possibly the biggest threat ever known to our rights as users of natural therapies.

Now is the time to contact your government & voice your concern about CODEX, & their intentions before it is too late or we may be forced to pay $39 for a packet of Disprin by prescription!
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Subject: Serious concerns for CAM Worldwide

Read this very important health message below and contact everyone. Your right to choose your vitamin, mineral and other supplements may end in June of this year (2005). After that U.S. supplements will be defined and controlled by the

World Trade Organization (WTO) and the World Health Organization (WHO). The CODEX ALIMENTARIUS (Food Code) is setting the supplement standards for all countries in the WTO. They will be enforced by the WTO and will over ride U.S. laws.

The U.S. President and Congress agreed to this take-over when the WTO Treaty was signed. Violations are punished by WTO trade sanctions. CODEX drastically restricts vitamins, minerals, herbs and other supplements. CODEX met secretly in November, 2004 and finalized ³Step 8 (the final stage)² to begin implementation in June, 2005.


The CODE includes:

(1) No supplement can be sold for preventive or therapeutic use.

(2) Any potency higher than RDA (minimal strength) is a ³drug² requiring a prescription and must be produced by drug companies. Over 5000 safe items now in health stores will be banned, terminating health stores as we now know them.

(3) CODEX regulations become binding internationally.

(4) New supplements are banned unless given very expensive CODEX testing and approval.

CODEX now applies to Norway and Germany, among others, where zinc tablets rose from $4 per bottle to $52. Echinacea (an ancient immune-enhancement herb) rose from $14 to $153 (both examples are now allowed by prescription only). They are now ³drugs². Vitamin C above 200 mg, niacin above 32 mg, vitamin B6 above 4 mg‹all are banned over-the-counter as drugs. No amino acids (arginine, lysine, carnitine, etc. = essential amino acids!), essential fatty acids (omegas 3, 6, 9, etc.), or other essential supplements such as DMEA, DHEA, CoQ10, MSM, beta-carotene, etc. are allowed.

The CODEX rules are not based on real science. They are made by a few people meeting in secret (see web sites below), not necessarily scientists. In 1993 the FDA and drug corporations tried to put all supplements under restriction and prescription. But over 4 million Americans told Congress and the President to protect their freedom of choice on health supplements. The DSHEA Law was passed in 1994, which does so. But this will be over ruled by CODEX and the World Trade Organization.

Virtually nothing about it has been in the media. What the drug corporations have failed to do through Congress they have gotten by sneak attack through CODEX with the help of a silent media. What can be done at this late hour?

(1) Spread the word as much as possible. Inform yourselves fully at www.ahha.org (www.codexinfo.org ), www.iahf.com , and www.alliance-natural-health.org.

(2) Oppose bills S.722 and H.R.3377. These support the CODEX restrictions with U.S. laws, changing the DSHEA law.

(3) Support H. R.1146 which would restore the sovereignty of the U.S. Constitution over CODEX, etc.

(4) Express your wishes to the President, Senators and Representatives (They got us into this!) ASAP.

(5) Contact multi-level health marketing groups that can get their members to inform the government.

(6) Send donations, however small, to the British Alliance for Natural Health (see web site above). It has succeeded in challenging the CODEX directives in World Court later this month or next. They need help financially, having carried the fight effectively for everyone. CODEX and the FDA wish to protect us by controlling supplements in the same way they do prescription drugs. A study of the latter by three medical scientists was reported in the Journal of the American Medical Association, April 15, 1998‹Vol. 279, No. 15, p. 1200 ³ŠIncidence of Adverse Drug Reactions (ADR¹s) was found to be extremely high.² Covering 30 years (1966 to 1996) it was found that in the U.S. an average of 106,000 hospitalized patients per year (290 per day) die from ADR¹s and 2,200,000 need more hospitalization for recovery. These were FDA approved drugs, properly administered by competent professionals in hospitals--none were considered malpractice. This is the number four cause of death in the U.S. When combined, these account for 7% of all hospitalized patients. This is equivalent to a 9-11 attack every ten days. There are very few fatalities from supplements or the news would be on every front page. There is no need for more FDA control of supplements than is already in place, which is substantial. Instead of drastically restricting supplements, why doesn¹t the FDA better control and restrict the extremely dangerous pharmaceutical drugs which are now killing us at the rate of a major airline crash per day?



Wallace G. Heath, Ph.D.
1145 Marine Drive Bellingham, WA 98225
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http://usenature.com/mangosteen.htm

 

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