WMD Lies Strike Again: The Skripal Incident

March 16, 2018 “Information Clearing House” –  As the West rallies around recent allegations by the UK against Russia regarding the alleged poisoning of former Russian military intelligence officer-turned British spy – Sergei Skripal – it is crucial to point out the alarming lack of actual evidence involved.

It is also important to point out the history of the accusers predicating entire wars on allegations now confirmed to have been intentional lies.

The Skripal Incident

The alleged poisoning of Sergei Skripal in Salisbury, UK on March 4 led to a lighting-fast escalation with Russia. Not even two weeks after the attack, UK Prime Minister Theresa May declared a deadline for Russia to provide an “explanation” for the incident the UK had squarely blamed on Moscow.

The Kremlin’s explanation was simple – it had nothing to do with the attack. Russia also offered to aid in the investigation, requesting samples of the poison used in the alleged attack.

However, the UK failed to produce any samples of the alleged poison – a Soviet-era nerve agent known as Novichok – either to the Russians to examine or to relevant international organizations as required under the Chemical Weapons Convention.

The UK also failed to explain why Russia would have carried out such an attack – or how the UK could have confirmed the use of Novichok agents without first possessing samples of the agents themselves. If the UK possessed Novichok agents to compare samples taken from the attack with, the entire rationale of accusing Russia because it is supposedly the only nation in possession of the agents is revealed as entirely false.

US, UK Certainly Have “Novichoks” 

The Daily Beast in its article, “Soviet Scientist Who Developed Novichok Poison Used on Sergei Skripal: ‘I’m Sorry’,” would admit:

For the prime minister to be able to publicly accuse the Russians of using a nerve agent like a novichok, British authorities at least must have had access to novichok’s unique chemical signature—which it legally could have had despite the Chemical Weapons Convention, due to the clause of countries being able to hold samples for testing in these incidences. 

Testing for novichoks, even based on a formula published by Mirzayanov in a memoir based on his work in the 1980s, is a potential sign that the British have potential access to newer variants of the nerve agent.

The Guardian too would admit in an article titled, “Novichok nerve agents – what are they?,” that:

The fact that so little is known about the novichoks may explain why Porton Down scientists took several days to identify the compound used in the attack against the Skripals. And while the agents were invented in the Soviet Union, other labs with access to the chemical structures would be able to manufacture them too.

The fact that the alleged creator of Novichok agents – Vil Mirzayanov – fled to and currently lives in the United States suggests the West has both knowledge of and the means to create Novichok agents themselves….

http://www.informationclearinghouse.info/48993.htm

Novichok Story Is Another Iraqi WMD Scam

March 16, 2018 “Information Clearing House” – As recently as 2016 Dr Robin Black, Head of the Detection Laboratory at the UK’s only chemical weapons facility at Porton Down, a former colleague of Dr David Kelly, published in an extremely prestigious scientific journal that the evidence for the existence of Novichoks was scant and their composition unknown.

In recent years, there has been much speculation that a fourth generation of nerve agents, ‘Novichoks’ (newcomer), was developed in Russia, beginning in the 1970s as part of the ‘Foliant’ programme, with the aim of finding agents that would compromise defensive countermeasures. Information on these compounds has been sparse in the public domain, mostly originating from a dissident Russian military chemist, Vil Mirzayanov. No independent confirmation of the structures or the properties of such compounds has been published. (Black, 2016)

Robin Black. (2016) Development, Historical Use and Properties of Chemical Warfare Agents. Royal Society of Chemistry

Yet now, the British Government is claiming to be able instantly to identify a substance which its only biological weapons research centre has never seen before and was unsure of its existence. Worse, it claims to be able not only to identify it, but to pinpoint its origin. Given Dr Black’s publication, it is plain that claim cannot be true.

The world’s international chemical weapons experts share Dr Black’s opinion. The Organisation for the Prohibition of Chemical Weapons (OPCW) is a UN body based in the Hague. In 2013 this was the report of its Scientific Advisory Board, which included US, French, German and Russian government representatives and on which Dr Black was the UK representative:

[The SAB] emphasised that the definition of toxic chemicals in the Convention would cover all potential candidate chemicals that might be utilised as chemical weapons. Regarding new toxic chemicals not listed in the Annex on Chemicals but which may nevertheless pose a risk to the Convention, the SAB makes reference to “Novichoks”. The name “Novichok” is used in a publication of a former Soviet scientist who reported investigating a new class of nerve agents suitable for use as binary chemical weapons. The SAB states that it has insufficient information to comment on the existence or properties of “Novichoks”. (OPCW, 2013)

OPCW: Report of the Scientific Advisory Board on developments in science and technology for the Third Review Conference 27 March 2013

Indeed the OPCW was so sceptical of the viability of “novichoks” that it decided – with US and UK agreement – not to add them nor their alleged precursors to its banned list. In short, the scientific community broadly accepts Mirzayanov was working on “novichoks” but doubts he succeeded.

Given that the OPCW has taken the view the evidence for the existence of “Novichoks” is dubious, if the UK actually has a sample of one it is extremely important the UK presents that sample to the OPCW. Indeed the UK has a binding treaty obligation to present that sample to OPCW. Russa has – unreported by the corporate media – entered a demand at the OPCW that Britain submit a sample of the Salisbury material for international analysis.

Yet Britain refuses to submit it to the OPCW….

http://www.informationclearinghouse.info/48995.htm

Chronic Disease Center Militantly Ignorant of Sexually Transmitted Lyme Disease

via govtslaves.info

The CDC’s Greatest Cover Up? Information About Lyme Disease They Don’t Want You To Know About

Lyme disease, do you have it? If you did, you probably wouldn’t know – unless you’re one of the chronic sufferers that have had to visit over 30 doctors to get a proper diagnosis. Lyme disease tests are highly inaccurate, often inconclusive or indicating false negatives.

Why? Because this clever bacteria has found a way to dumb down the immune system and white blood cells so that it’s not detectable until treatment is initiated. To diagnose Lyme properly you must see a “Lyme Literate MD (LLMD),” however, more and more doctors are turning their backs on patients due to sheer fear of losing their practices! Insurance companies and the CDC will do whatever it Ttakes to stop Chronic Lyme Disease from being diagnosed, treated, or widely recognized as an increasingly common issue.

Lyme is considered by the medical field to “only” transmit by way of a tick infected with bacteria. However, the CDC itself admits it is under-reported, and believes there are between 300,000 to half a million new cases each year. That makes Lyme disease almost twice as common as breast cancer and six times more common than HIV/AIDS. Where are all of these new cases coming from? (It’s interesting to note that since Avril Lavigne recently went public with her Chronic Lyme Disease battle, mainstream news outlets like The Daily Mail have been mentioning Lyme can be transmitted by mosquitoes, too!)

When Lyme isn’t detected in the early stages, it becomes Chronic Lyme, a condition which the CDC and IDSA both deny even exists. They will continue to deny it, because if there’s one thing insurance companies hate, it’s chronic disorders they have to spend time and money treating. Therefore, a panel with ties to insurance companies gathered to write up official Lyme guidelines that assure patients are only allowed a few weeks of antibiotic treatment and are not to be diagnosed with Chronic Lyme Disease (even if clear symptoms persist and invade the nervous system). Over half of the panelists who wrote the IDSA Lyme guidelines announcing that Chronic Lyme is not real — including the panel chairman — have obvious conflicts of interest including financial interests in drug companies, diagnostic tests, and patents, as well as consulting agreements with insurance companies. Researchers and scientists with evidence in support of Chronic Lyme were intentionally excluded from the panel. Because of these unjust Lyme guidelines, insurance companies have the “right” to deny coverage for the treatment of long-term Lyme disease. Doctors have even lost their practices for successfully diagnosing and treating Chronic Lyme, as shown in the film Under Our Skin. In the case of Dr. Joseph Jemsek of North Carolina, he not only lost his license, but also his livelihood. Dr. Jemsek can no longer practice simply because he gave antibiotics to Chronic Lyme sufferers, and was then sued by BCBS for 100 million dollars, following which he had to declare bankruptcy. You can read his closing remarks to the NC Medical Board just before they pulled his license here. You can also watch his story in the documentary at the end of this post.

Busted – Big Pharma bucks taint the IDSA

Connecticut Attorney General Richard Blumenthal investigated the IDSA panel members for possible violation of antitrust laws and conflicts of interest.

Of the 14 panel authors of the first edition guidelines: 6 of them or their universities held patents on Lyme or its co-infections, 4 received funding from Lyme or co-infection test kit manufacturers, 4 were paid by insurance companies to write Lyme policy guidelines or consult in Lyme legal cases, and 9 received money from Lyme disease vaccine manufacturers. Some of the authors were involved in more than one conflict of interest. (Source: ‘Under Our Skin‘ [2008])

Lyme disease, do you have it? If you did, you probably wouldn’t know – unless you’re one of the chronic sufferers that have had to visit over 30 doctors to get a proper diagnosis. Lyme disease tests are highly inaccurate, often inconclusive or indicating false negatives.

Why? Because this clever bacteria has found a way to dumb down the immune system and white blood cells so that it’s not detectable until treatment is initiated. To diagnose Lyme properly you must see a “Lyme Literate MD (LLMD),” however, more and more doctors are turning their backs on patients due to sheer fear of losing their practices! Insurance companies and the CDC will do whatever it Ttakes to stop Chronic Lyme Disease from being diagnosed, treated, or widely recognized as an increasingly common issue.

Lyme is considered by the medical field to “only” transmit by way of a tick infected with bacteria. However, the CDC itself admits it is under-reported, and believes there are between 300,000 to half a million new cases each year. That makes Lyme disease almost twice as common as breast cancer and six times more common than HIV/AIDS. Where are all of these new cases coming from? (It’s interesting to note that since Avril Lavigne recently went public with her Chronic Lyme Disease battle, mainstream news outlets like The Daily Mail have been mentioning Lyme can be transmitted by mosquitoes, too!)

When Lyme isn’t detected in the early stages, it becomes Chronic Lyme, a condition which the CDC and IDSA both deny even exists. They will continue to deny it, because if there’s one thing insurance companies hate, it’s chronic disorders they have to spend time and money treating. Therefore, a panel with ties to insurance companies gathered to write up official Lyme guidelines that assure patients are only allowed a few weeks of antibiotic treatment and are not to be diagnosed with Chronic Lyme Disease (even if clear symptoms persist and invade the nervous system). Over half of the panelists who wrote the IDSA Lyme guidelines announcing that Chronic Lyme is not real — including the panel chairman — have obvious conflicts of interest including financial interests in drug companies, diagnostic tests, and patents, as well as consulting agreements with insurance companies. Researchers and scientists with evidence in support of Chronic Lyme were intentionally excluded from the panel. Because of these unjust Lyme guidelines, insurance companies have the “right” to deny coverage for the treatment of long-term Lyme disease. Doctors have even lost their practices for successfully diagnosing and treating Chronic Lyme, as shown in the film Under Our Skin. In the case of Dr. Joseph Jemsek of North Carolina, he not only lost his license, but also his livelihood. Dr. Jemsek can no longer practice simply because he gave antibiotics to Chronic Lyme sufferers, and was then sued by BCBS for 100 million dollars, following which he had to declare bankruptcy. You can read his closing remarks to the NC Medical Board just before they pulled his license here. You can also watch his story in the documentary at the end of this post.

Busted – Big Pharma bucks taint the IDSA

Connecticut Attorney General Richard Blumenthal investigated the IDSA panel members for possible violation of antitrust laws and conflicts of interest.

Of the 14 panel authors of the first edition guidelines: 6 of them or their universities held patents on Lyme or its co-infections, 4 received funding from Lyme or co-infection test kit manufacturers, 4 were paid by insurance companies to write Lyme policy guidelines or consult in Lyme legal cases, and 9 received money from Lyme disease vaccine manufacturers. Some of the authors were involved in more than one conflict of interest. (Source: ‘Under Our Skin‘ [2008])

Study: Strong Evidence Of Sexual Transmission

The bacteria that causes Lyme disease is Borrelia burgdorferi, a type of corkscrew-shaped bacteria known as a spirochete. The Lyme spirochete is a cousin to Treponema pallidum, the spirochete that causes syphilis.

Dr. Alan MacDonald, MD who appears in the documentary ‘Under Our Skin’ (2008), says in the film that he found found Borrelia (Lyme) DNA in 7 out of 10 postmortem Alzheimers patients’ brains. This makes perfect sense, since syphilis, its cousin, also invades the brain in tertiary or neurosyphilis. Dr. Klinghardt, MD (also quoted from ‘Under Our Skin’) stated that he’s “never had a single patient with Alzheimer’s, ALS, Parkinson’s Disease or Multiple Sclerosis who tested negative for Borrelia.”

Dr. Alan MacDonald, MD talks about Lyme.

Why are so many people suffering from Lyme disease and its allegedly associated chronic disorders, such as Alzheimers and ALS? A new study suggests that just like its spirochete cousin that causes syphilis, Lyme disease may be sexually transmitted! The study was presented at the annual Western Regional Meeting of the American Federation for Medical Research, and an abstract of the research was published in the January issue of the Journal of Investigative Medicine….

http://www.collective-evolution.com/2018/03/15/the-cdcs-greatest-cover-up-information-about-lyme-disease-they-dont-want-you-to-know-about/