Fenbendazole (brand names Panacur C ®, Safe-Guard ®) is a veterinary medication introduced in 1974.
Worldwide, veterinarians commonly use fenbendazole, FBZ, to treat a variety of parasites in animals, such as tapeworms, hookworms, roundworms, lungworms, and whipworms.
Fenbendazole has been known to have a high safety margin for animal use as it is tolerated well, has low side effects, and has a low degree of toxicity.
Following anecdotal fenbendazole cancer success stories, researchers have been experimenting with the “repurposed” use of Fenbendazole for cancer – for animals and humans.
Drug “repurposing” is a new use for a medicine that is different from the original medical indication. Though the Fenbendazole studies are limited, what researchers have found so far is promising for patients with cancer.
Fenbendazole for Pancreatic Cancer
Despite the initial effectiveness of certain chemotherapies, pancreatic tumors frequently develop resistance to these treatments. Moreover, newer methods like immunotherapy have struggled to address this challenging disease effectively. All of which has led researchers to turn their attention to Fenbendazole as a possible treatment. And while there is a great need for further studies, early evidence is showing great promise.
The cancer cells in pancreatic cancer behave in a very specific way when it comes to getting energy and nutrients for their growth. They use special ways to process glucose, amino acids, and lipids, which helps them grow and spread quickly. Scientists believe that the key to using fenbendazole effectively in treating pancreatic cancer lies in figuring out how the drug targets the behavior of these cancer cells.
Fenbendazole for Breast Cancer
One study published in March 2023 investigated Fenbendazole’s ability to treat Breast Cancer while preserving healthy breast cells. This research tested the drug on three cell types: normal, low metastatic cancer, and highly metastatic cancer cells. The findings revealed that Fenbendazole induced significant stress in the highly metastatic cancer cells compared to the others. This suggests Fenbendazole could offer a new, targeted treatment for advanced breast cancer
Fenbendazole for Colorectal Cancer
Colorectal cancer occurs when cells in the colon or rectum grow out of control. Treatment typically involves a combination of surgery, chemotherapy, and radiation therapy. There have been a few very promising studies that looked at how these cells responded to fenbendazole.
Tests showed that fenbendazole not only caused cell death in the cancer cells but also stopped them from growing by blocking a specific stage of their growth cycle.
They also found that the resistant cancer cells behaved differently compared to normal cancer cells. They didn’t respond as much to a natural process called autophagy, but they were more sensitive to another process called ferroptosis, which involves cell death due to iron overload.
This suggests that fenbendazole could be a promising treatment for cancers that are resistant to 5-fluorouracil, a type of chemotherapy medicine that is often used to treat colorectal cancer
Fenbendazole for Lung Cancer
Perhaps the most well-known case of someone treating their cancer with Fenbendazole is a man named Joe Tippens was diagnosed with lung cancer in 2017 and given only a few months to live.
Tippens developed a protocol combining Fenbendazole with CBD oil, curcumin, and Vitamin E which proved successful for his case. He remains cancer-free today and his story has sparked interest in pursuing more in-depth trials of Fenben as a repurposed drug.
In principle, a molecule can act as an antiviral drug if it “inhibits some stage of the virus replication cycle, without being too toxic to the body’s cells.” [20]
The possible modes of action of antiviral agents would include the following:
(1)
Inactivate extracellular virus particles.
(2)
Prevent viral attachment and/or entry.
(3)
Prevent replication of the viral genome.
(4)
Prevent synthesis of specific viral protein(s).
(5)
Prevent assembly or release of new infectious virions.
The role of ivermectin against the SARS-CoV-2 virus
The targets of activity of ivermectin can be divided into the following four groups:
A. Direct action on SARS-CoV-2
Level 1: Action on SARS-CoV-2 cell entry.
Level 2: Action on importin (IMP) superfamily.
Level 3: Action as an ionophore.
B. Action on host targets important for viral replication
Level 4: Action as an antiviral.
Level 5: Action on viral replication and assembly.
Level 6: Action on posttranslational processing of viral polyproteins.
Level 7: Action on karyopherin (KPNA/KPNB) receptors.
C. Action on host targets important for inflammation
Level 8: Action on interferon (INF) levels.
Level 9: Action on Toll-like receptors (TLRs).
Level 10: Action on nuclear factor-κB (NF-κB) pathway.
Level 11: Action on the JAK-STAT pathway, PAI-1, that could be involved with COVID-19 sequalae.
Level 12: Action on P21 activated kinase 1 (PAK1).
Level 13: Action on interleukin-6 (IL-6) levels.
Level 14: Action on allosteric modulation of P2X4 receptor.
Level 15: Action on high mobility group box 1 (HMGB1).
Level 16: Action as an immunomodulator on lung tissue and olfaction.
Level 17: Action as an anti-inflammatory.
D. Action on other host targets
Level 18: Action on plasmin and annexin A2.
Level 19: Action on CD 147 on the red blood cell (RBC).
Level 20: Action on mitochondrial ATP under hypoxia on cardiac function.
The direct “antiviral targets” may be useful in the early stages while the anti-inflammatory targets might be addressed in the later stages of the disease.
Abstract
Considering the urgency of the ongoing COVID-19 pandemic, detection of new mutant strains and potential re-emergence of novel coronaviruses, repurposing of drugs such as ivermectin could be worthy of attention. This review article aims to discuss the probable mechanisms of action of ivermectin against SARS-CoV-2 by summarizing the available literature over the years. A schematic of the key cellular and biomolecular interactions between ivermectin, host cell, and SARS-CoV-2 in COVID-19 pathogenesis and prevention of complications has been proposed.
Introduction
A relatively recent surge in zoonotic diseases has been noted over the past few decades. Several reasons could be responsible for this “spill-over” of disease-causing agents from animals to humans. These include an exponential rise in the global population causing man to encroach new ecological habitats in search of space, food, and resources as well as improved opportunities for rampant wildlife trade causing interspecies pathogen jumps. The 1980s was known for HIV/AIDS crisis that originated from the great apes, while the avian flu pandemic in 2004–07 came from the birds. The pigs led to the swine flu pandemic in 2009 and bats were the original hosts of Ebola, severe acute respiratory syndrome (SARS), Middle Eastern respiratory syndrome, and probably SARS coronavirus 2 (SARS-CoV-2) outbreak as well.
COVID-19 has already caused millions of deaths worldwide and has paralyzed not only the world’s healthcare system but also the political and economic relations between countries [1]. The fact that the SARS-CoV-2 virus has been thought to have originated from wildlife and may have “jumped” into humans, not only highlights future risks from animal-borne diseases but also provides an important clue to its resolution. In such a scenario, where this “jump” has been made from animal to human, it seems only logical to review a drug that has worked efficiently against a disease-causing agent and is available in a form that is safe for human consumption since the early 1980s.
Ivermectin belongs to a group of avermectins, which is a group of 16 membered macrocyclic lactone compounds discovered at the Japanese Kitasato Institute in 1967 during actinomycetes cultures with Streptomyces avermitilis [2]. This drug radically lowered the incidence of river blindness and lymphatic filariasis and was discovered and developed by William C. Campbell and Satoshi Ōmura for which they received the Nobel Prize in Physiology or Medicine in 2015 [3, 4]. Ivermectin is enlisted in the World Health Organization’s Model List of Essential Medicines [5].
Drug repurposing, drug redirecting, or drug reprofiling is defined as the identification of novel uses for existing drugs. The development risks, costs as well as safety-related failure, are reduced with this approach since these drugs have a well-established formulation development, in vitro and in vivo screening, as well as pharmacokinetic and pharmacodynamic profiles. Moreover, the first clinical trial phases of many such drugs have been completed and can be bypassed to reduce several years of development. Therefore, drug repurposing has the potential to reduce the time frame for the whole process by up to 3–12 years and carries great potential [6].
Although several drugs received emergency use authorization for COVID-19 treatment with unsatisfactory supportive data, ivermectin, on the other hand, has been sidelined. Nevertheless, many countries adopted ivermectin as one of the first-line treatment options for COVID-19.
With the ongoing vaccine roll-out programs in full swing across the globe, the longevity of the immunity offered by these vaccines or their role in offering protection against new mutant strains is still a matter of debate. Thus, the search for new, effective antivirals continues.
Several doctor-initiated clinical trial protocols that aimed to evaluate outcomes, such as reduction in mortality figures, shortened length of intensive care unit stay and/or hospital stay, and elimination of the virus with ivermectin use have been registered at the US ClinicalTrials.gov [7]. Controlled clinical trials using ivermectin are underway, including one being conducted by the National Institutes of Health (ACTIV-6) [ClinicalTrials.gov Identifier: NCT04885530] in the USA and a second in the UK (PRINCIPLE) [ISRCTN registry: ISRCTN86534580] [8, 9].
Ivermectin has rapid oral absorption, high liposolubility, is widely distributed in the body, metabolized in the liver (cytochrome P450 system), and excreted almost exclusively in feces [4]. Following a standard oral dose in healthy humans, it reaches peak plasma levels at 3.4–5 h, and plasma half-life has been reported to be 12–66 h [10]. Despite its widespread use, there are relatively few studies on the pharmacokinetics of ivermectin in humans [11]. Ivermectin binds strongly to plasma proteins in healthy subjects (93.2%) [12]. Such an “avid binding” can be beneficial when administered in countries where malnutrition and hypoalbuminemia are common, leading to increased availability of “free fraction” of ivermectin [4]. Hypoalbuminemia is a frequent finding in patients with COVID‐19 and it also appears to be linked to the severity of lung injury [13]. Therefore, ivermectin could have sufficient bioavailability when used in such a setting.
This article aims to discuss the probable mechanisms of action by summarizing the in vitro and in vivo evidence demonstrating the role of ivermectin in COVID-19 based on the available literature over the years (Table 1). A schematic of the key cellular and biomolecular interactions between ivermectin, host cell, and SARS-CoV-2 in COVID-19 pathogenesis and prevention of complications has been proposed (Fig. 1).
In this candid video, I share my personal journey exploring an unconventional cancer treatment - Joe Tippens' fenbendazole protocol. During the process of being diagnosed with stage 4 pancreatic cancer but before formal diagnosis, I uncovered Joe's remarkable story of putting his late-stage small cell lung cancer into remission using fenbendazole, a common deworming medication for animals.
Inspired by his case, I decided to try incorporating fenbendazole into my treatment plan alongside other supplements like curcumin and CBD oil, just as Joe had done according to the protocol he published in 2022. However, my results were mixed - while what were potentially lung tumors seemed to respond, I soon developed aggressive new liver metastases.
In this first video of a series, I provide all the details on Joe's original protocol components, how I implemented it personally, the positives and negatives I experienced, and my overall thoughts on fenbendazole's potential role in a comprehensive metabolic approach.
Whether you're exploring all options as a cancer patient/caregiver or just interested in Joe's viral story, this video is my transparent first-hand account. The next video will dive deeper into the Science behind fenbendazole, exploring the potential anti-cancer mechanisms and research behind this dewormer drug.
Transcript:
0:02
two years ago I was diagnosed with stage
0:05
four inoperable pancreatic cancer
0:07
against the odds I'm still here in those
0:09
dark days I searched for Survivor
0:11
stories and came across Joe tippens a
0:14
stage four lung cancer patient who
0:16
incredibly sent his disease into
0:17
remission using an unconventional
0:19
protocol involving a dog dewormer drug as
0:22
many comments suggest I try Fenbendasol
0:24
over three videos I'll share why
0:27
Joe inspires me my reasons for trying
0:30
and my reasons for stopping
0:32
Fenbendasol after being diagnosed with stage
0:35
three small cell lung cancer which had
0:37
widely metastases to 40 or 50 locations
0:40
following standard treatments Joe
0:42
tippens was given just months to live in
0:44
January
0:45
2017 the hedge fund private Equity CEO
0:48
did the same thing I did he started
0:50
relentlessly researching how he could
0:53
turn this around the 59-year-old who
0:56
strongly believes in the power of
0:57
positive thinking and prayer had already
1:00
gone chemotherapy fasting and radiation
1:02
but the cancer had only spread further
1:04
to multiple
1:06
organs then Joe came across an
1:08
incredible post on an Oklahoma State
1:10
message board from a veterinarian
1:12
alumnist call me if you've got cancer
1:15
the vet told Joe how his research
1:18
scientist friend at MK had inadvertently
1:21
cured mice of cancer after worming them
1:23
with fendol a common deworming compound
1:26
the scientist herself then used fendol
1:29
and was cleared of her stage four G gleo
1:32
blastoma within weeks Joe was included
1:35
in the 1,100 person key truda
1:37
immunotherapy trial aimed at extending
1:40
Life by just 3 to 6 months but he also
1:43
decided to take the inexpensive pet
1:45
Dormer Fen bendol himself combining it
1:48
with supplements like CBD and circumin
1:51
the results were astonishing within 6
1:54
weeks Joe's widespread tumors had
1:56
disappeared on scans $1.2 million of
2:00
conventional treatments had failed but
2:02
this $5 dog medication seemed to have
2:04
worked a miracle Joe was the only
2:07
participant who finished the trial in
2:09
complete remission Joe soon took to
2:11
social media to share his protocol
2:14
inspiring many other late stage cancer
2:16
patients around the world to explore Fen
2:18
bendol as an unconventional last hope
2:21
this was my kind of story like Joe I'd
2:24
scoured to find anything that could help
2:26
with my stage 4 pancreatic cancer my
2:29
Research into antiparasitic drugs agreed
2:32
Fen bendol showed potential for
2:34
pancreatic cancer though par bendol
2:37
actually seem more effective for
2:38
pancreatic cancer specifically I tried
2:41
unsuccessfully to obtain parb benzol
2:44
before settling on the more accessible
2:46
fend Bend resol combined with other
2:48
supplements and off labels that I was
2:49
taking at that time Joe's protocol was
2:52
originally fenben every 3 days on four
2:55
off with thumin vitamin E and CBD oil
2:59
later adding fermented wheat germ and
3:01
berberine he credited positive thinking
3:04
as key I took fendol with avocados for
3:08
absorption using a high absorption
3:10
curcumin and lowd dose CBD alongside
3:13
other off labels this was when doctors
3:15
suspected stage 4 pancreatic cancer
3:18
before confirming with a biopsy so no
3:20
standard treatments yet I regret not
3:23
taking milk thistle then strongly
3:26
advised in Joe's group over time Joe
3:29
find tuned advising continuous Fen Bol
3:32
after a 2018 scare from reducing it he
3:35
now combines it with ultra botanicas
3:37
enco junct Botanicals specifically
3:40
formulated as a complimentary protocol I
3:43
started Fen bendol at the 220 milligram
3:47
dose in June 2022 though research showed
3:51
potential benefits really required 500
3:53
milligrams I only took the 222 milligram
3:56
dose 3 to 7 days per week until August
4:00
when low blood pressure after chemo
4:02
forced me to stop all off labels and
4:04
reset my mixed feelings stem from my
4:06
cancer aggressively metastasizing to my
4:09
liver soon after starting F bendil in
4:13
hindsight I didn't have all metabolic
4:15
pathways blocked nor was I protecting my
4:18
liver with milk thistle so when the lung
4:21
tumors may have initially responded I
4:23
think Fen Bend resol potentially allowed
4:26
the cancer to spread to my unprotected
4:28
liver however overhauling my protocol
4:31
which still included Fen Bend resol led
4:34
to significant tumor reductions on my
4:36
next scan overall I've stepped away from
4:38
most off labels for now and I've had my
4:40
best results without them but I'm open
4:42
to revisiting fenol as part of a
4:44
comprehensive metabolic approach down
4:46
the line not as a standalone therapy I
4:49
note the success others like Noel Watson
4:51
with stage four pancreatic have had with
4:53
Fen bendol in the next video I'll dive
4:56
deeper into the Science exploring the
4:58
mechanisms of how this worming drug
5:00
works against cancer cells and the
5:02
research investigating its anti-cancer
5:05
properties thanks for all your wonderful
5:07
comments on my last video I deeply
5:09
appreciate the messages of support
I came across your video--was not looking but it ”stands” out and have seen the affects of pancreatic cancer, parasites etc.
1. The average pancreatic duct is a ”protected” hotel for Liver Fluk ....
I came across your video--was not looking but it "stands" out and have seen the affects of pancreatic cancer, parasites etc.
1. The average pancreatic duct is a "protected" hotel for Liver Flukes, where they lay thousands of eggs, endlessly your entire lifetime....protected because of no blood flow in the duct and the duct is almost always "blocked" with mineral "stones" that act like a door protecting the Liver Flukes.
When Russia was building the first zappers so humans could stay in space with out "swelling-up", one of the first side affects was curing diabetes. I discovered that when taking the internal zappers properly 3x, on the second pass, often people expel a fist size amount of Liver Flukes following a flow of rock hard stones that flushed out of the pancreatic duct and pictured the stones and worms for Dr. Hulda Clark long ago...
2. Clark proved gold fillings affect the pancreas health badly leading to cancer---she was 100% correct.
3. A full mouth full of crowns and metal fillings is certainly asking for cancers.
4.If you have cancer anywhere, you had it first in the liver...when they tell you liver cancer "after" years of treating cancers elsewhere, they often say your hopeless once they do tell you your liver is full of it.
5. PARASITES---you surely have 3# of Lyme and never know it, all the endless other parasites will die easily in comparison to Lyme; Lyme has been the last great plague for the past 300 years and entered into just about everything with blood above and below the water.
6. Animal / Drug / Heavy Metals to kill worms----does not cure cancers and diseases, they are just "toxic" substances....professional / gimmick websites can not change cancers--- WHEN they are n ot addressing the endless reasons for cancers and "IF" parasites cause cancers and poisons that kill parasites is the cure for 1 of the deadliest cancers known---WOW, the cancer industry would crumble and all the hospitals would empty as everyone went on chemicals--- no one can take a poison and expect better health, what they can expect is that the poisoned blood cells defend themself and they kill/dissolve/expel parasites.
7. Not that long ago, every house had a very toxic parasite killer--- farmers used it to treat their horses, dogs, cats, kids.....vets still today use it for dog heart worm---injecting it in the front legs for 3 days-----it is always used by drops going up daily and then coming back down--because it is extremely toxic, but not long ago, every house had it in their bathroom---but after bad people used it to kill people they did not like---it became outlawed and only the vets use it....
8. Back in the days every family had the most powerful parasite killer known--- they also were plagued with cancers.
9. Cancers and Parasites: The parasites feast on the rot. They thrive on slow / low oxygen death.
10. 4th stage pancreatic cancer is no small deal and for anyone to survive after they did chemo-----is rare. Great M.D. always said no one do chemo after age 50, just for the fact it is too toxic for old people. Poisons can never cure anything, they just "force" a response.
11. The best cancer M.D. 15 years ago, said if you want to survive pancreatic cancer in America, you must leave America and got to China. Others will say Russia--both use a completely different approach. He said "if" your in america and want to try--1 M.D. in Texas doing extreme Pancreatic Hormone therapy has some success, but ignoring all the foundational problems and supplying hormones is insuring the pancreas will close down and become dependent on the synthetics..
12. Pancreatic Cancer ends up with orange colored eyes, degradation of the face and body and requires "STINTS" in the pancreas to allow the worms and fluids to flow out and down into the intestines and instantly their eyes lighten up as it drains down and out...and during that time period, is when people discover thy may need to pull every toxic tooth in their mouth. Stop all the toxic foods/drinks/drugs...stop everything bad....
13. the idea a person can continue what caused their cancer and just take some de-wormer----would be in the "Miracle" Class and YES, that happens;
"IF" a person believes--------their subconscious will CURE any disease, all cancers......you will become what your truly believed in..... long ago called POW WOW or just faith healing. The brain can make you or break you; we are what we believe.
SO YES, some scary cat, dog, horse de-wormer powders can indeed aid you to cure yourself; medical proved that over 100 years ago; Jesus proved it over 2,000 years ago, Elijah, Enoch etc. long long ago understood The Miracle Cure.
BEWARE animal products, the commercial types often ad poisons as a method to stop human consumption. EXAMPLE, Lugol'sIodine often used for animals, but they ad chemicals so no human can use it and actually, Lugol'sIodine since Dr. Lugol Synthetically made it in the 1800's was/is toxic and no human should ever touch it.
BE GLAD your miraculously self-cured; but something seems very fishy when you have the ability to make fancy websites.....
The Curezone foundation was all about Dr. Hulda Clark , I knew her well (enough) and her dental info surely saved allot of lives......I do not care how much magic powders a human consumes---if their dental disaster is the root cause for their cancers..that cancer is never staying away until all that rot is out and even then---the accumulated dental poisons in the cells takes years to cleanse...
Dental Disaster takes 100% of your immunity 100% of your day, every day until you die---by design. YOUR BLOOD will never stop dissolving your dental poisoned teeth and that fact, allows cancers to develop....it takes a professional dentist/dr that can cut all your rotted teeth out in 1 day...and those rotted teeth will be so dissolved they will break into pieces and take a full day for just 1 person...as cancerous puss oozes out of the jaw..
Then BEWARE! When the surgeons discover you learned how to cure pancreatic cancer and they replace your pancreatic stint with a permanent stint and say your next check up with be 1 year....do not be surprised that you never ever eat again--due to an aggressive Thrush that resulted from "dirty" instruments and they say--whoops, our bad. Go to your local hospital and get a thrush shot and if you make it past 3 days after your last ever stint--that would be a true miracle... "they" don't those that learn how to beat their system.
If your lucky enough to stop a cancer with a simple poison--use that time to CLEAN UP the dirty body....
The Hormones must be helped with true hormones---not synthetic /animal hormones...true hormones make old people act like they are young.
Joe Tippens - The hidden truth. How a cancer patient healed himself. Joe Tippens a cancer patient who was given three months to live, took a combination of nutrients including Fenbendazole, while deciding not to change his diet & it worked.
* Fenbendazole 222mg
* Vitamin E 800 IU daily
* Curcumin 600mg daily
* CBD oil 25mg daily
Joe Tippins' journey is one of unlikely twists and remarkable resilience.
Diagnosed with small cell lung cancer in 2016, his battle took him through the conventional treatments of chemotherapy and radiation. However, amidst the challenges, he faced an unexpected turn when his esophagus was severely damaged during treatment, leading him to make a bold decision to forgo a feeding tube and rely on his body's reserves. Despite the odds, Joe's perseverance paid off, and by January 2017, he embarked on a new path, inspired by a veterinarian's anecdote about an unconventional cancer treatment.
Turning to fenbendazole, a drug typically used in veterinary medicine, Joe's decision was met with skepticism from the medical community.
Yet, fueled by hope and a belief in the drug's potential, he began his regimen. Astonishingly, subsequent PET scans revealed a reversal in his condition, defying medical expectations. Joe's journey didn't end there; his story spread rapidly, captivating audiences globally and sparking conversations within the medical community.
Against all odds, Joe's adherence to the unconventional regimen resulted in a remarkable reversal of his condition, propelling his story to international recognition and prompting discussions within the medical community.
Joe shares anecdotes and insights about his unconventional journey with cancer treatment. One standout moment is when he humorously recounts how a misunderstanding led to him being dubbed "Uncle Joey" by people in China. The cultural quirk underscores the global impact of his story, highlighting the widespread interest and adoption of his protocol.
Another compelling aspect of Joe's narrative is his commitment to providing his protocol pro bono, driven by a desire to maintain credibility and authenticity. Despite the immense personal investment of time and effort, Joe's dedication to helping others shines through, fueled by the profound impact his protocol has had on countless lives.
Key points from Joe's discussion:
Joe's journey began with a diagnosis of small cell lung cancer, leading him through conventional treatments that took a toll on his health.
Facing unexpected complications from treatment, Joe made a courageous decision to explore unconventional therapies, including fenbendazole, inspired by a veterinarian's anecdote.
Against all odds, Joe's adherence to the unconventional regimen resulted in a remarkable reversal of his condition, propelling his story to international recognition and prompting discussions within the medical community.
He emphasizes the importance of not monetizing his protocol, citing feedback from followers who value his credibility due to this stance. This decision reflects his dedication to prioritizing the integrity and accessibility of his story over financial gain.
Joe shares fascinating success stories, such as miraculous recoveries from various cancer types, including prostate cancer. These anecdotes underscore the transformative potential of his protocol, which combines fenbendazole with other supplements curated for maximum effectiveness.
Reflecting on the challenges he faces, Joe discusses the proliferation of counterfeit fenbendazole products sold online, underscoring the need for caution and diligence when sourcing medications. Despite these obstacles, Joe remains steadfast in his mission to empower individuals with knowledge and access to his protocol, leveraging his platform to disseminate information transparently and responsibly.
----
At Least 55Undeclared Chemical Elements Found in
COVID-19 Vaccines from AstraZeneca, CanSino,
Moderna, Pfizer, Sinopharm and Sputnik V, with
Precise ICP-MS
The study was conducted in March 2023 and was published on October 11, 2024 in Research Gate.
The whole process is explained in the 27-page PDF:
(The summary, method, results, discussion, conclusion and 6 complete pages indicating the references associated with this study. )
This research team includes doctors, physicists, biotechnologists, cell and molecular biologists, and physicists.
List of doctors who conducted the study:
1) Lorena Diblasi, PhD: Biotechnologist, Faculty of Biochemistry, Chemistry and Pharmacy, National University of Tucuman, Argentina
2 ) Martín Monteverde, MD : Colegio Médico de Santa Fe, Argentina
3 ) David Nonis, PhD : Molecular and Cellular Biologist, PhD, California, USA
4 ) Marcela Sangorrin, PhD Biotechnologist, Faculty of Biochemistry, Chemistry and Pharmacy, National University of Tucuman, Argentina
For example, the increase in molybdenum in the blood is associated with a decrease in testosterone levels and a decrease in the number and quality of sperm.
You probably also notice that there is an onset of cancer turbos, sudden and unexplained deaths etc..
Skeptical about Alternative Cancer Therapies? Have skeptical questions? Go to Cancer Debate Forum.
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