March 4, 2008
www.eu-referendum.org
Six non-governmental organizations (NGOs), collectively representing consumers from all 27 European Union (EU) countries, today announced the official launch of a campaign for citizens to have the right to vote in referendums whenever significant changes to laws affecting them are made at either national or European level. In particular, they are demanding that all EU citizens should immediately be given the opportunity to vote in referendums on the Lisbon Treaty.
Arguing that the EU is increasingly favouring the interests of big business over those of its own citizens, the six organizations say that unless this situation is reversed and European citizens are given the right to be directly involved in political decision-making, the European political system will rapidly degenerate into a dictatorship where democracy, freedom of choice and the privacy rights of individuals are routinely violated.
Paul Anthony Taylor, External Relations Director of the Dr. Rath Health Foundation and the campaign’s coordinator, said: “Last November, for the thirteenth year in a row, the EU’s auditors refused to sign off its financial accounts citing errors of legality and presumed attempts at fraud. Then, only two weeks ago, EU politicians were openly accused of fraud and embezzlement on a massive scale and an official investigation was launched that could potentially lead to the imprisonment of a number of MEPs. Corruption, fraud and an overall lack of accountability are becoming increasingly rife amongst the European Union’s political elite and it is clearly time that ordinary citizens are given a direct say in the way that the EU is developing. Simply giving people one vote every four or five years - to elect their political representatives - is not nearly enough in any political system that still professes to be a democracy.”
... ContinueHEALTHY BODIES ARE NO GOOD TO BIG PHARMA
by Beldeu Singh*
Can your politician save you from the agenda and designs of Big Pharma? Will your health authorities bother to understand their designs and stand for your health interests?
I do not think so.
They have too much money to throw around and they have in some cases conspired to create organizations to front for them. They have been very successful in getting more and more toxic chemicals into human bodies in the name of treatment. Some of these chemicals are only marginally more effective than placebos, giving rise to the very good prospect of placebo therapy. No one has bothered to consider this, even though a placebo costs a tiny fraction compared to the drug and it comes with a bonus – no side effects.
Preventive medicine based on nutrition and high antioxidant intake from food sources does not seem to interest anyone except the science-literate consumer because healthy bodies do not contribute to the bottom-line of Big Pharma. On the other hand, toxic drugs, once they are legally categorized as medications, can create side-effects to be treated by more drugs that impact their bottom-lines positively. It is a gravely vicious cycle nurtured through a “cosy” relationship between Big Pharma and the regulatory authorities.
Officials have become so adversarial to ensuring health benefits that they have issued statements to the effect that doctors must only give pharmaceutical benefits to their patients and not health benefits. And, quite naturally, the number of deaths and hospitalizations from adverse drug reactions is increasing every year. But banning toxic drugs for therapy is out of the question. The system has many supporters and these people are in a position to ask for bans on clinical nutrition and to press for those in order to promote their business interests through legislation. Those ridiculous laws and legal definitions will help to stifle the application of nutrition and edible herbs to promote health and for use in therapy unless they are sold by Big Pharma!
The FDA would also like to harmonize our dietary supplement laws with the evolving international standards set by Codex, thus branding therapeutic nutrition as dangerous and risky and needing to be sold by Big Pharma or removed from the market altogether (if it competes with a blockbuster category of drugs). Codex is planning to use the same proteomics and biomarker technology that will be used by the FDA’s Critical Path Initiative to remove therapeutic dietary supplements from the international market and force their policies on America, thereby superseding the sovereignty of American law on threat of trade sanctions. The FDA fully supports draconian Codex guidelines to regulate dietary supplements and is working with the Germans to concoct technology to brand nutrients as drugs. (Life Extension Foundation as quoted in: Health Supreme, Oct 15, 2007, Codex Alimentarius: Will EU Laws Become World Standard).
The law can define animals as traffic as in the Road Traffic Acts in commonwealth countries. It can be used to distort and warp the natural order of things and a definition can be introduced to even say that vitamin C from fruits is a drug. Where will it all stop? If selling fruits is lucrative, the business can be put in the hands of Big Pharma, by changing the legal definitions. Anything that can be consumed that benefits health, whether it is a supplement or food or anything edible can be redefined in such a way as to make it a business solely of Big Pharma. If it makes money, it can be turned into a monopoly or controlled by changing the legal definitions.
Pharma has embarked on a dirty game because their drugs are not getting any better; they are getting more toxic. And more and more research is showing that these drugs do not work within the natural and healthy biochemistry to provide a health benefit. Hence, the Big Pharma producers are working hard to press for laws and regulations to ensure pharmaceutical benefits instead of health benefits. Let’s examine the issue of competition from natural medicine, clinical nutrition, ayurveda and their therapeutic and health benefits that improve quality of life or help to slow down the progression of degenerative conditions. This competition can be killed by legally defining nutrients as drugs so that only pharmaceutical companies can sell them. This becomes all the more critical for them to do as more and more people realize that drugs are D-form chemicals that cause harm in the mammalian L-form biochemistry. Many of these drugs disrupt healthy biochemical pathways by blocking the formation of the ATP molecule or the formation of antioxidant enzymes in the body. They deplete mitochondrial DNA in cells and stores of minerals in the body especially copper, manganese, zinc and iron. Those minerals work catalytically with the glutathione-catalase system to convert hydrogen peroxide produced by the cells’ metabolism into water and oxygen, a critical function for maintaining and restoring health. They also deplete magnesium or otherwise suppress your immune system. Some drugs that aim to deliver a pharmaceutical benefit, for example to reduce blood glucose levels by blocking the conversion of lipids into glucose, may end up altering the blood lipid profile, thereby creating a new risk for the patient especially if the patient’s antioxidant intake and consumption of soluble fiber through foods is low.
Many drugs generate free radicals in the body. Sometimes these dangers can be easily seen in diabetic patients with diabetic wounds who are given antibiotics resulting in blood sugar levels rising to double the original readings (eg from a reading of 7-9 going up to 16-18). On the other hand, Big Pharma companies are working to rebrand their toxic drugs and poisons into “well-tolerated” medications that somehow over time become “non-poisonous” or “cures” or are advertised to sound like supplements.
Would medical science prescribe a cancer causing drug to cancer patients? Last March, the U.S. federal government issued an unusually detailed alert to the nation’s 5.5 million health care workers: The powerful drugs used in chemotherapy can themselves cause cancer and pose a risk to nurses, pharmacists and others who handle them (The Washington Post, Tuesday, February 15, 2005; Page HE01, Jim Morris). Chemotherapy drugs in human and animal studies have shown they have the potential to cause cancer or reproductive problems, said Thomas Connor, a research biologist with the National Institute for Occupational Safety and Health (NIOSH).
Chemo-drugs, like radiation, generate huge amounts of the highly reactive hydroxyl radical that damages cell membranes and disrupts the electron transport system in cells as well as protein synthesis. Natural enzyme and micronutrient levels drop rapidly and that accelerates cell death. Such a new surge of free radicals is generated by chemo-drugs which are cytotoxic to cancer cells as well as normal cells. Thus many young normal cells die due to the treatment. Most of the known carcinogens, including benzene and at least 40 other toxic chemicals in cigarette smoke and pesticides generate free radicals that create oxidative stress in cells, impairing their aerobic respiration or damaging DNA and mitochondrial DNA, turning them into cancer cells. It is this very same toxicity that is common to carcinogens and chemotherapy-drugs. Hence the NOISH alert really comes as no surprise (see: Dangerous Philosophy of treatment in Medical Science).
How much control do they want? That depends on what and how the substance will impact the bottom-line.
"Britain is reviewing the laws on the regulation of tailored herbal treatments, but Dr Canter wants them banned, even at the risk of a backlash from Chinese or Indian communities. In some countries doctors practice phytotherapy, which uses extracts from a single plant and closely follows the principles of pharmacology" (see: Health Supreme, Oct 15, 2007, Codex Alimentarius: Will EU Laws Become World Standard).
So phytotherapy, using "extracts from a single plant" that "closely follow the principles of pharmacology" is all right, while individual attention from a herbalist is outright dangerous. If you recommend a glass juice made of orange plus carrot plus red spinach with a spoon of coconut oil and if the health of the person improves and they also lose some fat, well there you go…it is a drug! Can you see how Codex is slowly taking control of your kitchen?
There is another grave danger. While allopathic medicine is moving towards individual customization, they want to take that principle away from nutritional interventions. Developments and research in therapeutic approaches that improve or restore health will be stifled, if the principles of pharmacology are adopted as the only way to treat diseases and degenerative conditions in the human body. The mammalian biological system does not use pharmacological principles in generating an immune response or to activate cells that target pathogens or cancer cells, or in the production of antibodies or anti-pathogenic proteins such perforin, and neither in the repair of genetic material. When you legally only provide for pharmacological principles, you only create more drugs to be put into the human body. Such a law goes against the natural health processes of the human biological system. It only works towards the bottom-line of pharmaceutical companies at the expense of health. Society and its productivity is dependent on health, not on the number of drugs or the amount of pharmaceutical benefit one gets. When a system of law is put in place that makes pharmacological principles the only system of treatment, we can say good bye to the use of an orange or a lemon to cure scurvy. By then, it will be too good to own a pharmaceutical company but too late for mankind.
By then codex would have given full control of all home remedies and your kitchen and orchard to Big Pharma. Can we change the course of the engines that are steaming in this direction? Big Pharma can bank roll what they choose and all you have is a deaf or illiterate congressman or parliamentarian. Bear in mind that lobbies against health have been very successful. Take for instance, coconut oil – your doctor or even your consultant dietician may tell you that it is bad for your heart because it contains cholesterol!
The point is that governments are no longer in control of health as the pharmaceutical agenda to promote pharmaceutical benefits is spreading like a bad cancer. Greed has become their god.
... ContinueBy Byron J. Richards, CCN
The New Year brings a surprise for the FDA – a lawsuit filed by Public Citizen seeking to force the FDA to do its pretended job of protecting American citizens from the dangers of drugs. Of course, the real FDA job, as prioritized by top FDA management, is to protect the sales of Big Pharma and create new market opportunities for Big Pharma and Big Biotech while using Americans for experimental purposes.
The current suit revolves around the dangers of toxic fluoride-containing antibiotics. The two brand names involved are Johnson & Johnson’s Levaquin and Bayer’s Cipro. The German company, Bayer, has a long and colorful history of injuring Americans while its executives laugh all the way to the bank. ... Continue
PRESS RELEASE of the National Health Federation
Codex Meeting in Germany Set to Decide Future for
Vitamin Consumers Around the World
November 12, 2007
The U.S.-based National Health Federation (NHF), the world’s longest-standing international health-freedom organisation, is today beginning a week of meetings at the 29th session of the Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU) in Bad Neuenahr, Germany. Expected to be attended by over 300 delegates, observers and advisors, representing about 70 member countries and over 30 international organizations, the Committee, sponsored by the Food & Agriculture Organization and World Health Organization, is the world’s highest international body setting global standards and guidelines on nutrition
With consumer members all over the world, and a Board of Governors and Advisory Board containing representatives from six countries, the NHF is unique as being the only consumer health-freedom organization in the world to enjoy official observer delegate status at Codex. The NHF therefore has the opportunity to make representations on behalf of natural health interests all over the world, which are presently being threatened by over-regulation stimulated by spurious science, misinformed media attacks and corporate pressure from large food and pharmaceutical concerns.
... Continue
NewsWithViews.com
By Byron J. Richards, CCN
June 27, 2007
The FDA, emboldened by its transformation into a drug company, has embarked upon an anti-American plan of interfering with business and intentionally eliminating various dietary supplement companies from the market. The FDA announcement came on Friday, June 22, 2007 under the guise of a final rule for dietary supplement good manufacturing practices (CGMPs). Within this 800 page rule the FDA states, “We find that this final rule will have a significant economic impact on a substantial number of small entities.... Establishments with above average costs, and even establishments with average costs, could be hard pressed to continue to operate. Some of these may decide it is too costly and either change product lines or go out of business.... 140 very small [less than 20 employees] and 32 small dietary supplement manufacturers [less than 500 employees] will be at risk of going out of business.... costs per establishment are proportionally higher for very small than for large establishments....The regulatory costs of this final rule will also discourage new small businesses from entering the industry.”
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Codex






