Since I cant create a new thread, I will add another article to this one.
Since I can even post the link I will just copy and paste the whole thing......
Boston Hearald 5-11-09
They look like cigarettes, but unlike the real thing these are battery-powered devices that deliver nicotine using a vapor. Electronic cigarettes - now available online and at mall kiosks - contain no
tobacco and produce no smoke. Thus, their risk is minimal compared to conventional cigarettes, which deliver not only nicotine but also more than 4,000 chemical toxins and more than 60 carcinogens.
As an additional benefit, e-cigarettes produce no secondhand smoke. Many smokers are using e-cigarettes to stay off conventional cigarettes. And because they look like cigarettes and simulate the act of smoking, they are proving to be far more effective in keeping smokers off cigarettes than nicotine replacement therapy.
Sounds like a public health win-win proposition, no?
Not so, based on the actions of some lawmakers and health groups. Rather than embrace e-cigarettes as a potentially life-saving alternative for many smokers, Sen. Frank Lautenberg (D-N.J.) and a number of health groups - including the Campaign for
tobacco-Free Kids, American Lung Association, American Heart Association and the American Cancer Society - have called on the Food and Drug Administration to remove them from the market.
Lautenberg urges the FDA to ban the sale of e-cigarettes because they have not yet been proven safe.
At the same time that Lautenberg and the health groups are trying to keep e-cigarettes off the market, they are promoting legislation that would force the FDA to approve conventional cigarettes - which have been proven to be extremely hazardous - for sale and marketing in the United States. Proposed legislation would institutionalize all cigarettes now on the market and make it nearly impossible for new products - which might be much safer - from entering the market.
What’s behind the FDA regulatory scheme? Philip Morris, to be exact. The nation’s largest cigarette company is pushing this legislation because it would protect the existing cigarette market from potential competition like the e-cigarettes that are becoming popular.
It is clear that the real purpose and effect of the FDA
tobacco legislation is to protect the conventional cigarette market from competition. And unfortunately, that competition - in the absence of FDA legislation - would come from truly reduced risk products, such as e-cigarettes. This is precisely why Philip Morris was brilliant in enticing the Campaign for Tobacco-Free Kids and other health groups into supporting FDA regulation of tobacco products.
Today, in extreme irony, these health groups stand as the most vigorous protectors of the current market of conventional cigarettes. As such, they stand as protectors, rather than opponents, of the death and disease caused by the nation’s most hazardous consumer product.
Michael Siegel is physician, a tobacco researcher and professor at Boston University’s School of Public Health.