Press Release Summary = Ex-cancer patient exposes cover-up of cancer cure using
evidence on pubmed archives
Press Release Body =
This Kills Cancer - Triamazon - The Miracle Rainforest Drug
A miracle non toxic natural rainforest discovery wipes out deadly cancers !
Andrew Harris an ex-cancer patient exposes the big pharma industry cover-up of a
natural cancer killing miracle with astounding incriminating conclusive independent
evidence available via a direct link to pubmed archives on his website. Andrew is
the founder of www.thiskillscancer.com His strong entrepreneurial background in
business, marketing, research and management is combined with his personal
experiences in having gone through 14 lots of conventional toxic combination
chemotherapy to actually surviving cancer through an alternative natural, non toxic,
immune system boosting, cancer killing miracle.
Here you will learn about an astounding opportunity to kill cancer using the product
we offer which is made by a recipe of natural bioactive compounds, phytochemicals,
novel alkaloids and acetogenins that are anti-cancerous, anti-tumorous, and
non-toxic, anti-viral, anti-parasitic. The product is called Triamazon, it works
well enough on its own or while taken in combination with chemotherapy. Triamazon
supports many health benefits. It is most popular for supporting the immune system
as it promotes and turbocharges healthy cell division and good tissue growth, it
also supports blood pressure, the heart, mood, and digestion and is 100% natural
from the amazon rainforest, This all natural cancer killing recipe when put in an
edible capsule, is literally saving lives.
Triamazon worked really well combined with a natural detox product called ZNatural
which removes heavy metals along with the nasty toxins from the chemotherapy to
protect healthy cells that get an automatic turbocharge from Triamazon the Cancer
killing miracle. ZNatural is the most powerful detoxification product on the market.
ZNatural can be purchased from www.spiritofsunshine.co.uk
The future of cancer treatment and the chances of survival look more promising than
ever. As a result of confidential communications involving a researcher from one of
America’s largest pharmaceutical companies, this anti-cancerous, anti-tumorous
product Triamazon, is finally coming to public attention thanks to this website.
Vital ingredients in Triamazon have been studied in more than 20 laboratory tests,
which have been shown to...
• effectively target and kill malignant cells in 12 different types of cancer
including, breast cancer, lung cancer, liver cancer, colon cancer, lymphoma cancer,
non hodgkins lymphoma, ovarian cancer, pancreatic cancer, prostate cancer, and vital
ingredients upon testing have proven that Triamazon is non toxic to healthy cells
and is safe, Triamazon only kills cancer cells while boosting and protecting the
immune system, testing has also proven Triamazon to be...
• 10,000 times stronger in killing colon cancer cells than Adriamycin, a commonly
used chemotherapeutic drug
• it selectively hunts down and kills cancer cells, including (MDR - multi drug
resistant human breast adenocarcinoma) without harming healthy cells, unlike
chemotherapy.
With extracts from this powerful rainforest drug, people have actually experienced
it to…
• conquer cancer safely and effectively with an all-natural therapy that doesn’t
cause extreme nausea, weight loss, and hair loss
• protect your immune system and evade deadly infections
• feel strong and healthy throughout the course of treatment
• boost your energy and improve your outlook on life.
Natural plant Chemicals in Triamazon...
Many active compounds and natural chemicals have been found in ingredients in
triamazon, as scientists have been studying these properties since the 1940s. Most
of the research on these ingredients focuses on a novel set of natural chemicals
called Annonaceous acetogenins. Three separate research groups have confirmed that
these natural chemicals have significant antitumorous properties and selective
toxicity against various types of cancer cells (without harming healthy cells)
publishing eight clinical studies on their findings. Many of the acetogenins have
demonstrated selective toxicity to tumor cells at very low dosages—as little as 1
part per million. Four studies were published in 1998 which further specify the
chemicals and acetogenins which are demonstrating the strongest anticancerous,
antitumorous, and antiviral properties. In a 1997 clinical study, the same novel
alkaloids in triamazon exhibited antidepressive effects in animals.
These natural chemicals in general have been documented with antitumorous,
antiparasitic, insecticidal, and antimicrobial activities. Mode of action studies in
separate laboratories have recently determined that these acetogenins are superb
inhibitors of enzyme processes that are only found in the membranes of cancerous
tumor cells. This is why they are toxic to cancer cells but have no toxicity to
healthy cells. Purdue University, in West Lafayette, Indiana, has conducted a great
deal of the research on the acetogenins.
Since 1997, Purdue University has this information with promising news that several
of the Annonaceous acetogenins were effective in killing tumors that have proven
resistant to anti-cancer agents, but also seem to have a special affinity for such
resistant cells.\" In several interviews, the head pharmacologist in Purdue\'s
research explained how this worked. As he explains it, cancer cells that survive
chemotherapy can develop resistance to the agent originally used as well as to
other, even unrelated, drugs. This phenomenon is called multi-drug resistance (MDR).
One of the main ways that cancer cells develop resistance to chemotherapy drugs is
by creating an intercellular pump which is capable of pushing anticancer agents out
of the cell before they can kill it. On average, only about two percent of the
cancer cells in any given person might develop this pump—but they are the two
percent that can eventually grow and expand to create multi-drug-resistant tumors.
Some of the latest research on acetogenins reported that they were capable of
shutting down these intercellular pumps, thereby killing multi-drug-resistant
tumors. Purdue researchers reported that the acetogenins preferentially killed
multi-drug-resistant cancer cells by blocking the transfer of ATP—the chief source
of cellular energy—into them. A tumor cell needs energy to grow and reproduce, and a
great deal more to run its pump and expel attacking agents. By inhibiting energy to
the cell , it can no longer run its pump. When acetogenins block ATP to the tumor
cell over time, the cell no longer has enough energy to operate sustaining
processes—and it dies. Normal cells seldom develop such a pump; therefore, they
don\'t require large amounts of energy to run a pump and, generally, are not
adversely affected by ATP inhibitors. Purdue researchers reported that 14 different
acetogenins tested thus far demonstrate potent ATP-blocking properties. They also
reported that 13 of these 14 acetogenins tested were more potent against MDR breast
cancer cells than all three of the standard drugs (adriamycin, vincristine, and
vinblastine) they used as controls.
The Annonaceous acetogenins in Triamazon include: annocatalin, annohexocin,
annomonicin, annomontacin, annomuricatin A & B, annomuricin A thru E, annomutacin,
annonacin, annonacinone, annopentocin A thru C, cis-annonacin, cis-corossolone,
cohibin A thru D, corepoxylone, coronin, corossolin, corossolone, donhexocin,
epomuricenin A & B, gigantetrocin, gigantetrocin A & B, gigantetrocinone,
gigantetronenin, goniothalamicin, iso-annonacin, javoricin, montanacin,
montecristin, muracin A thru G, muricapentocin, muricatalicin, muricatalin,
muri-catenol, muricatetrocin A & B muricatin D, muricatocin A thru C muricin H,
muricin I, muricoreacin, murihexocin 3, murihexocin A thru C, murihexol, murisolin,
robustocin, rolliniastatin 1 & 2, saba-delin, solamin, uvariamicin I & IV,
xylomaticinBiological Activites and Clinical Research
In an 1976 plant screening program by the National Cancer Institute, showed active
toxicity against cancer cells and researchers have been following up on these
findings since. Thus far, specific acetogenins in the ingredients of Triamazon have
been reported to be selectively toxic in vitro to these types of tumor cells: lung
carcinoma cell lines; human breast solid tumor lines; prostate adenocarcinoma;
pancreatic carcinoma cell lines; colon adenocarcinoma cell lines; liver cancer cell
lines; human lymphoma cell lines; and multi-drug resistant human breast
adenocarcinoma.
There are plenty of sceptics that read these claims, but the non-believers soon
become shocked and stunned as they see the truth as they read independently from the
very genuine pages of The National Library of Medicine and the National Institutes
of Health that shows just one ingredient of Triamazon to be 10,000 times more lethal
to cancer than a commonly used chemotherapy drug Adriamycin. remember this number [
8991944 ] copy and paste it into the (right hand side) search box on this following
link http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD
Web Site = http://thiskillscancer.com
Contact Details = Andrew Harris 0044 161 775 5041email: snakey1959@aol.com
2008
