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CANCER CURE NEWS

The FDA Just Outlawed Hemp Oil — The #1 Cancer Treatment in The World

Hemp oil extracts containing CBD (cannabidiol) are such a threat to the pharmaceutical industry that the FDA is now invoking totally insane justifications for outlawing them.

According to the FDA’s website: “The cannabidiol products are excluded from the dietary supplement definition”. The FDA has also started sending aggressive warning letters to CBD product marketers.

CBDs are non-psychoactive compounds found naturally in hemp plants. They work so well as powerful natural medicine that people everywhere are realizing CBDs work better than pharmaceuticals for treating epilepsy, seizures, neurological disorders, HIV infections and It is even used as an alternative cancer treatment.

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Photo credit: Pinterest

So, this is crazy:
The FDA has just launched a massive regulatory assault against CBDs by invoking the most insane logic you’ve ever heard! Here’s how it goes:

1) CBDs work so well that drug companies are now investigating them to be approved by the FDA as medicines.

2) Because CBDs are being investigated by drug companies, the FDA has granted CBDs status as being “investigated as a new drug.”

The FDA just criminalized one of the most miraculous healing medicines in the world Click To Tweet

In the FDA’s own language from their website:

“FDA CONSIDERS A SUBSTANCE TO BE ‘AUTHORIZED FOR INVESTIGATION AS A NEW DRUG’ IF IT IS THE SUBJECT OF AN INVESTIGATIONAL NEW DRUG APPLICATION (IND) THAT HAS GONE INTO EFFECT.”

3) Because CBDs work so well and have been authorized for drug investigations, the FDA now OUTLAWS them being sold as dietary supplements. Per the FDA’s own website:

“FDA has concluded that cannabidiol products are excluded from the dietary supplement definition under section 201(ff)(3)(B)(ii) of the FD&C Act. Under that provision, if a substance (such as cannabidiol) has been authorized for investigation as a new drug for which substantial clinical investigations have been instituted and for which the existence of such investigations has been made public, then products containing that substance are outside the definition of a dietary supplement.”

4) Now the FDA has begun sending warning letters to CBD makers, claiming they are in violation of FDA regulations because they are selling “adulterated products.”

Adulterated with what, exactly? CBDs, of course!

“The debate over hemp CBD’s legal status continues after FDA sent eight warning letters to manufacturers of CBD dietary supplement and food products earlier this month,” reports Nutritional Outlook. “The warning letters cite impermissible health claims used to market the products, as well as CBD’s invalid status as a dietary ingredient due to its presence in two drug applications currently under consideration.”

 

The FDA just criminalized one of the most miraculous healing medicines in the world by handing it over to Big Pharma

Photo credit: Pinterest

In other words, the FDA just handed Big Pharma an absolute monopoly over CBDs (hemp oil extract) by ridiculously claiming such natural products are “adulterated” with molecules (CBDs) that the FDA says might one day become a drug.

“Drugs,” according to the FDA, are substances that are proven to treat, prevent or cure a disease, and thus the FDA’s own logic admits that CBDs must be able to treat, prevent or cure diseases, otherwise they would be useless as “drugs”.

 

But when a dietary supplement company makes the same claim, they are hit with aggressive warning letters from the FDA, threatening to shut them down, confiscate their products and seek criminal prosecution of the company executives.

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This is how the FDA can instantly criminalize any vitamin or plant extract

Do you see how this twisted, corrupt regulatory tactic can allow the FDA to instantly criminalize any dietary supplement, vitamin, herb or plant extract?

Vitamin D, for example, could be outlawed by the FDA announcing that it has granted “Investigational New Drug application (IND)” status to any drug company studying vitamin D.

Using this same corrupt, mafia-style tactic, the FDA could outlaw resveratrol or even vitamin C, denying Americans the right to access safe, affordable, natural substances that are routinely found in nature.

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It’s time to end the FDA’s monopolization over natural plant molecules

If humanity is ever to achieve medical freedom, we must end the FDA’s outrageous medical monopolization of plant molecules such as CBDs.

By allowing this corrupt, criminally-run regulatory agency to criminalize every molecule found in nature, our nation’s lawmakers condemn us all to life in what can only be called medical totalitarianism under FDA tyranny.

Any time a healing substances is found in nature, the FDA can simply assert that such molecules are now in the process of being studied as drugs and are therefore illegal to sell as dietary supplements even though they were developed by Mother Nature, not drug companies.

Photo credit: Pinterest

This FDA tactic is nothing more than the FDA proclaiming intellectual monopolies over all molecules of interest found in nature.

It is Monsanto-like in its arrogance and wickedness, and it deprives the People of their right to access medicinal plants and healing substances that have existed in nature for countless thousands of years long before the FDA ever came into existence (1906).

If we do not stop this FDA, we are all doomed to living under a totalitarian regulatory regime that will systematically criminalize every healing molecule found in nature, from the curcuminoids in turmeric root to green tea catechins and even phycocyanins found in spirulina.

That this federal agency has now resorted to such tactics of medical totalitarianism and outright tyranny is proof that we need to strip the FDA of regulatory powers over natural dietary supplements and limit its domain to pharmaceutical drugs only.

 The FDA has now declared war on CBDs and Hemp oil extracts Click To Tweet

FDA begins crackdown by targeting inaccurate label claims… but it won’t end there

The FDA has now declared war on CBDs and hemp oil extracts. Its first targets are those companies who have inaccurate label claims or are committing outright fraud in claiming CBD concentrations that don’t even exist in their products.

Photo credit: Pinterest

On this point, I must agree that inaccurate label claims deserve regulatory enforcement. The CBD industry is heavily populated with fraudulent sellers whose products often contain no CBDs at all.

“The FDA has turned its back on the cannabis industry, claiming that CBD products cannot be sold as dietary supplements,” reports Canna Business. “Companies affected by the latest crackdown include Cali Stores, Dose of Nature, Green Garden Gold, Healthy Hemp Oil, Michigan Herbal Remedies, Morgue Juice, Pain Bomb and Senate Premium Oils. According to the FDA’s analysis, all products contained different amounts of 9-THC, THCa, CBDa, CBN and CBD than they had claimed.”

The second target of the FDA is companies that made disease treatment claims that their CBD products might treat epilepsy, cancer or other conditions. The FDA, of course, routinely attacks any dietary supplement maker that tells the truth about the medicinal benefits of their products. According to the FDA, there is no such thing as any food, nutrient, herb or natural molecule that has any ability whatsoever to treat, prevent or cure any disease. This position is, of course, patently absurd and stands in total violation of nutritional science, but it is the “big lie” the FDA must maintain in order to keep putting dietary supplement companies out of business.

Once the FDA finishes destroying all the companies with inaccurate labels and disease marketing claims, it will target all the honest suppliers of CBDs who are selling genuine, honest products that contain accurate CBD labels. This is the real goal of the FDA: to threaten, intimidate and destroy the entire CBD industry and thereby protect the medical monopolies of drug companies that can’t wait to cash in on these amazing molecules that really do treat disease (otherwise, Big Pharma would have no interest in them).

This is how the FDA keeps the medical racket marching along

And so the great medical monopoly racket marches on, with the FDA giving a big “F-YOU” to the American people while handing lucrative medical monopolies to its greed-driven friends in the pharmaceutical industry.

Meanwhile, the American people are denied healing medicine that works at a fraction of the cost of overpriced pharmaceuticals.

 

Entrepreneurial companies that offer such hemp oil extracts containing CBDs — natural medicines that could help reduce human suffering while lowering health care costs nationwide — are threatened by the FDA with devastating enforcement actions that could land their executives in prison.

This is all part of the FDA’s war on natural medicine that systematically criminalizes molecules found in nature and the people who seek to make those molecules available to patients in need.

While disease suffering skyrockets across America and medical expenses push more and more families over the threshold of bankruptcy and destitution, isn’t it comforting to know that your federal government is doing everything in its power to deny you access to safe, affordable natural medicine while protecting the profits of the drug giants?

Now:

What can you do to oppose this medical tyranny by the FDA?

None of this is ever going to change, by the way, if we keep electing establishment politicians to the White House. If you want to see real change in the legalization of hemp extract components such as CBDs, you’d better vote for someone who terrifies the establishment and threatens to tear it down.

At the same time, you need to support health freedom organizations like the Alliance for Natural Health, which is fighting to keep dietary supplements legal in America.

You should also watch this video animation by  Alliance for Natural Health, that exposes the anti-dietary supplement bias of PBS Frontline, which recently ran a totally dishonest hit piece documentary attacking supplements.

There is a nationwide effort under way right now to criminalize ALL dietary supplements and force every plant extract, vitamin or food concentrate to be regulated by the FDA as if they were prescription drugs. This would utterly wipe out the entire dietary supplements industry and plunge America into an era of runaway disease, suffering and death as people are denying access to the healing nutrients that are presently preventing disease (and even reversing serious disease in some cases).

 

The FDA is anti science and anti human rights

Photo credit: Jantoo

We have a fundamental human right to access healing plants found in nature, and the FDA has systematically sought to destroy that right and criminalize those who seek to express it. Access to Mother Nature’s healing molecules is a fundamental human right that exists above and beyond the Bill of Rights. It is a DIVINE right.

To re-establish our access to these rights, we need a political revolution in Washington that puts people in power who are ready and willing to dismantle the FDA and end its devastating monopolies over dietary supplements, medicinal herbs and natural molecules found in nature.

We need to legalize health freedom in America and set this nation on a new path of disease prevention and drastically reduced healthcare costs through access to affordable, natural medicines. The only way to accomplish this is to end the FDA’s reign of tyranny over the dietary supplements industry.

We need a new health freedom revolution in America, and it starts at the ballot box. It’s time to start electing outsiders, not insiders… people who the terrify the Washington establishment because they know their insidious grip on regulatory power will be challenged. If you want medical marijuana legalized, or if you want access to CBD oil as an affordable dietary supplement, it’s time to start voting for people the establishment is desperately trying to destroy. Because it is only those people who have any real hope of achieving the kind of political and legislative goals that will end the FDA’s stranglehold on natural medicine in America.

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Key Takeaways

  • CBDs are non-psychoactive compounds found naturally in hemp plants. They work so well as powerful natural medicine that people everywhere are realizing CBDs work better than pharmaceuticals for treating epilepsy, seizures, neurological disorders and other serious health conditions (including HIV infections).
  • Hemp oil extracts containing CBD (cannabidiol) are such a threat to the pharmaceutical industry that the FDA is now invoking totally insane justifications for outlawing them.
  • According to the FDA’s website: “the cannabidiol products are excluded from the dietary supplement definition”. (source)

The FDA just criminalized one of the most miraculous healing medicines in the world by handing it over to Big Pharma

  • In other words, the FDA just handed Big Pharma an absolute monopoly over CBDs (hemp oil extract) by ridiculously claiming such natural products are “adulterated” with molecules (CBDs) that the FDA says might one day become a drug.
  • But when a dietary supplement company makes the same claim, they are hit with aggressive warning letters from the FDA, threatening to shut them down, confiscate their products and seek criminal prosecution of the company executives.

It’s time to end the FDA’s monopolization over natural plant molecules

  • Any time a healing substances is found in nature, the FDA can simply assert that such molecules are now in the process of being studied as drugs and are therefore illegal to sell as dietary supplements even though they were developed by Mother Nature, not drug companies.
  • If we do not stop this FDA, we are all doomed to living under a totalitarian regulatory regime that will systematically criminalize every healing molecule found in nature, from the curcuminoids in turmeric root to green tea catechins and even phycocyanins found in spirulina.

FDA begins crackdown by targeting inaccurate label claims… but it won’t end there

  • The FDA has now declared war on CBDs and hemp oil extracts. Its first targets are those companies who have inaccurate label claims or are committing outright fraud in claiming CBD concentrations that don’t even exist in their products.
  • The second target of the FDA is companies that made disease treatment claims that their CBD products might treat epilepsy, cancer or other conditions.
  • Once the FDA finishes destroying all the companies with inaccurate labels and disease marketing claims, it will target all the honest suppliers of CBDs who are selling genuine, honest products that contain accurate CBD labels. This is the real goal of the FDA: to threaten, intimidate and destroy the entire CBD industry and thereby protect the medical monopolies of drug companies that can’t wait to cash in on these amazing molecules that really do treat disease.

What can you do to oppose this medical tyranny by the FDA?

  • Support health freedom organizations like the Alliance for Natural Health, which is fighting to keep dietary supplements legal in America.

Sources

NaturalNews

 

Categories
CANCER CURE NEWS

FDA Announces That DTap Vaccine Can Cause Autism

The FDA has published conclusive proof on their website that the DTap vaccine can cause autism. According to the FDA’s online Biologics Blood Vaccines document, a vaccine manufacturer admits on its package insert that their vaccination can cause autism as one of many adverse reactions.

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These adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea. Events were included in this list because of the seriousness or frequency of reporting. Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequencies or to establish a causal relationship to components of Tripedia vaccine.

FDA: Vaccines can cause autism
The FDA’s online Biologics Blood Vaccines document admits on its package insert that their vaccination can cause autism as one of many adverse reactions.

In this sense, it should be noted that:

Acellular Pertussis Vaccine Concentrates (For Further Manufacturing Use) are produced by The Research Foundation for Microbial Diseases of Osaka University (BIKEN), Osaka, Japan, under United States (US) license, and are combined with diphtheria and tetanus toxoids manufactured by Sanofi Pasteur Inc. Tripedia vaccine is filled, labeled, packaged, and released by Sanofi Pasteur Inc.

 

What’s in Tripedia that probably can interfere with brain chemistry and neurology?

According to the Tripedia’s package insert, some ingredients include: Bovine extract, formaldehyde used to inactivate microorganisms a couple of times, ammonium sulfate, aluminum potassium sulfate and two growth mediums: modified Mueller and Miller is one; the other is Stainer-Scholte medium.

 

What is the content of these two growth mediums?

dtap-vaccine-autism
Tripedia’s ingredients include: Bovine extract, formaldehyde, ammonium sulfate, aluminum potassium sulfate, modified Mueller and Miller and Stainer-Scholte medium.

Mueller and Miller medium, contains:

Glucose, sodium chloride, sodium phosphate dibasic, monopotassium, phosphate, magnesium sulfate hydrate, ferrous sulfate heptahydrate, cysteine hydrochloride, tyrosine hydrochloride, uracil hydrochloride, Ca-pantothenate in ethanol, thiamine in ethanol, pyridoxine-hydrochloride in ethanol, riboflavin in ethanol, biotin in ethanol, sodium hydroxide, beef heart infusion (de- fatted beef heart and distilled water), casein [milk protein] solution. Basically a mixture of sugar, salt, amino acids, vitamins, and minerals.

While Stainer-Scholte medium has the following ingredients:

Tris hydrochloride, tris base, glutamate (monosodium salt) [MSG], proline, salt, monopotassium phosphate, potassium chloride, magnesium chloride, calcium chloride, ferrous sulfate, ascorbic acid, niacin, glutathione.

The vaccine is formulated without preservatives, but contains a trace amount of thimerosal [(mercury derivative), (≤0.3 μg mercury/dose)] from the manufacturing process. Each 0.5 mL dose also contains, by assay, not more than 0.170 mg of aluminum and not more than 100 μg(0.02%) of residual formaldehyde. The vaccine contains gelatin and polysorbate 80 (Tween-80), which are used in the production of the pertussis concentrate.

“Probable cause” ingredients for adverse reactions include: casein, to which some children are allergic; MSG—an excitotoxin; thimerosal-ethyl mercury; aluminum; formaldehyde; gelatin; and polysorbate 80.

 

You might be wondering:

 

Why the doctors don’t say anything about the risk of DTaP Vaccine?

That is a question that many of us, still wondering! Maybe they just is just not convenient for them that we know about the risk of these vaccine

To take the vaccine debacle further, most of the mandated vaccines for infants and children, contain many of the above ingredients, which must be stopped from being injected into infants, toddlers, teens and even adults!

efficacy-of-dtap
Most of the mandated vaccines for infants and children, contain many of the above ingredients

It’s time for Congress to rescind the “Get out of Jail Free” card for vaccine makers and stop the aggressive onslaught of the Autism Spectrum Disorder that is depriving children of a fulfilling life and ruining families emotionally, financially, and physically to the point of parents divorcing because of the stresses of ASD in a family.

It’s about time vaccines are publicly acknowledged by the feds and the media for all the health damages they have caused. Just check out the CDC’s VAERS reports and the vaccine damage payouts by the HHS/HRSA. According to a new report published on March 1, 2017, by the department of health and human services of the United States, about $ 3,363,282,409.21 have been paid for vaccine adverse reactions and deaths from 1989 to 2017 so far.

Finally, as another recommendation to get the whole and real picture of the vaccines (from both the anti and pro vaccination sides), you must check out: “The Truth About Vaccines”.

 

To conclude, what do you think about this? Tell us in the comment section below. Also, if you think this information should be known by more people, please share it with all your friends and help spread the word.

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Key Takeaways

  • The FDA has published conclusive proof on their website that the DTap vaccine can cause autism. This adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic purpura, SIDS, anaphylactic reaction, cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea.

Click here to download report.

  • What’s in Tripedia that probably can interfere with brain chemistry and neurology?

According to the Tripedia’s package insert, some ingredients include: Bovine extract, formaldehyde used to inactivate microorganisms a couple of times, ammonium sulfate, aluminum potassium sulfate and two growth mediums: modified Mueller and Miller is one; the other is Stainer-Scholte medium.

  • Why the doctors don’t say anything about the risk of DTaP Vaccine?

That is a question that many of us, are still wondering! Maybe it is just not convenient for them that we know about the risk of this vaccine.

Article Source

http://www.activistpost.com/2016/04/vaccine-maker-admits-on-fda-website-dtap-vaccine-causes-autism.html

Special Thanks to Savannah from ramblingsmom.com for bringing the FDA’s document back into life.