Connect with us

Awareness

Gulf War Illness Tied to Cipro Antibiotics

Published

on

gulfwarA U.S. military publication, The Air Force Times, made the connection that victims of Fluoroquinolone Toxicity Syndrome (“Floxies”) have been screaming about for years – that Gulf War Illness is tied to Cipro.  In an article entitled, “New FDA warnings on Cipro may tie into Gulf War Illness,” it was noted that the August, 2013 update to the warning labels of all fluoroquinolone antibiotics stating that PERMANENT peripheral neuropathy is a possible adverse effect, prompted The Air Force Times to make the connection.

advertisement - learn more

Civilians suffering from Fluoroquinolone Toxicity Syndrome (an adverse reaction to a fluoroquinolone – Cipro/Ciprofloxacin, Levaquin/Levofloxacin, Avelox/Moxifloxacin, Floxin/Ofloxacin and others) have noted the similarities between Gulf War illness and Fluoroquinolone Toxicity Syndrome for years.  It is beyond likely, it is probable, that they are one in the same.

The Symptoms

The VA defines Gulf War Illness as “chronic, unexplained symptoms existing for 6 months or more” that are at least ten percent disabling.  The CDC case definition of Gulf War Illness “requires chronic symptoms in two of three domains of fatigue, cognitive-mood, and musculoskeletal.”

Fluoroquinolone Toxicity Syndrome is a chronic, unexplained illness with symptoms lasting for months, years, or, as the updated warning label notes, permanently.  The symptoms of Fluoroquinolone Toxicity Syndrome are too numerous to list, but a cursory glance at the warning label for Cipro/Ciprofloxacin will tell you that the effects include musculoskeletal problems and central nervous system issues.  Additionally, as  pharmaceuticals that damage mitochondria, the energy centers of cells, severe fatigue is often induced by Fluoroquinolones.

A 1998 study entitled, “Chronic Multisymptom Illness Affecting Air Force Veterans of the Gulf War,” found that the most commonly reported symptoms of Gulf War Illness are sinus congestion, headache, fatigue, joint pain, difficulty remembering or concentrating, joint stiffness, difficulty sleeping, abdominal pain, trouble finding words, (feeling) moody or irritable, rash or sores, numbness or tingling and muscle pain.

advertisement - learn more

A 2011 study conducted by the Quinolone Vigilance Foundation found that the most commonly reported symptoms of Fluoroquinolone Toxicity Syndrome are tendon, joint, and muscle pain, fatigue, popping/cracking joints, weakness, neuropathic pain, paresthesia (tingling), muscle twitching, depression, anxiety, insomnia, back pain, memory loss, tinnitus, muscle wasting.

The symptoms are similar enough to raise a few eyebrows.  It should be noted that when a chronic, multi-symptom illness suddenly sickens a patient or a soldier, and he or she goes from being healthy and active to suddenly being exhausted and unable to move or think, it is difficult to pinpoint and describe exactly what is going wrong in his or her body.  Thus, even if the symptoms are identical, they may not be described in an identical way because of context and differing areas of focus.

For victims of fluoroquinolones, it is as if a bomb went off in the body of the victim, yet all tests come back “normal” so in addition to physical pain and suffering that the soldier/patient is going through, he or she has to suffer through dismissal and denial from medical professionals as well.  Neither Gulf War Illness nor Fluoroquinolone Toxicity Syndrome are detected by traditional medical tests and thus both diseases are systematically denied.  All blood and urine markers come back within the normal ranges, yet the patient or soldier is suddenly incapable of 90% of what he or she used to be able to do.  When a large number of patients or soldiers (nearly 30% of the soldiers serving in the Gulf reported symptoms.  Exact numbers of civilian patients suffering from Fluoroquinolone Toxicity Syndrome are unknown because of delayed reactions, misdiagnosing the illness, tolerance thresholds, etc.) experience adverse reactions that are undetectable using the tests available, there is something wrong with the tests.  The patients and soldiers aren’t lying and their loss of abilities isn’t “in their heads.”

Exposure to the same Poison

Another glaring similarity between Gulf War Illness and Fluoroquinolone Toxicity Syndrome is that everyone with either syndrome took a Fluoroquinolone.

Per a Veteran of the Marines who commented on healthboards.com about the use of Ciprofloxacin by soldiers in the Gulf:

“The Ciprofloxacin 500 mg were ordered to be taken twice a day. The Marines were the only service that I know for sure were given these orders. We were ordered to start them before the air war, and the order to stop taking them was giver at 0645 Feb 28th 1991 by General Myatt 1st Marine div commander. We were forced to take Cipro 500mg twice a day for 40 plus days. so the Marines were given NAPP (nerve agent protection pills) or pyridiostigmine bromide to protect us from nerve agent, and We were ordered to take the Cipro to protect from anthrax. We were part of the human research trial conducted by the Bayer corporation in the creation of their new anthrax pills. At that time they had no idea of the side effects of flouroquinolones. That’s the class of medications that Cipro falls into. After the Gulf War the FDA and Bayer co. started releasing the list of side effects.  You do need to know what was done to you so you will have to do your own research. Good luck to all of you and Semper Fi.”

By definition, everyone who suffers from Fluoroquinolone Toxicity Syndrome has taken a fluoroquinolone – Cipro/Ciprofloxacin, Levaquin/Levofloxacin, Avelox/Moxifloxacin or Floxin/Ofloxacin.  Civilians are also part of the “human research trial conducted by the Bayer corporation” as well as Johnson & Johnson, Merck and multiple generic drug manufacturers who peddle fluoroquinolones as “safe” antibiotics.

The Case Against Fluoroquinolones

Of course, there were multiple chemicals and poisons that Gulf War Veterans were exposed to in the 1990-91 Persian Gulf War and thus it has been difficult to pinpoint an exact cause of Gulf War Illness.  The ruling out of the following possible causes should certainly be questioned thoroughly, but “depleted uranium, anthrax vaccine, fuels, solvents, sand and particulates, infectious diseases, and chemical agent resistant coating” have been found not to cause Gulf War Illness.  Other potential causes of Gulf War Illness include oil fires, multiple vaccines, pesticides, and, of course, fluoroquinolone antibiotics (Cipro).  (It should be noted that non-deployed military personnel who served during the Gulf War period, but who were not deployed in the Middle East, have also been afflicted with Gulf War Illness and thus toxins that both deployed and non-deployed personnel have been exposed to should be the focus of investigations into the causes of Gulf War Illness.)

The Air Force Times article is one of the first official mentions of the relationship between Cipro and Gulf War Illness.  Officially, the link hasn’t been examined (though some very smart researchers are building a case as you read this).  Why Cipro hasn’t been looked at as a potential cause of Gulf War Illness is a question that I don’t know the answer to.  Perhaps it’s because most people think that all antibiotics are as safe as penicillin.  Perhaps it’s because most people have a tolerance threshold for fluoroquinolones and don’t react negatively to the first prescription that they receive.  Perhaps it’s because even today, more than 30 years after Cipro was patented by Bayer, the exact mechanism by which fluoroquinolones operate is still officially unknown (1).  Perhaps it’s because it is unthinkable that a commonly used antibiotic could cause a chronic syndrome of pain and suffering.  Perhaps it’s because the tests that show the damage done by fluoroquinolones aren’t used by the VA or civilian doctors’ offices.  Perhaps it’s because fluoroquinolones are the perfect drug – they take an acute problem – an infection, and convert it into a chronic disease-state that is systematically misdiagnosed as fibromyalgia, chronic fatigue syndrome, an autoimmune disease, leaky gut syndrome, insomnia, anxiety, depression, etc. and turns formerly healthy people into lifetime customers of the medical establishment / pharmaceutical companies.  Perhaps it is simply widespread ignorance about the way these dangerous drugs work.

The Cliffs Notes version of how fluoroquinolones work is as follows:

The fluoroquinolone depletes liver enzymes that metabolize drugs (CYP450) (2).  When the enzymes are depleted sufficiently, the fluoroquinolone forms a poisonous adduct to mitochondrial DNA (mtDNA) (3, 4), which destroys and depletes mtDNA (5).  While the mtDNA is being destroyed, the fluoroquinolone is also binding to cellular magnesium. (6, 7)  The mitochondria reacts to being assaulted by producing reactive oxygen species (ROS) (8, 9).  Some of the ROS, specifically hydrogen peroxide, combines with the excess calcium (there is a balance in cells of magnesium and calcium and the binding of the magnesium results in an excess of calcium) to induce the expression of CD95L/Fas Ligand (5) which then causes cell death (apoptosis) and immune system dysfunction (10) which leads the body to attack itself – like an autoimmune disease.

Damage is caused by every single step in the process.  Additional damage may be done by the fluorine atom that is added to fluoroquinolones to make them more potent.  It should be noted that the complexity of these cellular interactions is too vast to write up in this article.

Every symptom of Gulf War Illness is consistent with mitochondrial damage and oxidative stress (11), both of which have been shown to be brought on by fluoroquinolones.

Though the tests used in typical medical practice show no reason for victims of fluoroquinolones to be ill, that fact simply shows that the wrong tests are being used.  Tests of mitochondrial function, antioxidant/oxidant ratios and DNA will show the damage that is done by fluoroquinolones.  The way to determine whether Cipro is the cause of Gulf War Illness is to conduct a DNA mass spectrogram analysis on afflicted Gulf War Veterans.  If the DNA mass spectrogram analysis shows that quinolone molecules have adducted to the DNA of the Veterans, that’s a smoking gun of damage done by Cipro.

Millions of civilians have also been hurt by fluoroquinolones.  I can connect fluoroquinolones to almost every chronic disease that has increased in prevalence since the introduction of fluoroquinolones to the mass population in the mid-1980s.  Additionally, DNA is damaged and thus the effects are intergenerational and many of the chronic diseases that plague children can be linked to fluoroquinolone use by parents.

Some very well-respected researchers are working on more furthering  the case that Cipro is responsible for Gulf War Illness.  If any Gulf War Veterans want to take on Bayer before those studies are released, the way to do so is through obtaining a DNA mass spectrogram analysis and having it analyzed by a toxicologist.  It is proof of damage and it is necessary.  When that proof is obtained, I encourage all Gulf War Veterans to use it to fight those who poisoned them – Bayer and their corroborators in the DOD and the FDA.

To any Gulf War Veterans who read this – you are soldiers and you are warriors.  I know that you have been weakened, but you are still alive and those of you who can fight, should, because a grave injustice has been done to you.  It is an injustice that is also being inflicted on innocent civilians.  There is nothing okay about the poisoning of our military men and women, or the American public, with chemotherapy drugs masquerading as antibiotics.  I encourage you to fight Bayer and their corroborators like what they are – domestic terrorists.  It is a fight that you can win.  The truth, and a significant amount evidence, are on your side.

Post Script:  The author’s web site, with more information about fluoroquinolones, is www.floxiehope.com.  Further information about fluoroquinolones can be found through the Quinolone Vigilance Foundation – www.saferpills.org.

Numbered Sources:

  1. Inorganic Chemistry, “New uses for old drugs: attempts to convert quinolone antibacterials into potential anticancer agents containing ruthenium.
  2. FDA Warning Label for Ciprofloxacin
  3. The Journal of Biological Chemistry, “The Mechanism of Inhibition of Topoisomerase IV by Quinolone Antibacterials.”
  4. Findings of Toxicologist Joe King
  5. The Journal of Immunology, “Mitochondrial Reactive Oxygen Species Control T Cell Activation by Regulating IL-2 and IL-4 Expression: MechanismN of Ciprofloxacin Mediated Immunosuppression
  6. Antimicrobial Agents and Chemotherapy, “Effects of Magnesium Complexation by Fluoroquinolones on their Antibacterial Properties
  7. Proceedings of the National Academy of Sciences of the United States, Biochemistry, “Quinolone Binding to DNA Mediated by Magnesium Ions”
  8. Science Translational Medicine, “Bactericidal Antibiotics Induce Mitochondrial Dysfunction and Oxidative Damage in Mammalian Cells
  9. Journal of Young Pharmacists, “Oxidative Stress Induced by Fluoroquinolones on Treatment for Complicated Urinary Tract Infections in Indian Patients
  10. Antimicrobial Agents and Chemotherapy, “Ciprofloxacin Induces an Immunomodulatory Stress Response in Human T Lymphocytes
  11. Nature Precedings, “Oxidative Stress and Mitochondrial Injury in Chronic Multisymptom Conditions:  From Gulf War Illness to Autism Spectrum Disorder

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

cards

Advertisement
advertisement - learn more

Alternative News

The Reality of Vaccine Injury: A Much Needed Lesson for Carly Weeks

Published

on

In November, 1985, MPP for Rainy River, Jack Pierce stood in the Ontario legislature before second reading of a bill he had introduced. His words are recorded in the Hansard (the official report of proceedings of Parliament):

My bill deals with the occurrences and documentation of severe side-effects which can result from the vaccination of infants and children. Some members may not be aware that the routine vaccination called DPT, diphtheria, pertussis and tetanus, given to almost every one of our children, can lead to convulsions, brain damage and even death.

Today, if an MPP dared to shine light on vaccine injury, he would be eviscerated by the media. Today, anyone who broaches the issue of vaccine safety has to contend with the likes of Carly Weeks. In her Feb. 2019 attack on the Total Health Show, Ms. Weeks singled out “anti-vaccine activists” who by telling others about vaccination risks spread “false information.” In her to-the-point article, she implies that only medical professionals are qualified to speak about vaccination. In other words: you will be vaccinated and have no right to voice an opinion about it.

If injured families had not spoken up in the 1980s, we would not have Pierce’s bill that became the Health Protection and Promotion Act (1990). This law requires vaccinators to inform vaccine recipients of possible adverse outcomes and of the obligation to report these events.

Pierce explained why he brought the bill:

As a member of the riding in which eight children are thought to have sufferedpermanent mental retardation and physical handicap as a result of this inoculation, Ifeel compelled to see that something is done about this nightmare.

advertisement - learn more

I spoke with Jack Pierce, now in his 80s. He still lives in his old riding.  As an MPP in 1983, Pierce met with every member of parliament, one by one. He shared with each the need for a mandatory reporting of adverse reactions “so we can develop a complete and accurate picture of the benefits and risks of DPT.”

In 1985, MPPs could speak about vaccine injury without fear of reprisal from the media. Pierce continued:

While the diphtheria and tetanus components are mandatory and nonproblematic, the pertussis component, better known as whooping cough vaccine, has been responsible for severe reactions, including high fever, seizures, inflammation of the brain, permanent brain damage and sometimes death. Immunization against whooping cough is not mandatory. Parents have the right to refuse shots, and many are exercising this right.

… no one ever told him of the possibility of an adverse reaction to DPT

Pierce described the “heartbreaking stories of children who, despite the fact that they showed obvious adverse reactions to the pertussis vaccine, were given subsequent DPT shots.”

Patrick Rothwell of Burlington, Ontario, is six years old, blind, mentally retarded and speechless. His father said that no one ever told him of the possibility of an adverse reaction to DPT.

The Rothwell case is the lesson we failed to learn in Ontario.

In 1979, Patrick Rothwell received three doses of the whole cell DPT vaccine that caused him to regress. Patrick’s parents sued two doctors, the vaccine maker Connaught and the Crown alleging they had not been warned that the pertussis vaccine can cause brain damage.

Although 50 witnesses testified over 74 days at the 1988 trial their defeat was inevitable. The plaintiffs would never have been able to meet the burden of proof.

The presiding judge stated:

. . . the normal process of litigation is an utterly inappropriate procedure for dealing with claims of this nature. [Rothwell v. Raes (Ont. H.C.J.), 1988 CanLII 4636 (ON SC)]

In a review of the Rothwell case, the Manitoba Law Reform Commission agreed with the judge:

In practical terms, the tort process holds out very little promise for an efficient and fair remedy for those children who suffer vaccine-related injury and illness.

Pierce seemed to know that government needed to step in:

No one questions the need of a vaccine like DPT, but given the risks of paralysis, brain damage and death, the questions that might be addressed concern the levels of effort to find a safer drug and to make parents and doctors aware of the dangers and side-effects directly attributable to the vaccine. Where have the efforts been to make mandatory the reporting of adverse side-effects to the local medical officer of health?

Indeed.

At this point, after a trial and parliamentary debate with the passage of a law in 1990 to help reduce vaccine injuries, what interests kept the whole cell pertussis DPT vaccine in the schedule? Why were there still no warnings to parents of the risks?

… resulted in over 11,000 AEFI reports that described adverse reactions that included inconsolable screaming, head banging, seizures, anaphylaxis, paralysis and death. There was no follow-up on these children to determine long term injuries.

A familiar story.

In 1994, my son received three doses of the same Connaught DPT vaccine that Patrick Rothwell had received. Ours was mixed with two other vaccines. Use of this combination shot for 3 years resulted in over 11,000 AEFI reports that described adverse reactions that included inconsolable screaming, head banging, seizures, anaphylaxis, paralysis and death. There was no follow-up on these children to determine long term injuries.

Our story echoes those told by the Rainy River parents to Jack Pierce who then told the government. Like those parents, I had no real knowledge of vaccination when I took my son for his well baby visit and the nurse injected him. We were not warned of the documented risks before or after the procedure. Two laws intended to protect us were not observed: informed consent and Pierce’s health protection and promotion act.

An hour after vaccination, my two month old son began scream. He had never screamed before. I was terrified. And it continued for several hours. Through the night, I watched and listened. The next day, I called the GP who assured me that this was normal. I was persuaded by a medical professional to suppress my fears.

The second shot, two months later resulted in the same terrible reaction. And now, he had symptoms: rashes and he struggled to breathe through his nose.

His reaction to the third dose was violent.  He screamed and writhed in pain…

Nurses call this the neuro-scream, when the nervous system and brain are set on fire by the vaccine. And it changed him. The rhinitis and eczema that had developed I now know were red flags, precursors to life threatening allergies. He had his first anaphylactic reaction to peanut at 13 months. I have written extensively about the documented relationship between vaccination and allergy.

Meanwhile, the Ontario government continued to struggle with the issue of vaccine injury. In 1991, a bill was introduced by MPP Frankford, a physician, to compensate children and their families for vaccine-related injuries.

In the Hansard, MPP McLean agreed. The plan was “feasible” and “social conscience demands its enactment.”

The bill to compensate was quashed in 1991. Attempts to revive it have floundered in large measure on the altar of high cost. It is easier to download the costs to children and families. It is easier not to investigate, to deny injuries exist and ultimately block public access to AEFI reports if anyone tries to dig. (See note below.)

Fast forward to 2019.

The Canadian Medical Association has voted in favour of ending non-medical exemptions and making vaccination mandatory for Ontario children while at the same time voting against compensation for vaccine injuries.[9] As if on cue, the province amended its Immunization of School Pupils Act to withhold exemptions until a parent attends an education session designed to instill compliance. And anyone who tells parents of the documented risks, of the lack of consumer protections or speaks up on behalf of their own vaccine-injured children will be demonized as an “anti-vaxxer” who spreads “false information.”  In such a climate, it is not hyperbole to suggest that a law mandating the injection of children… will be followed by the same for adults.

And this dystopian reality — that Jack Pierce would have denounced — is something Ms. Weeks is paid to promote.

Note: We have an enormous deficit in information caused by a surveillance system that is passive, an under-reporting of adverse events and the fact that there is no follow-up on Adverse Events Following Immunization reports to determine long term injuries.  According to PHAC there were 115,837 AEFIs between 1987 and 2011 with 85% of them being children. If, as is generally recognized, this represents just 10% (some say it is 1%) of all adverse events, then we have upwards of one million events over 24 years about which we have no data.  In attempting to retrieve what information might be available to the public, I made an ATIP request in October 2016 for all AEFI reports (redacted) for the MMR II DIN#00466085 made by Merck Frosst Canada. This has still not been fulfilled. After lengthy email exchanges with various staffers at PHAC, I have had to conclude that either the records do not exist, they cannot access them or they are unwilling to send the redacted reports to me.

 Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. CHD is planning many strategies, including legal, in an effort to defend the health of our children and obtain justice for those already injured. Your support is essential to CHD’s successful mission.

 

Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

cards

Continue Reading

Awareness

Natural Herbal HPV “Cure” Discovered

Published

on

In Brief

  • The Facts:

    This article was written by Sayer Ji, founder of Greenmedinfo.com where it was originally published. Posted here with permission.

  • Reflect On:

    Despite the widespread belief that HPV infection is a lethal force against which we only have vaccination to defend ourselves, both ancient herbal medicine and our body's inherent immune defenses have newly been confirmed to help combat it.

A groundbreaking study published in the Asian Pacific Journal of Cancer Prevention, titled, “Clearance of Cervical Human Papillomavirus Infection by Topical Application of Curcumin and Curcumin Containing Polyherbal Cream: A Phase II Randomized Controlled Study,” reveals that vaccination and watchful waiting are not the only recourse against HPV infection.

The study is believed to be the first of its kind to find an effective and safe therapeutic intervention for the clearance of established cervical human papillomavirus (HPV) infection. Moreover, the study confirmed that HPV infection is self-limiting and clears on its own in 73.3% of the untreated placebo group within 37 days. 

The researchers evaluated the effectiveness of two herbal interventions in eliminating HPV infection from the cervix of women who were determined to have HPV infection through Pap smear and HPV DNA tests (PCR), but whose condition had not yet progressed to high grade cervical neoplasias (i.e. cervical pre-cancer).

The first intervention used was a polyherbal vaginal cream containing containing extracts of curcumin, reetha, amla and aloe vera, known by the trade name Basant. The second intervention was a curcumin vaginal capsule. The other two placebo groups received either a vaginal placebo cream or a placebo vaginal capsule.

All 287 subjects were instructed to use one application of the assigned formulation daily for 30 consecutive days except during menstruation. Seven days after the last application they were recalled for repeat HPV test, cytology and colposcopy.

The results were reported as follows:

advertisement - learn more

“HPV clearance rate in Basant arm (87.7%) was significantly higher than the combined placebo arms (73.3%). Curcumin caused higher rate of clearance (81.3%) than placebo though the difference was not statistically significant.”

Vaginal irritation and itching, mostly mild to moderate, was significantly higher after Basant application. No serious adverse events were noted.

While both of the herbal formulations clearly increased the rate of HPV clearance, it is noteworthy that the placebo group also experienced a 73.3% clearance rate, as it confirms that majority of HPV infections will clear from the body as a result of the immune system doing its job correctly. The researchers acknowledged that this is not a novel finding:

“It is already documented that the majority of HPV infections are self-limiting and cell-mediated immunity is responsible for spontaneous clearance.”

Indeed, we addressed this under appreciated fact in a previous article titled, The HPV Vaccine Debate: Don’t Ask, Don’t Tell:

[I]n 2004, Lancet published a study which found that low-grade squamous intra-epithelial cervical lesions (LSIL) commonly associated with HPV infection spontaneously regress in 61% of females within 12 months and 91% within 36 months.[i] LSIL is considered a mild form of cervical dysplasia (CIN), but is nonetheless often subject to more aggressive measures such as a colposcopy with biopsy,[ii] which sometimes leads to surgical treatment.

Another 2010 study published in the European Journal of Obstetrics, Gynecology and Reproductive Biology found that at the end of 12 months of follow-up, the CIN 2 regression rate was 74% (31/42), progression rate to CIN 3 was 24% (10/42) and in one case CIN 2 persisted (2%).  Finally, a 2011 study in the Journal of Lower Genital Tract Diseases found At 12 months, 70% of CIN 1 and 54% of CIN 2 lesions spontaneously regressed (p<.001).[iii]

The odds therefore are clearly in the favor of HPV-associated abnormal cell changes (so-called ‘precancerous’ lesions) regressing naturally like most self-limiting viral infections. Vaccines are clearly not responsible for the ‘protection’ conferred by our inbuilt immunity; nor is the HPV virus some inevitable force of lethality that only universal HPV vaccination campaigns can effectively countermand.

Given the widespread belief that HPV infection is a lethal force against which we have only vaccination and watchful waiting to defend ourselves, this latest encourages us to recognize both the power of the human body and natural plant allies to help us maintain our health, despite the constant threat of infection.

In actuality, the results of the intervention are not surprising, given the established body of research indicating curcumin’s value as an anti-cancer agent. Not only has this powerful turmeric polyphenol been extensively researched for its anti-cancer properties in over 100 difference cancer cell types, the GreeMedInfo database contains 11 studies specifically on curcumin’s anti-cervical cancer properties, which can be viewed here.

For additional information on HPV related concerns, view the following sections on our database:

Human Papillomavirus HPV

Vaccination: HPV Gardisil

Cervical Cancer


Sayer Ji is founder of Greenmedinfo.com, a reviewer at the International Journal of Human Nutrition and Functional Medicine, Co-founder and CEO of Systome Biomed, Vice Chairman of the Board of the National Health Federation, Steering Committee Member of the Global Non-GMO Foundation.


Original Article


Help Support Collective Evolution

The demand for Collective Evolution's content is bigger than ever, except ad agencies and social media keep cutting our revenues. This is making it hard for us to continue.

In order to stay truly independent, we need your help. We are not going to put up paywalls on this website, as we want to get our info out far and wide. For as little as $3 a month, you can help keep CE alive!

SUPPORT CE HERE!

cards

Continue Reading

Awareness

How To Care For Your Liver: Debunking The Popular & Harmful Liver Myths

Published

on

In Brief

  • The Facts:

    Your liver is #1 protector. There are many myths surrounding the liver that impede its ability to do its job. These myths include taking ox bile, doing liver flushes, doing coffee enemas, avoiding fructose, drinking apple cider vinegar, and more.

  • Reflect On:

    Besides avoiding the popular liver myths listed in this article, avoid eating too many fats, processed or raw, and increase your uptake of nutrient-dense, antioxidant-rich foods like fruit, vegetables, and herbs.

If you haven’t picked up a copy of Medical Medium’s new book, “Liver Rescue,” do yourself a favour today and get one. The book is a four-hundred page encyclopedia of in-depth knowledge regarding our liver, knowledge which has yet to be discovered by medical research, knowledge which could save you and your family’s and friends’ lives.

If you think that your liver is in pristine shape, you’re about to learn otherwise—in this day and age our livers are under tremendous pressure from the onslaught of pathogens and environmental toxins in our food, air, water, hygiene products, clothing, and households. And even if you grew up eating ‘clean,’ drinking clean water and living in a natural environment, your liver could be holding poisons (like toxic heavy metals) from many generations before you, passed down from your mother and grandmother.

What drove me to want to learn more about my liver came out of two factors. One, I grew up with a mouth full of amalgam (mercury) fillings, and two, in 2014 I had a severe mono and hepatitis A infection which nearly caused my liver to fail. So I knew that there was deep damage that had occurred from these two factors alone, not to mention that I grew up on a standard American diet (SAD) full of processed junk and void of fresh fruits and vegetables. Not to mention all of those years of binge drinking alcohol in my teens and early twenties (dare I say more).

Your liver is your number one protector

What I love most about Anthony William’s books is that they give us a unique understanding of the processes happening within the body. He humanizes our livers and helps us see how hard this organ is working for us at all times.

Our livers have been our number one protectors from the time we were in our mother’s wombs. That is its sole job—to protect us from the unfathomable amount of toxins in our environment. This protection code was passed down from your mother’s liver, to never give up on you, to take on the brunt of every pathogen, every toxin, and excess adrenaline that you come into contact with. It will do so with unwavering loyalty and commitment, even until its own demise. But we must not let this happen. At some point we must give back to this precious organ, we must swoop in and say enough is enough, it’s time to heal our livers.