...composing a response to Mr.Sielbeck's email. He'll never figure out that he didn't send the original message to me, as he has probably sent out hundreds. I have received word-for-word the same message from other ALA employess as well as the American Heart Assn.
Hi Mr. Sielback:
I'm writing to let you know that your scientific information on electronic cigarettes is outdated. There have been at least a dozen studies conducted on the chemical make-up of electronic cigarette liquid. CASAA.org
We should be able to rely on government agencies to provide us with factual scientific information. Unfortunately, the U.S. Food and Drug Administration (FDA) has fallen down on the job. It is unheard of for a toxicology report to leave out the quantitative data on potentially harmful substances discovered during testing -- but that's exactly what the FDA did.
The FDA press coference stirrred up a lot of excitement when they announced that they had found carcinogens in electronic cigarette cartridges. People would probably not have been so excited about it if the FDA had bothered to mention that the quantity matches the amount in the FDA approved nicotine patch. Obviously the FDA would not have approved the patch if 8 nanograms was considered dangerously carcinogenic, right? For verification of the quantity see the Health New Zealand report, especially the footnote under Table 2.2 on page 7. http://www.healthnz.co.nz/RuyanCartridgeReport30-Oct-08.pdf
You can also view a chart that compares the Tobaco-Specific Nitrosamine (TSNA) levels of electronic cigarettes to a variety of nicotine products and tobacco products, including popular brands of cigarettes. http://www.casaa.org/files/TSNA_Chart(1).pdf
The testing performed by Ben Thomas Group found that only one of the TSNAs identified by FDA actually makes it into the vapor phase of njoy, and that particular chemical is not considered a carcinogen.
To its credit, the FDA did specify an approximate quantity (1%) of the diethylene glycol (DEG) it claims to have found in one of the 18 cartridges tested. However, we know that "the dose makes the poison," and FDA failed to tell its audience whether or not the amount found is enough to be harmful. It turns out that 1% of the 1/2 ml. of liquid in a cartridge is approximately 5,000 times smaller than the toxic dose, which is calculated based on the person's weight in kg. The other thing that is very strange is that among all the tests that have been performed on many different brands of liquid, no other lab has found any DEG. Could it be that the FDA accidentally introduced some contamination?
The bottom line is that no tests on electronic cigarettes -- not even those conducted by FDA -- have identified any potentially harmful substances in large enough quantities to be carcinogenic or toxic.
So you see, continually quoting the FDA's study as "proof" that electronic cigarettes are dangerous makes it appear as if the American Lung Association doesn't know what it is talking about.
Furthermore, there are mixed messages coming from your organization If the ALA believes that Eissenberg's study proves that there is no nicotine coming out of an electronic cigarette, then what is the FDA's basis for banning the product as an unapproved drug-delivery device? An electronic cigarette cannot possbily be a drug-delivery device if it doesn't deliver a drug.
Perhaps this product is a wonderfully effective placebo. Thousands and thousands of people are reporting that they are finally able to achieve smoking abstinence by substituting the electronic cigarette for their tobacco cigarettes. If these people are no longer inhaling smoke, and they are managing to do that with a placebo, how can the ALA possibly justify trying to put a stop to it? I look forward to your answer.