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What Big Pharma Doesn’t Tell Parents: The Truth About Aluminum & Mercury In Children’s Vaccines

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Below are two previously published but important articles featured on our website that go into detail regarding mercury and aluminum. We are working to create more awareness on this topic as well as share an important documentary series about this subject that everyone should watch to stay informed.

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Chemicals that are commonly used in the production of vaccines, according to the CDC, are done so to improve the effectiveness of the vaccine. Adjuvants like aluminum (one of the most common) are a component of vaccines that potentates the immune response to an antigen. The adjuvant is basically used to invoke the desired immune response.

Aluminum has been added to vaccines for approximately 90 years, and since then, a lot of controversy, especially in recent years, has emerged regarding their safety and effectiveness.

This is precisely why we are raising awareness about this new docu-series which features a number of experts (doctors and scientists) discussing the topic of vaccines. Click here or on the image below to find out more about the series. 

 This controversy comes as a result of a number of recent studies (some of which are presented in this article) outlining clear concerns over the use of aluminum in this manner, as well as the fact that over the past few years, billions of dollars have been paid to families with vaccine injured children.

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There are a number of reasons why more parents are choosing not to vaccinate their children.

This is quite concerning, given the fact that recommended immunization rates have more than doubled in the past few decades. In some developed countries, by the time a child is 4 to 6 years old, they will have received a total of 126 antigenic compounds, along with high amounts of aluminum adjuvants through routine vaccinations.

Here are some eye opening reasons why so many people are starting to question the safety of administering vaccines that contain aluminum.

Below is a a video from Chris Shaw who you’ll more about later in the article

No Safety Assessments (Toxicity Studies) For Vaccine Ingredients

Again, aluminum has been added to vaccines for approximately 90 years, and one disturbing fact that many people still don’t know is that the Food and Drug Administration (FDA) and vaccine manufacturers themselves have not conducted or included appropriate toxicity studies/testing proving the safety of aluminum, or any other ingredients, for that matter. These ingredients have been put into vaccines based on the assumption that they are safe. Yes, you read that correctly. It’s kind of disturbing, isn’t it?

So because vaccines have been viewed as non-toxic substances, the FDA and vaccine manufactures have not conducted appropriate toxicity studies to prove the safety of vaccine ingredients – more specifically, aluminum.(source)

I have a document from 2002 from the US Food and Drug Administration (FDA)…discussing the assessment of vaccine ingredients…and testing specifically in animal models…Back then, the FDA states that the routine toxicity studies in animals with vaccine ingredients have not been conducted because it was assumed that these ingredients are safe, when I read this I was kind of pulling my hairs out [thinking] ‘So, this is your indisputable evidence of safety?’ – Dr. Lucija Tomlijenovic, PhD., a post-doctoral fellow at the University of British Columbia where she works in neurosciences and the Department of Medicine. (source)

She also has documents which reveal that vaccine manufacturers, pharmaceutical companies, and health authorities have known about multiple dangers associated with vaccines but chose to withhold them from the public. They show that health authorities and vaccine manufacturers made “continuous efforts to withhold critical data on severe adverse reactions and contraindications to vaccinations to both parents and health practitioners in order to reach overall vaccination rates, which they deemed were necessary for ‘herd immunity.’ ” (source)

If we take a look at the FDA’s website/guidelines, it’s not like this is a secret. The statement above (from Lucija) comes from their 2002 guidelines, which is a fairly recent document, but more than 10 years later, despite all of the studies demonstrating clear cause for concern, not much has changed.

Until recently, few licensed vaccines have been tested for developmental toxicity in animals prior to their use in humans. (source)

Despite their long use as active agents of medicines and fungicides, the safety levels of these substances have never been determined, either for animals or for adult humans—much less for fetuses, newborns, infants, and children. – Jose G. Dores, Professor at the University of Brasillia’s department of nutritional sciences. (source)

Aluminum Is An Experimentally Demonstrated Neurotoxin

A growing number of studies have linked the use of aluminum adjuvants to serious autoimmune outcomes in humans.  (source)(source)(source)(source)

The use of this adjuvant has been connected to all kinds of diseases, from autism to brain disease to Alzheimer’s and much more.

Experimental research … clearly shows that aluminum adjuvants have a potential to induce serious immunological disorders in humans –  Dr. Lucija Tomlijenovic (source)

There are numerous studies which have examined aluminum’s potential to induce toxic effects, and this is clearly established in medical literature, and has been for a long time. (source)

If significant aluminum load exceeds the body’s capacity to get rid of it, it is deposited into various tissues that include bone, brain, liver, heart, spleen, and muscle. Aluminum is found in cigarettes, cosmetics, food, medicines (aspirin), and much much more. It’s in our environment, and we are surrounded by it. This is concerning, because aluminum was not really around until the industrial revolution. Today, it shows up in so many products. And we know, from the work of Richard Flarend, that aluminum is commonly absorbed into the body, into areas it shouldn’t be, and has been found in various urine samples from multiple studies examining this topic… and that’s not just for aluminum in vaccines.

We increasingly have this compound that was not part of any biochemical process on Earth, that can now only go and do havoc, which is exactly what it does. It causes all kinds of unusual biochemical reactions. – Dr. Chris Shaw, a Neuroscientist and professor at the University of British Columbia

Here is a great video by Dr. Christopher Exley, Professor in Bioinorganic Chemistry at Keele University and Honorary Professor at UHI Millennium Institute. He is known as one of the world’s leading experts on aluminum toxicity.

Again, all of this information is exactly why we are promoting this new docu-series about vaccine safety. Here it for yourself from the mouth of a number of doctors and scientists from around teh world. 

The Body Reacts Differently To Aluminum Adjuvants In Vaccines Than To Aluminum Absorbed Into The Body From Food, Water, Medicine, etc…

Just imagine, you have a higher than normal body burden of aluminum. You are potentially accumulating it in certain areas in the body. You then receive multiple vaccinations, all of which contain some aluminum. In those multiple vaccinations, aluminum is acting as adjuvant and antigen, it sets off cascades of potential responses which I believe potentially can then cascade around the body, setting off potentially other stores of aluminum, whether they be in the brain, or the bone, the connective tissues, the places where we might expect to find high or raised levels of aluminum. Could this type of cascade effect explain why an aluminum adjuvant could then in some individuals only, produce such adverse effects? … Many of the adverse affects that you see in people who have suffered following vaccination are very similar to the known effects of aluminum intoxication. Dr. Christoper Exley (source)

One of the most common arguments to support the administration of aluminum into vaccines is the fact that a person usually accumulates more aluminum in their body each day from food alone, but what is not often considered is that your body has a different method of flushing it out of your system. They body is very good at doing this, usually through the kidneys, as illustrated by the video above.

But when you inject aluminum, it goes into a different compartment of your body. It doesn’t come into the same mechanism of excretion, and that’s the whole point of adjuvants, they are meant to stick around and allow that antigen to be presented over and over again. It can’t be excreted because it must provide that prolonged exposure of the antigen to your immune system. This is why they put it into vaccines in the first place. Something to think about.

Another great video here, a clip of Dr. Chris Shaw, a Neuroscientist and professor at the University of British Columbia, explaining the dangers of putting aluminum into vaccines as an adjuvant.

***HERE is an article that explores in depth (heavily sourced) why so many parents are choosing not to vaccinate their children. It’s important to present this information because these parents are often criticized and misunderstood.

Related CE Articles:

The Top 6 Reasons Why Parents Are Choosing Not To Vaccinate Their Children.

Neuroscientist Makes It Clear Why Aluminum Should Not Be Put Into Vaccines

MIT Scientist Shows What Can Happen To Children Who Receive Aluminum Containing Vaccines

Dr. Suzanne Humphries Has A Lot To Say About Aluminum In Vaccines

Mercury

Robert F. Kennedy Jr., Chairman of the World Mercury Project (WMP), announced a $100,000 challenge today aimed at putting an end to including mercury, a neurotoxin that is 100 times more poisonous than lead, in vaccines administered in the U.S and globally.

It’s offered to anybody, including journalists and scientists, who can provide a study showing that it is safe to inject mercury into babies. This will be difficult, as hundreds of studies (that were also present at the press conference in print form) suggest that it isn’t safe at all, and can significantly increase the risk of developing neurodegenerative disorders.

Robert De Niro and numerous other people support the World Mercury Project, many of which made a historical appearance at the National Press Club today bringing attention to an issue that more people are becoming aware of every single year. For nearly 100 years, appropriate safety assessments (toxicity studies) have not been conducted for the administration of vaccines containing mercury as an adjuvant, yet we continue to give them to the general public. Government health authorities have been putting mercury (and aluminum) in vaccines based solely on the assumption that it is safe to do so.

You can view the full press conference on the World Mercury Project Facebook Page.

Since vaccines have been perceived as non-toxic substances for decades, the Food and Drug Administration (FDA) has not attempted to prove the safety of this particular vaccine ingredient. Considering billions of dollars have been paid to families of children injured by vaccinations, it’s fair to say that this is an alarming state of affairs, so it’s about time that this press conference was held. (source)

Here is a quote from Dr. Jose G. Dores, a professor at the University of Brasilia’s Department of Nutritional Sciences who recently published a study in the International Journal of Environmental Research and Public Health. In the study, he offers the following observation: “Despite their long use as active agents of medicines and fungicides, the safety levels of these substances have never been determined, either for animals or for adult humans—much less for fetuses, newborns, infants, and children.”  (source)

A fairly recent Meta-Analysis published in the Journal Bio Med Research International found that:

 “The studies upon which the CDC relies and over which it exerted some level of control report that there is no increased risk of autism from exposure to organic Hg in vaccines, and some of these studies even reported that exposure to Thimerosal appeared to decrease the risk of autism. These six studies are in sharp contrast to research conducted by independent researchers over the past 75+ years that have consistently found Thimerosal to be harmful. As mentioned in the Introduction section, many studies conducted by independent investigators have found Thimerosal to be associated with neurodevelopmental disorders. Considering that there are many studies conducted by independent researchers which show a relationship between Thimerosal and neurodevelopmental disorders, the results of the six studies examined in this review, particularly those showing the protective effects of Thimerosal, should bring into question the validity of the methodology used in the studies.” (source)

Not only was the science (all from PubMed) present at the conference, facts about scientific fraud and industry influence were also brought up.

For example, Dr. William Thompson, a longtime senior CDC scientist, published some of the most commonly cited pro-vaccine studies, which showed that there was absolutely no link between the MMR vaccine and autism (Thompson, et al. 2007, Price, et al. 2010Destefano, et al. 2004). However, Dr. Thompson recently admitted that  it was “the lowest point” in his career when he “went along with that paper.” He went on to say that he and the other authors “didn’t report significant findings” and that he is “completely ashamed” of what he did. He was “complicit and went along with this,” and regrets that he has “been a part of the problem.” (source)(source)(source)

A  study with revised information and no data omitted was published by Dr. Brian Hooker (a contact of Dr. Thompson) in the peer reviewed journal Translational Neurodegeneration, and it found a 340% increased risk of autism in African American boys receiving the Measles-mumps-rubella (MMR) vaccine. The study has since been retracted around the same time of this controversy.

You can read the full study HERE; although, unsurprisingly, it has since been retracted.

Thompson’s attorneys, Robert F. Kennedy Jr. and Bryan Smith of Morgan & Morgan, also released a statement from Dr. Thompson, which mentioned Hooker: “I have had many discussions with Dr. Brian Hooker over the last 10 months regarding studies  the CDC has carried out regarding vaccines and neurodevelopmental outcomes including autism spectrum disorders. I share his belief that CDC decision-making and analyses should be transparent.” (source)

He had to invoke whistleblower protection and turned extensive agency files over to Congress. He said that for the past decade, his superiors have pressured him and his fellow scientists to lie and manipulate data to conceal a causal link between vaccines and brain injuries, including autism.

In addition to these, there are countless other concerns involving vaccines, which is precisely why more and more parents are choosing not to vaccinate their children.

For a more in-depth look into this topic, you can read this heavily sourced article we published about it, but keep in mind that more information is always coming to light, even since we published this one:

The Top 6 Reasons Why More and More Parents Are Choosing Not To Vaccinate Their Children

The World Mercury Project $100,000 Challenge & The Livestream

The World Mercury Project’s mission is to raise public awareness of the sources and dangers of mercury, help treat those who have been personally affected by mercury exposure, and to push for safe and responsible removal of mercury in all consumer products and industrial processes.

You can view the full press conference on the World Mercury Project Facebook Page.

“On the occasion of our announcement of the World Mercury Project’s $100K challenge, we want to address America’s reporters, journalists, columnists, editors, network anchors, on-air doctors and news division producers….

Despite the cascade of recent science confirming that thimerosal is a potent neurotoxin that damages children’s brains, the American media has fiercely defended the orthodoxy that mercury-based vaccines are safe. We believe that even a meagre effort at homework will expose that contention as unsupported by science. In just the past month, a Centers for Disease Control and Prevention (CDC) review confirmed thimerosal’s profound neurotoxicity and a Yale University study connected vaccines to neurological illnesses including OCD, anorexia and tics…

Journalists, we have discovered—even science and health journalists—don’t always read the science! On the vaccine issues, many of them have let government and industry officials tell them what the science supposedly says. Instead of questioning, digging and investigating, journalists, too often, have taken the easy course of repeating the safety assurances of the pharmaceutical industry and the regulators at CDC’s Immunization Safety Office, which they have good reason to doubt.” 

As you can see, there are many issues to create awareness about, and the fact that mainstream media continues to ignore this type of thing is a big concern, and means we should probably be paying even more attention to it.

“It’s our hope that this challenge will elevate this important debate beyond name-calling and prompt a genuine examination of the relevant science. The American public is entitled to an honest, probing and vigorous discussion about this critical public health issue – a debate based on facts, not rooted in fear, or on blind faith in regulators and the pharmaceutical industry,” wrote Kennedy in a letter addressed to America’s reporters, journalists, columnists, editors, network anchors, on-air doctors and news division producers that was handed out at the press conference.

Reminder: You can watch The Truth About Vaccines here for free

 

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12 Reasons Why Even Low Levels of Glyphosate Are Unsafe

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In Brief

  • The Facts:

    Decades of research have shown how Glyphosate is toxic in any amount, both for human and and the environment. This is not debatable.

  • Reflect On:

    Glyphosate is illegal in several dozen countries around the world due to health and environmental concerns. How can this product be approved for use when it's abundantly clear it's extremely unsafe, just like DDT was?

By Zen Honeycutt, Founding Executive Director Mom’s Across AmericaChildren’s Heath Defense Coalition Partner

Proponents of GMOs and Glyphosate-based herbicides and staunch believers in the EPA have long argued that low levels of glyphosate exposure are safe for humans. Even our own EPA tells us that Americans can consume 17 times more glyphosate in our drinking water than European residents. The EWG asserts that 160 ppb of glyphosate found in breakfast cereal is safe for a child to consume due to their own safety assessments, and yet renowned scientists and health advocates have long stated that no level is safe.  Confusion amongst consumers and the media is rampant.

Glyphosate is the declared active chemical ingredient in Roundup and Ranger Pro, which are both manufactured by Monsanto, the original manufacturer of Agent Orange and DDT. There are 750 brands of glyphosate-based herbicides.Glyphosate based herbicides are the most widely used in the world and residues of glyphosate have been found in tap water, children’s urine, breast milk, chips, snacks, beer, wine, cereals, eggs, oatmeal, wheat products, and most conventional foods tested.

The detection of glyphosate in these foods has set off alarms of concern in households and food manufacturers’ offices around the world. Lawsuits have sprung up against companies that make food products that claim to be “100% Natural” and yet contain glyphosate residues. These lawsuits have been successful. Debates, using the argument that “the dose makes the poison,” have been pushed by media. Speculation is that these media outlets are funded by advertisers that make or sell these chemicals or have sister companies that do, and threatening their profits would be unwise for all involved – except the consumers.

It is time to set the record straight

Here are 12 reasons why there is no safe level of glyphosate herbicide residue in our food or beverages.

  1. Babies, toddlers, and young children have kidneys and livers which are underdeveloped and do not have the ability to detox toxins the way adults doTheir bodies are less capable of eliminating toxins and therefore are particularly susceptible. The American Academy of Pediatrics (AAP) has stated that children, especially, should avoid pesticides because, “prenatal and early childhood exposure to pesticides is associated with pediatric cancers, decreased cognitive function and behavioral problems.”
  2. Glyphosate does not wash, dry or cook off, and has been shown to bioaccumulate in the bone marrow, tendons and muscle tissue. Bioaccumulation of low levels over time will result in levels which we cannot predict or determine; therefore there is no scientific basis to state that the low levels are not dangerous, as they can accumulate to high levels in an unforeseeable amount of time.
  3. “There is no current reliable way to determine the incidence of pesticide exposure and illness in US children.” -AAP  Children are exposed through food, air, contact with grass and pets. How much they are being exposed to daily from all these possibilities is simply not something that we have been able to determine. Therefore no one is capable of assessing what levels are safe from any one modality of exposure because an additional low level from other modalities could add up to a high level of exposure.
    1. Ultra-low levels of glyphosate herbicides have been proven to cause non-alcoholic liver disease in a long term animal study by Michael Antoniou, Giles Eric Seralini et al.  The levels the rats were exposed to, per kg of body weight, were far lower than what is allowed in our food supply. According to the Mayo Clinic 100 million, or 1 out of 3 Americans now have liver disease. These diagnoses are in some as young as 8 years old.
    2. Ultra-low levels of glyphosate have been shown to be  endocrine and hormone disrupting.Changes to hormones can lead to birth defects, miscarriage, autoimmune disease, cancer, mental and chronic illness.
    3. The  EPA Allowable Daily Intake Levels (ADIs) of glyphosate exposure were set for a 175-pound man, not a pregnant mother, infant, or child.
    4. Glyphosate alone has been shown to be chronically toxic causing organ and cell damage. Glyphosate herbicides final formulations, have been shown to be acutely toxic, causing immediate damage at low levels.
    5. The detection of glyphosate at low levels could mean the presence of the other toxic ingredients in glyphosate herbicides on our food. Until studies are done, one must practice the Precautionary Principle. The label on glyphosate herbicides does not specify the pesticide class or “other”/“inert” ingredients that may have significant acute toxicity and can account for up to 54% of the product.
    6. Regarding the label and low-level exposure: “Chronic toxicity information is not included, and labels are predominantly available in English. There is significant use of illegal pesticides(especially in immigrant communities), off-label use, and overuse, underscoring the importance of education, monitoring, and enforcement.” – AAP. Exposure to low levels of glyphosate herbicides can occur through pregnant wives or children hugging the father who is a pesticide applicator.  The chronic health impacts such as rashes which can, years later, result in non-Hodgkin lymphoma, are often ignored, especially by low income or non-English speaking users dependent on their pesticide application occupation for survival.
    7. The EPA has admitted to not having any long-term animal studies with blood analysis on the final formulation of any glyphosate herbicides.  The EPA cannot state that the final formulation is safe.
    8. For approval of pesticides and herbicides, the EPA only requires safety studies, by the manufacturer who benefits from the sales, on the one declared active chemical ingredient—in this case glyphosate. Glyphosate is never used alone.
    9. The main manufacturer, Monsanto, has been found to be guilty on all counts by a San Francisco Supreme Court Jury in the Johnson v Monsanto. This includes guilty of “malice and oppression” which means that the company executives knew that their glyphosate products could cause cancer and suppressed this information from the public.

    Clearly, it is time for food and beverage manufacturers to have a zero tolerance for glyphosate residue levels and for the US EPA and regulatory agencies everywhere to stop ignoring the science and to revoke the license of glyphosate immediately.

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    Moms Across America is a 501c3 non profit organization whose motto is “Empowered Moms, Healthy Kids.”

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.

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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!

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Cannabis Oil Was Used To Treat Epilepsy 176 Years Ago

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In Brief

  • The Facts:

    Cannabis has been used to treat people with Epilepsy for more than 100 years. Numerous people including children have had tremendous success with it, but it's not disclosed within the mainstream as much as it should be.

  • Reflect On:

    The medicinal properties of cannabis have been known for a long time, so why is it so difficult for patients to access? Today, things are changing, but big pharma is taking it over for themselves. How will they grow it? What will they spray it with?

Cannabinoids have been found to have antioxidant properties, unrelated to NMDA receptor antagonism. This new found property makes cannabinoids useful in the treatment and prophylaxis of a wide variety of oxidation associated diseases such as ischemic, age-related, inflammatory and autoimmune diseases. The cannabinoids are found to have particular application as neuroprotectants, for example in limiting neurological damage following ischemic issues such as strokes and trauma, or in the treatment of neurodegenerative diseases such as Alzheimer’s disease, Parkinson’s disease and HIV dementia. Non-psychoactive cannabinoids such as cannabidiol are particularly advantageous to use because they avoid toxicity that is encountered with psychoactive cannabinoids at high doses useful in the method of the present invention. A particular disclosed class of cannabinoids useful as neuroprotective antioxidants is formula (I) wherein the R group is independently selected from the group consisting of H, CH3, and COCH3. (Source)

The statement above comes from a patent owned by the United States government, which was assigned decades ago. Since then, countless amounts of studies have shown how the active constituents within cannabis, like cannabidiol for example,  completely obliterate cancer cells in the lab in vitro. As illustrated above, it has a wide variety of health applications, which begs the question when it comes to various diseases, why have we not seen any clinical trials? There are so many published studies warranting clinical trials when it comes to using cannabis to treat cancer, among several other diseases.

When the development of a drug shows even a quarter of the potential that cannabis has over the years, it seems that funding for clinical trials becomes instant. But when it comes to cannabis, which has obviously shown huge potential, we’ve seen nothing. I am more so referring to clinical trials with regards to cancer. Just imagine if we funded studies using natural remedies with the same amount of money we invest into pharmaceuticals. Would certain cancers be cured? Again, we don’t know, because the resources haven’t been adequately dished out, and if it did turn out that cannabis could obliterate multiple cancers in vivo (full living biological organisms), it would be against corporate interests.

However, this will likely change now that medical marijuana is being legalized across the world, the most recent example being Canada. This has brought up multiple concerns from citizens, as Big Pharma is now taking over the medical cannabis industry. How it’s grown, what pesticides are being put on it, and whether or not it’s genetically modified is still unknown. The truth is, pharmaceutical marijuana will not at all compare to marijuana that’s grown naturally in nature. If one were to study the medicinal properties comparing the two, I bet there would be a significant difference.

Big pharma is taking over the medical marijuana industry. Legalization in Canada and various US states was largely done in order to profit these big corporations who don’t really seem to care about our health at all. The main reason why cannabis has been illegal for so long is that powerful corporate interests have had a huge hand in keeping cannabis off the market. Cannabis can eliminate the need for many prescription drugs, for example, and these alone kill approximately 100,000 people a year, and that’s in the United States alone.

Cannabis & Epilepsy

Children and people with epilepsy have had a very hard time accessing medical marijuana to treat their condition. Again, this is largely because the use of it threatens corporate interests. This became even more evident a couple years ago when 12 year old Alexis Bortell sued Attorney General Jeff Sessions and The Drug Enforcement Administration (DEA). She needed access to clean, pure, natural cannabis for the treatment of her illnesses and medical conditions. The family had no choice but to relocate from Texas to Colorado and uproot their entire lives just to treat her severe epilepsy.

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The crazy thing about cannabis and epilepsy is the fact that it works, and that’s something that has been known for a number of years. Sure, it might take a lot of time to find the right strand, make it into oil, and get the dosage amounts exactly right, but that’s only because parents and doctors who are actively engaged in using this as medicine don’t have the resources to figure this out in an efficient way.

Cannabis and its ability to treat epilepsy has been known for a long time, probably much longer than we are aware of. Prior to Rockefeller creating medical education, it was probably used a lot. Rockefeller and other ‘philanthropists’ played a large role in shutting down all medical schools before they began funding and building their own medical education and treatment methods. During this process, an enormous amount of knowledge was lost, and the treatment methods that were most profitable became mainstream.

The first detailed modern description of cannabis as an anti-seizure medication was published in 1843 by W.B. O’Shaughnessy, a physician in the Bengal Army and Late Professor of Chemistry and Materia Medica at the Medical College of Calcutta. A perfect example of what I just referred to above with regards to medical education.

After testing the behavioural effects of various preparations of Cannabis indica in healthy fish, dogs, swines, vultures, crows, horses, deers, monkeys, goats, sheep, cows, and military assistants, he investigated the potential value of extracts of the plant in patients with different disorders, and reported remarkable anti-seizure effects in a 40-days-old baby girl with recurrent convulsive seizures. These observations were taken up by other physicians, including Sir William Gowers, who described the effectiveness of Cannabis Indica against seizures resistant to bromides. (source)

In the twentieth century the use of cannabis declined somewhat because cultivation of the plant was made illegal in many countries.

Below is a graph of  the number of articles retrieved in PubMed by using the search terms ‘cannabis and epilepsy’, grouped by year of publication.

One of Many Real World Examples

Alex Repetski, father of three year old daughter, Gwenevere, has spent a long time reading through studies and medical journals and researching CBD and its healing properties to help her with the tonic, myoclonic, and clinical seizures she was having — sometimes up to 50 a day. She was diagnosed with epilepsy and, as her EEGs revealed, was experiencing constant subclinical seizure activity throughout the day. It may not have looked like she was having a seizure from the outside, but at the brain level there were neurons firing constantly, and such activity can produce significant brain damage.

Gwenevere had a team of doctors that were trying an array of treatment methods to reduce the number of seizures she was having each day. At one point she was on 9 different medications. They kept hoping each subsequent medication would work, but nothing did. That’s when Alex decided to look into cannabis oil. “At that point, we really didn’t have anything to lose,” he said, as he recalled the struggle of trying to help his daughter achieve a better quality of life.

After acquiring the cannabis and reducing it down to its oil form, Alex proceeded with many rounds of trial and error, trying to find just the right dosage for Gwenevere. After five days, they noticed no seizures. Then another week went by, and then a month, and then two months of no seizures. Two Januaries ago, she went in for her 17th EEG after being on cannabis oil for 5 weeks.

This EEG was strikingly different from her previous ones. It seemed the cannabis oil had helped straighten out her brainwaves, working at the subclinical level. This was a huge moment for the Repetski family.

The Takeaway

Corporations have amassed so much power that plants and natural substances with unbelievable healing properties are being made illegal. Furthermore, many doctors are brainwashed to believe that this is still a controversial topic. And with legalization comes the takeover of this medicine by big pharmaceutical companies. If you want to know about the healing properties of cannabis, you don’t have to look far. It’s also important to acknowledge that theses benefits typically do not include smoking the plant, since that completely changes its chemical composition.

It’s very hard to find pure, healthy, and properly grown cannabis today. It requires a lot of research and a lot of work to find, which is in large part due to government regulations and big pharma. Anything that threatens corporate interests, no matter how helpful it can be for humanity, is often hidden from us or made illegal.

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!

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Awareness

Tylenol Damages The Brains of Children, Research Reveals

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In Brief

  • The Facts:

    Tylenol has a wide range of toxic side effects you should be aware of, especially if you are pregnant or use it with your children. Article written by William Parker, Ph.D for Greenmedinfo.com, published here with permission.

  • Reflect On:

    Why do we keep taking Tylenol and other over-the-counter drugs when it's unquestionable that they do more harm than good? Why don't we ever look into healthy ways to alleviate our symptoms?

Original Article Link

A number of non-peer-reviewed articles have been written and published on the web claiming that there is literally nothing to fear from acetaminophen during pregnancy. There are two types of articles that fall into this category. First, reputable watchdog organizations have weighed in on the issue, declaring acetaminophen use during pregnancy and during childhood to be proven safe. In particular, the National Health Service of the UK and the Center for Accountability in Science have both strongly criticized the Spanish study from 2016 showing a link between acetaminophen use during pregnancy and ADHD/autism.

The second type of article is generally written by a science writer working for an organization that runs a website. Often quoting one to three experts who claim that is perfectly safe and that pregnant women and families should not be concerned, many of these articles are published by reputable sources that are generally trustworthy. Typically, an expert is being asked to comment on one particular publication showing a link between acetaminophen use (usually during pregnancy) and some sort of neuropsychiatric problem (autism, lowered IQ, hyperactivity, and/or social/behavioral problems, depending on the study). There are several important things to consider when evaluating these articles:

1.  There are a number of University Professors who have studied the use of acetaminophen on the developing brain and who are keenly aware of the potential dangers. A partial list of these individuals is provided below.

2.  Being an expert in acetaminophen neurotoxicity during development means that considerable time has been invested in studying the issue. Any true expert in this issue will be aware of basic facts regarding acetaminophen neurotoxicity. These facts include the following:

(a) Studies in animal models (both in mice and in rats) demonstrate that acetaminophen use during a sensitive period of brain development causes long-term alterations in the brain and is manifested as problems with social function.

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(b)  Margaret McCarthy, Chair of Pharmacology at the University of Maryland, has worked out the probable mechanism by which acetaminophen-induced brain damage occurs. Her research team has found that the male brain is considerably more sensitive to acetaminophen than the female brain, possibly accounting for the gender bias in autism.

(c) There are (as of January 2017) a total of 8 published studies evaluating the long terms effects on children of acetaminophen use during pregnancy or during childhood. Two of these (one in 2014, one in 2016) were published in JAMA Pediatrics, one of the most highly respected pediatric journals. All studies point toward acetaminophen use being associated with long-term problems with neurological function. Each study design has included some attempt to control for indication. In all studies, acetaminophen use rather than indication has been identified as the key factor associated with cognitive problems. A formal meta-analysis is not currently possible because of the varied outcome measures and study designs, but all 8 studies point in the same direction: Acetaminophen is neurotoxic to the developing brain. The studies are not “cherry picked”, selecting only those which find an effect. All studies point toward a neurotoxic effect of acetaminophen in the developing brain.

(d)   Acetaminophen substantially alters brain chemistry and temporarily impairs awareness of social issues in adult humans.

(e)  Testing of acetaminophen safety in children did not include any evaluation of brain function, and no long-term studies were ever conducted. The primary manufacturer of acetaminophen in the US acknowledges that the drug has never been shown to be safe for brain development when used during pregnancy or in childhood. All safety tests were performed with the assumption that any side effects would be acute in nature (e.g., bleeding or acute organ damage). This assumption was based on observations made with acetaminophen in adults and with aspirin in children. It was not based on any experience with acetaminophen use in children.

3.     Having prescribed tens of thousands of doses of acetaminophen does not make anyone an expert on the neurotoxicity of acetaminophen, any more than eating thousands of pounds of chips makes somebody an expert in the effects of an inflammatory diet. Credentials and certifications that allow physicians to prescribe acetaminophen do not make them experts, and elevated positions in the medical community do not qualify anybody as an expert on the effects of acetaminophen. If somebody does not know those basic facts listed above, then they are not an expert on the neurotoxicity of acetaminophen. Usually, the experts will have published one or more peer-reviewed manuscripts on the topic. Those are the people to ask when an expert is needed.

4.     It is tempting to point accusing fingers at physicians who say that acetaminophen is safe when they literally have no grasp whatsoever of the relevant scientific literature. However, this would be a mistake. I have tracked down a few of these individuals who were quoted in a very public format, and one individual, in particular, didn’t even remember having made a comment on the topic. The most likely explanation is that a reporter asked them if acetaminophen was safe, and their response based on their training (not on the knowledge of the literature) was that it is safe. After all, if they didn’t think it was safe, they would not be administering it dozens of times per day. So, if a reporter asks a physician if something is safe, and they provide their knowledge based on what they have been taught and how they practice, then it is hard to blame them. The reporter didn’t ask them to spend days or even weeks reviewing the literature in detail, but rather assumed that any physician administering something dozens of times per day would know the literature. (This is a false assumption. No physician has the time to study all current literature on every drug they administer.) So, in a nutshell, a tragic propagation of incorrect information is occurring despite the best of intentions of all parties involved.

5.     Unless an organization such as the National Health Service has the time to review a topic thoroughly, they should remain silent on an issue. It took a team of us two years to put together our summary of the evidence, both direct and circumstantial, regarding the potential neurotoxicity of acetaminophen during development. It took the NHS only days to publish their recent criticism of the 2016 Spanish study. Offering questionable criticisms of a single paper without reviewing the literature to see how that publication fits into the big picture is a disservice to the public being served.

6. Reading the published quotes from many “experts” who exonerate acetaminophen, it is apparent that the logic falls into one of two categories.

(a) Everybody is doing it, so it must be OK.

(b) This single study is not perfect, so no change in practice should be made.

Neither of these criticisms is logically sound, of course. These two criticisms are often combined and were, in fact, part of the critical comments directed toward the first paper showing that acetaminophen probably has substantial neurotoxicity during development (published in 2008 by Steve Shultz). Further, the evaluation of study weaknesses is usually skewed and not entirely valid. Since the idea that acetaminophen is safe is being embraced, then any merit in the paper is often undermined to make the case. This is certainly true of the published (peer reviewed) criticisms of the 2008 Shultz paper.

7.     Many on-line sources support the view that acetaminophen can be very dangerous to the developing brain. Probably the most reliable source, the FDA, is remaining silent on the topic until something more definitive is done. The FDA knows that this is extremely urgent, but unfortunately, our FDA is not linked well (in a practical manner) with our NIH, and thus they can’t dictate research priorities.

8.     Here is a list (not comprehensive) of experts regarding the neurotoxicity of acetaminophen during brain development.

a) First, I’ll thank the wonderful team of individuals who helped put together our comprehensive review on this topic. Shu Lin, a professor with me in Duke’s Surgery Department, is a very dear and long-time friend of mine who has supported me through countless projects over the past 22 years. Staci Bilbo, director for research on Autism at Harvard, is a friend and collaborator who has helped me understand what causes inflammation and the role of inflammation in brain dysfunction. Chi Dang Hornik, a pediatric pharmacist at Duke, contributed greatly to our understanding of the frequency of acetaminophen administration and the available formulations of the drug. Many thanks to Martha Herbert. As a Harvard professor and clinician, she has a great appreciation for the clinical data obtained from patients with autism. Cindy Nevison, a professor at the University of Colorado at Boulder, rounds out our team, providing critical information about the epidemiology of autism. (Thanks also to our interns (Rasika Rao and Lauren Gentry) and research analyst (Zoie Holzknecht) who were a tremendous help in compiling information and preparing that information for publication.)

b) Margaret McCarthy, chair of Pharmacology at the University of Maryland, it the most knowledgeable person I know regarding the biochemistry of the human brain and how that is affected by acetaminophen and other drugs in that class.

c) Chittaranjan Andrade, Chair of Psychopharmacology at the National Institute of Mental Health and Neurosciences, Bangalore, India, has written a peer reviewed paper on the topic of acetaminophen induced brain damage. He nicely summarized a number of studies looking at the connection between acetaminophen and neurological damage. His final conclusion is that the drug is probably more associated with ADHD than autism, but the conclusion was limited to exposure during pregnancy and his work was conducted before some critical studies were published in 2016.

d) Henrik Viberg is a professor in the Department of Organismal Biology at Uppsala University in Sweden. He has studied how exposure of mice to acetaminophen during development can cause long term brain damage.

e) In 2015, a group of scientists working with Laurence de Fays at the Federal Agency for Medicines and Health Products in Brussels acknowledged the clinical studies and the studies in animal models which indicated that acetaminophen could be dangerous to the developing fetus, but concluded that paracetamol is “still to be considered safe in pregnancy”. At the same time, they state that “additional carefully designed studies are necessary to confirm or disprove the association (between acetaminophen and brain damage to children)”, and that “care should be taken to avoid raising poorly founded concerns among pregnant females”. We very strongly agree with the conclusion that more studies are needed, but very strongly disagree with the conclusion that women should be kept in the dark about the matter. It is important to point out that several more studies have come out since Laurence de Fays’ report. One of those is a 2016 manuscript in JAMA Pediatrics(see the next expert), a highly reputable peer reviewed journal, which addresses the concerns raised by de Fays, so it is possible that de Fays’ group may now have a different opinion.

f) A team of scientists and doctors working with Evie Stergiakouli at the University of Bristol analyzed data from a prospective birth cohort, and concluded that “children exposed to acetaminophen prenatally are at increased risk of multiple behavioral difficulties”. They found considerable evidence indicating that the association was not due to the confounding factors that concerned de Fays’ group (previous expert).

g) Jordi Julvez at the Centre for Research in Environmental Epidemiology in Barcelona, Spain worked with a team of a dozen clinicians and scientists to publish their 2016 study linking acetaminophen with autism and ADHD.

h) Amany A. Abdin, a professor in the Department of Pharmacology, Tanta University, Egypt, wrote a review of the acetaminophen/autism connection and published it in the journal Biochemistry and Pharmacology: Open Access. Her conclusion in 2013 was that the drug is not safe and that the acetaminophen/autism connection should receive attention.

i) The original paper that identified a connection between neuropsychiatric disorders and acetaminophen was published by Steve Shultz while at the University of California at San Diego. Coauthors on the paper included Hillary Klonoff-Cohen, currently an Endowed Professor and Director of the MPH program at the University of Illinois.

j) Four scientists, including research scientist Ragnhild Eek Brandlistuen and professors Hedvig Nordeng and Eivind Ystrom in the Department of Pharmacy at the University of Oslo, coauthored a study showing a connection between adverse neurodevelopment and acetaminophen use during pregnancy.

k) Jorn Olsen, Professor and Chair of the Department of Epidemiology at UCLA, published one of the more recent papers (2016) showing a connection between autism and acetaminophen use during pregnancy.

l) Five professors (John M. D. Thompson, Karen E. Waldie, Clare R. Wall, Rinky Murphy, and Edwin A. Mitchell) from four different departments at The University of Auckland published their findings in PLOSone in 2014 which “strengthen the contention that acetaminophen exposure in pregnancy increases the risk of ADHD-like behaviours. Our study also supports earlier claims that findings are specific to acetaminophen.”

For evidence-based research on the dangers of acetaminophen, visit the GreenMedInfo.com Research Dashboard.\

Read their related article on Tylenol: 

Tylenol Kills Emotions As Well As Pain, Study Reveals

Sign Up For The Greenmedinfo Newsletter HERE.


William Parker is an Associate Professor at Duke University, where he has worked in the Department of Surgery since 1993.  William is currently investigating a number of issues associated with inflammation and Western society, including vitamin D deficiency, heart disease and alteration of the symbionts of the human body (“biota alteration”). He has been interested in “natural” immune function for some time, which has led him down a path that includes the first studies of immune function in wild rats and the discovery of the function of the human appendix.

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