Howdy Doc, nice to meet you.
I have Ulcerative Colitis held in check for the 35 years that I smoked and diagnosed after I quit. I bled while waiting for diagnosis at 0mg. My first diagnosis was Crohn's so I stayed off nicotine and bled while taking mesalamine. It wasn't until dx'ed with UC when I increased my nicotine (I quit at 11mg and had to work my way up to 18mg) along with the mesalamine that I stopped bleeding.
Ulcerative colitis in smokers, non-smokers and ex-smokers
(edit) Oops, gave you the wrong link, that one is interesting and includes this one but it's long, this is the one with the study I meant to give,
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2014383/ (/edit)
Vaping IS part of my medicine and while I can go without nicotine as far as addiction goes eventually it does cross into going without medicine and I have to pay for it. I suspect the last flare was because I wasn't vaping enough, about 2 months of minor pain, 2 months of great pain and now 3 months of really fun methods of taking mesalamine.
Is an imaginary threat of second hand vapor or a real annoyance of the smell more important than my real health issue?
Should I be forced to pay $40/wk for patches when I can pay $1/wk to vape because some health orgs have brainwashed people against anything that even looks like smoking?
I already don't go places because of the disease. Do I have to limit that even further because people don't approve of my treatment?
I agree it's the look, but it's also propaganda. I could use a nicotine inhaler, hold it just like a cigarette, pretend I'm blowing smoke and nobody would have a problem. I could use an asthma inhaler and blow out wisps of vapor and nobody would have a problem. But blow out vapor getting nicotine in something called an ecig and suddenly people have an issue.
About your strawberry steak and wine. Would you have enjoyed the scent if the table next to you was having strawberry cake?