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STUDY GROUP AIDS THERAPY
c/o Felix A. de Fries
Eglistr. 7 CH-8004 Zürich, Tel. /FAX: 0041 1 401 34 24
E-Mail: felix.defries@bluewin.ch 
 
Zurich, 5th August 2002
 
The "HIV-vaccines" and the attempts to prevent the access to effective treatment and diagnostics.

 

Dear Sir or Madam
 
With parts from nacked DNA the promotors of the HIV-AIDS model try to produce "HIV-vaccines" that should prevent persons with a negative result in the HIV-antibody test from developing AIDS-defining illnessesif they get infected with the real HIV-virus. This effect would be demonstrated after 5 or 10 years if less of the participants in these tests (selected from risk groups) develop AIDS defining illnesses, say their producers. They state already that these vaccines could not bring a secure protection against the HIV viruses, "as these viruses mutate continuously".
These vaccines produced by leading multinational pharma companies, that are now tested under the control of the CDC, should induce a higher release of antibodies against the proteins of the cell skeleton, that have been defined to be the product of HIV-retroviruses. By this they could effect a positive result in HIV-antibody tests. In reality because of their formulation the HIV-antibody tests dedect a a hightened titer of antibodies to a defined scale of cellular protein particles said to characterise the presence of HIV above a certain level. (This scale of cellular proteins is defined differently in the HIV-antibody-tests administrated in African and Asian countries, than it is in antibody-tests administrated in Europe, the USA or in Australia).
After all the announcements made at the International AIDS conference in Barcelona the medical world and international media eagerly await to see if the postulated effects of these vaccines can be chieved.
At the same time as trials with these vaccines are being carried out the multinational pharma companies and their lobbyists are trying to prevent the access to the substances and tests that have been shown to be effective in the treatment of AIDS defining illnesses:
-multi-national pharma companies have tried to stop the distribution of  herbal preparations that showed good effects in the restitution of cellular immune reactions in Switzerland and in India, as they try to isolate potent substances from these plants and register patents on these substances.
- the pharma multinational Aventis, which is involved in the HIV vaccinetest, has cancelled the production of the DTH-multitest  (Mérieux-test, cutaneous anergy-test) that allowes measurement the cellular defence capability (in persons with a positive result in HIV-antibody-tests).
- the members of the European Parliament approved the EU Food Supplement Directive, that places access to substances(vitamins, minerals, food supplements, amino acids, herbal prepartions) that have shown good effects in the treatment of immune deficiencies under heavy restriction and have thereby strenghtened the position of the Rome-based Codex Alimentarius Commission, a drug- and  food-industry-controlled commission, that forces a rigid control over diatry supplements. This comission aims to establish its standards world-wide within the Gatt trade agreement and remove the supplement industry and the local producers of  herbal medicaments from the market. (The lobbyists of these multinational pharma companies (such as Pfizer, Glaxo, Merck, Astra Zeneca. Johnson &Johnson, Bristol-Myers  Squibb, Novartis, Aventis, Pharmacia and Abott) and important pharma shareholders (such as the Bush family as shareholder at Abott) will certainly use their influence to make ratification of these standards pass the US-congress. 
As these "HIV-vaccines" cannot have any influence on the  Th1-Th2 switch in the cytokine-profile of CD-4 helpercells, which is the common agent in most of the diseases that can define the AIDS syndrome, they can not inhibit the development of AIDS defining illnesses. The Th1-Th2 switch, that comes about with a hightened release of NO gas and a lack in glutathione molecules, induces an ongoing formation in the bone marrow of antibodies to external antigens, an ongoing inhibition of cellular immune reactions (the detection and destruction of cells containing viruses, fungi and mycobacteria) and subsequent the inhibition of the production of NO gas in the organism.
As it was demonstrated by various studies (that we have sent you earlier) the Th1-Th2 switch can be deblocked by the administraion ofherbal antioxidants, amino acids, fatty acids,  vitamins, enzymes and minerals. By this means cellular immune reactions can be restored and AIDS defining illnesses can be treated efficiently.
If access to these substances is prevented by the multi-national pharma industry and by international and national institutions, an effective treatment of AIDS-defining illnesses will not bepossible any more. The monopoly then established would end any freedom of medical treatment. 
We hope you do support health freedom
With our best regards
 
Felix de Fries
Study group AIDS therapy

 

FEATURE ARTICLE FROM THE ICHF NEWSLETTER 
Codex: worldwide battle shaping up over plans by pharma-globalists to ruin supplements industry
 
WORLDWIDE - Health-freedoms advocates worldwide are gearing up for the November meeting of the international Codex Alimentarius Commission at which, it is feared, the German proposal to essentially limit public access to dietary supplements in virtually all countries - as a prelude to knocking ut the industry globally - will advance.
Concerns have grown steadily that the dictates of the Rome-based, United Nations-aligned Codex Alimentarius Commission will be binding as nternational law and subvert the sovereignty of member nations, including the US.
Attempts to control the burgeoning global supplements industry -  perceived by international pharmaceutical interests as a major economic threat - by "harmonizing" and "standardizing" the doses and uses of the same have been strengthened by several factors: In February, the European Union (EU) parliament, while partially addressing dissidents’ views as mounted through a vigorous anti- "EU vitamin directive" petition unleashed continent-wide from Italy, nonetheless approved "safe upper levels"for supplements based on "science" which dissidents have found to be both flawed and fraudulent. EU decisions apparently are not binding until the Union’s Council of Ministers accept them, so European health-freedoms activists are continuing the petition campaign.
Witnesses in opposition to the planned Codex restrictions were reportedly snubbed at a March "Codex vitamin oversight hearing" of Rep. Dan Burton’s House Government Reform Committee, leaving the field essentially to organizations which are in alignment with the globalist supplement-control agenda.
Last November, the "dietary supplements sector working group" of the Transatlantic Business Dialogue (TABD) agreed on  several Codex-like elements involving the "harmonization" of a regulatory framework for vitamin/mineral food supplements on both sides of the Atlantic. TABD has described itself as "a results-oriented forum that seeks to increase trans-Atlantic trade and investment opportunities through the removal of costly inefficiencies from excessive regulation, duplication anddifferences in the EU and US regulatory systems and  procedures in a manner consistent with sustainable development. "Planned US participation in March at a conference of the International Alliance of Dietary/Food Supplement Associations (IADSA) in South Africa seemed to fly in the face of US governmental assertions that regulations approved by Codex will not supersede US laws and that concern over the same is a "non-issue." The South African conference topic was creation of  a "global regulatory model."
Codex Alimentarius, attached to the Food and Agricultural Organization (FAO) of the United Nations, ostensibly is a commission set up toestablish an international code of food standards through the UN and the World Health Organization (WHO). In fact, commission delegations largely reflect international drug and food-processing interests, though often interspersed with "citizen" groups which in turn are economically influenced by the same interests.
In prior Codex meetings, the German plan to advance total control over dietary supplements - leading to their removal as over-the-counter items and subject to stringent prescription regulation, as has happened in Germany itself and to a lesser extent in other countries - has been blocked by several delegations.
Should the German proposals ultimately be adopted by the Codex Committee on Nutrition and Foods for Special Dietary Uses (CCNFSDU) in Berlin in  November, the following draconian measures would be the "law" according to Codex:
- No dietary supplement could be sold for preventive or therapeutic use.
- No dietary supplement sold as a food could exceed potency levels set by
the commission.
- Codex regulations for dietary supplements would become binding.
- All new dietary supplements would automatically be banned unless they go
through the Codex approval process.
John Hammell, of International Advocates for Health Freedom (IAHF), has played a key international role in alerting the US, and the world, to Codex operations.
Not mincing words, Hammell said in an Internet posting in January that: ". . . The citizens of the EU (European Union) are being set up for genocide, and we don’t want it happening to us here (USA) via ‘harmonization’ of our laws to a rapidly emerging, grossly restrictive, Codex vitamin standard. 
"The EU Vitamin Directive is in the process of being shoved down the throats of people in Europe . . . This will cause all 15 EU nations towalk in lockstep with Germany and France. This is a full frontal assault on health freedoms worldwide by multinational pharmaceutical interests." 

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