That was exactly the reason I started this thread. What we need is for every one here to tell everyone else to get involved.
There's been some speculation that if we do that it may actually count against us. It's possible that the FDA will simply count the number of calls and report them all as adverse rather than actually counting the good reports separate from the bad.
The FDA is already against us. I think we all know that we're already screwed. The only hope we have of maintaining our rights is to raise our voices.
While looking around on that link, I found this FDA Seeks Your Input on Tobacco Regulation
Fda seeks your input on tobacco regulation. Toward the bottom you may click on comment on FDA's regulation to leave your own comment. You can also click on comments submitted by the public. There are some interesting comments there & yes some from smokers. Maybe we should all leave our letters & comments about how e-cigs have helped us.
Why would you say the FDA is against us?
Why would you say the FDA is against us? The FDA is against manufacturers like Smoking Everywhere who BLATANTLY advertise the PV as a drug device. They aren't against you, the user.
And in opposing them they're threatening to restrict or even ban e-cigarettes altogether, which would condemn a lot of people to an early grave. Some countries already have, you know.They're against these stupid companies who continue to make unfounded health claims.
Nonsense. Lots of companies have had their e-cigs and liquids tested to make sure they don't contain anything bad. I mean, they shouldn't have to; there is nothing new and unknown in e-cigarettes. PG is well-known to be safe. Nicotine is well-studied and not a controlled substance. All the flavourings used are approved by the FDA. Since no combustion occurs in an e-cigarette, the chemical makeup of the liquid doesn't change from its original components. So really there's no need. Yet lots of companies have independent tests done regardless, because they do care - if nothing else then independent testing is a selling point.Overall, in this whole thing, I think the FDA will try to work with the companies. HOWEVER, not ONE of the companies has invested ANY TIME OR RESOURCES towards scientific medical findings.
Pyrodoxamine is a drug developed, at great cost, by the pharmaceutical company Biostratum. It later turned out that it was really a common substance found in many existing foods. After this apparent screw-up, the FDA "naturally" ruled that only Biostratum may sell pyrodoxamine as a drug or dietary supplement, and nobody may mention the fact that foods like chicken breast contain it. Why? In the FDA's own words, it "would not be fair to the pharmaceutical company that brought, or intends to bring, the drug to the market" if farmers or brewers (ya it's in beer too) let their customers know of the newly discovered medicine in their products.Turn your anger towards the companies that didn't do their homework, not the enforcers who are required to keep you as safe as possible.
EDIT:
After numerous comments from others and a suggestion from smiley7 I retract my original suggestion of going to the MedWatch web page. Smiley7's suggestion of going to the FDA page FDA Seeks Your Input on Tobacco Regulationis a much better suggestion.
Bump
We need more people to send comments here. Yes a lot of their posts were just copy & paste (same comments)lol. Lets outdo them with our original comments!