From Hell To Veins

July 26, 2011

TV Networks Report Meningitis Mania, A One Sided Story.

After watching the local network snooze, I’m not sure if flesh eating meningitis is the ‘new polio’ or, is it the blob about to devour the movie theater downtown?

Yesterday the local network snooze was doing their typical playing ball for big pharma by promoting FEAR, FEAR, FEAR. The networks were showing grotesque images of babies whose flesh had been eaten by the blob called meningitis. Which strain of meningitis is flesh eating? Well, Your guess is as good as mine? The local snooze was reluctant to give out that information.

Yes, flesh eating meningitis is serious but, so is getting struck by lightning. As usual, the local networks gave a one sided story IGNORING obvious questions and facts about flesh eating meningitis but, thank God there is a silver bullet that will kill that mean old nasty blob in it’s tracks. Of course they then cut to ‘concerned parents’ getting their kids shot up with yet another vaccine. This means nine more shots to the ever growing vaccine schedule. With mandates for it waiting in the wings.

WHAT YOUR LOCAL SNOOZE DIDN’T BOTHER TO TELL YOU ABOUT THE NEW MENINGITIS VACCINE.

I just want to first mention that the local news acted as if no meningitis vaccines ever existed up until the release of the new vaccine when in fact the ‘OTHER’ meningitis vaccine was released in 1999.

Back then, similar promises were made about silver bullet protection against ALL strains of meningitis when the manufactures and doctors knew the vaccine was only for one strain.

Dr. KING PHD has worked in the vaccine industry and has testified before the meaningless FDA. Here are some excerpts from his report…
http://dr-king.com/docs/110128_DrftRevuNonCostEffectivenessOfVaxProgrmForN_MeningitidisAnd_b.pdf

… the annual number of case is, as of 2009, down to less than 1,000 a year.

…In addition, having testified to the FDA just before Sanofi’s Menactra was approved, this vaccine is not very effective (<85% based on the company’s choice of antibody titer with no proof that titer translates into protection)
OH? The local snooze called it a ‘silver bullet’!!

…Further, please read the package insert for Novartis’ MenVeo and ask yourself what are the undisclosed components in this 2-part, lyophilized vaccine and why does the FDA allow Novartis to conceal the nature of the other components in the vaccine besides the 4 antigens and a trace of formaldehyde?
DON’T ASK!!! DON’T TELL!!!

…In addition, N. Meningitidis is able, and has been shown, to change strains (by altering the polysaccharide on its surface).
It’s no wonder why the local snooze chose to ignore this fact.

The report goes on and on with subjects like… How the FDA approved the vaccine when they a.) threw out the stats on those injured by it and b.) where there was NO PROOF that antibody strains actually worked against the strain in the first place!

One other point needs to be made here.
In reading some of the recent deaths of youth by meningococcal meningitis bacteria it has been reported that family members were furious with the emergency care given at the hospitals that these youth ‘admitted themselves’ into, stating that had they been given ‘proper and immediate care’ their children would not have had to die. Here’s what the vaccine pusher’s (e.g. mainstream corporate TV…) don’t want people to get clued into. These family members are correct. These various bacteria that turn deadly for a few unfortunate individuals CAN BE TREATED BEFORE THEY TURN DEADLY. That is 100% correct.

I am not giving any medical advise here. I’m just going to relay to you what COMPETENT medical professionals say to do if you happen to show signs of sever meningitis. The symptoms are obvious to detect and once you have the symptoms you are on the clock. Yes! This IS an emergency. God help you if you go to a US hospital in this day and age. You’re going to have to talk some sense into someone at the ER to quickly admit you so you can get the proper ANTIBIOTICS as quickly as possible. If you can do that you will live. Same with an infant. You can detect the symptoms with them as well.

The problem is these hospitals are so lethargic their red tape will kill you before the meningitis will.

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February 18, 2010

FDA: Conflict of Interest in Vaccine Approval Confirmed

Filed under: HOME — nwqfk @ 3:15 p02
Tags: , , ,

My Commentary:
The headline is like a broken record. There really is NO conflict of interest at the FDA because the INTERESTS ‘ALL lies’ with the big pharmacological industrial machine which has NO ‘interest’ regarding the public and it’s safety.

Right now, Investigations are going on in Europe over the very same issue concerning the World Health Organization Mr. Rockefeller founded over the swine flu hoax.

WEHONEWS.com
Monday, February 15, 2010 – By Michael Mooney, West Hollywood
West Hollywood, California (February 15, 2010) – If you’ve read my two articles in WeHoNews.com questioning the safety and effectiveness of the swine flu vaccine, you know how I feel about it.

Michael Mooney writes on health issues, focusing on research and access. WeHo News.
I’d rather take high dose vitamin D to strengthen my immune system so I don’t have to worry about getting the flu than get vaccinated with a potentially toxic vaccine that was rushed into circulation even after World Health Organization balked at the lack of confirmed safety data, saying, “…with such a large amount of an experimental vaccine that contains mercury being distributed, keeping track of people that experience adverse effects will be difficult.”

What’s important to note is that FDA is once more not doing their job of protecting the public to the standards of modern science. They have seriously compromised their own approval process with dangerous medications. Think Vioxx.

Not only did they dumb down on what possible problems the swine flu vaccine could cause, but they went further by advocated for vaccine manufacturers and promoting the sales of the swine flu vaccine while ignoring safety concerns about solidly documented problems that other countries do not ignore.

For FDA to sell vaccines goes farther than what their official role is defined as, to protect the public from danger.

Story Continued…

December 22, 2009

FDA accused of international kidnapping. That’s How They Roll.

My Commentary
Even though this is a vaccine blog I feel it justified to post this FDA ‘event’, since this same FDA is responsible for the ‘pushing’ (or rubber stamping) of dangerous drugs AND vaccines onto an un-witted public.

It shouldn’t come as any surprise to those of us aware of the ‘CRIMINAL’ behavior of the FDA, that they would be unconstitutionally acting as ‘their own’ police department. What may surprise even the population with a clue is that the FDA is acting as CIA agents going abroad and kidnapping people.

The FDA is a cleaver COVER acronym for the pharmacological Rockefeller et.al monopoly to not only highjack the United States food and drug regulatory system but, to act as it’s own judicial system as well. If you ever had a doubt about this FACT read this ‘event’.

There can be NO DOUBT that the FDA was initially created for the Pharmacological Industrial Complex to take over and control when starring directly at the FACTS of the gross conflict of interest that resides within it. There can also be no doubt that the reason for the creation and control of such an agency is to STAMP OUT ALL NATURAL HEALING that COMPETES with big pharma’s drug monopoly. Of course it did NOT start out this way. The level of control, AS ALWAYS, happens INCREMENTALLY. This agency is so out of control today, had you told the public when it was created that the FDA would OUTLAW lime growers to ‘claim’ limes prevent a ‘disease’ called scurvy, most would have said that would be going “way too far” and could NEVER happen. Never say Never! Even though limes ‘preventing a disease’ is NOT A ‘CLAIM’ but a well known ‘FACT’, the FDA intentionally and purposefully distorts FACTS as claims to persecute anyone HEALING without AUTHORIZATION from this criminal organization.

So if anyone should be hauled in front of a FAIR and JUST court it would most certainly have to be the FDA itself for crimes BEYOND the ‘claims’ that this agency is working FOR THE BENEFIT of the general welfare of the U.S. population. Where such FALSE claims have in fact endangered the general welfare of the population.

www.PamRotella.com

FDA accused of international kidnapping, illegal detention of prominent Ecuadorian herbalist

21 December 2009
Pam Rotella

Allegations of kidnapping and illegal detention by the US Food and Drug Administration are being made after its seizure of a prominent herbalist from Ecuador.

Greg Caton, owner of Alpha Omega Labs, was seized from Ecuador in a move outside of extradition procedures, and against the orders of an Ecuadorian Federal judge. The alleged kidnapping occurred three days prior to a pending hearing for Caton, having the appearance of an attempt to evade compliance with the court’s expected ruling.

Christopher Kelly of the FDA refused comment on the FDA’s current actions in Ecuador, or its legal argument for subverting extradition procedures within Ecuador and removing Caton via police seizure. Kelly referred inquiries to the US Marshals and US Attorneys offices.

When contacted, a US Marshals spokesman denied involvement in the seizure of Caton from Ecuador, and said that the Marshals’ role in this case would be their usual duty of holding Federal prisoners, probably after Caton reached Florida. The US Attorneys office was also contacted for comment but has not responded.

Speaking via phone from Ecuador on Saturday, Caton’s wife Cathryn said that the FDA finally explained its reason for her husband’s abduction during Florida court proceedings. The FDA claimed that Greg Caton violated his supervised probation under a 2003 plea of selling “unapproved drugs.”

“Selling unapproved drugs” is a charge usually filed against herbalists who sell herbs and also make claims about the herbs’ medicinal properties. The FDA does not allow medicinal claims about food or herbal products by those who also sell them. No actual “drugs,” in the traditional sense of the term, were involved in the 2003 Caton case.

Cathryn Caton said that Caton’s company Alpha Omega Labs (AltCancer.com) had been selling herbal products after Caton’s release in the US, but that the herbs were sold from Ecuador where herb sales are legal along with information on their medicinal properties. In fact, Caton had moved his company to Ecuador specifically because he could continue working with herbal remedies without restrictions on the information provided to customers.

At issue is whether Caton’s herb sales in Ecuador would violate Caton’s probation in the United States. This legal issue could not be addressed in Ecuador, as Caton was seized before his court date there. It is possible that Caton’s abduction was meant to preempt such legal precedent from being set on this matter.

After arriving in Florida, Greg Caton was given a detention hearing and arraigned for violating his supervised release. A hearing is scheduled for December 28th to move him to Louisiana. According to his wife, Caton will probably be held in Florida until early next year, and then moved to Louisiana for hearings on probation violation charges. So far, Caton has been represented by a court-appointed attorney.

The method used to remove Caton from the country — kidnapping — is probably the most egregious charge leveled against the FDA. Before his scheduled court date, Ecuadorian police illegally removed Greg Caton from his cell in Ecuador without court authorization, and put him on an American Airlines jet. One of Cathryn Caton’s contacts at the airport recognized a US State Department employee, and happened to know the man’s identity due to his presence at Greg Caton’s hearings in Ecuador. Caton’s contact informed her that the State Department employee was directing the Ecuadorian police on how to slip Greg Caton out of Ecuador.

The Ecuadorian Federal Judge in charge of Caton’s appeal was contacted and went to the airport in person, where he informed American Airlines that they were engaged in an illegal action, and presented paperwork ordering the release of Greg Caton. American Airlines refused to allow Caton off of the plane, and claimed that they were not subject to Ecuadorian laws even while in Ecuador, that they were technically US soil (a privilege enjoyed by embassies). The jet was then allowed to leave the airport, and Caton was transported to Miami, Florida. The Ecuadorian police officers flew out of the country on the airplane with Caton according to witnesses, but the US State Department employee who directed the action stayed in Ecuador. Cathryn Caton wants to know who paid for their airline tickets.

Along with questions of why the FDA felt entitled to subvert the Ecuadorian legal system to capture a mere herbalist, tactics by the agency prior to Caton’s court appeal are also being scrutinized. The Catons claim that one FDA agent in particular, John Armand, seemed to be “rogue,” and engaged in questionable tactics such as using a witness accused of embezzling $20,000 from Caton’s company as a witness against Caton. Cathryn Caton suspected that the employee was led to believe that landing her bosses in jail would help her to avoid jail time herself. Caton witnessed the woman with the FDA agent in court, making claims that helped to build the agent’s case.

The FDA also refused to comment on whether Armand or other agents in charge of Caton’s case had past affiliations with pharmaceutical companies or competitors of Caton’s products. One well-known and widely criticized fault of the Food and Drug Administration is the “revolving door” between pharmaceutical companies and the agency charged with regulating them, the FDA. Employees of the FDA often are hired from drug companies, or are offered high-paid jobs at the very pharmaceutical companies whose drugs they helped to approve. This cozy relationship is seen as a major flaw in the way drugs are approved and regulated in the United States.

In addition to the FDA’s star witness being an accused embezzler, Caton was also told that the judge who signed her husband’s original deportation order had been bribed with promises of green cards for his relatives in the United States. (Caton will not identify the witness or the name/position of the US agent offering green cards, for the protection of her witness.)

The appeal of that judge’s deportation order was scheduled to be heard by a Federal Ecuadorian judge with no such questions surrounding his integrity. However, that higher judge’s orders at the airport in Guayaquil were ignored and Greg Caton was flown out of the country. Cathryn Caton is working with the political process in Ecuador to have the people responsible for her husband’s abduction investigated and prosecuted. President Correa of Ecuador had already expelled 2 diplomats after the FDA attempted a similar abduction of Greg Caton in 2008.

Caton’s company, Alpha Omega Labs (AltCancer.com), is the maker of anti-cancer herbal blends such as “Black Salve” (a bloodroot-based topical product) and “Cansema” (a chaparral-based capsule blend). Notably, a new cancer drug named “Chemex” based on chaparral was mentioned on Caton’s own web site:

“Chaparral (Larrea tridentata, Larrea mexicata) — An herb long reverred for its miraculous medicinal properties by Indians of the Southwest U.S., chaparral’s secret is known to be contained in a substance known as NDGA (nordihydroguauretic acid). This organic anti-oxidant is the basis of several recent cancer cures which have been filed with the U.S. patent office, most by Chemex Pharmaceutical of Fort Collins, Colorado (USA). The FDA has granted drug status to Chemex for a remedy for a pre-cancerous skin remedy (actinic keratosis) which uses NDGA as its base. Our products contain specially harvested chaparral which have been specimened and known to contain 16-18% NDGA by weight for maximum concentration.”

Bloodroot-based topical solutions are traditionally used to treat skin cancer patients. In his book “Spontaneous Healing,” Andrew Weil, MD, mentioned using bloodroot paste on his dog. Weil was satisfied with the results.

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