This is beyond TREASON, this is beyond ATTEMPTED FIRST DEGREE MURDER..... This is beyond anything I have ever experienced, and this proves that deep rooted, true EVIL does exist at a level I had no idea could exist in any human being. I now know. When I first got this it was before all the dead scientists were being murdered and before all the patented bioweapons we now know about that have been tried around the world.
I now know Yale University was involved and plum Island, so its an inside job with Israel as part of it due to the Yale connection. Please read this and see what they INTENTIONALLY DID TO OUR SOLDIERS DURING THE EARLY GULF WAR after 9-11. This is a crime and prosecutable and we better step up now or we are complicit and get everything we deserve. I can't image the impact on the children and old people in Iraq of this effort to kill and permanently damage our own soldiers..... our children, spouses, etc. This is beyond a crime, its deeply perverted.
Living Next Door To Plum Island; Lyme Disease - Denial of Treatment and Doctor Persecution
http://www.samento.com.ec/sciencelib/4lyme/plumisland.html
By Journal of Degenerative Diseases, August 6, 2002
The Lyme Disease
epidemic, along with it's many co-infections, is sweeping across North
America like Wildfire. At the same time doctors who are courageous
enough to treat the chronic Lyme patients till they are well, are being
picked off one by one.
In the
Connecticut/New York area where I live, doctors have to be very careful
concerning the number of Lyme patients they treat and also how long they
treat them for. Patients are not getting the antibiotics they require
and as a result their disease can become irreversible and progressively
more debilitating. People have died from Lyme Disease. When patients
begin to go downhill many of those who were originally diagnosed with
Lyme are now assigned different disease labels, according to what ever
organ system is affected. It appears that this is one method of
downplaying an epidemic.
Yale University
is one of the main forces behind Lyme patients' treatment denial. Yale
contends that 3 to 4 weeks of antibiotics is a sufficient protocol for
just about every case. If a patient is still sick with the exact same
symptoms on the 31st day of treatment, they now, according to Yale, no
longer have an active infection but automatically now have an autoimmune
problem....Fibromyalgia, Chronic Fatigue Syndrome, depression or
"antibiotic seeking behavior".
I have yet to see
any evidence provided by Yale that would support this theory or
speculation. Testing is very inaccurate which means it cannot be used as
definite proof of infection or noninfection. Many chronic lyme patients
will tell the same story of relapsing when antibiotics are
discontinued. Some doctors claim that patients continue to improve when
on extended antibiotics (after the approved one month period) because
the antibiotics may have an antinflammatory or immunomodulatory effect
and are not improving necessarily because the drugs are killing off an
active infection. It is possible that the antibiotics may be working by
some other mechanism that we are not yet aware of, but the point is
that, if the treatment is working and has minimal side effects, then
isn't it better to treat and prevent inevitable deterioration of the
patient.... at least until a better solution is found?
There is much
talk in the mainstream media concerning antibiotic resistance and this
concept is used many times to justify nontreatment. We all know that the
concept of antibiotic resistance has validity but it is never mentioned
that certain labs are intentionally creating antibiotic resistant
microbes for biowarfare purposes. These "modified" biologicals require
some sort of field testing. Could the Lyme Disease spirochete be
modified...a product of biowarfare research? Could this be the reason it
is so difficult to eradicate? Another troubling thought is why are
chronic acne patients allowed to recieve years of antibiotic treatment
with no hassle whatsoever, when those with a much more serious, often
progressive disease, are denied the same treatment?
Many place the
blame of this strange behavior from the medical community, mainly on the
insurance companies. I question this and feel that the reasons for
treatment denial go much deeper. Insurance companies most likely do play
a role. However, it appears to me that it would be many times more
expensive for insurance companies to refuse paying for long term
antibiotic treatment ( especially considering that oral antibiotics are
fairly inexpensive) than it would be to treat those patients. The
patients who are refused antibiotics and are told they have an
autoimmune disease or that it is 'all in their heads', proceed to go
from doctor to doctor and many end up recieving almost every medical
test known to man, including MRIs, X-Rays, tilt table tests, Spect
Scans,antidepressant medications...and I could go on almost
indefinitely. Costs for those denied antibiotics become astronomical.
As I was trying
to make sense of this extremely puzzling, nonsensical situation, I was
sent some information from a very reliable source, which stated that 60%
of chronic lyme patients are coinfected with several strains of
mycoplasma, the most common one being "mycoplasma fermentens" which is
patented by the U.S. Army and army pathologist Dr. Lo!
Lo, Shyh-Ching-Pathogenic mycoplasma-U.S. Patent 5,242,820 issued Sept. 7, 1993.
It is becoming
evident that any microbe that has been "modified" is considered "off
limits" for treatment and any physician that takes these chronic
infections seriously, is targeted for harassment. This same pathogen is
found in Gulf war Illness, Fibromyalgia and Chronic Fatigue patients!
Could this be the main reason why the symptoms of all these diseases
overlap to such a degree and all seem to have emerged around the same
time period?
As mentioned in
an earlier issue of the Journal of Degenerative Diseases, I live and
work almost directly across the water from Plum Island, off the tip of
Long Island, N.Y.. Years ago, in 1897, the War Dept. owned Plum Island
which was then called Fort Terry. In 1954 the Army officially
transferred Fort Terry over to the USDA to be used as an animal disease
laboratory. Fairly recently Plum Island requested 75 million dollars to
upgrade the facility to a bio-level 4 status for the express purpose of
reinstating biowarfare research.
It seems very coincidental that....
1) Lyme disease is endemic to all land areas surrounding Plum Island.
2) Many Lyme and
Gulf war Ilness patients are infected with the same genetically
engineered organism (mycoplasma fermentens) created and patented by the
US Government.
3) Lyme Disease and Gulf War Illness share almost identical symptoms.
4) Doxycycline is one of the drugs of choice for both diseases.
5) Both sets of patients are being denied antibiotic treatment.
6) I spoke with
Dr. Thomas, the previous Director of Plum Island, who admitted that an
Iraqi researcher (who has since been murdered) did his graduate training
at Plum Island, specifically involving different strains of mycoplasma.
He went back to Iraq and headed up the mycoplasma research program at
the University of Bagdad. I asked Dr. Thomas if Plum Island ever worked
with mycoplasmas in general. She denied this at the beginning but
gradually admitted researching 7 different different strains. I asked if
Plum Island researchers ever worked with mycoplasma fermentens. She was
immediately familiar with that particular genetically engineered strain
although she did deny that Plum Island researchers ever worked with it.
7) Yale University often works with Plum Island on various projects and they are in close proximity to each other.
8) Yale, again,
is one of the main opponents of long term antibiotic treatment for Lyme
Disease in spite of it's obvious benefits.
It is extremely
suspicious that one of the most Lyme-endemic areas in the country only
has a handful of doctors that will treat chronic patients. Syphilis is
also a spirochetal disease, as is lyme. and is known to sometimes
require open-ended antibiotic treatment. Webster's dictionary states
that untreated Syphilis may result in the degeneration of many organs
and tissues of the human body. Could Lyme disease be another Tuskegee
experiment?
Why is there so
much attention and propaganda directed at west Nile Virus and Anthrax
when these diseases have affected only a few people? I feel that all
this media attention to the above two disease causing pathogens involves
several agendas which include creating a smokescreen to divert our
attention from the more subtle biowarfare pathogens that are already in
our midst, destroying countless lives.
I am a
cofacilitator of one of the only Lyme Disease support groups in
southeastern CT. It is appalling and very frightening to witness the
massive numbers of previously intelligent and productive people whose
lives are being completely ruined by this disease and it's coinfections
such as mycoplasma. babesia and erichliosis. Lyme disease is very
misunderstood ( mainly due to media misinformation)and as a result
patients' families are disintegrating, patients are losing their jobs,
their homes, their insurance, their friends, their dignity and even
their minds. Many regret the loss of their minds the most.
Chronic lyme
disease can manifest itself with severe neurological symptoms, many
which originate in the brain. SPECT scans, which measure blood flow to
the brain, show decreased patchy perfusion to specific areas in the
patient's brain which usually correlates with their neurological
symptoms. Most patients, after sufficient antibiotic treatment, show
much improvement in symptoms and in perfusion. Those who have not
recieved sufficient treatment or who were treated too late in the
disease complain that they are not the same person that they used to be.
Many comment that this disease has taken away everything that they hold
dear, their brain and even their souls.
Our country is becoming disabled...perhaps intentionally?
The attack on our
concerned and compassionate Lyme literate physicians is equally
appalling. Our support group here in Connecticut only knows 5 or 6
doctors in the whole state that we can refer Chronic Lyme disease
patients to. Several of those few doctors are currently under
unwarranted investigation.
Massive numbers
of people sick with Chronic Lyme are flocking to these few doctors
looking for answers, which not only overwhelms the doctors, but also
attaches a stigma to them which then attracts State investigation and
sometimes the removal of their medical license.
The most
distressing case in the Notheast is that of Dr. Joseph Burrascano. Many
Lyme Disease patients owe their lives to him. Dr. Burrascano is
nationally renowned for his dedicated research and treatment of Lyme
disease. He is well respected by his colleagues and many doctors who
treat these patients, use his protocols. In 1993 Dr. Burrascano spoke at
a Senate Committee Hearing on Lyme disease. I am including several
excerpts from his testimony.
" There is a core
group of university-based Lyme Disease researchers whose opinions carry
a great deal of weight. Unfortunately many of them act unscientifically
and unethically. They adhere to outdated, self-serving views and
attempt to personally discredit those whose opinions differ from their
own. They exert strong ethically questionable influence on medical
journals, which enables them to publish and promote articles that are
badly flawed. They work with certain government agencies to bias the
agenda of consensus and have worked to exclude from these meetings and
scientific seminars those with alternate opinions. They behave this way
for reasons of personal or professional gain and are involved in obvious
conflicts of interest."
"Following the
lead of this group of physicians, a few state health departments have
begun to investigate, in a very threatening way, physicians who have
more open minded views on Lyme Disease diagnoses and treatment than they
do. Indeed, I must confess that I feel I am taking a large risk here
today by publically stating these views, for fear that I may suffer some
negative repercussions, despite the fact that many hundreds of
physicians all over the world agree with what i am saying here. Because
of this bias by this inner circle, Lyme Disease is both under diagnosed
and under treated, to the great detriment of many of our fellow
citizens."
"The very
existence of hundreds of Lyme Disease support groups in this country,
and tens of thousands of dissatisfied, mistreated and very ill patients
whom these groups represent, underscores the many problems that exist
out in the real world of Lyme Disease. I ask and plead with you to hear
their voices, listen to their stories and work in an honest and unbiased
way to help protect the many sufferers whose health is at risk from
what now has become a political disease."
Dr. Burrascano
has indeed suffered repercussions since his testimony in 1993. He has
spent the last couple of years defending himself and other Lyme literate
physicians. Burrascano was charged with professional misconduct for the
sole reason of treating Lyme patients with long term antibiotics, when
needed. In November of 2001 he was exonerated concerning the 39 charges
filed against him. However, this ordeal seriously affected him
emotionally, physically and financially. Is it any wonder that
physicians are acting so strangely when confronted with patients who
present with these "Unacceptable illnesses" such as Chronic Fatigue
syndrome, Gulf war Illness, Lyme , etc?
We must speak out
against this blatant bureaucratic bullying and harassment before all
our doctors are corporate owned and controlled and we are all too sick
to do anything about it.
The article is reproduced in accordance with Section 107 of title 17 of the Copyright Law of the United States relating to fair-use and is for the purposes of criticism, comment, news reporting, teaching, scholarship, and research.
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