
According to CHILD’s mother, this behavior continued over the next
ten days, and CHILD also began to arch her back when she cried. Id.

On July 31, 2000, CHILD presented to the Pediatric Center with a 101-
102 degree temperature, a diminished appetite, and small red dots on
her chest. Pet. Ex. 31 at 28. The nurse practitioner recorded that
CHILD was extremely irritable and inconsolable. Id. She was diagnosed
with a post-varicella vaccination rash. Id. at 29.

Two months later, on September 26, 2000, CHILD returned to the
Pediatric Center with a temperature of 102 degrees, diarrhea, nasal
discharge, a reduced appetite, and pulling at her left ear. Id. at
29. Two days later, on September 28, 2000, CHILD was again seen at
the Pediatric Center because her diarrhea continued, she was
congested, and her mother reported that CHILD was crying during
urination. Id. at 32. On November 1, 2000, CHILD received bilateral
PE tubes. Id. at 38. On November 13, 2000, a physician at ENT
Associates noted that CHILD was “obviously hearing better” and her
audiogram was normal. Id. at 38. On November 27, 2000, CHILD was seen
at the Pediatric Center with complaints of diarrhea, vomiting,
diminished energy, fever, and a rash on her cheek. Id. at 33. At a
follow-up visit, on December 14, 2000, the doctor noted that CHILD
had a possible speech delay. Id.

CHILD was evaluated at the Howard County Infants and Toddlers
Program, on November 17, 2000, and November 28, 2000, due to concerns
about her language development. Pet. Ex. 19 at 2, 7. The assessment
team observed deficits in CHILD’s communication and social
development. Id. at 6. CHILD’s mother reported that CHILD had become
less responsive to verbal direction in the previous four months and
had lost some language skills. Id. At 2.

On December 21, 2000, CHILD returned to ENT Associates because of an
obstruction in her right ear and fussiness. Pet. Ex. 31 at 39. Dr.
Grace Matesic identified a middle ear effusion and recorded that
CHILD was having some balance issues and not progressing with her
speech. Id. On December 27, 2000, CHILD visited ENT Associates, where
Dr. Grace Matesic observed that CHILD’s left PE tube was obstructed
with crust. Pet. Ex. 14 at 6. The tube was replaced on January 17,
2001. Id.

Dr. Andrew Zimmerman, a pediatric neurologist, evaluated CHILD at the
Kennedy Krieger Children’s Hospital Neurology Clinic (“Krieger
Institute”), on February 8, 2001. Pet. Ex. 25 at 1. Dr. Zimmerman
reported that after CHILD’s immunizations of July 19, 2000,
an “encephalopathy progressed to persistent loss of previously
acquired language, eye contact, and relatedness.” Id. He noted a
disruption in CHILD’s sleep patterns, persistent screaming and
arching, the development of pica to foreign objects, and loose
stools. Id. Dr. Zimmerman observed that CHILD watched the fluorescent
lights repeatedly during the examination and would not make eye
contact. Id. He diagnosed CHILD with “regressive encephalopathy with
features consistent with an autistic spectrum disorder, following
normal development.” Id. At 2. Dr. Zimmerman ordered genetic testing,
a magnetic resonance imaging test (“MRI”), and an
electroencephalogram (“EEG”). Id.

Dr. Zimmerman referred CHILD to the Krieger Institute’s Occupational
Therapy Clinic and the Center for Autism and Related Disorders
(“CARDS”). Pet. Ex. 25 at 40. She was evaluated at the Occupational
Therapy Clinic by Stacey Merenstein, OTR/L, on February 23, 2001. Id.
The evaluation report summarized that CHILD had deficits in “many
areas of sensory processing which decrease[d] her ability to
interpret sensory input and influence[d] her motor performance as a
result.” Id. at 45. CHILD was evaluated by Alice Kau and Kelley Duff,
on May 16, 2001, at CARDS. Pet. Ex. 25 at 17. The clinicians
concluded that CHILD was developmentally delayed and demonstrated
features of autistic disorder. Id. at 22.

CHILD returned to Dr. Zimmerman, on May 17, 2001, for a follow-up
consultation. Pet. Ex. 25 at 4. An overnight EEG, performed on April
6, 2001, showed no seizure discharges. Id. at 16. An MRI, performed
on March 14, 2001, was normal. Pet. Ex. 24 at 16. A G-band test
revealed a normal karyotype. Pet. Ex. 25 at 16. Laboratory studies,
however, strongly indicated an underlying mitochondrial disorder. Id.
at 4.

Dr. Zimmerman referred CHILD for a neurogenetics consultation to
evaluate her abnormal metabolic test results. Pet. Ex. 25 at 8. CHILD
met with Dr. Richard Kelley, a specialist in neurogenetics, on May
22, 2001, at the Krieger Institute. Id. In his assessment, Dr. Kelley
affirmed that CHILD’s history and lab results were consistent
with “an etiologically unexplained metabolic disorder that appear[ed]
to be a common cause of developmental regression.” Id. at 7. He
continued to note that children with biochemical profiles similar to
CHILD’s develop normally until sometime between the first and second
year of life when their metabolic pattern becomes apparent, at which
time they developmentally regress. Id. Dr. Kelley described this
condition as “mitochondrial PPD.” Id.

On October 4, 2001, Dr. John Schoffner, at Horizon Molecular Medicine
in Norcross, Georgia, examined CHILD to assess whether her clinical
manifestations were related to a defect in cellular energetics. Pet.
Ex. 16 at 26. After reviewing her history, Dr. Schoffner agreed that
the previous metabolic testing was “suggestive of a defect in
cellular energetics.” Id. Dr. Schoffner recommended a muscle biopsy,
genetic testing, metabolic testing, and cell culture based testing.
Id. at 36. A CSF organic acids test, on January 8, 2002, displayed an
increased lactate to pyruvate ratio of 28,1 which can be seen in
disorders of mitochondrial oxidative phosphorylation. Id. at 22. A
muscle biopsy test for oxidative phosphorylation disease revealed
abnormal results for Type One and Three. Id. at 3. The most prominent
findings were scattered atrophic myofibers that were mostly type one
oxidative phosphorylation dependent myofibers, mild increase in lipid
in selected myofibers, and occasional myofiber with reduced
cytochrome c oxidase activity. Id. at 7. After reviewing these
laboratory results, Dr. Schoffner diagnosed CHILD with oxidative
phosphorylation disease. Id. at 3. In February 2004, a mitochondrial
DNA (“mtDNA”) point mutation analysis revealed a single nucleotide
change in the 16S ribosomal RNA gene (T2387C). Id. at 11.

CHILD returned to the Krieger Institute, on July 7, 2004, for a
follow-up evaluation with Dr. Zimmerman. Pet. Ex. 57 at 9. He
reported CHILD “had done very well” with treatment for a
mitochondrial dysfunction. Dr. Zimmerman concluded that CHILD would
continue to require services in speech, occupational, physical, and
behavioral therapy. Id.

On April 14, 2006, CHILD was brought by ambulance to Athens Regional
Hospital and developed a tonic seizure en route. Pet. Ex. 10 at 38.
An EEG showed diffuse slowing. Id. At 40. She was diagnosed with
having experienced a prolonged complex partial seizure and
transferred to Scottish Rite Hospital. Id. at 39, 44. She experienced
no more seizures while at Scottish Rite Hospital and was discharged
on the medications Trileptal and Diastal. Id. at 44. A follow-up MRI
of the brain, on June 16, 2006, was normal with evidence of a left
mastoiditis manifested by distortion of the air cells. Id. at 36. An
EEG, performed on August 15, 2006, showed “rhythmic epileptiform
discharges in the right temporal region and then focal slowing during
a witnessed clinical seizure.” Id. At 37. CHILD continues to suffer
from a seizure disorder.

ANALYSIS

Medical personnel at the Division of Vaccine Injury Compensation,
Department of Health and Human Services (DVIC) have reviewed the
facts of this case, as presented by the petition, medical records,
and affidavits. After a thorough review, DVIC has concluded that
compensation is appropriate in this case.

In sum, DVIC has concluded that the facts of this case meet the
statutory criteria for demonstrating that the vaccinations CHILD
received on July 19, 2000, significantly aggravated an underlying
mitochondrial disorder, which predisposed her to deficits in cellular
energy metabolism, and manifested as a regressive encephalopathy with
features of autism spectrum disorder. Therefore, respondent
recommends that compensation be awarded to petitioners in accordance
with 42 U.S.C. § 300aa-11(c)(1)(C)(ii).

DVIC has concluded that CHILD’s complex partial seizure disorder,
with an onset of almost six years after her July 19, 2000
vaccinations, is not related to a vaccine-injury.

Respectfully submitted,

PETER D. KEISLER
Assistant Attorney General

TIMOTHY P. GARREN
Director
Torts Branch, Civil Division

MARK W. ROGERS
Deputy Director
Torts Branch, Civil Division

VINCENT J. MATANOSKI
Assistant Director
Torts Branch, Civil Division

s/ Linda S. Renzi by s/ Lynn E. Ricciardella
LINDA S. RENZI
Senior Trial Counsel
Torts Branch, Civil Division
U.S. Department of Justice
P.O. Box 146
Benjamin Franklin Station
Washington, D.C. 20044
(202) 616-4133

DATE: November 9, 2007

PS: On Friday, February 22, HHS conceded that this child’s complex
partial seizure disorder was also caused by her vaccines. Now we the
taxpayers will award this family compensation to finance her seizure
medication. Surely ALL decent people can agree that is a good thing.

By the way, it”s worth noting that her seizures did not begin until
six years after the date of vaccination, yet the government
acknowledges they were, indeed, linked to the immunizations of July,
2000, – David Kirby

Now I am going to prove to you, BEYOND A SHADOW OF A DOUBT, that
mercury is a distraction in the case of autism:

Please go to http://healthtruthrevealed.com/audio-interviews.php,
click on “inoculations the true weapons of mass destruction”, and
listen to the interview I did on this very subject on 3/4/08. You
will hear Greg Ciola mention research done at the University of
Calgary regarding mercury’s effect on brain neurons, and I thank him
for sending me a link to this information. He also mentions an
interview he did with John Moore, a researcher in the dangers of
mercury who himself was severely injured by mercury poisoning due to
multiple amalgam fillings. His interview is posted at
http://healthtruthrevealed.com/full-page.php?id=39&&page=news. You
will read on page 16 that Mr. Moore states that the research done at
the University of Calgary shows “the myelin sheathing simply stripped
away from the nerve”.

Now, go to http://www.youtube.com/watch?v=85tgwh3HpsM; this is
CRITICAL. You will hear and see the effect of mercury on brain
neurons demonstrated by the University of Calgary which Mr. Moore
refers to. Mercury causes DEATH of the nerve’s axon, as the actin &
tubulin which make up the neurofibrils are destroyed when mercury
binds to the tubulin molecules, causing the neurofibril to collapse,
and some neurofibrils form aggregates or tangles. THIS IS THE KEY
DIAGNOSTIC FEATURE SEEN IN ALZHEIMER’S DISEASE; NOT AUTISM! You will
also notice that these neurons in a culture dish do not have myelin
on then; in fact, THE MYELIN SHEATH IS NOT EVEN MENTIONED IN THIS
VIDEO. (Side note – when the brains of Alzheimer’s patients are
studied microscopically, ALUMINUM is found in the middle of these
neurofibrillary tangles).

I also encourage you to go to http://video.google.com/videoplay?
docid=1803137818942286763, and hear Dr Boyd Haley discuss autism &
thimerosol (be sure to watch all 4 videos in this series). Dr Haley
blames thimerosol for Gulf War Syndrome (GWS) as well as autism. I
have done many shows on GWS, which has many factors; Gulf War PLAGUE
(the infectious component of the SYNDROME) is due to mycoplasma
incognitas which was in the vaccines given to the soldiers. As
explained in my document “Inoculation the true weapons of mass
destruction” at www.drcarley.com, the injection of vaccines corrupts
the immune system and prevents any infective agent from being
eliminated from the body. GWS has many other aspects to it; depleted
uranium, pyridostigmine pills given to the soldiers, aspartame in
their beverages, etc. To blame thimerosol solely for GWS is
disinformation in its highest form.

Dr. Haley brings up the work of Dr Andrew Wakefield, whose medical
license was attacked because he demonstrated measles virus in the
lymphoid patches in the guts of autistic children. DR. BOYD ADMITS
HE DID NOT EVEN STUDY THE MEASLES VIRUS. Although Dr Wakefield did
not realize that these viruses’ significance as a chronic infection
is that this leads to a constant production of anti-measles antibody
which, through molecular mimicry, then attackes the myelin sheath
(causing demyelination), he was attacked because his work supports my
work; especially since the MMR has NEVER HAD MERCURY. Dr. Haley’s
work reinforces the notion that if you take mercury out of vaccines,
they will be safe. My work proves there is NO SUCH THING as a safe
vaccine, due to the corruption of the immune system caused by
injection of live viruses.

Dr. Haley also discusses how antibiotics further accelerate the
damage in these children. The question he does not address is why
are the vaccinated children on antibiotics? Answer…because they
have chronic infection caused by inoculation of live viruses; as
quoted from Harrison’s principles of medicine in my response to the
CDC (also on my website), “RARELY IS PREVENTION OF INFECTION PER SE
CONSIDERED TO BE AN IMPORTANT GOAL OF VACCINATION. In fact,
asymptomatic infection after vaccination can serve to enhance and
prolong the immune response”. (And this prolonged immune response IS
prolonged production of anti-measles antibody which then continue to
attack the myelin sheath, causing demyelination). As I also quote
from Harrison’s in my CDC response the symptoms of subacute
sclerosing panencephalitis (SSPE), you will see that autism is a non-
fatal form of SSPE. The way Dr. Haley gets around the fact that
almost every parent reports their child descended into autism
following their MMR shot is by saying that the children received
OTHER vaccines containing mercury at the same time as they received
the MMR.

Dr. Haley also discusses how mercury is more toxic in children with
immune disorders. Where did these immune disorders come from? From
the corruption of the immune system caused by the inoculation of live
viruses. He also discusses that mercury can cause toxicity which
affects genetics by decreased methylation of DNA & RNA. However, no
mention is made of the genetic mutations caused by injection of
plasmids of DNA from the organisms themselves and the tissues that
the viruses are cultured on, which is the whole basis of DNA
vaccines. That is why this court case focuses on the fact that the
child had a genetic defect which caused mitochondrial dysfunction.
Where this defect originated is not discussed…injection of foreign
DNA in prior vaccines (You will note in the court decision that the
parents were not tested for this defect, as that would have proven
that this is NOT an inherited genetic defect, but rather a mutation
that occurred in this child de novo).

Lastly, Dr. also states that oral vaccines would be safer, but does
not say this is because of the secretory IgA causing proper handling
of the antigen (as also explained in my inoculation paper), leading
to life long NATURAL immunity. Of course, if all vaccines were made
into oral forms, people may then ask the hard question…SO WHY ISN’T
NATURAL EXPOSURE TO THESE VIRUSES THE BEST WAY TO GO? This question
would stop vaccine production altogether, which would stop the
creation of all autoimmune diseases and cancer, which would shut down
Big Pharma. THAT IS THE POTENTIAL OF MY INFORMATION; which is why
the medical mafia has gone as far as taking my only child, not just
my medical license as they tried with Dr. Wakefield in an attempt to
shut me down.

Can you handle knowing the fact that all this is being done to the
children ON PURPOSE? Then gohere
and listen to the 2nd hour of my interview on 3/5/08 with Dr. True
Ott, where he discusses how the history of MediSIN goes back to the
1600’s as detailed in the Magnum Opus, with the creation of amulets
by sacrificing animals and mixing their blood with mercurial
compounds TO CAST A SPELL AND CONTROL THE MINDS OF THE POPULATIONS
(Dr Ott discusses this starting at 13 minutes of the 2nd hour of our
interview). He explains how the origins of the word “pharmaceutical”
in Latin is “pharmakia”, which translates to “SORCERY”. Yes,
folks…you have now entered the rabbit hole…because nothing has
changed since the 1600’s.

I have been trying for 10 years to stop the vaccination holocaust on
people and pets. I have proven, with the quoted studies and works of
the “mercury causes autism” disinformers themselves, that it is NOT
MERCURY WHICH CAUSES AUTISM. I leave it up to you to forward this e-
mail to all the individuals and groups which promote mercury as the
cause of autism, so you will see for YOURSELVES who is intentionally
misleading you, vs. who was misguided. You will know which is the
case by whether or not they respond. SILENCE IS CONSENT that I am
right; and if they do not join with me to stop this holocaust
altogether, you must then ask yourself WHY. IT IS TIME FOR THOSE
WITH HONORABLE INTENTIONS TO JOIN WITH ME TO STOP THIS EPIDEMIC OF
VIDS. Let’s roll….

Namaste,
Dr Carley

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