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The health freedom movement is a libertarian coalition that opposes regulation of health practices [1] and advocates for increased access to "non-traditional" health care. [2]
The right-wing John Birch Society has been a prominent advocate for health freedom since at least the 1970s, and the specific term "health freedom movement" has been used in the United States since the 1990s. [3] [4]
Vitamins and supplements have been exempted in the US from regulations requiring evidence of safety and efficacy, largely due to the activism of health freedom advocates. The belief that supplements and vitamins can demonstrably improve health or longevity and that there are no negative consequences from their use, is not widely accepted in the medical community. [5] Very rarely, large doses of some vitamins lead to vitamin poisoning (hypervitaminosis). [6]
Health freedom is a libertarian position not aligned to the conventional left/right political axis. Libertarian Republican Congressman Ron Paul introduced the Health Freedom Protection Act in the U.S. House of Representatives in 2005. [7] [8]
Prominent celebrity supporters of the movement include the musician Sir Paul McCartney, who says that people "have a right to buy legitimate health food supplements" and that "this right is now clearly under threat," [9] and the pop star/actress Billie Piper, who joined a march in London in 2003 to protest planned EU legislation to ban high dosage vitamin supplements. [10]
The Dietary Supplement Health and Education Act of 1994 (DSHEA) defines supplements as foods and thus permits marketing unless the United States Food and Drug Administration (FDA) proves that it poses significant or unreasonable risk of harm rather than requiring the manufacturer to prove the supplement’s safety or efficacy. The Food and Drug Administration can take action only if the producers make medical claims about their products or if consumers of the products become seriously ill. [11]
An October 2002 nationwide Harris poll showed that, at that time, consumers still had widespread confusion about the differences between supplements and pharmaceuticals. Here, 59% of respondents believed that supplements had to be approved by a government agency before they could be marketed; 68% believed that supplements had to list potential side effects on their labels; and 55% believed that supplement labels could not make claims of safety without scientific evidence. All of these beliefs are incorrect as a result of provisions of the DSHEA. [12]
A law in the U.S. State of Virginia allows teenagers 14 or older and their parents the right to refuse medical treatments for ailments such as cancer, and to seek alternative treatments so long as they have considered all other medical options, presented as "significant for health freedom in Virginia." [13]
In Europe, health freedom movement writers and campaigners believe that European Union (EU) laws such as the Food Supplements Directive and the Human Medicinal Products (Pharmaceuticals) Directive will reduce their access to food supplements and herbal "medicines". [14] European health food producers, retailers and consumers have been vocal in protesting against this legislation, with the health freedom movement inviting supporters to "Stop Brussels from killing natural medicine". [15] Euro-MPs were accosted by activists handing out a propaganda video accusing five European commissioners of corruptly colluding with big pharmaceutical firms in an attempt to destroy the alternative network of homeopathic and "natural medicines", [16] though it emerged that most homeopathic practice in the UK has been illegal for some years and proposed European regulatory changes do not materially affect this. [17] [18] [19]
In 2004, the Alliance for Natural Health (ANH) and two British trade associations introduced a legal challenge to the Food Supplements Directive referred to the European Court of Justice by the High Court in London. [20] European judges found the restrictions to be legal but stated that there must be clear procedures to allow substances to be added to the permitted list based on scientific evidence. They also said that any refusal to add a product to the list must be open to challenge in the courts. [21] Some media observers[ weasel words ] believe that, as a result of this legislation, a black market will emerge, and that controls over ingredients and quality will vanish. [22]
Health freedom-orientated writers and campaigners tend to see restrictive legislation on supplements as being designed to protect the interests of the pharmaceutical industry. [16] If herbal medicines and supplements are removed from sale, they argue, patients will have no alternative but to use conventional pharmaceutical medicines. [23] [24]
Pharmacist and skeptical writer Scott Gavura notes that the reverse is more often true, and that "governments around the world have consistently given manufacturers the upper hand, prioritizing a company’s desire to sell a product over a consumer’s right to a marketplace with safe, effective products". [25] In particular, the US Dietary Supplement Health and Education Act permitted existing supplements to be marketed without any evidence that they are effective or safe, and for new supplement ingredients required only that a new ingredient "should be safe". [26] This has resulted in a number of serious incidents including adulteration with synthetic drugs. [27] [28]
The health-freedom movement vehemently opposes [29] the Guidelines for Vitamin and Mineral Food Supplements, adopted by the Codex Alimentarius Commission as a voluntary standard at its meeting in Rome in July 2005, which includes requirements for the packaging and labelling of vitamin and mineral supplements. The text specifies that "supplements should contain vitamins/provitamins and minerals whose nutritional value for human beings has been proven by scientific data and whose status as vitamins and minerals is recognised by FAO and WHO." In addition, it states that the "sources of vitamins and minerals may be either natural or synthetic" and that "their selection should be based on considerations such as safety and bioavailability."
The United Nations' Food and Agriculture Organization (FAO) and World Health Organization (WHO) have stated that the guidelines are a consumer protection measure "to stop consumers overdosing on vitamin and mineral food supplements." The Codex Alimentarius Commission (CAC) has said that the guidelines call "for labelling that contains information on maximum consumption levels of vitamin and mineral food supplements." The WHO has also said that the Guidelines "ensure that consumers receive beneficial health effects from vitamins and minerals." [30]
The National Health Federation (NHF) is an international non-profit organization founded in January 1955, which describes its mission as protecting individuals' rights to use dietary supplements and alternative therapies without government restriction. The NHF also opposes interventions such as water fluoridation and childhood vaccines. The Federation has official observer status at meetings of the Codex Alimentarius Commission, the highest international body on food standards. Based in California, the Federation's board members include medical doctors, scientists, therapists and consumer advocates of natural health; and it is the only health-freedom organization with Codex credentials permitting it to participate actively at Codex Alimentarius meetings.
The Alliance for Natural Health (ANH) is an advocacy group founded in 2002 by Robert Verkerk and based in the United Kingdom. The ANH was initially founded to raise funds to finance a legal challenge of the EU Food Supplement Directive. The ANH lobbies against regulation of dietary supplements and in favor of alternative medical approaches such as homeopathy, and also advocates a healthy diet, exercise, and other lifestyle approaches to health. Verkerk rejects scientific research showing that megadoses of vitamins lack any health benefit.
The health freedom movement includes proponents such as Gary Null and convicted fraudster Kevin Trudeau.[ citation needed ]
Food additives are substances added to food to preserve flavor or enhance taste, appearance, or other sensory qualities. Some additives have been used for centuries as part of an effort to preserve food, for example vinegar (pickling), salt (salting), smoke (smoking), sugar (crystallization), etc. This allows for longer-lasting foods such as bacon, sweets or wines. With the advent of ultra-processed foods in the second half of the twentieth century, many additives have been introduced, of both natural and artificial origin. Food additives also include substances that may be introduced to food indirectly in the manufacturing process, through packaging, or during storage or transport.
A dietary supplement is a manufactured product intended to supplement a person's diet by taking a pill, capsule, tablet, powder, or liquid. A supplement can provide nutrients either extracted from food sources, or that are synthetic. The classes of nutrient compounds in supplements include vitamins, minerals, fiber, fatty acids, and amino acids. Dietary supplements can also contain substances that have not been confirmed as being essential to life, and so are not nutrients per se, but are marketed as having a beneficial biological effect, such as plant pigments or polyphenols. Animals can also be a source of supplement ingredients, such as collagen from chickens or fish for example. These are also sold individually and in combination, and may be combined with nutrient ingredients. The European Commission has also established harmonized rules to help insure that food supplements are safe and appropriately labeled.
In the U.S. and Canada, the Reference Daily Intake (RDI) is used in nutrition labeling on food and dietary supplement products to indicate the daily intake level of a nutrient that is considered to be sufficient to meet the requirements of 97–98% of healthy individuals in every demographic in the United States. While developed for the US population, it has been adopted by other countries, such as Canada.
A prescription drug is a pharmaceutical drug that is permitted to be dispensed only to those with a medical prescription. In contrast, over-the-counter drugs can be obtained without a prescription. The reason for this difference in substance control is the potential scope of misuse, from drug abuse to practicing medicine without a license and without sufficient education. Different jurisdictions have different definitions of what constitutes a prescription drug.
Herbal medicine is the study of pharmacognosy and the use of medicinal plants, which are a basis of traditional medicine. With worldwide research into pharmacology, some herbal medicines have been translated into modern remedies, such as the anti-malarial group of drugs called artemisinin isolated from Artemisia annua, a herb that was known in Chinese medicine to treat fever. There is limited scientific evidence for the safety and efficacy of many plants used in 21st-century herbalism, which generally does not provide standards for purity or dosage. The scope of herbal medicine sometimes includes fungal and bee products, as well as minerals, shells and certain animal parts.
A multivitamin is a preparation intended to serve as a dietary supplement with vitamins, dietary minerals, and other nutritional elements. Such preparations are available in the form of tablets, capsules, pastilles, powders, liquids, or injectable formulations. Other than injectable formulations, which are only available and administered under medical supervision, multivitamins are recognized by the Codex Alimentarius Commission as a category of food.
Nootropics, colloquially brain supplements, smart drugs and cognitive enhancers, are natural, semisynthetic or synthetic compounds which purportedly improve cognitive functions, such as executive functions, attention or memory.
The Codex Alimentarius is a collection of internationally recognized standards, codes of practice, guidelines, and other recommendations published by the Food and Agriculture Organization of the United Nations relating to food, food production, food labeling, and food safety.
Nutraceutical is a marketing term used to imply a pharmaceutical effect from a compound or food product that has not been scientifically confirmed or approved to have clinical benefits. In the United States, nutraceuticals are considered and regulated as a subset of foods by the Food and Drug Administration (FDA).
The United States Federal Food, Drug, and Cosmetic Act is a set of laws passed by the United States Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics. The FDA's principal representative with members of congress during its drafting was Charles W. Crawford. A principal author of this law was Royal S. Copeland, a three-term U.S. senator from New York. In 1968, the Electronic Product Radiation Control provisions were added to the FD&C. Also in that year the FDA formed the Drug Efficacy Study Implementation (DESI) to incorporate into FD&C regulations the recommendations from a National Academy of Sciences investigation of effectiveness of previously marketed drugs. The act has been amended many times, most recently to add requirements about bioterrorism preparations.
A health food store is a type of grocery store that primarily sells health foods, organic foods, local produce, and often nutritional supplements. Health food stores typically offer a wider or more specialized selection of foods than conventional grocery stores for their customers, for example people with special dietary needs, such as people who are allergic to the gluten in wheat or some other substance, and for people who observe vegetarian, vegan, raw food, organic, or other alternative diets.
The National Health Federation (NHF) is a lobbying group which promotes natural medicine. The NHF is based in California and describes its mission as protecting individuals' rights to use dietary supplements and alternative therapies without government restriction. The NHF also opposes mainstream public-health measures such as water fluoridation and compulsory childhood vaccines.
Health is the state of complete physical, mental, and social well-being and a positive concept emphasizing social and personal resources, as well as physical capacities. This article lists major topics related to personal health.
The Alliance for Natural Health (ANH) is an advocacy group founded in 2002 by Robert Verkerk and based in the United Kingdom. ANH was founded to raise funds to finance a legal challenge of the EU Food Supplement Directive. ANH lobbies against regulation of dietary supplements, in favour of pseudo-scientific alternative medicine, and advocates dietary and other lifestyle approaches to health. It also criticises established science showing that Megavitamin therapy lack any health benefit.
Sulfoaildenafil (thioaildenafil) is a synthetic drug that is a structural analog of sildenafil (Viagra). It was first reported in 2005, and it is not approved by any health regulation agency. Like sildenafil, sulfoaildenafil is a phosphodiesterase type 5 inhibitor.
The Alliance for Natural Health USA (ANH-USA), formerly known as the American Association for Health Freedom, is a 501(c)(4) nonprofit organization dedicated to promoting alternative medicine and is associated with the libertarian health freedom movement. Located in Charlottesville, Virginia, the organization was founded in 1992 as the American Preventive Medical Association (APMA) and became a part of the international Alliance for Natural Health organization, headquartered in the United Kingdom, in 2009.
Because of the uncertain nature of various alternative therapies and the wide variety of claims different practitioners make, alternative medicine has been a source of vigorous debate, even over the definition of "alternative medicine". Dietary supplements, their ingredients, safety, and claims, are a continual source of controversy. In some cases, political issues, mainstream medicine and alternative medicine all collide, such as in cases where synthetic drugs are legal but the herbal sources of the same active chemical are banned.
The PubMed Dietary Supplement Subset (PMDSS) is a joint project between the National Institutes of Health (NIH) National Library of Medicine (NLM) and the NIH Office of Dietary Supplements (ODS). PMDSS is designed to help people search for academic journal articles related to dietary supplement literature. The subset was created using a search strategy that includes terms provided by the Office of Dietary Supplements, and selected journals indexed for PubMed that include significant dietary supplement related content. It succeeds the International Bibliographic Information on Dietary Supplements (IBIDS) database, 1999–2010, which was a collaboration between the Office of Dietary Supplements and the U.S. Department of Agriculture's National Agricultural Library.
The Dietary Supplement Health and Education Act of 1994 ("DSHEA"), is a 1994 statute of United States Federal legislation which defines and regulates dietary supplements. Under the act, supplements are regulated by the FDA for Good Manufacturing Practices under 21 CFR Part 111. The act was intended to exempt the dietary and herbal supplement industry from most FDA drug regulations, allowing them to be sold and marketed without scientific backing for their health and medical claims.
The Proxmire Amendments were a series of legislation that prohibited the Food and Drug Administration from monitoring and limiting the potency of vitamins and minerals found in dietary supplements. The Proxmire Amendment also made it so that food supplements could not be classified as drugs, making their sale possible without a prescription from a doctor. According to a study done, "dietary supplements fall into the following categories: vitamins, minerals, herbs or other botanicals, amino acids, animal-derived products, hormones and hormone analogues, enzymes, and concentrates, metabolites, constituents, or extracts of these." They can be used by anyone wishing to purchase them as much or as little as they desire. Dietary supplements can be used to increase productivity, treat illness, help mental health such as depression and anxiety, enhancing mental abilities, building muscle, or losing weight, among many other uses. William Proxmire, a Senator for Wisconsin, was instrumental in influencing the passing the Proxmire Amendment. The Proxmire Amendment is also known as The Rogers-Proxmire Amendment of 1976, and The Vitamins and Minerals Amendments. This amendment became section 411 of the Federal Food, Drug, and Cosmetic Act.