ASPARTAME HAS BEEN RENAMED AND IS NOW BEING MARKETED AS A NATURAL SWEETENER

World Truth News

Artificial sweeteners especially aspartame has gotten a bad rap over the years, most likely due to studies showing they cause cancer. But not to worry Ajinomoto the company that makes

Aspartame has changed the name to AminoSweet. It has the same toxic ingredients but a nice new sounding name. And if you or your child happens to be allergic to Aspartame, well don’t take it personally it’s just business.

Despite the evidence gained over the years showing that aspartame is a dangerous toxin, it has remained on the global market . In continues to gain approval for use in new types of food despite evidence showing that it causes neurological brain damage, cancerous tumors, and endocrine disruption, among other things.

Most consumers are oblivious to the fact that Aspartame was invented as a drug but upon discovery of its’ sweet taste was magically transformed from a drug to a food additive. HFA wants to warn our readers to beware of a wolf dressed up in sheep’s clothing or in this case Aspartame dressed up as Aminosweet.

Over 25 years ago, aspartame was first introduced into the European food supply. Today, it is an everyday component of most diet beverages, sugar-free desserts, and chewing gums in countries worldwide. But the tides have been turning as the general public is waking up to the truth about artificial sweeteners like aspartame and the harm they cause to health. The latest aspartame marketing scheme is a desperate effort to indoctrinate the public into accepting the chemical sweetener as natural and safe, despite evidence to the contrary.

Aspartame was an accidental discovery by James Schlatter, a chemist who had been trying to produce an anti-ulcer pharmaceutical drug for G.D. Searle & Company back in 1965. Upon mixing aspartic acid and phenylalanine, two naturally-occurring amino acids, he discovered that the new compound had a sweet taste. The company merely changed its FDA approval application from drug to food additive and, voila, aspartame was born.

G.D. Searle & Company first patented aspartame in 1970. An internal memo released in the same year urged company executives to work on getting the FDA into the “habit of saying yes” and of encouraging a “subconscious spirit of participation” in getting the chemical approved.

G.D. Searle & Company submitted its first petition to the FDA in 1973 and fought for years to gain FDA approval, submitting its own safety studies that many believed were inadequate and deceptive. Despite numerous objections, including one from its own scientists, the company was able to convince the FDA to approve aspartame for commercial use in a few products in 1974, igniting a blaze of controversy.

300,000 Flu Vaccines Recalled Over Serious Adverse Reactions

Natural Society, Nov. 10, 2011

Baxter Healthcare Corp. has announced it is recalling around 300,000 doses of its Preflucel flu vaccine due to an ‘excessive’ amount of adverse reactions. Recalled from thousands of pharmacies and surgeries across Europe, the 300,000 units are to be immediately withdrawn. With seasonal flu vaccines already linked to nerve disease Guillain-Barre Syndrome and narcolepsy and still being given out liberally to citizens worldwide, the adverse reactions must be quite serious in order to prompt a recall.

Even more concerning is the fact that vaccine makers actually have been given legal immunity thanks to a law signed by Secretary of Health and Human Services Kathleen Sebelius.

Of course Baxter representatives are urging the public to stay calm, while also downplaying the risks associated with the shot. In the past NaturalSociety has revealed how Merck uses similar tactics to downplay the true side effects of the Gardasil vaccine, listing only minor side effects and ignoring the death link completely.

“The vaccine is being recalled because these side effects have been reported more frequently with this specific batch,” said a Baxter spokesmen. This spokesman also attempted to reassure the public that those who have already been vaccinated with Preflucel “should not be concerned (for their safety).”

Only time will tell what serious reactions are associated with this batch of Preflucel. In response to why the vaccine was recalled, Baxter states that “most of the side-effects are those usually associated with flu vaccines – they have started shortly after the vaccination and have been mild and short-lived.”

The problem with this statement is the fact that the seasonal flu shot has been repeatedly tied with serious adverse reactions. Therefore, it is not very reassuring that ‘most of the side-effects’ occur in the regular seasonal flu shot as well. Furthermore, it seems unlikely that Baxter would not recall flu vaccines, or at least investigate them further, after it was found that they are virtually ineffective and linked to nerve disease if they truly cared about your health. Therefore, it seems reasonable that despite the reassuring language of the Baxter spokesmen, this batch of Preflucel must be linked to something quite nasty.

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Related: Immune System Protects Against Flu, Not Vaccines