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Part 1 of 5
The Real Story
Hydrazine Sulfate
Article Extract from OPTIONS the alternative therapy book.
by Richard Walters
Hydrazine sulfate, a simple, off-the-shelf chemical, dramatically
reverses cachexia
(ka-KEK-si-a), the wasting-away process that kills two thirds of all
cancer patients.
This inexpensive drug, with little or no side effects, also has a
clinically documented
antitumor action. It causes malignant tumors to stop growing, to reduce
in size, and,
in some cases, to disappear. A growing number of cancer patients
diagnosed as
terminal have experienced tumor stabilization and remission through
hydrazine
sulfate therapy.
About half of all patients who take hydrazine sulfate experience weight
gain,
restored appetite, extended survival time, and a significant reduction
in pain and
suffering. Many patients report an increase in vigor and strength and
he
disappearance of symptoms of the disease, along with feelings of
well-being and
optimism.
While hydrazine sulfate may not be a sure-fire cancer cure, large-scale
clinical trials
suggest that it effects every type of tumor at every stage. It can be
administered
either alone or in combination with cytotoxic chemotherapy or radiation
to make the
cancer more vulnerable to these standard forms of treatment.
Hydrazine sulfate is now undergoing Phase III trials sponsored by the
National
Cancer Institute. It is available to patients as a "compassionate IND
(Investigational
New Drug)," a designation conferred by the Food and Drug Administration
on a
case by case basis, so it is no longer, strictly speaking, an
"unconventional therapy."
Yet even though hundreds of patients across the country are using the
drug, it is not
widely discussed or disseminated among practicing physicians and its
promise
remains largely untapped twenty-four years after it was first proposed
as an
anticancer treatment by Dr. ]oseph Gold. Meanwhile, hydrazine sulfate is
widely
available in the Commonwealth of Independent States (formerly the Soviet
Union),
where researchers have followed up on Gold' s pioneering work with over
ten years
of investigation supporting the drug's effectiveness.
"We've gone from a red lift to a yellow light, and hopefully will go to
a green light,"
says Dr. Gold, director of the Syracuse Cancer Research Institute in
Syracuse,
New York, which he founded in 1966. Since his discovery in 1968 that
hydrazine
sulfate can prevent the wasting-away process in cancer patients and
inhibit tumor
growth, Gold has waged courageous uphill battle to win acceptance for
his nontoxic
chemotherapy by the medical establishment.
The American Cancer Society put hydrazine sulfate on its Unproven
ethods
blacklist in 1976. It condemned and stigmatized the drug following a
clinical trial on
twenty-nine patients at Memorial Sloan-Kettering Cancer Center in New
York. But
it is now widely acknowledged that the Sloan Kettering tests were
botched.
When Dr. Gold made an unannounced visit to the hospital in 1974, he
discovered,
to his horror, that "many patients in the study were either being
underdosed or
overdosed. Some people who were beginning to show anticachexia response
were
suddenly being given 90 to 100 milligrams at one time. All this was in
clear violation
of the drug protocols and of our joint agreements," said Gold. The
study's protocol
called for patients to receive 60 milligrams once a day for the first
three days, twice
a day for the next three days, and three times a day for the following
six weeks.
Therefore, some patients were getting a 67 percent overdose.
In a letter of protest to Sloan Kettering, Gold pointed out that some
patients were
receiving a massive, single dose of approximately 120 to 190 milligrams
a day
(instead of the usual two or three 60 milligram doses), "which quickly
wiped out
whatever good response they were beginning to show." The study was so
poorly
See part 2 of 5
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