Natural Solutions Foundation
The Voice of Global Health Freedom™
www.HealthFreedomUSA.org
www.GlobalHealthFreedom.org
Congressional Hearing on FDA Lawlessness
Problem: FDA answers to its industrial constituency, not the Constitution and the well-being of the people of the United States.
Background: Article 16 of the enabling legislation which created what has become Food and Drug Administration in 1932 (who thought of combining foods and drugs?) says that the primary purpose of the Agency is to promote, protect and promulgate the Pharmaceutical Industry. The Agency is doing that job very, very well. Its other job, however, protecting the health and welfare of the American Public is not being served.
Summary: Despite Constitutional and explicit legal protection, the FDA has repeatedly created arbitrary, illogical and unlawful standards upon which to curtail First Amendment rights regarding health and food, nutrients, health devices and technologies and abused its considerable powers to stifle non-pharmaceutical, natural health options. FDA Marshals invade and terrorize small manufacturers of legal substances and devices. FDA lawyers bully and intimidate these same companies and individuals, jailing innocent people and destroying legitimate businesses which compete with drug company profits.
Action: http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3688
The FDA is a lawless, out-of-control agency terrorizing and killing Americans. We call on Congress to put a halt to this deadly reign of terror.
The Agency creates new standards never envisioned by Congress, approves deadly drugs, permits wildly dangerous food and contaminants and suppresses truthful, science-based information about health and food. In short, the FDA is conducting a war against freedom and the law.
Why is the Phase IV (drug/device approval) record of the FDA so dismal that approximately 50% of the drugs and devices which it approves for sale and use are withdrawn within 5 years due to deaths and other serious adverse events?
Why is the FDA not permitted to examine or conduct safety investigations on genetically modified foods and plants and animals modified to produce drugs?
Why does the FDA prohibit the accurate labeling of genetically modified foods, drugs, ingredients and products despite clear consumer demand for such labeling?
Why is the FDA unable to select experts for its Expert Panels who are free of professional and financial conflicts of interest? Without such freedom from conflicts of interest, the Expert Opinions upon which the FDA relies are dangerously self-interested?
Corruption in the Agency is nearly limitless: its scientists are routinely ignored and the decisions of its “experts” feather their own nests and harm the American public on a regular, daily basis.
So let’s ask Congress to use its investigative powers to hold investigative findings to end the reign of terror and corruption of the most lawless agency in the United States: the FDA, or, as it is tragically correctly called, the Fraud and Death Administration.
We set up an Action Item originally asking Congress to investigate the autism/mercury connection, but understand the issue is even broader than that tragic linkage. There is corruption at the very heart of the agency, corruption that cannot be cured by the best intentions.
Thus, we’ve modified that Action Item to petition Congress to redress our grievances against the lawless agency, an agency which Dr. Ron Paul has cited for “abuse of power…”
Please take action here NOW!
http://salsa.democracyinaction.org/o/568/p/dia/action/public/?action_KEY=3688
And please donate to help us continue to fight for your health freedom:
http://drrimatruthreports.com/?page_id=189
The questions we want Congress to ask the FDA include:
1. Is there any convincing evidence reviewed by FDA that the difference in autism incidence and prevalence between unvaccinated populations and vaccinated ones is NOT related to vaccination as the variable?
2. Is there any convincing evidence reviewed by FDA that sharp increases in autism incidence and prevalence is not related to the introduction of vaccines containing human fetal DNA?
3. Is there any convincing evidence reviewed by FDA that total body burden of mercury, from all sources (including vaccines, environmental contamination, dental amalgams, etc.) is not directly proportional to in utero and post partum neurological damage, including autism?
4. Is there any convincing epidemiological evidence reviewed by FDA that the exponential rise in the incidence and prevalence of autism in the last 40 years is not related to environmental toxicity, including vaccination contamination?
5. Is there any convincing evidence reviewed by FDA that a wide-spread genetic mutation has occurred in the last 40 years resulting in the exponential rise in incidence and prevalence of autism, supporting the assertion that autism is a genetic, not an environmental, disorder?
6. Is there any convincing evidence reviewed by FDA that psychotropic medication, much of which contains high levels of fluoride, is helpful in the long-term neurological and endocrine status of autistic persons and that these medications do not produce long term brain damage?
7. Is there any convincing evidence reviewed by FDA that autistic children do not benefit from natural medical therapies such as detoxification, chelation, enzymatic and dietary strategies?
8. Is there any convincing evidence reviewed by FDA that allopathically treated autistic persons have a better outcome than those receive natural remedies?
9. Is there any convincing evidence reviewed by FDA that the use of aluminum and other adjuvants, neurotransmitter analogues, formaldehyde, TWEEN 80 and other “inactive” ingredients in vaccines do not increase the incidence and prevalence of autism?
10. Is there any convincing evidence reviewed by FDA that vaccines prevent, mitigate or minimize infection with the diseases to which they are targeted or that they are safe when injected as formulated?
11. Upon what scientific basis does the FDA permit the fluoridation of water supplies, given the clear hazards of both sodium fluoride and hexafluoric acid, the type of fluoride most often used in municipal water supplies
12. Upon what scientific basis does the FDA permit the introduction of aluminum into municipal water supplies, given the known toxicity of aluminum to the central nervous system and the synergistic toxicity of aluminum and fluoride in the human body?
13. Upon what scientific basis does the CDC’s Advisory Committee on Imunization Practicies (ACIP) make its recommendatiions for child and adult vaccine schedules, given the deep conflicts of interest of its staff and experts?
14. Is the FDA, as an agency, hopelessly corrupt and in continual conflict of of interests with the drug industry? Is this agency, as charged by Dr. Ron Paul, engaged in “abuse of power?”
Further, in 1993 the FDA proclaimed its intention to “HARMonize” our nutrient and health freedoms to international restrictions. It continues to push this policy, rejected by Congress in the 1995 Anti-Harmonization Act. The FDA’s participation in such international agencies as Codex Alimentarius (the so-called World Food Code) is shameful, dishonorable, disgraces and damages the US around the world and contributes to the degredation of the food and health of not only the US but the entire world.
See these hard-hitting videos exposing the pretensions of Codex and the actions needed to protect our food supply:
Do you believe that the United States has no place in Codex Alimentarius? If you go to http://www.youtube.com/watch?v=AfCni-LuR_c you can watch a video in which Dr. Rima discusses that view.
You can also go to http://salsa.democracyinaction.org/o/568/t/1128/questionnaire.jsp?questionnaire_KEY=1042 and take our survey asking if you think that the US should participate in Codex Alimentarius.
Natural Solutions Foundation is the largest health freedom organization in the world: we are 100% supporter supported so we need your help in several ways. First of all, we need people to become informed about the origins and real function of Codex.
Please go to http://video.google.com/videoplay?docid=-5266884912495233634# to watch a Video on the German genocidalists’ creation of Codex after they got out of jail for their crimes against humanity.
Then sign up for our free, secure Health Freedom Action eAlerts on our home page, www.HealthFreedomUSA.org to take action to protect your health, food and freedom. There is little time to loose, as you can see from this thrust.
My brief video on the Globalist Eugenocidal Agenda is at: http://www.youtube.com/naturalsolutions#p/f/1/_gWmVtn5JsA
The original precursor to the FDA was established under the Wiley Act of 1906. The agency has had over a century to get it right… and has failed — and failed dismally, resulting in FDA-approved drug deaths that outnumber all other causes of death in the United States! Now it’s time for Congress to listen to the voice of the people and call FDA to account!
Health Freedom is our First Freedom!
The Trustees of the Natural Solutions Foundation
Maj. Gen. Albert N. Stubblebine (US Army Ret) – President
Dr. Rima E. Laibow MD – Medical Director
Ralph Fucetola JD – Counsel
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