I emailed Dr Siegal for suggestions on what I could do to advance the fight for
ecig use. Basically, he thinks its a good idea to continue to contact he FDA and our reps with our personal stories disputing the fantsy land the FDA 'experts' seem to be living in.
FDA created an online form to get comments from people. However, note the following instruction from the FDA: "
Health care professionals and consumers may report serious adverse events (side effects) or product quality problems with the use of e-cigarettes to the FDA's MedWatch Adverse Event Reporting program..."
Someone on ECF in a different
thread wrote a warning that FDA is not seeking "good" comments and it is very possible that if people use that form to report positive results, FDA can simply just count them as "problems" and claim that they received large XYZ number of complaints from people.
This could seriously hurt us.
Actually the Electronic Cigarette Association should be asking FDA to remove the restriction of reporting only "adverse events".