Archive for Big Pharma – Page 8
Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
Dr. Laibow’s Virtual Interview with HHS Secretary Sebelius
September 16, 2009 – URGENT NOTE: Your Action Required Now to Secure Your Right to Refuse the Swine Flu Vaccine Without Incarceration
Health Freedom’s best friend in Congress has responded to our Push Back. We’ve sent more than 2 million emails demanding the right to say “NO!” to vaccines without punishment, incarceration or involuntary quarantine. The Congressman knows how important that is to health, liberty and, we have to imagine, sanity. We have been in discussion with his office about introducing a bill modeled on our Draft Legislation to prevent pandemic vaccination which is mandatory, compulsory or taken under duress of any type.
We received a call today from the Congressman’s office telling us that he is close to introducing a new No Compulsory Vaccine Bill to the House. Given the fact that we have sent well over 2 million emails to our State and Federal legislators, HHS Secretary Sebelius, DHS Secretary Napolitano, President Obama and the Governors of every State in the Union, we anticipate that his bill will garner a good deal of support.
NOW IS THE TIME TO TURN UP THE HEAT. WE NEED 2 MILLION MORE EMAILS IN THE NEXT WEEK. CAN WE DO IT? YOU KNOW WE CAN! WE ARE THE NET ROOTS OF HEALTH FREEDOM!
Have you already sent this Action Item once for every member of your household demanding the right to self shield instead of facing mock-voluntary Swine Flu vaccination with incarceration as the consequence of vaccine refusal? If so, thank you. If not, now, more than ever, we need your help in taking this action right now. We need every bit of support we can muster. Once we get Dr. Paul’s bill number and text, we will publish it and then we’ll ask you to do the same thing again: click on the link we’ll give you to support that Action Item as if your life depended upon it. It will.
Click here once for each member of your family and then disseminate as widely as you can: http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275
And don’t forget that we are 100% supporter supported.
Please set up two (2) recurring donations, whether large or small: one tax deductible donation to support our legal challenge of the legality of the FDA’s approval of the vaccines Secretary Sebelius is referring to in her testimony below. That one should end in the number 6 to ear mark it for our legal fund. The other tax deductible donation can end in any number and it keeps the Natural Solutions Foundation keeping-on. Here is the link: http://drrimatruthreports.com/?page_id=189
Now, on to the all too real, but still very surreal, testimony authorizing the Pandemic Swine Flu vaccines without any, that’s right, any safety testing. On September 15, 2009, a terrible, tragic and tyrannical event in America’s history took place. HHS Secretary Kathleen Sebelius testified before the US House of Representatives Committee on Energy and Commerce and, in that testimony, announced the “licensing” of the “Swine Flu” vaccines. Secretary Sebelius, please allow me to remind you that it is a crime to provide false testimony before Congress.
I was not in the chamber when the Secretary announced the approval of several Swine Flu vaccines using a combination of untruth, falsehood, illogic and deceit. But I would like to present my virtual interview of Secretary Sebelius as she reads her testimony before that Committee and I question her about it. Remember that every word following SKS (Secretary Kathleen Sebelius) is her unedited testimony, with nothing altered or changed in context. I guess she is counting on the declining quality of the educational system in the US to see her through.
Watch for the new Youtube.com.naturalsolutions series in which Secretary Sebelius and I have a virtual interview. Here is the text of that virtual interview. Please read and share as widely as you can.
Thanks for your activism.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
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A virtual Interview with Secretary Sebelius on the “Swine Flu” Vaccine Licensing
My comments are in italics, labeled “REL”
Secretary Sebelius’ comments are labeled SKS.
SKS: Preparing for the 2009-2010 Influenza Season
Secretary of Health and Human Services Kathleen Sebelius
Secretary, U.S. Department of Health and Human Services
SKS: Chairman Waxman, Ranking Member Barton, Chairman Emeritus Dingell, members of the Committee, thank you for this opportunity to update you on the public health challenges of 2009 H1N1 influenza. I want to assure the Committee that the Administration is taking these challenges seriously…
REL: These challenges do not exist, Secretary Sebelius. They have been manufactured as a kind of, at best, a cynical windfall of unprecedented proportions for Big Pharma. At worst, you and your conspirators are playing Doctor Death with America, starting with our next generation, children and pregnant mothers.
SKS: and has mounted an aggressive plan to address H1N1 throughout this fall and winter.
REL: The challenges you speak of do not exist. Without any challenge, an aggressive plan is totally unnecessary.
SKS: HHS has a leading role because this is a health event, and we are working in close partnership with virtually every part of the federal government under a national preparedness and response framework for action that builds on the efforts and lessons learned from this spring. Working together with governors, mayors, tribal leaders, state and local health departments, the medical community and our private sector partners, the federal government has been actively preparing for possible H1N1 virus outbreak scenarios that may develop over the next few months.
REL: Madam Secretary, you are saying “MAY develop” but your use of the phrase, “MAY DEVELOP” shows there is no sufficient scientific evidence that the so-called “Swine Flu” is a pandemic threat. You have called it a “novel” virus, which is a condition for there to be a pandemic potential, but you are not treating this vaccine as thought it were a novel vaccine, requiring safety testing. Given the costs in human and financial terms, I am afraid that “MAY DEVELOP” is not sufficient for vaccination of the population, starting with our most vulnerable population.
SKS: Since the initial spring outbreak of 2009 H1N1 influenza, the virus has triggered a worldwide pandemic,
REL: Well, no. Actually a world wide pandemic has been declared without any clear evidence that there actually IS a world wide pandemic. There is NO world-wide pandemic; there is a only legally declared pandemic, made possible only because the W.H.O. changed the definition of a “pandemic” for political reasons. The “pandemic” has been declared without any clear evidence that there is any world-wide threat. How has the Secretary ascertained, in the absence of accurate testing, that H1N1 is the “DOMINANT” flu strain? Australian authorities do not confirm your claim.
SKS: and has been the dominant flu strain in the southern hemisphere during its winter flu season.
REL: Just how is this ascertained in the absence of accurate testing, not just testing, mind you, but accurate testing that H1N1 is the “DOMINANT” flu strain? Australian authorities do not agree with or substantiate your claim.
SKS: The evidence to date shows that the virus has not changed to become more deadly.
REL: At last, Madam Secretary, we have common ground. We agree, and therefore, since both WHO and CDC has said that this H1N1 virus causes a disease that is milder than seasonal flu, requiring no medical intervention, why is major medical intervention required for something that poses no dangers and may, MAY, become a problem at some time, somewhere in the future?
I am sorry, Madam Secretary, but this is absurd, unscientific, dangerous and a ferocious waste of money, sort of like TARP and other corporate welfare programs, but this time for Big Pharma.
SKS: Unlike our typical seasonal flu, we continued to see flu activity in the United States over the summer, notably in summer camps.
REL: But since diagnosis is not being carried out, is it Swine Flu? Allergies to GMO junk food fed to children, perhaps, common colds, maybe? How would you know? The best tests we have are wrong 9 times out of 10. WHO and CDC requested countries not to test for the virus and not to keep accurate counts, just to guess – and it is on these guesses that you apparently are making your pronouncements, judgments and decisions.
SKS: More recently, we have seen an increase in 2009 H1N1 influenza activity in several states
REL: Based on what independently verified data? If you have no lab tests, you would have no idea of what you are seeing.
SKS: and expect this to continue across the United States during the coming months.
REL: All respiratory cases are being assigned the unscientific label of “Swine Flu” without testing. No one has any idea if any of these cases are causes by H1N1, except, apparently you, Secretary Sebelius. Assuming, however, that all of them are, there are no deaths which are not caused by underlying disease or treatments with toxic, but approved drugs such as Tamiflu, which killed a pregnant mother and the baby she gave birth to in Mumbai, India recently.
Diagnosis by symptom picture alone. Right. That is not exactly good science and it certainly is terrible medicine. Swine Flu walks like a duck, coughs like a duck and has a fever like a duck. What makes it a swine? Public relations and nothing else!
SKS: As fall begins, we anticipate that even more communities may be affected than those that saw cases this past spring and summer.
REL: Again I ask you, Secretary, based on exactly, precisely, what?”
SKS: In addition, communities may be more severely affected, reflecting wider transmission and causing potentially greater impact.
REL: I am afraid I have to ask again, based on what? You say that communities may be more severely affected, but the truth is that they may also be less severely affected. Where do you get your crystal ball serviced, Madam Secretary? Could it be the same place that Novartis used when they decided to patent a vaccine for the Swine Flu in 2008 when CDC and WHO declare that this is a novel, never-before-seen virus which arose, de novo, like Athena from the forehead of Zeus, in April, 2009? Could the same shop be servicing Baxter’s decision-making Magic 8 Ball so that they were able to apply for a patent for a Swine Flu vaccine in 2007? If so, Madam Secretary, this crystal ball is a national treasure and should be made available to “We the People of These United States.”
SKS: Seasonal influenza viruses may cause illness concurrently with 2009 H1N1 this fall and winter and it will not be possible to determine quickly if ill individuals have 2009 H1N1 influenza, seasonal influenza, or other respiratory conditions based on symptoms alone.
REL: It may. Or, then again, it may not. There is no hard data on which to make these predictions and the consequences of these predictions, including vaccines are dangerous and unwarranted by any level of fact or reality. I repeat, there is simply no hard data, or at least none that you have presented on your websites, public statements, press releases or here today.
SKS: It is also difficult to predict the severity of the disease that we will see in the coming months from either 2009 H1N1 or seasonal influenza.
REL: Right again, Madam Secretary. So why poison the populace for something whose dreadful menace did not materialize and is not showing any signs of materializing. In fact, its dreadful menace is a lot like the bogyman under the bed: a product of your big brother’s desire to scare you witless so that you will do whatever he says. The parallel is uncanny.
SKS: Influenza is an unpredictable disease and we know that things will change and we will learn more throughout the fall.
REL: So unpredictable, in fact, that seasonal flu vaccines are accurate less than 40% of the time although the toxins injected (mercury, aluminum, formaldehyde, foreign protein, MSG, etc., fluoride, etc.) are toxic 100% of the time and become more so with more shots, which are increasingly r4commended by conflict-of-interest-laden ACIP (Advisory Committee on Immunization Practices) and others of their stripe. By the way, Secretary Sebelius, what is your financial interest in the medical and pharmaceutical industries?
SKS: Shared Responsibility and Science-Based Guidance Slowing the spread and reducing the impact of H1N1…
REL: From nothing to nothing?
SKS: …and seasonal flu is a shared responsibility…
REL: Exactly what does that mean? There is no meaningful impact from H1N1, but there certainly will be from yet another round of vaccines, even if those vaccines are, as falsely stated, but a strain change variation on a theme. Children vaccinated with attenuated live virus vaccines, specifically influenza vaccines, are many times more likely to be admitted to hospitals for all causes, many times more likely to develop serious asthma, etc. There is nothing trivial about influenza shots but, with the guidance of ACIP they are increasingly passed out as if they were either safe or effective. In fact they are neither and, if it is merely a strain change variation, then H1N1 is also neither safe nor effective. It it is a novel vaccine for a novel virus, it is clearly neither safe nor effective since it has never had any safety testing concluded. Were such safety testing to show that it were not safe or effective, then the sales and administration of it would pierce the veil of liability free manufacture, distribution and use which the Federal government has accorded to itself, its agents and to the manufacturers and distributors of these dangerous vaccines as we.. It is therefore in the ir best interest not to have any safety data (or data showing the lack of safety).
SKS: …and we all need to plan for what would need to be done when the flu impacts our community, school, business or home this fall.
REL: When? Shouldn’t the word be “IF” or “just in case” or “In the unlikely chance that it might, given the lack of evidence that it can”?
SKS: Given that flu already is circulating in the United States this fall, it’s important for every American family and business to prepare their own household and business plans and think through the steps they will have to take if a family member or co-worker contracts the flu.
REL: Tuberculosis is also circulating this fall. So are impetigo, gonorrhea, athlete’s foot, head lice and zits. Is the US Government offering a TARP bailout, at the expense of our lives, to the the very wealthy, very powerful Pharmaceutical Industry?
SKS: CDC has provided specific recommendations for what individuals, communities, clinicians, and other professionals can do.
REL: In the face of trivial disease, if it indeed exists in community distribution, for which there is no evidence that has forensic or scientific credibility, these common sense wash-yours-hands, cover your mouth and nose when you sneeze recommendations are more than sufficient the help out a perfectly unthreatened population. My mother taught me that, too, and it sufficed.
SKS: Individuals can take actions to prevent respiratory infections. We emphasize frequent hand-washing as an effective way to reduce transmission of disease. It is very important for sick individuals to stay at home,
REL: Really? Do employers know that and do they refrain from docking them?
SKS: and for parents to keep children who have a fever or flu-like illness home from school, childcare, the playground, or other places children gather.
REL: Flu is not necessarily Swine Flu.
SKS: Similarly, sick individuals should not get on an airplane or any public transport.
REL:This benign-sounding provision will result in persons who have not been vaccinated being denied boarding privileges on public transport in the United States unless we stop this medical fascism now. There is already talk of stainless steel RFID chipped bracelets at state trooper checkpoints. Where accurate or not, this suggestion illustrates how easily this type of tyranny would be to install. Tyrannical control never presents itself as that. it always wants to help, to take care of, to protect you. This process of constitutional abrogation, so well advanced at the state and federal levels, is receiving another set of supporting members in this document, Madam Secretary, and in this dangerous and unwarranted approval.
SKS: Taking personal responsibility for these things will help reduce the spread of this new virus as well as other respiratory illnesses.
We have issued new guidance from the CDC on www.flu.gov for schools, child care settings, colleges and universities, and large and small businesses that also includes strategies for preventing the spread of flu, especially in the early fall when the 2009 H1N1 vaccine will not yet be ready. These comprehensive guidelines provide advice on how individuals and institutions can guard against the flu and mitigate its spread. The CDC also has issued guidance for healthcare providers about appropriate use of anti-viral drugs to treat patients who are at highest risk from complications from the seasonal and 2009 H1N1 flu.
REL: These guidelines offer dangerous pharmacological usage practices which, like the vaccine approval itself, is not supported by science. In fact, the science of the antivirals suggests very strongly that they should not be used and their use, while increasing the liklihood of serious complications and death, does little or nothing to shorten or minimize the severity of the purported “Swine Flu” infection. Remember, it can only be purported because the laboratory testing is not being done, based on the recommendations of the CDC and W.H.O. Why? Because the testing is so inaccurate. Therefore any suggestion about incidence, prevalence or impact is mere fantasy. Tamiflu and Relenza have not been shown to bring about positive outcomes in this diagnostic fantasy matrix, in fact, quite the contrary.
SKS: Additional work is being done on critical guidelines to address infection control and worker safety in healthcare settings. Our recommendations and action plans are based on the best scientific information…
REL: Please refer to what I have said above and my comments below, Madam Secretary.
SKS: …available to help our nation respond aggressively and effectively to the 2009 H1N1 virus.
REL: This may sound awfully familiar by now, Madam Secretary, but why? Where is the justification for aggressive action or the demonstration that effective action is not achieved by the “Personal responsibility” suggestions and by the protection of the collective immune system through avoiding junk foods, chemicals, GMOs and other health degradation substances and processes permitted by your agency, the same FDA which is now so sanctimoniously declaring its benign intent here?
In fact, the same FDA has literally criminalized communications which offer non-vaccine, non-drug options to prevent, treat, mitigate or cure the Swine Flu. It is hard to see how the FDA is working to help our nation respond aggressively and effectively to anything except the need to make the population docile, obedient, sick and profitable in its chronic illness.
SKS: We are working to ensure that Americans are informed and consistently updated with information in clear language. This is a dynamic situation, but it is essential that the American people are fully engaged so they can be part of the response.
REL: Really? To my mind, being fully engaged would require clear, accurate information and, I am very much afraid that your testimony makes it clear that the intention of the FDA is to provide anything but that. You are providing information in easily understood words, but it is distorted and dangerous. If your FDA were interested in that goal, it would be offering abundant information on nutrition, antioxidants, homeopathy, Foods, nutrients, nano silver and supplements designed to support the immune system.
SKS: The federal government, particularly the CDC, will be conducting weekly and, when necessary, daily briefings that will be available at flu.gov to get critical information out to the American people.
Vaccination Campaign The federal government is also preparing for a voluntary national vaccination campaign for the 2009 H1N1 virus starting in October.
REL:The Federal Government has backed off from its earlier stance for mandatory vaccination, which was articulated by HHS on July 23, 2008 and by DHS on the following day in advisory communications.
SKS: With unprecedented speed, we have completed key steps in the vaccine development process — we have characterized the virus, identified a candidate strain, expedited manufacturing, and performed clinical trials.
REL: Clinical trials have not been performed. Brief dose response trials have been initiated, is some cases not even completed before this authorization.
SKS: The speed of this vaccine development was possible due to the investments made through ASPR/BARDA over the past six years in advanced research and development and infrastructure building.
REL: How convenient!
SKS: One-hundred ninety-five (195) million doses of H1N1 vaccine have been purchased from five manufacturers by the U.S. government.
REL:Vaccines have already been purchased, BEFORE their approval? That makes their approval sound very much as if it were pre arraigned. Why the haste? Why the collusion? Your agency declared a national state of health emergency on April 25, 2009, just 11 days after the first so-called death from the so-called novel virus in Mexico. A level 6 pandemic was declared on June 11, just shy of 2 months after the first alleged death. The death toll was reduced in Mexico from 168 to 16, a percentage decrease in mortality of 90.5%. This miracle of biblical proportions was not only ignored, but the decrease in observed mortality was apparently not factored into the response of either WHO or FDA.
SKS: Two types of vaccine will be available: vaccine made from killed virus for injection (flu shot) and vaccine with live, weakened virus administered by nasal spray.
REL: Madam Secretary, our information is that this is simply not correct. We have been informed that there is more than one inactivated live virus preparation. We are checking this out now.
SKS: The vaccines are being manufactured by the same methods used for the production of the seasonal flu vaccines administered every year.
REL: I am afraid that this is simply not true. Conventional influenza vaccines are cultured in eggs. Cell based, rather than egg based, vaccines are not the norm and are not just a simple “strain change” variation of the same old vaccine. MF59, and oil and water adjuvant, is not the norm. The virus is said by both WHO and FDA to be unpredictable and to be a totally novel virus. In that case, there is no possibility that all approved vaccines are merely strain change variations on a well proven, but not particularly safe, theme. FDA can only have it one way or the other, but not both, Madam Secretary.
SKS: NIH is conducting a series of clinical trials on the vaccine to determine the safety and number of doses needed to induce a protective immune response.
REL: Safety trials will not, according to the FDA< be completed until June, 2010. Approval of the novel vaccines before that point constitutes irresponsible dereliction of duty at the very least. Since full disclosure and informed consent are not possible under the conditions of secrecy which prevail in these tests, it is possible that they are illegal and that they constitute crimes against humanity.
SKS: Trials in healthy adults and the elderly began in the first week of August. Complete immune response data from the first trials—those studying two doses in healthy adults—are expected in late October.
REL: The approval of 5 different vaccines was announced today, September 15, 2009. There is no possibility that even the preliminary dosage trials in healthy adults have been completed. No trials in immuno compromised or suppressed people, vaccine injured persons, infants, people with atopic disorders like asthma, eczema, egg allergies, organ transplant recipients, cancer chemotherapy patients or those on steroids, etc., have been conducted. No safety information exists to guide usage or administration. This is consistent with the lack of information which would pierce the veil of liability protection as mentioned before.
SKS: Preliminary data indicate that the vaccines are safe
REL: What preliminary data. Is that sufficient to jeopardize the health of a nation for a non existent threat of a disease?
SKS: and that a single 15-microgram dose induces what is likely to be a protective immune response in healthy adults between the ages of 18 and 64.
REL: We should note that no one says that the dose will be protective since vaccines have never been shown to be protective of diseases for which they are administered. Not a single double blind, placebo controlled study on this question has ever been done. But the antibody production generated by vaccines is assumed, not know, to provide protection. Given the dangerous nature of these novel vaccines for a novel virus, don’t ou think, Madam Secretary, that more information about the conclusive results of carefully designed safety testing, with fully informed consent, would be in order before these vaccines were approved?
SKS: For adults aged 65 and over, the preliminary data indicate that the immune response to the 2009 H1N1 influenza vaccine is somewhat less robust, as is the case with seasonal influenza vaccine.
REL: And there is no intermediate or long term safety data on the adjuvanted vaccines whatsoever since no adjuvanted vaccine has ever been approved before in the US. the only two adjuvanted vaccines available in Europe are for patients on dialysis, whose immune function is so suppressed that they are deemed to need the extra “punch” of the squalene adjuvant and, according tot he controlling agency, have such a reduced life span that they are not expected to live long enough to develop side effects and complications from the vaccine and Cervavax, GSK’s competitor to Garadsil, the HPV vaccine.
Parents who continue to state that their daughters were either killed by, or seriously damaged by Cervavax administration are being warned that if they continue to disseminate that information their children will be taken from them.
The suggestions in this data is that although dangerous, the danger is being hidden. Without a good deal of further clarification, the approval of adjuvanted vaccines, or the potential administration of adjuvants by themselves or mixed with unadjuvanted vaccines, as being discussed now by CDC, makes the purchase some months ago of nearly $1/2 billion worth of squalene adjuvants make sense in the limited fashion that injecting a a known poison into large number of humans might be said to make sense.
Squalene, when injected into animals, causes such severe auto immune illness that its use is standard in laboratories where the induction of such disease is desired for research purposes. In that context, it is named after the scientist who discovered that it had that impact and is known as “Freund’s Adjuvant.
SKS: Trials in children began in mid-August, and trials in pregnant women have just begun.
REL:Does that mean that approval for the use of these vaccines for unrestricted use is based on …what? Certainly not science or data.
SKS: Our expectation is that vaccine will be a good match for the virus currently circulating in the United States based on intensive monitoring of the virus.
REL: But the expectation of the FDA and WHO for a “good match” between a circulating influenza virus and the next season’s disease is wrong well over 70% of the time. Secretray Sebelius, you and your Staff’s expectations are less than compelling. The regular administration of the seasonal flu vaccine that ACIP and CDC, both units of FDA, recommend year after year has been shown to increase the incidence of Alzheimer’s Disease by more than 600% while its accuracy in predictng which virus will be circulating is less than 30%.
FDA standards are not very high: according to your official website, the H1N1 vaccine will be considered a success if the anticipated antibody titer response (1:40) is found in 28% of the population. That means that these vaccines are being approved even if the number of people who do not show a robust laboratory antibody response (which is not associated with protection) is as high as 72%. So the risks of these vaccines are not accounted for and the efficacy is not required.
Furthermore, FDA has announced that the unadjuvanted vaccine, the strain change variety, is expected, under the best case scenario, to kill at least 30,000 people. The number who are expected to be maimed and crippled by this is not specified on the offical FDA website. If the 1976 disaster, which Secretary Sebelius says the FDA is looking to for guidance, is any indication, we can expect at least a thousand people sickened and crippled for each person who dies from the Vaccine. The math is hardly conducive to confidence in the FDA.
SKS: We are coordinating this 2009 H1N1 vaccination campaign with the seasonal influenza vaccination campaign, and are working hard with state and local authorities and the clinical community to address the challenges this presents.
From what we know as of today, 2009 H1N1 virus preferentially affects a population different from that affected by seasonal flu. In particular, this virus is infecting more young people including children, younger adults and pregnant women.
REL: What is this data based upon, given the lack of diagnostic specificity and the fact that symptoms are not distinguishable from all other types of colds or flus?
SKS: Typically these groups, particularly young children and pregnant women, are at greater risk of serious complications from any influenza, including the 2009 H1N1.
REL: Again I must ask, Secretary Sebelius, without diagnosis, how can that be ascertainined?
SKS: CDC’s Advisory Committee on Immunization Practices (ACIP) recommended on July 29 providing initial doses of the new H1N1 vaccine to five groups—approximately 159 million people.
REL: That is over one half of the entire population of the US. Wouldn’t it be more prudent, given that there is no legitimate health emergency, to not vaccinate more than half of the country, specifically the most vulnerable half, with an untested, unnecessary and uninsurable group of vaccines?
SKS: CDC endorsed these recommendations.
REL: Rather than reassuring me, this seems to me to be a clear cause for an overhaul of FDA and CDC with the possibility of criminal charges being investigated.
SKS: These groups are:
pregnant women,
people who live with or care for children younger than 6 months of age,
health care and emergency services personnel,
persons between the ages of 6 months through 24 years of age, and
people from ages 25 through 64 years who are at higher risk for novel H1N1.
REL: Note your use of the term “Novel”, Secretary Sebelius. As stated above, that precludes the claim that these vaccines are mere strain change variations on a well-worn theme.
SKS: because of chronic health disorders like asthma and diabetes or compromised immune systems.
REL: These are the very groups to whom squalene is the most dangerous and the crops to whom contaminates like leukemia-causing virus SV40, found in the line of monkey kidney cells that the Novartis Vaccine has been cultured.
SKS: The H1N1 virus is particularly dangerous to healthy women who are pregnant. Not only has this virus caused greater numbers of pregnant women to be hospitalized, it has also been fatal in a higher percentage of this population than in other affected groups.
REL: Does squalene cross the placenta. Does it damage the fetus? In what way? At what age? It is known that mercury does cross the placenta and does damage the Fetus. Yet the CDC is advising women to take the H1N1 vaccine(s) regardless of whether it has the preservative known as “Thimerisol” (49.6% mercury by weight). No mention has been made of the dangers of aluminum adjuvants, nor of the fact that polysorbate 80 (also called “Tween 80) is associated with infertility when injected?
SKS: The federal government will be working in partnership with states, territories, tribes, and local communities as well as the private sector to help distribute and administer the new H1N1 vaccine. Thanks to support from Congress, the federal government has allocated $1.444 billion for states and hospitals to support planning and preparation efforts. TARP AGAIN.
The large scale 2009 H1N1 vaccine program will begin mid-October with small amounts of vaccine becoming available the first full week in October. The vaccine itself will be available free of charge to the American people, but some public and private providers may charge an administration fee. It will be distributed to providers and state health departments in a manner similar to how federally purchased vaccines are distributed in the Vaccines For Children program. The CDC and states will work with a contractor to get vaccine to where it needs to go. The number of doses shipped will be reported to the CDC daily, and the number of doses administered will be reported to the CDC weekly.
REL: Where will the adverse relations be reported for the general public to track?
SKS: The fact that vaccine won’t begin distribution until October makes preventing the spread of flu even more critical. Again, we need to remind all Americans about the things they should be doing right now: washing hands, staying home if you’re sick, and taking the necessary precautions to stay healthy and avoid getting sick. Flu.gov has good tips for what you need to do to avoid getting the flu.
While the 2009 H1N1 flu virus has been the focus of attention since the spring, it is important that we do not forget the risks posed by the seasonal flu viruses. More than 36,000 people die each year from complications associated with the flu.
REL: This statistic is totally false and misleading. About 600 people per year from the complications of influenza, but marketing concerns have created this oft-repeated number from which bears little relationship to reality as the swine flu case numbers or death numbers.
SKS: CDC continues to recommend vaccination against seasonal influenza viruses, especially for all infants, children, and people at greater risk for influenza complications. Seasonal flu vaccine already is becoming available in many places.
It is not too early to get a seasonal flu shot as soon as it is available. The protection you get from the vaccine will not wear off before the flu season is over.
REL: There is no evidence that the seasonal flu strain in the vaccines is the one circulating but there is considerable evidence that the vaccines are dangerous, despite insistent government and industry denial.
SKS: Closing Remarks – At HHS, we are simultaneously working hard to understand and control this outbreak…
REL: What outbreak? See above.
SKS: …while also keeping the public and the Congress fully informed about the situation and our response. We are working in close collaboration with our federal partners as well as with other organizations with unique expertise that helps us provide guidance for multiple sectors of our economy and society. It is important to recognize that there have been enormous efforts in the United States and abroad to prepare for this kind of an outbreak and a pandemic.
REL: One would have to wonder why.
SKS: Our nation’s current preparedness is a direct result of the investments and support of the Congress and the hard work of state and local officials across the country. While we must remain vigilant throughout this and subsequent outbreaks, it is important to note that at no time in our nation’s history have we been more prepared to face this kind of challenge.
REL: Or more over-prepared to face a challenge which does exist.
SKS: But the government cannot solve this alone and, as I have noted, all of us must take constructive steps. Taking all of those reasonable measures will help us mitigate how many people actually get sick in our country.
We look forward to working closely with the Congress to best address the situation as it evolves in the weeks and months ahead. Again, Mr. Chairman, thank you for the opportunity to participate in this conversation with you and your colleagues. I look forward to taking your questions.
REL: Thank you Madam Secretary. I do think you have told us quite enough disinformation.
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Today there was a treat and a terror in my email box: a new article from William Engdahl. A treat, because William Engdahl is one of my heroes. I do not know whether to admire him most as a writer who researches or a researcher who writes. Looked at either way, however, he is an honest and fearless man whose works tell us what we need to know – and what the self-anointed elite does not want us to know. And they do so with passion, clarity but without the faintest hint of panic or hysteria.
A terror because of the subject: mercury and aluminum in our babies and our own bodies through the mechanism of vaccination. You have heard it before: mercury and aluminum are neurotoxins. The restatement of this information in the context of a clear and focused historical and scientific review of just what we are talking about when we talk about mercury, aluminum and autism. It must be read and shared.
There are a few more facts which help to frame the cataclysmic disaster called “Vaccine Injury”, which is by no means limited to children. Think for a moment of healthy young men and women in coma, developing demyelinating neurological disorders like MS, ALS (now seen in children and adolescents for the first time in history as a new disease called “Juvenile ALS, but only in girls and women who have received Gardasil), diabetes, encephalitis, meningitis, persistent and debilitating rashes, swollen, painful joints everywhere in the body, brain fog, memory loss, depression, loss of IQ, lupus and other auto immune disorders, Alzheimer’s Disease, etc.
They Would Have Died Anyway
Let’s start with the origins of Thimerisol, which is 49.6% mercury by weight. Mercury is more toxic by far to tissues, including the brain, than lead.
It was patented by Eli Lilly, a so called “ethical” drug company (so named because they sell patented medicines) in the 1920s. In 1930, it was administered IV to 22 meningococcal meningitis patients, all of whom were in coma. All 22 patients died.
Eli Lilly, an “ethical” drug company, concluded that Thimerisol was safe because although all patients died, none showed any adverse response to the injected Thimerisol since they WOULD HAVE DIED FROM OTHER CAUSES ANYWAY. Therefore, none died from Thimerisol and it was deemed to be safe. When the FDA was founded, this information was presented to it and accepted. Thimerisol was grandfathered into use. The FDA, always compliant to the desires of industry, bought the insane logic of the “ethical” drug company, to the endless tragedy of our children, our elders and ourselves. This horrific substance is added to our vaccines as a “preservative”.
As a simple side thought, if vaccine manufacturing were strictly clean and sterile, not careless, contaminated and dirty, why would a preservative be necessary? Thimerosal was subsequently introduced for use in vaccines and in over the counter remedies as a preservative to kill bacteria in the product without any additional safety testing of any kind since it had been “grandfathered”. The 1930 study, in which every patient died, remains the only safety testing done on the substance even after being in use for over 84 years.
Aluminum is added to vaccines in order to irritate the immune system and increase the production of antibodies which are ASSUMED to be associated with immune competence with respect to the disease entity on which the vaccine is focused. No compelling (or even non-compelling) scientific evidence exists which demonstrates that this type of antibody production is associated with protection from the disease. In fact, virtually every epidemic in modern times has occurred in fully vaccinated populations.
Aluminum is neurotoxic and is strongly associated with the epidemic of a previously unknown type of dementia which will impact more than half of those who reach the age of 80: Alzheimer’s Disease.
When combined with fluoride, also added to many vaccines, the two toxic metals are strongly synergistic, increasing the neurotoxicity of the other substance by many times, creating a much higher level of impact than either one alone could produce. Since nearly everyone in the US drinks fluoridated water and brushes their teeth with fluoride-containing toothpaste, even without added injected fluoride, the synergistic potential is both untested and very frightening.
These metals are not the only toxins found in vaccines, but they are, individually and in combination, enough to create the public health and private home tragedies which can be laid directly at the feet of Big Pharma and criminal regulators.
Please disseminate this blog as widely as possible with full attribution AND with the Action Items above: they are vital to our ability to stay unvaccinated, all of us, with the new and much deadlier Swine Flu vaccines. Safety testing, if you can call it that, will not be completed until July of 2010. Yet the WHO and FDA (CDC is part of FDA) are rushing to vaccinate our precious children, pregnant women and the chronically ill with a vaccine containing aluminum, mercury AND a million times more squalene than the wildly toxic anthrax Vaccine A which caused the horrific, and frequently lethal, Gulf War Syndrome in hundreds of thousands of Gulf War vets and is still causing the same damage in our soldiers now.
Despite that, the Department of Defense, Governor after Governor and employer after employer are making these untested vaccines mandatory even while the President and Secretary Sebelius of Health and Human Services intone solemnly that vaccinations will be “voluntary”, defining “voluntary” as one option of a pair of options which offer you the unsafe, untested, unnecessary and uninsurable vaccine, all liability for which both the government and the manufacturers have been relieve of in a convenient legislative and regulatory pirouette. The other option is involuntary internment or incarceration, as the public documents from Iowa, Florida, North Carolina and other states makes clear is already being prepared for you. Indeed, “vaccine refusers” in Massachusetts may, under a pending law, be liable to fines of $1000 per day for refusing to be vaccinated AND jailed for up to 30 days [Per day of refusal? For all days of refusal? – REL]
So, indeed, “it IS the Vaccines, Stupid!” as William Engdahl tells the FDA, the media and the rest of the deaf establishment.
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
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It’s The Vaccines Stupid!”
F. William Engdahl
Global Research
September 6, 2009
Part I: Evidence Linking Autism Rise in Children to Vaccinations
The WHO and US Government CDC are escalating a public psychological
conditioning to create hysteria and panic among an uninformed public about an
alleged “virus” H1N1 Influenza A, aka Swine Flu, whose alleged effects to
date appear comparable with a common cold. Before people line up in the
streets demanding their vaccinations for their children and themselves, it
would be wise to remember, to paraphrase a 1992 campaign statement of Bill
Clinton to George H.W. Bush: “It’s the vaccination, Stupid!”
By countless scientific accounts, far more dangerous to human health than any
reported incidences of Swine Flu are the dangers of severe health issues
including paralysis, brain damage and even death arising from what is added to
vaccines by virtually every major vaccine maker. Almost without exception, all
commercial vaccines today contain various substances known as adjuvants
designed to make the vaccine “work.” These adjuvants are the source of
horrendous and sometimes deadly damage.
It has been speculated for some time that there might be a link in the
alarming rise in cases of autism among tiny infants and children and massive
multiple vaccinations today given routinely to infants and children from the
first hours of birth. There is clear and
shocking evidence of the link between the two. If you do not have a strong
constitution, you are advised not to read further.
A new study shows a direct link between standard childhood vaccination series,
MMR, and autism-like symptoms in monkeys. The principal scientist involved in
the study, Dr. Laura Hewitson of the University of Pittsburgh, presented the
alarming conclusions as an abstract pending publication at the International
Meeting for Autism Research. It has been presented at scientific conferences
in both London and Seattle, USA.
The study compared vaccinated macaque monkeys with non-vaccinated macaques. No
major flaws in the study have been revealed by any attending scientist. The
vaccines included the popular MMR series. The study found a marked increase in
“gastrointestinal tissue gene expression” and “inflammation issues”
with those monkeys which received vaccinations. They are a common symptom of
children with regressive autism.
The study also found marked behavior changes and development differences in
those monkeys given the vaccines versus those who were not. “Compared with
unexposed animals, significant neuro-developmental deficits were evident for
exposed animals in survival reflexes, tests of color discrimination and
reversal, and learning sets,” the study`s authors reported. “Differences
in behaviors were observed between exposed and unexposed animals and within
the exposed group before and after MMR vaccination.”
US Government-mandated research approved by Congress was t
o begin this year, but the funds were rescinded in early January. Claiming
“conflict of interest” because of ongoing court cases, the Centers for
Disease Control and Prevention (CDC), a long-time supporter of infant
vaccinations, withdrew the research plans.
The most shocking of all is the recent and now common medical practice,
reinforced by an aggressive pharmaceutical industry, of giving multiple
vaccines, often virtually within hours of birth, to infants despite the fact
that no study including all of the vaccine series commonly given to children
in the US and UK, about 30 in all, has been conducted until now. The practice
of newborn multiple vaccinations has become widespread in Germany and other EU countries over the past decade. Significantly there have surfaced reports of dramatically increased instances of autism in newborn and infants in various German hospitals over the past decade, precisely the period multiple
vaccinations of newborn and infants has become routine.
US Government coverup
Tragically, the US Government agency theoretically entrusted with guarding
public health, the Food and Drug Administration (FDA), as with the case of
health dangers of GMO foods, as well with the dramatic evidence of the link
between autism and adjuvants used in typical vaccines, is accepting the
argument of big and politically powerful Pharmaceutical companies.
The Food and Drug Administration considers vaccines safe but, just as with
GMO, they have done no studies into the effects of multiple vaccinations as given in the common childhood series which started in the 1990s in
the USA and spread to the UK and now across the EU.
According to Robert F. Kennedy, Jr., son of the late Attorney General and an
attorney active in campaigning to expose mercury (Thimerosal) and other
toxicity dangers in vaccines, recently stated, “as autism is a behavioral
affliction rather than a precisely defined biological injury —
epidemiological studies are critical to establishing its causation. But the
greatest source of epidemiological data is the Vaccine Safety Datalink (VSD)
— the government maintained medical records of hundreds of thousands of
vaccinated children — which Health and Human Services Department has gone to great lengths to keep out of the hands of plaintiffs’ attorneys and
independent scientists…The raw data collected in the VSD would undoubtedly
provide the epidemiological evidence needed to understand the relationship
between vaccines and autism. The absence of such studies makes it easy for
judges to say to plaintiffs they have not met
their burden of proving causation.”
Autism was virtually unknown in the United States until 1943 when it was
diagnosed and identified eleven months after Thimerosal, a mercury-based
vaccine “adjuvant” was first added to baby vaccines along with various
aluminum compounds in the United States. Thimerosal is often used to stem
fungi and bacterial growth in vaccines despite massive evidence of its severe
effects as a potent neurotoxin. Following independent studies, Russia, Japan, Austria, Denmark, Sweden and Britain have banned Thimerisol from children’s vaccines. Germany to date has no such ban. The toxin was developed in 1930 by Eli Lilly. Tragically in 1991, despite overwhelming evidence to the contrary the US Government’s Center for Disease Control (CDC), the same agency fueling the current hysteria over the non-proven H1N1 Swine Flu virus danger, recommended that infants be injected with a series of mercury-containing vaccines in some cases within 24 hours of birth for Hepatitis B and two months for diphtheria-tetanus- pertussis.
Before 1989 US pre-school children received eleven vaccinations— polio,
diphtheria-tetanus- pertussis, measles-mumps- rubella (MMR). By 1999, because of the various CDC recommendations, the number of vaccinations was twenty two before first grade of school. Parallel with this explosive rise in
vaccinations of the very young in the United States, according to Kennedy, the
rate of autism among children. The state of Iowa reported a 700% increase in
autism in children beginning in the 1990’s and along with California has
banned mercury in vaccines. Despite evidence, however the US FDA continues to allow drug makers to include Thimerosal in numerous over-the-counter
non-prescription medications as well as steroids and injected collagen. The US
Government ships vaccines preserved with Thimerosal to numerous developing
countries as well, where some are reporting sudden explosion of autism rates
as well. In China,20where autism was unknown before introduction of Thimerosal by US drug makers in 1999, press reports indicate there are almost two million autistic children.
Instances of autism in the US exploded as some 40 million children were
injected during the 1990’s with Thimerisol-based vaccines, giving them
unprecedented accumulations of mercury poison. The level of ethylmercury in a
vaccine routinely given then to children of two months age was 99 times
greater than the US Government’s daily limit for exposure. As with the
current WHO pandemic declaration around H1N1 Swine Flu, the CDC Vaccine
Advisory Committee is filled with scientists with close ties to the
pharmaceutical industry. Dr. Sam Katz, chairman of the committee was a paid
consultant to most companies producing the vaccines he “recommended.”
The aluminum danger remains
While vaccines available in the US today exist with no Thimerosal (50%
mercury), virtually all vaccines still contain aluminum, which has been linked
to impaired neurological development in children. Aluminum has not replaced
thimerosal as a vaccine preservative; it has always been used in vaccines.
In the recent past, most US children got exposed to both thimerosal and
aluminum simultaneously with the hepatitis B, Hib, DTaP (diphtheria, tetanus
and pertussis) and pneumococcal vaccines. Combining mercury with aluminum
increases the likelihood that the mercury will damage human tissue.
According to a recent report by Michael Wagnitz, an American chemist, “Currently eight childhood vaccines that contain aluminum ranging from 125 to 850micrograms (mcg). These vaccines are administered 17 times in the first 18months of life, an almost six-fold increase compared to the vaccine schedule
of the 1980s.”
Wagnitz adds, “According to the American Society for Parenteral and Enteral
Nutrition, based on IV feeding solutions, a child should not exceed a maximum
daily dose of 5 mcg of aluminum per kilogram of weight per day. That means if
a child weighs 11 pounds, the child should not exceed 25 mcg in a day. This
level was determined to be the maximum safety limit based on a study publishedin the New England Journal of Medicine titled “Aluminum Neurotoxicity in Preterm Infants Receiving Intravenous Feeding Solutions.”
The hepatitis B vaccine, administered at birth, contains 250 mcg.
In a 1996 policy statement, “Aluminum Toxicity in Infants and Children,”
the American Academy of Pediatrics states, “Aluminum can cause neurological
harm. People with kidney disease who build up bloodstream levels of aluminum
greater than 100 mcg per liter are at risk of toxicity. The toxic threshold of
aluminum in the bloodstream may be lower than 100 mcg per liter.” What level
of aluminium toxicity is contained in vaccines routinely given German, French
and other children n the EU is not known. It might be time for a public demand
for such information to be disclosed, and before governments launch mass
vaccination campaigns for untested vaccines against a non-proven H1N1 Swine Flu threat.
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
www.Nutronix.com/naturalsolutions
Action Item: Support Ron Paul’s Bills to end FDA & FTC gag rules on free health speech: http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27732
Action Item: Support your right to turn down Swine Flu vaccines without facing incarceration: http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275
Natural Solutions Foundation proudly recommends Silver Biotics Nano Silver:
www.Nutronix.com/naturalsolutions
Index:
Dr. Rima’s Ballad: “Say Not Silver…”
Does Silver Causes Cytokine Storms? No
—————–
Say Not Silver
Say not “silver” for the flu of pig
Lest the Phama gods be angry.
Say not “echinaca sprig”
Says Sibelius. Sang she,
“Tamiflu and vaccines only
May you tout as cure for flu.
Nature’s cures, let them be lonely,
Nothing plant-ish may you do.”
“Worst of all, far worse than C
Colloid silver, or, worse, nano.
Squalene’s safe as safe can be:
Get sick and die. See? That’s the plan-O!”
Speaking with a silver tongue
Into major trouble gets you.
Staying healthy, staying young,
Means FDA will surely fret you
Some fear immune cell health
Storms of cytokines will bring you.
“Back off silver, save yourself
Lest Death’s keen dart surely sting you.”
“Pish”, I say, and “Tush” as well
Review the research deep with care.
Silver does not increase cell
Mediated immune share
So storms of cytokines, while real,
Are not involved. We need not fear
That silver will cease to appeal
As swine flu slayer without peer.
My advice to you, for feeling dandy,
Facing Flying Pig or other trouble
Is “Keep the nano silver handy
If you need it, just take double!”
——————————-
Index
Does Silver Causes Cytokine Storms? No
The US FDA, known in the circles in which I travel as the “Fraud and Death Administration”, has apparently decided that the First Amendment is neither binding upon it nor of much interest. It does that in two ways: first, it exerts gag order authority upon people who want to let you know the truth about what a natural product, substance, molecule or preparation does to enhance or support your health, whether you have any financial or other connection to the product or not. Only a very narrow type of health claim, called a “Structure/Function Claim” is “permitted” by the self designated “protectors” of your knowledge. They do not have the law on their side, but they do have the enormous might of the US Government, including their own legal department and the US Department of Justice. Small manufacturers rarely have the resources to fight their illegal, unconstitutional and absurd rulings. Occasionally, however, they do, and when they do, with attorneys like Natural Solutions Foundation Trustee Ralph Fucetola, JD, they often come out on the right side of justice. That road trip, however, is very, very expensive.
The Natural Solutions Foundation enthusiastically supports Rep. Ron Paul, MD (TX-R) in his bid to pass two laws which he has introduced into the US House of Representatives which would untie the gag which the FDA has unconstitutionally placed on us all. You can help by taking action here, http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27732, once for each member of your family.
The second way that the FDA stifles your knowledge is to tell you in advance, called ‘prior restraint’, what you may or may not say about something. In this case, they say that it is forbidden speech to tell anyone that ANYTHING except vaccines (which are totally unproven for EITHER safety or efficacy against the Swine Flu) or drugs, specifically the very dangerous Tamiflu (c) and Relenza (c) may be used to prevent, treat, mitigate or cure H1N1 virus.
Well, so much for immunology, biochemistry, virology, nutritional medicine and common sense. This amazing flu virus is so novel that not only does it travel through time, leading to at least two patents for the manufacture of the vaccines to “prevent” it to be applied for and granted BEFORE it appeared mysteriously, like Venus from the forehead of Zeus, from absolutely nowhere, but it also makes you sick by mechanisms that have nothing to do with physiology, pathology or any other “ology”. If it were not so astonishingly mysterious, the many ways in which the body counters viruses would apply. Alas, no vitamin, no nutrient, no immune support, nothing but two Big Pharma money makers will have any impact on the nasty, swiny, birdy, magical thing.
But wait! There’s ever so much more.
Now we have the Cytokine Storm which is the source of death in the Swine Flu! Never mind the fact that it is not clear from any forensically meaningful evidence of any kind that
1. The Swine Flu can be diagnosed with any degree of certainly since tests seem to be running about 90% inaccurate, making chicken entrails a better diagnostic system than the tests approved – and rapidly abandoned – by CDC and WHO.
2. The Swine Flu actually exists. No independent scientist of whom I am aware has actually characterized the virus, which requires isolating it from an organism, introducing it into another organism and reproducing the disease. That may have happened, but none of the scientists whom I know of have any reports that this has, indeed, occurred.
3. No one that I am aware of knows how the Swine Flu kills because there is no clear evidence that it ever has killed anyone. It appears, and this is not clear, that some people have died WITH the Swine Flu virus, assuming that it actually exists. However, all of them had underlying medical conditions which, as far as I am aware, is what killed them or, like the pregnant woman “with” Swine Flu (unconfirmed by lab tests) in India who was in Intensive Care in Mumbai (Bombay) when her baby was born and died, they may well have been killed by Tamiflu, a dangerous and ineffective anti-viral making Hoffman LaRoche, Donald Rumsfeld and, reportedly, President Obama and his cronies a great deal of money. So the idea that because the 1918 virus has been retroactively decided to kill by “Cytokine Storm” this flu kills the same way, given the fact that it does not actually seem to do very much killing, is beyond absurd. Hysterical, yes. Great press, yes. But science? Oh, I think not.
So now we come to the question of whether silver, especially nano silver, is the cause of a cytokine storm reaction and could, if it is, be the cause of a cytokine storm if one is infected with Swine Flu and then serve as a contributory factor in death.
That question was posed by a woman who had read something of the sort in the newsletter of a very popular health guru. Generally, I admire this person for his way of sharing information and for getting things right most of the time. This time, however, I am afraid that he got the information wrong. We all do sometimes, and his credibility should not be in the least tarnished by this, but he is not, I believe, correct. Silver, especially nano silver, is a wonderful help in dealing with all types of pathogens since it does NOT work by elevating inflammatory cytokines so even if the body does not have the resources to raise a cytokine response, nano silver is exceptionally helpful in combating disease causing organisms.
Here is the letter my correspondent (name removed) sent to me:
Dear Dr. Rima,
You are my Nutronix sponsor: Can you please respond to this from Dr. X:
“…there may be significant problems in using nano silver for swine flu. We were initially going to carry one of the finest silver products in our store, but I recently learned of new information that changed my mind.
“While silver will likely work to kill the swine flu virus, in many healthy individuals it is likely to elicit a severe cytokine storm reaction. This is basically a severe allergic inflammatory reaction that can occur in your lungs, and could be fatal….” [Emphasis added – REL]
I have healed my body of cancer without surgery chemo or radiation but I can not recommend this silver nor sell nor use it anymore without knowing about this allegation of the severe cytokine reaction that may lead to death. Please tell me what you know about this.
What I am reading is this, Thanks, [Name Removed – REL]
A cytokine storm, or hypercytokinemia is a potentially fatal immune reaction consisting of a positive feedback loop between cytokines and immune cells, with highly elevated levels of various cytokines.[Emphasis added – REL]
When the immune system is fighting pathogens, cytokines signal immune cells such as T-cells and macrophages to travel to the site of infection. In addition, cytokines activate those cells, stimulating them to produce more cytokines. Normally, this feedback loop is kept in check by the body. However, in some instances, the reaction becomes uncontrolled, and too many immune cells are activated in a single place. The precise reason for this is not entirely understood but may be caused by an exaggerated response when the immune system encounters a new and highly pathogenic invader. Cytokine storms have potential to do significant damage to body tissues and organs. If a cytokine storm occurs in the lungs, for example, fluids and immune cells such as macrophages may accumulate and eventually block off the airways, potentially resulting in death.
The cytokine storm (hypercytokinemia) is the systemic expression of a healthy and vigorous immune system resulting in the release of more than 150 known inflammatory mediators (cytokines, oxygen free radicals, and coagulation factors). Both pro-inflammatory cytokines (such as Tumor necrosis factor-alpha, Interleukin-1, and Interleukin-6) and anti-inflammatory cytokines (such as interleukin 10 and interleukin 1 receptor antagonist) are elevated in the serum of patients experiencing a cytokine storm.
It is believed that cytokine storms were responsible for many of the deaths during the 1918 influenza pandemic, which killed a disproportionate number of young adults.[1] In this case, a healthy immune system may have been a liability rather than an asset. Preliminary research results from Hong Kong also indicated this as the probable reason for many deaths during the SARS epidemic in 2003.[6] Human deaths from the bird flu H5N1 usually involve cytokine storms as well.[7]Recent reports of high mortality among healthy young adults in the 2009 swine flu outbreak has led to speculation that cytokine storms could be responsible for these deaths.[8] However, the Centers for Disease Control and Prevention (CDC) have indicated that symptoms reported from this strain so far are similar to those of normal seasonal flu,[9] with the CDC stating that there is “insufficient information to date about clinical complications of this variant of swine-origin influenza A (H1N1) virus infection”
I thought that was a totally fair, intelligent question.
The problem is that it is based on assumptions about the mechanism of action of silver that are incorrect. Here is my response to her:
Dear [Name Removed]
Good question. I am afraid that I believe Dr. X to be incorrect. A search of the available literature shows only one study in which silver has any impact on inflammatory cytokines, and the impact is negligible.
http://www.woundsresearch.com/content/effectiveness-inflammatory-cytokines-induced-sericin-compared-sericin-combination-with-silve
And here, a discussion of the nanocrystallin coating of Anticoat, a wound dressing at
http://www.worldwidewounds.com/News/News2003.html
This shows no impact, either.
See for example,
This article states:
“Interleukin-5 (IL-5), interferon-? (INF-?), and tumor necrosis factor-? (TNF-?) protein levels were measured to determine the activation state of PBMCs.
At levels of over 15 ppm, nano-silver was found to have a significant cytotoxic effect on PBMCs, and PHA-induced cytokine productions were significantly inhibited by nano-silver (IL-5: at 10 ppm, INF-? and TNF-? at 3 ppm).
Although nano-silver had a cytotoxic effect at high concentration, nano-silver modulated cytokine production in a concentration-dependent manner. These experimental data suggest that nano-silver could be used to treat immunologic and inflammatory diseases.”
Based on my study of the literature, I will continue to recommend nano silver for all infections, whether with bacteria, mycoplasma, parasites or viruses.
Thanks for bringing up this important question.
Yours in health and freedom,
Dr. Rima
So, as you can see, there is no credible evidence that silver, nano or otherwise, will initiate a cytokine storm. The Natural Solutions Foundation strongly recommends the Nano Silver at www.Nutronix.com/NaturalSolutions without hesitation, although the FDA does not want me to tell you that it would kill the H1N1 virus. So I am not telling you that. If you have a flu and take the Nano Silver dose I use, 1-2 cap fulls once or twice a day, either in the mouth for 2 minutes, then swallowed or in a bit of water and consumed, you will do so on your own. Since nobody is going to diagnose Swine Flu accurately, my guess is that you need to take it when you get symptoms that might be flu. Who know? It might be Swine Flu. Or not. Who cares? Only Big Pharma.
Yours in health and freedom,
Dr. Rima
By the way, your donations and your patronage of our two on-line stores are our only means of support. Please make your tax free, recurring donation at http://drrimatruthreports.com/?page_id=189 and make another donation ending in the number “6” to support our STOP THE SHOT lawsuit against the FDA to prevent their releasing untested, unsafe and uninsurable pandemic vaccines before any safety testing has been completed.
Thanks!
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
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Natural Solutions Foundation
Health Freedom Action eAlert
The Voice of Global Health Freedom™
Share this Action eAlert:
http://drrimatruthreports.com/?p=3339
August 20, 2009 – Welcome! In This Issue:
* FDA Petition: Stop the Shot!
* Don’t Forget 3 for Liberty Campaign
* Dr Rima: Health Freedom Silly Season
* Swine Flu Reports from Good Doctors
* Be a Natural Solutions Volunteer Sponsor
——————-
Special Action eAlert:
We Urgently Need Your Help!
Gary Null, PhD, Leads Demand that FDA
STOP THE SHOT
Individuals – Join Dr. Null Here:
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27791
Organizations Join Dr. Null Here:
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27793
——————-
Nano Silver Special!
Save $76 on 4 Bottles; Receive Spray, Nasal Attachments Free!
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24 -7 Information Online…
New Network Supports Natural Solutions
http://drrimatruthreports.com/?p=3332
——————-
Health Freedom Leaders Join Forces to
Stop FDA Approval of Swine Flu Vaccines Without ANY Safety Testing
Read Legal Call for Relief Here:
http://drrimatruthreports.com/?p=3312
Take Action! Help Prevent FDA from Approving Pandemic Vaccines for Use on All of Us Absent ALL Safety Testing
1. Say “NO!” to Forced Vaccination
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275
Join the New Citizens Petition! Stop FDA Approval for Untested Vaccines
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27791
At last! An effective and powerful legal action with the potential to stop the FDA’s planned approval of Swine Flu Vaccines without any, repeat ANY, safety testing. Three far sighted health freedom leaders have banded together to take action to protect us all and invite your help, and your organization’s help, too.
2. Join in: Demand FDA NOT Approve Vaccines Before Completion of Safety Testing
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27791
Remember: Take Actions 1 and 2 Once for Each Member of Your Household
3. Representatives of Organizations Click Here:
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27793
Note: Take action 3 in addition to Actions 1 and 2 if you represent an organization
Not the signatory for your organization? Contact your organization’s leaders and urge them to participate in this democratic legal exercise. No charge, no downside – just benefits for all!
4. Mere Days Left to Save Health Freedom…
Right, our 3 Weeks Nearly over. Senate Reconvenes Sept. 7.
We MUST Prevent Passage of HR 2749 Equivalent Bill
ACT HERE NOW!
http://drrimatruthreports.com/?p=3262
We, you and the Natural Solutions Foundation, ARE the net roots of health freedom. We can – and do! – produce literally millions of emails, raising our voices high enough to push back the madness. In fact, we’ve already sent more than 1.5 million emails demanding the right to say “No!” to pandemic vaccines. Well, it is time for more of same!
If you have not yet clicked on the Action Item demanding the right to say NO! to the vaccine without then going to jail, now is the right time to do so for every member of your family:
Click here, http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275
To safeguard your right to say “NO!” to dangerous vaccines and click here, http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27791
To tell the FDA that untested, unnecessary, unsafe and un-insurable vaccines are not acceptable.
Time for Health Freedom Silly Season to End
Silly Season Science is the product of shameless intellectual prostitution in which science for hire pumps out whatever it is told to produce. A prime example from the supposedly reputable British paper, The Guardian:
“Healthy Eating Can be Sign of Serious Psychological Disorder”
http://www.guardian.co.uk/society/2009/aug/16/orthorexia-mental-health-eating-disorder
Health Freedom Silly Season has to end, now. You see, Health Freedom organizations are notorious for NOT working together. You know, this one says this, and the other one says that and pretty soon you don’t care “who struck John” and you are sick of all the gore! That’s one of the classic disinformation techniques and juvenile people are easily stimulated to behave like tantrum-ing toddlers. You have noticed that the Natural Solutions Foundation does not waste its time, or yours, with that kind of sniping and in-fighting. Instead, we focus on the problems, find solutions and tell you what we think is going on, asking for your help.
But when the folks that like to call themselves part of the Health Freedom movement behave that way, it means they are notoriously shooting themselves in the foot. Since they are supposed to be working for you, that also means they are not doing their job protecting your interests. If they had been, perhaps we would not be in this mess and perhaps General Bert and I would still be running our drug-free practice of medicine.
This issue, mandatory/unapproved vaccination, is really the ultimate litmus test: either the other “Health Freedom” organizations actually get on board and join us in protecting your rights to stop this dangerous – possibly lethal – FDA idiocy or they are, in fact, NOT health freedom anythings.
High Road To Survival
You see, once again, as we continue to do, the Natural Solutions Foundation is offering the hand of literally life-saving collaboration to any and all other health freedom organizations and advocates. Those who join us are welcome, no matter how inappropriate or inflammatory their previous bad behavior and disinformation activities have been. This is literally a matter of YOUR life and death.
Those who do not join us are making who they are, and who they work for, clear by marginalizing themselves.
Please contact the health freedom organizations of your choice to urge them in the strongest terms to get on board with this powerful initiative. If they resist, ask them to explain, in writing, why they are not taking this opportunity to work for your health and freedom, and that of the other supporters/members of the group. Insist on real reasons for their inaction, not merely unsupported assertions and, if they cannot provide them, walk away. They are not on your side. They just proved it.
On the other hand, smart non-governmental organizations are happy to cooperate to make sure Health Freedom can survive. For example, we’ve just accepted DownSize DCs invitation to join its coalition partners in www.ConsumerCenteredHealthcare.org to “Stop current efforts to expand government control of health care – Roll back existing government involvement and restore free market competition” No matter what healthcare system exists, we want it to a system that allows people the freedom to make their own choices… and a politician and bureaucrat dominated system cannot do that! Whoever pays for it, your health care choices should be, must be, determined solely by you.
Real Health Freedom Leaders:
Koren, Laibow, Null…
Three leading health freedom advocate organizations banded together this week and, under the guidance of Ralph Fucetola, JD, Natural Solutions Foundation’s brilliant and skillful Counsel and Trustee, submitted a Citizens Petition (unlike an Internet Petition, a Citizens Petition is a powerful legal challenge which can have real impact on Policy) to the FDA demanding redress from the immanent harm posed by approval of attenuated and adjuvanted live virus vaccines for a trivial disease when not one of the vaccines have been tested for safety. You will recall that on July 23, 2009 the Fraud and Death Administration said that they will approve these vaccines in the absence of completed safety tests.
Remember, the pediatric tests of the vaccine now underway are to determine antibody response levels (dosage), NOT safety. And the vaccines being tested are NOT those with adjuvants.
The Health Freedom movement has been divided by disinformation and ego-based squabbles for decades. Enough. The issues are too important to let absurd accusations and personal turf struggles interfere any longer.
Health advocates, officials and doctors, along with and health freedom leaders, have all known for quite some time that the enormously profitable Swine Flu Vaccines are a vast windfall for Big Pharma and a horrific dangers for the rest of us.
The New York State Association of Nurses refused New York State’s Mandatory Vaccination regulation for mandatory health care worker vaccination without any provision for exemptions of any kind.
http://www.nysna.org/publications/newyorknurse/jul_aug/flu_shots.htm
In the UK, where the Daily Mail leaked two letters from their Health Protection Agency and a leading neurologist urging other neurologists to be on the lookout for an anticipated 800% rise in the incidence of Guillian Barre Syndrome, also known as Polio, following the upcoming MANDATORY Swine Flu vaccinations there. http://dailyexpress.co.uk/posts/view/120936/Alert-on-killer-side-effect-of-the-swine-flu-vaccine-/, nurses are so uneasy about the mandatory Swine Flu vaccine’s dangers, and the non-seriousness of the “Pandemic” disease, that 2/3 say they will either refuse the Swine Flu vaccine outright or are unsure that they will submit to it. In fact, only 1 nurse in 7 receives the seasonal flu vaccine in the UK anyway. Skepticism runs high among people in the know!
http://www.infowars.com/nationwide-revolt-against-mass-swine-flu-vaccination-accelerates/
Legal Legs and Limps
Quite a number of legal actions have been filed in response to these dangers. Some are good, some are marginal and some make no sense at all. Click here,
http://drrimatruthreports.com/?p=3170
for a look at the good, the bad and the just plain meaningless.
The Citizens Petition which we have filed with the FDA is, we believe, a highly effective way to exhaust our legal remedies so that we can rapidly and effectively move forward. We need your help, though. Your organizations and you (and your family, friends, contacts, etc.) all are invited to join the Petition and exercise your First Amendment Right for redress of grievances via a Petition to the Government.
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27791
Six for the Cemetery?
All 6 Swine Flu vaccines which the FDA has announced it will approve BEFORE the completion of any safety testing are unsafe. Some or all will have squalene-based adjuvants. Some or all will have live attenuated virus (LAIV) vaccines which have been shown to
* Increase hospitalizations of children for all causes by 300%
* Cause wheezing and asthma,
* Communicate the vaccine disease to those with health problems and weak immune systems
* Add new bits of other viruses in the warm, wet, nutrient rich environment of a cell
BUT
* They provide little or any real or lasting immunity against the target disease.
Oil in water adjuvants such as sqalene or its related compounds have never been approved for injection in the US and, in fact, have been rejected by the FDA itself because they were “too dangerous to test in the United States”. Tragically, they were used against our own military creating the cataclysmic auto immune disorder known as “Gulf War Syndrome”.
Health Without Freedom?
Let’s make an incorrect assumption for a moment, just for the sake of argument. let’s assume that untested LAIV vaccines with deadly adjuvants were safe and effective. Even if they worked and were safe, is it OK with you to force your kids and you, too, to be vaccinated at someone else’s choice? I think not and I am quite certain that you think not, too.
Health freedom IS our first freedom and making this type of decision for ourselves IS the hall mark of freedom. Take each of these Action Steps once for each member of your family, then alert all your contact to do the same to help keep health freedom free – and help keep yourself alive!
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27275
AND
Individuals:
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27791
AND
Organizations:
http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27793
Freedom to Stay Alive?
Justice Antonin Scalia
“Innocence Is No Reason Not To Execute”
I will bet that you thought that the Constitution of These United States gave you the right to a fair trial along with life, liberty and the pursuit of happiness, didn’t you? And you thought that innocence was a defense before the bar, didn’t you.
Well, Supreme Court Justice Antonin Scalia thinks differently – very differently. Justice Scalia recently wrote that that there is nothing inherently un-constitutional about executing an innocent person.
In his dissenting opinion in the appeal of convicted – but innocent – felon Troy Anthony Davis, Justice Antonin Scalia took his Supreme Court colleagues to task for thinking that mere innocence is grounds to overturn a conviction: “This Court has never held that the Constitution forbids the execution of a convicted defendant who has had a full and fair trial but is later able to convince a habeas court that he is “actually” innocent. Quite to the contrary, we have repeatedly left that question unresolved, while expressing considerable doubt that any claim based on alleged “actual innocence” is constitutionally cognizable.”
http://thinkprogress.org/2009/08/17/scalia-actual-innocence/
Change You Can’t Conceive Of…
You do not have to be a lawyer to understand that the very atoms of the molecules of the thread of the fabric of the Constitution of These United States are being destroyed from within the so-called “Justice System”. If you think that your right to protect your body from dangerous pharmaceutical interventions will be protected by the Justice System as it is now, in light of this madness, think again.
With a Supreme Court of this type, we clearly want to impact the regulations BEFORE we ever get to the point of needing the Court’s help! To protect us all from the vaccines, we need to grab the legal system, which means, in this case, the FDA, by its metaphoric parts, and force it to protect us while we have access to it and can still control some of its actions. And for that, we need your help, in force. NOW!
Speaking of Rights, Does the US Have As Much Freedom of Speech as India? Apparently Not!
In the US, we like to think that our Constitutional system assures us of freedom of speech that we can rely upon, more than any other country.
In fact, however, the FDA imposes a profoundly un-American gag rule on what you can or cannot say – or learn – about the health benefits of food and food components and will put manufactures out of business if they tell you the truth about health freedom with legal methods or with their ax-wielding, gun-toting, dog-using goons called FDA Marshals.
Take Swine Flu (NOT the Swine Flu vaccine, of course – don’t take that!): The FDA has criminalized the discussion of ALL options to prevent, treat, mitigate or cure Swine flu except Swine Flu Vaccines and the [quite dangerous] anti viral drugs Tamiflu and Relenza.
http://www.accessdata.fda.gov/scripts/h1n1flu/
But my friend in India, the noted Dr. Leo Rebello, notes that although doctors at Kasturba Hospital of Infectious Diseases in Mumbai (formerly Bombay) maintain, falsely, that they don’t know why a baby born to a mother who supposedly had Swine Flu [although tests for Swine Flu are wrong 90% of the time, so how could they tell?- REL], they do, in fact, know why the baby died: it died because its mother was given Tamiflu!
He states, “The adverse or side-effects of Tamiflu are – delirium, hallucination, delusion, disturbances in consciousness, abnormal behavior and convulsions. Allergic reaction including severe rash, nausea, dizziness are the common reactions. Children under 12 months and pregnant and nursing mothers and those who are allergic to oseltamivir phosphate – the main ingredient – or any other ingredients in Tamiflu should not be given Tamiflu. H1N1 is a bio-weapon and Tamiflu in combination is designed to control the population. We will have on hand another tragedy like Thalidomide if Tamiflu is given so recklessly.”
Dr. Rebello goes on, in what the FDA has previously announced would be criminal speech if, for example, I were to tell you this information,
“There are much better, safer and cheaper Flu medicines in Ayurveda and Homeopathy. Amla which contains the highest level of Vitamin C as also Mosambi (sweet lime) and Santra (orange) and simple Nimbu Pani bring immediate relief in Flu.
In Homeopathy, as I have already written :
We have Arsenic Album 200 — cold, running nose, cough and feverishness.
Gelsemium Sempervirens 200 — headache, cold, running nose, bodyache.
Eupatorium Perfollatum 200 — bone pain, bodyache.
Bellis Perennis 200 — muscle pain, bodyache.
Bryonia Alba 200 — cold, cough, fever, headache, giddiness.”
If I were to tell you in the USA, as I could in India, that Nano silver, www.Nutronix.com/naturalsolutions, is outstandingly effective in killing this virus (and all others against which it has been tested) and then point you to an article by Gordon Peterson, PH D, which states,
“Antibiotic Drugs:
Antibiotic drugs provide no solution against the virus but can be very beneficial for pneumonia that develops later. A broad spectrum antibiotic should be used because there are numerous bacteria that can produce pneumonia. According to a Penn State publication, silver sol can be given with the antibiotics and produce up to a tenfold increase in antibiotic activity.
Nutritional Supplements
There are hundreds of supplements that can be of significant benefit for the immune system and even some that claim to have antiviral activity. The best proven choices for nutritional supplements come in the form of immune stimulants and wellness products. These include: immunity Vit C, B complex, folic acid, vit D (prevention) ginseng, Echinacea, garlic, probiotics, expectorants and silver sol.
Air Filters:
CDC recommends one in every room. HEPA air filters use silver to inactivate viruses and can effectively kill 99% of all bacteria, and viruses in minutes.
Water Purifiers
Proper hygiene and a water purifier are recommended by the CDC because the influenza virus can survive 100 hours in water. Get one that has a silver filter that can actually destroy the virus. Carbon, filtration, reverse osmosis does not destroy or remove the virus.
Topical Disinfectants:
Topical disinfectants are recommended by the CDC for use between each patient and can kill germs for 4-6 hours. Patients and health care professionals should use these 4 times a day or as needed. Silver so gel demonstrates effectiveness against some of the worst pathogens including: MRSA, VRE, Strep, and the other bacteria that cause pneumonia.
Silver Sol: [Silver Solution, www.Nutronix.com/naturalsolutions – REL]
Prescription drugs and vaccines “treat” and [may -REL] help prevent viral infection and disease but are not capable of totally controlling a dangerous new or novel virus. Nutritional supplements such as Vitamins, Minerals, Echinacea, Ginseng, Probiotics and many others have the ability to help boost immune function and improve natural defenses which results in some defense against disease causing viruses and the associated secondary infections
Silver Sol provides proven prevention and treatment against viral and bacterial infections, while there is nothing else with such broad spectrum benefits. In addition, Silver Sol can be safely taken every day for prevention where it has been shown to provide protection against the very dangerous Bird flu H5N1.
The combination of antibiotics with Silver Sol has been shown to enhance antibiotic function by as much as ten fold due to the fact that Silver Sol kills the residual pathogens that the antibiotics cannot. Results of the combination of 19 different prescription antibiotics and silver sol demonstrate safe additive and/or synergistic benefits across 7 different pathogenic strains (Staphylococcus, MRSA, E coli, Pseudomonas arugenosa, Salmonella and Streptococcus). The results of this combination therapy result in significant pathogenic destruction while helping to reduce bacterial resistance (19). This can be attributed to the fact that Silver Sol does not produce resistance, nor does it destroy the beneficial intestinal probiotic bacteria.
Discussion:
…It is evident that the newly patented EPA certified and FDA approved Silver Sol technology provides tremendous treatment options for prevention and combination therapies. Silver Sol gel can help stop viral spread on the most contagious areas like hands, nose, mouth and skin. It is sufficiently documented and proven to be considered to be a first line of defense against Influenza and a significant companion to antiviral and antibacterial drug regimens topically and orally.”
Swine Flu Influenza Type A/H1N1 Protection for Health Care Practitioners and Their Patients, http://www.worldhealth.net/news/swine_flu_influenza_type_a_h1n1_protecti4
If I said that, I would be violating the FDA’s regulations which, in the US, have the strength of law.
Is this Your Kind of Democracy?
Not Mine, Either.
Happily, we’ve got Rep. Ron Paul, MD (Tx-R) on our side. He has introduced two bills to end this unconstitutional rule by edict by the Fraud and Death Administration (FDA) and the Fake Trade Commission (FTC).
We urge you to join the dozens of thousands of people who have already told their members of Congress that they co sponsor and support HR 3394 and HR 3395.
Please visit http://salsa.democracyinaction.org/o/568/campaign.jsp?campaign_KEY=27732
To lend your support (and do so once for every member of your Household) to real free speech, as defined in the Constitution of These United States.
For more information, please visit (and share!) our Three For Liberty Campaign, http://drrimatruthreports.com/?p=3209
Health freedom, your freedom, is facing enormous challenges right now. I cannot remember them coming so fast, or so furious. And the Natural Solutions Foundation is working on the most important ones of all:
1. Codex-i-fication of our Food Supply through really awful bills like HR 2749 which, if passed as a sister bill by the US Senate will be nothing short of a full blown disaster for health and freedom. You can take action by informing your Senator in person (use our talking points) and by email:
http://salsa.democracyinaction.org/o/568/t/1128/campaign.jsp?campaign_KEY=26714
Tell them this (sic) “food Safety” bill is NOT what you want. You can visit our Three for Liberty Campaign,
http://drrimatruthreports.com/?p=3209
for background information and talking points leaflets.
2. Free Health Speech being gagged
3. State and Federal mandated Swine Flu
You can imagine that keeping up with health freedom is an enormous job which requires diverse skills and talents. You can also imagine that we need hands, but not just any hands: hands that are connected minds, hearts and brains.
That is why we are asking for volunteers for the Natural Solutions Foundation and, at the same time, volunteers for our Valley of the Moon Eco Demonstration Project, www.NaturalSolutionsFoundation.org, in Volcan, Panama.
Click here, http://drrimatruthreports.com/?p=3283, to read about our Volunteer program and see if you are cut out to help change the world! If you are, please join us on our Yahoo! Forum, NSCC, at http://groups.yahoo.com/group/NSCC and on our weekly Wednesday night conference call (info in the “Calendar” section of the Forum).
We have building projects, marketing and development ones, administrative, communication, and a host of other needs. If you are interested in either an Expense Paid Volunteer Position (Room and Board in Volcan, Panama) or in joining the roll of Health Freedom Volunteer Sponsors, please join the Forum and contact Ralph Fucetola at ralph.fucetola “at” usa.net or me at dr.laibow “at” gmail.com with “Volunteer” as the subject.
Oh, yes, Money
You know that this battle is expensive. You know that we are fighting for you. That means that we need your support.
Whether you can volunteer or not, health freedom also requires your on-going support. Click here,
http://drrimatruthreports.com/?page_id=189
to set up your recurring, tax deductible donation now.
Please visit our donations page and help us in any way you can; of course, recurring donations are the most important, since that allows us to plan ahead and be prepared for the Health Freedom battles to come!
————————–
Mark Your Calendar!
The Truth About Natural Cancer Cures
Date: Wednesday, September 2nd at 8:00 PM ET
Time: 8:00 PM ET
Instructor: Dr. Leonard Coldwell
Tuition: No Cost
Dr. Leonard Coldwell, Board Certified NMD DNM PHD LCHC CNHP DIP.PHC is the leading authority for cancer and stress related illness and has the highest cure rate for terminal diseases in Europe. Dr. Coldwell is the most endorsed holistic doctor in America and 11 times bestselling author. His newest book, Instinct Based Medicine, www.instinctbasedmedicine.com, has just been released and is already in the second Edition. Dr. Coldwell’s most awaited book: The Only Answer to Cancer, will be available in September 09.
Don’t miss this chance to spend time with this renowned physician and activist.
3 Leaflets for the
3 Weeks to Save Health Freedom Campaign:
http://drrimatruthreports.com/?p=3241
Must Read – Dr. Laibow’s Hard Hitting
Push Back and the Ministry of Lies
http://drrimatruthreports.com/?p=3279
Don’t Forget to “Follow”
Us on Twitter!
For Up-to-the-Minute Developments
www.Twitter.com/HealthFreedomUS
www.Twitter.com/DrLaibow
Hashtags: #selfshielf #healthfreedom #foodfreedom #pandemic
Yours in health and freedom,
Dr. Rima
Rima E. Laibow, MD
Medical Director
Natural Solutions Foundation
www.HealthFreedomUSA.org
Natural Solutions Foundation
wwwHealthFreedomUSA.org
My nominee for the Hall of Shame: FDA with reference to its banning of Pyridoxamine, a form of Vitamin B-6.
Read on and see if you agree with me.
Big Pharma is part of a mega-cartel that makes its money when you are sick. We might want to call it “Big Sick.” The FDA serves the needs of that super cartel without so much as a second thought; it’s built into the bureaucratic structure. It is an agency that Dr. Ron Paul says engages in “abuses of power.” It is increasingly blatant about it, though, as if there is nothing that can be done to stop it.
Well, there is, but it takes a lot of effort. Push-back works. We’ve proven it!
The FDA has, for a long time, banned truthful claims and information about the health benefits you can expect from foods and nutrients. Nutrient benefits will cut into the drug pushers’ market substantially, after all. Unless you do not know the good things you can expect from those items, leaving you all the more vulnerable to the drug pushers who are permitted to sell their deadly wares to you over the TV, in magazines and through your doctor’s prescription pads.
Remember that the 1994 law which gives us the right to nutrients in whatever dose we want them, the Dietary Supplements Health and Education Act (DSHEA) also gives us the right to truthful information about nutrients, herbs and food components. In clear violation of that law, and the First Amendment of the Constitution, however, the FDA uses a variety of powers, real and assumed, to suppress both science and facts. Take away the information and you effectively kill the alternatives to the deadly drugs the Big Pharma cartel pushes…
To make matters worse, this same gag rule on truthful speech concerning nutrient health benefits has been brought — by the FDA, of course, to Codex Alimentarius (the “world food code”) where it has been globalized through the efforts of the US delegate (previous Hall of Shame “Honoree” Dr. Barbara Schneeman, head of the FDA’s Department of Dietary Supplements, no less!) and approved by the Codex Committee on Food Labeling and then by the Codex Commission.
Codex says that any information offered to consumers about the health benefits of food or food components is illegal because it is advertising as if advertising were banned. The whole thing lacks logic, but has reason: the reason is to kill nutritional medicine in favor of drugs. This process has gone dangerously far in the EU and is advancing through FDA “HARMonization” of US rules with Codex restrictions.
Remember, our video “Nutricide” is called that for two reasons.
First, “Nutricide” means the death of the body of knowledge of the relationship between health and food components
Second, “Nutricide” means the death of a large number of people through the manipulation of the food supply. You can watch this important lecture by going to www.HealthFreedomUSA.org and scrolling down the video section. It is well worth your time.
This effort to kill nutrients is blatant as blatant can be.
How blatant? This blatant. Read the excellent article below which discusses the absurd ban on a form of activated B6, Pyradoxamine, to see just how shameless this organization is. This form of B6 has been available for decades. Then remember that when we, in our numbers, push back against the FDA, experience shows that we deflect their plans. Yes, they come back again, but we do push them away from the brink time and time again. With your magnificent help.
We thank you for your activism. After reading this article, I am sure that you will agree that eternal vigilance is the price of protecting high potency nutrients and information about them, from those who want to take away our right to access natural health options, including foods that heal!
The Natural Solutions Foundation continues to fight for your health. Please “stay tuned” for action items to oppose the evil that FDA’s bureaucrats seek to perpetuate. Remember to open our Health Freedom Action eAlerts when we send them to you! Please give generously so that we can continue that fight, with you by our side.
Click here (http://drrimatruthreports.com/?page_id=189) to make your tax deductible recurring donation – large or small. Both help enormously.
Dr. Rima E. Laibow, MD
PS – Our Counsel and Co-Trustee, Ralph Fucetola JD blogged about this sordid story this past January:
http://vitaminlawyerhealthfreedom.blogspot.com/2009/01/change-fdas-plan-to-destroy-dshea.html
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Big Pharma and the FDA: Suppress the Science, Ban the Natural Substances, Sell the Drugs!
Michael D. Ostrolenk
Thu, Jun 11, 2009 at 12:31 AM
In 2005, an up-and-coming pharmaceutical company made a big mistake: they invested millions of dollars into developing a drug only to discover that the only active ingredient of the drug, pyridoxamine, was really a common, naturally occurring substance that has been sold for decades at low cost to consumers in the form of a dietary supplement, and has always been available in commonly consumed foods such as chicken and brewer’s yeast.
We’re taught as children that when you make a mistake, you should own up to it and face the consequences. Apparently the pharmaceutical company in question, Biostratum, Inc., has yet to learn that lesson. Instead of owning up to their mistake, Biostratum tried to game the system to their advantage by asking the US Food and Drug Administration (FDA) to declare supplements containing pyridoxamine “adulterated” and effectively ban anyone but Biostratum from selling pyridoxamine.
Sadly, Biostratum’s desperate ploy to save their investment worked. Earlier this year the FDA agreed to ban companies from selling pyridoxamine as a dietary supplement. They denied the request to declare products containing pyridoxamine “adulterated,” but instead they declared that such products are not dietary supplements at all—claiming they are excluded from the definition of dietary supplements under the “prior market clause” [21 U.S.C. 321(ff)(3)(B)(ii)] and so may not be marketed as such.
Please note that nowhere in the FDA’s response letter is anything said about safety concerns. In fact, the FDA’s letter specifically says that “to allow such an article to be marketed as a dietary supplement would not be fair to the pharmaceutical company that brought, or intends to bring, the drug to market.” Fair to the pharmaceutical companies? What about fairness to consumers, some of whom rely on affordable pyridozxamine supplements to provide the levels of vitamin B-6 required for their survival? Is it fair to force those consumers to pay for expensive prescription drugs and doctors’ visits to supply their B-6 needs when they could get the exact same thing for a fraction of the cost in the form of a supplement? Isn’t this why our health care system is so ineffective?
This is hardly the first time the FDA has attacked naturally occurring substances. On October 17, 2005, the FDA banned information about the health benefits of cherries from appearing on websites—scientifically proven benefits, such as tart cherries’ ability to reduce the risk of colon cancer because of the anthocyanins and cyanidin contained in the cherry. Cherries, according to the latest research, help ease the pain of arthritis and gout; reduce risk factors for heart disease and diabetes; help regulate the body’s natural sleep patterns, aid with jet lag, prevent memory loss, and delay the aging process; and helps lower body fat and cholesterol—risk factors associated with heart disease. Moreover, Scientists at Johns Hopkins have found that tart cherry anthocyanins reduced painful inflammation as well as a non-steroidal anti-inflammatory drug, indomethacin.
When the 2005 ban was instituted, the FDA sent warning letters to twenty-nine companies that market cherry products. In these letters, they ordered the companies to stop publicizing scientific data about cherries. According to the FDA, when cherry companies disseminate this peer-reviewed scientific information, the cherries become “unapproved new drugs” and are subject to seizure. The FDA warned that if those involved in “cherry trafficking” continue to inform consumers about these scientific studies, criminal prosecutions would ensue.
But fresh fruit and vegetables are not the FDA’s only target: As we reported in this newsletter recently, General Mills was recently issued a warning letter by the FDA for illegally marketing Cheerios Toasted Whole Grain Oat Cereal. The problem was the claim on the cereal box that Cheerios can lower cholesterol 4% in six weeks, and the statement on their website that “diets rich in whole grain foods can reduce the risk of heart disease.” The letter, dated May 5, 2009, called the above claims “serious violations” of the Federal Food, Drug, and Cosmetic Act and applicable regulations. FDA stated that based on the claims made, Cheerios is now an unapproved drug, and must go through FDA new drug approval process. Note that the FDA isn’t disputing the claim. It’s disputing the company’s right to make the claim.
As one newspaper columnist humorously put it, “One of these things is not like the others: morphine, penicillin, aspirin, Cheerios. Most drugs, if taken improperly, will kill the consumer or cause substantial bodily harm. An entire bottle of aspirin at one sitting will harm or kill. If Cheerios is a drug, therefore, one should be able to commit suicide by consuming the entire box.”
For years, the FDA barred health claims about the benefits of fish oil for heart, cancer, depression, body pain, and various other conditions until a drug company paid a great deal of money to go through the approval process. This type of enforcement effectively censors scientific information and greatly restricts consumer access to scientific studies that provide valuable information.
In the case of pyridoxamine, the FDA did not act out of concern for public safety. This is about money, and about a profit-seeking corporation taking advantage of what is supposed to be a public health organization in order to save their skins.
http://aahf.nonprofitsoapbox.com/index.php?option=com_content&task=view&id=798&Itemid=