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Seawater – A Safe Blood Plasma Substitute?
Diluted seawater contains almost the same concentration of minerals
and trace elements as blood plasma, and its sodium content matches
that of blood. It has been used successfully in animal tests as a
blood transfusion substitute, but human trials are long overdue.
Extracted from Nexus Magazine, Volume 13, Number 6 (October - November
2006) PO Box 30, Mapleton Qld 4560 Australia. editor@nexusmagazine.com
Telephone: +61 (0)7 5442 9280; Fax: +61 (0)7 5442 9381 From our web
page at: www.nexusmagazine.com
© 2006 by Dianne Jacobs Thompson Email: t_ospeaks@yahoo.com From the
web page: http://www.truthquest2.com/oceanplasma.htm
My long-time fear of having a blood transfusion or anything else
injected directly into my unprotected bloodstream has grown stronger
over the years. It's not a religious issue, but rather an occupational
hazard. Being a health researcher, I'm haunted by terrible visions of
what could go wrong—with good reason. I feel like the meat inspector
who becomes a vegetarian. I know things that forever destroyed my
innocent faith in all things medical. I no longer worship in "the
Church of Modern Medicine", nor tithe to its pseudo-gods voluntarily.
"They", the health (read disease) industry specialists, check blood
better these days to catch unsafe blood supplies contaminated with
HIV, hepatitis and other disease components, but blood products still
aren't completely safe, even with modern technology. They can't
sterilise blood any more than they can sterilise vaccines to kill all
the unwanted "bugs" without destroying the nature of these products.
They test blood and separate blood components through centrifugal
action and other methods to purify these substances as much as
possible, but it remains impossible for them to promise or deliver a
completely safe blood-related product. Blood is "alive": it cannot be
sterilised or rendered antiseptic. There are countless transfusion
horror stories dating back many decades, but we rarely ever hear about
them. For example, a neighbour down the street lost her husband about
four years ago. He had cancer, but became infected with viral
hepatitis from a blood transfusion and died from liver failure, not
the cancer. Many people know someone who suffered from the effects of
a blood transfusion gone bad. That's just a fact of life and one of
the known risks of surgery, no matter how minor.
Dangers Lurking in Vaccines Unfortunately, I've run across too many
stories of this nature. I've spent most of my adult life doing
research and writing in the field of alternative medicine
(www.truthquest2.com) with an early focus on viral and bacterial
diseases and problem vaccines, some of which are still made from
pooled human blood products or with "attenuated" vaccine viruses
created by "serial passage" through contaminated animal cell cultures.
That means they take human viruses and put them in layers of animal
cells over and over again, which forces them to adapt to the foreign
cells to survive. This "adaptation" requires an exchange of genetic
material between virus and host cells. When monkey kidney cells are
used, the exchange of genetic material that takes place forces the
human virus to become a little bit "monkey-like", supposedly so that
it cannot initiate full-blown disease—which doesn't always work. In
the process, native monkey viruses become a little bit "human-like",
giving them greater compatibility with human cells. Such may be the
case with the infamous Epstein–Barr virus, which is referred to as
"human"—although many scientists believe it originated in monkeys,
went on to infect humans through contaminated vaccines in mutated form
and then became associated with chronic fatigue syndrome and other
maladies. But then, there is less of a species barrier with monkeys
than with other animals, which gives us less protection from their
pathogens. The bio-hazards of monkey viruses are well known in certain
scientific circles, but little known by the general public. In the
course of my research, I came to study the subject of recombinant
virology: the combining of unlike viruses into new "tribes", usually
with more dangerous characteristics than the "parent" viruses, by men
in white coats playing God. Recombination events can also happen in
nature under certain conditions, particularly when helped along by bad
science. For example, a monkey virus called SV-40 (simian virus 40,
after becoming the 40th virus found in monkey tissues) was found to
have unique properties. This "naked virus" can penetrate any kind of
cell without the problem of a "species barrier", and it allows unlike
viruses to attach to it and ride piggyback into the genetic material
of a cell where they can take over the "machinery" and replicate new
recombined viruses on their own. The discovery of this virus gave rise
to the field of recombinant virology, with many dire consequences.
SV-40 became a well-documented but unpublicised contaminant in polio
vaccines (made with the use of monkey kidney-cell cultures) when it
was given in 1955 to 1963 to 95 million unsuspecting recipients. The
first official claim was that SV-40 viruses "do not have any
significance in the safety or efficacy of polio vaccines"; but when
the virus was first tested on guinea pigs after its discovery, the
animals developed salivary gland tumours and immune deficiency
symptoms. The corresponding organ in humans is the pancreas. Deadly
pancreatic cancer has since become epidemic in numbers. SV-40 is now
associated with numerous cancers, including human mesotheliomas,
ostoeosarcomas, brain tumours, ependymomas, choroid plexus tumours and
others. These same monkey cell cultures, used to make vaccines,
contained other viruses such as SIV (simian immuno-deficiency virus),
which figures prominently in the make-up of another recombinant virus
that we know as HIV. There's no proof offered publicly as to whether
HIV resulted from a naturally occurring recombination event, but the
sophistication of this virus and some documented government requests
for the creation of a similar biological weapon suggest otherwise.
However, a study generated at the request of the World Health
Organization (WHO) and then suppressed, linking African AIDS to the
WHO vaccination campaigns against smallpox, polio and other diseases,
theorised that viral vaccines "activated" dormant viruses, so this is
a possibility supporting natural recombination—unless HIV was
intentionally added to certain vaccines. The London Times printed this
story on May 11, 1986, but the story was withheld from the American
media. This kind of information seldom reaches the general public in
my country. The same thing happened when one of the most horrific
scientific "errors" ever made was hushed up. It involved "HeLa
cells"—the most aggressive cancer cell cultures ever known—which made
their way into science labs all over the world for research and then
contaminated many cell cultures used for vaccines…by accident. Think
about human vaccine viruses being grown in cancer cells and exchanging
genetic information with the cancerous host cells before being
injected into millions of unsuspecting victims!
Problems with blood transfusions That's just part of what a person
potentially faces when receiving blood from another person or persons
with undetected infection. Sam Biser, a researcher in the field of
alternative medicine, interviewed Dr William Donald Kelly, DDS, MS,
who related a conversation with Drs Friedman and Burton from the
former Immunological Center in Great Neck, New York. Their research
reportedly suggested that a blood transfusion may destroy your
resistance to cancer. Dr Burton believed, as many religious groups do,
that blood transfusions can cause cancer, in a manner of speaking. Dr
Burton claimed that a tumour, in order to survive, secretes compounds
called "blocking factors" which protect it from the natural defence
system of the body. He believed that a transfusion would result in
these blocking factors from a donor being passed on, able to suppress
the recipient's own immune system enough to allow a tumour to develop.
That new tumour would in turn create its own blocking factors. Cancer
wouldn't be transmitted directly, but, in this way, a blood
transfusion may increase one's susceptibility to cancer. While
possible "blocking factors" and contamination from human and animal
microbes in blood supplies worry me somewhat, there are other factors
that keep me awake at night… Someone I knew in college just happened
to mention in passing that a blood transfusion changed his life. He
described coming out of surgery after an accident and waking up with a
changed personality. He blamed his condition on the blood transfusion
he was given. Since I only knew him after this event, I can't say
whether the change was good or bad, but who wants something like that
to happen while under anaesthesia? But something far worse than a
personality change affected my opinion in 1981. That year, in Alaska,
I gave birth to my only child—a much anticipated arrival by me at age
34 and by the baby's godmother, Ceci Clark, an artist and gallery
owner of some renown in that State. Ceci developed bone cancer, which
wasn't diagnosed immediately. Before they found it, she had surgery
for something else and was given a blood transfusion. When she woke
up, her "brains" were scrambled, so to speak. She recognised me but
thought I was her sister, and she grew confused trying to figure out
where that newborn baby had come from. They eventually found the
cancer. She died soon after.
The Marine Treatment In the ensuing years, my research turned to
alternative cancer treatments and remedies for chronic degenerative
disease, particularly after my becoming desperately ill and having my
health, and that of other family members, restored without drugs or
surgery by an unusual naturopathic physician in Spokane, Washington:
the late Dr Harold Dick, ND. His extraordinary diagnostic and healing
skills were passed on and added to by his daughter, Dr Letitia Dick-Watrous,
ND, who completed a three-year residency with him, became his partner
and then took over his practice after his death. Dr Dick not only
turned my health around with a little-known diagnostic "tool" and an
updated treatment modality with roots in the old "water cure" of
Germany's famous Father Sebastian Kneipp, the O. G. Carroll Food
Intolerance Test and constitutional hydrotherapy, but mentored me and
lit a research fire in my belly that won't go out—and Dr Dick-Watrous
fanned the flames. In the course of researching natural healing
methods, I joined a membership website that featured little-known
alternative treatments for cancer and infection. These included "the
Marine Treatment", based on the work of French biologist/physiologist
René Quinton. He proved that seawater, properly formulated and under
certain conditions, is virtually identical to mammalian blood plasma.
With the assistance of many eminent physicians, he successfully used
seawater as a healing agent on thousands of patients in France and
Egypt in the early 1900s. Cancer was almost unknown in those days, but
many other disease conditions responded to injections of the diluted
ocean water—a true "marine plasma" which could remineralise a sick
body, normalise the pH (acid–alkali) level and balance the
electrolytes, thereby correcting the underlying cause of many disease
conditions by regenerating the "internal terrain", as Quinton called
it. The report included before-and-after photos of patients. Like most
people, I was drawn to the shocking 100-year-old photos first, and the
science came in a distant second. Babies brought back from near death
from cholera and other causes; cadaver-like bodies filled out to
healthy plumpness; raw, weeping skin from eczema made smooth and
lesion free…all by the power of seawater. Many early-20th-century
scourges such as tuberculosis were shown to be healed by this
remarkable marine plasma. Historically, ocean water (plasma) has had
numerous applications, based on the concept of renewing, purifying and
regenerating the internal fluid terrain as well as maintaining the
equilibrium of the body. It has proved to be a support for and
regenerator of cell functions. How important is the mineral and trace
mineral balance in the body? Many researchers, including Dr Joel
Wallach, author of the best-selling audiotape Dead Doctors Don't Lie,
claim that the absence of one single mineral needed by the body can
give rise to as many as 10 different disease symptoms. Of course, much
of modern medicine still blames germs and genetics for most human
disease, so the "mineral deficiency" theory is generally ignored. But
Dr Wallach believes that a common heart condition, cardiomyopathy—a
condition which has killed countless victims from professional
athletes to heart specialists, or made them candidates for heart
transplants—is caused by nothing more than a deficiency of the trace
mineral selenium, which can be cured or prevented by a few cents'
worth of selenium supplements a day. Enter seawater—the missing link
in deficient elemental nutrition! It contains every mineral and trace
mineral known, in organic form and in the proper ratios needed by
human tissues—and it's been there all along as a healing and
life-giving agent, hidden in plain sight. While the website where I
first found the Marine Treatment information had a good report and
impressive photos, a more complete website on the subject was under
construction. There, on his academic www.oceanplasma.org website, I
discovered that Dr Juergen Buche, ND, was in the process of
translating a large body of ocean-water research and supporting
documentation from the original French into English. What I found on
that site hit so close to home that I'm still reeling! My eye caught
something that resonated with my transfusion phobia. It turns out that
trials were run on stray dogs to test ocean plasma (diluted,
cold-filtered ocean water) as a transfusion substitute. In one
experiment, René Quinton and his medical team drained a dog of all of
its blood and replaced it with isotonic (diluted) seawater. The dog
should have died immediately, one would think, but the dog lived. On
day two after the transfusion, 50 per cent of the blood components had
reappeared. By day four, almost 100 per cent of the missing blood
components were restored in what appeared to be proof of biological
transmutation (a change from one element to another). Not only did the
blood completely regenerate, but soon after the procedure the dog
bounced around like a puppy with greater vitality than before, and it
lived for many years afterwards. Just think what a safe, effective,
plentiful substitute for blood transfusion would mean to the world: no
side effects, no blood-type matching needed, no pathogen screening
required, and it would be a true plasma with proven healing properties
in itself! So, what became of this wondrous marine treatment? World
War I got in the way of medical research, and Quinton was drafted. He
died in 1925. These events somewhat interrupted the continuance of
Marine Treatment hospitals and clinics, of which there were many.
However, the treatment was carried on by his medical co-workers and
ardent followers, and it experienced a resurgence after World War II
in several countries. Animal trials using seawater as a transfusion
substitute were repeated with the same results in 1969; but since then
the "marine treatment" has been used as a therapeutic agent on people,
mostly as a foundational treatment for chronic degenerative disease.
Also, it became known as a complete and readily assimilated liquid
mineral and trace mineral supplement for remineralisation, for
detoxification, for energy and for relieving stress. No human trials
for transfusion have ever been attempted. As for the healing
properties of seawater, in today's restrictive medical atmosphere
seawater can only be referred to as a "mineral drink". If the word
"cure" were uttered or written in relation to a brand name, the
"offence" would be legally actionable. Only a drug, toxic by its very
nature, can be called "curative". No FDA-sanctioned studies will be
funded or reported on the efficacy of seawater treatment for disease
because a supplement can be studied only in relation to its disease
"risk reduction" factor as defined by the government agency, and not
as a treatment for actual disease. Why haven't we heard of René
Quinton and his marine treatment?
A Sick Health System The USA has the worst national health of any
industrialised country in the world—in spite of spending the most
money on health research and health care. This country lags sadly
behind in many areas of medical science, particularly when those who
profit from bad science are called to arms for their own protection by
safer, more effective and less expensive remedies and methods such as
Quinton's modest but living ocean water. Look at the international
pharmaceutical industry. It has such wealth and power that it controls
not only the FDA but American health-related legislation and policies.
Take, for example, the case of the "cholesterol" caper. In the past,
the federal guidelines for managing cholesterol were this: someone
with 300 mg of dietary cholesterol per day, with an HDL (good
cholesterol) level of 35 mg per decilitre (dL) in the blood, was
considered to have unacceptable levels and be in need of treatment.
However, under the "guidance" of the powerful pharmaceutical industry,
those federal guidelines were recently changed. Now, less than 200 mg
of dietary cholesterol per day is considered "acceptable" and an HDL
(good cholesterol) level of anything less than 40 mg/dL is now
unacceptable (JAMA 2001; 285:2486-2497). To translate: under the old
guidelines, 13 million people were pushed into using
cholesterol-lowering drugs; under the new guidelines, 36 million
people are now buying those drugs, and that means billions of dollars
of additional revenue going to the pharmaceutical companies. At the
same time, these drug manufacturers have been particularly hesitant to
publish anything about the effects of drug-induced low cholesterol,
which can include depression, violent behaviour, suicide, aggression,
increased risk of stroke and poor immune system function according to
certain studies. It looks like we're being brainwashed by some kind of
drug mythology into believing that diseases are caused by a drug
deficiency and that they can only be cured by increased and expensive
drug consumption. What would happen to these international drug
cartels if an actual cure for cancer suddenly came on the market
outside of their control? Since they exist financially only for the
"treatment of symptoms" (disease management) rather than for curing
anything, it is possible that our entire financial/ medical
infrastructure might collapse as a consequence. The stockholders of
pharmaceutical companies want profits, not a cure to end human misery
and stop the flow of profits. We hear similar stories about fossil
fuel substitutes and other life-altering discoveries and inventions
that have never made it to the open market due to intervention by the
competition. Likewise, a safe blood transfusion substitute might
threaten too many rich and powerful areas of the medical market to
ever see the light of day…but one can visualise the possibilities.
However, "Vision without action is only a dream," according to Dr
Buche. Consider this article the start of action—maybe your action!
Harvesting the Living Solution Seawater can be ingested orally or can
be injected. However, harvesting seawater for consumption is not easy;
it requires knowledge, care and the right equipment. Seawater differs
in composition and can't be harvested randomly. Its make-up varies
according to the distance from the coastline, the climate and the
marine vegetation. During the entire process from ocean to bottle, the
seawater cannot touch metal; it must be kept cold, because heating
kills the invigorating living properties of seawater. It has to be
transported and kept in glass or food-grade plastic containers. Then
it has to be tested and cold-purified in a manner that protects it
from alteration and preserves its state as a living solution. (For
more details about seawater harvesting, see web page
http://www.truthquest2.com/oceanplasma.htm.) Seawater in its original
and primal state had only one-third the saline content it has now, and
this fact is still mirrored in the saline content of blood and tears.
The oceans have become more concentrated through the ages, and their
waters are now far too salty to drink in large amounts. To use ocean
water as blood plasma, it must be diluted with ultra-pure water to the
same concentration as blood plasma: namely, nine grams of salts per
litre. As the perfect mineral supplement, it can be consumed orally in
dilute form or full strength by those with no sodium sensitivities—but
only in small amounts, like an ounce [0.03 litres] at a time, several
times a day if necessary. However, it's extremely important to dilute
it with pure spring water for home use, because chlorinated water has
the same kind of damaging effect on ocean water as it has on the human
body according to several studies. The French got it right: they
ozonate their drinking water instead of adding (cheaper) bleach to it.
The exact properties of seawater remain a mystery to modern science.
In spite of our great technical expertise, the complete nature of
seawater defies analysis. It has some living quality beyond the sum of
its parts. It can't be dried and reconstituted or synthesised in a
chemistry lab. The great French scientist Antoine Béchamp looked at
blood as a kind of flowing tissue rather than just a liquid. Seawater
also has something about it that makes it more than "just water". It
sustains life, as proved by Nobel laureate Alexis Carroll who kept a
piece of chicken heart tissue alive in it for over 26 years, needing
only to change it daily to dispose of metabolic wastes. In fact, one
could actually say that we have internalised the ocean within
ourselves and that this nutrient-rich medium is the source of life.
Every cell in the body bathes and feeds in it. It picks up and carries
away the waste products of cell metabolism. It has a life force—unlike
the saline solution seen in familiar bags in every hospital, which is
nothing more than a solution of table salt and plain water. Processed
table salt bears little resemblance to the raw, unprocessed,
mineral-rich sea salt that we should be using, and our depleted bodies
suffer the consequences. If I had to have surgery, I'd want to see
"ocean plasma" in a drip bag above my head before the lights went out.
The world needs someone with courage and vision, willing to initiate
the first human trials of seawater transfusion; the world needs
someone to extend René Quinton's animal trials and to make that leap
into the future that signals true progress. ?
About the Author: Dianne Jacobs Thompson is a graduate of what is now
Western Washington State University with a degree in art in 1976,
after which she gained teaching credentials in art with a journalism
endorsement from Central Washington State University. She has taught
public school part time on and off for the last two decades and since
1981 has been doing research and writing about alternative medicine.
Most of the articles and reports were too controversial in
nature—usually dealing with the dangers of conventional medicine as
well as healing alternatives—to have been published in the past, but
the Internet has removed countless roadblocks that previously kept
such information from being made public in the mainstream media and
has allowed many such travellers access to the "information
superhighway". Dianne's website is at http://www.truthquest2.com. She
can be contacted by email at t_ospeaks@yahoo.com.
References: Alphabetical
1.Attkisson, Sharyl. Bad Blood Transfusion? CBS Evening News.
WASHINGTON, May 7, 2004. CBS Broadcasting Inc. http://www.cbsnews.com/stories/2004/05/07/eveningnews/main616279.shtml
2.Baskin, G.B. & E.D. Roberts, D. Kuebler, L.N. Martin, B. Blauw, J.
Heeney, C. Zurcher. Squamous epithelial proliferative lesions
associated with rhesus Epstein-Barr virus in simian immunodeficiency
virus-infected rhesus monkeys. J Infect Dis. Aug. 1995;172(2):535-9.
Department of Pathology, Tulane Regional Primate Research Center,
Tulane University, Covington, Louisiana 70433, USA. <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=7622899&dopt=Citation>
3.Better Blood: Heart of America Radio reports on a new technology is
being developed to kill viruses in donated blood. ACFNewsSource. Heart
of America Radio: A Project of ACF. December 10, 2005 <http://www.acfnewsource.org/science/better_blood.html>
4.Bizer, Sam. Cancer Signs: An Interview With Dr. William Donald
Kelly, D.D.S., M.S. (no longer available online) <http://www.sambiser.com/>
5.Blood transfusions or injections of factors from pooled-human blood.
<http://www.tuberose.com/Vaccinations.html>
6.Bloodbook.com: Information For Life. November 10, 2004 <http://www.bloodbook.com/>
7.Buche, N.D., Juergen. Private correspondence 2006
8.Buche, N.D., Juergen. Seawater. 2006 <http://www.oceanplasma.org>
9.Buttram, M.D., Harold E. "Live Virus Vaccines and Genetic Mutation."
Health Consciousness April, 1990
10.Cancer Strategy #7: Toxins (Including GMOs And Chlorine) Underlying
Cancer Cause... Reducing Toxic Overload Vital For Successfully
Fighting Cancer. <http://www.cancer-prevention.net/?engine=adwords!800&keyword=%2Acancer%2A&match_type=>
11.Cantwell, Jr., M.D., Alan. Are Vaccines Causing More Disease Than
They Are Curing? 1999 <http://www.whale.to/v/cantwell.html>
12.Cantwell, Jr., M.D., Alan. Are Vaccines Causing More Disease Than
They are Curing? New Dawn Magazine: A Journal of Alternative News &
Information. New Dawn No. 63 (November-December 2000). <http://www.newdawnmagazine.com/Articles/Vaccine_Genocide.html>
13.Cantwell, Jr., M.D., Alan. Dr. Alan Cantwell. M.D. quotes. <http://www.whale.to/m/cantwell9.html>
14.Carper, Jean. "The Race Against Rubella" The World Book Year Book.
A Review of the Events of 1969. 1970:104. Field Enterprises
Educational Corporation
15.Carlsen,William. Rogue virus in the vaccine: Early polio vaccine
harbored virus now feared to cause cancer in humans. San Francisco
Chronicle. <http://www.sfgate.com/cgi-bin/article.cgi?file=/chronicle/archive/2001/07/15
/MN193825.DTL> July 15, 2001. reprint <http://www.vaccinetruth.org/sv40.htm>
16.Caspari, Gregor. "Are inactivation procedures for blood products
good or bad?" BMJ. 2002 November 9; 325(7372): 1116. Head, transfusion
unit Institut für Transfusionsmedizin, 14770 Brandenburg an der Havel,
Germany
17.Cavanagh, Tom. Research Manager, Boehringer Mannheim. Cell Biology
(Re: Where can I find out more about HeLa cells?). April 7, 1997.
<http://www.madsci.org/posts/archives/may97/860431113.Cb.r.html>
18.DELALANDE Medical Research Center (France) under the directorship
of Dr. B. Pourrias and Dr. G. Raynod. EXPERIMENT ON A DOG WITH OCEAN
(Quinton) PLASMA DURING A STAGE OF HEMORRHAGIC SHOCK. May 1969
<http://oceanplasma.org> 2006
19.FRANKEN, MICHAEL,1, ODILE DEVERGNE,1,2, MICHAEL ROSENZWEIG,3,
BETHANY ANNIS,1, ELLIOTT KIEFF,1,2, & FRED WANG,1. "Comparative
Analysis Identifies Conserved Tumour Necrosis Factor
Receptor-Associated Factor 3 Binding Sites in the Human and Simian
Epstein-Barr Virus Oncogene LMP1." JOURNAL OF VIROLOGY, Vol. 70, No.
11. Nov. 1996: 7819–7826. American Society for Microbiology Department
of Medicine, Brigham & Women’s Hospital-1 and Department of
Microbiology and Molecular Genetics, Harvard Medical School-2 Boston,
Massachusetts 02115, and Department of Immunology, New England
Regional Primate Research Center-3, Southborough, Massachusetts 017723
20.Gillon, Raanan. A startling 19,000-word thesis on the origin of
AIDS: should the JME have published it? Editorial. Imperial College
Health Service and St Mary's Hospital Medical School, London
University Journal of Medical Ethics, 1992, Volume 18: 3-4. BMJ
Publishing Group. <http://www.uow.edu.au/arts/sts/bmartin/dissent/documents/AIDS/JME92.html>
21.Giradi, A.J., F. Jensen, & H. Koprowski. "SV40-induced
transformation of human diploid cells: crisis and recovery." J. cell.
comp. Physiol. 65, 1965: 69-83
22.Gold, Michael. Conspiracy of Cells: One Woman's Immortal Legacy-And
the Medical Scandal It Caused. State University of New York Press,
Albany, NY 12246, 1986
23.Hecht, Jeff. Chimps are human, gene study implies. NewScientist.com
news service. May 19, 2003. Journal reference: Proceedings of the
National Academy of Sciences (DOI: 10.1073/pnas.1232172100) <http://www.newscientist.com/article.ns?id=dn3744>
24.Ho, Dr., Mae-Wan. AIDS-Vaccines Trials Dangerous. ISIS Report
(Institute of Science in Society). July 29, 2001 <http://www.i-sis.org.uk/AIDS_virus.php>
November, 2005
25.Horvath, B.L. & F. Fornosi. "Excretion of SV-40 virus after oral
administration of contaminated polio vaccine." Acta Microbiologica
Scientaria Hungary. Vol. 11:271-5, 1964-65
26.JARRICOT, Dr. Jean. Le dispensaire Marin. Ed. Mason 1921 (out of
print)
27.JARRICOT, Dr. Jean - Practice and Results of the Quinton Marine
Method in Cases of Infantile Athrepsia and Cholera - Extrait de la
"CURE MARINE" Revue Internationale de Thalassothérapie - année 1938,
No. 1., Imp. Graphica, Rue des Pelletiers, 16, Bruges, Imprimé en
Belgique Translated from the French by the Ocean Plasma Team
28.Kalter, S.S., & R.L. Heberling. Biohazards and simian viruses. Bibl
Haematol. 1975;(40):759-69 <http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=169837&dopt=Citation>
29.Maiden, M.C. "Population genetics of a transformable bacterium: the
influence of horizontal genetic exchange on the biology of Neisseria
meningitidis." FEMS Microbiol Lett. Sept.15,1993;112(3):243-50
Division of Bacteriology, National Institute for Biological Standards
and Control, South Mimms, UK.
30.Martin, Jamie. Experts Cite Health Clinics as Source of HIV/AIDS in
Africa (Potentially high infection rate is "preventable"). Washington
File Staff Writer. August 1, 2003 <http://usinfo.org/wf-archive/2003/030801/epf512.htm>
31.McRearden, Bengamin. What's Coming Through That Needle? The Problem
of Pathogenic Vaccine Contamination. <http://www.newmediaexplorer.org/chris/vaccine_contamination_mcrearden.pdf>
32."New storm over polio vaccine?: Research detects 'strange viruses'
causing animal cancer in monkey kidneys like those used in making Salk
vaccine; there's no link to man but scientists are uneasy." Business
Week June 17th, 1961: 27
33.Nullis, Clare. German scandal stokes AIDS fears; Tainted blood
imperils third world. San Francisco Chronicle November 6, 1993
Associated Press <http://ww2.aegis.org/news/ap/1993/AP931102.html >
34.O'Malley, Jaclyn. Hep C from transfusion: "Strong will, sense of
humor keep Reno mother going after 10 years waiting for liver
transplant" RENO-GAZETTE JOURNAL Nov. 7, 2005
35.Outbreak: some other examples of cross-species virus transmission.
PBS Organ Farm Frontline.1995-2005 wgbh educational foundation.
<http://www.pbs.org/wgbh/pages/frontline/shows/organfarm/risks/outbreak.html>
36.Parsons, Vic. Book Review: Bad Blood: Tainted Blood Scandal (Bad
Blood: The Tragedy of the Canadian Tainted Blood Scandal). Author E.
KAYE FULTON. The Canadian Encyclopedia. Maclean's June 26, 1995
<http://www.thecanadianencyclopedia.com/index.cfm?PgNm=TCE&Params=M1ARTM0010440>
37.Pastian, Timothy. 8-3 DNA transfer by conjugation. Microbiology and
Bacteriology: The world of microbes. 1999-2006 <http://www.bact.wisc.edu/Microtextbook/index.php?module=Book&func=displayarticle&art_id=128>
November, 2005
38.Peters, W.P., "Biological and biochemical evidence for an
intereaction between Marek's disease, herpes virus and avian leukosis
virus in vitro." Proc. Nat. Acad. Sci. (Wash.) 70, 1973: 3175-3178
39.Pingel, Sabine 1, and Horst Hannig 1, Kerstin Mätz-Rensing 2,
Franz-Josef Kaup 2, Gerhard Hunsmann 1, Walter Bodemer 1 *
1-Department of Virology/Immunology, German Primate Center, Göttingen,
Germany
2-Department of Experimental Pathology, German Primate Center,
Göttingen, Germany. Detection of Epstein-Barr virus small RNAs EBER1
and EBER2 in lymphomas of SIV-infected rhesus monkeys by in situ
hybridization. International Journal of Cancer. Volume 72, Issue 1:
160-165. December 1998. John Wiley & Sons, Inc.
<http://www3.interscience.wiley.com/cgi-bin/abstract/41933/ABSTRACT?CRETRY=1&SRETRY=0>
40.Polio. Thinktwice: Global Vaccine Institute, New Atlantean Press
1986.<http://www.thinktwice.com/s_polio.htm> November, 2005
41.PRECAUTIONARY MEASURES ANNOUNCED FOR BLOOD PRODUCTS. The Scottish
Office, Press Release. February 26, 1998 <http://www.scotland.gov.uk/news/releas98/pr0382.htm>
42.QUINTON, René. L'eau de Mer milieu organique (1912: Ed. Masson)
Reprinted: Ed. ENCRE 1995
43.QUINTON, René & Dr. Robert SIMON. Seawater: injected subcutaneously
in the treatment of pulmonary tuberculosis. Paris, Éditions de la
Revue des Idées 1906 Translated from the French by the Ocean Plasma
Team
44.Redden. The Nazi Flu Interview With Dr. Leonard Horowitz. December
3, 2005 <http://bc.indymedia.org/newswire/display/8085/index.php>
45.Reitz, M.D., N.R. Miller, F. Wong-Staal, R.E. Gallagher, R.C.
Gallo, & D.H. Gillespie. "Primate type-C virus nucleic acid sequences
(woolly monkey and baboon types) in tissues from a patient with acute
myelogenous leukemia and in viruses isolated from cultured cells of
the same patient." Proc. Natl. Acad. Sci. USA 73, 1976: 2113-2117
46.Sneed, M.D., Eva Lee. "AIDS-IMMUNIZATION RELATED SYNDROME." Health
Freedom News July, 1987, National Health Federation
47.Stary, A. & A Sarasin. "Simian virus 40 (SV40) large T
antigen-dependent amplification of an Epstein-Barr virus-SV40 hybrid
shuttle vector integrated into the human HeLa cell genome" Journal of
General Virology, Vol 73, 1992: 1679. Society for General Microbiology
48.The Canadian Red Cross Used Blood Contaminated With the HIV Virus.
Press Interpreter. May 31, 2005 <http://www.pressinterpreter.org/node/168>
49.Wang, M.D., Frederick C.S. Epstein-Barr Virus. Channing
Laboratories. Brigham and Women's Hospital /Harvard Medical
School.<http://www.channing.harvard.edu/wang_f.htm>
50.Wong-Staal, F., D. Gillespie, & R.C. Gallo. "Provirual sequences of
baboon endogenous type-C RNA virus in DNA of human leukeaemic
tissues." Nature 262, 1976: 190-195
51.Wright, Pearce. "Smallpox vaccine 'triggered Aids virus.'" Science
Editor. London Times May 11, 1987
52.Xi'an Works To Keep Its Blood Supply Safe. U.S. Embassy Beijing.
April 2000 <http://www.usembassy-china.org.cn/sandt/xian-blood.htm>
53.Youngner, J.S. "Poliomyelitis" The American Peoples Encyclopedia
Year Book. Events of 1955. 1956: 883-84. The Spencer Press, Inc.,
Chicago, Ill.
54.Zacky, Elaine. AIDS/Ebola Author Defends Embattled African
Presidents: Reports Outbreaks May Be "Man-made" and CIA-linked.
Lightstream Productions Press Release. October 19, 2000 <http://www.lightstreamers.com/Horowitz/PressAIDS.html> |
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